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EP1389999A1 - Cosmetic composition comprising a dispersion of polymer particles and a dispersion of pigments - Google Patents

Cosmetic composition comprising a dispersion of polymer particles and a dispersion of pigments

Info

Publication number
EP1389999A1
EP1389999A1 EP01985790A EP01985790A EP1389999A1 EP 1389999 A1 EP1389999 A1 EP 1389999A1 EP 01985790 A EP01985790 A EP 01985790A EP 01985790 A EP01985790 A EP 01985790A EP 1389999 A1 EP1389999 A1 EP 1389999A1
Authority
EP
European Patent Office
Prior art keywords
composition
polymer
composition according
dispersion
particles
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP01985790A
Other languages
German (de)
French (fr)
Inventor
Veronique Ferarri
Rolf Klucker
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LOreal SA
Original Assignee
LOreal SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from FR0014790A external-priority patent/FR2816500B1/en
Application filed by LOreal SA filed Critical LOreal SA
Publication of EP1389999A1 publication Critical patent/EP1389999A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241Containing particulates characterized by their shape and/or structure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8105Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • A61K8/8111Homopolymers or copolymers of aliphatic olefines, e.g. polyethylene, polyisobutene; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/87Polyurethanes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/90Block copolymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • A61Q1/04Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06Lipsticks
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/42Colour properties
    • A61K2800/43Pigments; Dyes

Definitions

  • Cosmetic composition comprising a dispersion of polymer particles and a dispersion of pigments
  • the present invention relates to a composition containing a polymer dispersible in an oily phase, intended in particular for the cosmetic field. More specifically, the invention relates to a composition for caring for and / or making up and / or treating keratin materials such as the skin of the face as well as of the human body, including the scalp, the integuments such as the eyelashes, eyebrows, nails and hair but also lips, lower or upper eyelids of humans.
  • This composition leads in particular to a shiny, homogeneous and non-sticky deposit on the keratin materials and / or the lips.
  • compositions for making up or caring for the skin or the lips of human beings such as foundations or lipsticks generally contain fatty phases such as waxes and oils, pigments and / or fillers and optionally additives such as cosmetic or dermatological active ingredients. They can also contain so-called "pasty" products, of flexible consistency, making it possible to obtain pastes, colored or not, to be applied with a brush.
  • compositions tend to migrate, that is to say to propagate over time inside the wrinkles and fine lines of the skin which surround in particular the lips and the eyes, causing an unsightly effect.
  • This migration is often cited by women as a major defect in conventional lipsticks.
  • migration is meant an overflow of the composition and in particular of the color, outside the initial trace of the makeup.
  • it exhibits poor resistance over time and in particular to color.
  • This poor behavior is characterized by a change in color (toning, paling) generally as a result of an interaction with the sebum and sweat secreted by the skin in the case of foundation and make-up or of an interaction with saliva. in the case of lipsticks.
  • This poor behavior requires the user to make-up very often, which can be a waste of time.
  • compositions containing a siloxysilicate resin (with three-dimensional network), a volatile silicone oil with a cyclic silicone chain and powdery charges Although having improved hold properties have the disadvantage of leaving on the lips, after evaporation of the silicone oils, a film which becomes uncomfortable over time (feeling of drying and tightness), eliminating a certain number of women of this type of lipstick.
  • compositions based on silicone oils and silicone resins lead to matt colored films.
  • women are now looking for products, in particular lip gloss, that are shiny.
  • composition is in solid form because it then has an inhomogeneous appearance in terms of color. In particular, white streaks are observed.
  • composition is a makeup product. Indeed, the makeup obtained is inhomogeneous and unsightly, accentuating the defects of the support and in particular of the skin, which is quite the opposite of what consumers are looking for.
  • the subject of the invention is precisely a composition for caring for and / or making up and / or treating keratin materials such as the skin and / or integuments but also the lips and the face, making it possible to remedy the various drawbacks mentioned above.
  • the composition of the invention makes it possible to obtain a non-sticky deposit, of good coverage having a more or less shiny appearance, adapted to the desire of the consumer, not migrating and of good behavior, not drying out the skin or lips to which it is applied, both during application and over time. It also has good stability properties and, when it is in the form of a stick, a limitation in color heterogeneity. It thus allows a homogeneous and aesthetic makeup.
  • the invention applies not only to lip makeup products but also to lip care and / or treatment products such as balms, skin, including the scalp, such as daily care and protection creams.
  • lip care and / or treatment products such as balms, skin, including the scalp, such as daily care and protection creams.
  • of the facial skin to make-up products for the skin, both of the face and of the human body, such as foundations, in particular cast in stick or in a cup, concealer products and ephemeral tattoo products, body hygiene products such as deodorants, in particular sticks, and eye makeup products, such as eyeliners, in particular in the form of a pencil, and mascaras, in particular in the form of bread.
  • the applicant has " found, quite surprisingly, that the use of a polymer dispersible in an oily phase, associated with a colloidal dispersion of particularly colored solid particles, in a composition in particular cosmetic, made it possible to obtain a glossy film, very good hold, of uniform color, non-migrating, water-resistant, while being very pleasant to apply and to wear throughout the day.
  • the film is in particular flexible, flexible and
  • the present invention therefore relates to a composition for application to keratin materials, comprising a physiologically acceptable medium containing at least one liquid fatty phase, a colloidal dispersion of particles solid at room temperature and a dispersion of polymer particles stabilized on the surface. in said liquid fatty phase by a stabilizer.
  • liquid fatty phase in the sense of the request, is meant any non-aqueous medium liquid at room temperature (25 ° C) and atmospheric pressure (760 mm Hg), corn- applied with one or more fatty substances liquid at room temperature, also called oils.
  • This fatty phase is macroscopically homogeneous (that is to say homogeneous when naked).
  • This fatty phase may contain a volatile liquid fatty phase and / or a non-volatile fatty phase.
  • non-volatile fatty phase any medium capable of remaining on the skin or the lips for several hours.
  • a nonvolatile fatty phase has in particular a vapor pressure at ambient temperature and atmospheric pressure, non-zero less than 0.02 mm Hg and better still less than 10 "3 mm Hg.
  • volatile fatty phase any non-aqueous medium capable of evaporating from the skin or the lips, in less than an hour at room temperature and atmospheric pressure.
  • This volatile phase notably comprises oils having a vapor pressure, at ambient temperature (25 ° C) and atmospheric pressure (760mm Hg) ranging from 10 '3 to 300 mm Hg (0.3 Pa to 40,000 Pa), particular ranging from 0.02 to 300 mm Hg (2.66 Pa to 40,000 Pa).
  • This composition is in particular a cosmetic, dermatological, hygienic or pharmaceutical composition. It therefore contains ingredients compatible with the skin, lips and integuments such as keratin fibers. It can be in the form of an anhydrous gel, an oil-in-water or water-in-oil emulsion or dispersion or also in the form of a multiple emulsion. It can be in the form of a paste, a more or less rigid solid, cream, ointment. Preferably, it is in anhydrous form, and more especially in the form of an anhydrous gel, in particular poured in a stick or in a dish.
  • this composition is stable over time and at temperature.
  • no segregation of the dispersed solid particles nor any phase shift is observed, even after 2 months at ambient temperature and atmospheric pressure and at 45 ° C.
  • its appearance to the naked eye is homogeneous and free from white streaks.
  • the polymer is a solid insoluble in (a fatty phase even at its softening temperature, unlike a wax even of polymeric origin which is soluble in the fatty phase at its melting temperature. furthermore, allows the formation of a deposit which is in particular continuous and homogeneous film-forming and / or is characterized by the entanglement of the polymer chains.With the same wax obtained by polymerization, recrystallization is obtained after melting in the fatty phase. This recrystallization is in particular responsible for the loss of the gloss of the composition.
  • the polymer in dispersion used in the present invention can be of any kind. It is thus possible to use a radical polymer, a polycondensate, or even a polymer of natural origin and their mixtures. This polymer can be chosen by a person skilled in the art according to its properties and according to the subsequent application desired for the composition.
  • the polymer used is film-forming, that is to say capable of forming, alone or in combination with a plasticizing agent, an isolable film. It is however possible to use a non-film-forming polymer.
  • non-film-forming polymer means a polymer which is not capable of forming, on its own, an isolable film.
  • This polymer makes it possible, in association with a non-volatile compound of the oil type, to form a continuous and homogeneous deposit on the skin and / or the lips.
  • the composition contains at least one ingredient chosen from cosmetic, dermatological, hygienic and pharmaceutical active ingredients, coloring matters and their mixtures. Thanks to the dispersion of polymer particles stabilized on the surface present in the liquid fatty phase, the composition of the invention makes it possible to maintain these active agents and / or coloring matters where they have been deposited.
  • the quantity of polymer in dispersion must be sufficient to form on the skin and / or the lips and / or the keratin fibers a film capable of trapping the coloring matters and or the cosmetic or dermatological active agents and / or the oils. with a view to limiting their migration and increasing the hold of the composition.
  • the amount of polymer is a function of the amount of coloring matter and / or active ingredients and / or oils, contained in the composition. In practice, the amount of polymer can be greater than 2% by weight (in active material), relative to the total weight of the composition.
  • Another subject of the invention is the cosmetic use in a composition for application to the skin, the hares and the integuments and more particularly cosmetic, hygienic or the use for the manufacture of a dermatological or pharmaceutical composition for application to the skin, the lips and the integuments, of particles of at least one polymer dispersed in a liquid fatty phase and stabilized on the surface by a stabilizing agent and of a colloidal dispersion of solid particles at room temperature, in particular colored to limit the migration of the composition and / or increase its resistance over time and / or obtain a homogeneous make-up and / or maintain the gloss of said composition.
  • the subject of the invention is also a method of cosmetic care or of making up keratin materials and in particular of the lips, integuments or of the skin, consisting in applying to the lips, the integuments or the skin respectively, a cosmetic composition as defined above.
  • the subject of the invention is also a cosmetic method for limiting the migration of a makeup or care composition for the skin or the lips and / or increasing the resistance over time of this composition and / or its stability, containing a phase liquid fat and at least one ingredient chosen from coloring matters in the form of solid particles at room temperature, colored, consisting in introducing into the liquid fatty phase particles of polymer dispersible in the liquid fatty phase and surface stabilized by an agent stabilizing and introducing into said liquid fatty phase said colored particles in the form of a colloidal dispersion.
  • a subject of the invention is also a process for the manufacture of a stable composition for application to keratin materials, comprising introducing into a physiologically acceptable liquid medium a) a dispersion of polymer particles stabilized at the surface in a phase fatty liquid by a stabilizer, b) a colloidal dispersion of particles welded at room temperature, chosen from pigments, nacres and (es fillers and their mixtures and to mix said medium supplemented with said dispersions a) and b).
  • the dispersion of polymer particles stabilized on the surface by a stabilizer and the colloidal dispersion of solid particles are prepared separately and beforehand, before their introduction into the composition.
  • Another subject of the invention is the use of a colloidal dispersion of solid particles at room temperature, chosen from pigments, nacres, fillers and their mixtures in a composition for application to keratin materials, containing a dispersion of polymer particles stabilized on the surface in a liquid fatty phase with a stabilizer, to stabilize said composition and / or give it a homogeneous appearance.
  • An advantage of the use of a polymer particle dispersion in a compo- "sition of the invention is that these particles remain in the form of elementary particles, without forming agglomerates in the fatty phase.
  • Another advantage of the polymer dispersion is the possibility of obtaining very fluid compositions (of the order of 130 centipoises), even in the presence of a high level of polymer.
  • Yet another advantage of such a polymer dispersion is that it is possible to calibrate the size of the polymer particles at will, and to modulate their "polydispersity" in size during the synthesis. It is thus possible to obtain particles of very small size, which are invisible to the naked eye when they are in the composition and when they are applied to the skin or the lips.
  • composition according to the invention exhibits qualities of spreading and adhesion to the skin, the lips, the eyelashes or the mucous membranes, which are particularly advantageous, as well as a smooth and pleasant touch.
  • This composition also has the advantage of removing makeup easily, in particular with a conventional cleansing milk.
  • composition according to the invention therefore advantageously comprises one or more stable dispersions of particles of generally spherical polymers of one or more polymers, in a physiologically acceptable liquid fatty phase.
  • These dispersions are generally called NAD (Non-Aqueous Dispersion) of polymer by opposition to latexes which are aqueous dispersions of polymer.
  • These dispersions can in particular be in the form of nanoparticles of polymers in stable dispersion in said fatty phase.
  • the nanoparticles are preferably of a size between 5 and 600 nm. It is however possible to obtain polymer particle sizes of up to 1 ⁇ m.
  • Another advantage of the polymer dispersion of the composition of the invention is the possibility of varying the glass-transition temperature (Tg) of the polymer or of the polymer system (polymer more additive of the plasticizer type), and thus to pass d a hard polymer to a more or less soft polymer, making it possible to adjust the mechanical properties of the composition as a function of the intended application and in particular of the film deposited.
  • Tg glass-transition temperature
  • the dispersion polymers which can be used in the composition of the invention preferably have a molecular weight of the order of 2000 to 10 000 000 and a Tg of -100 ° C to 300 ° C and better still of -50 ° to 50 ° C , preferably from -10 ° C to 100 ° C.
  • a plasticizer can be associated with it so as to lower this temperature of the mixture used.
  • the plasticizer can be chosen from the plasticizers commonly used in the field of application and in particular from the compounds capable of being solvents for the polymer. It is possible to use film-forming polymers, preferably having a low Tg, less than or equal to the skin temperature and in particular less than or equal to 40 ° C. A dispersion is thus obtained which can film when applied to a support, which is not the case when dispersions of mineral pigments according to the prior art are used.
  • film-forming polymers mention may be made of radical, acrylic or vinyl homopolymers or copolymers, preferably having a Tg of less than or equal to 40 ° C and in particular ranging from - 10 ° to 30 ° C, used alone or as a mixture.
  • radical, vinyl or acrylic homopolymers or copolymers optionally crosslinked, preferably having a Tg greater than 40 ° C and in particular ranging from 45 ° to 150 ° C, used alone or as a mixture.
  • radical polymer is meant a polymer obtained by polymerization of unsaturated monomers, in particular ethylenic, each monomer being capable of homopolymerizing (unlike polycondensates).
  • the radical polymers can be in particular vinyl polymers or copolymers, in particular acrylic polymers.
  • the vinyl polymers can result from the polymerization of ethylenically unsaturated monomers having at least one acid group and / or esters of these acid monomers and / or amides of these acids.
  • monomer carrying an acid group ⁇ , ⁇ -ethylenic unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid can be used.
  • (meth) acrylic acid and crotonic acid are used, and more preferably (meth) acrylic acid.
  • esters of acidic monomers are advantageously chosen from esters of (meth) acrylic acid (also called (meth) acrylates), such as alkyl (meth) acrylates, in particular C 1 -C 20 alkyl, of preferably in Cj-Cg, aryl (meth) acrylates, in particular C 6 -C 10 aryl, hydroxyalkyl (meth) acrylates, in particular C 2 -C 6 hydroxyalkyl.
  • alkyl (meth) acrylates mention may be made of methyl, ethyl, butyl, isobutyl, 2-ethylhexyl and lauryie (meth) acrylate.
  • hydroxyalkyl (meth) acrylates mention may be made of hydroxyethyl (meth) acrylate and 2-hydroxypropyl (meth) acrylate.
  • aryl (meth) acrylates mention may be made of benzyl or phenyl acrylate.
  • esters of (meth) acrylic acid are alkyl (meth) acrylates.
  • radical polymer use is preferably made of copolymers of (meth) acrylic acid and of (meth) acrylate, in particular C 1 -C alkyl. More preferably, methyl acrylates may be used, optionally copolymerized with acrylic acid.
  • amides of the acid monomers mention may be made of (meth) acrylamides, and in particular N-alkyl (nneth) acrylamides, in particular of C 2 -C 12 alkyl such as N-ethyl acrylamide, Nt-butyl acrylamide , N-octyl acrylamide; N-dialkyl (CC 4 ) (meth) acrylamides.
  • the vinyl polymers can also result from the polymerization of ethylenically unsaturated monomers having at least one amino group, in free form or else partially or totally neutralized, or even partially or totally quaternized.
  • Such monomers can be, for example, dimethylaminoethyl (meth) acrylate, dimethylaminoethyl ethacrylamide, vinylamine, vinylpyridine, d.allyldimethylammonium chloride.
  • the vinyl polymers can also result from the homopolymerization or from the copolyerization of at least one monomer chosen from vinyl esters and styrene monomers.
  • these monomers can be polymerized with acidic monomers and / or their esters and / or their amides, such as those mentioned above.
  • vinyl esters include vinyl acetate, vinyl propionate, vinyl neodecanoate, vinyl pivalate, vinyl benzoate and vinyl t-butyl benzoate.
  • styrene monomers mention may be made of styrene and aipha-methyl styrene.
  • - olefins such as ethylene, propylene, butylene, isoprene, butadiene.
  • the vinyl polymer can be crosslinked using one or more difunctional monomers, in particular comprising at least two ethylenic unsaturations, such as ethylene glycol dimethacrylate or diallyl phthalate.
  • the dispersion polymers of the invention can be chosen from the following polymers or copolymers: polyurethanes, polyurethanes-acrylics, polyureas, polyurea-polyurethanes, polyester-polyurethanes, polyether-polyurethanes, polyesters, polyester amides, polyesters fatty chain, alkyds; acrylic and / or vinyl polymers or copolymers; acrylic-silicone copolymers; polyacrylamides; silicone polymers such as polyurethanes or silicone acrylics, fluoropolymers and mixtures thereof.
  • the polymer (s) in oily dispersion can represent (in dry matter or active material) from 0.1 to 60% of the weight of the composition, preferably from 2 to 40% and better still from 4 to 25%.
  • the amount of dry matter in the dispersion represents the total amount of polymer + stabilizer.
  • the liquid fatty phase of the composition can consist of any cosmetically or dermatologically acceptable oil, and generally physiologically acceptable oil, in particular chosen from oils of mineral, animal, vegetable or synthetic origin, carbonaceous, hydrocarbonaceous, fluorinated and / or silicone-based, alone or as a mixture insofar as they form a homogeneous and macroscopically stable mixture and where they are compatible with the intended use.
  • hydrocarbon-based oil is meant oils mainly containing carbon atoms and hydrogen atoms and in particular alkyl or alkenyl chains such as alkanes or alkenes but also oils with alkyl or alkenyl chains comprising one or more ether groups , ester or carboxylic acid.
  • the total liquid fatty phase of the composition may represent from 5% to 99.40% of the total weight of the composition and preferably from 20 to 85%. Advantageously, it represents at least 30% of the total weight of the composition. Preferably, this fatty phase contains at least one non-volatile oil (namely several non-volatile oils).
  • the non-volatile part can represent from 0 to 80% of the total weight of the composition and better still from 1 to 50%.
  • hydrocarbon oils of mineral or synthetic origin such as linear or branched hydrocarbons, volatile or not, such as paraffin oil or its derivatives, petrolatum oil, polydecenes, hydrogenated polyisobutene such as parlameam, squalane; oils of animal origin such as mink, turtle oil, perhydrosqualene; oils of vegetable origin; hydrocarbons with a high triglyceride content made up of fatty acid and glycerol esters, the fatty acids of which can have various chain lengths, the latter possibly being linear or branched, saturated or unsaturated, such as sweet almond oil, calophyllum, palm, grapeseed, sesame, arara, rapeseed, sunflower, cotton, apricot, castor, alfalfa, squash, blackcurrant, macadamia, rosebush muscat, hazelnut, avocado, jojoba, olive or germ of cereals (corn,
  • one or more volatile solvents can be used at room temperature such as volatile cosmetic oils. These volatile solvents are favorable for obtaining a deposit of good performance. After evaporation of these solvents, a flexible film-forming deposit is obtained, which does not stick to the skin or the lips. These volatile solvents also facilitate the application of the composition to the skin, the lips and the integuments. They can be hydrocarbon or silicone and optionally comprise alkyl or alkoxy groups, pendant or at the end of the silicone chain.
  • volatile oil which can be used in the invention, mention may be made of linear or cyclic silicone oils having a viscosity at room temperature of less than 8 cSt and having in particular from 2 to 7 silicon atoms, these silicones optionally comprising alkyl or alkoxy groups having from 1 to 10 carbon atoms.
  • volatile silicone oil which can be used in the invention, mention may in particular be made of octamethylcyclo-tetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, heptamethyl hexyltrisiloxane, heptamethyloctyl trisiloxane, hexamethyldisethyloxane tranethylamethane, octamethylane tetrasiloxane, dodecamethyl pentasiloxane and mixtures thereof.
  • volatile solvent used in the invention include volatile hydrocarbon oils having from 8 to 16 carbon atoms and their mixtures and in particular branched alkanes, C 8 -C 16 isoalkanes (also called isoparaffins) C 8 -C ⁇ 6 , isododecane, isodecane, isohexadecane and for example the oils sold under the trade names of isopars 'or Permyls', the branched esters of C 8 -C 18 such as neo isano pentanoate -hexyl and their mixtures.
  • volatile hydrocarbon oils having from 8 to 16 carbon atoms and their mixtures and in particular branched alkanes, C 8 -C 16 isoalkanes (also called isoparaffins) C 8 -C ⁇ 6 , isododecane, isodecane, isohexadecane and for example the oils sold under the trade names of isopars 'or Permyls'
  • liquid fatty phase is chosen from the group comprising:
  • oils of vegetable origin formed by fatty acid esters and polyols, especially triglycerides, such as sunflower oil, sesame oil or rapeseed *, or esters derived from acids or long-chain alcohols (ie having from 6 to 20 carbon carbon), including the esters of formula R 1 COOR 2 in which R represents the residue of a higher fatty acid containing from 7 to 40 carbon atoms and R 2 represents a hydrocarbon chain comprising from 3 to 40 carbon atoms, such as palmitates , adipates and benzoates, in particular diisopropyl adipate.
  • silicone oils such as polydimethylsiloxanes and polymethylphenylsiloxanes, optionally substituted by aliphatic and / or aromatic groups, optionally fluorinated, or by functional groups such as hydroxyl, thiol and / or amino groups, and volatile silicone oils, in particular cyclic oils.
  • solvents alone or as a mixture, chosen from (i) linear, branched or cyclic esters, having more than 6 carbon atoms, (ii) ethers having more than 6 carbon atoms, (iii) ketones having more than 6 carbon atoms.
  • monoalcohols having a global solubility parameter according to the HANSEN solubility space of less than or equal to 20 (MPa) 1 ′ 2 is meant aliphatic fatty alcohols having at least 6 carbon atoms, fa hydrocarbon chain not comprising a group of substitution.
  • oleic alcohol decanol, dodecanol, octadecanol and linoleic alcohol.
  • non-aqueous medium it is also possible to use those described in document FR-A-2 710 646 by LVMH
  • non-aqueous medium is made by a person skilled in the art depending on the nature of the monomers constituting the polymer and / or the nature of the stabilizer, as indicated below.
  • the polymer dispersion can be manufactured as described in document EP-A-749747.
  • the polymerization can be carried out in dispersion, that is to say by precipitation of the polymer during formation, with protection of the particles formed by stabilizer.
  • a mixture is therefore prepared comprising the initial monomers and a radical initiator.
  • This mixture is dissolved in a solvent called, in (following (a present description, "synthesis solvent”.
  • synthesis solvent a solvent that is a non-volatile oil
  • the polymerization can be carried out in an apolar organic solvent (synthesis solvent) then add the non-volatile oil (which must be miscible with said synthesis solvent) and selectively distil the synthesis solvent.
  • a synthetic solvent such as the initial monomers and the radical initiator are therefore chosen to be soluble therein, and the polymer particles obtained therein are insoluble so that they precipitate thereon during their formation.
  • the synthesis solvent can be chosen from alkanes such as heptane, isododecane or cyclohexane.
  • the polymerization can be carried out directly in said oil which therefore also plays the role of synthetic solvent.
  • the monomers must also be soluble therein, as well as the radical initiator, and the polymer obtained must be insoluble therein.
  • the monomers are preferably present in the synthesis solvent, before polymerization, in an amount of 5-20% by weight of the reaction mixture). All of the monomers may be present in the solvent before the start of the reaction, or a portion of the monomers may be added as the polymerization reaction proceeds.
  • the radical initiator can in particular be azo-bis-isobutyronitrile or tert-butylpyroxy-2-ethyl hexanoate.
  • the polymer particles are surface stabilized, as the polymerization progresses, thanks to a stabilizer which can be a block polymer, a graft polymer, and / or a random polymer, alone or as a mixture.
  • Stabilization can be carried out by any known means, and in particular by direct addition of the block polymer, graft polymer and / or random polymer, during the polymerization.
  • the stabilizer is preferably also present in the mixture before polymerization. However, it is also possible to add it continuously, in particular when the monomers are also added continuously.
  • 2-30% by weight of stabilizer relative to the initial mixture of monomers can be used, and preferably 5-20% by weight.
  • the synthetic solvent is chosen in such a way that at least part of the grafts or blocks of said polymer stabilizer is soluble in said solvent, the other part of the grafts or sequences not being soluble therein.
  • the polymer stabilizer used during the polymerization must be soluble, or dispersible, in the synthetic solvent.
  • a stabilizer is preferably chosen whose insoluble blocks or grafts have a certain affinity for the polymer formed during the polymerization.
  • grafted polymers mention may be made of silicone polymers grafted with a hydrocarbon chain; hydrocarbon polymers grafted with a silicone chain. Also suitable are graft copolymers having, for example, an insoluble skeleton of polyacrylic type with soluble grafts of poly-12- (hydroxystearic) acid type.
  • graft or block block copolymers comprising at least one block of polyorganosiloxane type and at least one block of a radical polymer can be used, such as graft copolymers of acrylic / silicone type which can be used in particular when the non-aqueous medium is silicone.
  • graft or block copolymers comprising at least one block of the polyorganosiloxane type and at least one polyether.
  • the polyorganopoly-siioxane block can in particular be a polydimethylsiloxane or alternatively a poly (C 2 -C 18 ) alkyl methyl siloxane; the polyether block may be a poly alkylene C z -C a, in particular polyoxyethylene and / or polyoxypropylene.
  • copolyof dimethicones or of alkyl (C 2 ⁇ C 18 ) copolyol dimethicones such as those sold under the name “Dow Corning 3225C” by the company Dow Corning, lauryl methicones such as those sold under name “Dow Corning Q2-5200 by the company” Dow Corning ".
  • graft or block block copolymers mention may also be made of those comprising at least one block resulting from the polymerization of at least one ethylenic monomer, with one or more optionally conjugated ethylenic bonds, such as ethylene or dienes such as butadiene and isoprene, and at least one block of a vinyl and better styrenic polymer.
  • ethylenic monomer has more than one ethylenic bond that possibly combined, the residual ethylenic unsaturations after the polymerization are generally hydrogenated.
  • block copolymers in particular of the "diblock” or “triblock” type of the polystyrene / polyisoprene (SI), polystyrene / polybutadiene (SB) type such as those sold under the name of "LUVITOL HSB" by BASF, of the polystyrene copoly (ethylene-propylene) type (SEP) such as those sold under the name 'Kraton' by Shell Chemical Co or also of the polystyrene / copoly (ethylene-butylene) (SEB) type.
  • SI polystyrene / polyisoprene
  • SB polystyrene / polybutadiene
  • SEP polystyrene copoly (ethylene-propylene) type
  • SEB polystyrene / copoly (ethylene-butylene)
  • Kraton G1650 SEBS
  • Kraton G1651 SEBS
  • Kraton G1652 SEBS
  • Kraton G1657X SEBS
  • Kraton G1701X SEP
  • Kraton G1702X SEP
  • Kraton G1726X SEB
  • Kraton CM 101 SBS
  • SBS Kraton D-1102
  • SBS Kraton D-107
  • Polymers are generally called copolymers of hydrogenated or non-hydrogenated dienes.
  • Gelled Permethyl 99A-750, 99A-753-59 and 99A-753-58 mixture of triblock and star polymer
  • Versagel 5960 from Penreco (triblock + star polymer)
  • OS129880, OS129881 and ⁇ S84383 from Lubrizol (styrene / methacrylate copolymer).
  • graft or block block copolymers comprising at least one block resulting from the polymerization of at least one ethylenic monomer with one or more ethylenic bonds and of at least one block of an acrylic polymer
  • graft or block block copolymers comprising at least one block resulting from the polymerization of at least one ethylenic monomer with one or more ethylenic bonds and of at least one block of a polyether such as a C 2 -C 18 polykylene (polyethylenated and / or polyoxypropylenated in particular), mention may be made of two or three-block polyoxyethylene / polybutadiene or polyoxyethylene / polyisobutylene copolymers.
  • a polyether such as a C 2 -C 18 polykylene
  • a random polymer When a random polymer is used as a stabilizer, it is chosen so that it has a sufficient quantity of groups making it soluble in the intended synthetic solvent.
  • copolymers based on alkyl acrylates or methacrylates derived from C 1 -C 4 alcohols and alkyl acrylates or methacrylates derived from C 8 -C 30 alcohols Mention may in particular be made of the stearyl methacrylate / methyl methacryate copolymer.
  • the synthetic solvent is apolar
  • the stabilizing agent is preferably chosen from the group consisting of grafted or block block copolymers comprising at least one block of polyorganosiloxane type and at least one block of a polymer radical or of a polyether or of a polyester such as polyoxypropylenated and / or oxyethylenated blods.
  • the stabilizing agent is preferably chosen from the group consisting of:
  • grafted or block copolymers comprising at least one block resulting from the polymerization of at least one ethylenic monomer, with conjugated ethylenic bonds, and at least one block of a vinyl or acrylic polymer or of a polyether or polyester, or mixtures thereof.
  • diblock polymers are used as the stabilizing agent.
  • the dispersions of gelled polymers obtained according to the invention can then be used in a composition, in particular cosmetic, dermatological, pharmaceutical and / or hygienic, such as a composition for caring for or making up the skin or the lips, or even a hair composition. or a sunscreen composition or artificial coloring or tanning of the skin.
  • a composition in particular cosmetic, dermatological, pharmaceutical and / or hygienic, such as a composition for caring for or making up the skin or the lips, or even a hair composition. or a sunscreen composition or artificial coloring or tanning of the skin.
  • composition according to the invention also contains particles solid at room temperature, dispersed in the physiologically acceptable medium introduced into the composition in the form of a colloidal dispersion, also called "particulate paste”.
  • colloidal dispersion or “particulate paste” is meant within the meaning of the invention a concentrated colloidal dispersion of particles coated or not in a continuous medium, surface stabilized using a dispersing agent.
  • particles can be chosen from pigments, nacres, solid fillers and their mixtures.
  • These particles can be of any shape, in particular of spherical or elongated shape like fibers. They are insoluble in the medium.
  • the dispersing agent serves to protect the dispersed particles against their agglomeration or flocculation.
  • concentration of dispersant generally used to stabilize a colloidal dispersion is 0.3 to 5 mg / m 2 , preferably 0.5 to 4 mg / m 2 , of surface area of particles.
  • This dispersing agent can be a surfactant, an oligomer, a polymer or a mixture of several of them, carrying one or more functionalities having a strong affinity for the surface of the particles to be dispersed. In particular, they can physically or chemically cling to the surface of the pigments.
  • These dispersants also have at least one functional group which is compatible or soluble in the continuous medium.
  • esters of 12-hydroxy stearic acid in particular and of acid are used.
  • polyol such as glycerol, diglycerin
  • poly (12-hydroxystearic) acid stearate with a molecular weight of approximately 750 g / mole such as that sold under the name of Solsperse 21,000 by the company Avecia
  • CTFA polygyceryl-2 dipolyhydroxystearate
  • the polydihydroxystearic acid and the esters of hydroxy12-stearic acid are preferably intended for a hydrocarbon or fluorinated medium, while the mixtures of dimethylsiloxane oxyethylene / oxypropyiene are preferably intended for a silicone medium.
  • the colloidal dispersion is a suspension of particles of generally micron size ( ⁇ 10 ⁇ m) in a continuous medium.
  • the volume fraction of particles in a concentrated dispersion is from 20% to 40%, preferably greater than 30%, which corresponds to a weight content of up to 70% depending on the density of the particles.
  • the particles dispersed in the medium can consist of mineral or organic particles or their mixtures such as those described below.
  • the continuous medium of the paste can be any and contain any solvent or liquid fatty substance and their mixtures.
  • the liquid medium of the particulate paste is one of the liquid fatty substances or oils which it is desired to use in the composition, thus forming part of the liquid fatty phase.
  • the "particulate paste" or colloidal dispersion is a "pigmentary paste” containing a colloidal dispersion of colored particles, coated or not, surface stabilized. These colored particles are pigments, nacres or a mixture of pigments and / or nacres.
  • the colloidal dispersion represents from 0.5 to 60% by weight of the composition and better still from 2 to 40% and even better still from 2 to 30%.
  • the pigments can be white or colored, mineral and / or organic, interference or not. Mention may be made, among the mineral pigments, of titanium dioxide, optionally surface-treated, zirconium or cerium oxides, as well as oxides of zinc, iron (black, yellow or red or chromium, manganese violet , ultramarine blue, chromium hydrate and ferric blue.
  • the organic pigments mention may be made of carbon black, pigments of the organic lacquer type of barium, strontium, calcium or aluminum, including those subject to certification by the Food and Drug Administration (FDA) (example D&C or FD&C) and those exempt from FDA certification such as cochineal carmine lacquers.
  • FDA Food and Drug Administration
  • Pigments can represent from 0.1 to 50% in active matter and in particular 0.5 at 35% and better still from 2 to 25% of the total weight of the composition.
  • the pearlescent pigments can be chosen from white pearlescent pigments such as mica coated with titanium, or bismuth oxychloride, colored pearlescent pigments such as titanium mica with iron oxides, titanium mica with in particular ferric blue or chromium oxide, titanium mica with an organic pigment of the aforementioned type as well as pearlescent pigments based on bismuth oxychloride. They can represent from 0 to 25% (in active material) of the total weight of the composition and better still from 0.1 to 15% (if present). Pigments with goniochromatic properties can thus be used.
  • the fillers can be mineral or organic, lamellar or spherical. Mention may be made of talc, mica, silica, kaolin, powders of Nylon® (Orgasol® from Atochem), of poly- ⁇ -alanine and of polyethylene, the powders of polymers of tetrafluoroethyiene (Teflon ®), lauroyl-lysine, starch, boron nitride, hollow microspheres such as Expancel® (Nobel industry), Polytrap® (Dow Corning) and silicone resin microbeads (Tospearls® from Toshiba , for example), precipitated calcium carbonate, magnesium carbonate and hydro-carbonate, hydroxyapatite, hollow silica microspheres (Silica Beads® from Maprecos), glass or ceramic microcapsules, metallic soaps derivatives of organic carboxylic acids having from 8 to 22 carbon atoms, preferably from 12 to 18 carbon atoms, for example zinc,
  • the fillers and the pearlescent pigments or not are non-polymeric.
  • the colloidal dispersion of the solid particles is prepared beforehand by mixing the solid particles, the dispersant and the continuous medium of the dispersion, with a view to obtaining adsorption of the stabilizer on the solid particles. This dispersion is then mixed with the other constituents of the composition. This step of prior preparation of the dispersion of solid particles is necessary to solve the problem of the stability of the composition.
  • the simple addition of a dispersant in the composition without its prior adsorption on the solid particles and in particular on the pigments, does not make it possible to solve the problem of destabilization of a composition containing a dispersion of polymer particles stabilized on the surface.
  • the composition of the invention may, inter alia, contain dyes soluble in the physiological medium and in particular liposoluble or water-soluble dyes.
  • the liposoluble dyes are for example Sudan red, D&C Red n ° 17, D&C Green n ° 6, ⁇ -carotene, (soybean oil, Sudan brown, D&C Yellow n ° 11, D&C Violet n ° 2, orange D&C n ° 5, quinoline yellow, bromoacids They can represent from 0 to 20% and in particular 0.01 to 20% of the weight of the composition and better still from 0.1 to 6% (if present).
  • the water-soluble dyes are for example beet juice, methylene blue and can represent up to 6% of the total weight of the composition.
  • the composition of the invention can, in addition, contain one or more cosmetic active agents or dermatological such as those conventionally used.
  • moisturizers As cosmetic, dermatological, hygienic or pharmaceutical active agents which can be used in the composition of the invention, mention may be made of moisturizers, vitamins, essential fatty acids, sphingolipids, sun filters. These assets are used in the usual amount for those skilled in the art and especially at concentrations of 0 to 20% and especially from 0.001 to 15% by total weight of a composition.
  • the polymer of the composition of the invention allows the formation of a film on the skin, the lips and / or the integuments, forming a network trapping the coloring matters (including the fillers) and / or the active agents.
  • the coloring matters including the fillers
  • composition according to the invention can, moreover, comprise, depending on the type of application envisaged, the constituents conventionally used in the fields under consideration, which are present in an amount appropriate to the desired dosage form.
  • the liquid fatty phase in which the polymer particles are stabilized can comprise, in addition, the liquid fatty phase in which the polymer particles are stabilized, additional fatty phases which can be chosen from waxes, oils, gums and / or pasty fatty, hydrocarbon-based, silicone and / or fluorinated, of vegetable, animal, mineral or synthetic origin and their mixtures.
  • waxes solid at room temperature which may be present in the composition according to the invention, mention may be made of hydrocarbon waxes such as beeswax, Carnauba, Candellila, Ouricoury, Japanese wax, cork or sugar cane fiber waxes, paraffin waxes, lignite waxes, microcrystalline waxes, lanolin wax, Montan wax, ozokerites, polyethylene waxes, waxes obtained by Fischer synthesis Tropsch, hydrogenated oils, fatty esters and concrete glycerides at 25 ° C. It is also possible to use silicone waxes, among which mention may be made of alkyl, alkoxy and / or polymethylsiloxane esters.
  • hydrocarbon waxes such as beeswax, Carnauba, Candellila, Ouricoury, Japanese wax, cork or sugar cane fiber waxes, paraffin waxes, lignite waxes, microcrystalline waxes, lanolin wax, Montan wax, ozokerites, poly
  • the waxes can be in the form of stable dispersions of colloidal particles of wax as they can be prepared according to known methods, such as those of "Microemulsions Theory and Practice", LM Prince Ed., Académie Press (1977), pages 21-32.
  • the waxes used have a melting temperature at least equal to 45 ° C.
  • the waxes can be present in an amount of 0-50% by weight in the composition and better still from 5 to 25%, in order not to decrease too much the gloss of the composition and of the film deposited on the lips and / or the skin.
  • composition can also comprise any other additive usually used in such compositions, such as water, oil or aqueous thickeners, antioxidants, perfumes, preservatives, surfactants, oils essential, liposoluble polymers (PolyVinyIPyrrolidone / eicosene copolymer).
  • additives such as water, oil or aqueous thickeners, antioxidants, perfumes, preservatives, surfactants, oils essential, liposoluble polymers (PolyVinyIPyrrolidone / eicosene copolymer).
  • compositions according to the invention can be prepared in the usual manner by a person skilled in the art. They can be in the form of a cast product and for example in the form of a stick or stick, or in the form of a dish usable by direct contact or with a sponge. In particular, they find application as a poured foundation, blush or eyeshadow, lipstick, base or lip care balm, concealer product. They can also be in the form of a flexible paste or else a gel, a more or less fluid cream. They can then constitute foundations or lipsticks, sunscreen or skin coloring products.
  • compositions of the invention are advantageously anhydrous and can contain less than 5% of water relative to the total weight of the composition. They can then be in particular in the form of an oily gel, an oily liquid or oil, a paste or a stick or also in the form of a vesicular dispersion containing ionic and / or nonionic lipids. They can also be in the form of a single or multiple emulsion with an oily or aqueous continuous phase, an oily dispersion in a phase aqueous thanks to vesicles containing ionic and / or nonionic lipids. These dosage forms are prepared according to the usual methods of the fields considered.
  • compositions for topical application may especially constitute a cosmetic, dermatological, hygienic or pharmaceutical composition for protection, treatment or care for the face, for the neck, for the hands or for the body (for example care cream, sun oil, body gel), a makeup composition (for example makeup gel, cream, stick) or an artificial tanning or skin protection composition.
  • a cosmetic, dermatological, hygienic or pharmaceutical composition for protection, treatment or care for the face, for the neck, for the hands or for the body for example care cream, sun oil, body gel
  • a makeup composition for example makeup gel, cream, stick
  • an artificial tanning or skin protection composition for topical application.
  • composition according to the invention may be in the form of a dermatological composition or for caring for the skin and / or integuments or in the form of a composition for sun protection, for personal hygiene, in particular in the form of a deodorant. It is then presented in particular in non-colored form. It can then be used as a care base for the skin, the integuments or the lips (lip balms, protecting the lips from the cold and / or the sun and / or the wind, care cream for the skin, the nails or the hair. ).
  • composition of the invention may also be in the form of a colored product in particular for making up the skin, optionally having care or treatment properties, and in particular a foundation, a blush, a blush or eyeshadow, concealer, eyeliner, body makeup; lip makeup such as a lipstick, a lip gloss or a lip pencil possibly having care or treatment properties; make-up of headlights such as nails, eyelashes in the form of mascara, eyebrows and hair.
  • composition of the invention must be cosmetically or dermatologically acceptable, ie contain a physiologically acceptable medium which is non-toxic and capable of being applied to the skin, the integuments or the lips of the face of human beings.
  • cosmetically acceptable is meant within the meaning of the invention a composition of pleasant appearance, odor and feel.
  • the invention is illustrated in more detail in the following examples.
  • the percentages are percentages by weight.
  • a dispersion of polymethyl methacrylate crosslinked with ethylene glycol dimethacrylate is prepared in hydrogenated polyisobutene (containing 6-8 moles of isobutylene) sold under the name Parieam by the company Nippon Oil Fat, according to the method of the example. 2 of document EP-A-749 746, by replacing Isopar L with the Parieam.
  • a dispersion of polymethyl methacrylate particles stabilized on the surface in Parieam is thus obtained by a polystyrene / copoly (ethylene-propylene) block copolymer sold under the name Kraton G1701 (Shell), having a dry matter content of 22- 25% by weight and a Tg of 100 ° C. This copolymer is not film-forming at room temperature.
  • a dispersion of uncrosslinked copolymer of methyl acrylate and acrylic acid in an 85/15 ratio is prepared in Parieam, according to the method of example 1 of document EP-A-749 746, replacing the heptane by the Parieam.
  • This copolymer is film-forming.
  • This dispersion is prepared beforehand before it is mixed with the other constituents of the composition according to the invention.
  • phase A In a pan, all the components of phase A are introduced (which are heated to 100 ° C. with magnetic stirring in order to obtain a homogeneous mixture.
  • Phase B is then ground in a three-cylinder mill. This grinding is then added to phase A.
  • the mixture is left under stirring for 1 hour and then poured into suitable lipstick molds.
  • the mixture is left under stirring for 1 hour and then poured into suitable lipstick molds. freezer at -18 ° C for 30 minutes to obtain a lipstick stick.
  • phase B grinding of pigment in the three-cylinder
  • this formula looks like an inhomogeneous stick on the surface: presence of mottling on the stick.
  • Phase B corresponding to the pigment paste, mixed with lanolin is then added.
  • the pigment paste contains 8.66% of pigments, 0.58% of poly (12-hydroxystearic) acid stearate and 8.48% of Parieam .
  • the color change is less pronounced than in the mixture of the counterexample.
  • the mixture is left under stirring for one hour and then poured into suitable lipstick molds. The molds are then placed in the freezer at -18 ° C for 30 minutes.
  • the lipstick stick obtained has no mottling and is uniform in color.
  • phase A All the components of phase A are introduced into a pan, which is heated to 100 ° C. with magnetic stirring in order to obtain a homogeneous mixture.
  • Phase B corresponding to the pigment paste, Parieam mixed, is then added.
  • the pigment paste contains 8.66% of pigments, 0.58% of poly (12-hydroxystearic acid) stearate and 8.48% of Parieam.
  • the stick obtained has no mottling and is uniform in color. Its application is easy: the deposit obtained is comfortable, homogeneous, shiny, non-migrating and of good performance, especially in color.

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Abstract

The invention concerns a composition in particular cosmetic for care or make-up of the skin and/or skin appendages and/or lips, capable of being in the form of a cast product comprising in a physiologically acceptable medium containing at least a fatty liquid, a colloidal dispersion of solid particles at room temperature in particular coloured and a dispersion of polymer particles surface-stabilised in said fatty liquid phase by a stabilising agent. The invention is characterised in that, depending on the amount of polymer, it enables to obtain on the skin or skin appendages or the lips a brilliant soft film coat, while providing great comfort. The invention also concerns a method for care or make-up of the skin, skin appendages and the lips using said composition.

Description

Composition cosmétique comprenant une dispersion de particules de polymère et une dispersion de pigments Cosmetic composition comprising a dispersion of polymer particles and a dispersion of pigments
La présente invention a trait à une composition contenant un polymère dispersible dans une phase grasse, destinée en particulier au domaine cosmétique. Plus spécialement, l'invention se rapporte à une composition de soin et/ou de maquillage et/ou de traitement des matières kératiniques comme la peau aussi bien du visage que du corps humain, y compris du cuir chevelu, les phanères comme les cils, les sourcils, les ongles et les cheveux mais aussi des lèvres, des paupières inférieures ou supérieures des êtres humains. Cette composition conduit en particulier à un dépôt brillant, couvrant homogène et non collant sur les matières kératiniques et/ou les lèvres.The present invention relates to a composition containing a polymer dispersible in an oily phase, intended in particular for the cosmetic field. More specifically, the invention relates to a composition for caring for and / or making up and / or treating keratin materials such as the skin of the face as well as of the human body, including the scalp, the integuments such as the eyelashes, eyebrows, nails and hair but also lips, lower or upper eyelids of humans. This composition leads in particular to a shiny, homogeneous and non-sticky deposit on the keratin materials and / or the lips.
Cette composition peut se présenter notamment sous forme de produit coulé en stick ou en coupelle comme les rouges ou baumes à lèvres, les fonds de teint coulés, les produits anti-cernes, les fards à paupières ou à joues, sous forme de pâte ou de crème plus ou moins fluide comme les fonds de teint ou rouges à lèvres fluides, les eyes liners, les mascaras, les compositions de protection solaire ou de coloration de la peau ou encore de maquillage du corps. Les compositions de maquillage ou de soin de la peau ou des lèvres des êtres humains comme les fonds de teint ou les rouges à lèvres contiennent généralement des phases grasses telles que des cires et des huiles, des pigments et/ou charges et éventuellement des additifs comme des actifs cosmétiques ou dermatologiques. Elles peuvent aussi contenir des produits dits "pâteux", de consistance souple, permettant d'obtenir des pâ- tes, colorées ou non, à appliquer au pinceau.This composition can be presented in particular in the form of a product cast in a stick or in a cup such as lipsticks or lip balms, cast foundations, concealer products, eyeshadows or blushes, in the form of paste or more or less fluid cream such as foundations or fluid lipsticks, eye liners, mascaras, sun protection or skin coloring compositions or even body makeup. The compositions for making up or caring for the skin or the lips of human beings such as foundations or lipsticks generally contain fatty phases such as waxes and oils, pigments and / or fillers and optionally additives such as cosmetic or dermatological active ingredients. They can also contain so-called "pasty" products, of flexible consistency, making it possible to obtain pastes, colored or not, to be applied with a brush.
Ces compositions ont tendance à migrer, c'est-à-dire à se propager au cours du temps à l'intérieur des rides et des ridules de la peau qui entourent notamment les lèvres et les yeux, entraînant un effet inesthétique. Cette migration est souvent citée par les femmes comme un défaut majeur des rouges à lèvres classiques. Par "migration", on entend un débordement de la composition et en particulier de la couleur, hors du tracé initial du maquillage. En outre, elle présente une mauvaise tenue dans le temps et en particulier de la couleur. Cette mauvaise tenue se caractérise par une modification de la couleur (virage, palissement) généralement par suite d'une interaction avec le sébum et la sueur sécrétés par la peau dans le cas de fond de teint et fard ou d'une interaction avec la salive dans le cas des rouges à lèvres. Cette mauvaise tenue oblige l'utilisateur à se remaquiller très souvent, ce qui peut constituer une perte de temps.These compositions tend to migrate, that is to say to propagate over time inside the wrinkles and fine lines of the skin which surround in particular the lips and the eyes, causing an unsightly effect. This migration is often cited by women as a major defect in conventional lipsticks. By "migration" is meant an overflow of the composition and in particular of the color, outside the initial trace of the makeup. In addition, it exhibits poor resistance over time and in particular to color. This poor behavior is characterized by a change in color (toning, paling) generally as a result of an interaction with the sebum and sweat secreted by the skin in the case of foundation and make-up or of an interaction with saliva. in the case of lipsticks. This poor behavior requires the user to make-up very often, which can be a waste of time.
Pour augmenter la tenue dans le temps, la société Shiseido a envisagé, dans la demande JP-A-61-65809, des compositions de rouge à lèvres contenant une résiné siloxysilicate (à réseau tridimensionnel), une huile de silicone volatile à chaîne silicone cyclique et des charges pulvérulentes. Ces compositions, bien que présentant des propriétés de tenue améliorées ont l'inconvénient de laisser sur les lèvres, après évaporation des huiles de silicone, un film qui devient inconfortable au cours du temps (sensation de dessèchement et de tiraillement), écartant un certain nombre de femmes de ce type de rouge à lèvres.To increase the resistance over time, the Shiseido company considered, in application JP-A-61-65809, lipstick compositions containing a siloxysilicate resin (with three-dimensional network), a volatile silicone oil with a cyclic silicone chain and powdery charges. These compositions, although having improved hold properties have the disadvantage of leaving on the lips, after evaporation of the silicone oils, a film which becomes uncomfortable over time (feeling of drying and tightness), eliminating a certain number of women of this type of lipstick.
En outre, ces compositions à base d'huiles de silicones et de résines siliconées conduisent à des films colorés mats. Or, la femme est aujourd'hui à la recherche de produits notamment de coloration des lèvres, brillants.In addition, these compositions based on silicone oils and silicone resins lead to matt colored films. However, women are now looking for products, in particular lip gloss, that are shiny.
Pour remédier à ces inconvénients, le demandeur a envisagé la fabrication de compositions de maquillage contenant des particules de polymère dispersées et stabilisées en surface par un stabilisant dans une phase grasse liquide, telles que décrites dans le document EP-A-930060. Malheureusement, le demandeur s'est trouvé face à la difficulté d'introduire dans certaines phases grasses liquides comme les polyisosobutènes hydrogénés (Parleam) une grande quantité des particules solides notamment colorées insolubles dans le milieu de ces compositions, comme les pigments et les nacres. En effet, les inventeurs ont constaté qu'au-dessus de quelques pour-cent de particules solides, celles-ci floculaient et s'agrégeaient ou interagissaient avec le stabilisant des particules de polymère, déstabilisant ainsi rapidement les compositions lors de leur fabrication. Ceci est particulièrement gênant lorsque la composition est sous forme solide car elle présente alors un aspect inhomogène en terme de couleur. On observe notamment des traînées blanches. Ceci est particulièrement gênant lorsque la composition est un produit de maquillage. En effet, le maquillage obtenu est inhomogène et inesthétique, accentuant les défauts du support et notamment de la peau, ce qui est tout le contraire de ce que recherchent les consommateurs. L'invention a justement pour objet une composition de soin et/ou de maquillage et/ou de traitement des matières kératiniques comme la peau et/ou phanères mais aussi des lèvres, du visage permettant de remédier aux différents inconvénients mentionnés ci- dessus. En particulier, la composition de l'invention permet l'obtention d'un dépôt non collant, de bonne couvrance ayant un aspect plus ou moins brillant, adapté au désir de la consommatrice, ne migrant pas et de bonne tenue, ne desséchant pas la peau ou les lèvres sur lesquelles il est appliqué, aussi bien lors de l'application qu'au cours du temps. Elle présente, en outre de bonnes propriétés de stabilité et, lorsqu'elle est sous forme de stick, une limitation de l'hétérogénéité de couleur. Elle permet, ainsi, un maquillage homogène et esthétique.To remedy these drawbacks, the applicant has considered the manufacture of makeup compositions containing dispersed polymer particles and surface stabilized with a stabilizer in a liquid fatty phase, as described in document EP-A-930060. Unfortunately, the plaintiff was faced with the difficulty to introduce into certain fatty fatty phases such as hydrogenated polyisosobutenes (Parleam) a large amount of solid particles, in particular colored insoluble in the medium of these compositions, such as pigments and nacres. In fact, the inventors have found that above a few percent of solid particles, these flocculate and aggregate or interact with the stabilizer of the polymer particles, thus rapidly destabilizing the compositions during their manufacture. This is particularly troublesome when the composition is in solid form because it then has an inhomogeneous appearance in terms of color. In particular, white streaks are observed. This is particularly troublesome when the composition is a makeup product. Indeed, the makeup obtained is inhomogeneous and unsightly, accentuating the defects of the support and in particular of the skin, which is quite the opposite of what consumers are looking for. The subject of the invention is precisely a composition for caring for and / or making up and / or treating keratin materials such as the skin and / or integuments but also the lips and the face, making it possible to remedy the various drawbacks mentioned above. In particular, the composition of the invention makes it possible to obtain a non-sticky deposit, of good coverage having a more or less shiny appearance, adapted to the desire of the consumer, not migrating and of good behavior, not drying out the skin or lips to which it is applied, both during application and over time. It also has good stability properties and, when it is in the form of a stick, a limitation in color heterogeneity. It thus allows a homogeneous and aesthetic makeup.
L'invention s'applique non seulement aux produits de maquillage des lèvres mais aussi aux produits de soin et/ou de traitement des lèvres comme les baumes, de la peau, y compris du cuir chevelu, comme les crèmes de soin journalier et de protection solaire de la peau du visage, aux produits de maquillage de la peau, aussi bien du visage que du corps humain, comme les fonds de teints notamment coulés en stick ou en coupelle, les produits anti-cerne et les produits de tatouage éphémère, aux produits d'hygiène corporelle comme les déodorants notamment en stick, et aux produits de maquillage des yeux comme les eye-liners en particulier sous forme de crayon et les mascaras notamment sous forme de pain.The invention applies not only to lip makeup products but also to lip care and / or treatment products such as balms, skin, including the scalp, such as daily care and protection creams. of the facial skin, to make-up products for the skin, both of the face and of the human body, such as foundations, in particular cast in stick or in a cup, concealer products and ephemeral tattoo products, body hygiene products such as deodorants, in particular sticks, and eye makeup products, such as eyeliners, in particular in the form of a pencil, and mascaras, in particular in the form of bread.
Le demandeur a "constaté, de façon tout à fait surprenante, que l'utilisation d'un polymère dispersible dans une phase grasse, associé à une dispersion colloïdale de particules soli- des notamment colorées, dans une composition notamment cosmétique, permettait d'obtenir un film brillant, de très bonne tenue, de couleur homogène, ne migrant pas, résistant à l'eau, tout en étant très agréable à l'application et à porter tout au long de la journée. Le film est notamment souple, flexible et homogène. La présente invention a donc pour objet une composition à application sur les matières kératiniques, comprenant un milieu physiologiquement acceptable contenant au moins une phase grasse liquide, une dispersion colloïdale de particules solides à température ambiante et une dispersion de particules de polymère stabilisées en surface dans ladite phase grasse liquide par un stabilisant.The applicant has " found, quite surprisingly, that the use of a polymer dispersible in an oily phase, associated with a colloidal dispersion of particularly colored solid particles, in a composition in particular cosmetic, made it possible to obtain a glossy film, very good hold, of uniform color, non-migrating, water-resistant, while being very pleasant to apply and to wear throughout the day. The film is in particular flexible, flexible and The present invention therefore relates to a composition for application to keratin materials, comprising a physiologically acceptable medium containing at least one liquid fatty phase, a colloidal dispersion of particles solid at room temperature and a dispersion of polymer particles stabilized on the surface. in said liquid fatty phase by a stabilizer.
Par "phase grasse liquide", au sens de la demande, on entend tout milieux non aqueux liquide à température ambiante (25°C) et pression atmosphérique (760 mm de Hg), corn- posé d'un ou plusieurs corps gras liquides à température ambiante, appelés aussi huiles. Cette phase grasse est macroscopiquement homogène (à savoir homogène à fceii nu). Cette phase grasse peut contenir une phase grasse liquide volatile et/ou une phase grasse non volatiie.By "liquid fatty phase", in the sense of the request, is meant any non-aqueous medium liquid at room temperature (25 ° C) and atmospheric pressure (760 mm Hg), corn- applied with one or more fatty substances liquid at room temperature, also called oils. This fatty phase is macroscopically homogeneous (that is to say homogeneous when naked). This fatty phase may contain a volatile liquid fatty phase and / or a non-volatile fatty phase.
Par "phase grasse non volatile", on entend tout milieu susceptible de rester sur la peau ou les lèvres pendant plusieurs heures. Une phase grasse non volatile a en particulier une pression de vapeur à température ambiante et pression atmosphérique, non nulle inférieure à 0,02 mm de Hg et mieux inférieur à 10"3 mm de Hg.By "non-volatile fatty phase" is meant any medium capable of remaining on the skin or the lips for several hours. A nonvolatile fatty phase has in particular a vapor pressure at ambient temperature and atmospheric pressure, non-zero less than 0.02 mm Hg and better still less than 10 "3 mm Hg.
Par "phase grasse volatile", on entend tout milieu non aqueux susceptible de s'évaporer de la peau ou des lèvres, en moins d'une heure à température ambiante et pression atmosphérique. Cette phase volatile comporte notamment des huiles ayant une pression de vapeur, à température ambiante (25°C) et pression atmosphérique (760mm Hg) allant de 10'3 à 300 mm de Hg (0, 3 Pa à 40 000 Pa), en particulier allant de 0,02 à 300 mm de Hg (2,66 Pa à 40 000 Pa).By "volatile fatty phase" is meant any non-aqueous medium capable of evaporating from the skin or the lips, in less than an hour at room temperature and atmospheric pressure. This volatile phase notably comprises oils having a vapor pressure, at ambient temperature (25 ° C) and atmospheric pressure (760mm Hg) ranging from 10 '3 to 300 mm Hg (0.3 Pa to 40,000 Pa), particular ranging from 0.02 to 300 mm Hg (2.66 Pa to 40,000 Pa).
Cette composition est en particulier une composition cosmétique, dermatologique, hygiénique ou pharmaceutique. Elle contient donc des ingrédients compatibles avec la peau, les lèvres et les phanères comme les fibres kératiniques. Elle peut se présenter sous forme de gel anhydre, d'émulsion ou de dispersion huile-dans-eau ou eau-dans-huile ou encore sous forme d'émulsion multiple. Elle peut se présenter sous forme de pâte, de solide plus ou moins rigide, de crème, de pommade. De préférence, elle se présente sous forme anhydre, et plus spécialement sous forme de gel anhydre, notamment coulée en stick ou en coupelle.This composition is in particular a cosmetic, dermatological, hygienic or pharmaceutical composition. It therefore contains ingredients compatible with the skin, lips and integuments such as keratin fibers. It can be in the form of an anhydrous gel, an oil-in-water or water-in-oil emulsion or dispersion or also in the form of a multiple emulsion. It can be in the form of a paste, a more or less rigid solid, cream, ointment. Preferably, it is in anhydrous form, and more especially in the form of an anhydrous gel, in particular poured in a stick or in a dish.
Selon l'invention, cette composition est stable dans le temps et en température. En particulier, aucune ségrégation des particules solides dispersées ni aucun déphasage est constaté, même au bout de 2 mois à température ambiante et pression atmosphérique et à 45°C. En outre, lorsqu'elle est sous forme de stick, son aspect à l'œil nu est homogène et exempt de traînées blanches.According to the invention, this composition is stable over time and at temperature. In particular, no segregation of the dispersed solid particles nor any phase shift is observed, even after 2 months at ambient temperature and atmospheric pressure and at 45 ° C. In addition, when in stick form, its appearance to the naked eye is homogeneous and free from white streaks.
Selon l'invention le polymère est un solide insoluble dans (a phase grasse même à sa température de ramollissement, à l'inverse d'une cire même d'origine polymérique qui est elle soluble dans la phase grasse à sa température de fusion. Il permet, en outre, la formation d'un dépôt notamment filmogène continu et homogène et/ou est caractérisé par l'enchevêtrement des chaînes polymériques. Avec une- cire même obtenue par polymérisation on obtient, après fusion dans la phase grasse, une recristallisation. Cette recristallisation est en particulier responsable de la perte de la brillance de la composition.According to the invention, the polymer is a solid insoluble in (a fatty phase even at its softening temperature, unlike a wax even of polymeric origin which is soluble in the fatty phase at its melting temperature. furthermore, allows the formation of a deposit which is in particular continuous and homogeneous film-forming and / or is characterized by the entanglement of the polymer chains.With the same wax obtained by polymerization, recrystallization is obtained after melting in the fatty phase. This recrystallization is in particular responsible for the loss of the gloss of the composition.
Le polymère en dispersion utilisé dans la présente invention peut être de toute nature. On peut ainsi employer un polymère radicalaire, un polycondensat, voire un polymère d'origine naturelle et leurs mélanges. Ce polymère peut être choisi par l'homme du métier en fonction de ses propriétés et selon l'application ultérieure souhaitée pour la composition. De préférence le polymère utilisé est filmifiable, c'est-à-dire apte à former seul ou en association avec un agent plastifiant, un film isolable. Il est toutefois possible d'utiliser un polymère non filmifiable.The polymer in dispersion used in the present invention can be of any kind. It is thus possible to use a radical polymer, a polycondensate, or even a polymer of natural origin and their mixtures. This polymer can be chosen by a person skilled in the art according to its properties and according to the subsequent application desired for the composition. Preferably, the polymer used is film-forming, that is to say capable of forming, alone or in combination with a plasticizing agent, an isolable film. It is however possible to use a non-film-forming polymer.
Par polymère non filmifiable, on entend un polymère non capable de former, seul, un film isolable. Ce polymère permet, en association avec un composé non volatil du type huile, de former un dépôt continu et homogène sur la peau et/ou les lèvres. Avantageusement, la composition contient au moins un ingrédient choisi parmi les actifs cosmétiques, dermatologiques, hygiéniques et pharmaceutiques, les matières colorantes et leurs mélanges. Grâce à la dispersion de particules de polymère stabilisées en surface présente dans la phase grasse liquide, la composition de l'invention permet de maintenir ces actifs et/ou matières colorantes là où ils ont été déposés.The term “non-film-forming polymer” means a polymer which is not capable of forming, on its own, an isolable film. This polymer makes it possible, in association with a non-volatile compound of the oil type, to form a continuous and homogeneous deposit on the skin and / or the lips. Advantageously, the composition contains at least one ingredient chosen from cosmetic, dermatological, hygienic and pharmaceutical active ingredients, coloring matters and their mixtures. Thanks to the dispersion of polymer particles stabilized on the surface present in the liquid fatty phase, the composition of the invention makes it possible to maintain these active agents and / or coloring matters where they have been deposited.
Selon l'invention, la quantité de polymère en dispersion doit être suffisante pour former sur la peau et/ou les lèvres et/ou les fibres kératiniques un film apte à piéger les matières colorantes et ou les actifs cosmétiques ou dermatologiques et/ou les huiles en vue de li- miter leur migration et d'augmenter la tenue de la composition. La quantité de polymère est fonction de la quantité de matières colorantes et/ou d'actifs et/ou d'huiles, contenue dans la composition. En pratique, la quantité de polymère peut être supérieure à 2 % en poids (en matière active), par rapport au poids total de la composition. Un autre objet de l'invention est l'utilisation cosmétique dans une composition à application sur !a peau, les ièvres et les phanères et plus spécialement cosmétique, hygiénique ou l'utilisation pour la fabrication d'une composition dermatologique ou pharmaceutique à application sur la peau, les lèvres et les phanères, de particules d'au moins un polymère dispersées dans une phase grasse liquide et stabilisées en surface par un agent stabili- sant et d'une dispersion colloïdale de particules solides à température ambiante, notamment colorées pour limiter la migration de la composition et/ou augmenter sa tenue dans le temps et/ou obtenir un maquillage homogène et/ou conserver la brillance de ladite composition. L'invention a encore pour objet un procédé de soin cosmétique ou de maquillage des matières kératiniques et notamment des lèvres, des phanères ou de fa peau, consistant à appliquer sur respectivement les lèvres, les phanères ou la peau une composition cosmétique telle définie précédemment. L'invention a encore pour objet un procédé cosmétique pour limiter la migration d'une composition de maquillage ou de soin de la peau ou des lèvres et/ou augmenter la tenue dans le temps de cette composition et/ou sa stabilité, contenant une phase grasse liquide et au moins un ingrédient choisi parmi les matières colorantes sous forme de particules solides à température ambiante, colorées, consistant à introduire dans la phase grasse liquide des particules de polymère dispersibles dans la phase grasse liquide et stabilisa- blés en surface par un agent stabilisant et à introduire dans ladite phase grasse liquide lesdites particules colorées sous forme de dispersion colloïdale.According to the invention, the quantity of polymer in dispersion must be sufficient to form on the skin and / or the lips and / or the keratin fibers a film capable of trapping the coloring matters and or the cosmetic or dermatological active agents and / or the oils. with a view to limiting their migration and increasing the hold of the composition. The amount of polymer is a function of the amount of coloring matter and / or active ingredients and / or oils, contained in the composition. In practice, the amount of polymer can be greater than 2% by weight (in active material), relative to the total weight of the composition. Another subject of the invention is the cosmetic use in a composition for application to the skin, the hares and the integuments and more particularly cosmetic, hygienic or the use for the manufacture of a dermatological or pharmaceutical composition for application to the skin, the lips and the integuments, of particles of at least one polymer dispersed in a liquid fatty phase and stabilized on the surface by a stabilizing agent and of a colloidal dispersion of solid particles at room temperature, in particular colored to limit the migration of the composition and / or increase its resistance over time and / or obtain a homogeneous make-up and / or maintain the gloss of said composition. The subject of the invention is also a method of cosmetic care or of making up keratin materials and in particular of the lips, integuments or of the skin, consisting in applying to the lips, the integuments or the skin respectively, a cosmetic composition as defined above. The subject of the invention is also a cosmetic method for limiting the migration of a makeup or care composition for the skin or the lips and / or increasing the resistance over time of this composition and / or its stability, containing a phase liquid fat and at least one ingredient chosen from coloring matters in the form of solid particles at room temperature, colored, consisting in introducing into the liquid fatty phase particles of polymer dispersible in the liquid fatty phase and surface stabilized by an agent stabilizing and introducing into said liquid fatty phase said colored particles in the form of a colloidal dispersion.
L'invention a encore pour objet un procédé de fabrication d'une composition stable à ap- plicatîon sur les matières kératiniques, consistant à introduire dans un milieu physioiogi- quement acceptable liquide a) une dispersion de particules de polymère stabilisées en surface dans une phase grasse liquide par un stabilisant, b) une dispersion colloïdale de particules soudes à température ambiante, choisies parmi les pigments, les nacres et (es charges et leurs mélanges et à mélanger ledit milieu supplémenté desdites dispersions a) et b)..A subject of the invention is also a process for the manufacture of a stable composition for application to keratin materials, comprising introducing into a physiologically acceptable liquid medium a) a dispersion of polymer particles stabilized at the surface in a phase fatty liquid by a stabilizer, b) a colloidal dispersion of particles welded at room temperature, chosen from pigments, nacres and (es fillers and their mixtures and to mix said medium supplemented with said dispersions a) and b).
Selon l'invention, la dispersion de particules de polymères stabilisées en surface par un stabilisant et la dispersion colloïdale de particules solides sont préparées séparément et au préalable, avant leur introduction dans \a composition.According to the invention, the dispersion of polymer particles stabilized on the surface by a stabilizer and the colloidal dispersion of solid particles are prepared separately and beforehand, before their introduction into the composition.
L'invention a encore pour objet l'utilisation d'une dispersion colloïdale de particules solides à température ambiante, choisies parmi les pigments, les nacres, les charges et leurs mélanges dans une composition à application sur les matières kératiniques, contenant une dispersion de particules de polymère stabilisées en surface dans une phase grasse liquide par un stabilisant, pour stabiliser ladite composition et/ou lui conférer un aspect homogène.Another subject of the invention is the use of a colloidal dispersion of solid particles at room temperature, chosen from pigments, nacres, fillers and their mixtures in a composition for application to keratin materials, containing a dispersion of polymer particles stabilized on the surface in a liquid fatty phase with a stabilizer, to stabilize said composition and / or give it a homogeneous appearance.
Un avantage de l'utilisation d'une dispersion de particules de polymère dans une compo- ' sition de l'invention est que ces particules restent à l'état de particules élémentaires, sans former d'agglomérats, dans la phase grasse. Un autre avantage de la dispersion de polymère est la possibilité d'obtenir des compositions très fluides (de l'ordre de 130 centipoi- ses), même en présence d'un taux élevé de polymère.An advantage of the use of a polymer particle dispersion in a compo- "sition of the invention is that these particles remain in the form of elementary particles, without forming agglomerates in the fatty phase. Another advantage of the polymer dispersion is the possibility of obtaining very fluid compositions (of the order of 130 centipoises), even in the presence of a high level of polymer.
Encore un autre avantage d'une telle dispersion de polymère est qu'il est possible de calibrer à volonté la taille des particules de polymère, et de moduler leur "polydispersité" en taille lors de la synthèse. Il est ainsi possible d'obtenir des particules de très petite taille, qui sont invisibles à l'oeil nu lorsqu'elles sont dans la composition et lorsqu'elles sont appliquées sur la peau ou les lèvres.Yet another advantage of such a polymer dispersion is that it is possible to calibrate the size of the polymer particles at will, and to modulate their "polydispersity" in size during the synthesis. It is thus possible to obtain particles of very small size, which are invisible to the naked eye when they are in the composition and when they are applied to the skin or the lips.
On a de plus constaté que la composition selon l'invention, présente des qualités d'étalement et d'adhésion sur la peau, les lèvres, les cils ou les muqueuses, particulière- ment intéressantes, ainsi qu'un toucher onctueux et agréable. Cette composition a, en outre, l'avantage de se démaquiller facilement notamment avec un lait démaquillant classique.It has also been found that the composition according to the invention exhibits qualities of spreading and adhesion to the skin, the lips, the eyelashes or the mucous membranes, which are particularly advantageous, as well as a smooth and pleasant touch. This composition also has the advantage of removing makeup easily, in particular with a conventional cleansing milk.
Polymères en dispersionDispersion polymers
La composition selon l'invention comprend donc avantageusement une ou plusieurs dispersions stables de particules de polymères généralement sphériques d'un ou plusieurs polymères, dans une phase grasse liquide physiologiquement acceptable. Ces dispersions sont généralement appelées NAD (Non-Aqueous Dispersion) de polymère par op- position à des latex qui sont des dispersions aqueuses de polymère. Ces dispersions peuvent notamment se présenter sous forme de nanoparticules de polymères en dispersion stable dans ladite phase grasse. Les nanoparticules sont de préférence d'une taille comprise entre 5 et 600 nm. Il est toutefois possible d'obtenir des tailles de particules de polymère allant jusqu'à 1μm.The composition according to the invention therefore advantageously comprises one or more stable dispersions of particles of generally spherical polymers of one or more polymers, in a physiologically acceptable liquid fatty phase. These dispersions are generally called NAD (Non-Aqueous Dispersion) of polymer by opposition to latexes which are aqueous dispersions of polymer. These dispersions can in particular be in the form of nanoparticles of polymers in stable dispersion in said fatty phase. The nanoparticles are preferably of a size between 5 and 600 nm. It is however possible to obtain polymer particle sizes of up to 1 μm.
Encore un avantage de la dispersion de polymère de la composition de l'invention est la possibilité de faire varier la température de transition -vitreuse (Tg) du polymère ou du système polymérique (polymère plus additif du type plastifiant), et de passer ainsi d'un polymère dur à un polymère plus ou moins mou, permettant de régler les propriétés mé- caniques de la composition en fonction de l'application envisagée et en particulier du film déposé. 'Another advantage of the polymer dispersion of the composition of the invention is the possibility of varying the glass-transition temperature (Tg) of the polymer or of the polymer system (polymer more additive of the plasticizer type), and thus to pass d a hard polymer to a more or less soft polymer, making it possible to adjust the mechanical properties of the composition as a function of the intended application and in particular of the film deposited. '
Les polymères en dispersion utilisables dans la composition de l'invention ont de préférence un poids moléculaire de l'ordre de 2000 à 10 000 000 et une Tg de -100°C à 300°C et mieux de -50° à 50°C, de préférence de -10°C à 100°C.The dispersion polymers which can be used in the composition of the invention preferably have a molecular weight of the order of 2000 to 10 000 000 and a Tg of -100 ° C to 300 ° C and better still of -50 ° to 50 ° C , preferably from -10 ° C to 100 ° C.
Lorsque le polymère présente une température de transition vitreuse trop élevée pour l'application souhaitée, on peut lui associer un plastifiant de manière à abaisser cette température du mélange utilisé. Le plastifiant peut être choisi parmi les plastifiants usuel- lement utilisés dans le domaine d'application et notamment parmi les composés susceptibles d'être des solvants du polymère. Il est possible d'utiliser des polymères filmifiables, de préférence ayant une Tg basse, inférieure ou égale à la température de la peau et notamment inférieure ou égale à 40°C. On obtient ainsi une dispersion qui peut filmifier lorsqu'elle est appliquée sur un support, ce qui n'est pas le cas lorsqu'on utilise des dispersions de pigments minéraux selon l'art antérieur.When the polymer has a glass transition temperature too high for the desired application, a plasticizer can be associated with it so as to lower this temperature of the mixture used. The plasticizer can be chosen from the plasticizers commonly used in the field of application and in particular from the compounds capable of being solvents for the polymer. It is possible to use film-forming polymers, preferably having a low Tg, less than or equal to the skin temperature and in particular less than or equal to 40 ° C. A dispersion is thus obtained which can film when applied to a support, which is not the case when dispersions of mineral pigments according to the prior art are used.
Parmi les polymères filmifiables, on peut citer des homopolymères ou des copolymères radicalaires, acryliques ou vinyliques, de préférence ayant une Tg inférieure ou égale à 40°C et notamment allant de - 10° à 30°C, utilisés seul ou en mélange.Among the film-forming polymers, mention may be made of radical, acrylic or vinyl homopolymers or copolymers, preferably having a Tg of less than or equal to 40 ° C and in particular ranging from - 10 ° to 30 ° C, used alone or as a mixture.
Parmi les polymères non filmifiables, on peut citer des homopolymères ou copolymères radicalaires, vinyliques ou acryliques, éventuellement réticulés, ayant de préférence une Tg supérieure à 40°C et notamment allant de 45° à 150°C, utilisés seul ou en mélange. Par polymère radicalaire, on entend un polymère obtenu par polymérisation de monomères à insaturation notamment éthylénique, chaque monomère étant susceptible de s'ho- mopolymériser (à l'inverse des polycondensats). Les polymères radicalaires peuvent être notamment des polymères, ou des copolymères, vinyliques, notamment des polymères acryliques.Among the non-film-forming polymers, mention may be made of radical, vinyl or acrylic homopolymers or copolymers, optionally crosslinked, preferably having a Tg greater than 40 ° C and in particular ranging from 45 ° to 150 ° C, used alone or as a mixture. By radical polymer is meant a polymer obtained by polymerization of unsaturated monomers, in particular ethylenic, each monomer being capable of homopolymerizing (unlike polycondensates). The radical polymers can be in particular vinyl polymers or copolymers, in particular acrylic polymers.
Les polymères vinyliques peuvent résulter de la polymérisation de monomères à insaturation éthylénique ayant au moins un groupement acide et/ou des esters de ces monomères acides et/ou des amides de ces acides. Comme monomère porteur de groupement acide, on peut utiliser des acides carboxyli- ques insaturés α,β-éthyléniques tels que l'acide acrylique, l'acide méthacrylique, l'acide crotonique, l'acide maléique, l'acide itaconique. On utilise de préférence l'acide (méth)acrylique et l'acide crotonique, et plus préférentiellement l'acide (méth)acryiique. Les esters de monomères acides sont avantageusement choisis parmi les esters de l'acide (méth)acrylique (encore appelé les (méth)acrylates), comme les (méth)acryîates d'alkyle, en particulier d'alkyle en CrC2o, de préférence en Cj-Cg, les (méth)acrylates d'aryle, en particulier d'aryle en C6-C10, les (méth)acrylates d'hydroxyalkyle, en particulier d'hydroxyalkyle en C2-C6. Comme (méth)acrylates d'alkyle, on peut citer le (méth)acrylate de méthyle, d'éthyle, de butyle, d'isobutyle, d'éthyl-2 hexyle et de lauryie. Comme (méth)acrylates d'hydroxyalkyle, on peut citer le (méth)acrylate d'hydroxyéthyle, le (méth)acrylate de 2-hydroxypropyle. Comme (méth)acrylates d'aryle, on peut citer l'acry- late de benzyle ou de phényle. Les esters de l'acide (méth)acrylique particulièrement préférés sont les (méth)acrylates d'alkyle.The vinyl polymers can result from the polymerization of ethylenically unsaturated monomers having at least one acid group and / or esters of these acid monomers and / or amides of these acids. As monomer carrying an acid group, α, β-ethylenic unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid can be used. Preferably (meth) acrylic acid and crotonic acid are used, and more preferably (meth) acrylic acid. The esters of acidic monomers are advantageously chosen from esters of (meth) acrylic acid (also called (meth) acrylates), such as alkyl (meth) acrylates, in particular C 1 -C 20 alkyl, of preferably in Cj-Cg, aryl (meth) acrylates, in particular C 6 -C 10 aryl, hydroxyalkyl (meth) acrylates, in particular C 2 -C 6 hydroxyalkyl. As alkyl (meth) acrylates, mention may be made of methyl, ethyl, butyl, isobutyl, 2-ethylhexyl and lauryie (meth) acrylate. As hydroxyalkyl (meth) acrylates, mention may be made of hydroxyethyl (meth) acrylate and 2-hydroxypropyl (meth) acrylate. As aryl (meth) acrylates, mention may be made of benzyl or phenyl acrylate. Particularly preferred esters of (meth) acrylic acid are alkyl (meth) acrylates.
Comme polymère radicalaire, on utilise de préférence les copolymères d'acide (méth)acrylique et de (méth)acrylate d'alkyle, notamment d'alkyle en C C . Plus préféren- tiellement, on peut utiliser les acrylates de méthyle éventuellement copolymérisés avec l'acide acrylique.As radical polymer, use is preferably made of copolymers of (meth) acrylic acid and of (meth) acrylate, in particular C 1 -C alkyl. More preferably, methyl acrylates may be used, optionally copolymerized with acrylic acid.
Comme amides des monomères acides, on peut citer les (méth)acrylamides, et notamment les N-alkyl (nnéth)acrylamides, en particulier d'alkyle en C2-C12 tels que le N-éthyl acrylamide, le N-t-butyl acrylamide, le N-octyl acrylamide ; les N- dialkyl (C C4) (méth)acrylamides. Les polymères vinyliques peuvent également résulter de la polymérisation de monomères à insaturation éthylénique ayant au moins un groupe aminé, sous forme libre ou bien partiellement ou totalement neutralisée, ou bien encore partiellement ou totalement quaterni- sée. De tels monomères peuvent être par exemple le (méth)acrylate de diméthylaminoé- thyle, le éthacrylamide de diméthylaminoéthyle, la vinylamine, la vinylpyridine, le chlorure de d.allyldiméthylammonium.As amides of the acid monomers, mention may be made of (meth) acrylamides, and in particular N-alkyl (nneth) acrylamides, in particular of C 2 -C 12 alkyl such as N-ethyl acrylamide, Nt-butyl acrylamide , N-octyl acrylamide; N-dialkyl (CC 4 ) (meth) acrylamides. The vinyl polymers can also result from the polymerization of ethylenically unsaturated monomers having at least one amino group, in free form or else partially or totally neutralized, or even partially or totally quaternized. Such monomers can be, for example, dimethylaminoethyl (meth) acrylate, dimethylaminoethyl ethacrylamide, vinylamine, vinylpyridine, d.allyldimethylammonium chloride.
Les polymères vinyliques peuvent également résulter de l'homopolymérisation ou de la copoly érisation d'au moins un monomère choisi parmi les esters vinyliques et les mo- nomères styrèniques. En particulier, ces monomères peuvent être polymérisés avec des monomères acides et/ou leurs esters et/ou leurs amides, tels que ceux mentionnés précédemment. Comme exemple d'esters vinyliques, on peut citer l'acétate de vinyle, le pro- pionate de vinyle, le néodécanoate de vinyle, le pivalate de vinyle, le benzoate de vinyle et le t-butyl benzoate de vinyle. Comme monomères styrèniques, on peut citer le styrène et l'aipha-méthyl styrène.The vinyl polymers can also result from the homopolymerization or from the copolyerization of at least one monomer chosen from vinyl esters and styrene monomers. In particular, these monomers can be polymerized with acidic monomers and / or their esters and / or their amides, such as those mentioned above. Examples of vinyl esters include vinyl acetate, vinyl propionate, vinyl neodecanoate, vinyl pivalate, vinyl benzoate and vinyl t-butyl benzoate. As styrene monomers, mention may be made of styrene and aipha-methyl styrene.
La liste des monomères donnée n'est pas limitative et il est possible d'utiliser tout monomère connu de l'homme du métier entrant dans les catégories de monomères acryliques et vinyliques (y compris les monomères modifiés par une chaîne siliconée).The list of monomers given is not exhaustive and it is possible to use any monomer known to a person skilled in the art falling within the categories of acrylic and vinyl monomers (including the monomers modified by a silicone chain).
Comme autres monomères vinyliques utilisables, on peut encore citer .As other vinyl monomers which can be used, mention may also be made.
- la N-vinylpyrrolidone, la vinylcaprolactame, les vinyl -alky C Cg) pyrroles, les vinyl- oxazoles, les vinyl-thiazoles, les vinylpyrimidines, les vi nyl i mi d azotes,- N-vinylpyrrolidone, vinylcaprolactam, vinyl -alky C Cg) pyrroles, vinyl-oxazoles, vinyl-thiazoles, vinylpyrimidines, vi nyl i mi d nitrogen,
- les oléfines tels que l'éthylène, le propylène, le butylène, l'isoprène, le butadiène.- olefins such as ethylene, propylene, butylene, isoprene, butadiene.
Le polymère vinylique peut être réticulé à l'aide d'un ou plusieurs monomères difonction- nels, notamment comprenant au moins deux insaturations éthyléniques, tel que le dimé- thacrylate d'éthylène glycol ou le phtalate de diallyle. De façon non limitative, les polymères en dispersion de l'invention peuvent être choisis parmi, les polymères ou copolymères suivants : polyuréthannes, polyuréthannes- acryliques, polyurées, polyurée-polyuréthannes, polyester-polyuréthannes, polyéther- polyuréthannes, polyesters, polyesters amides, polyesters à chaîne grasse, alkydes ; polymères ou copolymères acryliques et/ou vinyliques ; copolymères acryliques-silicone ; polyacrylamides ; polymères siliconés comme les polyuréthannes ou acryliques siliconés, polymères fluorés et leurs mélanges.The vinyl polymer can be crosslinked using one or more difunctional monomers, in particular comprising at least two ethylenic unsaturations, such as ethylene glycol dimethacrylate or diallyl phthalate. Without limitation, the dispersion polymers of the invention can be chosen from the following polymers or copolymers: polyurethanes, polyurethanes-acrylics, polyureas, polyurea-polyurethanes, polyester-polyurethanes, polyether-polyurethanes, polyesters, polyester amides, polyesters fatty chain, alkyds; acrylic and / or vinyl polymers or copolymers; acrylic-silicone copolymers; polyacrylamides; silicone polymers such as polyurethanes or silicone acrylics, fluoropolymers and mixtures thereof.
Le ou les polymères en dispersion huileuse peuvent représenter (en matière sèche ou matière active) de 0,1 à 60 % du poids de la composition, de préférence de 2 à 40 % et mieux de 4 à 25 %. Pour un stabilisant solide à température ambiante, la quantité en matière sèche de la dispersion représente la quantité totale de polymère + stabilisant.The polymer (s) in oily dispersion can represent (in dry matter or active material) from 0.1 to 60% of the weight of the composition, preferably from 2 to 40% and better still from 4 to 25%. For a solid stabilizer at room temperature, the amount of dry matter in the dispersion represents the total amount of polymer + stabilizer.
Phase grasse La phase grasse liquide de la composition peut être constituée de toute huile cosméti- quement ou dermatologiquemeπt acceptable, et de façon générale physiologiquement acceptable, notamment choisie parmi les huiles d'origine minérale, animale, végétale ou synthétique, carbonées, hydrocarbonées, fluorées et/ou siliconées, seules ou en mélange dans fa mesure où elles forment un mélange homogène et stable macroscopiquement et où elles sont compatibles avec l'utilisation envisagée. Par "huile hydrocarbonée", on entend des huiles contenant majoritairement des atomes de carbone et des atomes d'hydrogène et en particulier des chaînes alkyle ou alcényle comme les alcanes ou alcènes mais aussi les huiles à chaîne alkyle ou alcényle comportant un ou des groupements éther, ester ou acide carboxylique.Fat phase The liquid fatty phase of the composition can consist of any cosmetically or dermatologically acceptable oil, and generally physiologically acceptable oil, in particular chosen from oils of mineral, animal, vegetable or synthetic origin, carbonaceous, hydrocarbonaceous, fluorinated and / or silicone-based, alone or as a mixture insofar as they form a homogeneous and macroscopically stable mixture and where they are compatible with the intended use. By “hydrocarbon-based oil” is meant oils mainly containing carbon atoms and hydrogen atoms and in particular alkyl or alkenyl chains such as alkanes or alkenes but also oils with alkyl or alkenyl chains comprising one or more ether groups , ester or carboxylic acid.
La phase grasse liquide totale de la composition peut représenter de 5 % à 99,40 % du poids total de la composition et de préférence de 20 à 85 %. Avantageusement, elle représente au moins 30 % du poids total de la composition. De préférence, cette phase grasse contient au moins une huile non volatile (à savoir plusieurs huiles non volatiles). La partie non volatile peut représenter de 0 à 80 % du poids total de la composition et mieux de 1 à 50%.The total liquid fatty phase of the composition may represent from 5% to 99.40% of the total weight of the composition and preferably from 20 to 85%. Advantageously, it represents at least 30% of the total weight of the composition. Preferably, this fatty phase contains at least one non-volatile oil (namely several non-volatile oils). The non-volatile part can represent from 0 to 80% of the total weight of the composition and better still from 1 to 50%.
Comme phase grasse liquide utilisable dans l'invention, on peut ainsi citer les huiles hydrocarbonées d'origine minérale ou synthétique telles les hydrocarbures linéaires ou ra- mifiés volatils ou non comme l'huile de paraffine ou ses dérivés, l'huile de vaseline, les polydécènes, le polyisobutène hydrogéné tel que le parléam, le squalane ; les huiles d'origine animale comme l'huile de vison, de tortue, le perhydrosqualène ; les huiles d'origine végétale ; hydrocarbonées à forte teneur en triglycérides constitués d'esters d'acides gras et de glycérol dont les acides gras peuvent avoir des longueurs de chaînes variées, ces dernières pouvant être linéaires ou ramifiées, saturées ou insaturées, comme l'huile d'amande douce, de calophyllum, de palme, de pépins de raisin, de sésame, d'ara- ra, de colza, de tournesol, de coton, d'abricot, de ricin, de luzerne, de courge, de cassis, de macadamia, de rosier muscat, de noisette, d'avocat, de jojoba, d'olive ou de germes de céréales (maïs, blé, orge, seigle) ; des esters d'acide gras et notamment d'acide lano- lique, d'acide oléique, d'acide laurique, d'acide stéarique ; les esters de synthèse de formule R-,COQR2 dans laquelle R, représente le reste d'un acide gras supérieur linéaire ou ramifié comportant de 7 à 40 atomes de carbone et R2 représente une chaîne hydrocarbonée ramifiée contenant de 3 à 40 atomes de carbone, comme par exemple l'huile de Pur- cellin (octanoate de cétostéaryle), l'isononanoate d'isononyle, le benzoate d'alcool en C12 à C15, le palmitate d'éthyl 2-hexyle, des octanoates, décanoates ou ricinoléates d'alcools ou de polyalcools, le myristate d'isopropyle, le palmitate d'isopropyle, le stéarate de butyle, le laurate d'hexyle, l'adipate de diisopropyîe, le palmitate de 2-éthyl-hexyle, le laurate de 2-hexyl-décyle, le palmitate de 2-octyl-décyle, le myristate de 2-octyl-dodécyle, le suc- cinate de 2-diéthyl-hexyle, le malate de diisostéaryle, le triisostéarate de glycérine ou de diglycérine ; les esters hydroxylés comme le lactate d'isostéaryle, le malate de diisostéaryle ; les esters du pentaérythritol ; les acides gras supérieurs en C8-C26 tels que l'acide myristique, l'acide palmitique, l'acide stéarique, -l'acide béhénique, l'acide oléique, l'acide linoléique, l'acide linolénique ou l'acide isostéarique ; les alcools gras supérieurs en C3-C26 tels que l'alcool stéarylique ou oléique, l'alcool linoléique ou linolénique, l'alcool isostéarique ou l'octyl dodécanol ; les éthers de synthèse à au moins 7 atomes de carbone les huiles siliconées telles que les polydiméthylsiloxanes (PD S) liquides à température ambiante, linéaires ou cycliques, volatiles ou non, éventuellement phénylés tels que les phényltriméthicones, les phényl triméthylsiloxy diphénylsiloxanes, les diphényl diméthicones, les diphényl méthyldiphényl trisiloxanes, tes 2-phényléthyl triméthylsiloxysi- licates liquides, éventuellement substitués par des groupements aliphatiques et/ou aromatiques comme les groupes alkyle, alcoxy ou phényle, pendant et/ou en bout de chaîne siliconée, groupements ayant de 2 à 24 atomes de carbone et éventuellement fluorés, ou par des groupements fonctionnels tels que des groupements hydroxyle, thiol et/ou aminé ; les polysiloxanes modifiés par des acides gras, des alcools gras ou des polyoxyalkylènes ; les siliconés fluorées ; ou encore les triglycérides des acides caprylique/caprique comme ceux vendus par la société Stearineries Dubois ou ceux vendus sous les dénominations Miglyol 810, 812 et 818 par la société Dynamit Nobel ; et leurs mélanges. Avantageusement, on peut utiliser une ou plusieurs solvants volatils à température ambiante comme des huiles volatiles cosmétiques. Ces solvants volatils sont favorables à l'obtention d'un dépôt de bonne tenue. Après évaporation de ces solvants, on obtient un dépôt filmogène souple, non collant sur la peau ou les lèvres. Ces solvants volatils facilitent, en outre, l'application de la composition sur la peau, les lèvres et les phanères. Ils peuvent être hydrocarbonés ou siliconés et comportés éventuellement des groupements alkyle ou alkoxy, pendants ou en bout de chaîne siliconée. Comme huile volatile utilisable dans l'invention, on peut citer les huiles de siliconés linéaires ou cycliques ayant une viscosité à température ambiante inférieure à 8 cSt et ayant notamment de 2 à 7 atomes de silicium, ces siliconés comportant éventuellement des groupes alkyle ou alkoxy ayant de 1 à 10 atomes dé carbone. Comme huile de silicone volatile utilisable dans l'invention, on peut citer notamment l'octaméthylcyclo-tétrasiloxane, le décaméthylcyclopentasiloxane, le dodécamethylcyclohexasiloxane, l'heptaméthyl hexyltrisiloxane, l'heptaméthyloctyl trisiloxane, l'hexaméthyldisiloxane, l'octaméthyl trisi- loxane, le décaméthyl tétrasiloxane, le dodécaméthyl pentasiloxane et leurs mélanges.As liquid fatty phase which can be used in the invention, mention may therefore be made of hydrocarbon oils of mineral or synthetic origin, such as linear or branched hydrocarbons, volatile or not, such as paraffin oil or its derivatives, petrolatum oil, polydecenes, hydrogenated polyisobutene such as parlameam, squalane; oils of animal origin such as mink, turtle oil, perhydrosqualene; oils of vegetable origin; hydrocarbons with a high triglyceride content made up of fatty acid and glycerol esters, the fatty acids of which can have various chain lengths, the latter possibly being linear or branched, saturated or unsaturated, such as sweet almond oil, calophyllum, palm, grapeseed, sesame, arara, rapeseed, sunflower, cotton, apricot, castor, alfalfa, squash, blackcurrant, macadamia, rosebush muscat, hazelnut, avocado, jojoba, olive or germ of cereals (corn, wheat, barley, rye); esters of fatty acid and in particular of lanoic acid, oleic acid, lauric acid, stearic acid; the synthetic esters of formula R-, COQR 2 in which R represents the remainder of a linear or branched higher fatty acid containing from 7 to 40 carbon atoms and R 2 represents a branched hydrocarbon chain containing from 3 to 40 carbon atoms carbon, such as Purcellin oil (ketostearyl octanoate), isononyl isononanoate, C 12 to C 15 alcohol benzoate, ethyl 2-hexyl palmitate, octanoates, decanoates or ricinoleates of alcohols or polyalcohols, isopropyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, diisopropyl adipate, 2-ethyl-hexyl palmitate, laurate of 2-hexyl-decyl, 2-octyl-decyl palmitate, 2-octyl-dodecyl myristate, 2-diethyl-hexyl succinate, diisostearyl malate, glycerin or diglycerin triisostearate; hydroxylated esters such as isostearyl lactate, diisostearyl malate; pentaerythritol esters; higher C 8 -C 26 fatty acids such as myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, linoleic acid, linolenic acid or isostearic acid; higher C 3 -C 26 fatty alcohols such as stearyl or oleic alcohol, linoleic or linolenic alcohol, isostearic alcohol or octyl dodecanol; synthetic ethers with at least 7 carbon atoms silicone oils such as polydimethylsiloxanes (PD S) liquid at room temperature, linear or cyclic, volatile or not, optionally phenylated such as phenyltrimethicones, phenyl trimethylsiloxy diphenylsiloxanes, diphenyl dimethicones , diphenyl methyldiphenyl trisiloxanes, 2-phenylethyl trimethylsiloxysilicates liquid, optionally substituted by aliphatic and / or aromatic groups such as alkyl, alkoxy or phenyl groups, during and / or at the end of the silicone chain, groups having from 2 to 24 carbon atoms and optionally fluorinated, or by functional groups such as hydroxyl, thiol and / or amino groups; polysiloxanes modified with fatty acids, fatty alcohols or polyoxyalkylenes; fluorinated silicones; or the triglycerides of caprylic / capric acids such as those sold by the company Stearineries Dubois or those sold under the names Miglyol 810, 812 and 818 by the company Dynamit Nobel; and their mixtures. Advantageously, one or more volatile solvents can be used at room temperature such as volatile cosmetic oils. These volatile solvents are favorable for obtaining a deposit of good performance. After evaporation of these solvents, a flexible film-forming deposit is obtained, which does not stick to the skin or the lips. These volatile solvents also facilitate the application of the composition to the skin, the lips and the integuments. They can be hydrocarbon or silicone and optionally comprise alkyl or alkoxy groups, pendant or at the end of the silicone chain. As volatile oil which can be used in the invention, mention may be made of linear or cyclic silicone oils having a viscosity at room temperature of less than 8 cSt and having in particular from 2 to 7 silicon atoms, these silicones optionally comprising alkyl or alkoxy groups having from 1 to 10 carbon atoms. As volatile silicone oil which can be used in the invention, mention may in particular be made of octamethylcyclo-tetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, heptamethyl hexyltrisiloxane, heptamethyloctyl trisiloxane, hexamethyldisethyloxane tranethylamethane, octamethylane tetrasiloxane, dodecamethyl pentasiloxane and mixtures thereof.
Comme autre solvant volatil utilisable dans l'invention, on peut citer les huiles volatiles hydrocarbonées ayant de 8 à 16 atomes de carbone et leurs mélanges et notamment les alcanes ramifiés en C8-C16 comme les isoalcanes (appelées aussi isoparaffines) en C8-Cι6, l'isododécane, l'isodécane, l'isohexadécane et par exemple les huiles vendues sous les noms commerciaux d'isopars' ou de Permetyls', les esters ramifiés en C8-C18 comme le néo pentanoate d'iso-hexyle et leurs mélanges.As other volatile solvent used in the invention include volatile hydrocarbon oils having from 8 to 16 carbon atoms and their mixtures and in particular branched alkanes, C 8 -C 16 isoalkanes (also called isoparaffins) C 8 -Cι 6 , isododecane, isodecane, isohexadecane and for example the oils sold under the trade names of isopars 'or Permyls', the branched esters of C 8 -C 18 such as neo isano pentanoate -hexyl and their mixtures.
Dans un mode particulier de réalisation de l'invention, on choisit le phase grasse liquide dans le groupe comprenant :In a particular embodiment of the invention, the liquid fatty phase is chosen from the group comprising:
- les composés liquides non aqueux ayant un paramètre de solubilité global selon l'espace de solubilité de HANSEN inférieur à 17 (IVIPa)1'2, - ou les monoalcools ayant un paramètre de solubilité global selon l'espace de solubilité de HANSEN inférieur ou égal à 20 (MPa)1'2,- non-aqueous liquid compounds having a global solubility parameter according to the HANSEN solubility space of less than 17 (IVIPa) 1 ' 2 , - or monoalcohols having a global solubility parameter according to the lower HANSEN solubility space or equal to 20 (MPa) 1 ' 2 ,
- ou leurs mélanges.- or their mixtures.
Le paramètre de solubilité global δ global selon l'espace de solubilité de HANSEN est dé- fini dans l'article "Solubility parameter values" de Eric A. Grulke de l'ouvrage "Polymer Handbook" 3ême édition, Chapitre VII, pages 519-559 par la relation : δ = ( dD 2+ dp2 + dH 2)1 2 , dans laquelle : - dD caractérise les forces de dispersion de LONDON issues de la formation de dipôles induits lors des chocs moléculaires,The total overall solubility parameter δ according to the Hansen solubility space is de- fined in the article "Solubility parameter values" by Eric A. Grulke of the book "Polymer Handbook" 3 ven edition, Chapter VII, pages 519 -559 by the relation: δ = (d D 2 + dp 2 + d H 2 ) 1 2 , in which: - d D characterizes the LONDON dispersion forces resulting from the formation of dipoles induced during molecular shocks,
- dp caractérise les forces d'interactions de DEBYE entre dipôies permanents,- dp characterizes the DEBYE interaction forces between permanent dipoiies,
- dH caractérise les forces d'interactions spécifiques (type liaisons hydrogène, acide/base, donneur/accepteur, etc.). La définition des solvants dans l'espace de solubilité tridimen- sionnel selon HANSEN est donnée dans l'article de C. M. HANSEN : "The three dimen- sional solubility parameters" J. Paint Technol. 39, 105 (1967).- d H characterizes the specific interaction forces (such as hydrogen bonds, acid / base, donor / acceptor, etc.). The definition of solvents in the three-dimensional solubility space according to HANSEN is given in the article by CM HANSEN: "The three dimensional solubility parameters" J. Paint Technol. 39, 105 (1967).
Parmi les phases grasses liquides ayant un paramètre de solubilité global selon l'espace de solubilité de HANSEN, inférieur ou égal à 17 (MPa)"1'2, on peut citer des huiles d'origine végétale formées par des esters d'acides gras et de polyols, en particulier les triglycérides, telles que l'huile de tournesol, de sésame ou* de colza, ou les esters dérivés d'acides ou d'alcools à longue chaîne (c'est à dire ayant de 6 à 20 atomes de carbone), notam- ment les esters de formule R1COOR2 dans laquelle R, représente le reste d'un acide gras supérieur comportant de 7 à 40 atomes de carbone et R2 représente une chaîne hydrocarbonée comportant de 3 à 40 atomes de carbone, tels que les palmitates, les adipates et les benzoates, notamment l'adipate de diisopropyle. On peut également citer les hydro- carbures et notamment des huiles de paraffine, de vaseline, ou le polyisobutylène hydrogéné, l'isododécane, ou encore les "Isopars" (isoparaffines volatiles). On peut encore citer les huiles de silicone telles que les polydiméthylsiloxanes et les polyméthylphénylsiloxa- nes, éventuellement substitués par des groupements aliphatiques et/ou aromatiques, éventuellement fluorés, ou par des groupements fonctionnels tels que des groupements hydroxyle, thiol et/ou aminé, et les huiles siliconées volatiles, notamment cycliques. On peut également citer les solvants, seuls ou en mélange, choisis parmi (i) les esters linéaires, ramifiés ou cycliques, ayant plus de 6 atomes de carbone, (ii) les éthers ayant plus de 6 atomes de carbone, (iii) les cétones ayant plus de 6 atomes de carbone. Par monoalcools ayant un paramètre de solubilité global selon l'espace de solubilité de HANSEN inférieur ou égal à 20 (MPa)1'2, on entend les alcools gras aliphatiques ayant au moins 6 atomes de carbone, fa chaîne hydrocarbonée ne comportant pas de groupement de substitution. Comme monoalcools selon l'invention, on peut citer l'alcool oléique, le déca- nol, le dodécanol, l'octadécanol et l'alcool linoléique. Comme milieu non aqueux, on peut aussi utiliser ceux décrits dans le document FR-A-2 710 646 de L.V.M.H.Among the liquid fatty phases having a global solubility parameter according to the HANSEN solubility space, less than or equal to 17 (MPa) "12 , mention may be made of oils of vegetable origin formed by fatty acid esters and polyols, especially triglycerides, such as sunflower oil, sesame oil or rapeseed *, or esters derived from acids or long-chain alcohols (ie having from 6 to 20 carbon carbon), including the esters of formula R 1 COOR 2 in which R represents the residue of a higher fatty acid containing from 7 to 40 carbon atoms and R 2 represents a hydrocarbon chain comprising from 3 to 40 carbon atoms, such as palmitates , adipates and benzoates, in particular diisopropyl adipate. Mention may also be made of hydrocarbons and in particular paraffin oils, petrolatum, or hydrogenated polyisobutylene, isododecane, or also "Isopars" (volatile isoparaffins). Mention may also be made of silicone oils such as polydimethylsiloxanes and polymethylphenylsiloxanes, optionally substituted by aliphatic and / or aromatic groups, optionally fluorinated, or by functional groups such as hydroxyl, thiol and / or amino groups, and volatile silicone oils, in particular cyclic oils. Mention may also be made of the solvents, alone or as a mixture, chosen from (i) linear, branched or cyclic esters, having more than 6 carbon atoms, (ii) ethers having more than 6 carbon atoms, (iii) ketones having more than 6 carbon atoms. By monoalcohols having a global solubility parameter according to the HANSEN solubility space of less than or equal to 20 (MPa) 12 , is meant aliphatic fatty alcohols having at least 6 carbon atoms, fa hydrocarbon chain not comprising a group of substitution. As monoalcohols according to the invention, there may be mentioned oleic alcohol, decanol, dodecanol, octadecanol and linoleic alcohol. As non-aqueous medium, it is also possible to use those described in document FR-A-2 710 646 by LVMH
Le choix du milieu non aqueux est effectué par l'homme du métier en fonction de la nature des monomères constituant le polymère et/ou de la nature du stabilisant, comme indiqué ci-après.The choice of the non-aqueous medium is made by a person skilled in the art depending on the nature of the monomers constituting the polymer and / or the nature of the stabilizer, as indicated below.
La dispersion de polymère peut être fabriquée comme décrit dans le document EP-A- 749747. La polymérisation peut être effectuée en dispersion, c'est-à-dire par précipitation du polymère en cours de formation, avec protection des particules formées par stabilisant.The polymer dispersion can be manufactured as described in document EP-A-749747. The polymerization can be carried out in dispersion, that is to say by precipitation of the polymer during formation, with protection of the particles formed by stabilizer.
On prépare donc un mélange comprenant les monomères initiaux ainsi qu'un amorceur radicalaire. Ce mélange est dissous dans un solvant appelé, dans (a suite de (a présente description, "solvant de synthèse". Lorsque la phase grasse est une huile non volatile, on peut effectuer la polymérisation dans un solvant organique apolaire (solvant de synthèse) puis ajouter l'huile non volatile (qui doit être miscible avec ledit solvant de synthèse) et distiller sélectivement le solvant de synthèse.A mixture is therefore prepared comprising the initial monomers and a radical initiator. This mixture is dissolved in a solvent called, in (following (a present description, "synthesis solvent". When the fatty phase is a non-volatile oil, the polymerization can be carried out in an apolar organic solvent (synthesis solvent) then add the non-volatile oil (which must be miscible with said synthesis solvent) and selectively distil the synthesis solvent.
On choisit donc un solvant de synthèse tel que les monomères initiaux, et l'amorceur radicalaire, y sont solubles, et les particules de polymère obtenues y sont insolubles afin qu'elles y précipitent lors de leur formation. En particulier, on peut choisir le solvant de synthèse parmi les alcanes tels que l'heptane, l'isododécane ou le cyclohexane.A synthetic solvent such as the initial monomers and the radical initiator are therefore chosen to be soluble therein, and the polymer particles obtained therein are insoluble so that they precipitate thereon during their formation. In particular, the synthesis solvent can be chosen from alkanes such as heptane, isododecane or cyclohexane.
Lorsque la phase grasse choisie est une huile volatile, on peut directement effectuer la polymérisation dans ladite huile qui joue donc également le rôle de solvant de synthèse. Les monomères doivent également y être solubles, ainsi que l'amorceur radicalaire, et le polymère obtenu doit y être insoluble.When the fatty phase chosen is a volatile oil, the polymerization can be carried out directly in said oil which therefore also plays the role of synthetic solvent. The monomers must also be soluble therein, as well as the radical initiator, and the polymer obtained must be insoluble therein.
Les monomères sont de préférence présents dans le solvant de synthèse, avant polymérisation, à raison de 5-20% en poids du mélange réactionne). La totalité des monomères peut être présente dans le solvant avant le début de la réaction, ou une partie des monomères peut être ajoutée au fur et à mesure de l'évolution de la réaction de polymérisation. L'amorceur radicalaire peut être notamment l'azo-bis-isobutyronitrile ou le tertiobutylpe- roxy-2-éthyl hexanoate.The monomers are preferably present in the synthesis solvent, before polymerization, in an amount of 5-20% by weight of the reaction mixture). All of the monomers may be present in the solvent before the start of the reaction, or a portion of the monomers may be added as the polymerization reaction proceeds. The radical initiator can in particular be azo-bis-isobutyronitrile or tert-butylpyroxy-2-ethyl hexanoate.
StabilisantStabilizing
Les particules de polymère sont stabilisées en surface, au fur et à mesure de la polymérisation, grâce à un stabilisant qui peut être un polymère séquence, un polymère greffé, et/ou un polymère statistique, seul ou en mélange. La stabilisation peut être effectuée par tout moyen connu, et en particulier par ajout direct du polymère séquence, polymère greffé et/ou polymère statistique, lors de la polymérisation.The polymer particles are surface stabilized, as the polymerization progresses, thanks to a stabilizer which can be a block polymer, a graft polymer, and / or a random polymer, alone or as a mixture. Stabilization can be carried out by any known means, and in particular by direct addition of the block polymer, graft polymer and / or random polymer, during the polymerization.
Le stabilisant est de préférence également présent dans le mélange avant polymérisation. Toutefois, il est également possible de l'ajouter en continu, notamment lorsqu'on ajoute également les monomères en continu.The stabilizer is preferably also present in the mixture before polymerization. However, it is also possible to add it continuously, in particular when the monomers are also added continuously.
On peut utiliser 2-30% en poids de stabilisant par rapport au mélange initial de monomères, et de préférence 5-20% en poids.2-30% by weight of stabilizer relative to the initial mixture of monomers can be used, and preferably 5-20% by weight.
Lorsqu'on utilise un polymère greffé et/ou séquence en tant que stabilisant, on choisit le solvant de synthèse de telle manière qu'au moins une partie des greffons ou séquences dudit polymère-stabilisant soit soluble dans ledit solvant, l'autre partie des greffons ou séquences n'y étant pas soluble. Le polymère-stabilisant utilisé lors de la polymérisation doit être soluble, ou dispersible, dans le solvant de synthèse. De plus, on choisit de préférence un stabilisant dont les séquences ou greffons insolubles présentent une certaine affinité pour le polymère formé lors de la polymérisation.When a grafted and / or block polymer is used as stabilizer, the synthetic solvent is chosen in such a way that at least part of the grafts or blocks of said polymer stabilizer is soluble in said solvent, the other part of the grafts or sequences not being soluble therein. The polymer stabilizer used during the polymerization must be soluble, or dispersible, in the synthetic solvent. In addition, a stabilizer is preferably chosen whose insoluble blocks or grafts have a certain affinity for the polymer formed during the polymerization.
Parmi les polymères greffés, on peut citer les polymères siliconés greffés avec une chaîne hydrocarbonée ; les polymères hydrocarbonés greffés avec une chaîne siliconée. Conviennent également les copolymères greffés ayant par exemple un squelette insoluble de type polyacrylique avec des greffons solubles de type acide poly-12- (hydroxystéarique).Among the grafted polymers, mention may be made of silicone polymers grafted with a hydrocarbon chain; hydrocarbon polymers grafted with a silicone chain. Also suitable are graft copolymers having, for example, an insoluble skeleton of polyacrylic type with soluble grafts of poly-12- (hydroxystearic) acid type.
Ainsi on peut utiliser des copolymères blocs greffés ou séquences comprenant au moins un bloc de type polyorganosiloxane et au moins un bloc d'un polymère radicalaire, comme les copolymères greffés de type acrylique/silicone qui peuvent être employés notamment lorsque le milieu non aqueux est silicone.Thus, graft or block block copolymers comprising at least one block of polyorganosiloxane type and at least one block of a radical polymer can be used, such as graft copolymers of acrylic / silicone type which can be used in particular when the non-aqueous medium is silicone. .
On peut aussi utiliser des copolymères blocs greffés ou séquences comprenant au moins un bloc de type polyorganosiloxane et au moins d'un polyéther. Le bloc polyorganopoly- siioxane peut être notamment un polydiméthylsiloxane ou bien encore un poly alkyl(C2- C18) méthyi siloxane ; le bloc polyéther peut être un poly alkylène en Cz-C a, en particulier polyoxyéthylène et/ou polyoxypropylène. En particulier, on peut utiliser les diméthicones copolyof ou des alkyl (C2~C18) diméthicones copolyol tels que ceux vendu sous la dénomi- nation "Dow Corning 3225C" par la société Dow Corning, les lauryl méthicones tels que ceux vendu sous la dénomination "Dow Corning Q2-5200 par la société "Dow Corning".It is also possible to use graft or block copolymers comprising at least one block of the polyorganosiloxane type and at least one polyether. The polyorganopoly-siioxane block can in particular be a polydimethylsiloxane or alternatively a poly (C 2 -C 18 ) alkyl methyl siloxane; the polyether block may be a poly alkylene C z -C a, in particular polyoxyethylene and / or polyoxypropylene. In particular, use may be made of copolyof dimethicones or of alkyl (C 2 ~ C 18 ) copolyol dimethicones such as those sold under the name "Dow Corning 3225C" by the company Dow Corning, lauryl methicones such as those sold under name "Dow Corning Q2-5200 by the company" Dow Corning ".
Comme copolymères blocs greffés ou séquences, on peut citer aussi ceux comprenant au moins un bloc résultant de la polymérisation d'au moins un monomère éthylénique, à une ou plusieurs liaisons éthyléniques éventuellement conjuguées, comme l'éthylène ou les diènes tels que le butadiène et l'isoprène, et d'au moins un bloc d'un polymère vinylique et mieux styrénique. Lorsque le monomère éthylénique comporte plusieurs liaisons éthyléni- ques éventuellement conjuguées, les insaturations éthyléniques résiduelles après la polymérisation sont généralement hydrogénées. Ainsi, de façon connue, la polymérisation de l'isoprène conduit, après hydrogénation, à la formation de bloc éthylène-propylène, et la polymérisation de butadiène conduit, après hydrogénation, à la formation de bloc éthy- iène-butylène. Parmi ces polymères, on peut citer les copolymères séquences, notamment de type "dibloc" ou "tribloc" du type polystyrène/polyisoprène (SI), polysty- rène/polybutadiène (SB) tels que ceux vendus sous le nom de 'LUVITOL HSB" par BASF, du type polystyrène copoly(éthylène-propylène) (SEP) tels que ceux vendus sous le nom de 'Kraton' par Shell Chemical Co ou encore du type polystyrène/copoly(éthylène- butylène) (SEB). En particulier, on peut utiliser le Kraton G1650 (SEBS), le Kraton G1651 (SEBS), le Kraton G1652 (SEBS), le Kraton G1657X (SEBS), le Kraton G1701X (SEP), le Kraton G1702X (SEP), le Kraton G1726X (SEB), le Kraton CM 101 (SBS), le Kraton D- 1102 (SBS), le Kraton D- 107 (SIS). Les polymères sont généralement appelés des copolymères de diènes hydrogénés ou non.As graft or block block copolymers, mention may also be made of those comprising at least one block resulting from the polymerization of at least one ethylenic monomer, with one or more optionally conjugated ethylenic bonds, such as ethylene or dienes such as butadiene and isoprene, and at least one block of a vinyl and better styrenic polymer. When the ethylenic monomer has more than one ethylenic bond that possibly combined, the residual ethylenic unsaturations after the polymerization are generally hydrogenated. Thus, in known manner, the polymerization of isoprene leads, after hydrogenation, to the formation of ethylene-propylene block, and the polymerization of butadiene leads, after hydrogenation, to the formation of ethylene-butylene block. Among these polymers, mention may be made of block copolymers, in particular of the "diblock" or "triblock" type of the polystyrene / polyisoprene (SI), polystyrene / polybutadiene (SB) type such as those sold under the name of "LUVITOL HSB" by BASF, of the polystyrene copoly (ethylene-propylene) type (SEP) such as those sold under the name 'Kraton' by Shell Chemical Co or also of the polystyrene / copoly (ethylene-butylene) (SEB) type. can use Kraton G1650 (SEBS), Kraton G1651 (SEBS), Kraton G1652 (SEBS), Kraton G1657X (SEBS), Kraton G1701X (SEP), Kraton G1702X (SEP), Kraton G1726X (SEB) , Kraton CM 101 (SBS), Kraton D-1102 (SBS), Kraton D-107 (SIS). Polymers are generally called copolymers of hydrogenated or non-hydrogenated dienes.
On peut aussi utiliser les Gelled Permethyl 99A-750, 99A-753-59 et 99A-753-58 (mélange de tribloc et de polymère en étoile), Versagel 5960 de chez Penreco (tribloc + polymère en étoile) ; OS129880, OS129881 et ÛS84383 de chez Lubrizol (copolymère sty- rène/méthacrylate).One can also use Gelled Permethyl 99A-750, 99A-753-59 and 99A-753-58 (mixture of triblock and star polymer), Versagel 5960 from Penreco (triblock + star polymer); OS129880, OS129881 and ÛS84383 from Lubrizol (styrene / methacrylate copolymer).
Comme copolymères blocs greffés ou séquences comprenant au moins un bloc résultant de la polymérisation d'au moins un monomère éthylénique à une ou plusieurs liaisons éthyléniques et d'au moins un bloc d'un polymère acrylique, on peut citer les copolymères bi- ou triséquencés poly(méthy!acrylate de méthyle)/polyisobutylène ou les copolymères greffés à squelette poly(méthylacrylate de méthyle) et à greffons polyisobutylène.As graft or block block copolymers comprising at least one block resulting from the polymerization of at least one ethylenic monomer with one or more ethylenic bonds and of at least one block of an acrylic polymer, mention may be made of bi- or triblock copolymers poly (methyl methyl acrylate) / polyisobutylene or graft copolymers with poly (methyl methyl acrylate) backbone and with polyisobutylene grafts.
Comme copolymères blocs greffés ou séquences comprenant au moins un bloc résultant de la polymérisation d'au moins un monomère éthylénique à une ou plusieurs liaisons éthyléniques et d'au moins un bloc d'un polyéther tel qu'un polylkylène en C2-C18 (poly- éthyléné et/ou polyoxypropyléné notamment), on peut citer (es copolymères bi- ou triséquencés polyoxyéthylène/polybutadiène ou polyoxyéthylène/polyisobutylène.As graft or block block copolymers comprising at least one block resulting from the polymerization of at least one ethylenic monomer with one or more ethylenic bonds and of at least one block of a polyether such as a C 2 -C 18 polykylene (polyethylenated and / or polyoxypropylenated in particular), mention may be made of two or three-block polyoxyethylene / polybutadiene or polyoxyethylene / polyisobutylene copolymers.
Lorsqu'on utilise un polymère statistique en tant que stabilisant, on le choisit de manière à ce qu'il possède une quantité suffisante de groupements le rendant soluble dans le sol- vant de synthèse envisagé.When a random polymer is used as a stabilizer, it is chosen so that it has a sufficient quantity of groups making it soluble in the intended synthetic solvent.
On peut ainsi employer des copolymères à base d'acrylates ou de méthacrylates d'alkyle issus d'alcools en C^C^ et d'acrylates ou de méthacrylates d'alkyle issus d'alcools en C8- C30. On peut en particulier citer le copolymère méthacrylate de stéaryle/méthacryiate de méthyle.It is thus possible to use copolymers based on alkyl acrylates or methacrylates derived from C 1 -C 4 alcohols and alkyl acrylates or methacrylates derived from C 8 -C 30 alcohols. Mention may in particular be made of the stearyl methacrylate / methyl methacryate copolymer.
Lorsque le solvant de synthèse est apolaire, il est préférabfe de choisir en tant que stabilisant, un polymère apportant une couverture des particules la plus complète possible, plusieurs chaînes de polymères-stabilisants venant alors s'adsorber sur une particule de po- lymère obtenu par polymérisation.When the synthetic solvent is apolar, it is preferable to choose as stabilizer, a polymer providing the most complete coverage of the particles possible, several chains of polymer-stabilizers then being adsorbed on a polymer particle obtained by polymerization.
Dans ce cas, on préfère alors utiliser comme stabilisant, soit un polymère greffé, soit un polymère séquence, de manière à avoir une meilleure activité interfaciale. En effet, les séquences ou greffons insolubles dans le solvant de synthèse apportent une couverture plus volumineuse à la surface des particules. Lorsque le solvant de synthèse liquide comprend au moins une huile de silicone, l'agent stabilisant est de préférence choisi dans le groupe constitué par les copolymères blocs greffés ou séquences comprenant au moins un bloc de type polyorganosiloxane et au moins un bloc d'un polymère radicalaire ou d'un polyéther ou d'un polyester comme les blods polyoxypropyléné et/ou oxyéthyléné.In this case, it is then preferred to use, as stabilizer, either a grafted polymer or a block polymer, so as to have better interfacial activity. In fact, the sequences or grafts which are insoluble in the synthesis solvent provide more voluminous coverage on the surface of the particles. When the liquid synthetic solvent comprises at least one silicone oil, the stabilizing agent is preferably chosen from the group consisting of grafted or block block copolymers comprising at least one block of polyorganosiloxane type and at least one block of a polymer radical or of a polyether or of a polyester such as polyoxypropylenated and / or oxyethylenated blods.
Lorsque la phase grasse liquide né comprend pas d'huile de silicone, l'agent stabilisant est de préférence choisi dans le groupe constitué par :When the liquid fatty phase born does not comprise silicone oil, the stabilizing agent is preferably chosen from the group consisting of:
- (a) les copolymères blocs greffés ou séquences comprenant au moins un bloc de type polyorganosiloxane et au moins un bloc d'un polymère radicalaire ou d'un polyéther ou d'un polyester,- (a) grafted or block copolymers comprising at least one block of polyorganosiloxane type and at least one block of a radical polymer or of a polyether or of a polyester,
- (b) les copolymères d'acrylates ou de méthacrylates d'alkyle issus d'alcools en C C4, et d'acrylates ou de méthacrylates d'alkyle issus d'alcools en C8-C30,(b) copolymers of alkyl acrylates or methacrylates derived from CC 4 alcohols, and alkyl acrylates or methacrylates derived from C 8 -C 30 alcohols,
- (c) les copolymères blocs greffés ou séquences comprenant au moins un bloc résultant de la polymérisation d'au moins un monomère éthylénique, à liaisons éthyléniques conjuguées, et au moins un bloc d'un polymère vinylique ou acrylique ou d'un polyéther ou d'un polyester, ou leurs mélanges. De préférence, on utilise des polymères dibloc comme agent stabilisant.- (c) grafted or block copolymers comprising at least one block resulting from the polymerization of at least one ethylenic monomer, with conjugated ethylenic bonds, and at least one block of a vinyl or acrylic polymer or of a polyether or polyester, or mixtures thereof. Preferably, diblock polymers are used as the stabilizing agent.
Les dispersions de polymères gélifiées obtenues selon l'invention peuvent alors être utilisées dans une composition notamment cosmétique, dermatologique, pharmaceutique et/ou hygiénique, telle qu'une composition de soin ou de maquillage de la peau ou des lèvres, ou encore une composition capillaire ou une composition solaire ou de coloration ou de bronzage artificiel de la peau.The dispersions of gelled polymers obtained according to the invention can then be used in a composition, in particular cosmetic, dermatological, pharmaceutical and / or hygienic, such as a composition for caring for or making up the skin or the lips, or even a hair composition. or a sunscreen composition or artificial coloring or tanning of the skin.
Suivant l'application, on pourra choisir d'utiliser des dispersions de polymères filmifiables ou non filmifiables, dans des huiles volatiles ou non volatiles.Depending on the application, it will be possible to choose to use dispersions of film-forming or non-film-forming polymers in volatile or non-volatile oils.
Dipersion colloïdaleColloidal dispersion
La composition selon l'invention contient, en outre, des particules solides à température ambiante, dispersées dans le milieu physiologiquement acceptable introduites dans la composition sous forme d'une dispersion colloïdale, appelé aussi "pâte particulaire".The composition according to the invention also contains particles solid at room temperature, dispersed in the physiologically acceptable medium introduced into the composition in the form of a colloidal dispersion, also called "particulate paste".
Par dispersion colloïdale ou "pâte particulaire", on entend au sens de l'invention une dispersion colloïdale concentrée de particules enrobées ou non dans un milieu continu, stabilisées en surface à l'aide d'un agent dispersant. Ces particules peuvent être choisies parmi les pigments, les nacres, les charges solides et leurs mélanges. Ces particules peuvent être de toute forme notamment de forme sphériqué ou allongée comme des fibres. Elles sont insolubles dans le milieu.By colloidal dispersion or "particulate paste" is meant within the meaning of the invention a concentrated colloidal dispersion of particles coated or not in a continuous medium, surface stabilized using a dispersing agent. These particles can be chosen from pigments, nacres, solid fillers and their mixtures. These particles can be of any shape, in particular of spherical or elongated shape like fibers. They are insoluble in the medium.
L'agent dispersant sert à protéger les particules dispersées contre leur agglomération ou floculation. La concentration en dispersant généralement utilisée pour stabiliser une dispersion colloïdale est de 0,3 à 5 mg/m2, de préférence de 0,5 à 4 mg/m2, de surface de particules. Cet agent dispersant peut être un tensioactif, un oligomère, un polymère ou un mélange de plusieurs d'entre eux, portant une ou des fonctionnalités ayant une affinité forte pour la surface des particules à disperser. En particulier, ils peuvent s'accrocher physiquement ou chimiquement à la surface des pigments. Ces dispersants présentent, en outre, au moins un groupe fonctionnel compatible ou soluble dans le milieu continu. En particulier, on utilise les esters de l'acide hydroxy-12 stéarique en particulier et d'acide gras en C8 à C20 et de polyol comme le glycérol, la diglycérine, tel que le stéarate d'acide poly(12-hydroxystéarique) de poids moléculaire d'environ 750g/mole tel que celui vendu sous le nom de Solsperse 21 000 par la société Avecia, le polygycéryl-2 dipolyhydroxys- téarate (nom CTFA) vendu sous la référence Dehymyls PGPH par la société Henkel ou encore l'acide polyhydroxystéarique tel que celui vendu sous la référence Arlacel P100 par la société Uniqema et leurs mélanges.The dispersing agent serves to protect the dispersed particles against their agglomeration or flocculation. The concentration of dispersant generally used to stabilize a colloidal dispersion is 0.3 to 5 mg / m 2 , preferably 0.5 to 4 mg / m 2 , of surface area of particles. This dispersing agent can be a surfactant, an oligomer, a polymer or a mixture of several of them, carrying one or more functionalities having a strong affinity for the surface of the particles to be dispersed. In particular, they can physically or chemically cling to the surface of the pigments. These dispersants also have at least one functional group which is compatible or soluble in the continuous medium. In particular, esters of 12-hydroxy stearic acid in particular and of acid are used. C 8 to C 20 fatty acids and polyol such as glycerol, diglycerin, such as poly (12-hydroxystearic) acid stearate with a molecular weight of approximately 750 g / mole such as that sold under the name of Solsperse 21,000 by the company Avecia, the polygyceryl-2 dipolyhydroxystearate (name CTFA) sold under the reference Dehymyls PGPH by the company Henkel or else the polyhydroxystearic acid such as that sold under the reference Arlacel P100 by the company Uniqema and their mixtures.
Comme autre dispersant utilisable dans la composition de l'invention, on peut citer les dérivés ammonium quaternaire d'acides gras polycondensés comme le Solsperse 17 000 vendu par la société Avecia, les mélanges de poly diméthylsiloxane/oxypropylène tels que ceux vendus par la société Dow Corning sous les références DC2-5185, DC2-5225 C.As another dispersant which can be used in the composition of the invention, mention may be made of quaternary ammonium derivatives of polycondensed fatty acids such as Solsperse 17,000 sold by the company Avecia, mixtures of poly dimethylsiloxane / oxypropylene such as those sold by the company Dow Corning under the references DC2-5185, DC2-5225 C.
L'acide polydihydroxystéarique et les esters de l'acide hydroxy12-stéarique sont de préférence destinés à un milieu hydrocarboné ou fluoré, alors que les mélanges de diméthyl- siloxane oxyéthylène/oxypropyiéné sont de préférence destinés à un milieu silicone.The polydihydroxystearic acid and the esters of hydroxy12-stearic acid are preferably intended for a hydrocarbon or fluorinated medium, while the mixtures of dimethylsiloxane oxyethylene / oxypropyiene are preferably intended for a silicone medium.
La dispersion colloïdale est une suspension de particules de taille généralement micronique (<10 μm) dans un milieu continu. La fraction volumique de particules dans une dispersion concentrée est de 20 % à 40 %, de préférence supérieure à 30 %, ce qui corres- pond à une teneur pondérale pouvant aller jusqu'à 70 % selon la densité des particules.The colloidal dispersion is a suspension of particles of generally micron size (<10 μm) in a continuous medium. The volume fraction of particles in a concentrated dispersion is from 20% to 40%, preferably greater than 30%, which corresponds to a weight content of up to 70% depending on the density of the particles.
Les particules dispersées dans le milieu peuvent être constituées de particules minérales ou organiques ou de leurs mélanges tels que ceux décrits ci-après. Le milieu continu de la pâte peut être quelconque et contenir tout solvant ou corps gras liquide et leurs mélanges. Avantageusement, le milieu liquide de la pâte particulaire est l'un des corps gras liquides ou huiles que l'on souhaite utiliser dans la composition, faisant ainsi partie de la phase grasse liquide. De façon avantageuse, la "pâte particulaire" ou dispersion colloïdale est une "pâte pig- mentaire" contenant une dispersion colloïdale de particules colorées, enrobées ou non, stabilisées en surface. Ces particules colorées sont des pigments, des nacres ou un mélange de pigments et/ou de nacres. Avantageusement, la dispersion colloïdale représente de 0,5 à 60 % en poids de la composition et mieux de 2 à 40 % et encore mieux de 2 à 30 %.The particles dispersed in the medium can consist of mineral or organic particles or their mixtures such as those described below. The continuous medium of the paste can be any and contain any solvent or liquid fatty substance and their mixtures. Advantageously, the liquid medium of the particulate paste is one of the liquid fatty substances or oils which it is desired to use in the composition, thus forming part of the liquid fatty phase. Advantageously, the "particulate paste" or colloidal dispersion is a "pigmentary paste" containing a colloidal dispersion of colored particles, coated or not, surface stabilized. These colored particles are pigments, nacres or a mixture of pigments and / or nacres. Advantageously, the colloidal dispersion represents from 0.5 to 60% by weight of the composition and better still from 2 to 40% and even better still from 2 to 30%.
Les pigments peuvent être blancs ou colorés, minéraux et/ou organiques, interférentiels ou non. On peut citer, parmi les pigments minéraux, le dioxyde de titane, éventuellement traité en surface, les oxydes de zirconium ou de cérium, ainsi que les oxydes de zinc, de fer (noir, jaune ou rouge ou de chrome, le violet de manganèse, le bleu outremer, l'hydrate de chrome et le bleu ferrique. Parmi les pigments organiques, on peut citer le noir de carbone, les pigments de type laques organiques de baryum, strontium, calcium ou aluminium dont celles soumises à une certification par la Food and Drug Administration (FDA) (exemple D&C ou FD&C) et ceux exempts de la certification FDA comme les laques à base de carmin de cochenille. Les pigments peuvent représenter de 0,1 à 50 % en matière active et notamment de 0,5 à 35 % et mieux de 2 à 25 % du poids total de la composition. Les pigments nacrés peuvent être choisis parmi les pigments nacrés blancs tels que le mica recouvert de titane, ou d'oxychlorure de bismuth, les pigments nacrés colorés tels que le mica titane avec des oxydes de fer, le mica titane avec notamment du bleu ferrique ou de l'oxyde de chrome, le mica titane avec un pigment organique du type précité ainsi que les pigments nacrés à base d'oxychlorure de bismuth. Ils peuvent représenter de 0 à 25 % (en matière active) du poids total de la composition et mieux de 0,1 à 15 % (si présents). On peut ainsi utiliser des pigments à propriétés goniochromatiques.The pigments can be white or colored, mineral and / or organic, interference or not. Mention may be made, among the mineral pigments, of titanium dioxide, optionally surface-treated, zirconium or cerium oxides, as well as oxides of zinc, iron (black, yellow or red or chromium, manganese violet , ultramarine blue, chromium hydrate and ferric blue. Among the organic pigments, mention may be made of carbon black, pigments of the organic lacquer type of barium, strontium, calcium or aluminum, including those subject to certification by the Food and Drug Administration (FDA) (example D&C or FD&C) and those exempt from FDA certification such as cochineal carmine lacquers. Pigments can represent from 0.1 to 50% in active matter and in particular 0.5 at 35% and better still from 2 to 25% of the total weight of the composition. The pearlescent pigments can be chosen from white pearlescent pigments such as mica coated with titanium, or bismuth oxychloride, colored pearlescent pigments such as titanium mica with iron oxides, titanium mica with in particular ferric blue or chromium oxide, titanium mica with an organic pigment of the aforementioned type as well as pearlescent pigments based on bismuth oxychloride. They can represent from 0 to 25% (in active material) of the total weight of the composition and better still from 0.1 to 15% (if present). Pigments with goniochromatic properties can thus be used.
Les charges peuvent être minérales ou organiques, lamellaires ou sphériques. On peut citer le talc, le mica, la silice, le kaolin, les poudres de Nylon® (Orgasol® de chez Ato- chem), de poly-β-alanine et de polyéthylène, les poudres de polymères de tétrafluoroé- thyiène (Téflon®), la lauroyl-lysine, l'amidon, le nitrure de bore, les microsphères creuses telles que l'Expancel® (Nobel industrie), le Polytrap® (Dow Corning) et les microbilles de résine de silicone (Tospearls® de Toshiba, par exemple), le carbonate de calcium précipité, le carbonate et l'hydro-carbonate de magnésium, l'hydroxyapatite, les microsphères de silice creuses (Silica Beads® de Maprecos), les microcapsules de verre ou de céramique, les savons métalliques dérivés d'acides organiques carboxyliques ayant de 8 à 22 atomes de carbone, de préférence de 12 à 18 atomes de carbone, par exemple le stéarate de zinc, de magnésium ou de lithium, le laurate de zinc, le myristate de magnésium.The fillers can be mineral or organic, lamellar or spherical. Mention may be made of talc, mica, silica, kaolin, powders of Nylon® (Orgasol® from Atochem), of poly-β-alanine and of polyethylene, the powders of polymers of tetrafluoroethyiene (Teflon ®), lauroyl-lysine, starch, boron nitride, hollow microspheres such as Expancel® (Nobel industry), Polytrap® (Dow Corning) and silicone resin microbeads (Tospearls® from Toshiba , for example), precipitated calcium carbonate, magnesium carbonate and hydro-carbonate, hydroxyapatite, hollow silica microspheres (Silica Beads® from Maprecos), glass or ceramic microcapsules, metallic soaps derivatives of organic carboxylic acids having from 8 to 22 carbon atoms, preferably from 12 to 18 carbon atoms, for example zinc, magnesium or lithium stearate, zinc laurate, magnesium myristate.
De préférence, les charges et les pigments nacrés ou non sont non polymériques. Selon l'invention, la dispersion colloïdale des particules solides est préparée au préalable par mélange des particules solides, du dispersant et du milieu continu de la dispersion, en vue d'obtenir une adsorption du stabilisant sur les particules solides. Cette dispersion est ensuite mélangée aux autres constituants de la composition. Cette étape de préparation préalable de la dispersion de particules solides est nécessaire pour résoudre le problème de la stabilité de la composition. L'ajout simple d'un dispersant dans la composition, sans son adsorption préalable sur les particules solides et en particulier sur (es pigments ne permet pas de résoudre le problème de déstabilisation d'une composition contenant une dispersion de particules de polymères stabilisées en surface. La composition de l'invention peut, entre autre, contenir des colorants solubles dans le milieu physiologique et en particulier des colorants liposolubles ou hydrosolubles.Preferably, the fillers and the pearlescent pigments or not are non-polymeric. According to the invention, the colloidal dispersion of the solid particles is prepared beforehand by mixing the solid particles, the dispersant and the continuous medium of the dispersion, with a view to obtaining adsorption of the stabilizer on the solid particles. This dispersion is then mixed with the other constituents of the composition. This step of prior preparation of the dispersion of solid particles is necessary to solve the problem of the stability of the composition. The simple addition of a dispersant in the composition, without its prior adsorption on the solid particles and in particular on the pigments, does not make it possible to solve the problem of destabilization of a composition containing a dispersion of polymer particles stabilized on the surface. The composition of the invention may, inter alia, contain dyes soluble in the physiological medium and in particular liposoluble or water-soluble dyes.
Les colorants liposolubles sont par exemple le rouge Soudan, le D&C Red n° 17, le D&C Green n° 6, le β-carotène, ('huile de soja, le brun Soudan, le D&C Yellow n° 11, le D&C Violet n° 2, le D&C orange n° 5, le jaune quïnoléine, les bromoacides. Ils peuvent représenter de 0 à 20 % et notamment 0,01 à 20 % du poids de la compositions et mieux de 0,1 à 6 % (si présents). Les colorants hydrosolubles sont par exemple le jus de betterave, le bleu de méthylène et peuvent représenter jusqu'à 6 % du poids total de la composition. La composition de l'invention peut, en outre, contenir un ou plusieurs actifs cosmétiques ou dermatologiques tels que ceux classiquement utilisés.The liposoluble dyes are for example Sudan red, D&C Red n ° 17, D&C Green n ° 6, β-carotene, (soybean oil, Sudan brown, D&C Yellow n ° 11, D&C Violet n ° 2, orange D&C n ° 5, quinoline yellow, bromoacids They can represent from 0 to 20% and in particular 0.01 to 20% of the weight of the composition and better still from 0.1 to 6% (if present The water-soluble dyes are for example beet juice, methylene blue and can represent up to 6% of the total weight of the composition. The composition of the invention can, in addition, contain one or more cosmetic active agents or dermatological such as those conventionally used.
Comme actifs cosmétiques, dermatologiques, hygiéniques ou pharmaceutiques, utilisables dans la composition de l'invention, on peut citer les hydratants, vitamines, acides gras essentiels, sphingolipides, filtres solaires. Ces actifs sont utilisés en quantité habituelle pour l'homme de l'art et notamment à des concentrations de 0 à 20 % et notamment de 0,001 à 15 % du poids total de l'a composition.As cosmetic, dermatological, hygienic or pharmaceutical active agents which can be used in the composition of the invention, mention may be made of moisturizers, vitamins, essential fatty acids, sphingolipids, sun filters. These assets are used in the usual amount for those skilled in the art and especially at concentrations of 0 to 20% and especially from 0.001 to 15% by total weight of a composition.
Le polymère de la composition de l'invention permet la formation d'un film sur la peau, les lèvres et/ou les phanères, formant un réseau piégeant les matières colorantes (y compris les charges) et/ou les actifs. Selon la quantité relative de matières colorantes, utilisée par rapport à la quantité de polymère stabilisé, utilisée, il est possible d'obtenir un film plus ou moins briffant, de bonne tenue, résistant à l'eau, de couleur homogène.The polymer of the composition of the invention allows the formation of a film on the skin, the lips and / or the integuments, forming a network trapping the coloring matters (including the fillers) and / or the active agents. Depending on the relative amount of coloring matter used by relative to the amount of stabilized polymer used, it is possible to obtain a more or less briffant film, of good performance, water resistant, of uniform color.
La composition selon l'invention peut, de plus, comprendre, selon le type d'application en- visagée, les constituants classiquement utilisés dans les domaines considérés, qui sont présents en une quantité appropriée à la forme galénique souhaitée.The composition according to the invention can, moreover, comprise, depending on the type of application envisaged, the constituents conventionally used in the fields under consideration, which are present in an amount appropriate to the desired dosage form.
En particulier, elle peut comprendre, outre, la phase grasse liquide dans laquelle les particules de polymère sont stabilisées des phases grasses additionnelles qui peuvent être choisies parmi les cires, les huiles, les gommes et/ou les corps gras pâteux, hydrocarbonés, siliconés et/ou fluorés, d'origine végétale, animale, minérale ou de synthèse et leurs mélanges.In particular, it can comprise, in addition, the liquid fatty phase in which the polymer particles are stabilized, additional fatty phases which can be chosen from waxes, oils, gums and / or pasty fatty, hydrocarbon-based, silicone and / or fluorinated, of vegetable, animal, mineral or synthetic origin and their mixtures.
Parmi les cires solides à température ambiante, susceptibles d'être présentes dans la composition selon l'invention, on peut citer les cires hydrocarbonées telles que la cire d'abeilles, la cire de Carnauba, de Candellila, d'Ouricoury, du Japon, les cires de fibres de liège ou de canne à sucre, les cires de paraffine, de lignite, les cires microcristallines, la cire de lanoline, la cire de Montan, les ozokérites, les cires de polyéthylène, les cires obtenues par synthèse de Fischer-Tropsch, les huiles hydrogénées, les esters gras et les glycérides concrets à 25°C. On peut également utiliser des cires de silicone, parmi lesquelles on peut citer les alkyl, alcoxy et/ou esters de polyméthylsiloxane. Les cires peuvent se présenter sous forme de dispersions stables de particules colloïdales de cire telles qu'elles peuvent être préparées selon des méthodes connues, telles que celles de "Microemulsions Theory and Practice", L. M. Prince Ed., Académie Press (1977), pages 21-32. De préférence, les cires utilisées ont une température de fusion au moins égale à 45°C.Among the waxes solid at room temperature, which may be present in the composition according to the invention, mention may be made of hydrocarbon waxes such as beeswax, Carnauba, Candellila, Ouricoury, Japanese wax, cork or sugar cane fiber waxes, paraffin waxes, lignite waxes, microcrystalline waxes, lanolin wax, Montan wax, ozokerites, polyethylene waxes, waxes obtained by Fischer synthesis Tropsch, hydrogenated oils, fatty esters and concrete glycerides at 25 ° C. It is also possible to use silicone waxes, among which mention may be made of alkyl, alkoxy and / or polymethylsiloxane esters. The waxes can be in the form of stable dispersions of colloidal particles of wax as they can be prepared according to known methods, such as those of "Microemulsions Theory and Practice", LM Prince Ed., Académie Press (1977), pages 21-32. Preferably, the waxes used have a melting temperature at least equal to 45 ° C.
Les cires peuvent être présentes à raison de 0-50% en poids dans la composition et mieux de 5 à 25%, en vue de ne pas trop diminuer la brillance de la composition et du film déposé sur les lèvres et/ou la peau.The waxes can be present in an amount of 0-50% by weight in the composition and better still from 5 to 25%, in order not to decrease too much the gloss of the composition and of the film deposited on the lips and / or the skin.
La composition peut comprendre, en outre, tout autre additif usuellement utilisé dans de telles compositions, tel que de l'eau, des épaississants d'huile ou de phase aqueuse, des antioxydants, des parfums,, des conservateurs, des tensioactifs, des huiles essentielles, des polymères liposolubles (copolymère de PolyVinyIPyrrolidone/eicosène).The composition can also comprise any other additive usually used in such compositions, such as water, oil or aqueous thickeners, antioxidants, perfumes, preservatives, surfactants, oils essential, liposoluble polymers (PolyVinyIPyrrolidone / eicosene copolymer).
Dans un mode de réalisation particulier de l'invention, .les compositions selon l'invention peuvent être préparées de manière usuelle par l'homme du métier. Elles peuvent se présenter sous forme d'un produit coulé et par exemple sous la forme d'un stick ou bâton, ou sous la forme de coupelle utilisable par contact direct ou à l'éponge. En particulier, elles trouvent une application en tant que fond de teint coulé, fard à joues ou à paupières coulé, rouge à lèvres, base ou baume de soin pour les lèvres, produit anti-cernes. Elles peuvent aussi se présenter sous forme d'une pâte souple ou encore de gel, de crème plus ou moins fluide. Elles peuvent alors constituer des fonds de teint ou des rouges à lèvres, des produits solaires ou de coloration de la peau.In a particular embodiment of the invention, the compositions according to the invention can be prepared in the usual manner by a person skilled in the art. They can be in the form of a cast product and for example in the form of a stick or stick, or in the form of a dish usable by direct contact or with a sponge. In particular, they find application as a poured foundation, blush or eyeshadow, lipstick, base or lip care balm, concealer product. They can also be in the form of a flexible paste or else a gel, a more or less fluid cream. They can then constitute foundations or lipsticks, sunscreen or skin coloring products.
Les compositions de l'invention sont avantageusement anhydres et peuvent contenir moins de 5 % d'eau par rapport au poids total de la composition. Elles peuvent alors se présenter notamment sous forme de gel huileux, de liquide huileux ou huile, de pâte ou de stick ou encore sous forme de dispersion vésiculaire contenant des lipides ioniques et/ou non ioniques. Elles peuvent aussi se présenter sous forme d'une émulsion simple ou multiple à phase continue huileuse ou aqueuse, de dispersion huileuse dans une phase aqueuse grâce à des vésicules contenant des lipides ioniques et/ou non ioniques. Ces formes galéniques sont préparées selon les méthodes usuelles des domaines considérés.The compositions of the invention are advantageously anhydrous and can contain less than 5% of water relative to the total weight of the composition. They can then be in particular in the form of an oily gel, an oily liquid or oil, a paste or a stick or also in the form of a vesicular dispersion containing ionic and / or nonionic lipids. They can also be in the form of a single or multiple emulsion with an oily or aqueous continuous phase, an oily dispersion in a phase aqueous thanks to vesicles containing ionic and / or nonionic lipids. These dosage forms are prepared according to the usual methods of the fields considered.
Ces compositions à application topique peuvent constituer notamment une composition cosmétique, dermatologique, hygiénique ou pharmaceutique de protection, de traitement ou de soin pour le visage, pour le cou, pour les mains ou pour le corps (par exemple crème de soin, huile solaire, gel corporel), une composition de maquillage (par exemple gel de maquillage, crème, stick) ou une composition de bronzage artificiel ou de protection de la peau.These compositions for topical application may especially constitute a cosmetic, dermatological, hygienic or pharmaceutical composition for protection, treatment or care for the face, for the neck, for the hands or for the body (for example care cream, sun oil, body gel), a makeup composition (for example makeup gel, cream, stick) or an artificial tanning or skin protection composition.
La composition selon l'invention peut se présenter sous la forme d'une composition dermatologique ou de soin de la peau et/ou des phanères ou sous forme d'une composition de protection solaire, d'hygiène corporelle, notamment sous forme de déodorant. Elle se présente alors notamment sous forme non colorée. Elle peut alors être utilisée comme base de soin pour la peau, les phanères ou les lèvres (baumes à lèvres, protégeant les lèvres du froid et/ou du soleil et ou du vent, crème de soin pour la peau, les ongles ou les cheveux).The composition according to the invention may be in the form of a dermatological composition or for caring for the skin and / or integuments or in the form of a composition for sun protection, for personal hygiene, in particular in the form of a deodorant. It is then presented in particular in non-colored form. It can then be used as a care base for the skin, the integuments or the lips (lip balms, protecting the lips from the cold and / or the sun and / or the wind, care cream for the skin, the nails or the hair. ).
La composition de l'invention peut également se présenter sous la forme d'un produit colo- ré en particulier de maquillage de la peau, présentant éventuellement des propriétés de soin ou de traitement, et en particulier un fond de teint, un blush, un fard à joues ou à paupières, un produit anti-cerne, un eye-liner, un produit de maquillage du corps ; de maquillage des lèvres comme un rouge à lèvres, un brillant à lèvres ou un crayon à lèvres présentant éventuellement des propriétés de soin ou de traitement ; de maquillage des pha- nères comme les ongles, les cils sous forme de mascara, les sourcils et les cheveux.The composition of the invention may also be in the form of a colored product in particular for making up the skin, optionally having care or treatment properties, and in particular a foundation, a blush, a blush or eyeshadow, concealer, eyeliner, body makeup; lip makeup such as a lipstick, a lip gloss or a lip pencil possibly having care or treatment properties; make-up of headlights such as nails, eyelashes in the form of mascara, eyebrows and hair.
Bien entendu la composition de l'invention doit être cosmétiquement ou dermatologique- ment acceptable, à savoir contenir un milieu physioiogiquement acceptable non toxique et susceptible d'être appliqué sur la peau, les phanères ou les lèvres du visage d'êtres hu- mains. Par cosmétiquement acceptable, on entend au sens de l'invention une composition d'aspect, d'odeur et de toucher agréables.Of course, the composition of the invention must be cosmetically or dermatologically acceptable, ie contain a physiologically acceptable medium which is non-toxic and capable of being applied to the skin, the integuments or the lips of the face of human beings. By cosmetically acceptable is meant within the meaning of the invention a composition of pleasant appearance, odor and feel.
Bien entendu l'homme du métier veillera à choisir ce ou ces éventuels composés complémentaires, et/ou leur quantité, de manière telle que les propriétés avantageuses de la composition selon l'invention ne soient pas, ou substantiellement pas, altérées par l'adjonction envisagée.Of course, those skilled in the art will take care to choose this or these optional additional compounds, and / or their quantity, in such a way that the advantageous properties of the composition according to the invention are not, or not substantially, affected by the addition considered.
L'invention est illustrée plus en détail dans les exemples suivants. Les pourcentages sont des pourcentages en poids.The invention is illustrated in more detail in the following examples. The percentages are percentages by weight.
Exemple 1 de dispersion de polymèreExample 1 of polymer dispersion
On prépare une dispersion de polyméthacrylate de méthyle réticulé par du diméthacrylate d'éthylène glycol, dans du polyisobutène hydrogéné (à 6-8 moles d'isobutylène) vendu sous le nom Parieam par la société Nippon Oil Fat, selon la méthode de l'exemple 2 du document EP-A-749 746, en remplaçant L'Isopar L par le Parieam. On obtient ainsi une dispersion de particules de polyméthacrylate de méthyle stabilisées en surface dans du Parieam par un copolymère dibloc séquence polystyrène/copoly(éhylène-propylène) vendu sous le nom de Kraton G1701 (Shell), ayant un taux de matière sèche de 22-25% en poids et une Tg de 100°C. Ce copolymère est non filmifiable à température ambiante.A dispersion of polymethyl methacrylate crosslinked with ethylene glycol dimethacrylate is prepared in hydrogenated polyisobutene (containing 6-8 moles of isobutylene) sold under the name Parieam by the company Nippon Oil Fat, according to the method of the example. 2 of document EP-A-749 746, by replacing Isopar L with the Parieam. A dispersion of polymethyl methacrylate particles stabilized on the surface in Parieam is thus obtained by a polystyrene / copoly (ethylene-propylene) block copolymer sold under the name Kraton G1701 (Shell), having a dry matter content of 22- 25% by weight and a Tg of 100 ° C. This copolymer is not film-forming at room temperature.
Cette dispersion est préparée au préalable avant son mélange avec les autres constituants de la composition selon l'invention Exemple 2 de dispersion de polymèreThis dispersion is prepared beforehand before it is mixed with the other constituents of the composition according to the invention. Example 2 of polymer dispersion
On prépare une dispersion de copolymère non réticulé d'acrylate de méthyle et d'acide acrylique dans un rapport 85/15, dans du Parieam, selon la méthode de l'exemple 1 du document EP-A-749 746, en remplaçant l'heptane par le Parieam. On obtient ainsi une dispersion de particules de poly(acrylate de méthyle/acide acrylique) stabilisées en surface dans le Parieam par un copolymère dibloc séquence polystyrène/copoly(éhylène- propylène) vendu sous le nom de Kraton G1701 (Shell), ayant un taux de matière sèche de 22-25% en poids et une taille moyenne de particules de 165 nm (polydispersité : 0,05) et une Tg de 13°C. Ce copolymère est filmifiable.A dispersion of uncrosslinked copolymer of methyl acrylate and acrylic acid in an 85/15 ratio is prepared in Parieam, according to the method of example 1 of document EP-A-749 746, replacing the heptane by the Parieam. This gives a dispersion of poly (methyl acrylate / acrylic acid) particles surface stabilized in Parieam by a diblock block polystyrene / copoly (ethylene-propylene) copolymer sold under the name Kraton G1701 (Shell), having a dry matter of 22-25% by weight and an average particle size of 165 nm (polydispersity: 0.05) and a Tg of 13 ° C. This copolymer is film-forming.
Cette dispersion est préparée au préalable avant son mélange avec les autres constituants de la composition selon l'invention.This dispersion is prepared beforehand before it is mixed with the other constituents of the composition according to the invention.
Contre-exemple 1 : rouge à lèvresCounterexample 1: lipstick
Phase APhase A
Cire de polyéthylène 13 % Cire de camauba 2 %Polyethylene wax 13% Camauba wax 2%
Malate de di-isostéaryle 6 % Dispersion de l'exemple 2 50 % Parieam 3 %Di-isostearyl malate 6% Dispersion of Example 2 50% Parieam 3%
Phase BPhase B
Lanoline 6 . %Lanolin 6. %
Pigments 8,66 %Pigments 8.66%
Dispersant 2 %Dispersing 2%
Parieam 9,34 %Parieam 9.34%
Dans un poêlon, on introduit tous les composants de la phase A que ('on chauffe à 100°C sous agitation magnétique afin d'obtenir un mélange homogène. La phase B est ensuite broyée dans un broyeur tricylindre. On ajoute alors ce broyage à la phase A. Le mélange est laissé sous agitation pendant 1 heure puis coulé dans des moules de rouge à lèvres appropriés. Le mélange est laissé sous agitation pendant une heure puis coulé dans des moules de rouge à lèvres appropriés. Les moules sont ensuite placés au congélateur à - 18°C pendant 30 minutes. On obtient un stick de rouge à lèvres.In a pan, all the components of phase A are introduced (which are heated to 100 ° C. with magnetic stirring in order to obtain a homogeneous mixture. Phase B is then ground in a three-cylinder mill. This grinding is then added to phase A. The mixture is left under stirring for 1 hour and then poured into suitable lipstick molds. The mixture is left under stirring for 1 hour and then poured into suitable lipstick molds. freezer at -18 ° C for 30 minutes to obtain a lipstick stick.
Lorsqu'on introduit la phase B (broyage de pigment à la tricylindre), on note un virage de la teinte à chaud. Une fois mise en forme dans les moules, cette formule se présente sous l'aspect d'un stick inhomogène en surface : présence de marbrures sur le stick.When phase B (grinding of pigment in the three-cylinder) is introduced, there is a change in color when hot. Once shaped in the molds, this formula looks like an inhomogeneous stick on the surface: presence of mottling on the stick.
Exemple 3 : rouge à lèvres >Example 3: lipstick>
Phase APhase A
Cire de polyéthylène 13 % Cire de camauba 2 %Polyethylene wax 13% Camauba wax 2%
Mafate de di-isostéaryle 6 % Dispersion de l'exemple 2 50 % Parieam 5,28 %Di-isostearyl mafate 6% Dispersion of Example 2 50% Parieam 5.28%
Phase BPhase B
Lanoline 6 %Lanolin 6%
Pâte pigmentaire 17,72 % Dans un poêlon on introduit tous les composants de la phase'A que l'on chauffe à 100°C sous agitation magnétique afin d'obtenir un mélange homogène. On ajoute alors la phase B correspondant à la pâte pigmentaire, mélangée à la lanoline .La pâte pigmentaire contient 8,66 % de pigments, 0,58 % de stéarate d'acide poly(12-hydroxystéarique) et 8,48 % de Parieam. Lorsqu'on introduit la pâte pigmentaire dans la phase A, on note que le virage de la teinte est moins prononcé que dans le mélange du contre-exemple. Le mélange est laissé sous agitation pendant une heure puis coulé dans des moules de rouge à lèvres appropriés. Les moules sont ensuite placés au congélateur à - 18°C pendant 30 minutes. Le stick de rouge à lèvres obtenu ne présente pas de marbrures et est homogène en teinte. Il conduit à un dépôt coloré sur les lèvres de bonne tenue, ne migrant pas, confortable et homogène. Cette différence d'aspect est due à l'adsorption du dispersant au préalable sur les pigments avant son introduction dans le mélange fondu des autres ingrédients de la composition. Contre-exemple 2 : Rouge à lèvresPigment paste 17.72% All the components of phase ' A are introduced into a pan which is heated to 100 ° C. with magnetic stirring in order to obtain a homogeneous mixture. Phase B corresponding to the pigment paste, mixed with lanolin is then added. The pigment paste contains 8.66% of pigments, 0.58% of poly (12-hydroxystearic) acid stearate and 8.48% of Parieam . When the pigment paste is introduced in phase A, it is noted that the color change is less pronounced than in the mixture of the counterexample. The mixture is left under stirring for one hour and then poured into suitable lipstick molds. The molds are then placed in the freezer at -18 ° C for 30 minutes. The lipstick stick obtained has no mottling and is uniform in color. It leads to a colored deposit on the lips of good behavior, not migrating, comfortable and homogeneous. This difference in appearance is due to the adsorption of the dispersant beforehand on the pigments before its introduction into the molten mixture of the other ingredients of the composition. Counterexample 2: Lipstick
Phase APhase A
Cire de polyéthylène 13 %13% polyethylene wax
Cire de camauba 2 % Malate de di-isostéaryle 6 %Camauba wax 2% Di-isostearyl malate 6%
Dispersion de l'exemple 2 50 %Dispersion of Example 2 50%
Parieam 9 %Parieam 9%
Phase B Pigments 8,66 %Phase B Pigments 8.66%
Dispersant 2 %Dispersing 2%
Parieam 9,34 %Parieam 9.34%
Le mode opératoire et ('aspect du rouge à lèvres sont identiques à ceux du rouge à lèvres du contre-exemple 1.The procedure and the appearance of the lipstick are identical to those of the lipstick of counterexample 1.
Exemple 4 : Rouge à lèvresExample 4: Lipstick
Phase APhase A
Cire de polyéthylène 13 % Cire de camauba 2 %Polyethylene wax 13% Camauba wax 2%
Malate de di-isostéaryle 6 %Di-isostearyl malate 6%
Dispersion de l'exemple 2 50 %Dispersion of Example 2 50%
Phase B Parieam 11,3 %Phase B Parieam 11.3%
Pâte pigmentaire > 17,7 %Pigment paste> 17.7%
Dans un poêlon on introduit tous les composants de la phase A que l'on chauffe à 100°C sous agitation magnétique afin d'obtenir un mélange homogène. On ajoute alors la phase B correspondant à la pâte pigmentaire, mélangée Parieam. La pâte pigmentaire contient 8,66 % de pigments, 0,58 % de stéarate d'acide poly(12-hydroxystéarique) et 8,48 % de Parieam. Le stick obtenu ne présente pas de marbrures et est homogène en teinte. Son application est aisée : le dépôt obtenu est confortable, homogène, brillant, non migrant et de bonne tenue notamment en couleur. All the components of phase A are introduced into a pan, which is heated to 100 ° C. with magnetic stirring in order to obtain a homogeneous mixture. Phase B corresponding to the pigment paste, Parieam mixed, is then added. The pigment paste contains 8.66% of pigments, 0.58% of poly (12-hydroxystearic acid) stearate and 8.48% of Parieam. The stick obtained has no mottling and is uniform in color. Its application is easy: the deposit obtained is comfortable, homogeneous, shiny, non-migrating and of good performance, especially in color.

Claims

REVENDICATIONS
1. Composition à application sur les matières kératiniques, comprenant un milieu physio- logiquement acceptable contenant au moins une phase grasse liquide, une dispersion colloïdale de particule solides à température ambiante et une dispersion de particules de polymère stabilisées en surface dans ladite phase grasse liquide par un stabilisant.1. Composition for application to keratin materials, comprising a physiologically acceptable medium containing at least one liquid fatty phase, a colloidal dispersion of particles solid at room temperature and a dispersion of polymer particles stabilized on the surface in said liquid fatty phase by a stabilizer.
2. Composition selon la revendication 1 , caractérisée en ce que les particules de la dispersion colloïdale sont des particules choisies parmi les pigments, des nacres, (es char- ges et leurs mélanges.2. Composition according to claim 1, characterized in that the particles of the colloidal dispersion are particles chosen from pigments, nacres, (fillers and their mixtures).
3. Composition selon la revendication 1 ou 2, caractérisée en ce que les particules de la dispersion colloïdale contiennent des particules colorées. 3. Composition according to claim 1 or 2, characterized in that the particles of the colloidal dispersion contain colored particles.
4. Composition selon l'une des revendications précédentes, caractérisée en ce que la dispersion colloïdale représente de 0,5 à 60 % en poids de la composition et mieux de 2 à 40 % et mieux encore de 2 à 50 %.4. Composition according to one of the preceding claims, characterized in that the colloidal dispersion represents from 0.5 to 60% by weight of the composition and better still from 2 to 40% and better still from 2 to 50%.
5. Composition selon l'une des revendications précédentes, caractérisée en ce que la dispersion colloïdale comprend un dispersant des particules.5. Composition according to one of the preceding claims, characterized in that the colloidal dispersion comprises a dispersant of the particles.
6. Composition selon la revendication 5, caractérisée en ce que le dispersant représente de 0,3 à 5 mg/m2, de préférence de 0,5 à 4 mg/m2, de surface de particules. 6. Composition according to claim 5, characterized in that the dispersant represents from 0.3 to 5 mg / m 2 , preferably from 0.5 to 4 mg / m 2 , of surface of particles.
7. Composition selon la revendication 5 ou 6, caractérisée en ce que le dispersant est choisi parmi le stéarate de l'acide poly(12-hydroxystéarique), l'acide poly (12- hydroxystéarique), le 2-dipolyhydroxystéarate de diglycéryle et leurs mélanges.7. Composition according to claim 5 or 6, characterized in that the dispersant is chosen from poly (12-hydroxystearic acid) stearate, poly (12-hydroxystearic acid), diglyceryl 2-dipolyhydroxystearate and their mixtures.
8. Composition selon l'une des revendications précédentes, caractérisée en ce que la dispersion colloïdale contient un corps gras liquide à température ambiante faisant partie de la phase grasse liquide.8. Composition according to one of the preceding claims, characterized in that the colloidal dispersion contains a fatty substance liquid at room temperature forming part of the liquid fatty phase.
9. Composition selon l'une des revendications précédentes, caractérisée en ce que le polymère en dispersion est filmifiable.9. Composition according to one of the preceding claims, characterized in that the polymer in dispersion is film-forming.
10. Composition selon l'une des revendications précédentes, dans laquelle au moins un ingrédient choisi parmi les actifs cosmétiques, dermatologiques, et leurs mélanges est prévu. 10. Composition according to one of the preceding claims, in which at least one ingredient chosen from cosmetic and dermatological active agents and their mixtures is provided.
11. Composition selon l'une des revendications précédentes, dans laquelle le polymère en dispersion est choisi parmi (es polymères radicalaires, les polycondensats, les polymères d'origine naturelle et leurs mélanges.11. Composition according to one of the preceding claims, in which the polymer in dispersion is chosen from (radical polymers, polycondensates, polymers of natural origin and their mixtures.
12. Composition selon l'une des revendications précédentes, dans laquelle le polymère en dispersion est choisi parmi les polyuréthannes, polyuréthannes-acryliques* polyurées, polyurèe/polyuréthannes, polyester-polyuréthannes, polyéther-polyuréthannes, polyesters, polyesters amides, polyesters à chaîne grasse, alkydes ; polymères ou copolymères acryliques et/ou vinyliques ; copolymères acryliques-silicone ; polyacrylamides ; polymères siliconés, polymères fluorés et leurs mélanges. 12. Composition according to one of the preceding claims, in which the polymer in dispersion is chosen from polyurethanes, polyurethanes-acrylics * polyureas, polyurethanes / polyurethanes, polyester-polyurethanes, polyether-polyurethanes, polyesters, polyester amides, polyesters with a fatty chain. , alkyds; acrylic and / or vinyl polymers or copolymers; acrylic-silicone copolymers; polyacrylamides; silicone polymers, fluoropolymers and mixtures thereof.
13. Composition selon l'une des revendications précédentes, dans laquelle la phase grasse liquide est constituée d'huiles d'origine minérale, animale, végétale ou synthétique, carbonées, hydrocarbonées, fluorées et/ou siliconées, seules ou en mélange. 13. Composition according to one of the preceding claims, in which the liquid fatty phase consists of oils of mineral, animal, vegetable or synthetic origin, carbonaceous, hydrocarbon-based, fluorinated and / or silicone-based, alone or as a mixture.
14. Composition selon l'une des revendications précédentes, dans laquelle la phase grasse liquide est choisie parmi les huiles de paraffine ou de vaseline, les isoparaffines volatiles ou non, l'huile de vison, de tortue, de soja, le perhydrosqualène, l'huile d'amande douce, de calophyllum, de palme, de parieam, de pépins de raisin, de sésame, de colza, de tournesol, de coton, d'abricot, de ricin, d'avocat, de jojoba, d'olive ou de germes de cé- réaies ; des esters d'acide lanolique, d'acide oléique, d'acide laurique, d'acide stéarique ; le myristate d'isopropyle, le palmitate d'isopropyle, le stéarate de butyle, le laurate d'hexyle, l'adipate de diisopropyle, l'isononate d'isononyle, le palmitate de 2-éthyl-hexyle, le laurate de 2-hexyl-décyle, le palmitate de 2-octyl-décyle, le myristate ou le lactate de 2- octyl-dodécyle, le succinate de 2-diéthyl-hexyle, le malate de diisostéaryle, le triisostéa- rate de glycérine ou de diglycérine ; l'acide myristique, l'acide palmitique, l'acide stéarique, l'acide béhénique, l'acide oléique, l'acide linoléique, l'acide linolénique ou l'acide isostéarique ; l'alcool stéarylique ou oléique, linoléique, linolénique, isostéarique ou octyl dodécanol ; les huiles siliconées volatiles ou non de type PDMS éventuellement phénylés ou éventuellement substitués par des groupements aliphatiques et/ou aromatiques, ou par des groupements fonctionnels ; les polysiloxanes modifiés par des acides gras, des alcools gras ou des polyoxyalkylènes ; les siliconés fluorées, les huiles perfluorées et leurs mélanges.14. Composition according to one of the preceding claims, in which the liquid fatty phase is chosen from paraffin or petrolatum oils, isoparaffins, volatile or not, mink, turtle, soybean oil, perhydrosqualene, l oil of sweet almond, calophyllum, palm, parieam, grape seed, sesame, rapeseed, sunflower, cotton, apricot, castor, avocado, jojoba, olive or of sprouts of cairies; esters of lanolic acid, oleic acid, lauric acid, stearic acid; isopropyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, diisopropyl adipate, isononyl isononate, 2-ethylhexyl palmitate, 2- laurate hexyl-decyl, 2-octyl-decyl palmitate, 2-octyl-dodecyl myristate or lactate, 2-diethyl-hexyl succinate, diisostearyl malate, glycerin or diglycerin triisostearate; myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, linoleic acid, linolenic acid or isostearic acid; stearyl or oleic, linoleic, linolenic, isostearic or octyl dodecanol alcohol; volatile or non-PDMS type silicone oils optionally phenylated or optionally substituted by aliphatic and / or aromatic groups, or by functional groups; polysiloxanes modified with fatty acids, fatty alcohols or polyoxyalkylenes; fluorinated silicones, perfluorinated oils and their mixtures.
15. Composition selon l'une des revendications précédentes, caractérisée en ce que la phase .grasse contient au moins une huile non volatile à température ambiante et pression atmosphérique.15. Composition according to one of the preceding claims, characterized in that the fatty phase contains at least one non-volatile oil at room temperature and atmospheric pressure.
16. Composition selon ('une des revendications précédentes, dans laquelle le stabilisant est choisi parmi les polymères séquences, les polymères greffés, les polymères statisti- ques et leurs mélanges.16. Composition according to (one of the preceding claims, in which the stabilizer is chosen from block polymers, graft polymers, static polymers and their mixtures.
17. Composition selon l'une des revendications précédentes, dans laquelle le stabilisant est choisi parmi les polymères siliconés greffés avec une chaîne hydrocarbonée ; les polymères hydrocarbonés greffés avec une chaîne siiiconée ; les copolymères greffés ayant un squelette insoluble de type polyacryiique avec des greffons solubles de type acide poly-12(hydroxystéarique) ; les copolymères blocs greffés ou séquences comprenant au moins un bloc de type polyorganosiloxane et au moins .un bloc d'un polymère radicalaire ; les copolymères blocs greffés ou séquences comprenant au moins un bloc de type polyorganosiloxane et au moins d'un polyéther ; les copolymères d'acrylates ou de métha- crylates d'alkyle en CrC4, ou d'acrylates ou de méthacrylates d'alkyle en C8-C3Q ; les copolymères blocs greffés ou séquences comprenant au moins un bloc résultant de la polymérisation de monomères éthyléniques comportant éventuellement des liaisons conjuguées et au moins un bloc d'un polymère vinylique ; les copolymères blocs greffés ou séquences comprenant au moins un bloc résultant de la polymérisation de monomères éthyléniques comportant éventuellement des liaisons conjuguées et au moins un bloc d'un polymère acrylique ; les copolymères blocs greffés ou séquences comprenant au moins un bloc résultant de la polymérisation de diène et au moins un bloc d'un polyéther, et leurs mélanges. 17. Composition according to one of the preceding claims, in which the stabilizer is chosen from silicone polymers grafted with a hydrocarbon chain; hydrocarbon polymers grafted with a siiiconée chain; grafted copolymers having an insoluble backbone of polyacrylic type with soluble grafts of poly-12 (hydroxystearic) acid type; grafted or block copolymers comprising at least one block of polyorganosiloxane type and at least one block of a radical polymer; grafted or block copolymers comprising at least one block of polyorganosiloxane type and at least one polyether; copolymers of acrylates or alkyl methacrylates of C r C 4, or of acrylates or alkyl methacrylates of C 8 -C 3Q; graft or block block copolymers comprising at least one block resulting from the polymerization of ethylenic monomers optionally comprising conjugated bonds and at least one block of a vinyl polymer; graft or block block copolymers comprising at least one block resulting from the polymerization of ethylenic monomers optionally comprising conjugated bonds and at least one block of an acrylic polymer; graft or block block copolymers comprising at least one block resulting from the polymerization of diene and at least one block of a polyether, and their mixtures.
18. Composition selon l'une des revendications précédentes, caractérisée en ce que le stabilisant est un polymère bloc greffé ou séquence, comprenant au moins un bloc résultant de la polymérisation de diène et au moins un bloc d'un polymère vinylique. 18. Composition according to one of the preceding claims, characterized in that the stabilizer is a graft or block block polymer, comprising at least one block resulting from the polymerization of diene and at least one block of a vinyl polymer.
19. Composition selon l'une des revendications précédentes, dans laquelle le stabilisant est un polymère dibloc. 19. Composition according to one of the preceding claims, in which the stabilizer is a diblock polymer.
20. Composition selon l'une des revendications précédentes, comprenant, en outre, au moins une phase grasse additionnelle choisie parmi les cires, les gommes et/ou les corps gras pâteux, hydrocarbonés, siliconés et/ou fluorés d'origine végétale, animale, minérale ou de synthèse, et leurs mélanges. 20. Composition according to one of the preceding claims, further comprising at least one additional fatty phase chosen from waxes, gums and / or pasty, hydrocarbon, silicone and / or fluorinated fatty substances of vegetable or animal origin. , mineral or synthetic, and mixtures thereof.
21. Composition selon l'une des revendications précédentes, caractérisée en ce que le polymère en dispersion représente (en matière sèche) jusqu'à 60 % du poids total de la composition.21. Composition according to one of the preceding claims, characterized in that the polymer in dispersion represents (in dry matter) up to 60% of the total weight of the composition.
22. Composition selon l'une des revendications précédentes, caractérisée en ce que le polymère en dispersion représente (en matière sèche) de 2 à 60 % du poids total de la composition, de préférence-de 4 à 2,5.22. Composition according to one of the preceding claims, characterized in that the polymer in dispersion represents (in dry matter) from 2 to 60% of the total weight of the composition, preferably from 4 to 2.5.
23. Composition selon l'une des revendications précédentes, se présentant sous forme d'un stick ou bâton, sous forme d'une pâte souple, sous forme de coupelle, de gel huileux, de liquide huileux, de dispersion vésiculaire contenant des lipides ioniques et/ou non ioniques, d'émulsion eau-dans-huile, huile-dans-eau ou multiple.23. Composition according to one of the preceding claims, which is in the form of a stick or stick, in the form of a flexible paste, in the form of a cup, of oily gel, of oily liquid, of vesicular dispersion containing ionic lipids. and / or nonionic, water-in-oil, oil-in-water or multiple emulsion.
24. Composition selon l'une des revendications précédentes, se présentant sous forme anhydre.24. Composition according to one of the preceding claims, which is in anhydrous form.
25. Composition selon l'une des revendications précédentes, se présentant sous fa forme d'un produit de soin et/ou de maquillage de la peau et/ou des lèvres.25. Composition according to one of the preceding claims, which is in the form of a product for caring for and / or making up the skin and / or the lips.
26. Composition selon l'une dès revendications précédentes, se présentant sous forme d'un fond de teint, d'un fard à joues ou à paupières; d'un rouge à lèvres, d'une base ou baume de soin pour les lèvres, d'un produit anti-cernes, d'un eye iiner, d'un mascara.26. Composition according to one of the preceding claims, in the form of a foundation, a blusher or an eyeshadow; a lipstick, a lip care base or balm, a concealer, an eye iiner, a mascara.
27. Composition selon l'une des revendications 5 à 26 caractérisée en ce que le dispersant est adsorbé sur les particules solides de la dispersion colloïdale.27. Composition according to one of claims 5 to 26 characterized in that the dispersant is adsorbed on the solid particles of the colloidal dispersion.
28. Procédé de soin cosmétique ou de maquillage des lèvres ou de la peau, consistant à appliquer sur respectivement les lèvres ou la peau une .composition cosmétique telle définie aux revendications précédentes. 28. A method of cosmetic care or of making up the lips or of the skin, consisting in applying a cosmetic composition as defined in the preceding claims to the lips or the skin respectively.
29. Procédé pour limiter, la migration d'une composition de maquillage ou de soin de la peau ou des lèvres et/ou d'augmenter la tenue dans le temps de cette composition et/ou sa stabilité, contenant une phase grasse liquide et au moins un ingrédient choisi parmi les matières colorantes sous forme de particules solides à température ambiante, colorées, consistant à introduire dans la phase grasse (iquide des particules de polymère dispersi- blés dans la phase grasse liquide et stabilisables en surface par un agent stabilisant et à introduire dans ladite phase grasse liquide lesdites particules colorées sous forme de dispersion colloïdale.29. Process for limiting, the migration of a makeup or care composition for the skin or the lips and / or for increasing the resistance over time of this composition and / or its stability, containing a liquid fatty phase and at at least one ingredient chosen from coloring matters in the form of solid particles at room temperature, colored, consisting in introducing into the fatty phase (liquid polymer particles dispersed in the liquid fatty phase and stabilized at the surface by a stabilizing agent and at introducing said colored particles into said liquid fatty phase in the form of a colloidal dispersion.
30. Utilisation cosmétique dans une composition à application sur la peau, les lèvres et sur les phanères, de particufes d'au moins un polymère dispersées dans une phase grasse (iquide et stabilisées en surface par un agent stabilisant et d'une dispersion colloïdale de particules solides à température ambiante, notamment colorées, pour (imiter la migration de la composition et/ou augmenter sa tenue dans le temps et/ou obtenir un maquillage homogène.30. Cosmetic use in a composition for application to the skin, the lips and the integuments, of particles of at least one polymer dispersed in a fatty phase (liquid and surface stabilized by a stabilizing agent and of a colloidal dispersion of solid particles at room temperature, in particular colored, to (mimic the migration of the composition and / or increase its resistance over time and / or obtain a homogeneous makeup.
31. Utilisation cosmétique dans une composition à application sur la peau, les lèvres et sur les phanères, de particules d'au moins un polymère dispersées dans une phase , grasse liquide et stabilisées en surface par un agent stabilisant et d'une dispersion colloïdale de particules solides à température ambiante, notamment colorées, pour conserver la brillance de ladite composition. 31. Cosmetic use in a composition for application to the skin, the lips and the integuments, of particles of at least one polymer dispersed in a liquid fatty phase and stabilized on the surface by a stabilizing agent and of a colloidal dispersion of solid particles at room temperature, in particular colored, to maintain the gloss of said composition.
32. Procédé de fabrication d'une composition stable à application sur les matières kératiniques, consistant à introduire dans un milieu physiologiquement acceptable liquide a) une dispersion de particules de polymère stabilisées en surface dans une phase grasse liquide par un stabilisant, b) une dispersion colloïdale de particules solides à température ambiante, choisies parmi les pigments, les nacres, les charges et leurs mélanges et à mélanger ledit milieu supplémenté desdites dispersions a) et b).32. Process for the manufacture of a stable composition for application to keratin materials, consisting in introducing into a physiologically acceptable liquid medium a) a dispersion of polymer particles surface-stabilized in a liquid fatty phase with a stabilizer, b) a dispersion colloidal of solid particles at room temperature, chosen from pigments, nacres, fillers and their mixtures and to mix said medium supplemented with said dispersions a) and b).
33. Procédé selon la revendication 32, caractérisé en ce que la dispersion colloïdale est préparée au préalable, avant son introduction dans la composition. 33. Method according to claim 32, characterized in that the colloidal dispersion is prepared beforehand, before its introduction into the composition.
34. Utilisation d'une dispersion colloïdale de particules solides à température ambiante, choisies parmi les pigments, les nacres, les charges et leurs mélanges dans une composition à application sur les matières kératiniques, contenant une dispersion de particules de polymère stabilisées en surface dans une phase grasse liquide par un stabilisant, pour stabiliser ladite composition et/ou lui conférer un aspect homogène.34. Use of a colloidal dispersion of solid particles at room temperature, chosen from pigments, nacres, fillers and their mixtures in a composition for application to keratin materials, containing a dispersion of polymer particles stabilized at the surface in a liquid fatty phase with a stabilizer, to stabilize said composition and / or give it a homogeneous appearance.
35. Procédé cosmétique pour limiter la migration d'une composition de maquillage ou de soin de la peau ou des lèvres et/ou augmenter la tenue dans le temps de cette composition et/ou sa stabilité, contenant une phase grasse liquide et au moins un ingrédient choisi parmi les matières colorantes sous forme de particules solides à température ambiante, colorées, consistant à introduire dans la phase grasse liquide des particules de polymère dispersibles dans la phase grasse liquidé et stabilisables en surface par un agent stabilisant et à introduire dans ladite phase grasse liquide lesdites particules colorées sous forme de dispersion colloïdale. 35. Cosmetic method for limiting the migration of a makeup or care composition for the skin or the lips and / or increasing the resistance over time of this composition and / or its stability, containing a liquid fatty phase and at least one ingredient selected from the coloring matter in the form of solid particles at room temperature, colored, consisting in introducing into the liquid fatty phase particles of polymer dispersible in the liquid fatty phase and stabilizable at the surface by a stabilizing agent and in introducing into said fatty phase liquid said colored particles in the form of a colloidal dispersion.
EP01985790A 2000-11-15 2001-11-08 Cosmetic composition comprising a dispersion of polymer particles and a dispersion of pigments Withdrawn EP1389999A1 (en)

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FR1400790 2000-11-15
FR0014790A FR2816500B1 (en) 2000-11-15 2000-11-15 COSMETIC COMPOSITION COMPRISING A DISPERSION OF POLYMER PARTICLES AND A DISPERSION OF PIGMENTS
US29497901P 2001-06-04 2001-06-04
US294979 2001-06-04
PCT/FR2001/003472 WO2002039961A1 (en) 2000-11-15 2001-11-08 Cosmetic composition comprising a dispersion of polymer particles and a dispersion of pigments

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WO2002039961A1 (en) 2002-05-23
AU2002223041A1 (en) 2002-05-27

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