CH649915A5 - COSMETIC COMPOSITION BASED ON AN AQUEOUS DISPERSION OF LIPID SPHERULES. - Google Patents
COSMETIC COMPOSITION BASED ON AN AQUEOUS DISPERSION OF LIPID SPHERULES. Download PDFInfo
- Publication number
- CH649915A5 CH649915A5 CH4357/81A CH435781A CH649915A5 CH 649915 A5 CH649915 A5 CH 649915A5 CH 4357/81 A CH4357/81 A CH 4357/81A CH 435781 A CH435781 A CH 435781A CH 649915 A5 CH649915 A5 CH 649915A5
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- CH
- Switzerland
- Prior art keywords
- composition according
- spherules
- esters
- oil
- phase
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 56
- 150000002632 lipids Chemical class 0.000 title claims description 52
- 239000006185 dispersion Substances 0.000 title claims description 48
- 239000002537 cosmetic Substances 0.000 title claims description 32
- 239000012071 phase Substances 0.000 claims description 46
- 239000003921 oil Substances 0.000 claims description 34
- 239000000126 substance Substances 0.000 claims description 31
- -1 hydrocarbon radical Chemical class 0.000 claims description 23
- 150000002148 esters Chemical class 0.000 claims description 17
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 15
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 14
- 239000000194 fatty acid Substances 0.000 claims description 14
- 229930195729 fatty acid Natural products 0.000 claims description 14
- 150000004665 fatty acids Chemical class 0.000 claims description 14
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 12
- 239000002304 perfume Substances 0.000 claims description 12
- 239000008346 aqueous phase Substances 0.000 claims description 11
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 10
- 229950005143 sitosterol Drugs 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 150000001298 alcohols Chemical class 0.000 claims description 7
- 239000003349 gelling agent Substances 0.000 claims description 7
- 229920005862 polyol Polymers 0.000 claims description 7
- 150000003077 polyols Chemical class 0.000 claims description 7
- 235000012000 cholesterol Nutrition 0.000 claims description 6
- 235000011187 glycerol Nutrition 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 235000010469 Glycine max Nutrition 0.000 claims description 4
- 229930182558 Sterol Natural products 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims description 4
- 235000003702 sterols Nutrition 0.000 claims description 4
- 230000000475 sunscreen effect Effects 0.000 claims description 4
- 239000000516 sunscreening agent Substances 0.000 claims description 4
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 235000009854 Cucurbita moschata Nutrition 0.000 claims description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 3
- 229940124091 Keratolytic Drugs 0.000 claims description 3
- 206010040829 Skin discolouration Diseases 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 230000001166 anti-perspirative effect Effects 0.000 claims description 3
- 239000003213 antiperspirant Substances 0.000 claims description 3
- 239000003212 astringent agent Substances 0.000 claims description 3
- 239000012752 auxiliary agent Substances 0.000 claims description 3
- 239000003086 colorant Substances 0.000 claims description 3
- 239000002781 deodorant agent Substances 0.000 claims description 3
- 230000002951 depilatory effect Effects 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- 239000000284 extract Substances 0.000 claims description 3
- 150000002191 fatty alcohols Chemical class 0.000 claims description 3
- 230000035876 healing Effects 0.000 claims description 3
- 239000003906 humectant Substances 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 230000001530 keratinolytic effect Effects 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 229920000223 polyglycerol Polymers 0.000 claims description 3
- 102000004169 proteins and genes Human genes 0.000 claims description 3
- 108090000623 proteins and genes Proteins 0.000 claims description 3
- 229940079889 pyrrolidonecarboxylic acid Drugs 0.000 claims description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 150000003432 sterols Chemical class 0.000 claims description 3
- 230000001256 tonic effect Effects 0.000 claims description 3
- 150000003626 triacylglycerols Chemical class 0.000 claims description 3
- 241000195493 Cryptophyta Species 0.000 claims description 2
- 235000009852 Cucurbita pepo Nutrition 0.000 claims description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 2
- MNQZXJOMYWMBOU-VKHMYHEASA-N D-glyceraldehyde Chemical compound OC[C@@H](O)C=O MNQZXJOMYWMBOU-VKHMYHEASA-N 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 2
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 claims description 2
- 239000004166 Lanolin Substances 0.000 claims description 2
- 244000044822 Simmondsia californica Species 0.000 claims description 2
- 235000004433 Simmondsia californica Nutrition 0.000 claims description 2
- 240000008042 Zea mays Species 0.000 claims description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 2
- 150000001299 aldehydes Chemical class 0.000 claims description 2
- 150000001414 amino alcohols Chemical class 0.000 claims description 2
- 210000004381 amniotic fluid Anatomy 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 235000005822 corn Nutrition 0.000 claims description 2
- 229940120503 dihydroxyacetone Drugs 0.000 claims description 2
- 150000002009 diols Chemical class 0.000 claims description 2
- UQPHVQVXLPRNCX-UHFFFAOYSA-N erythrulose Chemical compound OCC(O)C(=O)CO UQPHVQVXLPRNCX-UHFFFAOYSA-N 0.000 claims description 2
- 150000004676 glycans Chemical class 0.000 claims description 2
- 229940087559 grape seed Drugs 0.000 claims description 2
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 claims description 2
- 229960000367 inositol Drugs 0.000 claims description 2
- 229940039717 lanolin Drugs 0.000 claims description 2
- 235000019388 lanolin Nutrition 0.000 claims description 2
- 229920001206 natural gum Polymers 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 229920001282 polysaccharide Polymers 0.000 claims description 2
- 239000005017 polysaccharide Substances 0.000 claims description 2
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 claims description 2
- 239000000600 sorbitol Substances 0.000 claims description 2
- 235000020354 squash Nutrition 0.000 claims description 2
- 229920001059 synthetic polymer Polymers 0.000 claims description 2
- 239000003643 water by type Substances 0.000 claims description 2
- 240000004244 Cucurbita moschata Species 0.000 claims 1
- 244000020551 Helianthus annuus Species 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- 229960005150 glycerol Drugs 0.000 claims 1
- 150000002430 hydrocarbons Chemical group 0.000 claims 1
- 208000021267 infertility disease Diseases 0.000 claims 1
- 229940059574 pentaerithrityl Drugs 0.000 claims 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
- 229960002920 sorbitol Drugs 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- 235000019198 oils Nutrition 0.000 description 27
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 10
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 10
- 229960002216 methylparaben Drugs 0.000 description 10
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 9
- 210000003491 skin Anatomy 0.000 description 9
- 239000012530 fluid Substances 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 235000019486 Sunflower oil Nutrition 0.000 description 6
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 6
- 239000002600 sunflower oil Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 4
- 241000416162 Astragalus gummifer Species 0.000 description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
- 229920001615 Tragacanth Polymers 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 239000000196 tragacanth Substances 0.000 description 3
- 235000010487 tragacanth Nutrition 0.000 description 3
- 229940116362 tragacanth Drugs 0.000 description 3
- 240000001980 Cucurbita pepo Species 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000001815 facial effect Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 239000002502 liposome Substances 0.000 description 2
- 238000010907 mechanical stirring Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 235000000832 Ayote Nutrition 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 229930186217 Glycolipid Natural products 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 244000025272 Persea americana Species 0.000 description 1
- 235000008673 Persea americana Nutrition 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229930183167 cerebroside Natural products 0.000 description 1
- 150000001784 cerebrosides Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 210000004087 cornea Anatomy 0.000 description 1
- 239000008278 cosmetic cream Substances 0.000 description 1
- 239000008341 cosmetic lotion Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- RNPXCFINMKSQPQ-UHFFFAOYSA-N dicetyl hydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(=O)OCCCCCCCCCCCCCCCC RNPXCFINMKSQPQ-UHFFFAOYSA-N 0.000 description 1
- 229940093541 dicetylphosphate Drugs 0.000 description 1
- XRWMGCFJVKDVMD-UHFFFAOYSA-M didodecyl(dimethyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC XRWMGCFJVKDVMD-UHFFFAOYSA-M 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 210000000245 forearm Anatomy 0.000 description 1
- 239000008169 grapeseed oil Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 229940099367 lanolin alcohols Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229940068065 phytosterols Drugs 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 210000000434 stratum corneum Anatomy 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/42—Ethers, e.g. polyglycol ethers of alcohols or phenols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0084—Antioxidants; Free-radical scavengers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
- A61K9/1271—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers
- A61K9/1272—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers with substantial amounts of non-phosphatidyl, i.e. non-acylglycerophosphate, surfactants as bilayer-forming substances, e.g. cationic lipids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
- A61K9/1277—Processes for preparing; Proliposomes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D19/00—Degasification of liquids
- B01D19/02—Foam dispersion or prevention
- B01D19/04—Foam dispersion or prevention by addition of chemical substances
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0026—Structured liquid compositions, e.g. liquid crystalline phases or network containing non-Newtonian phase
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/022—Well-defined aliphatic compounds saturated
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/024—Well-defined aliphatic compounds unsaturated
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/04—Well-defined cycloaliphatic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/26—Amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/10—Phosphatides, e.g. lecithin, cephalin
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/46—Textile oils
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
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Description
La présente invention concerne une composition cosmétique consistant en une dispersion de sphérules lipidiques. Des dispersions aqueuses de ce genre ont déjà été décrites dans le brevet français N° 2315991 déposé le 30 juin 1975. The present invention relates to a cosmetic composition consisting of a dispersion of lipid spherules. Aqueous dispersions of this kind have already been described in French patent No. 2315991 filed on June 30, 1975.
Les sphérules lipidiques de ces dispersions sont caractérisées par leur structure en feuillets constitués de deux ou plusieurs couches lipidiques séparées les unes des autres par des couches de phase aqueuse. Elles peuvent ainsi servir à encapsuler, dans les compartiments aqueux compris entre les couches lipidiques, des substances actives hydrosolubles, par exemple pharmaceutiques ou cosmétiques, et à les protéger des conditions extérieures. The lipid spherules of these dispersions are characterized by their structure in sheets made up of two or more lipid layers separated from each other by layers of aqueous phase. They can thus be used to encapsulate, in the aqueous compartments comprised between the lipid layers, water-soluble active substances, for example pharmaceutical or cosmetic, and to protect them from external conditions.
Le brevet français précité décrit également un nouveau procédé de préparation d'une dispersion aqueuse de sphérules lipidiques consistant, en premier lieu, à mettre en contact les lipides destinés à constituer les feuillets concentriques des sphérules avec la solution aqueuse à encapsuler, le rapport lipophile/hydrophile des lipides choisis étant tel que ces derniers gonflent dans l'eau ou dans la phase aqueuse à encapsuler pour former une phase lamellaire plane, en second lieu, à ajouter à la phase lamellaire une solution aqueuse destinée à constituer la phase externe continue de la dispersion et, en troisième lieu, à soumettre le tout à une agitation énergique pour obtenir une dispersion de sphérules entre les feuillets concentriques desquelles est emprisonnée la phase aqueuse à encapsuler. The aforementioned French patent also describes a new process for preparing an aqueous dispersion of lipid spherules consisting, first of all, in bringing the lipids intended to constitute the concentric sheets of the spherules into contact with the aqueous solution to be encapsulated, the lipophilic / hydrophilic of the lipids chosen being such that the latter swell in water or in the aqueous phase to be encapsulated to form a planar lamellar phase, secondly, to add to the lamellar phase an aqueous solution intended to constitute the continuous external phase of the dispersion and, thirdly, to subject the whole to vigorous stirring to obtain a dispersion of spherules between the concentric sheets of which is trapped the aqueous phase to be encapsulated.
Pour former les feuillets concentriques des sphérules, on peut, selon l'enseignement du brevet français considéré, utiliser des lipides amphiphiles ou bien ioniques ou bien non ioniques. Parmi les lipides amphiphiles non ioniques, on préfère: To form the concentric sheets of the spherules, it is possible, according to the teaching of the French patent considered, to use amphiphilic lipids or either ionic or nonionic lipids. Among the nonionic amphiphilic lipids, preference is given to:
— les éthers de polyglycérol linéaires ou ramifiés de formules respectives: - linear or branched polyglycerol ethers of respective formulas:
R-f OCH2CHOH - CH2)j- OH R-f OCH2CHOH - CH2) j- OH
et and
R-f OCH2—CH)j-OH CH2OH R-f OCH2 — CH) j-OH CH2OH
n étant un entier compris entre 1 et 6, R étant une chaîne aliphatique linéaire ou ramifiée, saturée ou insaturée de 12 à 30 atomes de carbone, les radicaux hydrocarbonés des alcools de lanoline ou les restes hydroxy-2-alkyle des a-diols à longue chaîne; n being an integer between 1 and 6, R being a linear or branched, saturated or unsaturated aliphatic chain of 12 to 30 carbon atoms, the hydrocarbon radicals of lanolin alcohols or the hydroxy-2-alkyl radicals of the α-diols to long chain;
— les alcools gras polyoxyéthylénés; - polyoxyethylenated fatty alcohols;
— les esters de polyols oxyéthylénés ou non et, en particulier, les esters de sorbitol polyoxyéthylénés; - esters of polyols, oxyethylenated or not and, in particular, polyoxyethylenated sorbitol esters;
— les glycolipides d'origine naturelle ou synthétique, par exemple les cérébrosides. - glycolipids of natural or synthetic origin, for example cerebrosides.
Parmi les substances actives cosmétiques qui peuvent être encapsulées dans les sphérules lipidiques, le brevet français précité donne à titre d'exemple des substances destinées aux soins du revêtement Among the cosmetic active substances which can be encapsulated in lipid spherules, the aforementioned French patent gives by way of example substances intended for the care of the coating.
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cutané telles que des humectants, des agents de brunissage artificiels, des agents de coloration de la peau, des filtres solaires hydrosolu-bles, des antiperspirants, des déodorants, des astringents, des produits rafraîchissants, toniques, cicatrisants, kératolytiques, dépilatoires, des eaux parfumées et des extraits de tissus animaux ou végétaux. skin products such as humectants, artificial browning agents, skin coloring agents, water-soluble sunscreens, antiperspirants, deodorants, astringents, refreshing, tonic, healing, keratolytic, depilatory, water perfumed and extracts of animal or vegetable tissues.
On a observé que les compositions cosmétiques visées ci-dessus sous forme de dispersion aqueuse de sphérules lipidiques présentent l'avantage, par rapport aux préparations classiques sous forme d'émulsion d'huile et d'eau, de présenter un effet moins agressif et, par suite, d'entraîner une irritation moindre lorsqu'elles sont appliquées sur le revêtement cutané. It has been observed that the cosmetic compositions referred to above in the form of an aqueous dispersion of lipid spherules have the advantage, compared with conventional preparations in the form of an oil and water emulsion, of exhibiting a less aggressive effect and, as a result, cause less irritation when applied to the skin.
La présente invention vise à décrire une composition cosmétique à base d'une dispersion aqueuse de sphérules lipidiques permettant de conjuguer à la fois les avantages des dispersions de sphérules et ceux résultant de la présence d'huiles cosmétiques. The present invention aims to describe a cosmetic composition based on an aqueous dispersion of lipid spherules making it possible to combine both the advantages of spherule dispersions and those resulting from the presence of cosmetic oils.
La présente invention a donc pour objet une composition cosmétique consistant en une dispersion aqueuse de sphérules composées de couches moléculaires organisées entre lesquelles est encapsulée une phase aqueuse interne, ces couches étant constituées d'au moins un lipide amphiphile non ionique, caractérisée par le fait qu'au moins une huile est dispersée dans la phase aqueuse externe qui entoure les sphérules, ladite huile étant prise dans le groupe formé par les esters d'acides gras et de polyols, notamment les triglycérides liquides, et par les esters d'acides gras et d'alcools ramifiés de formule R—COOR', formule dans laquelle R représente le reste d'un acide gras supérieur comportant de 8 à 20 atomes de carbone et R' représente une chaîne hydrocarbonée ramifiée contenant de 3 à 20 atomes de carbone. The subject of the present invention is therefore a cosmetic composition consisting of an aqueous dispersion of spherules composed of organized molecular layers between which an internal aqueous phase is encapsulated, these layers consisting of at least one nonionic amphiphilic lipid, characterized in that at least one oil is dispersed in the external aqueous phase which surrounds the spherules, said oil being taken from the group formed by esters of fatty acids and of polyols, in particular liquid triglycerides, and by esters of fatty acids and branched alcohols of formula R — COOR ', formula in which R represents the residue of a higher fatty acid containing from 8 to 20 carbon atoms and R' represents a branched hydrocarbon chain containing from 3 to 20 carbon atoms.
On observe de façon inattendue que les sphérules d'amphiphiles non ioniques permettent de stabiliser la dispersion d'huile dans l'eau sans requérir l'addition d'un agent émulsifiant traditionnel ni entraîner la destruction des sphérules. Pourtant, on sait que la stabilité d'une émulsion dépend pour l'essentiel de la présence d'un émulsifiant, dont les molécules vont s'adsorber à la surface des gouttelettes d'huile en formant une sorte de membrane continue qui empêche le contact direct de deux gouttelettes voisines, au cours d'un choc par exemple. Ainsi, dans le cas présent, l'homme du métier aurait été conduit à penser que les lipides amphiphiles non ioniques des sphérules pouvaient certes jouer le rôle d'un émulsifiant en venant s'adsorber à la surface des gouttelettes d'huile, mais que cette stabilisation avait aussi pour effet d'entraîner la destruction des feuillets concentriques des sphérules. Or, il n'en est rien et l'on constate, de façon surprenante, que les sphérules d'amphiphiles non ioniques de l'invention sont capables de stabiliser une dispersion d'au moins une huile végétale définie ci-dessus dans une phase aqueuse externe en venant se disperser autour des gouttelettes d'huile en gardant leur intégrité. It is unexpectedly observed that the spherules of nonionic amphiphiles make it possible to stabilize the dispersion of oil in water without requiring the addition of a traditional emulsifying agent or causing the destruction of the spherules. However, it is known that the stability of an emulsion depends essentially on the presence of an emulsifier, the molecules of which will adsorb on the surface of the oil droplets, forming a sort of continuous membrane which prevents contact direct from two neighboring droplets, during a shock for example. Thus, in the present case, a person skilled in the art would have been led to think that the nonionic amphiphilic lipids of the spherules could certainly play the role of an emulsifier by being adsorbed on the surface of the oil droplets, but that this stabilization also had the effect of destroying the concentric sheets of the spherules. However, this is not the case and it is found, surprisingly, that the spherules of nonionic amphiphiles of the invention are capable of stabilizing a dispersion of at least one vegetable oil defined above in a phase external aqueous by dispersing around the oil droplets while maintaining their integrity.
Dans le brevet des Etats Unis d'Amérique N° 3957971, on décrit des dispersions de sphérules d'amphiphiles ioniques ou liposomes entrant dans la composition de crèmes ou de lotions cosmétiques, c'est-à-dire d'émulsions eau-dans-huile ou huile-dans-eau. Dans la présente invention, les sphérules sont composées non pas d'amphiphiles ioniques, mais d'amphiphiles non ioniques. En outre, on a constater que les liposomes ne permettent pas de stabiliser une dispersion dans l'eau d'une huile végétale prise dans la classe visée ci-dessus, alors que, de façon tout à fait inattendue, les sphérules d'amphiphiles non ioniques de l'invention permettent de stabiliser une telle dispersion. In the patent of the United States of America No. 3957971, dispersions of spherules of ionic amphiphiles or liposomes used in the composition of cosmetic creams or lotions, that is to say water-in emulsions, are described. oil or oil-in-water. In the present invention, the spherules are composed not of ionic amphiphiles, but of nonionic amphiphiles. In addition, it has been found that the liposomes do not make it possible to stabilize a dispersion in water of a vegetable oil taken in the class referred to above, whereas, quite unexpectedly, the spherules of amphiphiles not ionic of the invention allow to stabilize such a dispersion.
La préparation de la composition cosmétique selon l'invention se fait en deux temps: dans un premier temps, on prépare une dispersion aqueuse de sphérules à partir des lipides amphiphiles non ioniques en mettant en œuvre ou bien le procédé revendiqué dans le brevet français N° 2315991, ou bien les modes opératoires décrits dans le brevet français N° 2221122. Dans un second temps, une fois que la dispersion aqueuse de sphérules est réalisée, on y ajoute notamment de l'huile. Puis, par agitation, on disperse l'huile dans la phase aqueuse externe. The preparation of the cosmetic composition according to the invention is done in two stages: firstly, an aqueous dispersion of spherules is prepared from nonionic amphiphilic lipids by implementing either the process claimed in French patent N ° 2315991, or else the procedures described in French patent No. 2221122. In a second step, once the aqueous dispersion of spherules is produced, oil is especially added thereto. Then, by stirring, the oil is dispersed in the external aqueous phase.
De préférence, la composition cosmétique selon l'invention contient de 2 à 10% de lipide(s) amphiphile(s) non ionique(s), constituant les parois des sphérules, et de 2 à 40% d'huile(s) dispersée(s), ces pourcentages étant exprimés en poids par rapport au poids total de la composition. Avantageusement, la proportion pondérale relative de lipide(s) amphiphile(s) non ionique(s) par rapport à l'huile (ou aux huiles) dispersée(s) est comprise entre 0,2:1 et 1:1. Preferably, the cosmetic composition according to the invention contains from 2 to 10% of non-ionic amphiphilic lipid (s), constituting the walls of the spherules, and from 2 to 40% of dispersed oil (s) (s), these percentages being expressed by weight relative to the total weight of the composition. Advantageously, the relative weight proportion of non-ionic amphiphilic lipid (s) relative to the dispersed oil (or oils) is between 0.2: 1 and 1: 1.
Les huiles qui peuvent être incorporées dans la composition selon l'invention sont prises dans le groupe formé par les esters d'acides gras et de polyols, notamment des triglycérides liquides et les esters d'acides gras et d'alcools ramifiés de formule R—COO—R', formule dans laquelle R représente le reste d'un acide gras supérieur comportant de 8 à 20 atomes de carbone et R' représente une chaîne hydrocarbonée ramifiée contenant de 3 à 20 atomes de carbone. Parmi les esters d'acides gras et de polyols, on peut mentionner des huiles de tournesol, de maïs, de soja, de courge, de pépins de raisin, de jojoba et le tricaprocaprylate de glycérol. Parmi les esters d'acides gras supérieurs et d'alcools ramifiés, on peut mentionner l'huile de purcellin. The oils which can be incorporated into the composition according to the invention are taken from the group formed by esters of fatty acids and of polyols, in particular liquid triglycerides and esters of fatty acids and branched alcohols of formula R— COO — R ', formula in which R represents the remainder of a higher fatty acid containing from 8 to 20 carbon atoms and R' represents a branched hydrocarbon chain containing from 3 to 20 carbon atoms. Among the esters of fatty acids and polyols, mention may be made of sunflower, corn, soybean, squash, grapeseed, jojoba and glycerol tricaprocaprylate oils. Among the esters of higher fatty acids and branched alcohols, mention may be made of purcellin oil.
Les substances actives cosmétiques de la composition selon l'invention peuvent être encapsulées à l'intérieur ou à l'extérieur des sphérules. C'est ainsi que, dans un mode préféré de réalisation, la phase huileuse de la composition contient une ou plusieurs substances cosmétiques liposolubles. Ces dernières sont, lors de la préparation de la composition selon l'invention, préalablement dissoutes dans l'huile qui est destinée à être ajoutée à la dispersion de sphérules lipidiques. Parmi ces substances cosmétiques actives liposolubles, on peut notamment citer des filtres antisolaires tels que le paradimé-thylaminobenzoates de 2-éthylhexyle ou des substances destinées à améliorer l'état des peaux sèches ou séniles, en particulier des insa-ponifiables tels que des insaponifiables de soja, d'avocat, des toco-phérols, des vitamines E, F, des antioxydants. The cosmetic active substances of the composition according to the invention can be encapsulated inside or outside the spherules. Thus, in a preferred embodiment, the oily phase of the composition contains one or more liposoluble cosmetic substances. The latter are, during the preparation of the composition according to the invention, previously dissolved in the oil which is intended to be added to the dispersion of lipid spherules. Among these liposoluble active cosmetic substances, mention may in particular be made of sunscreen filters such as 2-ethylhexyl paradimyl-thylaminobenzoates or substances intended to improve the condition of dry or senile skin, in particular unsaponifiables such as unsaponifiables of soy, avocado, toco-pherols, vitamins E, F, antioxidants.
La dispersion d'huile dans l'eau qui constitue le milieu externe de la dispersion de sphérules peut contenir au moins un additif, notamment un gélifiant ou un parfum. L'additif est ajouté à la dispersion en même temps que l'huile. Le gélifiant peut être introduit à une concentration variant entre 0,1 et 2%, ces pourcentages étant exprimés en poids par rapport au poids total de la composition. Parmi les gélifiants utilisables, on peut citer les dérivés de cellulose tels que l'hydroxyéthylcellulose; des polymères synthétiques; des dérivés d'algues tels que le satiagum ou encore des gommes naturelles telles que l'adragante. On préfère utiliser, à titre de gélifiants, l'hydroxyéthylcellulose, un mélange d'acides carboxyvinyliques disponible dans le commerce sous le nom de Carbopol 940, du satiagum ou encore de l'adragante. The dispersion of oil in water which constitutes the external medium of the dispersion of spherules may contain at least one additive, in particular a gelling agent or a perfume. The additive is added to the dispersion at the same time as the oil. The gelling agent can be introduced at a concentration varying between 0.1 and 2%, these percentages being expressed by weight relative to the total weight of the composition. Among the gelling agents which can be used, mention may be made of cellulose derivatives such as hydroxyethylcellulose; synthetic polymers; algae derivatives such as satiagum or natural gums such as tragacanth. It is preferred to use, as gelling agents, hydroxyethylcellulose, a mixture of carboxyvinyl acids commercially available under the name of Carbopol 940, satiagum or else the tragacanth.
Les lipides amphiphiles non ioniques qui sont destinés à constituer les feuillets concentriques des sphérules dans la composition cosmétique selon l'invention sont: The nonionic amphiphilic lipids which are intended to constitute the concentric sheets of the spherules in the cosmetic composition according to the invention are:
— des éthers ou esters de polyglycérol linéaires ou ramifiés, de formules respectives: - linear or branched polyglycerol ethers or esters, of respective formulas:
R-f OCH2CHOH—CH2 )j OH R-f OCH2CHOH — CH2) j OH
et and
R-f OCH2—CH)gOH CH2OH R-f OCH2 — CH) gOH CH2OH
formules dans lesquelles n est un nombre compris entre 2 et 6 et R représente une chaîne aliphatique saturée, linéaire ou ramifiée, comportant de 16 à 20 atomes de carbone ou le radical hydrocarboné d'un alcool de lanoline; formulas in which n is a number between 2 and 6 and R represents a saturated, linear or branched aliphatic chain, comprising from 16 to 20 carbon atoms or the hydrocarbon radical of a lanolin alcohol;
— des stérols polyoxyéthylénés. - polyoxyethylenated sterols.
Au moment de la formation de la phase lamellaire plane obtenue en mettant en contact les lipides amphiphiles non ioniques avec la phase aqueuse à encapsuler, on peut associer divers agents auxiliaires auxdits lipides en vue de modifier, par exemple, la perméabilité ou la charge superficielle des sphérules. On peut citer à cet égard l'addition éventuelle des alcools et diols à longue chaîne, des stérols, notamment le cholestérol et le P-sitostérol, des aminés à longue At the time of formation of the planar lamellar phase obtained by bringing the nonionic amphiphilic lipids into contact with the aqueous phase to be encapsulated, various auxiliary agents can be combined with said lipids in order to modify, for example, the permeability or the surface charge of the spherules. In this regard, mention may be made of the possible addition of long-chain alcohols and diols, sterols, in particular cholesterol and P-sitosterol, long-chain amines.
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chaîne et de leurs dérivés ammonium quaternaire, notamment le bromure de didodêcyldiméthylammonium, des hydroxyalkylamines, des aminés grasses polyoxyéthylénées, des esters d'aminoalcools à longue chaîne et leurs sels et dérivés ammonium quaternaire, des esters phosphoriques d'alcools gras, notamment de dicétylphos-phate, des alkylsulfates, par exemple le cétylsulfate de sodium, de certains polymères tels que les polypeptides et les protéines. chain and their quaternary ammonium derivatives, in particular didodeccyldimethylammonium bromide, hydroxyalkylamines, polyoxyethylenated fatty amines, esters of long chain amino alcohols and their salts and quaternary ammonium derivatives, phosphoric esters of fatty alcohols, in particular of diketylphos- phate, alkyl sulphates, for example sodium cetyl sulphate, certain polymers such as polypeptides and proteins.
Outre les agents auxiliaires énoncés ci-dessus, on peut ajouter un agent conservateur tel que du parahydroxybenzoate de méthyle par exemple. In addition to the auxiliary agents listed above, a preservative can be added such as methyl parahydroxybenzoate for example.
La phase aqueuse, qu'elle soit interne ou externe, peut renfermer une substance cosmétique hydrosoluble habituellement utilisée pour les soins du visage, des mains ou du corps. Parmi ces substances, on peut citer des humectants tels que la glycérine, le sorbitol, le pentaé-rythritol, l'inositol, l'acide pyrrolidonecarboxylique et ses sels; des agents de brunissage artificiels tels que la dihydroxyacétone, l'éry-thrulose, le glycéraldéhyde, les y-dialdéhydes tels que l'aldéhyde tar-trique; des agents de coloration de la peau; des filtres solaires, des antiperspirants, des déodorants, des astringents, des produits rafraîchissants, toniques, cicatrisants, kératolytiques, dépilatoires, des eaux parfumées, des extraits de tissus animaux ou végétaux, tels que protéines, liquide amniotique, Polysaccharides, et des agents antiséborrhéiques. The aqueous phase, whether internal or external, may contain a water-soluble cosmetic substance usually used for the care of the face, hands or body. Among these substances, mention may be made of humectants such as glycerin, sorbitol, pentaé-rythritol, inositol, pyrrolidonecarboxylic acid and its salts; artificial browning agents such as dihydroxyacetone, erythrulose, glyceraldehyde, γ-dialdehydes such as tarric aldehyde; skin coloring agents; sunscreens, antiperspirants, deodorants, astringents, refreshing, tonic, healing, keratolytic, depilatory, scented waters, extracts of animal or plant tissues, such as proteins, amniotic fluid, Polysaccharides, and antiseborrhoeic agents .
Pour mieux faire comprendre l'objet de l'invention, on va en décrire maintenant à titre d'exemples purement illustratifs et non limitatifs plusieurs modes de réalisation. To better understand the object of the invention, several embodiments will now be described by way of purely illustrative and nonlimiting examples.
La préparation des formulations cosmétiques données dans les exemples ci-après s'effectue en deux phases. Dans une première phase, on fabrique une dispersion aqueuse selon le procédé décrit dans le brevet français N° 2315991. La dispersion aqueuse de sphérules lipidiques est préparée à partir: The preparation of the cosmetic formulations given in the examples below is carried out in two phases. In a first phase, an aqueous dispersion is produced according to the process described in French patent No. 2315991. The aqueous dispersion of lipid spherules is prepared from:
— d'un lipide amphiphile non ionique; - a nonionic amphiphilic lipid;
— de stérols comme le cholestérol ou le p-sitostérol; - sterols such as cholesterol or p-sitosterol;
— éventuellement de dicétylphosphate; - possibly diketylphosphate;
— éventuellement de substances cosmétiques actives de nature hydrosoluble, et - optionally active cosmetic substances of water-soluble nature, and
— d'eau déminéralisée pouvant contenir un conservateur. - demineralized water which may contain a preservative.
Dans une seconde phase, on ajoute l'huile, que l'on disperse par agitation mécanique intense à la température ambiante, de préférence à une température d'environ 40° C. C'est au cours de cette deuxième phase que l'on peut éventuellement incorporer des substances cosmétiques liposolubles, des parfums et/ou des gélifiants. In a second phase, the oil is added, which is dispersed by intense mechanical stirring at room temperature, preferably at a temperature of about 40 ° C. It is during this second phase that may optionally incorporate liposoluble cosmetic substances, perfumes and / or gelling agents.
Exemple 1 Example 1
Essais comparatifs entre une composition cosmétique selon l'invention et une composition cosmétique de type connu. Comparative tests between a cosmetic composition according to the invention and a cosmetic composition of known type.
On prépare deux compositions A et B rigoureusement identiques, à cette différence près que la préparation de la composition B ne comporte pas de seconde phase d'addition d'huile. Two strictly identical compositions A and B are prepared, with the difference that the preparation of composition B does not include a second phase of oil addition.
La composition A contient les ingrédients suivants : Composition A contains the following ingredients:
1" Phase 1 "Phase
— Lipide amphiphile non ionique de formule: - Nonionic amphiphilic lipid of formula:
R-f 00^-0% OH R-f 00 ^ -0% OH
CH2OH CH2OH
dans laquelle R est un radical hexadêcyl et n a une valeur statistique moyenne égale à 3 3,8 g in which R is a hexadecyl radical and n has a mean statistical value equal to 3 3.8 g
— P-Sitostérol 3,8 g - P-Sitosterol 3.8 g
— Dicétylphosphate 0,4 g - Diketylphosphate 0.4 g
— Parahydroxybenzoate de méthyle 0,3 g - Methyl parahydroxybenzoate 0.3 g
— Eau déminéralisée 66,7 g - Demineralized water 66.7 g
2 Phase 2 Phase
On ajoute à la dispersion ci-dessus 25 g d'huile de tournesol; on soumet le tout à une agitation mécanique pour obtenir la dispersion finale. 25 g of sunflower oil are added to the above dispersion; the whole is subjected to mechanical stirring to obtain the final dispersion.
On prépare de la même façon la composition cosmétique B mais sans seconde phase d'addition d'huile de tournesol, les 25 g d'huile étant alors remplacés par une quantité identique d'eau déminéralisée. Cosmetic composition B is prepared in the same way but without the second phase of adding sunflower oil, the 25 g of oil then being replaced by an identical amount of demineralized water.
5 La composition cosmétique A se distingue par conséquent de la composition cosmétique B en ce qu'elle contient 25% d'huile de tournesol. 5 Cosmetic composition A is therefore distinguished from cosmetic composition B in that it contains 25% sunflower oil.
1. Mesures du coefficient de friction de la peau au cours de l'êtale-0 ment des compositions cosmétiques A et B. 1. Measurements of the coefficient of friction of the skin during the plating of the cosmetic compositions A and B.
On mesure le coefficient de friction de la peau au cours de l'étalement des compositions cosmétiques A ou B sur l'avant-bras d'un sujet à l'aide d'un palpeur animé d'un mouvement de rotation; on enregistre l'évolution du couple résistant au niveau du palpeur lors 15 de sa rotation sur lui-même; le palpeur est appliqué à force constante (20 ou 50 g). The coefficient of friction of the skin is measured during the spreading of cosmetic compositions A or B on the forearm of a subject using a feeler animated with a rotary movement; the evolution of the resisting torque is recorded at the level of the probe during its rotation on itself; the probe is applied at constant force (20 or 50 g).
On obtient les résultats suivants: The following results are obtained:
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Variation du coefficient de friction de la peau mesuré 15 min après l'application Change in the coefficient of friction of the skin measured 15 min after application
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Sous une force de 20 g Under a force of 20 g
Sous une force de 50 g Under a force of 50 g
Composition B Composition B
+209 +209
+245 +245
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Composition A selon l'invention (contenant 25% d'huile de tournesol) Composition A according to the invention (containing 25% sunflower oil)
- 40 - 40
- 60 - 60
On observe que la composition B, c'est-à-dire la dispersion 35 aqueuse de sphérules lipidiques qui ne contient pas d'huile, augmente sensiblement le coefficient de friction de la peau, alors que la composition A selon l'invention, c'est-à-dire une dispersion de sphérules qui contient de l'huile, permet d'obtenir un effet inverse. Cet abaissement significatif du cœfficient de friction de la peau traduit 40 sur le plan cosmétique l'effet de douceur apporté par la formulation A selon l'invention. It is observed that composition B, that is to say the aqueous dispersion of lipid spherules which does not contain oil, appreciably increases the coefficient of friction of the skin, while composition A according to the invention, c that is to say a dispersion of spherules which contains oil, makes it possible to obtain an opposite effect. This significant reduction in the coefficient of friction of the skin reflects 40 on the cosmetic level the effect of softness provided by formulation A according to the invention.
2. Mesure du module d'élasticité du Stratum corneum humain effectué in vitro avant et après application des compositions cosmétiques 2. Measurement of the modulus of elasticity of the human Stratum corneum carried out in vitro before and after application of the cosmetic compositions
.. A et B ci-dessus. .. A and B above.
45 45
Ces mesures ont été réalisées sur un appareil de laboratoire destiné à mesurer le module d'élasticité de la peau. Un tel appareil de laboratoire se trouve décrit dans le brevet français N° 78. 25149 demandé le 31 août 1978. These measurements were carried out on a laboratory device intended to measure the elastic modulus of the skin. Such a laboratory device is described in French patent No. 78. 25149 applied for on August 31, 1978.
50 Les conditions expérimentales sont les suivantes: 50 The experimental conditions are as follows:
humidité relative: 72% + 2 relative humidity: 72% + 2
température: 30°C ± 0,2 temperature: 30 ° C ± 0.2
quantité de produit appliqué: 5 mg/cm2 On obtient les résultats suivants: amount of product applied: 5 mg / cm2 The following results are obtained:
Produits testés Products tested
Réduction moyenne du module d'élasticité 1 !4 h après l'application (%) Average reduction in elastic modulus 1! 4 h after application (%)
Composition B Composition A selon l'invention Composition B Composition A according to the invention
0 0
+ 15 + 15
Les résultats ci-dessus montrent de façon significative la différence de plasticité de la cornée, selon que l'on y applique une disper The above results show significantly the difference in plasticity of the cornea, depending on whether one applies a disper
5 5
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sion de sphérules sans phase huileuse ou une dispersion de sphérules avec une phase huileuse. sion of spherules without oily phase or a dispersion of spherules with an oily phase.
Exemple 2 Example 2
Fluide de soins pour le corps. Body care fluid.
I" Phase I "Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes: As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
— Lipide amphiphile non ionique de formule générale: - Nonionic amphiphilic lipid of general formula:
R -f OCH2 — CH OH R -f OCH2 - CH OH
CH2OH CH2OH
dans laquelle R est un radical hexadécyl et n a une valeur statistique moyenne égale à 3 4,5 g in which R is a hexadecyl radical and n has a mean statistical value equal to 3 4.5 g
P-Sitostérol 4,5 g P-Sitosterol 4.5 g
Dicétylphosphate 1,0 g Diketylphosphate 1.0 g
Parahydroxybenzoate de méthyle 0,3 g Methyl parahydroxybenzoate 0.3 g
Sel de sodium de l'acide pyrrolidonecarboxylique 2,0 g Sodium salt of pyrrolidonecarboxylic acid 2.0 g
Eau déminéralisée 56,5 g Demineralized water 56.5 g
2 Phase 2 Phase
On ajoute à la dispersion de sphérules obtenue dans la lre phase les substances suivantes: The following substances are added to the dispersion of spherules obtained in the 1st phase:
Parfum 0,4 g Perfume 0.4 g
Huile de tournesol 10,0 g Mélange d'acides carboxyvinyliques commercialisé Sunflower oil 10.0 g Mixture of carboxyvinyl acids sold
sous le nom de Carbopol 940 0,4 g under the name Carbopol 940 0.4 g
Triéthanolamine 0,4 g Triethanolamine 0.4 g
Eau déminéralisée 20,0 g Demineralized water 20.0 g
Exemple 3 Example 3
Fluide de soins pour le visage. Facial care fluid.
1" Phase 1 "Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes: As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
— Lipide amphiphile non ionique de formule générale: - Nonionic amphiphilic lipid of general formula:
R-f 0CH2 —CH)jOH R-f 0CH2 —CH) jOH
CH2OH CH2OH
dans laquelle R est un radical hexadécyl et n a une valeur égale à 2 6,0 g in which R is a hexadecyl radical and n has a value equal to 2 6.0 g
Cholestérol 1,6 g Cholesterol 1.6 g
Dicétylphosphate 0,4 g Diketylphosphate 0.4 g
Parahydroxybenzoate de méthyle 0,3 g Methyl parahydroxybenzoate 0.3 g
Eau déminéralisée 61,1g Demineralized water 61.1g
2 Phase 2 Phase
On ajoute à la dispersion de sphérules obtenue dans la 1" phase les substances suivantes : The following substances are added to the dispersion of spherules obtained in the 1 "phase:
Parfum 0,2 g Perfume 0.2 g
Huile de pépins de raisin 20,0 g Mélange d'acides carboxyvinyliques commercialisé Grapeseed oil 20.0 g Mixture of carboxyvinyl acids sold
sous le nom de Carbopol 940 0,2 g as Carbopol 940 0.2 g
Triéthanolamine 0,2 g 0.2 g triethanolamine
Eau déminéralisée 10,0 g Demineralized water 10.0 g
Exemple 4 Example 4
Fluide de soins pour les mains. Hand care fluid.
1" Phase 1 "Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes : As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
Phytostérols polyoxyéthylénés (répartition statistique de valeur moyenne égale à 5) 6,0 g Polyoxyethylenated phytosterols (statistical distribution with an average value of 5) 6.0 g
Cholestérol 2,0 g Cholesterol 2.0 g
Parahydroxybenzoate de méthyle 0,3 g Methyl parahydroxybenzoate 0.3 g
Eau déminéralisée 45,7 g Demineralized water 45.7 g
2 Phase 2 Phase
On ajoute à la dispersion de sphérules obtenue dans la lre phase les substances suivantes: The following substances are added to the dispersion of spherules obtained in the 1st phase:
Parfum 0,2 g Perfume 0.2 g
Huile de jojoba 25,0 g Mélange d'acides carboxyvinyliques commercialisé Jojoba oil 25.0 g Mixture of carboxyvinyl acids sold
sous le nom de Carbopol 940 _ 0,4 g under the name of Carbopol 940 _ 0.4 g
Triéthanolamine 0,4 g Triethanolamine 0.4 g
Eau déminéralisée 20,0 g Demineralized water 20.0 g
Exemple 5 Example 5
Fluide de soins pour le corps. Body care fluid.
F'Phase F'Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes: As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
— Lipide amphiphile non ionique de formule générale: - Nonionic amphiphilic lipid of general formula:
R -f OCH2 — CH)=- OH I " R -f OCH2 - CH) = - OH I "
CH2OH CH2OH
dans laquelle R est un radical hexadécyl et n a une valeur statistique moyenne égale à 3 4,0 g in which R is a hexadecyl radical and n has a mean statistical value equal to 3 4.0 g
Cholestérol 4,0 g Cholesterol 4.0 g
Parahydroxybenzoate de méthyle 0,3 g Methyl parahydroxybenzoate 0.3 g
Eau déminéralisée 45,5 g Demineralized water 45.5 g
2' Phase 2 'Phase
On ajoute à la dispersion de sphérules obtenue dans la lre phase les substances suivantes: The following substances are added to the dispersion of spherules obtained in the 1st phase:
Parfum 0,4 g Perfume 0.4 g
Huile de maïs 25,0 g Mélange d'acides carboxyvinyliques commercialisé Corn oil 25.0 g Mixture of carboxyvinyl acids sold
sous le nom de Carbopol 940 0,4 g under the name Carbopol 940 0.4 g
Triéthanolamine 0,4 g Triethanolamine 0.4 g
Eau déminéralisée 20,0 g Demineralized water 20.0 g
Exemple 6 Example 6
Fluide de soins pour le visage. Facial care fluid.
1" Phase 1 "Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes : As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
— Lipide amphiphile non ionique de formule générale: - Nonionic amphiphilic lipid of general formula:
R -f OCH2 — CH)= OH R -f OCH2 - CH) = OH
I " I "
ch2oh dans laquelle R est un radical hexadécyl et n a une valeur statistique moyenne égale à 3 0,95 g ch2oh in which R is a hexadecyl radical and n has a mean statistical value equal to 30.95 g
P-Sitostérol 0,95 g P-Sitosterol 0.95 g
Dicétylphosphate 0,10 g Dicetylphosphate 0.10 g
Parahydroxybenzoate de méthyle 0,30 g Methyl parahydroxybenzoate 0.30 g
Eau déminéralisée 64,80 g Demineralized water 64.80 g
2 Phase 2 Phase
On ajoute à la dispersion de sphérules obtenue dans la lre phase les substances suivantes : The following substances are added to the dispersion of spherules obtained in the 1st phase:
Parfum 0,4 g Perfume 0.4 g
Huile de soja 10,0 g Soybean oil 10.0 g
Insaponifiables de soja 2,0 g Hydroxyéthylcellulose commercialisée sous le nom de Natrosol 250 HHR 0,5 g Soy unsaponifiables 2.0 g Hydroxyethylcellulose marketed under the name of Natrosol 250 HHR 0.5 g
Eau déminéralisée 20,0 g Demineralized water 20.0 g
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649 915 649,915
Exemple 7 Example 7
Fluide de soins solaire. Sun care fluid.
1" Phase 1 "Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes: As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
— Lipide amphiphile non ionique de formule générale: R -f OCH2 — CHW OH - Nonionic amphiphilic lipid of general formula: R -f OCH2 - CHW OH
I I
ch2oh dans laquelle R est un radical hexadécyl et n a une valeur statistique moyenne égale à 3 3,6 g ch2oh in which R is a hexadecyl radical and n has a mean statistical value equal to 3 3.6 g
P-Sitostérol 3,6 g P-Sitosterol 3.6 g
Bromure de didodécyldiméthylammonium 0,8 g Didodecyldimethylammonium bromide 0.8 g
Parahydroxybenzoate de méthyle 0,3 g Methyl parahydroxybenzoate 0.3 g
Eau déminéralisée 45,9 g Demineralized water 45.9 g
2 Phase 2 Phase
On ajoute à la dispersion de sphérules obtenue dans la 1™ phase les substances suivantes : The following substances are added to the dispersion of spherules obtained in the 1st phase:
Parfum 0,4 g Perfume 0.4 g
Huile de courge 22,0 g Pumpkin oil 22.0 g
Paradiméthylaminobenzoate de 2-éthylhexyle 3,0 g 2-ethylhexyl paradimethylaminobenzoate 3.0 g
Gomme adragante 0,4 g Tragacanth 0.4 g
Eau déminéralisée 20,0 g Demineralized water 20.0 g
Exemple 8 Example 8
Fluide de soins pour les mains. Hand care fluid.
1" Phase 1 "Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes: As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
— Lipide amphiphile non ionique de formule générale: - Nonionic amphiphilic lipid of general formula:
R -f OCH2—CH)=- OH CH2OH R -f OCH2 — CH) = - OH CH2OH
dans laquelle R est un radical hexadécyl et n a une valeur statistique moyenne égale à 3 3,8 g in which R is a hexadecyl radical and n has a mean statistical value equal to 3 3.8 g
P-Sitostérol 3,8 g P-Sitosterol 3.8 g
Dicétylphosphate 0,4 g Diketylphosphate 0.4 g
Parahydroxybenzoate de méthyle 0,3 g Methyl parahydroxybenzoate 0.3 g
Glycérine 3,0 g Glycerin 3.0 g
Eau déminéralisée 42,5 g Demineralized water 42.5 g
2 Phase 2 Phase
On ajoute à la dispersion de sphérules obtenue dans la lre phase les substances suivantes: The following substances are added to the dispersion of spherules obtained in the 1st phase:
Parfum 0,2 g Perfume 0.2 g
Huile de purcellin 25,0 g Purcellin oil 25.0 g
Satiagum - 1,0 g Satiagum - 1.0 g
Eau déminéralisée 20,0 g Demineralized water 20.0 g
Exemple 9 Example 9
Fluide de soins pour le corps. Body care fluid.
1" Phase 1 "Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes: As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
— Lipide amphiphile non ionique de formule générale: - Nonionic amphiphilic lipid of general formula:
R -f OCH2—CH)=- OH R -f OCH2 — CH) = - OH
CH2OH CH2OH
dans laquelle R est un radical hexadécyl et n a une valeur statistique moyenne égale à 3 3,8 g in which R is a hexadecyl radical and n has a mean statistical value equal to 3 3.8 g
P-Sitostérol 3,8 g P-Sitosterol 3.8 g
Dicétylphosphate 0,4 g Diketylphosphate 0.4 g
Parahydroxybenzoate de méthyle 0,3 g Methyl parahydroxybenzoate 0.3 g
Eau déminéralisée 60,5 g Demineralized water 60.5 g
2 Phase 2 Phase
On ajoute à la dispersion de sphérules obtenue dans la lre phase les substances suivantes: The following substances are added to the dispersion of spherules obtained in the 1st phase:
Parfum 0,4 g Perfume 0.4 g
Tricaprocaprylate de glycérol 10,0 g Mélange d'acides carboxyvinyliques commercialisé Glycerol tricaprocaprylate 10.0 g Mixture of carboxyvinyl acids marketed
sous le nom de Carbopol 940 0,4 g under the name Carbopol 940 0.4 g
Triéthanolamine 0,4 g Triethanolamine 0.4 g
Eau déminéralisée 20,0 g Demineralized water 20.0 g
Exemple 10 Example 10
Crème de soins pour le visage. Face care cream.
1" Phase 1 "Phase
Comme indiqué ci-dessus, on fabrique une dispersion aqueuse de sphérules lipidiques à partir des substances suivantes: As indicated above, an aqueous dispersion of lipid spherules is produced from the following substances:
— Lipide amphiphile non ionique de formule générale: - Nonionic amphiphilic lipid of general formula:
R-f OCH2 — CH)=- OH CH2OH R-f OCH2 - CH) = - OH CH2OH
dans laquelle R est un radical hexadecyl et n a une valeur statistique moyenne égale à 3 3,8 g in which R is a hexadecyl radical and n has a mean statistical value equal to 3 3.8 g
P-Sitostérol 3,8 g P-Sitosterol 3.8 g
Dicétylphosphate 0,4 g Diketylphosphate 0.4 g
Conservateur 0,3 g Preservative 0.3 g
Eau déminéralisée 47,6 g Demineralized water 47.6 g
2 Phase 2 Phase
On ajoute à la dispersion de sphérules obtenue dans la lre phase les substances suivantes: The following substances are added to the dispersion of spherules obtained in the 1st phase:
Huile de tournesol 35,0 g Sunflower oil 35.0 g
Parfum 0,6 g Mélange d'acides carboxyvinyliques commercialisé Perfume 0.6 g Mixture of carboxyvinyl acids sold
sous le nom de Carbopol 940 0,2 g as Carbopol 940 0.2 g
Triéthanolamine 0,2 g 0.2 g triethanolamine
Eau déminéralisée 8,1 g Demineralized water 8.1 g
Il est bien entendu que les modes de réalisation décrits ci-dessus ne sont aucunement limitatifs et pourront donner lieu à toutes modifications désirables sans sortir pour cela du cadre de l'invention. It is understood that the embodiments described above are in no way limiting and may give rise to any desirable modifications without departing from the scope of the invention.
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R R
Claims (13)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8014657A FR2485921A1 (en) | 1980-07-01 | 1980-07-01 | COSMETIC COMPOSITION BASED ON AN AQUEOUS DISPERSION OF LIPID SPHERULES |
Publications (1)
Publication Number | Publication Date |
---|---|
CH649915A5 true CH649915A5 (en) | 1985-06-28 |
Family
ID=9243726
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH4357/81A CH649915A5 (en) | 1980-07-01 | 1981-07-01 | COSMETIC COMPOSITION BASED ON AN AQUEOUS DISPERSION OF LIPID SPHERULES. |
Country Status (8)
Country | Link |
---|---|
JP (2) | JPS5794326A (en) |
BE (2) | BE889451A (en) |
CA (1) | CA1168158A (en) |
CH (1) | CH649915A5 (en) |
DE (1) | DE3125710A1 (en) |
FR (1) | FR2485921A1 (en) |
GB (1) | GB2079179B (en) |
IT (1) | IT1144739B (en) |
Families Citing this family (42)
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FR2509988B1 (en) * | 1981-07-23 | 1986-05-30 | Oreal | MIXTURE OF VEGETABLE OILS BASED ON JOJOBA OIL AS AN OXIDATION STABILIZING AGENT AND COSMETIC COMPOSITIONS CONTAINING THE SAME |
FR2569561B1 (en) * | 1984-08-30 | 1990-05-18 | Oreal | STABLE ANTHRALIN COMPOSITION IN SATURATED FATTY ACID TRIGLYCERIDES OF PLANT ORIGIN WITH 6 TO 12 CARBON ATOMS |
FR2571963B1 (en) * | 1984-10-24 | 1987-07-10 | Oreal | COMPOSITION FOR COSMETIC OR PHARMACEUTICAL USE CONTAINING NIOSOMES AND AT LEAST ONE WATER-SOLUBLE POLYAMIDE AND PROCESS FOR PREPARING THE SAME. |
JPH0676308B2 (en) * | 1985-06-18 | 1994-09-28 | ポーラ化成工業株式会社 | External skin preparation |
US4777035A (en) * | 1985-11-15 | 1988-10-11 | Bristol-Myers Company | Antiperspirant composition and process |
MY101125A (en) * | 1985-12-23 | 1991-07-31 | Kao Corp | Gel-like emulsion and o/w emulsions obtained from gel-like emulsion |
US5234767A (en) * | 1987-03-13 | 1993-08-10 | Micro-Pak, Inc. | Hybrid paucilamellar lipid vesicles |
US4911928A (en) * | 1987-03-13 | 1990-03-27 | Micro-Pak, Inc. | Paucilamellar lipid vesicles |
US4917951A (en) * | 1987-07-28 | 1990-04-17 | Micro-Pak, Inc. | Lipid vesicles formed of surfactants and steroids |
US5628936A (en) * | 1987-03-13 | 1997-05-13 | Micro-Pak, Inc. | Hybrid paucilamellar lipid vesicles |
US5000960A (en) * | 1987-03-13 | 1991-03-19 | Micro-Pak, Inc. | Protein coupling to lipid vesicles |
US4855090A (en) * | 1987-03-13 | 1989-08-08 | Micro-Pak, Inc. | Method of producing high aqueous volume multilamellar vesicles |
US5023086A (en) * | 1987-03-13 | 1991-06-11 | Micro-Pak, Inc. | Encapsulated ionophore growth factors |
US5019392A (en) * | 1988-03-03 | 1991-05-28 | Micro-Pak, Inc. | Encapsulation of parasiticides |
US5160669A (en) * | 1988-03-03 | 1992-11-03 | Micro Vesicular Systems, Inc. | Method of making oil filled paucilamellar lipid vesicles |
US5019174A (en) * | 1988-03-03 | 1991-05-28 | Micro Vesicular Systems, Inc. | Removing oil from surfaces with liposomal cleaner |
US5032457A (en) * | 1988-03-03 | 1991-07-16 | Micro Vesicular Systems, Inc. | Paucilamellar lipid vesicles using charge-localized, single chain, nonphospholipid surfactants |
US6132763A (en) * | 1988-10-20 | 2000-10-17 | Polymasc Pharmaceuticals Plc | Liposomes |
DE3836971C1 (en) * | 1988-10-31 | 1990-05-17 | Weck, Wolfgang, Dr.Med., 6990 Bad Mergentheim, De | |
FR2648462B1 (en) * | 1989-06-15 | 1994-01-28 | Oreal | PROCESS FOR IMPROVING THE THERAPEUTIC EFFICIENCY OF LIPOSOLUBLE CORTICOSTEROIDS AND COMPOSITION FOR CARRYING OUT SAID METHOD |
FR2655540B1 (en) * | 1989-12-13 | 1994-02-11 | Oreal | COSMETIC COMPOSITION FOR HAIR CARE AND USE OF THE SAME. |
FR2655542B1 (en) * | 1989-12-13 | 1994-02-11 | Oreal | COSMETIC COMPOSITION FOR TOPICAL APPLICATION CONTAINING ESSENTIAL OILS. |
FR2657607B1 (en) * | 1990-01-30 | 1992-04-30 | Durand Muriel | METHOD FOR PROTECTING DIHYDROXYACETONE, DIHYDROXYACETONE PROTECTED BY THIS PROCESS AND COSMETIC PRODUCT CONTAINING SUCH PROTECTED DIHYDROXYACETONE. |
US5256422A (en) * | 1991-03-28 | 1993-10-26 | Micro Vesicular Systems, Inc. | Lipid vesicle containing water-in-oil emulsions |
US5213805A (en) * | 1991-07-25 | 1993-05-25 | Micro Vesicular Systems, Inc. | Lipid vesicles having n,n-dimethylamide derivatives as their primary lipid |
US5260065A (en) * | 1991-09-17 | 1993-11-09 | Micro Vesicular Systems, Inc. | Blended lipid vesicles |
US5405615A (en) * | 1991-09-17 | 1995-04-11 | Micro Vesicular Systems, Inc. | Sucrose distearate lipid vesicles |
FR2701396B1 (en) * | 1993-02-12 | 1995-04-21 | Oreal | Method for stabilizing vesicles of amphiphilic lipid (s) and composition for topical application containing said stabilized vesicles. |
FR2722102B1 (en) | 1994-07-11 | 1996-08-23 | Cird Galderma | USE OF DEFORMABLE HOLLOW PARTICLES IN A COSMETIC AND / OR DERMATOLOGICAL COMPOSITION CONTAINING FAT MATERIALS |
FR2723848B1 (en) | 1994-08-31 | 1997-06-20 | Oreal | COSMETIC OR DERMATOLOGICAL COMPOSITION CONTAINING ENCAPSULATED PLANT EXTRACTS |
FR2730928B1 (en) * | 1995-02-23 | 1997-04-04 | Oreal | COMPOSITION BASED ON LIPIDIC VESICLES WITH ACIDIC PH AND USE THEREOF IN TOPICAL APPLICATION |
FR2742674B1 (en) | 1995-12-21 | 1998-02-06 | Oreal | STABLE DISPERSION OF A PHASE NOT MISCIBLE IN WATER, IN AN AQUEOUS PHASE BY MEANS OF VESICLES BASED ON SILICONE SURFACTANT |
DE19703368C1 (en) * | 1997-01-30 | 1998-10-01 | Klaus Dr Goebel | Rapid production of homogeneous stable cream from storage-stable powder without mechanical work |
AU8053898A (en) * | 1997-05-28 | 1998-12-30 | Jenner Biotherapies, Inc. | Immunogenic compositions |
FR2790975B1 (en) * | 1999-03-16 | 2001-06-01 | Capsulis | MEDIA IN THE FORM OF COMPLEX DISPERSIONS, THEIR PREPARATION PROCESS AND THEIR USES |
KR100903896B1 (en) * | 1999-07-13 | 2009-06-19 | 체엘에르-헤미쉐스 라보라토리움 독토르 쿠르트 리히터 게엠베하 | Uv-protection composition protecting against harmful uv radiation and reinforcing the natural skin barrier |
CN102258959B (en) | 2004-04-05 | 2015-09-23 | 学校法人神奈川大学 | Emulsifying dispersant and use its emulsion dispersion method, emulsion and emulsion fuel |
FR2885808B1 (en) * | 2005-05-19 | 2007-07-06 | Oreal | VECTORIZATION OF DSRNA BY CATIONIC PARTICLES AND TOPICAL USE. |
US9139850B2 (en) | 2005-05-19 | 2015-09-22 | L'oreal | Vectorization of dsRNA by cationic particles and topical use |
JP6274477B2 (en) * | 2010-12-21 | 2018-02-07 | 学校法人神奈川大学 | Manufacturing method of emulsifier manufacturing material, emulsifying material, and manufacturing method of emulsifier |
US9549891B2 (en) | 2012-03-19 | 2017-01-24 | The Procter & Gamble Company | Superabsorbent polymers and sunscreen actives for use in skin care compositions |
CA2988808C (en) | 2015-06-29 | 2021-05-25 | The Procter & Gamble Company | Superabsorbent polymers, waxes, oils, and starch powders for use in skincare compositions |
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Publication number | Priority date | Publication date | Assignee | Title |
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DE3161962D1 (en) * | 1980-07-01 | 1984-02-23 | Oreal | Process for obtaining stable dispersions in an aqueous phase of at least a water immiscible liquid phase, and corresponding dispersions |
-
1980
- 1980-07-01 FR FR8014657A patent/FR2485921A1/en active Granted
-
1981
- 1981-06-30 IT IT67906/81A patent/IT1144739B/en active
- 1981-06-30 CA CA000380902A patent/CA1168158A/en not_active Expired
- 1981-06-30 BE BE0/205268A patent/BE889451A/en not_active IP Right Cessation
- 1981-06-30 DE DE19813125710 patent/DE3125710A1/en active Granted
- 1981-06-30 BE BE0/205269A patent/BE889452A/en not_active IP Right Cessation
- 1981-06-30 GB GB8120182A patent/GB2079179B/en not_active Expired
- 1981-07-01 CH CH4357/81A patent/CH649915A5/en not_active IP Right Cessation
- 1981-07-01 JP JP56101398A patent/JPS5794326A/en active Granted
- 1981-07-01 JP JP56101397A patent/JPS5777613A/en active Granted
Also Published As
Publication number | Publication date |
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JPH0210803B2 (en) | 1990-03-09 |
DE3125710A1 (en) | 1982-03-25 |
BE889451A (en) | 1981-12-30 |
JPS5794326A (en) | 1982-06-11 |
CA1168158A (en) | 1984-05-29 |
DE3125710C2 (en) | 1988-09-22 |
JPS6333414B2 (en) | 1988-07-05 |
FR2485921A1 (en) | 1982-01-08 |
GB2079179B (en) | 1984-03-07 |
IT8167906A0 (en) | 1981-06-30 |
FR2485921B1 (en) | 1983-07-22 |
JPS5777613A (en) | 1982-05-15 |
BE889452A (en) | 1981-12-30 |
IT1144739B (en) | 1986-10-29 |
GB2079179A (en) | 1982-01-20 |
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