KR102099074B1 - 자외 방사선-흡수 폴리에스테르를 함유하는 썬스크린 조성물 - Google Patents
자외 방사선-흡수 폴리에스테르를 함유하는 썬스크린 조성물 Download PDFInfo
- Publication number
- KR102099074B1 KR102099074B1 KR1020157001810A KR20157001810A KR102099074B1 KR 102099074 B1 KR102099074 B1 KR 102099074B1 KR 1020157001810 A KR1020157001810 A KR 1020157001810A KR 20157001810 A KR20157001810 A KR 20157001810A KR 102099074 B1 KR102099074 B1 KR 102099074B1
- Authority
- KR
- South Korea
- Prior art keywords
- composition
- absorbing
- polyester
- weight
- water
- 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.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 130
- 229920000728 polyester Polymers 0.000 title claims abstract description 88
- 239000000516 sunscreening agent Substances 0.000 title claims abstract description 37
- 230000000475 sunscreen effect Effects 0.000 title claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 66
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 39
- 239000000178 monomer Substances 0.000 claims abstract description 23
- 150000003852 triazoles Chemical class 0.000 claims abstract description 21
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims abstract description 12
- 150000002009 diols Chemical class 0.000 claims abstract description 11
- 229920005862 polyol Polymers 0.000 claims abstract description 11
- 125000000129 anionic group Chemical group 0.000 claims abstract description 10
- 150000003077 polyols Chemical class 0.000 claims abstract description 10
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims abstract description 10
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims abstract description 10
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims abstract description 10
- DJOWTWWHMWQATC-KYHIUUMWSA-N Karpoxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1(O)C(C)(C)CC(O)CC1(C)O)C=CC=C(/C)C=CC2=C(C)CC(O)CC2(C)C DJOWTWWHMWQATC-KYHIUUMWSA-N 0.000 claims abstract description 8
- 150000005690 diesters Chemical class 0.000 claims abstract description 5
- 239000002954 polymerization reaction product Substances 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 19
- 239000012875 nonionic emulsifier Substances 0.000 claims description 7
- WMYINDVYGQKYMI-UHFFFAOYSA-N 2-[2,2-bis(hydroxymethyl)butoxymethyl]-2-ethylpropane-1,3-diol Chemical compound CCC(CO)(CO)COCC(CC)(CO)CO WMYINDVYGQKYMI-UHFFFAOYSA-N 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 claims description 5
- 239000000539 dimer Substances 0.000 claims description 5
- 239000012874 anionic emulsifier Substances 0.000 claims description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 235000015250 liver sausages Nutrition 0.000 claims 1
- 239000012071 phase Substances 0.000 description 45
- 229920000642 polymer Polymers 0.000 description 35
- 239000003921 oil Substances 0.000 description 28
- 235000019198 oils Nutrition 0.000 description 28
- 238000002156 mixing Methods 0.000 description 26
- 230000000052 comparative effect Effects 0.000 description 17
- -1 polyacids Polymers 0.000 description 16
- 239000000049 pigment Substances 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 12
- 150000002148 esters Chemical group 0.000 description 12
- 239000002537 cosmetic Substances 0.000 description 11
- 239000010408 film Substances 0.000 description 11
- 239000008346 aqueous phase Substances 0.000 description 10
- 238000009472 formulation Methods 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 230000005855 radiation Effects 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 238000005227 gel permeation chromatography Methods 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 230000000699 topical effect Effects 0.000 description 6
- 238000002211 ultraviolet spectrum Methods 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 239000008367 deionised water Substances 0.000 description 5
- 229910021641 deionized water Inorganic materials 0.000 description 5
- 238000000338 in vitro Methods 0.000 description 5
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000004926 polymethyl methacrylate Substances 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 238000000149 argon plasma sintering Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000010445 mica Substances 0.000 description 4
- 229910052618 mica group Inorganic materials 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000004408 titanium dioxide Substances 0.000 description 4
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- PKPOVTYZGGYDIJ-UHFFFAOYSA-N dioctyl carbonate Chemical compound CCCCCCCCOC(=O)OCCCCCCCC PKPOVTYZGGYDIJ-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 150000004702 methyl esters Chemical class 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000005809 transesterification reaction Methods 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical class C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- ISDGWTZFJKFKMO-UHFFFAOYSA-N 2-phenyl-1,3-dioxane-4,6-dione Chemical compound O1C(=O)CC(=O)OC1C1=CC=CC=C1 ISDGWTZFJKFKMO-UHFFFAOYSA-N 0.000 description 2
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 description 2
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 206010015150 Erythema Diseases 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000004909 Moisturizer Substances 0.000 description 2
- YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical class CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 229960000250 adipic acid Drugs 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 125000003158 alcohol group Chemical group 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229940073609 bismuth oxychloride Drugs 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- 229940008099 dimethicone Drugs 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 239000003974 emollient agent Substances 0.000 description 2
- 231100000321 erythema Toxicity 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001034 iron oxide pigment Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000004005 microsphere Substances 0.000 description 2
- 230000001333 moisturizer Effects 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- RMGVATURDVPNOZ-UHFFFAOYSA-M potassium;hexadecyl hydrogen phosphate Chemical compound [K+].CCCCCCCCCCCCCCCCOP(O)([O-])=O RMGVATURDVPNOZ-UHFFFAOYSA-M 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- 230000037072 sun protection Effects 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- HEOCBCNFKCOKBX-RELGSGGGSA-N (1s,2e,4r)-4,7,7-trimethyl-2-[(4-methylphenyl)methylidene]bicyclo[2.2.1]heptan-3-one Chemical compound C1=CC(C)=CC=C1\C=C/1C(=O)[C@]2(C)CC[C@H]\1C2(C)C HEOCBCNFKCOKBX-RELGSGGGSA-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
- OVUBDKNXJHOLMI-ZVAWYAOSSA-N (2s)-n,n'-dibutyl-2-(2-ethylhexanoylamino)pentanediamide Chemical compound CCCCNC(=O)CC[C@@H](C(=O)NCCCC)NC(=O)C(CC)CCCC OVUBDKNXJHOLMI-ZVAWYAOSSA-N 0.000 description 1
- QIVRABJQTNPYAI-QFIPXVFZSA-N (2s)-n,n'-dibutyl-2-(dodecanoylamino)pentanediamide Chemical compound CCCCCCCCCCCC(=O)N[C@H](C(=O)NCCCC)CCC(=O)NCCCC QIVRABJQTNPYAI-QFIPXVFZSA-N 0.000 description 1
- 0 *c1cc2n[n](-c(cccc3*)c3O)nc2cc1 Chemical compound *c1cc2n[n](-c(cccc3*)c3O)nc2cc1 0.000 description 1
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- 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
- 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
- JGUMTYWKIBJSTN-UHFFFAOYSA-N 2-ethylhexyl 4-[[4,6-bis[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)OCC(CC)CCCC)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 JGUMTYWKIBJSTN-UHFFFAOYSA-N 0.000 description 1
- 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 1
- OXOHMAPRQAJJIR-UHFFFAOYSA-N 3-(2,3-dihydroxypropoxy)propane-1,2-diol;sulfuric acid Chemical class OS(O)(=O)=O.OCC(O)COCC(O)CO OXOHMAPRQAJJIR-UHFFFAOYSA-N 0.000 description 1
- 208000002874 Acne Vulgaris Diseases 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241000195940 Bryophyta Species 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 206010051246 Photodermatosis Diseases 0.000 description 1
- 229920003171 Poly (ethylene oxide) Chemical class 0.000 description 1
- 229920002732 Polyanhydride Polymers 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- 208000000453 Skin Neoplasms Diseases 0.000 description 1
- 206010040799 Skin atrophy Diseases 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 238000011481 absorbance measurement Methods 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000001720 action spectrum Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 229920013820 alkyl cellulose Polymers 0.000 description 1
- 229960002709 amiloxate Drugs 0.000 description 1
- UBNYRXMKIIGMKK-RMKNXTFCSA-N amiloxate Chemical compound COC1=CC=C(\C=C\C(=O)OCCC(C)C)C=C1 UBNYRXMKIIGMKK-RMKNXTFCSA-N 0.000 description 1
- 229940024606 amino acid Drugs 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229960005193 avobenzone Drugs 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 229960001716 benzalkonium Drugs 0.000 description 1
- CYDRXTMLKJDRQH-UHFFFAOYSA-N benzododecinium Chemical compound CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 CYDRXTMLKJDRQH-UHFFFAOYSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-aminopropionic acid Natural products NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- VQWFNAGFNGABOH-UHFFFAOYSA-K chromium(iii) hydroxide Chemical compound [OH-].[OH-].[OH-].[Cr+3] VQWFNAGFNGABOH-UHFFFAOYSA-K 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000003581 cosmetic carrier Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000007854 depigmenting agent Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 229960004960 dioxybenzone Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- HUVYTMDMDZRHBN-UHFFFAOYSA-N drometrizole trisiloxane Chemical compound C[Si](C)(C)O[Si](C)(O[Si](C)(C)C)CC(C)CC1=CC(C)=CC(N2N=C3C=CC=CC3=N2)=C1O HUVYTMDMDZRHBN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 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
- 229960000655 ensulizole Drugs 0.000 description 1
- 229960004697 enzacamene Drugs 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 229940075529 glyceryl stearate Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229960004881 homosalate Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 201000001441 melanoma Diseases 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
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 229960001679 octinoxate Drugs 0.000 description 1
- 229960003921 octisalate Drugs 0.000 description 1
- 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 description 1
- 229960000601 octocrylene 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
- 239000002674 ointment Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 229960001173 oxybenzone Drugs 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229940100460 peg-100 stearate Drugs 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical class O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 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
- 208000017983 photosensitivity disease Diseases 0.000 description 1
- 229920000765 poly(2-oxazolines) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002282 polysilicones-15 Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 229940071089 sarcosinate Drugs 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 230000009759 skin aging Effects 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 229940086735 succinate Drugs 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- AGGIJOLULBJGTQ-UHFFFAOYSA-N sulfoacetic acid Chemical compound OC(=O)CS(O)(=O)=O AGGIJOLULBJGTQ-UHFFFAOYSA-N 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003458 sulfonic acid derivatives Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 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
- 239000000725 suspension Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 229910000314 transition metal oxide Inorganic materials 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 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
- 238000009849 vacuum degassing Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 229940075420 xanthine Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 239000004711 α-olefin Substances 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
- A61K8/72—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
-
- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/85—Polyesters
-
- 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
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
-
- 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
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/062—Oil-in-water emulsions
-
- 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
- A61K8/817—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 a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
- A61K8/8182—Copolymers of vinyl-pyrrolidones. 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Dispersion Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/535,890 US20140004054A1 (en) | 2012-06-28 | 2012-06-28 | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
| US13/535,890 | 2012-06-28 | ||
| US13/710,531 US20140004057A1 (en) | 2012-06-28 | 2012-12-11 | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
| US13/710,531 | 2012-12-11 | ||
| PCT/US2013/046316 WO2014004169A2 (en) | 2012-06-28 | 2013-06-18 | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20150023866A KR20150023866A (ko) | 2015-03-05 |
| KR102099074B1 true KR102099074B1 (ko) | 2020-04-09 |
Family
ID=48699339
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020157001810A Active KR102099074B1 (ko) | 2012-06-28 | 2013-06-18 | 자외 방사선-흡수 폴리에스테르를 함유하는 썬스크린 조성물 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US20140004057A1 (enExample) |
| EP (1) | EP2866770B1 (enExample) |
| KR (1) | KR102099074B1 (enExample) |
| CN (1) | CN104427965A (enExample) |
| AU (1) | AU2013280908B2 (enExample) |
| BR (1) | BR112014032792A8 (enExample) |
| CA (1) | CA2877464C (enExample) |
| ES (1) | ES2642887T3 (enExample) |
| IN (1) | IN2014DN10613A (enExample) |
| RU (1) | RU2648756C2 (enExample) |
| WO (1) | WO2014004169A2 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20140004057A1 (en) | 2012-06-28 | 2014-01-02 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
| US9255180B2 (en) | 2012-06-28 | 2016-02-09 | Johnson & Johnson Consumer Inc. | Ultraviolet radiation absorbing polyethers |
| WO2014004474A2 (en) | 2012-06-28 | 2014-01-03 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions containing an ultraviolet radiation-absorbing polymer |
| US10709650B2 (en) * | 2014-03-27 | 2020-07-14 | Inolex Investment Corporation | Sprayable sunscreen compositions and methods |
| KR102402780B1 (ko) * | 2015-06-04 | 2022-05-27 | 삼성전자 주식회사 | 메모리 관리 방법 및 장치 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110104078A1 (en) * | 2009-11-02 | 2011-05-05 | Inolex Investment Corporation | Uv absorbing complex polyester polymers, compositions containing uv absorbing complex polyester polymers, and related methods |
Family Cites Families (106)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4107290A (en) | 1972-06-29 | 1978-08-15 | L'oreal | Anti-solar polymers, method of making the same and cosmetic compositions containing the same |
| US4322522A (en) | 1980-07-08 | 1982-03-30 | Akzona Incorporated | Polyester/polyether segmented copolymers stabilized against degradation by UV light via copolymerization with analogs of 2,2,6,6-tetramethylpiperidine derivatives |
| US4528311A (en) | 1983-07-11 | 1985-07-09 | Iolab Corporation | Ultraviolet absorbing polymers comprising 2-hydroxy-5-acrylyloxyphenyl-2H-benzotriazoles |
| JPS6099186A (ja) | 1983-11-04 | 1985-06-03 | Pola Chem Ind Inc | 高分子量紫外線吸収及びこれを含有する化粧料 |
| FR2596400B1 (fr) * | 1986-03-28 | 1988-08-26 | Oreal | Nouveaux polymeres capables d'absorber le rayonnement ultraviolet, leur preparation et leur application notamment en cosmetologie |
| US5138089A (en) | 1986-06-27 | 1992-08-11 | The Procter & Gamble Company | Chromophores, sunscreen compositions and methods for preventing sunburn |
| US4810489A (en) * | 1986-12-04 | 1989-03-07 | Bristol-Myers Company | High oil phase pharmaceutical vehicles and sunscreen compositions having waterproof sun protection factors |
| US4897259A (en) * | 1986-12-04 | 1990-01-30 | Bristol-Myers Company | High oil phase pharmaceutical vehicles and sunscreen compositions having waterproof sun protection factors |
| WO1989003402A1 (fr) | 1987-10-07 | 1989-04-20 | Terumo Kabushiki Kaisha | Materiau polymere absorbant les ultraviolets et procede de photogravure |
| US5166234A (en) | 1988-05-19 | 1992-11-24 | E. I. Du Pont De Nemours And Company | Bisurea light stabilizer for organic polymers |
| US5039782A (en) | 1990-12-11 | 1991-08-13 | Lever Brothers Company, Division Of Conopco, Inc. | Polymeric whitening agent |
| JPH04288010A (ja) | 1991-03-15 | 1992-10-13 | Max Fuakutaa Kk | 化粧料 |
| US5219559A (en) * | 1991-08-26 | 1993-06-15 | Isp Investments Inc. | Copolymer of vinyl pyrrolidone and a C30 alpha-olefin in flake or powder form, process for making same, and personal care compositions therewith |
| FR2680684B1 (fr) | 1991-08-29 | 1993-11-12 | Oreal | Composition cosmetique filtrante comprenant un nanopigment d'oxyde metallique et un polymere filtre. |
| US5250652A (en) | 1992-07-30 | 1993-10-05 | Lever Brothers Company, Division Of Conopco, Inc. | High loading water-dispersible UVA and/or UVB light-absorbing copolymer |
| US6123928A (en) | 1992-12-21 | 2000-09-26 | Biophysica, Inc. | Sunblocking polymers and their novel formulations |
| US5487885A (en) | 1992-12-21 | 1996-01-30 | Biophysica, Inc. | Sunblocking polymers and their formulation |
| US5459222A (en) | 1993-06-04 | 1995-10-17 | Ciba-Geigy Corporation | UV-absorbing polyurethanes and polyesters |
| GB9403451D0 (en) | 1994-02-23 | 1994-04-13 | Ciba Geigy Ag | Sunscreen compositions |
| ES2170116T3 (es) | 1994-10-14 | 2002-08-01 | Hoffmann La Roche | Composiciones de filtrado de luz cosmeticas fotoestables. |
| ZA964872B (en) | 1995-06-08 | 1997-12-08 | Johnson & Johnson Consumer | Sunscreen compositions. |
| KR100236388B1 (ko) | 1995-11-28 | 1999-12-15 | 성재갑 | 신규한 고분자 자외선 차단제 및 그 제조방법 |
| US5716602A (en) * | 1996-06-26 | 1998-02-10 | S. C. Johnson & Sons, Inc. | Insect repellent sunscreen |
| DE19634399A1 (de) | 1996-08-26 | 1998-03-05 | Basf Ag | Kosmetisches Mittel mit polymergebundenen Benzophenonchromophoren |
| DE19634401A1 (de) | 1996-08-26 | 1998-03-05 | Basf Ag | Kosmetisches Mittel mit polymergebundenen Benzophenonchromophoren |
| CA2241645A1 (en) | 1997-07-14 | 1999-01-14 | F. Hoffmann-La Roche Ag | Light-screening agents |
| DE19734445A1 (de) | 1997-08-08 | 1999-02-11 | Basf Ag | Lipophile polymere UV-Absorber |
| US5904917A (en) * | 1997-09-12 | 1999-05-18 | Colgate-Palmolive Company | Sun protection composition |
| DE19834819A1 (de) | 1998-08-01 | 2000-02-03 | Beiersdorf Ag | Emulgatorfreie feindisperse Systeme vom Typ Öl-in-Wasser und Wasser-in-Öl |
| DE19834820A1 (de) | 1998-08-01 | 2000-02-03 | Beiersdorf Ag | Emulgatorfreie feindisperse Systeme vom Typ Öl-in-Wasser und Wasser-in-Öl |
| DE19842730A1 (de) | 1998-09-18 | 2000-03-23 | Beiersdorf Ag | Emulgatorfreie feindisperse Systeme vom Typ Öl-in-Wasser und Wasser-in-Öl |
| DE19842786A1 (de) | 1998-09-18 | 2000-03-23 | Beiersdorf Ag | Emulgatorfreie feindisperse Systeme vom Typ Öl-in-Wasser und Wasser-in-Öl |
| DE19842787A1 (de) | 1998-09-18 | 2000-03-23 | Beiersdorf Ag | Emulgatorfreie feindisperse Systeme vom Typ Öl-in-Wasser und Wasser-in-Öl |
| ES2306532T3 (es) | 1998-12-10 | 2008-11-01 | Color Access, Inc. | Composiciones con efecto fotoprotector potenciado y procedimiento de utilizacion de las mismas. |
| FR2793139B1 (fr) | 1999-05-06 | 2001-06-29 | Oreal | Composition renfermant au moins un compose bicyclique aromatique et au moins un filtre solaire lipophile, et ses utilisations |
| US7427640B1 (en) | 1999-06-28 | 2008-09-23 | Nippon Fine Chemical Co., Ltd. | Oil materials comprising dimerdiol ester and cosmetics comprising the ester |
| US6413393B1 (en) | 1999-07-07 | 2002-07-02 | Minimed, Inc. | Sensor including UV-absorbing polymer and method of manufacture |
| BR0012445A (pt) | 1999-07-13 | 2002-04-02 | Pharmasol Gmbh | Agentes com ação absorvente e/ou refletora de radiação uv para proteção contra radiação uv nociva à saúde e para reforçar a barreira natural da pele |
| ATE328571T1 (de) | 1999-07-20 | 2006-06-15 | Beiersdorf Ag | Emulgatorfreie feindisperse systeme vom typ wasser-in-öl |
| JP2001288064A (ja) | 2000-04-10 | 2001-10-16 | Kao Corp | 化粧料 |
| EP1275669A4 (en) | 2000-04-13 | 2006-03-08 | Sanyo Chemical Ind Ltd | NETWORKED POLYMER, PROCESS FOR ITS MANUFACTURE, ABSORBENT STRUCTURE AND ABSORBENT ARTICLE |
| FR2811554B1 (fr) | 2000-07-12 | 2002-09-13 | Oreal | Composition comprenant au moins un filtre uv et un sel de flavylium non substitue en position 3 pour la coloration de la peau et utilisations |
| DE10046927A1 (de) | 2000-09-21 | 2002-04-25 | Basf Ag | Farbmittelhaltige wässrige Polymerdispersion |
| DE10053375C1 (de) | 2000-10-27 | 2002-01-24 | Lohmann Therapie Syst Lts | Transdermale therapeutische Systeme mit lichtempfindlichen Wirkstoffen |
| US6867250B1 (en) | 2000-10-30 | 2005-03-15 | Cytec Technology Corp. | Non-yellowing ortho-dialkyl aryl substituted triazine ultraviolet light absorbers |
| FR2816834B1 (fr) | 2000-11-20 | 2005-06-24 | Oreal | Composition de traitement des fibres keratiniques comprenant un polymere polyurethane associatif cationique et un agent protecteur ou conditionneur |
| FR2824266B1 (fr) | 2001-05-04 | 2005-11-18 | Oreal | Composition cosmetique de soin ou de maquillage des matieres keratiniques comprenant un ester a groupement aromatique et un agent photoprotecteur et utilisations |
| US7097828B2 (en) | 2001-06-29 | 2006-08-29 | Schering-Plough Healthcare Products, Inc. | Sunscreen formulations containing waterborne polyurethane polymers |
| WO2003011239A2 (en) | 2001-07-31 | 2003-02-13 | Merck Patent Gmbh | Sunscreen composition |
| JP2003063932A (ja) | 2001-08-24 | 2003-03-05 | Catalysts & Chem Ind Co Ltd | 化粧料用改質無機微粒子およびそれを配合した化粧料 |
| FR2832060B1 (fr) | 2001-11-09 | 2004-07-09 | Oreal | Composition contenant un ester n-acyle d'acide amine et un filtre uv structuree par un polyamide |
| US7854925B2 (en) | 2002-04-04 | 2010-12-21 | Akzo Nobel N.V. | Use of solubilized, anionic polyurethanes in skin care compositions |
| US20050008598A1 (en) | 2003-07-11 | 2005-01-13 | Shaoxiang Lu | Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent |
| US6899866B2 (en) | 2002-09-06 | 2005-05-31 | Cph Innovations Corporation | Photostabilization of a sunscreen composition with a combination of an α-cyano-β, β-diphenylacrylate compound and a dialkyl naphithalate |
| US6800274B2 (en) | 2002-09-17 | 2004-10-05 | The C.P. Hall Company | Photostabilizers, UV absorbers, and methods of photostabilizing a sunscreen composition |
| US20040096406A1 (en) | 2002-09-30 | 2004-05-20 | L'oreal | Composition containing ascorbic acid compound and screening agent, method of use |
| US7153494B2 (en) | 2002-10-21 | 2006-12-26 | L'oreal | Dibenzoylmethane sunscreen compositions photostabilized with amphiphilic block copolymers |
| US7008618B1 (en) | 2002-11-08 | 2006-03-07 | Nalco Company | Water soluble monomers and polymers for protecting substrates from ultraviolet light |
| US7087692B2 (en) | 2002-11-27 | 2006-08-08 | Galaxy Surfactants Ltd | Salt and heat sensitive, substantive UV-absorbing polymers |
| RU2359657C2 (ru) * | 2002-12-24 | 2009-06-27 | Оксоника Лимитед | Солнцезащитные фильтры |
| US20040126339A1 (en) | 2002-12-31 | 2004-07-01 | Roszell James A. | Sunscreen composition and methods for manufacturing and using a sunscreen composition |
| EP1596819A1 (en) | 2003-02-26 | 2005-11-23 | Fuji Photo Film B.V. | Cosmetic uv-screen compositions and aminobutadiene-based uv-absorbing complexes therefor |
| US6902722B2 (en) | 2003-04-14 | 2005-06-07 | L'oreal | Aqueous antisun/sunscreen compositions comprising amphiphilic 2-acrylamidomethylpropanesulfonic acid polymers and water-soluble silicones |
| US6905674B2 (en) | 2003-04-14 | 2005-06-14 | L'oreal | Aqueous photoprotective compositions comprising acrylamido-2-methylpropanesulfonic acid polymers and 4,4-diarylbutadiene UV-A sunscreens |
| US20040223925A1 (en) | 2003-04-14 | 2004-11-11 | L'oreal | Water-in-oil photoprotective emulsions comprising polyolefinic surfactants and 4,4-diarylbutadiene UV-A sunscreens |
| MXPA06001474A (es) | 2003-08-07 | 2006-05-15 | Procter & Gamble | Composiciones para el cuidado personal. |
| US20050036961A1 (en) | 2003-08-13 | 2005-02-17 | Societe L'oreals S.A. | Aesthetically and SPF improved UV-sunscreens comprising glass microspheres |
| US8609784B2 (en) | 2003-09-04 | 2013-12-17 | Nalco Company | Water-soluble polyaminoamides as sunscreen agents |
| US6887400B1 (en) | 2003-10-30 | 2005-05-03 | Nalco Company | Water-soluble polyaminoamides comprising 1,3-diimines as sunscreen agents |
| US7534420B2 (en) | 2004-02-25 | 2009-05-19 | Hallstar Innovations Corp. | Compounds derived from polyanhydride resins with film-forming, UV-absorbing, and photostablizing properties, compositions containing same, and methods of using the same |
| US20080311234A1 (en) | 2004-03-24 | 2008-12-18 | Tadashi Yoneda | Oil-in-Water Emulsified Composition, and External Preparation for Skin and Cosmetics Using the Composition |
| KR101158942B1 (ko) | 2004-03-25 | 2012-06-21 | 디에스엠 아이피 어셋츠 비.브이. | 과도하게 분지된 중합체에 공유 결합된 자외선 흡수 발색단 |
| FR2868069B1 (fr) | 2004-03-25 | 2007-06-29 | Oreal | Composes monomeriques possedant des proprietes optiques, polymeres les comprenant et utilisation |
| DE102004018510A1 (de) | 2004-04-14 | 2005-11-03 | Goldschmidt Gmbh | Verbesserte Lösungsvermittler/Lösungsmittel für organische UV-Filter |
| EP1807452B1 (en) | 2004-11-02 | 2013-05-08 | DSM IP Assets B.V. | Additive for uv-sunscreen preparations |
| JP2006265389A (ja) | 2005-03-24 | 2006-10-05 | Nippon Zeon Co Ltd | 紫外線吸収剤、その製造方法、樹脂組成物及び成形体 |
| WO2007001484A2 (en) | 2005-06-20 | 2007-01-04 | Playtex Products, Inc. | Non-irritating compositions |
| JP2007126530A (ja) | 2005-11-02 | 2007-05-24 | Taisei Fine Chemical Co Ltd | 紫外線吸収能を有する非水液状組成物 |
| US20070134174A1 (en) | 2005-11-03 | 2007-06-14 | Christopher Irwin | Personal care composition |
| JP5137503B2 (ja) | 2006-09-15 | 2013-02-06 | 株式会社日本触媒 | 化粧料用紫外線カット剤およびそれを用いた化粧料 |
| CN101677937A (zh) | 2007-04-05 | 2010-03-24 | 巴斯夫欧洲公司 | 包含所选共聚物的防晒剂和个人护理组合物 |
| FR2918563B1 (fr) | 2007-07-12 | 2009-12-04 | Oreal | Composition photoprotectrice fluide aqueuse a base d'un polymere polyamide a terminaison amide tertiaire. |
| WO2009016046A2 (en) | 2007-07-27 | 2009-02-05 | Basf Se | Sunless tanning compositions comprising substituted polyamine compounds |
| EP2194958B1 (en) | 2007-08-31 | 2012-02-29 | Playtex Products, Inc. | Sunless tanning composition with photostabilized sunscreen |
| US8454941B2 (en) | 2007-09-19 | 2013-06-04 | Symrise Ag | O/W-emulsifiers, O/W-emulsions and methods of manufacture thereof |
| WO2009040917A1 (ja) | 2007-09-27 | 2009-04-02 | Lead Chemical Co. , Ltd. | 紫外線吸収剤 |
| JP5270134B2 (ja) | 2007-11-12 | 2013-08-21 | 株式会社コーセー | 紫外線吸収剤水分散組成物 |
| FR2924930A1 (fr) | 2007-12-18 | 2009-06-19 | Oreal | Emulsions photoprotectrices huile-dans-eau fluides contenant des agents tensioactifs gemines et un copolymere reticule d'acide methacrylique et d'acrylate d'alkyle en c1-c4; procede de preparation de ces emulsions |
| JP5312922B2 (ja) | 2007-12-19 | 2013-10-09 | ロート製薬株式会社 | 有機紫外線吸収剤内包マイクロカプセル |
| US7989572B2 (en) | 2008-01-17 | 2011-08-02 | Eastman Chemical Company | Polyvinyl ultraviolet light absorbers for personal care |
| JP5402063B2 (ja) | 2008-03-13 | 2014-01-29 | 信越化学工業株式会社 | 化粧料 |
| EP2105124A1 (de) | 2008-03-26 | 2009-09-30 | Bayer MaterialScience AG | Sonnenschutz-Zusammensetzungen |
| US20090258230A1 (en) | 2008-04-11 | 2009-10-15 | Kobo Products, Inc. | Porous and/or hollow material containing uv attenuating nanoparticles, method of production and use |
| US8003132B2 (en) | 2008-06-30 | 2011-08-23 | Johnson & Johnson Consumer Companies, Inc. | Compositions comprising an ultraviolet radiation-absorbing polymer |
| US20100129303A1 (en) | 2008-10-17 | 2010-05-27 | Dueva-Koganov Olga V | Sunscreen and personal care compositions comprising a random terpolymer |
| US9044623B2 (en) | 2009-01-27 | 2015-06-02 | Isp Investments Inc. | Polymer-bound UV absorbers in personal care compositions |
| US8475774B2 (en) * | 2010-02-08 | 2013-07-02 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions comprising an ultraviolet radiation-absorbing polymer |
| US20140004057A1 (en) | 2012-06-28 | 2014-01-02 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
| US9469725B2 (en) | 2012-06-28 | 2016-10-18 | Johnson & Johnson Consumer Inc. | Ultraviolet radiation absorbing polymers |
| WO2014004474A2 (en) | 2012-06-28 | 2014-01-03 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions containing an ultraviolet radiation-absorbing polymer |
| US20140004054A1 (en) | 2012-06-28 | 2014-01-02 | Susan Daly | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
| US20140004058A1 (en) | 2012-06-28 | 2014-01-02 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
| US20140004059A1 (en) | 2012-06-28 | 2014-01-02 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
| US9255180B2 (en) | 2012-06-28 | 2016-02-09 | Johnson & Johnson Consumer Inc. | Ultraviolet radiation absorbing polyethers |
| US20140004056A1 (en) | 2012-06-28 | 2014-01-02 | Susan Daly | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
| US20140004055A1 (en) | 2012-06-28 | 2014-01-02 | Susan Daly | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
-
2012
- 2012-12-11 US US13/710,531 patent/US20140004057A1/en not_active Abandoned
-
2013
- 2013-06-18 CA CA2877464A patent/CA2877464C/en active Active
- 2013-06-18 EP EP13731623.8A patent/EP2866770B1/en active Active
- 2013-06-18 AU AU2013280908A patent/AU2013280908B2/en active Active
- 2013-06-18 ES ES13731623.8T patent/ES2642887T3/es active Active
- 2013-06-18 BR BR112014032792A patent/BR112014032792A8/pt not_active Application Discontinuation
- 2013-06-18 WO PCT/US2013/046316 patent/WO2014004169A2/en not_active Ceased
- 2013-06-18 IN IN10613DEN2014 patent/IN2014DN10613A/en unknown
- 2013-06-18 KR KR1020157001810A patent/KR102099074B1/ko active Active
- 2013-06-18 RU RU2015102579A patent/RU2648756C2/ru active
- 2013-06-18 CN CN201380034715.2A patent/CN104427965A/zh active Pending
-
2014
- 2014-12-10 US US14/565,909 patent/US9592190B2/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110104078A1 (en) * | 2009-11-02 | 2011-05-05 | Inolex Investment Corporation | Uv absorbing complex polyester polymers, compositions containing uv absorbing complex polyester polymers, and related methods |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2014004169A3 (en) | 2014-09-25 |
| EP2866770B1 (en) | 2017-08-23 |
| US9592190B2 (en) | 2017-03-14 |
| CA2877464A1 (en) | 2014-01-03 |
| BR112014032792A2 (pt) | 2017-06-27 |
| EP2866770A2 (en) | 2015-05-06 |
| AU2013280908B2 (en) | 2018-02-15 |
| US20140004057A1 (en) | 2014-01-02 |
| RU2015102579A (ru) | 2016-08-20 |
| WO2014004169A2 (en) | 2014-01-03 |
| ES2642887T3 (es) | 2017-11-20 |
| IN2014DN10613A (enExample) | 2015-09-11 |
| CN104427965A (zh) | 2015-03-18 |
| KR20150023866A (ko) | 2015-03-05 |
| CA2877464C (en) | 2021-06-01 |
| BR112014032792A8 (pt) | 2022-08-16 |
| AU2013280908A1 (en) | 2015-01-22 |
| RU2648756C2 (ru) | 2018-03-28 |
| US20150093341A1 (en) | 2015-04-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2021202557B2 (en) | Sunscreen composition | |
| KR102099074B1 (ko) | 자외 방사선-흡수 폴리에스테르를 함유하는 썬스크린 조성물 | |
| WO2014004170A2 (en) | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester | |
| US20190192391A1 (en) | Sprayable compositions containing metal oxides | |
| AU2013280910A1 (en) | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester | |
| AU2013280912A1 (en) | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester | |
| WO2014004168A2 (en) | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester | |
| WO2014004172A2 (en) | Sunscreen compositions containing an ultraviolet radiation-absorbing polyester |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20150122 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20180615 Comment text: Request for Examination of Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20190827 Patent event code: PE09021S01D |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20200108 |
|
| PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20200403 Patent event code: PR07011E01D |
|
| PR1002 | Payment of registration fee |
Payment date: 20200406 End annual number: 3 Start annual number: 1 |
|
| PG1601 | Publication of registration | ||
| PR1001 | Payment of annual fee |
Payment date: 20240319 Start annual number: 5 End annual number: 5 |
|
| PR1001 | Payment of annual fee |
Payment date: 20250317 Start annual number: 6 End annual number: 6 |