PT100338A - Composicoes em emulsao estabilizadas para dar uma tonalidade bronzeada artificial a pele humana que contem dihidroxiacetona e, pelo menos,um alquil fosfato e um copolimero de acido carboc - Google Patents

Composicoes em emulsao estabilizadas para dar uma tonalidade bronzeada artificial a pele humana que contem dihidroxiacetona e, pelo menos,um alquil fosfato e um copolimero de acido carboc Download PDF

Info

Publication number: PT100338A
Authority: PT; Portugal
Prior art keywords: emulsion composition; composition according; ethylhexyl; skin; phosphate
Prior art date: 1991-04-03

Application number

PT10033892A

Other languages

English (en)

Portuguese (pt)

Inventor

Frederick Winfield Woodin Jr

Original Assignee

Richardson Vicks Inc

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.)

1991-04-03

Filing date

1992-04-02

Publication date

1993-10-29

1992-04-02 Application filed by Richardson Vicks Inc filed Critical Richardson Vicks Inc

1993-10-29 Publication of PT100338A publication Critical patent/PT100338A/pt

Links

239000000203 mixture Substances 0.000 title claims description 81
229910019142 PO4 Inorganic materials 0.000 title claims description 22
229920001577 copolymer Polymers 0.000 title claims description 20
239000010452 phosphate Substances 0.000 title claims description 15
239000002253 acid Substances 0.000 title description 7
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title description 3
RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims description 84
239000000839 emulsion Substances 0.000 claims description 54
-1 alkyl phosphate Chemical compound 0.000 claims description 42
229940120503 dihydroxyacetone Drugs 0.000 claims description 41
229920002125 Sokalan® Polymers 0.000 claims description 24
238000000034 method Methods 0.000 claims description 19
239000000516 sunscreening agent Substances 0.000 claims description 19
NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical group OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 14
230000005855 radiation Effects 0.000 claims description 14
229920002126 Acrylic acid copolymer Polymers 0.000 claims description 12
229960001631 carbomer Drugs 0.000 claims description 9
GKKMCECQQIKAHA-UHFFFAOYSA-N hexadecyl dihydrogen phosphate;2-(2-hydroxyethylamino)ethanol Chemical compound OCCNCCO.CCCCCCCCCCCCCCCCOP(O)(O)=O GKKMCECQQIKAHA-UHFFFAOYSA-N 0.000 claims description 9
239000007764 o/w emulsion Substances 0.000 claims description 7
230000000699 topical effect Effects 0.000 claims description 7
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 6
230000000694 effects Effects 0.000 claims description 6
RMGVATURDVPNOZ-UHFFFAOYSA-M potassium;hexadecyl hydrogen phosphate Chemical compound [K+].CCCCCCCCCCCCCCCCOP(O)([O-])=O RMGVATURDVPNOZ-UHFFFAOYSA-M 0.000 claims description 6
YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 claims description 5
229940031766 diethanolamine cetyl phosphate Drugs 0.000 claims description 5
ZUVCYFMOHFTGDM-UHFFFAOYSA-N hexadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(O)=O ZUVCYFMOHFTGDM-UHFFFAOYSA-N 0.000 claims description 5
229960001679 octinoxate Drugs 0.000 claims description 5
229960000601 octocrylene Drugs 0.000 claims description 5
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 4
FMJSMJQBSVNSBF-UHFFFAOYSA-N octocrylene Chemical group C=1C=CC=CC=1C(=C(C#N)C(=O)OCC(CC)CCCC)C1=CC=CC=C1 FMJSMJQBSVNSBF-UHFFFAOYSA-N 0.000 claims description 4
230000004224 protection Effects 0.000 claims description 4
229940085237 carbomer-980 Drugs 0.000 claims description 3
239000004408 titanium dioxide Substances 0.000 claims description 3
HSEXOZXVUZVSDZ-UHFFFAOYSA-N 2-[2-ethylhexyl(methyl)amino]benzoic acid Chemical compound CCCCC(CC)CN(C)C1=CC=CC=C1C(O)=O HSEXOZXVUZVSDZ-UHFFFAOYSA-N 0.000 claims description 2
INKBCSHTYYRDHU-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;hexadecyl dihydrogen phosphate Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCCCCCOP(O)(O)=O INKBCSHTYYRDHU-UHFFFAOYSA-N 0.000 claims description 2
UVCJGUGAGLDPAA-UHFFFAOYSA-N ensulizole Chemical compound N1C2=CC(S(=O)(=O)O)=CC=C2N=C1C1=CC=CC=C1 UVCJGUGAGLDPAA-UHFFFAOYSA-N 0.000 claims description 2
239000011787 zinc oxide Substances 0.000 claims description 2
BGNGWHSBYQYVRX-UHFFFAOYSA-N 4-(dimethylamino)benzaldehyde Chemical compound CN(C)C1=CC=C(C=O)C=C1 BGNGWHSBYQYVRX-UHFFFAOYSA-N 0.000 claims 2
229960003921 octisalate Drugs 0.000 claims 2
WCJLCOAEJIHPCW-UHFFFAOYSA-N octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O WCJLCOAEJIHPCW-UHFFFAOYSA-N 0.000 claims 2
QLIBJPGWWSHWBF-UHFFFAOYSA-N 2-aminoethyl methacrylate Chemical compound CC(=C)C(=O)OCCN QLIBJPGWWSHWBF-UHFFFAOYSA-N 0.000 claims 1
PINYIMREBAFXFI-UHFFFAOYSA-N 2-ethylhexyl 2-(dimethylamino)benzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1N(C)C PINYIMREBAFXFI-UHFFFAOYSA-N 0.000 claims 1
HRCTWBSVGHLFKF-UHFFFAOYSA-N 4-[bis(2-ethylhexyl)amino]benzoic acid Chemical compound CCCCC(CC)CN(CC(CC)CCCC)C1=CC=C(C(O)=O)C=C1 HRCTWBSVGHLFKF-UHFFFAOYSA-N 0.000 claims 1
229920006243 acrylic copolymer Polymers 0.000 claims 1
125000005907 alkyl ester group Chemical group 0.000 claims 1
229940075509 carbomer 1342 Drugs 0.000 claims 1
239000003223 protective agent Substances 0.000 claims 1
230000000191 radiation effect Effects 0.000 claims 1
229960005196 titanium dioxide Drugs 0.000 claims 1
239000012071 phase Substances 0.000 description 31
210000003491 skin Anatomy 0.000 description 28
239000004615 ingredient Substances 0.000 description 20
235000021317 phosphate Nutrition 0.000 description 18
230000000475 sunscreen effect Effects 0.000 description 14
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239000000178 monomer Substances 0.000 description 12
229920000642 polymer Polymers 0.000 description 12
238000009472 formulation Methods 0.000 description 11
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 10
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238000006243 chemical reaction Methods 0.000 description 8
WSDISUOETYTPRL-UHFFFAOYSA-N dmdm hydantoin Chemical compound CC1(C)N(CO)C(=O)N(CO)C1=O WSDISUOETYTPRL-UHFFFAOYSA-N 0.000 description 8
230000009931 harmful effect Effects 0.000 description 8
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 8
238000002156 mixing Methods 0.000 description 8
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
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239000004721 Polyphenylene oxide Substances 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
230000003711 photoprotective effect Effects 0.000 description 6
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XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 5
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125000000217 alkyl group Chemical group 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
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239000003974 emollient agent Substances 0.000 description 5
239000003906 humectant Substances 0.000 description 5
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 5
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150000003839 salts Chemical class 0.000 description 5
239000000126 substance Substances 0.000 description 5
230000037072 sun protection Effects 0.000 description 5
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
125000003342 alkenyl group Chemical group 0.000 description 4
229960000541 cetyl alcohol Drugs 0.000 description 4
239000002537 cosmetic Substances 0.000 description 4
239000003205 fragrance Substances 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
239000000243 solution Substances 0.000 description 4
150000005846 sugar alcohols Polymers 0.000 description 4
229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 description 3
WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
125000005210 alkyl ammonium group Chemical class 0.000 description 3
150000001413 amino acids Chemical class 0.000 description 3
UPOYFZYFGWBUKL-UHFFFAOYSA-N amiphenazole Chemical compound S1C(N)=NC(N)=C1C1=CC=CC=C1 UPOYFZYFGWBUKL-UHFFFAOYSA-N 0.000 description 3
229950001798 amiphenazole Drugs 0.000 description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
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239000003795 chemical substances by application Substances 0.000 description 3
239000003086 colorant Substances 0.000 description 3
239000006071 cream Substances 0.000 description 3
239000000017 hydrogel Substances 0.000 description 3
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150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
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AFDXODALSZRGIH-QPJJXVBHSA-N (E)-3-(4-methoxyphenyl)prop-2-enoic acid Chemical compound COC1=CC=C(\C=C\C(O)=O)C=C1 AFDXODALSZRGIH-QPJJXVBHSA-N 0.000 description 2
GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical class C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
XMFXBMLFOSSELI-UHFFFAOYSA-N 2-octyldodecyl 12-octadecanoyloxyoctadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(CCCCCC)CCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC XMFXBMLFOSSELI-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
235000019489 Almond oil Nutrition 0.000 description 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
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AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
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WYWZRNAHINYAEF-UHFFFAOYSA-N Padimate O Chemical compound CCCCC(CC)COC(=O)C1=CC=C(N(C)C)C=C1 WYWZRNAHINYAEF-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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238000010521 absorption reaction Methods 0.000 description 2
230000002411 adverse Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
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150000003863 ammonium salts Chemical class 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
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229940082484 carbomer-934 Drugs 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
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239000000539 dimer Substances 0.000 description 2
231100000321 erythema Toxicity 0.000 description 2
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
FOYKKGHVWRFIBD-UHFFFAOYSA-N gamma-tocopherol acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 FOYKKGHVWRFIBD-UHFFFAOYSA-N 0.000 description 2
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150000002430 hydrocarbons Chemical class 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
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VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
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125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 2
JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical group N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 2
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125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
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229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Chemical group 0.000 description 1
LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
229910000160 potassium phosphate Inorganic materials 0.000 description 1
235000011009 potassium phosphates Nutrition 0.000 description 1
229940091888 ppg-20 methyl glucose ether distearate Drugs 0.000 description 1
230000002028 premature Effects 0.000 description 1
238000004321 preservation Methods 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
102000004196 processed proteins & peptides Human genes 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
229960003415 propylparaben Drugs 0.000 description 1
230000001012 protector Effects 0.000 description 1
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000003873 salicylate salts Chemical class 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
230000009759 skin aging Effects 0.000 description 1
229940035044 sorbitan monolaurate Drugs 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
150000003432 sterols Chemical class 0.000 description 1
235000003702 sterols Nutrition 0.000 description 1
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
235000021286 stilbenes Nutrition 0.000 description 1
101150035983 str1 gene Proteins 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 1
229960000368 sulisobenzone Drugs 0.000 description 1
LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
229940033123 tannic acid Drugs 0.000 description 1
235000015523 tannic acid Nutrition 0.000 description 1
229920002258 tannic acid Polymers 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
229910052721 tungsten Inorganic materials 0.000 description 1
239000010937 tungsten Substances 0.000 description 1
ORHBXUUXSCNDEV-UHFFFAOYSA-N umbelliferone Chemical compound C1=CC(=O)OC2=CC(O)=CC=C21 ORHBXUUXSCNDEV-UHFFFAOYSA-N 0.000 description 1
HFTAFOQKODTIJY-UHFFFAOYSA-N umbelliferone Natural products Cc1cc2C=CC(=O)Oc2cc1OCC=CC(C)(C)O HFTAFOQKODTIJY-UHFFFAOYSA-N 0.000 description 1
235000019155 vitamin A Nutrition 0.000 description 1
239000011719 vitamin A Substances 0.000 description 1
235000019156 vitamin B Nutrition 0.000 description 1
239000011720 vitamin B Substances 0.000 description 1
235000019166 vitamin D Nutrition 0.000 description 1
239000011710 vitamin D Substances 0.000 description 1
150000003710 vitamin D derivatives Chemical class 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
229940045997 vitamin a Drugs 0.000 description 1
229940046008 vitamin d Drugs 0.000 description 1

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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- 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
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers

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)
Emergency Medicine (AREA)
Cosmetics (AREA)
Medicinal Preparation (AREA)

PT10033892A 1991-04-03 1992-04-02 Composicoes em emulsao estabilizadas para dar uma tonalidade bronzeada artificial a pele humana que contem dihidroxiacetona e, pelo menos,um alquil fosfato e um copolimero de acido carboc PT100338A (pt)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US67989291A	1991-04-03	1991-04-03

Publications (1)

Publication Number	Publication Date
PT100338A true PT100338A (pt)	1993-10-29

Family

ID=24728815

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PT10033892A PT100338A (pt)	1991-04-03	1992-04-02	Composicoes em emulsao estabilizadas para dar uma tonalidade bronzeada artificial a pele humana que contem dihidroxiacetona e, pelo menos,um alquil fosfato e um copolimero de acido carboc

Country Status (8)

Country	Link
CN (1)	CN1066182A (fr)
AU (1)	AU1775592A (fr)
IE (1)	IE921053A1 (fr)
MA (1)	MA22491A1 (fr)
MX (1)	MX9201525A (fr)
PT (1)	PT100338A (fr)
TR (1)	TR25613A (fr)
WO (1)	WO1992017159A2 (fr)

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EP0608320B1 (fr) *	1991-10-16	1998-01-28	Richardson-Vicks, Inc.	Systeme ameliore de penetration cutanee utilise dans l'administration locale efficace de medicaments
GB9204387D0 (en) *	1992-02-29	1992-04-15	Tioxide Specialties Ltd	Oil-in-water emulsions
GB9204388D0 (en) *	1992-02-29	1992-04-15	Tioxide Specialties Ltd	Water-in-oil emulsions
US5232688A (en) *	1992-06-17	1993-08-03	Chesebrough-Pond's Usa Co., Division Of Conopco, Inc.	Self-tanner cosmetic compositions
GB9215178D0 (en) *	1992-07-16	1992-08-26	Glaxo Group Ltd	Antiviral combinations
FR2698267B1 (fr) *	1992-11-24	1995-02-10	Oreal	Compositions à base de dihydroxyacétone et leur utilisation cosmétique.
EP0678015B2 (fr) *	1993-01-11	2001-01-31	The Procter & Gamble Company	Compositions cosmetiques contenant des pigments traites en surface
US5603863A (en) *	1993-03-01	1997-02-18	Tioxide Specialties Limited	Water-in-oil emulsions
ATE162706T1 (de) *	1993-04-16	1998-02-15	Procter & Gamble	Mittel zum künstlichen sonnenbräunen und zum schutz der haut gegen uv-strahlen
US5747012A (en) *	1993-06-11	1998-05-05	Tioxide Specialties Limited	Compositions containing sunscreens
ES2152397T3 (es) *	1994-03-29	2001-02-01	Procter & Gamble	Composiciones para el bronceado artificial que tienen un desarrollo del color mejorado.
US5514437A (en) *	1994-03-29	1996-05-07	The Procter & Gamble Company	Artificial tanning compositions having improved stability
DE4415051A1 (de) *	1994-04-28	1995-11-02	Merck Patent Gmbh	Hautfärbende Zubereitung
FR2731152B1 (fr) *	1995-03-03	1997-05-30	Roussel Uclaf	Compositions cosmetiques pour la protection solaire
DE19603018C2 (de) *	1996-01-17	1998-02-26	Lancaster Group Gmbh	Kosmetisches Selbstbräunungsmittel mit Lichtschutzwirkung
DE19733625A1 (de) *	1997-07-28	1999-02-04	Lancaster Group Gmbh	Dekorative kosmetische O/W-Emulsion
US6464965B1 (en)	1997-09-24	2002-10-15	Noveon Ip Holdings Corp.	Sunscreen composition
DE19750029A1 (de) *	1997-11-12	1999-05-20	Merck Patent Gmbh	Stabile kosmetische Formulierung enthaltend Butylmethoxydibenzoylmethan
EP1481663A1 (fr) *	2003-05-27	2004-12-01	The Procter & Gamble Company	Composition cosmétique stable contenant un agent autobronzant
BRPI0700674A2 (pt) *	2007-03-01	2009-03-17	Johnson & Johnson Ind Ltda	composição autobronzeadora, uso de dha em combinação com óleo mineral e método de autobronzeamento da pele
US8686033B2 (en)	2007-08-02	2014-04-01	Clariant Finance (Bvi) Limited	Phosphoric acid esters containing phosphorus atoms bridged by diol units
DE102007036188A1 (de)	2007-08-02	2008-06-19	Clariant International Limited	Verfahren zur Herstellung alkoxylierter Phosphorsäuretriester
DE102008006857A1 (de) *	2008-01-31	2009-01-29	Clariant International Ltd.	Zusammensetzungen enthaltend Phosphorsäureester und hydrophob modifizierte vernetzte, anionische Polymere
US8241614B2 (en) *	2009-11-30	2012-08-14	Conopco, Inc	Compositions and methods for imparting a sunless tan
ES2644442T3 (es) *	2010-03-26	2017-11-29	Merck Patent Gmbh	Formulaciones que comprenden dihidroxiacetona
US8821839B2 (en)	2010-10-22	2014-09-02	Conopco, Inc.	Compositions and methods for imparting a sunless tan with a vicinal diamine
US8961942B2 (en)	2011-12-13	2015-02-24	Conopco, Inc.	Sunless tanning compositions with adjuvants comprising sulfur comprising moieties
FR3060307B1 (fr)	2016-12-16	2019-01-25	L'oreal	Composition cosmetique comprenant des corps gras solides et un polymere gelifiant
WO2018237218A1 (fr)	2017-06-23	2018-12-27	The Procter & Gamble Company	Composition et procédé permettant d'améliorer l'aspect de la peau
KR20210011964A (ko)	2018-07-03	2021-02-02	더 프록터 앤드 갬블 캄파니	피부 병태를 치료하는 방법
CN115843238B (zh)	2020-06-01	2025-06-10	宝洁公司	改善维生素b3化合物渗透到皮肤中的方法
US10959933B1 (en)	2020-06-01	2021-03-30	The Procter & Gamble Company	Low pH skin care composition and methods of using the same

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Publication number	Priority date	Publication date	Assignee	Title
MY101125A (en) *	1985-12-23	1991-07-31	Kao Corp	Gel-like emulsion and o/w emulsions obtained from gel-like emulsion
JPS63225312A (ja) *	1986-10-02	1988-09-20	Kao Corp	透明ないし半透明のジエリー状の化粧料
US4939179A (en) *	1989-06-22	1990-07-03	Chesebrough-Pond's Inc.	Cosmetic emulsions with hydrocarbon thickening agents
FR2651126B1 (fr) *	1989-08-29	1991-12-06	Oreal	Association de dihydroxyacetone et de derives indoliques pour conferer a la peau une coloration similaire au bronzage naturel et procede de mise en óoeuvre.

1992
- 1992-03-13 WO PCT/US1992/001980 patent/WO1992017159A2/fr not_active Ceased
- 1992-03-13 AU AU17755/92A patent/AU1775592A/en not_active Abandoned
- 1992-03-25 TR TR25492A patent/TR25613A/xx unknown
- 1992-04-02 IE IE921053A patent/IE921053A1/en unknown
- 1992-04-02 MX MX9201525A patent/MX9201525A/es unknown
- 1992-04-02 CN CN 92102944 patent/CN1066182A/zh active Pending
- 1992-04-02 PT PT10033892A patent/PT100338A/pt not_active Application Discontinuation
- 1992-04-02 MA MA22772A patent/MA22491A1/fr unknown

Also Published As

Publication number	Publication date
IE921053A1 (en)	1992-10-07
CN1066182A (zh)	1992-11-18
WO1992017159A3 (fr)	1993-01-07
WO1992017159A2 (fr)	1992-10-15
MX9201525A (es)	1992-10-01
MA22491A1 (fr)	1992-12-31
AU1775592A (en)	1992-11-02
TR25613A (tr)	1993-07-01

Legal Events

Date	Code	Title	Description
1993-10-29	BB1A	Laying open of patent application	Effective date: 19930209
1999-06-30	FC3A	Refusal	Effective date: 19990330

Publication	Publication Date	Title
PT100338A (pt)	1993-10-29	Composicoes em emulsao estabilizadas para dar uma tonalidade bronzeada artificial a pele humana que contem dihidroxiacetona e, pelo menos,um alquil fosfato e um copolimero de acido carboc
US5318774A (en)	1994-06-07	Composition and method for imparting an artificial tan to human skin
US5505935A (en)	1996-04-09	Sunscreen compositions
JP3615759B2 (ja)	2005-02-02	人工日焼け色を形成して、ｕｖ光から皮膚を保護するための組成物
US5219558A (en)	1993-06-15	Photoprotection compositions having improved substantivity
US5229104A (en)	1993-07-20	Artificial tanning compositions containing positively charged paucilamellar vesicles
US5306485A (en)	1994-04-26	Suncare compositions
US5073371A (en)	1991-12-17	Leave-on facial emulsion compositions
US5073372A (en)	1991-12-17	Leave-on facial emulsion compositions
US5573754A (en)	1996-11-12	Photoprotective compositions
US5547659A (en)	1996-08-20	Photoprotection compositions
US5026540A (en)	1991-06-25	Sunscreen composition
AU774670B2 (en)	2004-07-01	Compositions with enhanced photoprotective effect and method for using same
CA2029045C (fr)	1995-02-07	Composes de protection contre le rayonnement solaire a efficacite accrue
US5516508A (en)	1996-05-14	Photoprotection compositions having improved efficiency
CA2029240C (fr)	1998-12-01	Compositions de photoprotection ayant une meilleure substantivite
HK1007505B (en)	1999-04-16	Leave-on facial emulsion compositions
HK1007505A1 (en)	1999-04-16	Leave-on facial emulsion compositions