JPH09501666A - 日焼け止め剤 - Google Patents
日焼け止め剤Info
- Publication number
- JPH09501666A JPH09501666A JP7506739A JP50673995A JPH09501666A JP H09501666 A JPH09501666 A JP H09501666A JP 7506739 A JP7506739 A JP 7506739A JP 50673995 A JP50673995 A JP 50673995A JP H09501666 A JPH09501666 A JP H09501666A
- Authority
- JP
- Japan
- Prior art keywords
- benzophenone
- hydroxy
- anion
- anions
- hydroxy salt
- 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.)
- Pending
Links
- 239000000516 sunscreening agent Substances 0.000 title claims abstract description 24
- 230000000475 sunscreen effect Effects 0.000 title claims abstract description 22
- 150000001450 anions Chemical group 0.000 claims abstract description 42
- 239000000203 mixture Substances 0.000 claims abstract description 18
- 239000011701 zinc Substances 0.000 claims abstract description 17
- 239000010949 copper Chemical group 0.000 claims abstract description 13
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 13
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052802 copper Inorganic materials 0.000 claims abstract description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 5
- -1 3-imidazole-4-yl-acrylate salicylate p-methoxycinnamate Chemical compound 0.000 claims description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 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 claims description 7
- 230000008033 biological extinction Effects 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 230000005855 radiation Effects 0.000 claims description 6
- 229960000368 sulisobenzone Drugs 0.000 claims description 5
- 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 claims description 4
- 229960004881 homosalate Drugs 0.000 claims description 4
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 claims description 4
- OMWSZDODENFLSV-UHFFFAOYSA-N (5-chloro-2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=C(Cl)C=C1C(=O)C1=CC=CC=C1 OMWSZDODENFLSV-UHFFFAOYSA-N 0.000 claims description 3
- 229940079894 benzophenone-9 Drugs 0.000 claims description 3
- WXNRYSGJLQFHBR-UHFFFAOYSA-N bis(2,4-dihydroxyphenyl)methanone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1O WXNRYSGJLQFHBR-UHFFFAOYSA-N 0.000 claims description 3
- SODJJEXAWOSSON-UHFFFAOYSA-N bis(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C=C1O SODJJEXAWOSSON-UHFFFAOYSA-N 0.000 claims description 3
- QDCHWIWENYCPIL-UHFFFAOYSA-L disodium;4-hydroxy-5-(2-hydroxy-4-methoxy-5-sulfonatobenzoyl)-2-methoxybenzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC(S([O-])(=O)=O)=C(OC)C=C1O QDCHWIWENYCPIL-UHFFFAOYSA-L 0.000 claims description 3
- MJVGBKJNTFCUJM-UHFFFAOYSA-N mexenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(C)C=C1 MJVGBKJNTFCUJM-UHFFFAOYSA-N 0.000 claims description 3
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 3
- MEZZCSHVIGVWFI-UHFFFAOYSA-N 2,2'-Dihydroxy-4-methoxybenzophenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1O MEZZCSHVIGVWFI-UHFFFAOYSA-N 0.000 claims description 2
- KERMUFCCTOREID-UHFFFAOYSA-N 5-methyl-2-[(4,7,7-trimethyl-3-oxo-2-bicyclo[2.2.1]heptanylidene)methyl]benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(C)=CC=C1C=C1C(=O)C2(C)CCC1C2(C)C KERMUFCCTOREID-UHFFFAOYSA-N 0.000 claims description 2
- RQQINPZVZGNJGE-UHFFFAOYSA-N C1(=CC=CC=C1)C=1NC2=C(N1)C=CC(=C2)S(=O)(=O)O.C(#N)C(C(=O)O)=CC2=CC=C(C=C2)OC Chemical compound C1(=CC=CC=C1)C=1NC2=C(N1)C=CC(=C2)S(=O)(=O)O.C(#N)C(C(=O)O)=CC2=CC=C(C=C2)OC RQQINPZVZGNJGE-UHFFFAOYSA-N 0.000 claims description 2
- 229940111759 benzophenone-2 Drugs 0.000 claims description 2
- 229960001173 oxybenzone Drugs 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- KJCLYACXIWMFCC-UHFFFAOYSA-M sodium;5-benzoyl-4-hydroxy-2-methoxybenzenesulfonate Chemical compound [Na+].C1=C(S([O-])(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 KJCLYACXIWMFCC-UHFFFAOYSA-M 0.000 claims description 2
- PDHSAQOQVUXZGQ-JKSUJKDBSA-N (2r,3s)-2-(3,4-dihydroxyphenyl)-3-methoxy-3,4-dihydro-2h-chromene-5,7-diol Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2OC)=CC=C(O)C(O)=C1 PDHSAQOQVUXZGQ-JKSUJKDBSA-N 0.000 claims 1
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical group OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 claims 1
- ZZGVYXFYYYIGEG-UHFFFAOYSA-N COC1=C(C=CC2=C1C=CO2)C(CC(=O)C2=CC=CC=C2)=O.C(CCC)C(C(C2=CC=CC=C2)=O)(C(C2=CC=CC=C2)=O)OC Chemical compound COC1=C(C=CC2=C1C=CO2)C(CC(=O)C2=CC=CC=C2)=O.C(CCC)C(C(C2=CC=CC=C2)=O)(C(C2=CC=CC=C2)=O)OC ZZGVYXFYYYIGEG-UHFFFAOYSA-N 0.000 claims 1
- SXAKRCIHMLAQQJ-UHFFFAOYSA-N COC=1C=C(C=CC1OC)C(C(=O)O)=O.NC1=CC=C(C(=O)O)C=C1.C(C=CC1=CC=CC=C1)(=O)O Chemical compound COC=1C=C(C=CC1OC)C(C(=O)O)=O.NC1=CC=C(C(=O)O)C=C1.C(C=CC1=CC=CC=C1)(=O)O SXAKRCIHMLAQQJ-UHFFFAOYSA-N 0.000 claims 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical group C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims 1
- FMJSMJQBSVNSBF-UHFFFAOYSA-N octocrylene Chemical compound C=1C=CC=CC=1C(=C(C#N)C(=O)OCC(CC)CCCC)C1=CC=CC=C1 FMJSMJQBSVNSBF-UHFFFAOYSA-N 0.000 claims 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 29
- 239000000047 product Substances 0.000 description 27
- 238000010521 absorption reaction Methods 0.000 description 22
- 238000002835 absorbance Methods 0.000 description 19
- 239000000463 material Substances 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 239000000126 substance Substances 0.000 description 15
- 239000000725 suspension Substances 0.000 description 14
- 210000003491 skin Anatomy 0.000 description 11
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 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 8
- 238000004458 analytical method Methods 0.000 description 8
- 239000004743 Polypropylene Substances 0.000 description 7
- 238000005342 ion exchange Methods 0.000 description 7
- 229920001155 polypropylene Polymers 0.000 description 7
- 238000000634 powder X-ray diffraction Methods 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 238000000862 absorption spectrum Methods 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 239000011787 zinc oxide Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000012265 solid product Substances 0.000 description 4
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 4
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 3
- UVCJGUGAGLDPAA-UHFFFAOYSA-N ensulizole Chemical compound N1C2=CC(S(=O)(=O)O)=CC=C2N=C1C1=CC=CC=C1 UVCJGUGAGLDPAA-UHFFFAOYSA-N 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000002211 ultraviolet spectrum Methods 0.000 description 3
- ALYNCZNDIQEVRV-UHFFFAOYSA-M 4-aminobenzoate Chemical compound NC1=CC=C(C([O-])=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-M 0.000 description 2
- 101150057104 MCIDAS gene Proteins 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 210000004207 dermis Anatomy 0.000 description 2
- 125000005594 diketone group Chemical group 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- AFDXODALSZRGIH-UHFFFAOYSA-N p-coumaric acid methyl ether Natural products COC1=CC=C(C=CC(O)=O)C=C1 AFDXODALSZRGIH-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- TYYHDKOVFSVWON-UHFFFAOYSA-N 2-butyl-2-methoxy-1,3-diphenylpropane-1,3-dione Chemical compound C=1C=CC=CC=1C(=O)C(OC)(CCCC)C(=O)C1=CC=CC=C1 TYYHDKOVFSVWON-UHFFFAOYSA-N 0.000 description 1
- AXZDITJWGFHAAA-UHFFFAOYSA-N 2-ethylhexyl 2-hydroxybenzoate;octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O.CCCCC(CC)COC(=O)C1=CC=CC=C1O AXZDITJWGFHAAA-UHFFFAOYSA-N 0.000 description 1
- HCSDAMGBOVWGEO-UHFFFAOYSA-N 3-oxo-3-phenylpropanal Chemical compound O=CCC(=O)C1=CC=CC=C1 HCSDAMGBOVWGEO-UHFFFAOYSA-N 0.000 description 1
- IEPXIXQWFCUFOL-UHFFFAOYSA-N 4-aminobenzoic acid;benzoic acid Chemical compound OC(=O)C1=CC=CC=C1.NC1=CC=C(C(O)=O)C=C1 IEPXIXQWFCUFOL-UHFFFAOYSA-N 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- 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 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 208000012641 Pigmentation disease Diseases 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 206010042496 Sunburn Diseases 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000008135 aqueous vehicle Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 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 description 1
- 229960005193 avobenzone Drugs 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 125000002587 enol group Chemical group 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000002245 particle Substances 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
- 230000000258 photobiological effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 230000009759 skin aging Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- DXIHILNWDOYYCH-UHDJGPCESA-M sodium;(e)-3-phenylprop-2-enoate Chemical compound [Na+].[O-]C(=O)\C=C\C1=CC=CC=C1 DXIHILNWDOYYCH-UHDJGPCESA-M 0.000 description 1
- BHLQWVRSTSGMPR-UHFFFAOYSA-M sodium;2-methoxy-3-phenylprop-2-enoate Chemical compound [Na+].COC(C([O-])=O)=CC1=CC=CC=C1 BHLQWVRSTSGMPR-UHFFFAOYSA-M 0.000 description 1
- XETSAYZRDCRPJY-UHFFFAOYSA-M sodium;4-aminobenzoate Chemical compound [Na+].NC1=CC=C(C([O-])=O)C=C1 XETSAYZRDCRPJY-UHFFFAOYSA-M 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
Classifications
-
- 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
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/27—Zinc; Compounds thereof
-
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
-
- 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
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/413—Nanosized, i.e. having sizes below 100 nm
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Nanotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Biotechnology (AREA)
- Emergency Medicine (AREA)
- Medical Informatics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Pharmacology & Pharmacy (AREA)
- Crystallography & Structural Chemistry (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB939316901A GB9316901D0 (en) | 1993-08-13 | 1993-08-13 | Sunscreen agents |
| GB9316901.9 | 1993-08-13 | ||
| PCT/EP1994/002669 WO1995005150A1 (en) | 1993-08-13 | 1994-08-10 | Sunscreen agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH09501666A true JPH09501666A (ja) | 1997-02-18 |
Family
ID=10740476
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7506739A Pending JPH09501666A (ja) | 1993-08-13 | 1994-08-10 | 日焼け止め剤 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5573755A (en, 2012) |
| EP (1) | EP0713383B1 (en, 2012) |
| JP (1) | JPH09501666A (en, 2012) |
| AU (1) | AU7652994A (en, 2012) |
| CA (1) | CA2166467C (en, 2012) |
| DE (1) | DE69411174T2 (en, 2012) |
| ES (1) | ES2119223T3 (en, 2012) |
| GB (1) | GB9316901D0 (en, 2012) |
| IN (2) | IN181735B (en, 2012) |
| WO (1) | WO1995005150A1 (en, 2012) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9424445D0 (en) * | 1994-12-02 | 1995-01-18 | Unilever Plc | Cosmetic composition |
| AU701182B2 (en) * | 1995-04-10 | 1999-01-21 | Kyowa Chemical Industry Co., Ltd. | Ultraviolet protective agent |
| US6019990A (en) * | 1997-11-21 | 2000-02-01 | Natural Nutrition Ltd. As | Conjugated linoleic acid delivery system in cosmetic preparations |
| FR2803224B1 (fr) * | 1999-12-30 | 2002-09-27 | Rhodia Chimie Sa | Dispersion colloidale aqueuse a base d'au moins un compose d'un metal et d'un complexant, procede de preparation et utilisation |
| US6866841B2 (en) * | 2001-08-09 | 2005-03-15 | Epatentmanager.Com | Non-endocrine disrupting cytoprotective UV radiation resistant substance |
| FR2833164B1 (fr) | 2001-12-07 | 2004-07-16 | Oreal | Compositions cosmetiques antisolaires a base d'un melange synergique de filtres et utilisations |
| US20040126337A1 (en) * | 2002-12-30 | 2004-07-01 | Singleton Laura C. | Sunscreen compositions |
| US20070218021A1 (en) * | 2006-03-20 | 2007-09-20 | Azur Skin International | Non-irritating sunscreen composition |
| US20080219939A1 (en) * | 2007-03-07 | 2008-09-11 | Grune Guerry L | Sunblock formulations |
| EP2569377A4 (en) | 2010-05-10 | 2015-01-21 | Segetis Inc | ALKYLCETALS ESTERS AS DISPERSANTS AND SLURRIES FOR PARTICULATE SOLIDS, PROCESSES FOR PREPARING THE SAME, AND USES THEREOF |
| MX348556B (es) | 2011-01-28 | 2017-06-16 | Momentive Performance Mat Gmbh | Composicion cosmetica fotoprotectora de rayos ultravioleta. |
| US11266584B2 (en) | 2012-07-13 | 2022-03-08 | L'oreal | Cosmetic composition comprising composite sunscreen particles |
| FR2993176B1 (fr) | 2012-07-13 | 2014-06-27 | Oreal | Composition cosmetique contenant des particules composites filtrantes de taille moyenne superieure a 0,1 micron et des particules de filtre inorganique et une phase aqueuse |
| JP6100897B2 (ja) | 2012-07-13 | 2017-03-22 | ロレアル | 複合顔料及びその調製方法 |
| US20150157539A1 (en) | 2012-07-13 | 2015-06-11 | L'oreal | Cosmetic composition comprising composite particles |
| JP6100896B2 (ja) | 2012-07-13 | 2017-03-22 | ロレアル | 複合顔料及びその調製方法 |
| AU2013352172A1 (en) | 2012-11-29 | 2015-06-11 | Gfbiochemicals Limited | Carboxy ester ketals, methods of manufacture, and uses thereof |
| BR112015017269B1 (pt) | 2013-01-21 | 2020-03-10 | L'oreal | Composição cosmética e processos cosméticos não terapêuticos |
| EP3185843B2 (fr) | 2014-08-28 | 2025-07-02 | L'oreal | Composition gel/gel comprenant un filtre uv |
| EP3223777A1 (fr) | 2014-11-24 | 2017-10-04 | L'Oréal | Composition cosmetique comprenant un phyllosilicate synthetique et un polyol et/ou un filtre uv |
| FR3037243B1 (fr) | 2015-06-11 | 2018-11-16 | L'oreal | Composition comprenant un filtre uv, un polymere hydrophile reticule anionique, un tensioactif ayant une hlb inferieure ou egale a 5 et un copolymere silicone |
| FR3073408B1 (fr) | 2017-11-15 | 2019-10-11 | L'oreal | Compositions comprenant au moins un polymere acrylique et au moins un filtre organique insoluble |
| FR3083093A1 (fr) | 2018-06-28 | 2020-01-03 | L'oreal | Composition photoprotectrice comprenant des particules de silice colloidale |
| FR3090329B1 (fr) | 2018-12-21 | 2020-12-04 | Oreal | Composition comprenant un filtre UV, un polymère hydrophile réticulé anionique, un tensioactif ayant une HLB inférieure ou égale à 5 et un alcane non volatil |
| FR3103704B1 (fr) | 2019-11-29 | 2022-07-08 | Oreal | Composition comprenant un filtre UV, un polymère éthylénique à groupe acide phosphonique et une huile hydrocarbonée |
| FR3103705B1 (fr) | 2019-11-29 | 2021-12-17 | Oreal | Composition comprenant un filtre UV, un polymère séquencé à groupe acide phosphonique et une huile hydrocarbonée |
| GB2634313A (en) * | 2023-10-06 | 2025-04-09 | Scg Chemicals Public Company Ltd | Cosmetic composition |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4664843A (en) * | 1985-07-05 | 1987-05-12 | The Dow Chemical Company | Mixed metal layered hydroxide-clay adducts as thickeners for water and other hydrophylic fluids |
| GB8925473D0 (en) * | 1989-11-10 | 1989-12-28 | Unilever Plc | Sunscreen compositions |
| FR2662079B1 (fr) * | 1990-05-18 | 1993-11-05 | Oreal | Emulsion cosmetique filtrante comprenant un filtre uv-a et un filtre uv-b et son utilisation pour la protection de la peau contre les radiations ultraviolettes. |
| DE4018628A1 (de) * | 1990-06-11 | 1991-12-12 | Henkel Kgaa | Koagulationsmittel auf der basis von doppelschichthydroxid-verbindungen |
| DE4020272A1 (de) * | 1990-06-26 | 1992-01-02 | Henkel Kgaa | Pigmente auf basis von doppelschicht-hydroxiden, verfahren zu deren herstellung sowie deren verwendung |
| AU3132193A (en) * | 1991-11-27 | 1993-06-28 | Richardson-Vicks Inc. | Uva-absorbing sunscreen metal complexes |
| GB9203806D0 (en) * | 1992-02-21 | 1992-04-08 | Unilever Plc | Sunscreen agents |
-
1993
- 1993-08-13 GB GB939316901A patent/GB9316901D0/en active Pending
-
1994
- 1994-08-10 JP JP7506739A patent/JPH09501666A/ja active Pending
- 1994-08-10 CA CA002166467A patent/CA2166467C/en not_active Expired - Fee Related
- 1994-08-10 AU AU76529/94A patent/AU7652994A/en not_active Abandoned
- 1994-08-10 EP EP94926830A patent/EP0713383B1/en not_active Expired - Lifetime
- 1994-08-10 WO PCT/EP1994/002669 patent/WO1995005150A1/en active IP Right Grant
- 1994-08-10 ES ES94926830T patent/ES2119223T3/es not_active Expired - Lifetime
- 1994-08-10 DE DE69411174T patent/DE69411174T2/de not_active Expired - Fee Related
- 1994-08-11 IN IN388BO1994 patent/IN181735B/en unknown
- 1994-08-11 US US08/289,042 patent/US5573755A/en not_active Expired - Fee Related
-
1998
- 1998-03-24 IN IN175BO1998 patent/IN187150B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0713383A1 (en) | 1996-05-29 |
| IN181735B (en, 2012) | 1998-09-12 |
| CA2166467A1 (en) | 1995-02-23 |
| WO1995005150A1 (en) | 1995-02-23 |
| US5573755A (en) | 1996-11-12 |
| GB9316901D0 (en) | 1993-09-29 |
| AU7652994A (en) | 1995-03-14 |
| DE69411174T2 (de) | 1998-10-29 |
| IN187150B (en, 2012) | 2002-02-16 |
| CA2166467C (en) | 2006-11-21 |
| DE69411174D1 (de) | 1998-07-23 |
| ES2119223T3 (es) | 1998-10-01 |
| EP0713383B1 (en) | 1998-06-17 |
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