CA2673743A1 - Emulsion product for use as sunscreen, cosmetic agent or a carrier for an active ingredient - Google Patents
Emulsion product for use as sunscreen, cosmetic agent or a carrier for an active ingredient Download PDFInfo
- Publication number
- CA2673743A1 CA2673743A1 CA002673743A CA2673743A CA2673743A1 CA 2673743 A1 CA2673743 A1 CA 2673743A1 CA 002673743 A CA002673743 A CA 002673743A CA 2673743 A CA2673743 A CA 2673743A CA 2673743 A1 CA2673743 A1 CA 2673743A1
- Authority
- CA
- Canada
- Prior art keywords
- product
- water
- range
- sunscreen
- emulsion
- 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.)
- Abandoned
Links
- 239000000516 sunscreening agent Substances 0.000 title claims abstract description 175
- 230000000475 sunscreen effect Effects 0.000 title claims abstract description 138
- 239000002537 cosmetic Substances 0.000 title claims abstract description 15
- 239000004480 active ingredient Substances 0.000 title claims abstract description 11
- 239000000839 emulsion Substances 0.000 title description 10
- 239000000203 mixture Substances 0.000 claims abstract description 80
- 238000004519 manufacturing process Methods 0.000 claims abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 316
- 230000037072 sun protection Effects 0.000 claims description 104
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 102
- 238000000034 method Methods 0.000 claims description 62
- 230000003068 static effect Effects 0.000 claims description 57
- 125000004432 carbon atom Chemical group C* 0.000 claims description 44
- 239000000084 colloidal system Substances 0.000 claims description 32
- 238000003756 stirring Methods 0.000 claims description 30
- 150000002148 esters Chemical class 0.000 claims description 25
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 24
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 22
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 22
- 229910000077 silane Inorganic materials 0.000 claims description 22
- 238000009738 saturating Methods 0.000 claims description 20
- -1 PPG-15 stearyl ether Chemical compound 0.000 claims description 19
- 229920001059 synthetic polymer Polymers 0.000 claims description 17
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 15
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 15
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 15
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 14
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 13
- 239000012965 benzophenone Substances 0.000 claims description 13
- 150000002576 ketones Chemical class 0.000 claims description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 12
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims description 12
- 238000002156 mixing Methods 0.000 claims description 12
- 229960001679 octinoxate Drugs 0.000 claims description 12
- 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 12
- 229960000601 octocrylene Drugs 0.000 claims description 12
- 229940078491 ppg-15 stearyl ether Drugs 0.000 claims description 12
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 12
- 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 11
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 11
- ZQCIPRGNRQXXSK-UHFFFAOYSA-N 1-octadecoxypropan-2-ol Chemical compound CCCCCCCCCCCCCCCCCCOCC(C)O ZQCIPRGNRQXXSK-UHFFFAOYSA-N 0.000 claims description 10
- 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 claims description 10
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 10
- 229960001173 oxybenzone Drugs 0.000 claims description 10
- SFFVATKALSIZGN-UHFFFAOYSA-N hexadecan-7-ol Chemical compound CCCCCCCCCC(O)CCCCCC SFFVATKALSIZGN-UHFFFAOYSA-N 0.000 claims description 8
- OOHTWBUKWQKKEE-UHFFFAOYSA-N [6-(diethylamino)-6-hydroxy-7-oxo-7-phenylheptyl] benzoate Chemical compound C=1C=CC=CC=1C(=O)C(O)(N(CC)CC)CCCCCOC(=O)C1=CC=CC=C1 OOHTWBUKWQKKEE-UHFFFAOYSA-N 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 7
- 229960001630 diethylamino hydroxybenzoyl hexyl benzoate Drugs 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 6
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 6
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- UUGLJVMIFJNVFH-UHFFFAOYSA-N Hexyl benzoate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1 UUGLJVMIFJNVFH-UHFFFAOYSA-N 0.000 claims description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 4
- 229940114081 cinnamate Drugs 0.000 claims description 4
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 4
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- 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 2
- 229960004881 homosalate Drugs 0.000 claims description 2
- 229940093476 ethylene glycol Drugs 0.000 claims 2
- 238000009472 formulation Methods 0.000 abstract description 13
- 239000000047 product Substances 0.000 description 307
- 235000019441 ethanol Nutrition 0.000 description 74
- 238000012360 testing method Methods 0.000 description 74
- 238000007654 immersion Methods 0.000 description 56
- 238000010998 test method Methods 0.000 description 25
- 239000007788 liquid Substances 0.000 description 21
- 239000012071 phase Substances 0.000 description 21
- 230000004224 protection Effects 0.000 description 20
- 239000002244 precipitate Substances 0.000 description 13
- 230000014759 maintenance of location Effects 0.000 description 12
- 150000001298 alcohols Chemical class 0.000 description 11
- 102100035174 SEC14-like protein 2 Human genes 0.000 description 10
- 101710188106 SEC14-like protein 2 Proteins 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- 238000002372 labelling Methods 0.000 description 8
- 206010015150 Erythema Diseases 0.000 description 7
- 238000011835 investigation Methods 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- 230000005855 radiation Effects 0.000 description 7
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- 231100000321 erythema Toxicity 0.000 description 6
- 230000003711 photoprotective effect Effects 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000004904 UV filter Substances 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 5
- 238000004364 calculation method Methods 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 239000007908 nanoemulsion Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 230000009182 swimming Effects 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 230000006870 function Effects 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 230000004044 response Effects 0.000 description 4
- 150000004756 silanes Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 4
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
- ZKYCLDTVJCJYIB-UHFFFAOYSA-N 2-methylidenedecanamide Chemical compound CCCCCCCCC(=C)C(N)=O ZKYCLDTVJCJYIB-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 125000003158 alcohol group Chemical group 0.000 description 3
- 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 3
- 238000003287 bathing Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 230000005284 excitation Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000036555 skin type Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 229910052724 xenon Inorganic materials 0.000 description 3
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 3
- IFVQFBULOVQQCH-UHFFFAOYSA-N 1,3,5,7,9,11,13-heptaoxa-2,4,6,8,10,12,14-heptasilacyclotetradecane 1,3,5,7,9,11-hexaoxa-2,4,6,8,10,12-hexasilacyclododecane 1,3,5,2,4,6-trioxatrisilinane Chemical compound O1[SiH2]O[SiH2]O[SiH2]1.O1[SiH2]O[SiH2]O[SiH2]O[SiH2]O[SiH2]O[SiH2]1.O1[SiH2]O[SiH2]O[SiH2]O[SiH2]O[SiH2]O[SiH2]O[SiH2]1 IFVQFBULOVQQCH-UHFFFAOYSA-N 0.000 description 2
- TURGQPDWYFJEDY-UHFFFAOYSA-N 1-hydroperoxypropane Chemical compound CCCOO TURGQPDWYFJEDY-UHFFFAOYSA-N 0.000 description 2
- SOJKBVIEJXRQQT-UHFFFAOYSA-N 11-hexyloctacosan-11-ol Chemical compound CCCCCCCCCCCCCCCCCC(O)(CCCCCC)CCCCCCCCCC SOJKBVIEJXRQQT-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
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 101001013208 Homo sapiens Mediator of RNA polymerase II transcription subunit 15 Proteins 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 102100029663 Mediator of RNA polymerase II transcription subunit 15 Human genes 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 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
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 238000007605 air drying Methods 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- CWJNMKKMGIAGDK-UHFFFAOYSA-N amtolmetin guacil Chemical compound COC1=CC=CC=C1OC(=O)CNC(=O)CC(N1C)=CC=C1C(=O)C1=CC=C(C)C=C1 CWJNMKKMGIAGDK-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 229940086555 cyclomethicone Drugs 0.000 description 2
- DDJSWKLBKSLAAZ-UHFFFAOYSA-N cyclotetrasiloxane Chemical compound O1[SiH2]O[SiH2]O[SiH2]O[SiH2]1 DDJSWKLBKSLAAZ-UHFFFAOYSA-N 0.000 description 2
- 239000003398 denaturant Substances 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 239000003974 emollient agent Substances 0.000 description 2
- 238000000695 excitation spectrum Methods 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
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- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 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
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229940096956 ppg-11 stearyl ether Drugs 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000000750 progressive effect Effects 0.000 description 2
- 230000001737 promoting effect Effects 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
- 239000004576 sand Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
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- 239000007787 solid Substances 0.000 description 2
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- 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 description 1
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 101100361281 Caenorhabditis elegans rpm-1 gene Proteins 0.000 description 1
- 101100478119 Caenorhabditis elegans spe-6 gene Proteins 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 206010040799 Skin atrophy Diseases 0.000 description 1
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- 235000021355 Stearic acid Nutrition 0.000 description 1
- 206010042496 Sunburn Diseases 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 1
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000032912 absorption of UV light Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
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- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
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- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- CMDKPGRTAQVGFQ-RMKNXTFCSA-N cinoxate Chemical compound CCOCCOC(=O)\C=C\C1=CC=C(OC)C=C1 CMDKPGRTAQVGFQ-RMKNXTFCSA-N 0.000 description 1
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- VWTINHYPRWEBQY-UHFFFAOYSA-N denatonium Chemical compound [O-]C(=O)C1=CC=CC=C1.C=1C=CC=CC=1C[N+](CC)(CC)CC(=O)NC1=C(C)C=CC=C1C VWTINHYPRWEBQY-UHFFFAOYSA-N 0.000 description 1
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- UVCJGUGAGLDPAA-UHFFFAOYSA-N ensulizole Chemical compound N1C2=CC(S(=O)(=O)O)=CC=C2N=C1C1=CC=CC=C1 UVCJGUGAGLDPAA-UHFFFAOYSA-N 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
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- 238000011049 filling Methods 0.000 description 1
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- 229940075507 glyceryl monostearate Drugs 0.000 description 1
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- 229920001519 homopolymer Polymers 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010982 kinetic investigation Methods 0.000 description 1
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- 230000002045 lasting effect Effects 0.000 description 1
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- 239000006210 lotion Substances 0.000 description 1
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- 230000001404 mediated effect Effects 0.000 description 1
- SOXAGEOHPCXXIO-DVOMOZLQSA-N menthyl anthranilate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)C1=CC=CC=C1N SOXAGEOHPCXXIO-DVOMOZLQSA-N 0.000 description 1
- 229960002248 meradimate Drugs 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960003921 octisalate Drugs 0.000 description 1
- WCJLCOAEJIHPCW-UHFFFAOYSA-N octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O WCJLCOAEJIHPCW-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229950000516 padimate Drugs 0.000 description 1
- LXTZRIBXKVRLOA-UHFFFAOYSA-N padimate a Chemical compound CCCCCOC(=O)C1=CC=C(N(C)C)C=C1 LXTZRIBXKVRLOA-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 231100000760 phototoxic Toxicity 0.000 description 1
- 230000037081 physical activity Effects 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000012545 processing Methods 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
- 150000003839 salts Chemical class 0.000 description 1
- 238000011012 sanitization Methods 0.000 description 1
- 210000001991 scapula Anatomy 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 230000009759 skin aging Effects 0.000 description 1
- 231100000075 skin burn Toxicity 0.000 description 1
- 230000035483 skin reaction Effects 0.000 description 1
- 231100000430 skin reaction Toxicity 0.000 description 1
- 229940036051 sojourn Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 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
- 230000035900 sweating Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229960005196 titanium dioxide Drugs 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- UEVAMYPIMMOEFW-UHFFFAOYSA-N trolamine salicylate Chemical compound OCCN(CCO)CCO.OC(=O)C1=CC=CC=C1O UEVAMYPIMMOEFW-UHFFFAOYSA-N 0.000 description 1
- 229940030300 trolamine salicylate Drugs 0.000 description 1
- 238000010200 validation analysis Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229960001296 zinc oxide Drugs 0.000 description 1
Classifications
-
- 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
- A61K8/34—Alcohols
-
- 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
- A61K8/73—Polysaccharides
- A61K8/731—Cellulose; Quaternized cellulose derivatives
-
- 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
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)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US84575306P | 2006-09-20 | 2006-09-20 | |
| DKPA200601213 | 2006-09-20 | ||
| DKPA200601213 | 2006-09-20 | ||
| US60/845,753 | 2006-09-20 | ||
| PCT/DK2007/050131 WO2008034447A1 (en) | 2006-09-20 | 2007-09-20 | Emulsion |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2673743A1 true CA2673743A1 (en) | 2008-03-27 |
Family
ID=37964529
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002673743A Abandoned CA2673743A1 (en) | 2006-09-20 | 2007-09-20 | Emulsion product for use as sunscreen, cosmetic agent or a carrier for an active ingredient |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20100040566A1 (https=) |
| EP (2) | EP2066286B1 (https=) |
| JP (1) | JP2010504291A (https=) |
| CN (1) | CN101557794A (https=) |
| AT (1) | ATE536166T1 (https=) |
| AU (1) | AU2007299376B2 (https=) |
| BR (1) | BRPI0718454A2 (https=) |
| CA (1) | CA2673743A1 (https=) |
| MX (1) | MX2009003060A (https=) |
| NO (1) | NO20091517L (https=) |
| NZ (1) | NZ575783A (https=) |
| WO (1) | WO2008034447A1 (https=) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2497457A1 (en) * | 2009-11-06 | 2012-09-12 | Kao Corporation | Emulsion cosmetic |
| KR101769170B1 (ko) * | 2009-11-06 | 2017-08-17 | 카오카부시키가이샤 | 수중유형 유화 화장료 |
| US10732171B2 (en) | 2011-12-20 | 2020-08-04 | The Procter & Gamble Company | Human skin sample methods and models for validating hypotheses for mechanisms driving skin pigmentation |
| US9089536B2 (en) | 2012-06-06 | 2015-07-28 | Brian J. Smith | Ophthalmic solution for absorbing ultraviolet radiation and method for absorbing ultraviolet radiation |
| DE102013215828A1 (de) | 2013-08-09 | 2015-02-12 | Beiersdorf Ag | Gelförmiges Sonnenschutzmittel mit Fettalkoholen |
| DE102013215831A1 (de) * | 2013-08-09 | 2015-02-12 | Beiersdorf Ag | Gelförmiges, alkoholisches Sonnenschutzmittel |
| WO2016068300A1 (ja) * | 2014-10-31 | 2016-05-06 | 株式会社 資生堂 | 日焼け止め化粧料 |
| CN107072919A (zh) * | 2014-10-31 | 2017-08-18 | 株式会社资生堂 | 油包水型乳化防晒化妆品 |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3529055A (en) * | 1966-03-18 | 1970-09-15 | Nat Starch Chem Corp | Suntan composition and method containing alkali soluble polymeric sun screening agents |
| US4193989A (en) * | 1976-09-27 | 1980-03-18 | Anheuser-Busch, Incorporated | Sunscreen gel |
| US4686099A (en) * | 1985-12-10 | 1987-08-11 | Victor Palinczar | Aerosol waterproof sunscreen compositions |
| US4731242A (en) * | 1986-03-21 | 1988-03-15 | Victor Palinczar | Waterproof sunscreen compositions |
| 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 |
| US5017366A (en) * | 1988-12-29 | 1991-05-21 | Stiefel Laboratories, Inc. | Pharmaceutical compositions |
| FR2650824B1 (fr) * | 1989-07-18 | 1993-01-22 | Cird | Thioesters bi-aromatiques, leur procede de preparation et leur utilisation en medecine humaine ou veterinaire et en cosmetique |
| ES2227563T3 (es) * | 1994-11-03 | 2005-04-01 | Estee Lauder Inc. | Composiciones pulverizables que contienen polvos dispersos y procedimientos para usar los mismos. |
| US5630723A (en) * | 1994-11-30 | 1997-05-20 | Nihon Plast Co., Ltd. | Cable type electric connector |
| US5993787A (en) * | 1996-09-13 | 1999-11-30 | Johnson & Johnson Consumer Products, Inc. | Composition base for topical therapeutic and cosmetic preparations |
| FR2758982B1 (fr) * | 1997-02-06 | 1999-12-10 | Oreal | Emulsions eau-dans-huile a base de deux emulsionnants particuliers et apllications cosmetiques |
| US5908631A (en) * | 1997-02-27 | 1999-06-01 | L'oreal S.A. | Monohydric alcohol-free composition for topical use comprising solubilized ethylcellulose |
| DE19748921C2 (de) * | 1997-10-30 | 2001-02-22 | Stockhausen Chem Fab Gmbh | Hautverträgliche Handreiniger, insbesondere Grobhandreiniger |
| DE19950711A1 (de) * | 1999-10-21 | 2001-05-03 | Wella Ag | Klares Wasser-in-Silikonöl Haarkonditioniermittel |
| CA2362613C (en) * | 1999-12-13 | 2010-09-28 | Ethicon, Inc. | Stabilized antimicrobial systems and methods of making the same |
| MXPA02011024A (es) * | 2000-05-12 | 2003-03-10 | Unilever Nv | Composiciones cosmeticas acondicionadas que se enjuagan. |
| US20030228267A1 (en) * | 2001-07-09 | 2003-12-11 | Aust Duncan T. | Suncreen composition wit enhanced spf and water resistant properties |
| US6540987B2 (en) * | 2001-03-15 | 2003-04-01 | Ethox Chemicals Llc | Polyesters based on hydroxy fatty acids and lower hydroxy alkyl acids and uses thereof |
| DE10162697A1 (de) * | 2001-12-19 | 2003-07-03 | Cognis Deutschland Gmbh | Kosmetische und/oder pharmazeutische Sonnenschutzmittel |
| JP3515559B2 (ja) * | 2002-01-09 | 2004-04-05 | 日本アンテナ株式会社 | 多周波用アンテナ |
| JP2003212747A (ja) * | 2002-01-15 | 2003-07-30 | Nisshin Oillio Ltd | 油中水型乳化皮膚外用剤 |
| US20040115159A1 (en) * | 2002-03-29 | 2004-06-17 | Tadlock Charles C | Novel nanoemulsions |
| DE10238649A1 (de) * | 2002-08-23 | 2004-03-11 | Beiersdorf Ag | Dünnflüssige kosmetische oder dermatologische Zubereitungen von Typ Öl-in Wasser |
| DE102004014704A1 (de) * | 2004-03-25 | 2005-10-13 | Wacker-Chemie Gmbh | Partikelstabilisierte Emulsionen |
| AU2006331192B2 (en) * | 2005-12-29 | 2010-08-05 | Riemann Trading Aps | Alcohol-in-oil type emulsion comprising a multivalent metal salt |
| US20070274932A1 (en) * | 2006-05-15 | 2007-11-29 | The Procter & Gamble Company | Water in oil emulsion compositions containing sunscreen actives and siloxane elastomers |
| BRPI0712700A2 (pt) * | 2006-05-31 | 2012-07-10 | Neutrogena Corp | composições de protetor claras |
-
2007
- 2007-09-20 MX MX2009003060A patent/MX2009003060A/es not_active Application Discontinuation
- 2007-09-20 NZ NZ575783A patent/NZ575783A/en not_active IP Right Cessation
- 2007-09-20 CN CNA2007800348855A patent/CN101557794A/zh active Pending
- 2007-09-20 BR BRPI0718454-9A patent/BRPI0718454A2/pt not_active IP Right Cessation
- 2007-09-20 JP JP2009528598A patent/JP2010504291A/ja active Pending
- 2007-09-20 EP EP07801396A patent/EP2066286B1/en not_active Revoked
- 2007-09-20 WO PCT/DK2007/050131 patent/WO2008034447A1/en not_active Ceased
- 2007-09-20 CA CA002673743A patent/CA2673743A1/en not_active Abandoned
- 2007-09-20 AU AU2007299376A patent/AU2007299376B2/en not_active Ceased
- 2007-09-20 AT AT07801396T patent/ATE536166T1/de active
- 2007-09-20 EP EP11179538A patent/EP2397119A1/en not_active Withdrawn
- 2007-09-27 US US12/441,882 patent/US20100040566A1/en not_active Abandoned
-
2009
- 2009-04-17 NO NO20091517A patent/NO20091517L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US20100040566A1 (en) | 2010-02-18 |
| AU2007299376B2 (en) | 2011-05-12 |
| CN101557794A (zh) | 2009-10-14 |
| EP2066286B1 (en) | 2011-12-07 |
| JP2010504291A (ja) | 2010-02-12 |
| AU2007299376A1 (en) | 2008-03-27 |
| EP2397119A1 (en) | 2011-12-21 |
| ATE536166T1 (de) | 2011-12-15 |
| NO20091517L (no) | 2009-06-05 |
| MX2009003060A (es) | 2009-06-01 |
| BRPI0718454A2 (pt) | 2013-11-26 |
| NZ575783A (en) | 2011-04-29 |
| WO2008034447A1 (en) | 2008-03-27 |
| EP2066286A1 (en) | 2009-06-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |
Effective date: 20130920 |