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FR2673373A1 - COMPOSITIONS FOR MAKEUP COMPRISING FATTY ACID-BASIC AMINO ACID ASSOCIATIONS FOR FIXING WATER-SOLUBLE COLORING MATERIALS TO THE SKIN. - Google Patents

COMPOSITIONS FOR MAKEUP COMPRISING FATTY ACID-BASIC AMINO ACID ASSOCIATIONS FOR FIXING WATER-SOLUBLE COLORING MATERIALS TO THE SKIN. Download PDF

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Publication number
FR2673373A1
FR2673373A1 FR9102446A FR9102446A FR2673373A1 FR 2673373 A1 FR2673373 A1 FR 2673373A1 FR 9102446 A FR9102446 A FR 9102446A FR 9102446 A FR9102446 A FR 9102446A FR 2673373 A1 FR2673373 A1 FR 2673373A1
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Prior art keywords
skin
associations
lysine
make
arginine
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FR9102446A
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French (fr)
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FR2673373B1 (en
Inventor
Bague Jean Claude
Lauzanne-Morelle Eliane
Morelle Jean
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Individual
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Application filed by Individual filed Critical Individual
Priority to FR9102446A priority Critical patent/FR2673373B1/en
Priority to EP19920907569 priority patent/EP0528014A1/en
Priority to JP92506898A priority patent/JPH05506460A/en
Priority to PCT/FR1992/000184 priority patent/WO1992015277A1/en
Publication of FR2673373A1 publication Critical patent/FR2673373A1/en
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Publication of FR2673373B1 publication Critical patent/FR2673373B1/en
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Classifications

    • 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • 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
    • 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
    • A61Q1/10Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
    • 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
    • A61Q1/14Preparations for removing make-up
    • 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

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Abstract

A cosmetic composition used for make-up or make-up removal contains, as active agent helping fix the colourings, 2 to 25 % by weight of a compound produced by associating a saturated or unsaturated C14 to C22 fatty acid either with a basic amino acid without water elimination or with a biological base with water elimination. This composition may be either a make-up cosmetic giving much improved fixation of colouring agents to the skin, or may be a make-up removal cosmetic for cleaning a skin surface treated with said make-up cosmetic, in order to remove the colouring agents.

Description

Il est connu que la fixation de matières colorantes contenues dans les produits de maquillage, en particulier au niveau des lèures, pose un certain nombre de problèmes: difficultés de maintenir la coloration,ou action désagreable de dessèchement ou de tiraillement des levures. It is known that the fixing of coloring matters contained in make-up products, in particular at the level of the lips, poses a certain number of problems: difficulties in maintaining the coloration, or unpleasant action of drying or tightening of the yeasts.

Jusqutici,pour fixer et solubiliser les matières colorantes hydrosolubles particulières, telles les dérivés bromés de la fluoresceine,on avait recours à différents polyalcools, comme les glycols.Or le pouvoir de fixation de ces colorants dépend du rapport existant entre glycols et corps gras généralement utilisés dans la confection des batons de rouge ou autres produits de maquillage tels par exemple les masacara. L'augmentation des glycols améliore la fixation des colorants, mais peut provoquer des incompatibilités avec les autres corps gras: exsudation, marbrage etc. Until now, to fix and dissolve particular water-soluble coloring matters, such as brominated derivatives of fluorescein, we had recourse to different polyalcohols, like glycols. Now the fixing power of these dyes depends on the existing relationship between glycols and fatty substances generally used in the making of red sticks or other makeup products such as masacara for example. The increase in glycols improves the fixation of dyes, but can cause incompatibilities with other fatty substances: exudation, marbling etc.

..ainsi . a nsi que des tiraillements et déssèchement des niuqueuses. ..so . as well as tightness and dryness of the niuqueuses.

Or, il il a eté constaté d'une façon inattendue,que des acides aminés basiques comme la lysine ou l'arginine, associés à des acides gras étaient meilleurs dissolvants des bromofluoresceines que les glycols, sans en auoir les inconvénients. Que de plus, leur activité tinctoriale sur la peau et plus particulièrement au niveau des sèvres est-très nettement superieure à celle des slYcols,celle-ci se manifestant encore,24 heures apres applicati.on.However, it was unexpectedly found that basic amino acids such as lysine or arginine, combined with fatty acids, were better solvents for bromofluoresceins than glycols, without having the disadvantages. That moreover, their dyeing activity on the skin and more particularly at the level of the sèvres is very clearly superior to that of the slYcols, this latter still being manifested, 24 hours after applicati.on.

La présente invention est caractérisée en ce qu'elle permet d'obtenir des produits de maquillage par dissolution de matières colorantes spécifiques à cet usage,grace aux sels d'acides gras de lysine ou d'arsinine répondant aux structures suivantes:

Figure img00010001
The present invention is characterized in that it makes it possible to obtain make-up products by dissolving dyestuffs specific for this use, by virtue of the fatty acid salts of lysine or arsinine corresponding to the following structures:
Figure img00010001

Dans laquelle R représente un radical gras saturé, insaturé, ramifié ou une fonction hydroxyle > comportant de IO à 22 atonies de carbone,
R2 représentant la fraction guanidyle de l'arginine ou un chainon hydrocarboné de la lysine ou de l'ariginine,
La dissolution des bromofluorescéines dans de tels sels d'acides aminés basiques conduit à une très forte et durable fixation de la matière colorante sur la peau, jamais atteinte jusqu'ici ainsi qu'une ameliorat-ion importante de l'effet émollient.
In which R represents a saturated, unsaturated, branched fatty radical or a hydroxyl function> comprising from 10 to 22 carbon atoms,
R2 representing the guanidyle fraction of arginine or a hydrocarbon chain of lysine or ariginine,
The dissolution of bromofluoresceins in such salts of basic amino acids leads to a very strong and lasting fixation of the coloring matter on the skin, never achieved until now as well as a significant improvement in the emollient effect.

Pour réaliser à titre d'exemple des produits cosmétiques destinées au maquillage des lèvres, on procedera comme suit:
On dissout au bain marie les bromofluorescéines à raison de 5 à 20% soit dans de l'oléate de lysine ou d'arginine, soit dans du ri ci nol éate de lysine ou dtarginine,ou encore,selon le niveau émollient recherché, dans des mélanges variables des deux sel s. On obtient une masse colorante qui sera introduite dans un milieu constitué de corps gras variables généralement utilisés dans la confection des produits de maquillage contenant des pigments.
To make, by way of example, cosmetic products intended for making up the lips, the procedure will be as follows:
Bromofluoresceins are dissolved in a water bath at a rate of 5 to 20% either in lysine or arginine oleate, in ri ci nol lysine or dtarginine oleate, or, depending on the desired emollient level, in variable mixtures of the two salt s. A coloring mass is obtained which will be introduced into a medium consisting of variable fatty substances generally used in the preparation of makeup products containing pigments.

A titre d'exemples non limitatifs de compositions de maquillage, on réalise, selon l'invention, dans le cas de la coloration des lèvres, une base dite inclélébile,selon la nature des constituants acides bras-acides aminés; bases indélébiles: exemple 1 Oléate de lysine.....,..K0
Dibromofluorescéine.....20
exemple 2 Ricinoléate de lysine...90
Tetrabromofluorescéine..10
exemple 3 Oléate d'arginine.......80
Dibromofluorescéine.....20
exemple 4 Ricinolétate d'arginine, 85
Tétrabromofluorescéine..15
Composition de rouge à lèvres indélébile:
On réalise une base grasse comportant ou non des pigments correspondant à titre d'exemple non limitatif à la formule suivante: :
Alcool oléique...............................0,100
Cire d'abeille..............................34,050
Stéarate de polyoxyéthylèneglycol............7,130
Cire de carnauba.............................4,660
Myristate de propylèneglycol.................9,200
Huile de vaseline............................16,300
Huile de Ricin...............................4,200
Selon les nuances racherchées, par exemple à 800 grs de cette base grasse pigmentée ou non, on ajoutera à une température se situant entre 600 et 80 200 gr d'une des bases indélébiles des exemples donnés.On obtiendra ainsi un produit pour maquillage des lèvres dont la coloration se maintiendre durant 24 heures.
By way of nonlimiting examples of makeup compositions, there is produced, according to the invention, in the case of the coloring of the lips, a base known as tilting base, depending on the nature of the arm-amino acid constituents; indelible bases: example 1 Lysine oleate ....., .. K0
Dibromofluorescein ..... 20
Example 2 Lysine Ricinoleate ... 90
Tetrabromofluorescein..10
Example 3 Arginine oleate ....... 80
Dibromofluorescein ..... 20
Example 4 Arginine Ricinoletate, 85
Tetrabromofluorescein..15
Composition of indelible lipstick:
An oily base is produced, with or without pigments corresponding, by way of nonlimiting example, to the following formula:
Oleic alcohol ............................... 0.100
Beeswax .............................. 34,050
Polyoxyethylene glycol stearate ............ 7,130
Carnauba wax ............................. 4,660
Propylene glycol myristate ................. 9,200
Vaseline oil ............................ 16,300
Castor oil ............................... 4,200
Depending on the nuances sought, for example at 800 g of this fatty base, pigmented or not, we will add at a temperature between 600 and 80,200 g of one of the indelible bases of the examples given. This will thus give a product for making up the lips. whose coloring is maintained for 24 hours.

Claims (3)

REVENDICATIONS i-Compositions cosmétiques pour maquillage caractérisées en ce que les colorants hydrosolubles tels les bromofluorescéines se fixent sur la peau et en particulier sur les lèvres par le fait de 1 a présence dans ces conipositions d'associations .d'acides gras avec des acides aminés basiques commue la lysine ou l'arginine. i-Cosmetic compositions for make-up characterized in that the water-soluble dyes such as bromofluoresceins are fixed on the skin and in particular on the lips by the fact of the presence in these conipositions of associations of fatty acids with basic amino acids. like lysine or arginine. 2-Compositions pour maquillage selon la revendication 1 caractéri sées en ce que ces associations aci desgras-aci des ami nés.2-Makeup compositions according to claim 1 characterized in that these aci desgras-aci associations of born friends. dans laquelle R1 represente un radical gras saturé insaturé ramifié ou hydroxylé, comportant de 10 à 22 atomes de carbone R2 représentant la fraction guanidyle de l'arigine ou un chai non hydrocarboné de la lysine ou de l'arginine. in which R1 represents a branched or hydroxylated saturated unsaturated fatty radical comprising from 10 to 22 carbon atoms R2 representing the guanidyl fraction of origin or a non-hydrocarbon chai of lysine or arginine.
Figure img00030001
Figure img00030001
basiques correspondent aux strutures suivantes:basic correspond to the following structures:
3-Compositions pour maquillage, selon les revendication 1 et 2 caractérisées en ce que les colorants hydrosolubles tels les bromofluorescéines sont solubilisés aisément dans des associations acides gras-arginine ou lysine,telles que l'oléáte ou le ricinoléate de lysine ou d'arginine ou leur mélange doués d'un haut pouvoir émollients, pour dissoudre ces matières colorantes et les fixer intensivement sur la peau et plus particulièrement sur les lèvres.  3-Makeup compositions according to claims 1 and 2 characterized in that the water-soluble dyes such as bromofluoresceins are easily dissolved in fatty acid-arginine or lysine associations, such as oleate or lysine or arginine ricinoleate or their mixture endowed with a high emollient power, to dissolve these coloring matters and fix them intensively on the skin and more particularly on the lips.
FR9102446A 1991-03-01 1991-03-01 COMPOSITIONS FOR MAKEUP COMPRISING FATTY ACID-BASIC AMINO ACID ASSOCIATIONS FOR FIXING WATER-SOLUBLE COLORING MATERIALS TO THE SKIN. Expired - Lifetime FR2673373B1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
FR9102446A FR2673373B1 (en) 1991-03-01 1991-03-01 COMPOSITIONS FOR MAKEUP COMPRISING FATTY ACID-BASIC AMINO ACID ASSOCIATIONS FOR FIXING WATER-SOLUBLE COLORING MATERIALS TO THE SKIN.
EP19920907569 EP0528014A1 (en) 1991-03-01 1992-02-28 Cosmetic compositions for make-up and make-up removal
JP92506898A JPH05506460A (en) 1991-03-01 1992-02-28 Cosmetic composition containing a fatty acid/basic amino acid association or combination that acts on the fixation of a water-soluble colorant to the skin
PCT/FR1992/000184 WO1992015277A1 (en) 1991-03-01 1992-02-28 Cosmetic compositions for make-up and make-up removal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9102446A FR2673373B1 (en) 1991-03-01 1991-03-01 COMPOSITIONS FOR MAKEUP COMPRISING FATTY ACID-BASIC AMINO ACID ASSOCIATIONS FOR FIXING WATER-SOLUBLE COLORING MATERIALS TO THE SKIN.

Publications (2)

Publication Number Publication Date
FR2673373A1 true FR2673373A1 (en) 1992-09-04
FR2673373B1 FR2673373B1 (en) 1995-02-03

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FR9102446A Expired - Lifetime FR2673373B1 (en) 1991-03-01 1991-03-01 COMPOSITIONS FOR MAKEUP COMPRISING FATTY ACID-BASIC AMINO ACID ASSOCIATIONS FOR FIXING WATER-SOLUBLE COLORING MATERIALS TO THE SKIN.

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EP (1) EP0528014A1 (en)
JP (1) JPH05506460A (en)
FR (1) FR2673373B1 (en)
WO (1) WO1992015277A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006097350A1 (en) * 2005-03-15 2006-09-21 L'oreal Anhydrous cosmetic composition containing an agent for promoting the microcirculation and a polyol, uses thereof
FR2883164A1 (en) * 2005-03-15 2006-09-22 Oreal Anhydrous cosmetic composition for caring for or making up the skin, lips, or nails, comprises fatty phase(s) containing polyol(s) and agent(s) for promoting blood microcirculation of keratin materials to which composition is applied
FR3117832A1 (en) * 2020-12-21 2022-06-24 L'oreal Two-step makeup process comprising on the one hand an amino acid and on the other hand an acid dye and kit
FR3117833A1 (en) * 2020-12-21 2022-06-24 L'oreal Three-step makeup process comprising on the one hand a basic amino acid and on the other hand an acid dye and kit

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1920760A1 (en) * 2006-11-10 2008-05-14 L'Oréal Cosmetic composition comprising a compound chosen from amino acid salts and derivatives
FR2908300B1 (en) * 2006-11-10 2012-08-24 Oreal COSMETIC COMPOSITION COMPRISING C16-C-30 FATTY ACID AND BASIC ACID, METHODS AND USES.

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1459818A (en) * 1965-07-08 1966-06-17 Beauty cream
US3873687A (en) * 1973-09-21 1975-03-25 Avon Prod Inc Cosmetic coloring compositions
JPS52156787A (en) * 1976-06-23 1977-12-27 Shiseido Co Ltd Oil-in-water type emulsified composition
GB2181647A (en) * 1985-10-01 1987-04-29 Jean Morelle Compositions based on lysine and arginine salts

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1007474B (en) * 1955-03-28 1957-05-02 Ewald Klein Dipl Chem Process for the manufacture of skin care products
JPS5923287B2 (en) * 1976-09-01 1984-06-01 株式会社資生堂 Production method of oil-based colorant

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1459818A (en) * 1965-07-08 1966-06-17 Beauty cream
US3873687A (en) * 1973-09-21 1975-03-25 Avon Prod Inc Cosmetic coloring compositions
JPS52156787A (en) * 1976-06-23 1977-12-27 Shiseido Co Ltd Oil-in-water type emulsified composition
GB2181647A (en) * 1985-10-01 1987-04-29 Jean Morelle Compositions based on lysine and arginine salts

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN, vol. 2, no. 46, 28 mars 1978; & JP-A-52 156 787 (SHISEIDO K.K.) 27-12-1977 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006097350A1 (en) * 2005-03-15 2006-09-21 L'oreal Anhydrous cosmetic composition containing an agent for promoting the microcirculation and a polyol, uses thereof
FR2883164A1 (en) * 2005-03-15 2006-09-22 Oreal Anhydrous cosmetic composition for caring for or making up the skin, lips, or nails, comprises fatty phase(s) containing polyol(s) and agent(s) for promoting blood microcirculation of keratin materials to which composition is applied
FR3117832A1 (en) * 2020-12-21 2022-06-24 L'oreal Two-step makeup process comprising on the one hand an amino acid and on the other hand an acid dye and kit
FR3117833A1 (en) * 2020-12-21 2022-06-24 L'oreal Three-step makeup process comprising on the one hand a basic amino acid and on the other hand an acid dye and kit

Also Published As

Publication number Publication date
WO1992015277A1 (en) 1992-09-17
EP0528014A1 (en) 1993-02-24
FR2673373B1 (en) 1995-02-03
JPH05506460A (en) 1993-09-22

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