LU87814A1 - Composition cosmetique comportant une dispersion de vesicules lipidiques ainsi que des pigments melaniques,et son utilisation - Google Patents

Composition cosmetique comportant une dispersion de vesicules lipidiques ainsi que des pigments melaniques,et son utilisation Download PDF

Info

Publication number: LU87814A1
Authority: LU; Luxembourg
Prior art keywords: composition according; hydroxy; amino; chosen; polymers
Prior art date: 1990-09-27

Application number

LU87814A

Other languages

English (en)

French (fr)

Inventor

Jean-Francois Grollier

Original Assignee

Oreal

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1990-09-27

Filing date

1990-09-27

Publication date

1992-05-25

1990-09-27 Application filed by Oreal filed Critical Oreal

1990-09-27 Priority to LU87814A priority Critical patent/LU87814A1/fr

1991-09-19 Priority to EP91916995A priority patent/EP0504347B1/de

1991-09-19 Priority to DE69106340T priority patent/DE69106340T2/de

1991-09-19 Priority to ES91916995T priority patent/ES2066474T3/es

1991-09-19 Priority to PCT/FR1991/000738 priority patent/WO1992005761A1/fr

1991-09-19 Priority to CA002068537A priority patent/CA2068537C/fr

1991-09-19 Priority to JP51577691A priority patent/JP3336432B2/ja

1991-09-19 Priority to AU86238/91A priority patent/AU639375B2/en

1991-09-19 Priority to AT91916995T priority patent/ATE116129T1/de

1992-05-25 Publication of LU87814A1 publication Critical patent/LU87814A1/fr

1994-07-08 Priority to US08/271,990 priority patent/US5874091A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 115
239000000049 pigment Substances 0.000 title claims abstract description 47
239000006185 dispersion Substances 0.000 title claims abstract description 16
239000002537 cosmetic Substances 0.000 title claims abstract description 8
150000002632 lipids Chemical class 0.000 title claims description 47
229920000642 polymer Polymers 0.000 claims abstract description 20
230000004224 protection Effects 0.000 claims abstract description 6
230000005855 radiation Effects 0.000 claims abstract description 6
229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 5
239000011707 mineral Substances 0.000 claims abstract description 4
XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 claims description 85
-1 trimethylsilyloxy Chemical group 0.000 claims description 39
239000001257 hydrogen Substances 0.000 claims description 20
229910052739 hydrogen Inorganic materials 0.000 claims description 20
150000002431 hydrogen Chemical group 0.000 claims description 18
239000002245 particle Substances 0.000 claims description 18
239000000945 filler Substances 0.000 claims description 15
108010076876 Keratins Proteins 0.000 claims description 14
102000011782 Keratins Human genes 0.000 claims description 14
239000003755 preservative agent Substances 0.000 claims description 14
230000003647 oxidation Effects 0.000 claims description 13
238000007254 oxidation reaction Methods 0.000 claims description 13
239000002304 perfume Substances 0.000 claims description 13
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 11
239000012071 phase Substances 0.000 claims description 11
SGNZYJXNUURYCH-UHFFFAOYSA-N 5,6-dihydroxyindole Chemical compound C1=C(O)C(O)=CC2=C1NC=C2 SGNZYJXNUURYCH-UHFFFAOYSA-N 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 10
230000001590 oxidative effect Effects 0.000 claims description 10
125000000204 (C2-C4) acyl group Chemical group 0.000 claims description 9
238000006116 polymerization reaction Methods 0.000 claims description 9
229920001296 polysiloxane Polymers 0.000 claims description 9
239000003381 stabilizer Substances 0.000 claims description 9
239000002562 thickening agent Substances 0.000 claims description 9
229920002101 Chitin Polymers 0.000 claims description 8
239000002243 precursor Substances 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 7
239000000499 gel Substances 0.000 claims description 7
239000000654 additive Substances 0.000 claims description 6
GEHJBWKLJVFKPS-UHFFFAOYSA-N bromochloroacetic acid Chemical compound OC(=O)C(Cl)Br GEHJBWKLJVFKPS-UHFFFAOYSA-N 0.000 claims description 6
239000006071 cream Substances 0.000 claims description 6
RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims description 6
125000004356 hydroxy functional group Chemical group O* 0.000 claims description 6
239000010445 mica Substances 0.000 claims description 6
229910052618 mica group Inorganic materials 0.000 claims description 6
239000004005 microsphere Substances 0.000 claims description 6
239000002480 mineral oil Substances 0.000 claims description 6
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
229910052582 BN Inorganic materials 0.000 claims description 5
PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 5
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230000000996 additive effect Effects 0.000 claims description 5
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229920001577 copolymer Polymers 0.000 claims description 4
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RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 4
BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 claims description 4
230000019612 pigmentation Effects 0.000 claims description 4
229920000223 polyglycerol Polymers 0.000 claims description 4
230000000087 stabilizing effect Effects 0.000 claims description 4
150000003432 sterols Chemical class 0.000 claims description 4
235000003702 sterols Nutrition 0.000 claims description 4
229920001059 synthetic polymer Polymers 0.000 claims description 4
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QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
239000003513 alkali Substances 0.000 claims description 3
239000001913 cellulose Substances 0.000 claims description 3
229920002678 cellulose Polymers 0.000 claims description 3
235000010980 cellulose Nutrition 0.000 claims description 3
239000003086 colorant Substances 0.000 claims description 3
229920006037 cross link polymer Polymers 0.000 claims description 3
235000014113 dietary fatty acids Nutrition 0.000 claims description 3
229940120503 dihydroxyacetone Drugs 0.000 claims description 3
238000006872 enzymatic polymerization reaction Methods 0.000 claims description 3
239000000194 fatty acid Substances 0.000 claims description 3
229930195729 fatty acid Natural products 0.000 claims description 3
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
235000013336 milk Nutrition 0.000 claims description 3
239000008267 milk Substances 0.000 claims description 3
210000004080 milk Anatomy 0.000 claims description 3
239000012764 mineral filler Substances 0.000 claims description 3
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150000003077 polyols Chemical class 0.000 claims description 3
239000000126 substance Substances 0.000 claims description 3
239000004408 titanium dioxide Substances 0.000 claims description 3
PBTPMXPHNHNPPD-UHFFFAOYSA-N (5-methoxy-1h-indol-6-yl) acetate Chemical compound C1=C(OC(C)=O)C(OC)=CC2=C1NC=C2 PBTPMXPHNHNPPD-UHFFFAOYSA-N 0.000 claims description 2
FSYSJTXGNHBKHU-UHFFFAOYSA-N (6-hydroxy-1h-indol-5-yl) acetate Chemical compound C1=C(O)C(OC(=O)C)=CC2=C1NC=C2 FSYSJTXGNHBKHU-UHFFFAOYSA-N 0.000 claims description 2
CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 claims description 2
KILNVBDSWZSGLL-KXQOOQHDSA-N 1,2-dihexadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCC KILNVBDSWZSGLL-KXQOOQHDSA-N 0.000 claims description 2
TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 claims description 2
OOOVRUXKQGYTPJ-UHFFFAOYSA-N 1-methylindol-6-ol Chemical compound C1=C(O)C=C2N(C)C=CC2=C1 OOOVRUXKQGYTPJ-UHFFFAOYSA-N 0.000 claims description 2
ZCBIFHNDZBSCEP-UHFFFAOYSA-N 1H-indol-5-amine Chemical compound NC1=CC=C2NC=CC2=C1 ZCBIFHNDZBSCEP-UHFFFAOYSA-N 0.000 claims description 2
WTFWZOSMUGZKNZ-UHFFFAOYSA-N 1H-indol-7-amine Chemical compound NC1=CC=CC2=C1NC=C2 WTFWZOSMUGZKNZ-UHFFFAOYSA-N 0.000 claims description 2
MIMYTSWNVBMNRH-UHFFFAOYSA-N 1h-indol-6-amine Chemical compound NC1=CC=C2C=CNC2=C1 MIMYTSWNVBMNRH-UHFFFAOYSA-N 0.000 claims description 2
ORVPXPKEZLTMNW-UHFFFAOYSA-N 1h-indol-7-ol Chemical compound OC1=CC=CC2=C1NC=C2 ORVPXPKEZLTMNW-UHFFFAOYSA-N 0.000 claims description 2
KJWHNCIWSFQFCA-UHFFFAOYSA-N 2,3,4,5-tetramethyl-1h-indol-6-amine Chemical compound NC1=C(C)C(C)=C2C(C)=C(C)NC2=C1 KJWHNCIWSFQFCA-UHFFFAOYSA-N 0.000 claims description 2
UWLICOAZFWOHBB-UHFFFAOYSA-N 2,3,4-trimethyl-1h-indol-6-amine Chemical compound NC1=CC(C)=C2C(C)=C(C)NC2=C1 UWLICOAZFWOHBB-UHFFFAOYSA-N 0.000 claims description 2
HMOWERPAXOQSFI-UHFFFAOYSA-N 2,3,5-trimethyl-1h-indol-6-amine Chemical compound NC1=C(C)C=C2C(C)=C(C)NC2=C1 HMOWERPAXOQSFI-UHFFFAOYSA-N 0.000 claims description 2
XOVMMAWNQMPAGS-UHFFFAOYSA-N 2,3,6-trimethylindol-6-amine Chemical compound CC1(N)C=CC2=C(C)C(C)=NC2=C1 XOVMMAWNQMPAGS-UHFFFAOYSA-N 0.000 claims description 2
YPDHDSNSNZOPLI-UHFFFAOYSA-N 2,3-dimethyl-1h-indol-6-amine Chemical compound NC1=CC=C2C(C)=C(C)NC2=C1 YPDHDSNSNZOPLI-UHFFFAOYSA-N 0.000 claims description 2
PYFVEIDRTLBMHG-UHFFFAOYSA-N 2,3-dimethyl-1h-indole Chemical compound C1=CC=C2C(C)=C(C)NC2=C1 PYFVEIDRTLBMHG-UHFFFAOYSA-N 0.000 claims description 2
HMTUVSJLXALWIU-UHFFFAOYSA-N 2,3-dimethyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2C(C)=C(C)NC2=C1 HMTUVSJLXALWIU-UHFFFAOYSA-N 0.000 claims description 2
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 2
QGJCWKNNWOVPTJ-UHFFFAOYSA-N 2-methyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2NC(C)=CC2=C1 QGJCWKNNWOVPTJ-UHFFFAOYSA-N 0.000 claims description 2
NPHFOFOYWYLBTF-UHFFFAOYSA-N 3-methyl-1h-indol-5-ol Chemical compound C1=C(O)C=C2C(C)=CNC2=C1 NPHFOFOYWYLBTF-UHFFFAOYSA-N 0.000 claims description 2
AIMWCCSARFYZCK-UHFFFAOYSA-N 3-methyl-1h-indol-7-ol Chemical compound C1=CC=C2C(C)=CNC2=C1O AIMWCCSARFYZCK-UHFFFAOYSA-N 0.000 claims description 2
LUNUNJFSHKSXGQ-UHFFFAOYSA-N 4-Aminoindole Chemical compound NC1=CC=CC2=C1C=CN2 LUNUNJFSHKSXGQ-UHFFFAOYSA-N 0.000 claims description 2
NLMQHXUGJIAKTH-UHFFFAOYSA-N 4-hydroxyindole Chemical compound OC1=CC=CC2=C1C=CN2 NLMQHXUGJIAKTH-UHFFFAOYSA-N 0.000 claims description 2
JEUGWNYIRZKHDS-UHFFFAOYSA-N 5,6-bis(phenylmethoxy)-1h-indole Chemical compound C=1C=CC=CC=1COC1=CC=2C=CNC=2C=C1OCC1=CC=CC=C1 JEUGWNYIRZKHDS-UHFFFAOYSA-N 0.000 claims description 2
YFTGOBNOJKXZJC-UHFFFAOYSA-N 5,6-dihydroxyindole-2-carboxylic acid Chemical compound OC1=C(O)C=C2NC(C(=O)O)=CC2=C1 YFTGOBNOJKXZJC-UHFFFAOYSA-N 0.000 claims description 2
BIMHWDJKNOMNLD-UHFFFAOYSA-N 5-Hydroxyindole-2-carboxylic acid Chemical compound OC1=CC=C2NC(C(=O)O)=CC2=C1 BIMHWDJKNOMNLD-UHFFFAOYSA-N 0.000 claims description 2
VASQXZIEEJSNHC-UHFFFAOYSA-N 5-ethoxy-1-methylindol-4-ol Chemical compound CCOC1=CC=C2N(C)C=CC2=C1O VASQXZIEEJSNHC-UHFFFAOYSA-N 0.000 claims description 2
LYZYLCBKDYUUES-UHFFFAOYSA-N 5-ethoxy-1h-indol-4-ol Chemical compound CCOC1=CC=C2NC=CC2=C1O LYZYLCBKDYUUES-UHFFFAOYSA-N 0.000 claims description 2
LMIQERWZRIFWNZ-UHFFFAOYSA-N 5-hydroxyindole Chemical compound OC1=CC=C2NC=CC2=C1 LMIQERWZRIFWNZ-UHFFFAOYSA-N 0.000 claims description 2
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RWEBZZKCIMKUTO-UHFFFAOYSA-N 5-methoxy-1h-indol-6-ol Chemical compound C1=C(O)C(OC)=CC2=C1NC=C2 RWEBZZKCIMKUTO-UHFFFAOYSA-N 0.000 claims description 2
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KCZRTDKNQXMPHR-UHFFFAOYSA-N 5-methoxy-2-methyl-1h-indol-6-ol Chemical compound C1=C(O)C(OC)=CC2=C1NC(C)=C2 KCZRTDKNQXMPHR-UHFFFAOYSA-N 0.000 claims description 2
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HXCHORPNRVSDCD-UHFFFAOYSA-N 5h-[1,3]dioxolo[4,5-f]indole Chemical compound C1=C2OCOC2=CC2=C1NC=C2 HXCHORPNRVSDCD-UHFFFAOYSA-N 0.000 claims description 2
HJUFFOMJRAXIRF-UHFFFAOYSA-N 6-hydroxy-1h-indole-2-carboxylic acid Chemical compound C1=C(O)C=C2NC(C(=O)O)=CC2=C1 HJUFFOMJRAXIRF-UHFFFAOYSA-N 0.000 claims description 2
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WZARGPVIAOAKMH-UHFFFAOYSA-N 6-methoxy-1h-indol-5-ol Chemical compound C1=C(O)C(OC)=CC2=C1C=CN2 WZARGPVIAOAKMH-UHFFFAOYSA-N 0.000 claims description 2
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108010022355 Fibroins Proteins 0.000 claims description 2
ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 claims description 2
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125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
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229940000635 beta-alanine Drugs 0.000 claims 1
QQXQAEWRSVZPJM-UHFFFAOYSA-N ethyl 1h-indole-2-carboxylate Chemical compound C1=CC=C2NC(C(=O)OCC)=CC2=C1 QQXQAEWRSVZPJM-UHFFFAOYSA-N 0.000 claims 1
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RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
229910000464 lead oxide Inorganic materials 0.000 description 1
239000002502 liposome Substances 0.000 description 1
210000002752 melanocyte Anatomy 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000003863 metallic catalyst Substances 0.000 description 1
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229940057867 methyl lactate Drugs 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
230000001333 moisturizer Effects 0.000 description 1
LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 1
YBGZDTIWKVFICR-UHFFFAOYSA-N octinoxate Chemical compound CCCCC(CC)COC(=O)C=CC1=CC=C(OC)C=C1 YBGZDTIWKVFICR-UHFFFAOYSA-N 0.000 description 1
NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
239000003002 pH adjusting agent Substances 0.000 description 1
230000035699 permeability Effects 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
230000003711 photoprotective effect Effects 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
229910052761 rare earth metal Inorganic materials 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910001923 silver oxide Inorganic materials 0.000 description 1
230000008591 skin barrier function Effects 0.000 description 1
230000036555 skin type Effects 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
QKHBMQWPOUUMQZ-BDQAORGHSA-M sodium;hydron;(2s)-2-(octadecanoylamino)pentanedioate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC([O-])=O QKHBMQWPOUUMQZ-BDQAORGHSA-M 0.000 description 1
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Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/04—Preparations for care of the skin for chemically tanning the skin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/14—Liposomes; Vesicles
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds

Landscapes

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)
Dermatology (AREA)
Cosmetics (AREA)
Automotive Seat Belt Assembly (AREA)

LU87814A 1990-09-27 1990-09-27 Composition cosmetique comportant une dispersion de vesicules lipidiques ainsi que des pigments melaniques,et son utilisation LU87814A1 (fr)

Priority Applications (10)

Application Number	Priority Date	Filing Date	Title
LU87814A LU87814A1 (fr)	1990-09-27	1990-09-27	Composition cosmetique comportant une dispersion de vesicules lipidiques ainsi que des pigments melaniques,et son utilisation
EP91916995A EP0504347B1 (de)	1990-09-27	1991-09-19	Eine lipidvesikeldispersion und melaninpigmente enthaltendes kosmetikum
DE69106340T DE69106340T2 (de)	1990-09-27	1991-09-19	Eine lipidvesikeldispersion und melaninpigmente enthaltendes kosmetikum.
ES91916995T ES2066474T3 (es)	1990-09-27	1991-09-19	Composicion cosmetica que comprende una dispersion de vesiculas lipidicas asi como pigmentos melanicos.
PCT/FR1991/000738 WO1992005761A1 (fr)	1990-09-27	1991-09-19	Composition cosmetique comportant une dispersion de vesicules lipidiques ainsi que des pigments melaniques
CA002068537A CA2068537C (fr)	1990-09-27	1991-09-19	Composition cosmetique comportant une dispersion de vesicules lipidiques ainsi que des pigments melaniques
JP51577691A JP3336432B2 (ja)	1990-09-27	1991-09-19	脂質小胞並にメラニン顔料の分散系を含む化粧品組成物
AU86238/91A AU639375B2 (en)	1990-09-27	1991-09-19	Cosmetic composition comprising a dispersion of lipidic vesicles as well as melanic pigments
AT91916995T ATE116129T1 (de)	1990-09-27	1991-09-19	Eine lipidvesikeldispersion und melaninpigmente enthaltendes kosmetikum.
US08/271,990 US5874091A (en)	1990-09-27	1994-07-08	Cosmetic composition comprising a dispersion of lipid vesicles as well as melanin pigments

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
LU87814A LU87814A1 (fr)	1990-09-27	1990-09-27	Composition cosmetique comportant une dispersion de vesicules lipidiques ainsi que des pigments melaniques,et son utilisation

Publications (1)

Publication Number	Publication Date
LU87814A1 true LU87814A1 (fr)	1992-05-25

Family

ID=19731256

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU87814A LU87814A1 (fr)	1990-09-27	1990-09-27	Composition cosmetique comportant une dispersion de vesicules lipidiques ainsi que des pigments melaniques,et son utilisation

Country Status (9)

Country	Link
EP (1)	EP0504347B1 (de)
JP (1)	JP3336432B2 (de)
AT (1)	ATE116129T1 (de)
AU (1)	AU639375B2 (de)
CA (1)	CA2068537C (de)
DE (1)	DE69106340T2 (de)
ES (1)	ES2066474T3 (de)
LU (1)	LU87814A1 (de)
WO (1)	WO1992005761A1 (de)

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2681329B1 (fr) *	1991-09-18	1995-06-23	Oreal	Dispersion fine de pigments melaniques, sa preparation et son utilisation en cosmetique.
WO1995007276A1 (en) *	1993-09-10	1995-03-16	Eisai Co., Ltd.	Bicyclic heterocyclic sulfonamide and sulfonic ester derivatives
GB9420535D0 (en) *	1994-10-12	1994-11-30	Procter & Gamble	Cosmetic make-up compositions
FR2742988B1 (fr) *	1996-01-03	1998-01-30	Oreal	Composition aqueuse contenant des vesicules lipidiques non-ioniques et au moins un pigment non-enrobe disperse dans la phase aqueuse, procede de preparation, utilisations
US5846551A (en) *	1996-06-10	1998-12-08	E-L Management Corp.	Water-based makeup compositions and methods for their preparation
DE19923648A1 (de) *	1999-05-22	2000-11-23	Beiersdorf Ag	Kosmetische und dermatologische Hydrodispersion mit einem Gehalt an Bornitrid
FR2816852B1 (fr) *	2000-11-21	2005-08-26	Nuxe Lab	Association stabilisee d'un colorant et d'un emulsionnant, composition cosmetique et/ou dermatologique la contenant et procede de preparation
DE10105139A1 (de)	2001-02-06	2002-08-22	Wella Ag	Elektrisch leitfähige Polymere in kosmetischen Mitteln
JP5866278B2 (ja) *	2009-08-25	2016-02-17	ロレアル	ケラチン繊維のための化粧用組成物

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
LU86946A1 (fr) *	1987-07-17	1989-03-08	Oreal	Poudre ultrafine comportant des pigments melaniques,son procede de preparation et son utilisation en cosmetique
US4855144A (en) *	1987-10-23	1989-08-08	Advanced Polymer Systems	Synthetic melanin aggregates
LU87429A1 (fr) *	1989-01-17	1990-07-24	Oreal	Produit a base de particules de polymere comportant des pigments melaniques,son procede de preparation et son utilisation,en particulier en cosmetique
AU5195090A (en) *	1989-03-07	1990-10-09	Plough Inc.	Liposome compositions

1990
- 1990-09-27 LU LU87814A patent/LU87814A1/fr unknown
1991
- 1991-09-19 EP EP91916995A patent/EP0504347B1/de not_active Expired - Lifetime
- 1991-09-19 ES ES91916995T patent/ES2066474T3/es not_active Expired - Lifetime
- 1991-09-19 CA CA002068537A patent/CA2068537C/fr not_active Expired - Lifetime
- 1991-09-19 AT AT91916995T patent/ATE116129T1/de not_active IP Right Cessation
- 1991-09-19 WO PCT/FR1991/000738 patent/WO1992005761A1/fr not_active Ceased
- 1991-09-19 AU AU86238/91A patent/AU639375B2/en not_active Ceased
- 1991-09-19 JP JP51577691A patent/JP3336432B2/ja not_active Expired - Fee Related
- 1991-09-19 DE DE69106340T patent/DE69106340T2/de not_active Expired - Lifetime

Also Published As

Publication number	Publication date
EP0504347A1 (de)	1992-09-23
ATE116129T1 (de)	1995-01-15
EP0504347B1 (de)	1994-12-28
CA2068537A1 (fr)	1992-03-28
AU639375B2 (en)	1993-07-22
JP3336432B2 (ja)	2002-10-21
JPH05502461A (ja)	1993-04-28
ES2066474T3 (es)	1995-03-01
CA2068537C (fr)	2005-07-26
AU8623891A (en)	1992-04-28
WO1992005761A1 (fr)	1992-04-16
DE69106340D1 (de)	1995-02-09
DE69106340T2 (de)	1995-08-03

Publication	Publication Date	Title
EP0379409B1 (de)	1993-09-15	Produkte auf der Basis von Melaninpigmente enthaltenden Polymerpartikeln, Verfahren zu ihrer Herstellung und ihre Verwendung, insbesondere in der Kosmetik
CA2071276C (fr)	2006-05-23	Composition cosmetique contenant un melange de nanopigments d'oxydes metalliques et de pigments melaniques
EP0575605B1 (de)	1996-11-27	Mittel auf basis von anorganischen oder organischen partikeln mit einer indolinverbindung
EP0587837B1 (de)	1998-06-03	Melanin-Pigmente zusammen mit Tocopherol enthaltende kosmetische Zusammensetzung und Verfahren zum Schutz der Haut, des Haares
EP0467767B1 (de)	1994-09-21	Produkte auf Basis von Melaninpigment enthaltenden plättchenförmigen Partikeln und Verfahren zu ihrer Herstellung
US5874091A (en)	1999-02-23	Cosmetic composition comprising a dispersion of lipid vesicles as well as melanin pigments
EP0575603B1 (de)	1996-10-23	Produkt, bazierend auf gefaerbten mineralteilchen, die ein melanin-pigment enthalten, sein herstellungsverfahren und seine verwendung in der kosmetik
EP0504347B1 (de)	1994-12-28	Eine lipidvesikeldispersion und melaninpigmente enthaltendes kosmetikum
EP0659069B1 (de)	1996-11-20	Kosmetische zusammensetzung, die feste organische, mit einem kationischen polymer überzogene partikel enthält
CA2106192A1 (fr)	1993-07-17	Produits indoliniques, leurs procedes de preparation et leur utilisation en cosmetique
EP0647255B1 (de)	1999-12-15	Herstellungsverfahren eines melaninpigments von geringer korngrösse sowie seine anwendung in der kosmetik
WO2002102333A1 (fr)	2002-12-27	Pigment organique enrobe et composition cosmetique contenant ce pigment