CN1274577A - 光稳定的化妆品遮光组合物 - Google Patents
光稳定的化妆品遮光组合物 Download PDFInfo
- Publication number
- CN1274577A CN1274577A CN00108286A CN00108286A CN1274577A CN 1274577 A CN1274577 A CN 1274577A CN 00108286 A CN00108286 A CN 00108286A CN 00108286 A CN00108286 A CN 00108286A CN 1274577 A CN1274577 A CN 1274577A
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- CN
- China
- Prior art keywords
- sunscreen
- polymer
- composition according
- methoxycinnamate
- particles
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000203 mixture Substances 0.000 title claims abstract description 59
- 239000002537 cosmetic Substances 0.000 title claims abstract description 13
- 230000004888 barrier function Effects 0.000 title 1
- 239000000516 sunscreening agent Substances 0.000 claims abstract description 115
- 230000000475 sunscreen effect Effects 0.000 claims abstract description 112
- 229920000642 polymer Polymers 0.000 claims abstract description 80
- 239000004816 latex Substances 0.000 claims abstract description 51
- 229920000126 latex Polymers 0.000 claims abstract description 51
- NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical compound C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 claims abstract description 31
- 150000003839 salts Chemical class 0.000 claims abstract description 28
- 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 claims abstract description 27
- 238000000034 method Methods 0.000 claims abstract description 17
- 239000002245 particle Substances 0.000 claims description 62
- 239000000178 monomer Substances 0.000 claims description 42
- -1 benzene Ethylene, ethylene, propylene, butene Chemical class 0.000 claims description 34
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 claims description 24
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 20
- 239000000839 emulsion Substances 0.000 claims description 19
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 claims description 17
- 229940119545 isobornyl methacrylate Drugs 0.000 claims description 17
- 239000000243 solution Substances 0.000 claims description 17
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 16
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 16
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 16
- 230000009477 glass transition Effects 0.000 claims description 16
- 238000006116 polymerization reaction Methods 0.000 claims description 16
- 238000002360 preparation method Methods 0.000 claims description 16
- 239000011159 matrix material Substances 0.000 claims description 13
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 7
- 239000007771 core particle Substances 0.000 claims description 7
- 230000008569 process Effects 0.000 claims description 7
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 6
- 239000010420 shell particle Substances 0.000 claims description 6
- QTKPMCIBUROOGY-UHFFFAOYSA-N 2,2,2-trifluoroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)F QTKPMCIBUROOGY-UHFFFAOYSA-N 0.000 claims description 5
- XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 claims description 5
- 238000001246 colloidal dispersion Methods 0.000 claims description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 4
- 239000003995 emulsifying agent Substances 0.000 claims description 4
- 229920002313 fluoropolymer Polymers 0.000 claims description 4
- 229920001477 hydrophilic polymer Polymers 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 230000001804 emulsifying effect Effects 0.000 claims description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 2
- 150000001253 acrylic acids Chemical class 0.000 claims 1
- 125000005399 allylmethacrylate group Chemical group 0.000 claims 1
- 230000000176 photostabilization Effects 0.000 abstract description 2
- 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 description 45
- 229960001679 octinoxate Drugs 0.000 description 42
- 239000011257 shell material Substances 0.000 description 22
- 239000007787 solid Substances 0.000 description 15
- 229920001296 polysiloxane Polymers 0.000 description 12
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 238000009472 formulation Methods 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- 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 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 229920006254 polymer film Polymers 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 235000013772 propylene glycol Nutrition 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 102100026735 Coagulation factor VIII Human genes 0.000 description 3
- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920001213 Polysorbate 20 Polymers 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 239000011258 core-shell material Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 229940086555 cyclomethicone Drugs 0.000 description 3
- 229940008099 dimethicone Drugs 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 239000003605 opacifier Substances 0.000 description 3
- 125000005375 organosiloxane group Chemical group 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 3
- 210000003491 skin Anatomy 0.000 description 3
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 2
- LALVCWMSKLEQMK-UHFFFAOYSA-N 1-phenyl-3-(4-propan-2-ylphenyl)propane-1,3-dione Chemical compound C1=CC(C(C)C)=CC=C1C(=O)CC(=O)C1=CC=CC=C1 LALVCWMSKLEQMK-UHFFFAOYSA-N 0.000 description 2
- JKXYOQDLERSFPT-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-octadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO JKXYOQDLERSFPT-UHFFFAOYSA-N 0.000 description 2
- WSSJONWNBBTCMG-UHFFFAOYSA-N 2-hydroxybenzoic acid (3,3,5-trimethylcyclohexyl) ester Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C1=CC=CC=C1O WSSJONWNBBTCMG-UHFFFAOYSA-N 0.000 description 2
- QMIBDVOQOZDSEN-UHFFFAOYSA-N 2-phenylbenzimidazole-2-sulfonic acid Chemical compound N1=C2C=CC=CC2=NC1(S(=O)(=O)O)C1=CC=CC=C1 QMIBDVOQOZDSEN-UHFFFAOYSA-N 0.000 description 2
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
- QFOHBWFCKVYLES-UHFFFAOYSA-N Butylparaben Chemical compound CCCCOC(=O)C1=CC=C(O)C=C1 QFOHBWFCKVYLES-UHFFFAOYSA-N 0.000 description 2
- 241000723346 Cinnamomum camphora Species 0.000 description 2
- FMRHJJZUHUTGKE-UHFFFAOYSA-N Ethylhexyl salicylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1O FMRHJJZUHUTGKE-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229910010413 TiO 2 Inorganic materials 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
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- 150000001298 alcohols Chemical class 0.000 description 2
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- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical class [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
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- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
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- 229910044991 metal oxide Inorganic materials 0.000 description 2
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
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- 239000012074 organic phase Substances 0.000 description 2
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- 150000003141 primary amines Chemical class 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
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- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical class [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 2
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- JQKOUPZLFGRFLI-UHFFFAOYSA-N (1,2,2-trimethylcyclohexyl) 2-hydroxybenzoate Chemical compound CC1(C)CCCCC1(C)OC(=O)C1=CC=CC=C1O JQKOUPZLFGRFLI-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
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- LUKQUIZLFXGUKZ-UHFFFAOYSA-N (3-benzylidene-1,7,7-trimethyl-2-oxo-4-bicyclo[2.2.1]heptanyl)methanesulfonic acid Chemical compound CC1(C)C(C2=O)(C)CCC1(CS(O)(=O)=O)C2=CC1=CC=CC=C1 LUKQUIZLFXGUKZ-UHFFFAOYSA-N 0.000 description 1
- AALXZHPCKJILAZ-UHFFFAOYSA-N (4-propan-2-ylphenyl)methyl 2-hydroxybenzoate Chemical compound C1=CC(C(C)C)=CC=C1COC(=O)C1=CC=CC=C1O AALXZHPCKJILAZ-UHFFFAOYSA-N 0.000 description 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
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- BEXQNGUXPFGRDC-UHFFFAOYSA-N 2,2-dimethoxy-1,3-diphenylpropane-1,3-dione Chemical compound C=1C=CC=CC=1C(=O)C(OC)(OC)C(=O)C1=CC=CC=C1 BEXQNGUXPFGRDC-UHFFFAOYSA-N 0.000 description 1
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- WMJBVALTYVXGHW-UHFFFAOYSA-N 3,3-diphenylprop-2-enoic acid Chemical class C=1C=CC=CC=1C(=CC(=O)O)C1=CC=CC=C1 WMJBVALTYVXGHW-UHFFFAOYSA-N 0.000 description 1
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- IPNFHEWNDOORKH-UHFFFAOYSA-N 6-methylheptyl 2-hydroxybenzoate Chemical compound CC(C)CCCCCOC(=O)C1=CC=CC=C1O IPNFHEWNDOORKH-UHFFFAOYSA-N 0.000 description 1
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical class CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 1
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- 108010082495 Dietary Plant Proteins Proteins 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
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- 235000005305 Nypa fruticans Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 description 1
- YSIALVLPAPHPRR-UHFFFAOYSA-N [2-[[8-amino-4,6-dimethyl-7-oxo-1,9-bis[[7,11,14-trimethyl-2,5,9,12,15-pentaoxo-3,10-di(propan-2-yl)-8-oxa-1,4,11,14-tetrazabicyclo[14.3.0]nonadecan-6-yl]carbamoyl]phenoxazin-3-yl]amino]-2-oxoethyl] 2-amino-3-methylbutanoate Chemical compound CC1OC(=O)C(C(C)C)N(C)C(=O)CN(C)C(=O)C2CCCN2C(=O)C(C(C)C)NC(=O)C1NC(=O)C1=C(N)C(=O)C(C)=C2C1=NC1=C(C(=O)NC3C(NC(C(=O)N4CCCC4C(=O)N(C)CC(=O)N(C)C(C(C)C)C(=O)OC3C)C(C)C)=O)C=C(NC(=O)COC(=O)C(N)C(C)C)C(C)=C1O2 YSIALVLPAPHPRR-UHFFFAOYSA-N 0.000 description 1
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- BOXCWTMAYIFDQP-UHFFFAOYSA-N benzo[l]pyrene-8-sulfonic acid Chemical compound C=1(C=CC=2C=CC=3C=CC=C4C5=C(C=1C=2C4=3)C=CC=C5)S(=O)(=O)O BOXCWTMAYIFDQP-UHFFFAOYSA-N 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940067596 butylparaben Drugs 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
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- 239000003086 colorant Substances 0.000 description 1
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- 238000011161 development Methods 0.000 description 1
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- BMOAQMNPJSPXIU-UHFFFAOYSA-N ethyl 2-(3-fluoro-4-nitrophenyl)propanoate Chemical compound CCOC(=O)C(C)C1=CC=C([N+]([O-])=O)C(F)=C1 BMOAQMNPJSPXIU-UHFFFAOYSA-N 0.000 description 1
- 229960001617 ethyl hydroxybenzoate Drugs 0.000 description 1
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- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
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- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
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- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
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- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 229960004881 homosalate Drugs 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
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- IWVKTOUOPHGZRX-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.COC(=O)C(C)=C IWVKTOUOPHGZRX-UHFFFAOYSA-N 0.000 description 1
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- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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- 229960003921 octisalate Drugs 0.000 description 1
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- WCJLCOAEJIHPCW-UHFFFAOYSA-N octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O WCJLCOAEJIHPCW-UHFFFAOYSA-N 0.000 description 1
- RPQUGMLCZLGZTG-UHFFFAOYSA-N octyl cyanoacrylate Chemical compound CCCCCCCCOC(=O)C(=C)C#N RPQUGMLCZLGZTG-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical class [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
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- 159000000001 potassium salts Chemical class 0.000 description 1
- OEEUOVDUVFUJCL-KQGICBIGSA-M potassium;(e)-3-(4-methoxyphenyl)prop-2-enoate Chemical compound [K+].COC1=CC=C(\C=C\C([O-])=O)C=C1 OEEUOVDUVFUJCL-KQGICBIGSA-M 0.000 description 1
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- 108091008025 regulatory factors Proteins 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- VOKPJLHFFYVQNS-UHFFFAOYSA-M sodium;3-(4-methoxyphenyl)prop-2-enoate Chemical compound [Na+].COC1=CC=C(C=CC([O-])=O)C=C1 VOKPJLHFFYVQNS-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
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- 238000011105 stabilization Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
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Classifications
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- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4946—Imidazoles or their condensed derivatives, e.g. benzimidazoles
-
- 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
- A61K8/11—Encapsulated compositions
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- 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
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
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)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Medicinal Preparation (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99109515.9 | 1999-05-12 | ||
| EP99109515 | 1999-05-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1274577A true CN1274577A (zh) | 2000-11-29 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN00108286A Pending CN1274577A (zh) | 1999-05-12 | 2000-05-10 | 光稳定的化妆品遮光组合物 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6338838B1 (enExample) |
| EP (1) | EP1051963B1 (enExample) |
| JP (1) | JP2000351721A (enExample) |
| KR (1) | KR20000077250A (enExample) |
| CN (1) | CN1274577A (enExample) |
| AT (1) | ATE334723T1 (enExample) |
| AU (1) | AU779064B2 (enExample) |
| BR (1) | BR0002414A (enExample) |
| CA (1) | CA2307721A1 (enExample) |
| DE (1) | DE60029672T2 (enExample) |
| ES (1) | ES2269040T3 (enExample) |
| ID (1) | ID25985A (enExample) |
| NO (1) | NO20002309L (enExample) |
| TW (1) | TW536406B (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103328582A (zh) * | 2011-01-25 | 2013-09-25 | 住友大阪水泥股份有限公司 | 含有有机系紫外线吸收剂的树脂粒子及其制造方法、含有有机系紫外线吸收剂的树脂粒子分散液、水系分散体和油系分散体、以及化妆料 |
| CN103998559A (zh) * | 2011-12-20 | 2014-08-20 | 住友大阪水泥股份有限公司 | 紫外线遮蔽复合粒子、含有紫外线遮蔽复合粒子的分散液和含有紫外线遮蔽复合粒子的树脂组合物、多层紫外线遮蔽复合粒子和紫外线遮蔽分散液以及化妆料 |
| CN107440918A (zh) * | 2017-08-15 | 2017-12-08 | 成都新柯力化工科技有限公司 | 一种可结膜抗过敏防晒乳护肤品及制备方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2322345A1 (en) * | 1999-10-14 | 2001-04-14 | Rohm And Haas Company | Method for preparing ultraviolet radiation-absorbing compositions |
| JP2001288064A (ja) * | 2000-04-10 | 2001-10-16 | Kao Corp | 化粧料 |
| EP1280505B1 (de) * | 2000-05-12 | 2007-05-02 | Ciba SC Holding AG | Photostabilisierung von dibenzoylmethan-derivaten |
| FR2818126B1 (fr) | 2000-12-18 | 2003-02-07 | Oreal | Composition filtrante photostable contenant un derive de 1,3,5,-triazine, un derive du dibenzoylmethane et un compose 4,4-diarylbutadiene |
| CA2390952C (en) * | 2001-07-02 | 2006-07-11 | Rohm And Haas Company | Compositions and process for retaining active ingredients comprising networked structured polymers |
| US6440402B1 (en) | 2001-12-14 | 2002-08-27 | Avon Products, Inc. | Photostable sunscreen compositions and methods of stabilizing |
| GB0129886D0 (en) * | 2001-12-14 | 2002-02-06 | Medtrade Products Ltd | Scar management composition |
| JP4020680B2 (ja) * | 2002-04-12 | 2007-12-12 | 株式会社ルネサステクノロジ | 半導体集積回路 |
| US7108860B2 (en) * | 2002-06-06 | 2006-09-19 | Playtex Products, Inc. | Sunscreen compositions |
| WO2004069216A1 (en) * | 2003-02-03 | 2004-08-19 | Dsm Ip Assets B.V. | Novel stabilized cinnamic ester sunscreen compositions |
| CA2526626C (en) * | 2003-05-29 | 2012-08-28 | Sun Pharmaceuticals Corporation | Emulsion base for skin care compositions |
| BRPI0415684B1 (pt) * | 2003-11-03 | 2015-12-08 | Ciba Sc Holding Ag | composição estabilizada e processo para estabilizar um produto para tratamento do corpo ou produto para o lar |
| EP1682228B1 (en) * | 2003-11-05 | 2009-12-02 | DSM IP Assets B.V. | Light protecting composition with reduced total amount of uv filter containing a polysiloxane-based uv filter |
| US20070242124A1 (en) * | 2004-05-18 | 2007-10-18 | Mitsui Chemicals, Inc. | Organic Particle for Inkjet Recording Sheet and Recording Sheet |
| FR2895240A1 (fr) * | 2005-12-26 | 2007-06-29 | Dermatologiques D Uriage Sa La | Compositions cosmetiques et dermatologiques pour la protection solaire |
| EP1815844B1 (fr) * | 2005-12-26 | 2015-04-29 | Laboratoires Dermatologiques d'Uriage | Compositions photoprotectrices réduisant les risques de sensibilisation cutanée |
| US20080066773A1 (en) * | 2006-04-21 | 2008-03-20 | Anderson Daniel G | In situ polymerization for hair treatment |
| RU2499607C2 (ru) * | 2006-09-19 | 2013-11-27 | Басф Се | Косметические препараты на основе молекулярно впечатанных полимеров |
| US8680176B2 (en) * | 2007-03-21 | 2014-03-25 | The University Of Southern Mississippi | Nanoencapsulation of isocyanates via aqueous media |
| CN101686909A (zh) | 2007-07-09 | 2010-03-31 | 巴斯夫欧洲公司 | 油溶性有机紫外吸收剂的水基浓缩产品形式 |
| EP2211825B1 (en) * | 2007-11-16 | 2014-08-20 | Dow Global Technologies LLC | Encapsulated low viscosity hydrophobic liquid actives |
| BRPI0905684A2 (pt) * | 2008-01-16 | 2015-07-07 | Dow Global Technologies Inc | Método para melhorar a estética de uma composição de cuidado pessoal e método para melhorar a facilidade de espalhamento, melhorar a adsorção pela pele, reduzir a pegajosidade e a sensação de oleosidade de uma composição de cuidado pessoal |
| EP2135598B1 (en) * | 2008-06-16 | 2011-08-03 | Rohm and Haas Company | Particle Containing Ultraviolet Absorber |
| US8003132B2 (en) | 2008-06-30 | 2011-08-23 | Johnson & Johnson Consumer Companies, Inc. | Compositions comprising an ultraviolet radiation-absorbing polymer |
| JP4299878B1 (ja) | 2008-10-06 | 2009-07-22 | 株式会社パラエルモサ | 化粧料 |
| US8475774B2 (en) * | 2010-02-08 | 2013-07-02 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions comprising an ultraviolet radiation-absorbing polymer |
| JP5058351B2 (ja) * | 2010-04-13 | 2012-10-24 | 株式会社 資生堂 | 水中油型乳化組成物 |
| JP5058352B2 (ja) | 2010-04-13 | 2012-10-24 | 株式会社 資生堂 | 油中水型乳化組成物 |
| EP2559481A1 (de) | 2011-08-16 | 2013-02-20 | Basf Se | Verfahren zur Verkapselung von Substanzen unter Ausbildung der Kapselhülle durch Grenzflächenreaktion im Zentrifugalreaktor |
| US9549891B2 (en) | 2012-03-19 | 2017-01-24 | The Procter & Gamble Company | Superabsorbent polymers and sunscreen actives for use in skin care compositions |
| FR2991684B1 (fr) * | 2012-06-08 | 2015-05-22 | Soc De Developpement Et De Recherche Industrielle | Dispersion aqueuse de particules de polymeres, composition filmogene la contenant et ses utilisations |
| US9255180B2 (en) | 2012-06-28 | 2016-02-09 | Johnson & Johnson Consumer Inc. | Ultraviolet radiation absorbing polyethers |
| BR112014032798B8 (pt) | 2012-06-28 | 2022-08-16 | Chenango Two Llc | Composição |
| US10874603B2 (en) | 2014-05-12 | 2020-12-29 | Johnson & Johnson Consumer Inc. | Sunscreen compositions containing a UV-absorbing polyglycerol and a non-UV-absorbing polyglycerol |
| WO2016210044A1 (en) * | 2015-06-24 | 2016-12-29 | Rohm And Haas Company | Particles containing ultraviolet absorber |
| WO2017004108A1 (en) | 2015-06-29 | 2017-01-05 | The Procter & Gamble Company | Superabsorbent polymers and starch powders for use in skin care compositions |
| KR101833612B1 (ko) * | 2016-03-30 | 2018-02-28 | 선진뷰티사이언스(주) | 다량의 유기계 자외선 차단제를 함유하는 고분자 복합입자 및 그의 제조방법 |
| KR102377585B1 (ko) | 2016-06-16 | 2022-03-24 | 존슨 앤드 존슨 컨수머 인코포레이티드 | 선형 자외 방사선-흡수 폴리에테르 및 다른 자외선-스크리닝 화합물의 배합물을 함유하는 선스크린 조성물 |
| US10596087B2 (en) | 2016-10-05 | 2020-03-24 | Johnson & Johnson Consumer Inc. | Ultraviolet radiation absorbing polymer composition |
| KR102239412B1 (ko) * | 2018-09-28 | 2021-04-12 | 카오카부시키가이샤 | 화장료 |
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| FR2658075B1 (fr) | 1990-02-14 | 1992-05-07 | Oreal | Composition cosmetique filtrante photostable contenant un filtre uv-a et un beta,beta-diphenylacrylate ou alpha-cyano-beta,beta-diphenylacrylate d'alkyle. |
| FR2681248B1 (fr) * | 1991-09-13 | 1995-04-28 | Oreal | Composition pour un traitement cosmetique et/ou pharmaceutique de longue duree des couches superieures de l'epiderme par une application topique sur la peau. |
| FR2687914B1 (fr) * | 1992-03-02 | 1994-05-13 | Isd | Procede pour obtenir un effet anti-uv prolonge, composition conforme a ce procede contenant un composant non enrobe et un composant enrobe. |
| GB9211708D0 (en) | 1992-06-03 | 1992-07-15 | Unilever Plc | Cosmetic composition |
| US5399342A (en) * | 1993-02-03 | 1995-03-21 | Dow Corning Corporation | Cosmetics with enhanced durability |
| DE4336407A1 (de) * | 1993-10-21 | 1995-04-27 | Rotring Int Gmbh | Wasserfeste Kosmetik |
| EP0669124A1 (en) * | 1994-02-28 | 1995-08-30 | Rohm And Haas Company | Ultraviolet radiation absorbing composition |
| US6033649A (en) * | 1995-12-18 | 2000-03-07 | Roche Vitamins Inc. | Light screening agents |
| US5876699A (en) * | 1996-05-14 | 1999-03-02 | Disomma; Joseph | Sunblock composition suitable for sensitive skin areas |
| FR2755856B1 (fr) * | 1996-11-21 | 1999-01-29 | Merck Clevenot Laboratoires | Microcapsules de chitine ou de derives de chitine contenant une substance hydrophobe, notamment un filtre solaire et procede de preparation de telles microcapsules |
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2000
- 2000-04-28 NO NO20002309A patent/NO20002309L/no not_active Application Discontinuation
- 2000-05-05 AT AT00109584T patent/ATE334723T1/de not_active IP Right Cessation
- 2000-05-05 DE DE60029672T patent/DE60029672T2/de not_active Expired - Fee Related
- 2000-05-05 EP EP00109584A patent/EP1051963B1/en not_active Expired - Lifetime
- 2000-05-05 ES ES00109584T patent/ES2269040T3/es not_active Expired - Lifetime
- 2000-05-08 CA CA002307721A patent/CA2307721A1/en not_active Abandoned
- 2000-05-09 US US09/567,652 patent/US6338838B1/en not_active Expired - Fee Related
- 2000-05-10 CN CN00108286A patent/CN1274577A/zh active Pending
- 2000-05-11 ID IDP20000396D patent/ID25985A/id unknown
- 2000-05-11 AU AU34032/00A patent/AU779064B2/en not_active Ceased
- 2000-05-11 JP JP2000137933A patent/JP2000351721A/ja active Pending
- 2000-05-11 BR BR0002414-7A patent/BR0002414A/pt not_active IP Right Cessation
- 2000-05-12 KR KR1020000025458A patent/KR20000077250A/ko not_active Ceased
- 2000-05-26 TW TW089110266A patent/TW536406B/zh active
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103328582A (zh) * | 2011-01-25 | 2013-09-25 | 住友大阪水泥股份有限公司 | 含有有机系紫外线吸收剂的树脂粒子及其制造方法、含有有机系紫外线吸收剂的树脂粒子分散液、水系分散体和油系分散体、以及化妆料 |
| CN103998559A (zh) * | 2011-12-20 | 2014-08-20 | 住友大阪水泥股份有限公司 | 紫外线遮蔽复合粒子、含有紫外线遮蔽复合粒子的分散液和含有紫外线遮蔽复合粒子的树脂组合物、多层紫外线遮蔽复合粒子和紫外线遮蔽分散液以及化妆料 |
| CN107440918A (zh) * | 2017-08-15 | 2017-12-08 | 成都新柯力化工科技有限公司 | 一种可结膜抗过敏防晒乳护肤品及制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| BR0002414A (pt) | 2001-01-02 |
| AU3403200A (en) | 2000-11-23 |
| US6338838B1 (en) | 2002-01-15 |
| ES2269040T3 (es) | 2007-04-01 |
| ATE334723T1 (de) | 2006-08-15 |
| KR20000077250A (ko) | 2000-12-26 |
| DE60029672T2 (de) | 2007-10-31 |
| JP2000351721A (ja) | 2000-12-19 |
| CA2307721A1 (en) | 2000-11-12 |
| TW536406B (en) | 2003-06-11 |
| ID25985A (id) | 2000-11-16 |
| NO20002309L (no) | 2000-11-13 |
| EP1051963B1 (en) | 2006-08-02 |
| NO20002309D0 (no) | 2000-04-28 |
| AU779064B2 (en) | 2005-01-06 |
| EP1051963A1 (en) | 2000-11-15 |
| DE60029672D1 (de) | 2006-09-14 |
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