JP6139867B2 - Skin cosmetics - Google Patents
Skin cosmetics Download PDFInfo
- Publication number
- JP6139867B2 JP6139867B2 JP2012263591A JP2012263591A JP6139867B2 JP 6139867 B2 JP6139867 B2 JP 6139867B2 JP 2012263591 A JP2012263591 A JP 2012263591A JP 2012263591 A JP2012263591 A JP 2012263591A JP 6139867 B2 JP6139867 B2 JP 6139867B2
- Authority
- JP
- Japan
- Prior art keywords
- mass
- component
- skin
- mixture
- preferable
- 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
- 239000002537 cosmetic Substances 0.000 title claims description 53
- 239000000203 mixture Substances 0.000 claims description 57
- 239000003921 oil Substances 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 22
- 230000008569 process Effects 0.000 claims description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 238000002156 mixing Methods 0.000 claims description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000002736 nonionic surfactant Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
- 238000010438 heat treatment Methods 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 239000003093 cationic surfactant Substances 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 6
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 5
- 239000010696 ester oil Substances 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 230000002087 whitening effect Effects 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 3
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 3
- -1 halogen ions Chemical class 0.000 description 30
- 235000019198 oils Nutrition 0.000 description 23
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 14
- 230000035699 permeability Effects 0.000 description 13
- 235000014113 dietary fatty acids Nutrition 0.000 description 12
- 239000000194 fatty acid Substances 0.000 description 12
- 229930195729 fatty acid Natural products 0.000 description 12
- XADJWCRESPGUTB-UHFFFAOYSA-N apigenin Natural products C1=CC(O)=CC=C1C1=CC(=O)C2=CC(O)=C(O)C=C2O1 XADJWCRESPGUTB-UHFFFAOYSA-N 0.000 description 9
- 235000008714 apigenin Nutrition 0.000 description 9
- KZNIFHPLKGYRTM-UHFFFAOYSA-N apigenin Chemical compound C1=CC(O)=CC=C1C1=CC(=O)C2=C(O)C=C(O)C=C2O1 KZNIFHPLKGYRTM-UHFFFAOYSA-N 0.000 description 9
- 229940117893 apigenin Drugs 0.000 description 9
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 8
- VOFUROIFQGPCGE-UHFFFAOYSA-N nile red Chemical compound C1=CC=C2C3=NC4=CC=C(N(CC)CC)C=C4OC3=CC(=O)C2=C1 VOFUROIFQGPCGE-UHFFFAOYSA-N 0.000 description 7
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- XMFUMMRWIFOQDQ-UHFFFAOYSA-N 1-(4-methylpentan-2-yloxy)hexadecane Chemical compound CCCCCCCCCCCCCCCCOC(C)CC(C)C XMFUMMRWIFOQDQ-UHFFFAOYSA-N 0.000 description 5
- 239000004359 castor oil Substances 0.000 description 5
- 235000019438 castor oil Nutrition 0.000 description 5
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 235000008390 olive oil Nutrition 0.000 description 5
- 239000004006 olive oil Substances 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- BJDAUCLANVMIOB-UHFFFAOYSA-N (3-decanoyloxy-2,2-dimethylpropyl) decanoate Chemical compound CCCCCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCCCCC BJDAUCLANVMIOB-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 229940058015 1,3-butylene glycol Drugs 0.000 description 3
- NJLYCNZOTQCQMC-UHFFFAOYSA-N 2-hexa-2,4-diynyl-1,6-dioxaspiro[4.4]non-3-ene Chemical compound C1=CC(CC#CC#CC)OC11OCCC1 NJLYCNZOTQCQMC-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 150000005215 alkyl ethers Chemical class 0.000 description 3
- 235000019437 butane-1,3-diol Nutrition 0.000 description 3
- 229960000541 cetyl alcohol Drugs 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- ZCPCLAPUXMZUCD-UHFFFAOYSA-M dihexadecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC ZCPCLAPUXMZUCD-UHFFFAOYSA-M 0.000 description 3
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- BGRXBNZMPMGLQI-UHFFFAOYSA-N 2-octyldodecyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC BGRXBNZMPMGLQI-UHFFFAOYSA-N 0.000 description 2
- ZFGOPJASRDDARH-UHFFFAOYSA-N 3-[[10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthrene Chemical compound C12CCC3(C)C(C(C)CCCC(C)C)CCC3C2CC=C(C2)C1(C)CCC2OC1CC2=CCC3C4CCC(C(C)CCCC(C)C)C4(C)CCC3C2(C)CC1 ZFGOPJASRDDARH-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- ZONYXWQDUYMKFB-UHFFFAOYSA-N SJ000286395 Natural products O1C2=CC=CC=C2C(=O)CC1C1=CC=CC=C1 ZONYXWQDUYMKFB-UHFFFAOYSA-N 0.000 description 2
- GAMYVSCDDLXAQW-AOIWZFSPSA-N Thermopsosid Natural products O(C)c1c(O)ccc(C=2Oc3c(c(O)cc(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O4)c3)C(=O)C=2)c1 GAMYVSCDDLXAQW-AOIWZFSPSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 229940008099 dimethicone Drugs 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 230000001815 facial effect Effects 0.000 description 2
- 229930003949 flavanone Natural products 0.000 description 2
- 150000002207 flavanone derivatives Chemical class 0.000 description 2
- 235000011981 flavanones Nutrition 0.000 description 2
- 229930003944 flavone Natural products 0.000 description 2
- 150000002212 flavone derivatives Chemical class 0.000 description 2
- 235000011949 flavones Nutrition 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 229940073665 octyldodecyl myristate Drugs 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 235000015277 pork Nutrition 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 2
- QYIXCDOBOSTCEI-QCYZZNICSA-N (5alpha)-cholestan-3beta-ol Chemical compound C([C@@H]1CC2)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CC1 QYIXCDOBOSTCEI-QCYZZNICSA-N 0.000 description 1
- NKJOXAZJBOMXID-UHFFFAOYSA-N 1,1'-Oxybisoctane Chemical compound CCCCCCCCOCCCCCCCC NKJOXAZJBOMXID-UHFFFAOYSA-N 0.000 description 1
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- CZWWITYVYJRTOX-UHFFFAOYSA-N 1-(2-methylpropoxy)hexadecane Chemical compound CCCCCCCCCCCCCCCCOCC(C)C CZWWITYVYJRTOX-UHFFFAOYSA-N 0.000 description 1
- WAYINTBTZWQNSN-UHFFFAOYSA-N 11-methyldodecyl 3,5,5-trimethylhexanoate Chemical compound CC(C)CCCCCCCCCCOC(=O)CC(C)CC(C)(C)C WAYINTBTZWQNSN-UHFFFAOYSA-N 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-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
- ZIIVEKCKOPDBLT-UHFFFAOYSA-N 2-octyldodecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCC(COC(=O)C(C)O)CCCCCCCC ZIIVEKCKOPDBLT-UHFFFAOYSA-N 0.000 description 1
- UIVPNOBLHXUKDX-UHFFFAOYSA-N 3,5,5-trimethylhexyl 3,5,5-trimethylhexanoate Chemical compound CC(C)(C)CC(C)CCOC(=O)CC(C)CC(C)(C)C UIVPNOBLHXUKDX-UHFFFAOYSA-N 0.000 description 1
- XPFCZYUVICHKDS-UHFFFAOYSA-N 3-methylbutane-1,3-diol Chemical compound CC(C)(O)CCO XPFCZYUVICHKDS-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 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
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- QYIXCDOBOSTCEI-UHFFFAOYSA-N alpha-cholestanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 QYIXCDOBOSTCEI-UHFFFAOYSA-N 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 238000001574 biopsy Methods 0.000 description 1
- HGKOWIQVWAQWDS-UHFFFAOYSA-N bis(16-methylheptadecyl) 2-hydroxybutanedioate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CC(O)C(=O)OCCCCCCCCCCCCCCCC(C)C HGKOWIQVWAQWDS-UHFFFAOYSA-N 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- VKKVMDHHSINGTJ-UHFFFAOYSA-M di(docosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCCCC VKKVMDHHSINGTJ-UHFFFAOYSA-M 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 235000019797 dipotassium phosphate Nutrition 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229940100554 isononyl isononanoate Drugs 0.000 description 1
- 229940093629 isopropyl isostearate Drugs 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- 229940078812 myristyl myristate Drugs 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 229940077397 octyldodecyl lactate Drugs 0.000 description 1
- 230000037368 penetrate the skin Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- NEOZOXKVMDBOSG-UHFFFAOYSA-N propan-2-yl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC(C)C NEOZOXKVMDBOSG-UHFFFAOYSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000010729 system oil Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
本発明は、皮膚化粧料に関する。 The present invention relates to a skin cosmetic.
皮膚化粧料には、美白作用、消炎作用等を発揮する種々の有効成分を配合し、経皮吸収させることにより、その効果を得ることが行われている。しかしながら、有効成分を単に化粧料に配合するのみでは、十分に経皮吸収されず、その成分本来の効果を得ることは困難である。
一方、水中油型乳化化粧料では、油溶性の成分を安定に乳化して配合することが課題であり、種々の検討がなされている。例えば、特許文献1〜3には、カチオン界面活性剤を用いて乳化することが記載されている。
In skin cosmetics, various active ingredients exhibiting a whitening action, an anti-inflammatory action and the like are blended and percutaneously absorbed to obtain the effect. However, if the active ingredient is simply blended into the cosmetic, it cannot be absorbed percutaneously and it is difficult to obtain the original effect of the ingredient.
On the other hand, oil-in-water emulsified cosmetics have a problem of stably emulsifying and blending oil-soluble ingredients, and various studies have been made. For example, Patent Documents 1 to 3 describe emulsification using a cationic surfactant.
本発明者は、カチオン界面活性剤を用いると、得られる組成物が硬くなり、肌の上で広がりにくく、ぬるつく、べたつくなど、使用感に課題があることを見出した。 The present inventor has found that when a cationic surfactant is used, the resulting composition becomes hard and difficult to spread on the skin, and there are problems in the feeling of use such as sliminess and stickiness.
本発明者らは、特定のカチオン界面活性剤と、非イオン界面活性剤、特定の油剤及び高級アルコールとを組み合わせて用いることにより、安定性に優れ、有効成分の経皮吸収効果を向上させると共に、使用感の良好な皮膚化粧料が得られることを見出した。 By using a specific cationic surfactant in combination with a nonionic surfactant, a specific oil and a higher alcohol, the present inventors have excellent stability and improve the transdermal absorption effect of the active ingredient. The present inventors have found that a skin cosmetic having a good feeling of use can be obtained.
本発明は、次の成分(A)、(B)、(C)、(D)、(E)及び(F):
(A)次の一般式(1)
The present invention includes the following components (A), (B), (C), (D), (E) and (F):
(A) The following general formula (1)
(式中、R1及びR2は同一又は異なって、炭素数16〜22の直鎖又は分岐鎖の飽和又は不飽和の炭化水素基を示し、R3及びR4は同一又は異なって、炭素数1〜3のアルキル基を示し、X-は、塩形成陰イオンを示す)
で表されるカチオン界面活性剤 0.1〜1質量%、
(B)HLB12.5〜15の非イオン界面活性剤、
(C)SP値が15.5〜18.5であり、25℃で液状のエステル油及びエーテル油から選ばれる油剤 1〜10質量%、
(D)高級アルコール 0.7〜2質量%、
(E)SP値が23〜30である化合物 0.0001〜0.1質量%、
(F)水
を含有し、成分(A)と成分(B)の質量比(A)/(B)が、0.5〜5である皮膚化粧料を提供するものである。
(In the formula, R 1 and R 2 are the same or different and each represents a linear or branched saturated or unsaturated hydrocarbon group having 16 to 22 carbon atoms, and R 3 and R 4 are the same or different and represent carbon. Represents an alkyl group of 1 to 3, and X − represents a salt-forming anion)
0.1 to 1% by mass of a cationic surfactant represented by
(B) HLB 12.5-15 nonionic surfactant,
(C) 1 to 10% by mass of an oil agent having an SP value of 15.5 to 18.5 and selected from ester oil and ether oil which are liquid at 25 ° C.
(D) 0.7-2 mass% higher alcohol,
(E) Compound having an SP value of 23 to 30 0.0001 to 0.1% by mass,
(F) The skin cosmetics which contain water and whose mass ratio (A) / (B) of a component (A) and a component (B) is 0.5-5 are provided.
本発明の皮膚化粧料は、油溶性成分の浸透性が向上し、使用感に優れるとともに、安定性も良好である。 The skin cosmetic of the present invention has improved permeability of oil-soluble components, excellent usability, and good stability.
本発明で用いる成分(A)のカチオン界面活性剤は、前記一般式(1)で表されるものであり、油溶性成分の浸透性を向上させることができる。
式(1)中、R1及びR2で示される炭化水素基としては、直鎖又は分岐鎖のアルキル基又はアルケニル基が挙げられる。また、塩形成陰イオンとしては、ハロゲンイオン、リン酸イオン、酢酸イオン、乳酸イオン、モノアルキル硫酸イオン等が挙げられる。
The component (A) cationic surfactant used in the present invention is represented by the general formula (1), and can improve the permeability of the oil-soluble component.
In the formula (1), examples of the hydrocarbon group represented by R 1 and R 2 include linear or branched alkyl groups or alkenyl groups. Examples of salt-forming anions include halogen ions, phosphate ions, acetate ions, lactate ions, monoalkyl sulfate ions, and the like.
カチオン界面活性剤の具体例としては、塩化ジセチルジメチルアンモニウム、塩化ジステアリルジメチルアンモニウム、塩化ジアラキルジメチルアンモニウム、塩化ジベヘニルジメチルアンモニウム等が挙げられる。これらのうち、皮膚に対する親和性を有する点から、塩化ジセチルジメチルアンモニウム、塩化ジステアリルジメチルアンモニウム等が好ましい。また、これらの市販品としては、VARISOFT 432 PPG(エボニック社),VARISOFT TA 100(EVONIK エボニック社)が挙げられる。 Specific examples of the cationic surfactant include dicetyldimethylammonium chloride, distearyldimethylammonium chloride, diaralkyldimethylammonium chloride, dibehenyldimethylammonium chloride, and the like. Of these, dicetyldimethylammonium chloride, distearyldimethylammonium chloride and the like are preferable from the viewpoint of affinity for the skin. Examples of these commercially available products include VARISOFT 432 PPG (Evonik) and VARISOFT TA 100 (EVONIK Evonik).
成分(A)は、1種又は2種以上を組み合わせて用いることができ、含有量は、後述する成分(E)の浸透性の向上と乳化組成物の安定性を向上させる点から、全組成中に0.1質量%以上であり、0.2質量%以上が好ましく、1質量%以下であり、0.6質量%以下が好ましい。また、成分(A)の含有量は、全組成中に0.1〜1質量%であり、0.2〜0.6質量%が好ましい。 Component (A) can be used alone or in combination of two or more, and the content is the total composition from the viewpoint of improving the permeability of component (E) described later and improving the stability of the emulsion composition. It is 0.1% by mass or more, preferably 0.2% by mass or more, preferably 1% by mass or less, and preferably 0.6% by mass or less. Moreover, content of a component (A) is 0.1-1 mass% in the whole composition, and 0.2-0.6 mass% is preferable.
本発明で用いる成分(B)の非イオン界面活性剤は、塗布時の化粧料の広がりを向上させることができ、HLB12.5〜15のものであり、HLB12.5〜14のものが好ましい。 The nonionic surfactant of the component (B) used in the present invention can improve the spread of the cosmetic at the time of application, and is HLB 12.5-15, and preferably HLB 12.5-14.
ここで、HLB(親水性−親油性のバランス〈Hydrophilic-Lypophilic Balance〉)は、界面活性剤の全分子量に占める親水基部分の分子量を示すものであり、非イオン界面活性剤については、グリフィン(Griffin)の式により求められるものである。
2種以上の非イオン界面活性剤から構成される混合界面活性剤のHLBは、次のようにして求められる。混合界面活性剤のHLBは、各非イオン界面活性剤のHLB値をその配合比率に基づいて相加算平均したものである。
Here, HLB (hydrophilic-lipophilic balance <Hydrophilic-Lypophilic Balance>) indicates the molecular weight of the hydrophilic group portion in the total molecular weight of the surfactant. For nonionic surfactants, Griffin ( Griffin).
The HLB of the mixed surfactant composed of two or more kinds of nonionic surfactants is obtained as follows. The HLB of the mixed surfactant is obtained by averaging the HLB values of the nonionic surfactants based on the blending ratio.
混合HLB=Σ(HLBx×Wx)/ΣWx
HLBxは、非イオン界面活性剤XのHLB値を示す。
Wxは、HLBxの値を有する非イオン界面活性剤Xの質量(g)を示す。
Mixed HLB = Σ (HLBx × Wx) / ΣWx
HLBx indicates the HLB value of the nonionic surfactant X.
Wx represents the mass (g) of the nonionic surfactant X having a value of HLBx.
成分(B)の非イオン界面活性剤としては、例えば、ソルビタン脂肪酸エステル、グリセリン脂肪酸エステル、ポリグリセリン脂肪酸エステル、プロピレングリコール脂肪酸エステル、ポリエチレングリコール脂肪酸エステル、ショ糖脂肪酸エステル、ポリオキシエチレン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、ポリオキシエチレンアルキルエーテル、ポリオキシエチレンソルビトール脂肪酸エステル、ポリオキシエチレングリセリン脂肪酸エステル、ポリオキシエチレンプロピレングリコール脂肪酸エステル、ポリオキシエチレンヒマシ油、ポリオキシエチレン硬化ヒマシ油、ポリオキシエチレン硬化ヒマシ油脂肪酸エステル、ポリオキシエチレンフィトスタノールエーテル、ポリオキシエチレンフィトステロースエーテル、ポリオキシエチレンコレスタノールエーテル、ポリオキシエチレンコレステリルエーテル、ポリオキシアルキレン変性オルガノポリシロキサン、ポリオキシアルキレン・アルキル共変性オルガノポリシロキサン等が挙げられる。
これらのうち、ポリオキシエチレンアルキルエーテル、ポリオキシエチレン硬化ヒマシ油が好ましい。
Examples of the nonionic surfactant of the component (B) include sorbitan fatty acid ester, glycerin fatty acid ester, polyglycerin fatty acid ester, propylene glycol fatty acid ester, polyethylene glycol fatty acid ester, sucrose fatty acid ester, polyoxyethylene fatty acid ester, poly Oxyethylene sorbitan fatty acid ester, polyoxyethylene alkyl ether, polyoxyethylene sorbitol fatty acid ester, polyoxyethylene glycerin fatty acid ester, polyoxyethylene propylene glycol fatty acid ester, polyoxyethylene castor oil, polyoxyethylene hydrogenated castor oil, polyoxyethylene Hardened castor oil fatty acid ester, polyoxyethylene phytostanol ether, polyoxyethylene phytosterol Ether, polyoxyethylene cholestanol ether, polyoxyethylene cholesteryl ether, polyoxyalkylene-modified organopolysiloxane, polyoxyalkylene-alkyl co-modified organopolysiloxanes, and the like.
Of these, polyoxyethylene alkyl ether and polyoxyethylene hydrogenated castor oil are preferred.
成分(B)は、1種又は2種以上を組み合わせて用いることができ、含有量は、カチオン活性剤と組み合わせた場合の塗布時の化粧料の広がりを向上、及び使用感(ぬるつきのなさ、べたつきのなさ)の向上の点から、全組成中に0.02質量%以上が好ましく、0.07質量%以上がより好ましく、2質量%以下が好ましく、0.4質量%以下がより好ましい。また、成分(B)の含有量は、全組成中に0.02〜2質量%が好ましく、0.07〜0.4質量%がより好ましい。 Component (B) can be used alone or in combination of two or more, and the content improves the spread of the cosmetic when applied in combination with a cationic active agent, and the feeling of use (no sliminess, From the point of improvement of non-stickiness), 0.02% by mass or more is preferable in the total composition, 0.07% by mass or more is more preferable, 2% by mass or less is preferable, and 0.4% by mass or less is more preferable. Moreover, 0.02-2 mass% is preferable in the whole composition, and, as for content of a component (B), 0.07-0.4 mass% is more preferable.
本発明の皮膚化粧料において、成分(A)と(B)の質量比(A)/(B)は、浸透性、化粧料の塗布時の広がりが向上する点から、0.5以上であり、1.5以上が好ましく、5以下であり、3以下が好ましい。また、成分(A)と(B)の質量比(A)/(B)は、0.5〜5であり、1.5〜3が好ましい。 In the skin cosmetic of the present invention, the mass ratio (A) / (B) of the components (A) and (B) is 0.5 or more from the viewpoint of improving the permeability and the spread when the cosmetic is applied. 1.5 or more, preferably 5 or less, and preferably 3 or less. Moreover, mass ratio (A) / (B) of component (A) and (B) is 0.5-5, and 1.5-3 are preferable.
本発明で用いる成分(C)の油剤は、油溶性成分の浸透性が向上する点から、SP値が15.5〜18.5のものであり、浸透性と系の安定性の観点から、16.3〜18.2のものがより好ましい。
ここで、SP値とは、溶解度パラメーターδであって、液体の分子凝集エネルギーEと分子容Vからδ=(E/V)1/2(J/cm3)で与えられる物質定数である。SP値は、各種方法で求められるが、本発明においては、Fedorsの方法(J.BRANDRUP著「POLYMER HANDBOOK 4th 」JHON WILEY & SONS,INC 1999年発行、VII685〜686項に示されるパラメーター)及びコンピューターソフトMolecular modeling Pro(Norgwyn Montgomery Software Inc.)を用いて求めた。
The oil agent of the component (C) used in the present invention has an SP value of 15.5 to 18.5 from the viewpoint of improving the permeability of the oil-soluble component, and from the viewpoint of permeability and system stability, Those of 16.3 to 18.2 are more preferable.
Here, the SP value is a solubility parameter δ, which is a material constant given by δ = (E / V) 1/2 (J / cm 3 ) from the molecular cohesive energy E and molecular volume V of the liquid. The SP value can be determined by various methods. In the present invention, the method of Fedors (J. BRANDRUP, “POLYMER HANDBOOK 4 th ”, JHON WILEY & SONS, INC, 1999, published in paragraphs VII685 to 686) and It calculated | required using computer software Molecular modeling Pro (Norgwyn Montgomery Software Inc.).
また、成分(C)の油剤は、25℃で液状のエステル油及びエーテル油から選ばれるものである。かかる油剤としては、通常の化粧料に用いられるものであれば、制限されずに使用することができる。
かかる油剤としては、例えば、リンゴ酸ジイソステアリル(SP値:18.17)、乳酸オクチルドデシル(SP値:18.53)、イソノナン酸イソノニル(SP値:16.44)、イソノナン酸イソトリデシル(SP値:16.56)、ミリスチン酸オクチルドデシル(SP値:16.74)、パルミチン酸イソプロピル(SP値:16.75)、イソステアリン酸イソプロピル(SP値:16.63)、ステアリン酸ブチル(SP値:16.74)、ミリスチン酸ミリスチル(SP値:16.75)、ミリスチン酸イソプロピル(SP値:17.0)、ミリスチン酸オクチルドデシル(SP値:16.74)、ジカプリン酸ネオペンチルグリコール(SP値:18.15)、トリカプロイン、2−エチルヘキサン酸ペンタエリスリチル、メドフォーム油、オリーブ油(SP値:16.3)等のエステル油;セチル−1,3−ジメチルブチルエーテル(SP値:16.57)、セチルイソブチルエーテル(SP値:16.83)、ジオクチルエーテル(SP値:16.85)等のエーテル油が挙げられる。
The oil agent of component (C) is selected from ester oil and ether oil that are liquid at 25 ° C. Such oil agents can be used without limitation as long as they are used in ordinary cosmetics.
Examples of the oil include diisostearyl malate (SP value: 18.17), octyldodecyl lactate (SP value: 18.53), isononyl isononanoate (SP value: 16.44), and isotridecyl isononanoate (SP). Value: 16.56), octyldodecyl myristate (SP value: 16.74), isopropyl palmitate (SP value: 16.75), isopropyl isostearate (SP value: 16.63), butyl stearate (SP value) : 16.74), myristyl myristate (SP value: 16.75), isopropyl myristate (SP value: 17.0), octyldodecyl myristate (SP value: 16.74), neopentyl glycol dicaprate (SP) Value: 18.15), tricaproine, pentaerythrityl 2-ethylhexanoate Ester oils such as medfoam oil and olive oil (SP value: 16.3); cetyl-1,3-dimethylbutyl ether (SP value: 16.57), cetyl isobutyl ether (SP value: 16.83), dioctyl ether ( And ether oils such as SP value: 16.85).
成分(C)の油剤としては、油溶性成分の浸透性と系の安定性の観点から、オリーブ油、セチル−1,3−ジメチルブチルエーテル、ジカプリン酸ネオペンチルグリコール等が好ましく、オリーブ油、セチル−1,3−ジメチルブチルエーテルがより好ましい。 As the oil agent of component (C), olive oil, cetyl-1,3-dimethylbutyl ether, neopentyl glycol dicaprate and the like are preferable from the viewpoint of the permeability of the oil-soluble component and the stability of the system, and olive oil, cetyl-1, 3-dimethylbutyl ether is more preferred.
成分(C)は、1種又は2種以上を用いることができ、後述する成分(E)の浸透性の向上と使用感の点から、含有量は、全組成中に1質量%以上であり、2質量%以上が好ましく、4質量%以上がより好ましく、10質量%以下であり、8質量%以下が好ましく、7質量%以下がより好ましい。また、成分(C)の含有量は、全組成中に1〜10質量%であり、2〜8質量%が好ましく、4〜7質量%がより好ましい。 Component (C) can be used singly or in combination of two or more, and the content is 1% by mass or more in the total composition from the viewpoint of improving the permeability of component (E) described later and the feeling of use. 2 mass% or more is preferable, 4 mass% or more is more preferable, it is 10 mass% or less, 8 mass% or less is preferable, and 7 mass% or less is more preferable. Moreover, content of a component (C) is 1-10 mass% in the whole composition, 2-8 mass% is preferable, and 4-7 mass% is more preferable.
成分(D)の高級アルコールは、炭素数12〜22の高級アルコールが好ましく、炭素数14〜18の直鎖高級アルコールがより好ましく、油溶性成分の浸透性を向上させることができる。
成分(D)としては、ミリスチルアルコール、セチルアルコール、ステアリルアルコール、ベヘニルアルコール等が挙げられる。これらのうち、セチルアルコール、ステアリルアルコールが好ましい。
The higher alcohol of component (D) is preferably a higher alcohol having 12 to 22 carbon atoms, more preferably a linear higher alcohol having 14 to 18 carbon atoms, and can improve the permeability of the oil-soluble component.
Examples of component (D) include myristyl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol and the like. Of these, cetyl alcohol and stearyl alcohol are preferred.
成分(D)は、1種又は2種以上を組み合わせて用いることができ、油溶性の成分の浸透性と使用感(べたつき、ぬるつき)の向上の点から、含有量は、全組成中に0.7質量%以上であり、1.3質量%以上が好ましく、2質量%以下であり、1.7質量%以下が好ましい。また、成分(D)の含有量は、全組成中に0.7〜2質量%であり、1.3〜1.7質量%が好ましい。 Component (D) can be used singly or in combination of two or more. From the viewpoint of improving the penetrability of oil-soluble components and the feeling of use (stickiness, sliminess), the content is in the total composition. It is 0.7 mass% or more, preferably 1.3 mass% or more, preferably 2 mass% or less, and preferably 1.7 mass% or less. Moreover, content of a component (D) is 0.7-2 mass% in the whole composition, and 1.3-1.7 mass% is preferable.
また、本発明の皮膚化粧料において、成分(A)と(D)の質量比(A)/(D)は、成分(E)の浸透性の点から、0.1以上が好ましく、0.24以上がより好ましく、0.57以下が好ましく、0.3以下がより好ましい。また、成分(A)と(D)の質量比(A)/(D)は、0.1〜0.57好ましく、0.24〜0.3がより好ましい。 In the skin cosmetic of the present invention, the mass ratio (A) / (D) of the components (A) and (D) is preferably 0.1 or more from the viewpoint of the permeability of the component (E). 24 or more is more preferable, 0.57 or less is preferable, and 0.3 or less is more preferable. Moreover, 0.1-0.57 are preferable and, as for mass ratio (A) / (D) of a component (A) and (D), 0.24-0.3 are more preferable.
成分(E)は、SP値が23〜30である化合物である。
成分(E)としては、美白剤、消炎剤、血行促進剤等の有用成分が挙げられる。本発明においては、成分(A)〜(D)を特定の割合で組み合わせて用いることにより、これらの有用成分の浸透性を向上させることができる。
なお、成分(E)のSP値は、成分(C)と同様の方法で求められる。
Component (E) is a compound having an SP value of 23-30.
Examples of the component (E) include useful components such as a whitening agent, an anti-inflammatory agent, and a blood circulation promoter. In the present invention, by using the components (A) to (D) in combination at a specific ratio, the permeability of these useful components can be improved.
In addition, SP value of a component (E) is calculated | required by the method similar to a component (C).
かかるSP値を有する化合物としては、例えば、ナイルレッド(SP値=23.6)、下記式(2)で表されるスピロエーテル(SP値=23.64)、フラバノン(SP値=24.49)、フラボン(SP値=25.2)、アピゲニン(SP値=29.4)などが挙げられる。 Examples of the compound having such SP value include Nile Red (SP value = 23.6), spiro ether represented by the following formula (2) (SP value = 23.64), and flavanone (SP value = 24.49). ), Flavone (SP value = 25.2), apigenin (SP value = 29.4), and the like.
(式中、波線は当該結合状態がZ又はEのいずれでもよいことを示す)
成分(E)としては、美白剤が好ましい。また、成分としては、下記式(2)で表されるスピロエーテル、アピゲニンがより好ましい。
本発明において、成分(E)は、皮膚に浸透されるためには、成分(A)〜(D)、(F)の混合物に混合されていれば良く、成分(C)中に分散、溶解していても良く、また、成分(F)中に分散されていても良い。従って、製造方法に大きく影響されることはない。
(Wherein the wavy line indicates that the binding state may be either Z or E)
As the component (E), a whitening agent is preferable. Moreover, as a component, the spiro ether and apigenin represented by following formula (2) are more preferable.
In the present invention, the component (E) may be mixed in the mixture of the components (A) to (D) and (F) in order to penetrate the skin, and is dispersed and dissolved in the component (C). Or may be dispersed in the component (F). Therefore, it is not greatly influenced by the manufacturing method.
また、成分(E)の含有量は、浸透性を考慮すれば、多い程良いが、全組成中に、0.0001質量%以上であり、0.001質量%以上が好ましく、0.1質量%以下が好ましく、0.09質量%以下が好ましい。また、成分(E)の含有量は、全組成中に、0.0001〜0.1質量%であり、0.001〜0.09質量%が好ましい。 Further, the content of the component (E) is preferably as long as the permeability is taken into consideration, but is 0.0001% by mass or more, preferably 0.001% by mass or more, and preferably 0.1% by mass in the total composition. % Or less is preferable, and 0.09 mass% or less is preferable. Moreover, content of a component (E) is 0.0001-0.1 mass% in the whole composition, and 0.001-0.09 mass% is preferable.
成分(F)の水の含有量は、皮膚上での感触のみずみずしさの点から、全組成中に、30質量%以上が好ましく、45質量%以上がより好ましく、95質量%以下が好ましく、90質量%以下がより好ましい。また、水の含有量は、全組成中に、30〜95質量%が好ましく、45〜90質量%がより好ましい。 The water content of the component (F) is preferably 30% by mass or more, more preferably 45% by mass or more, and preferably 95% by mass or less in the total composition from the viewpoint of freshness on the skin. 90 mass% or less is more preferable. Moreover, 30-95 mass% is preferable in the whole composition, and, as for content of water, 45-90 mass% is more preferable.
本発明の皮膚化粧料は、さらに、(G)ジメチルポリシロキサンを含有することができ、塗布時のベタツキを抑制し、塗布時のなめらかさを向上させることができる。
成分(G)のジメチルポリシロキサンとしては、25℃における粘度が、5〜7mm2/sのものが好ましい。
The skin cosmetic of the present invention can further contain (G) dimethylpolysiloxane, can suppress stickiness during application, and can improve smoothness during application.
The component (G) dimethylpolysiloxane preferably has a viscosity at 25 ° C. of 5 to 7 mm 2 / s.
成分(G)は、1種又は2種以上を用いることができ、含有量は、塗布時のベタツキを抑制し、塗布時のなめらかさを向上させる点から、全組成中に0.1質量%以上が好ましく、0.5質量%以上がより好ましく、0.8質量%以上が更に好ましく、5質量%以下が好ましく、3質量%以下がより好ましく、1.5質量%以下が更に好ましい。また、成分(G)の含有量は、全組成中に0.1〜5質量%が好ましく、0.5〜3質量%がより好ましく、0.8〜1.5質量%が更に好ましい。 Component (G) can be used alone or in combination of two or more, and the content is 0.1% by mass in the total composition from the point of suppressing stickiness during coating and improving smoothness during coating. The above is preferable, 0.5 mass% or more is more preferable, 0.8 mass% or more is further preferable, 5 mass% or less is preferable, 3 mass% or less is more preferable, and 1.5 mass% or less is further preferable. Moreover, 0.1-5 mass% is preferable in the whole composition, content of a component (G) has more preferable 0.5-3 mass%, and 0.8-1.5 mass% is still more preferable.
本発明の皮膚化粧料は、さらに、(H)架橋型メチルポリシロキサンを含有することができ、塗布後の肌のなめらかさを向上させることができる。
架橋型メチルポリシロキサンは、(ジメチコン/ビニルジメチコン)クロスポリマー(INCI名)であり、常法に従って製造することができる。架橋型メチルポリシロキサンは、水や、アルコール、油剤等に不溶性のシリコーン粉体で、数平均粒径が1〜30μmのものが好ましく、2〜6μmのものがより好ましい。
The skin cosmetic of the present invention can further contain (H) a crosslinked methylpolysiloxane, and can improve the smoothness of the skin after application.
Cross-linked methylpolysiloxane is a (dimethicone / vinyl dimethicone) crosspolymer (INCI name) and can be produced according to a conventional method. The cross-linked methylpolysiloxane is a silicone powder that is insoluble in water, alcohol, oil, etc., and preferably has a number average particle size of 1 to 30 μm, more preferably 2 to 6 μm.
成分(H)は、粉体として配合してもよい。例えば、KM9729(信越化学工業社);トレフィルE−506c、トレフィルE−508(東レ・ダウコーニング社)などが挙げられる。また、各種の溶媒に界面活性剤等を用いて分散させた分散液として配合することもできる。このような分散液としては、例えば、シリコーンBY29−119、シリコーンBY29−129(東レ・ダウコーニング社)等の市販品を用いることができる。 Component (H) may be blended as a powder. For example, KM9729 (Shin-Etsu Chemical Co., Ltd.); Trefil E-506c, Trefil E-508 (Toray Dow Corning), etc. are mentioned. Moreover, it can also mix | blend as a dispersion liquid disperse | distributed using surfactant etc. in various solvents. As such a dispersion, for example, commercially available products such as silicone BY29-119 and silicone BY29-129 (Toray Dow Corning) can be used.
成分(H)は、1種又は2種以上を組み合わせて用いることができ、含有量は、塗布後の肌のなめらかさの点から、全組成中に1質量%以上が好ましく、2質量%以上がより好ましく、3質量%以上が更に好ましく、10質量%以下が好ましく、8質量%以下がより好ましく、6質量%以下が更に好ましい。また、成分(H)の含有量は、全組成中に1〜10質量%が好ましく、2〜8質量%がより好ましく、3〜6質量%が更に好ましい。 Component (H) can be used singly or in combination of two or more, and the content is preferably 1% by mass or more, preferably 2% by mass or more in the total composition from the point of smoothness of the skin after application. Is more preferably 3% by mass or more, preferably 10% by mass or less, more preferably 8% by mass or less, and further preferably 6% by mass or less. Moreover, 1-10 mass% is preferable in the whole composition, as for content of a component (H), 2-8 mass% is more preferable, and 3-6 mass% is still more preferable.
本発明の皮膚化粧料は、更に、多価アルコールを含有することができる。成分(E)などの分散剤として機能するだけでなく、保湿効果を付与することができる。
多価アルコールとしては、グリセリン、ジグリセリン、ポリエチレングリコール、1,3−ブチレングリコール、イソプレングリコール、プロピレングリコール、ジプロピレングリコールなどが挙げられる。
多価アルコールは、1種又は2種以上を用いることができ、含有量は、分散剤及び使用感の点から、0.1質量%以上が好ましく、1質量%以上がより好ましく、30質量%以下が好ましく、25質量%以下がより好ましい。また、多価アルコールの含有量は、全組成中に0.1〜30質量%が好ましく、1〜25質量%がより好ましい。
The skin cosmetic of the present invention can further contain a polyhydric alcohol. In addition to functioning as a dispersant such as the component (E), a moisturizing effect can be imparted.
Examples of the polyhydric alcohol include glycerin, diglycerin, polyethylene glycol, 1,3-butylene glycol, isoprene glycol, propylene glycol, and dipropylene glycol.
The polyhydric alcohol can be used singly or in combination of two or more, and the content is preferably 0.1% by mass or more, more preferably 1% by mass or more, and 30% by mass from the viewpoint of the dispersant and the feeling of use. The following is preferable, and 25% by mass or less is more preferable. Moreover, 0.1-30 mass% is preferable in the whole composition, and, as for content of a polyhydric alcohol, 1-25 mass% is more preferable.
本発明の皮膚化粧料は、前記成分のほか、通常の化粧料に用いられるその他の成分を含有することができる。例えば、前記以外の油性成分、前記以外の非イオン界面活性剤、アニオン界面活性剤、両性界面活性剤、低級アルコール、保湿剤、水溶性高分子、酸化防止剤、防腐剤、キレート剤、紫外線吸収剤、粉体、香料、色材、成分(E)以外の美白剤、成分(E)以外のビタミン類、成分(E)以外のその他各種薬効成分などが挙げられる。 The skin cosmetic of the present invention can contain other components used in ordinary cosmetics in addition to the above components. For example, oily components other than the above, nonionic surfactants other than the above, anionic surfactants, amphoteric surfactants, lower alcohols, humectants, water-soluble polymers, antioxidants, preservatives, chelating agents, UV absorption Agents, powders, fragrances, coloring materials, whitening agents other than component (E), vitamins other than component (E), and various other medicinal components other than component (E).
本発明の皮膚化粧料は、以下のいずれかの方法で水中油型乳化化粧料を製造することができる。
(製造方法1)
工程1:成分(A)〜(E)及びその他の油剤成分を含む油相を、成分中最も融点が高い成分の温度以上に加熱し、撹拌して混合物(1)を得る工程。
工程2:成分(F)及び、その他水溶性成分を混合し、混合物(1)と略同温に加熱し、混合物(1)と混合し、混合物(2)得る工程。
工程3:混合物(2)を15〜35℃まで冷却する工程。
The skin cosmetic of the present invention can produce an oil-in-water emulsified cosmetic by any of the following methods.
(Manufacturing method 1)
Step 1: A step of heating the oil phase containing the components (A) to (E) and other oil agent components to a temperature equal to or higher than the component having the highest melting point and stirring to obtain a mixture (1).
Step 2: A step of mixing the component (F) and other water-soluble components, heating to about the same temperature as the mixture (1), and mixing with the mixture (1) to obtain the mixture (2).
Process 3: The process of cooling a mixture (2) to 15-35 degreeC.
(製造方法2)
工程1:成分(A)〜(D)及びその他の油剤成分を含む油相を、成分中最も融点が高い成分の温度以上に加熱し、撹拌して混合物(3)を得る工程。
工程2:成分(F)及び、その他水溶性成分を混合し、混合物(3)と略同温に加熱し、混合物(3)と混合し、混合物(4)を得る工程。
工程3:混合物(4)を15〜35℃まで冷却し、成分(E)を混合し、均一にする工程。
なお、成分(E)の安定性を考慮した場合、製造方法2で行うことが好ましい。
(Manufacturing method 2)
Step 1: A step of heating the oil phase containing the components (A) to (D) and other oil agent components to a temperature equal to or higher than the component having the highest melting point and stirring to obtain a mixture (3).
Process 2: The process of mixing a component (F) and another water-soluble component, heating to substantially the same temperature as a mixture (3), and mixing with a mixture (3), and obtaining a mixture (4).
Process 3: The process of cooling a mixture (4) to 15-35 degreeC, mixing a component (E), and making it uniform.
In consideration of the stability of the component (E), the production method 2 is preferable.
本発明の皮膚化粧料は、例えば、化粧下地、日焼け止め化粧料、ローション、クリーム、乳液、化粧水等の皮膚化粧料として適用することができる。
本発明の皮膚化粧料を用いて、スキンケアを行う場合、本発明の皮膚化粧料を肌に塗布し、薄く伸ばすことができる。このようにすることで、化粧料中の有効成分を肌に浸透させることができる。
上述した実施形態に関し、本発明は、更に以下の組成物、製造方法、使用方法を開示する。
The skin cosmetics of the present invention can be applied as skin cosmetics such as makeup bases, sunscreen cosmetics, lotions, creams, milky lotions, and lotions.
When performing skin care using the skin cosmetic of the present invention, the skin cosmetic of the present invention can be applied to the skin and stretched thinly. By doing in this way, the active ingredient in cosmetics can be penetrated into skin.
This invention discloses the following compositions, manufacturing methods, and usage methods further regarding embodiment mentioned above.
<1>次の成分(A)、(B)、(C)、(D)、(E)及び(F):
(A)次の一般式(1)
<1> The following components (A), (B), (C), (D), (E) and (F):
(A) The following general formula (1)
(式中、R1及びR2は同一又は異なって、炭素数16〜22の直鎖又は分岐鎖の飽和又は不飽和の炭化水素基を示し、R3及びR4は同一又は異なって、炭素数1〜3のアルキル基を示し、X-は、塩形成陰イオンを示す)
で表されるカチオン界面活性剤 0.1〜1質量%、
(B)HLB12.5〜15の非イオン界面活性剤、
(C)25℃で液状のエステル油及びエーテル油から選ばれる油剤 1〜10質量%、
(D)高級アルコール 0.7〜2質量%、
(E)SP値が23〜30である化合物 0.0001〜0.1質量%、
(F)水
を含有し、成分(A)と成分(B)の質量比(A)/(B)が、0.5〜5である皮膚化粧料。
(In the formula, R 1 and R 2 are the same or different and each represents a linear or branched saturated or unsaturated hydrocarbon group having 16 to 22 carbon atoms, and R 3 and R 4 are the same or different and represent carbon. Represents an alkyl group of 1 to 3, and X − represents a salt-forming anion)
0.1 to 1% by mass of a cationic surfactant represented by
(B) HLB 12.5-15 nonionic surfactant,
(C) 1 to 10% by mass of an oil agent selected from ester oil and ether oil which are liquid at 25 ° C.
(D) 0.7-2 mass% higher alcohol,
(E) Compound having an SP value of 23 to 30 0.0001 to 0.1% by mass,
(F) A skin cosmetic containing water and having a mass ratio (A) / (B) of the component (A) to the component (B) of 0.5 to 5.
<2>成分(A)が、塩化ジステアリルジメチルアンモニウムであり、その含有量が、全組成中に、好ましくは0.1〜1質量%であって、0.2〜0.6質量%がより好ましい前記<1>記載の皮膚化粧料。
<3>成分(B)が、ポリオキシエチレンアルキルエーテル、ポリオキシエチレン硬化ヒマシ油から選ばれる少なくとも1種又は2種以上であり、その含有量が、全組成中に、好ましくは0.02質量%以上であり、0.07質量%以上がより好ましく、2質量%以下が好ましく、0.4質量%以下がより好ましい前記<1>又は<2>記載の皮膚化粧料。
<4>成分(C)の油剤が、SP値15.5〜18.5であって、16.3〜18.2が好ましい前記<1>〜<3>のいずれか1記載の皮膚化粧料。
<2> Component (A) is distearyldimethylammonium chloride, and its content is preferably 0.1 to 1% by mass, and 0.2 to 0.6% by mass in the total composition. The skin cosmetic according to <1>, which is more preferable.
<3> Component (B) is at least one or two or more selected from polyoxyethylene alkyl ether and polyoxyethylene hydrogenated castor oil, and the content thereof is preferably 0.02 mass in the total composition. % Or more, 0.07% by mass or more is more preferable, 2% by mass or less is preferable, and 0.4% by mass or less is more preferable. The skin cosmetic according to <1> or <2>.
<4> The skin cosmetic according to any one of <1> to <3>, wherein the oil of component (C) has an SP value of 15.5 to 18.5, and preferably 16.3 to 18.2. .
<5>成分(C)が、オリーブ油、セチル−1,3−ジメチルブチルエーテル、ジカプリン酸ネオペンチルグリコールであり、好ましくは、オリーブ油及びセチル−1,3−ジメチルブチルエーテルから選ばれる少なくとも1種又は2種以上であり、その含有量は、全組成中に1質量%以上であり、2質量%以上が好ましく、4質量%以上がより好ましく、10質量%以下であり、8質量%以下が好ましく、7質量%以下がより好ましい前記<1>〜<4>のいずれか1記載の皮膚化粧料。
<6>成分(D)が、炭素数12〜22の高級アルコールであって、セチルアルコール、ステアリルアルコールが好ましい前記<1>〜<5>のいずれか1記載の皮膚化粧料。
<7>成分(E)が、ナイルレッド、式(2)
<5> Component (C) is olive oil, cetyl-1,3-dimethylbutyl ether, or neopentyl glycol dicaprate, preferably at least one or two selected from olive oil and cetyl-1,3-dimethylbutyl ether The content thereof is 1% by mass or more in the total composition, preferably 2% by mass or more, more preferably 4% by mass or more, and preferably 10% by mass or less, preferably 8% by mass or less, The skin cosmetic according to any one of <1> to <4>, wherein the content is more preferably at most% by mass.
<6> The skin cosmetic according to any one of <1> to <5>, wherein the component (D) is a higher alcohol having 12 to 22 carbon atoms, and preferably cetyl alcohol and stearyl alcohol.
<7> Component (E) is Nile Red, Formula (2)
(式中、波線は当該結合状態がZ又はEのいずれでもよいことを示す)
で表されるスピロエーテル、フラバノン、フラボン及びアピゲニンから選ばれる少なくとも1種又は2種以上を含み、その含有量が、0.0001質量%以上であり、0.001質量%以上が好ましく、0.1質量%以下が好ましく、0.09質量%以下が好ましい前記<1>〜<6>のいずれか1記載の皮膚化粧料。
<8>成分(A)と成分(D)の質量比(A)/(D)が、0.1〜0.57であり、0.24〜0.3が好ましい前記<1>〜<7>のいずれか1記載の皮膚化粧料。
<9>さらに、(G)ジメチルポリシロキサンを含有し、その含有量は、全組成中に0.1質量%以上が好ましく、0.5質量%以上がより好ましく、0.8質量%以上が更に好ましく、5質量%以下が好ましく、3質量%以下がより好ましく、1.5質量%以下が更に好ましい前記<1>〜<8>のいずれか1記載の皮膚化粧料。
(Wherein the wavy line indicates that the binding state may be either Z or E)
And at least one or more selected from spiroether, flavanone, flavone and apigenin, the content of which is 0.0001% by mass or more, preferably 0.001% by mass or more, and 1 mass% or less is preferable and 0.09 mass% or less is preferable The skin cosmetics in any one of said <1>-<6>.
<8> Mass ratio (A) / (D) of component (A) to component (D) is 0.1 to 0.57, and preferably 0.24 to 0.3 <1> to <7 > The skin cosmetic according to any one of the above.
<9> Furthermore, (G) dimethylpolysiloxane is contained, and the content thereof is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and more preferably 0.8% by mass or more in the total composition. The skin cosmetic according to any one of <1> to <8>, more preferably 5% by mass or less, more preferably 3% by mass or less, and further preferably 1.5% by mass or less.
<10>さらに、(H)架橋型メチルポリシロキサンを含有し、架橋型メチルポリシロキサンの数平均粒径が1〜30μm、好ましくは2〜6μmであり、その含有量は、全組成中に、好ましくは1質量%以上であり、2質量%以上がより好ましく、3質量%以上が更に好ましく、10質量%以下が好ましく、8質量%以下がより好ましく、6質量%以下が更に好ましい前記<1>〜<9>のいずれか1記載の皮膚化粧料。
<11>前記<1>〜<10>いずれか1記載の皮膚化粧料を、肌に塗布し、肌に保持するスキンケアのための使用。
<10> Further, (H) a crosslinked methylpolysiloxane is contained, and the number average particle diameter of the crosslinked methylpolysiloxane is 1 to 30 μm, preferably 2 to 6 μm. Preferably it is 1 mass% or more, 2 mass% or more is more preferable, 3 mass% or more is further more preferable, 10 mass% or less is preferable, 8 mass% or less is more preferable, and 6 mass% or less is further more preferable <1 The skin cosmetic according to any one of> to <9>.
<11> Use for skin care in which the skin cosmetic according to any one of <1> to <10> is applied to the skin and retained on the skin.
<12>以下の工程を備えた前記<1>〜<10>のいずれか1記載の皮膚化粧料の製造方法。
工程1:成分(A)〜(E)及びその他の油剤成分を含む油相を、成分中最も高い融点以上に加熱し、撹拌し混合物(1)を得る工程。
工程2:成分(F)及び、その他水溶性成分を混合し、混合物(1)と略同温に加熱し、混合物(1)と混合し、混合物(2)得る工程。
工程3:混合物(2)を15〜35℃まで冷却する工程。
<12> The method for producing a skin cosmetic according to any one of <1> to <10>, comprising the following steps.
Step 1: A step of heating the oil phase containing the components (A) to (E) and other oil agent components to a temperature higher than the highest melting point of the components and stirring to obtain a mixture (1).
Step 2: A step of mixing the component (F) and other water-soluble components, heating to about the same temperature as the mixture (1), and mixing with the mixture (1) to obtain the mixture (2).
Process 3: The process of cooling a mixture (2) to 15-35 degreeC.
<13>以下の工程を備えた前記<1>〜<10>のいずれか1記載の皮膚化粧料の製造方法。
工程1:成分(A)〜(D)及びその他の油剤成分を含む油相を、成分中最も高い融点以上に加熱し、撹拌し混合物(3)を得る工程。
工程2:成分(F)及び、その他水溶性成分を混合し、混合物(3)と略同温に加熱し、混合物(3)と混合し、混合物(4)を得る工程。
工程3:混合物(4)を15〜35℃まで冷却し、成分(E)を混合し、均一にする工程。
<13> The method for producing a skin cosmetic according to any one of <1> to <10>, comprising the following steps.
Step 1: A step of heating an oil phase containing the components (A) to (D) and other oil agent components to a temperature higher than the highest melting point of the components and stirring to obtain a mixture (3).
Process 2: The process of mixing a component (F) and another water-soluble component, heating to substantially the same temperature as a mixture (3), and mixing with a mixture (3), and obtaining a mixture (4).
Process 3: The process of cooling a mixture (4) to 15-35 degreeC, mixing a component (E), and making it uniform.
実施例1〜14、比較例1〜5
表1〜表4に示す組成の水中油型乳化化粧料を製造し、浸透性、保存安定性及び使用感(塗布時の広がり、ぬるぬるしない、べたつかない、塗布時のなめらかさ、塗布後の肌のなめらかさ)を評価した。結果を表1〜表4に併せて示す。
Examples 1-14, Comparative Examples 1-5
Manufactures oil-in-water emulsified cosmetics having the compositions shown in Tables 1 to 4 and has penetrability, storage stability and feeling of use (spreading when applied, not slimy, not sticky, smooth when applied, skin after application Smoothness). The results are also shown in Tables 1 to 4.
(製造方法)
(1)成分(E)が、アピゲニンの場合:
成分(A)〜(D)、(G)及び(H)を混合し、80℃に加熱し、撹拌して均一にした。この混合液に、80℃に加熱した成分(F)(成分(F)から、1質量%をのぞいたもの)を加え、撹拌して均一にした。この後、撹拌しながら25℃まで冷却し、乳化物を得た。この乳化物に、成分(E)アピゲニンと1,3−ブチレングリコール及び成分(F)1質量%の混合物と混合し、均一にして、水中油型乳化化粧料を得た。
(Production method)
(1) When component (E) is apigenin:
Components (A) to (D), (G), and (H) were mixed, heated to 80 ° C., and stirred to make uniform. To this mixture, component (F) heated to 80 ° C. (excluding 1% by mass from component (F)) was added and stirred to make it uniform. Then, it cooled to 25 degreeC, stirring, and obtained the emulsion. This emulsion was mixed with a mixture of component (E) apigenin, 1,3-butylene glycol and component (F) 1% by mass to obtain a uniform oil-in-water emulsion cosmetic.
(2)成分(E)が、ナイルレッドである場合:
成分(A)〜(E)を混合し、80℃に加熱し、撹拌して均一にした。この混合液に、80℃に加熱した成分(F)を加え、撹拌し均一にした。この後、撹拌しながら25℃まで冷却し、水中油型乳化化粧料を得た。
(2) When component (E) is Nile Red:
Components (A) to (E) were mixed, heated to 80 ° C., and stirred to make uniform. To this mixture, component (F) heated to 80 ° C. was added and stirred to make it uniform. Then, it cooled to 25 degreeC, stirring, and obtained the oil-in-water type emulsion cosmetic.
(評価方法)
(1)浸透性:
(i)豚皮(ランドレース♀)を洗顔料(ソフィーナ ボーテ ミルク洗顔料、花王社製)で洗浄した後、水分を拭きとり、アセトン/エーテル(1/1)の混液に皮膚表面を3分間浸した。
(ii)豚皮をフランツ拡散セルに挟み込み、表面側に評価物質(アピゲニン又はナイルレッド)を配合した各化粧料を0.4mL/cm2となるように塗布し、30℃の環境下にて、16時間遮光して静置した。
(iii)豚皮表面を洗顔料(ソフィーナ ボーテ ミルク洗顔料、花王社製)で洗い流して化粧料を除去し、バイオプシパンチ(8mmΦ)で皮膚をくり抜き、1.5mLの抽出溶媒に浸し、超音波で10分間処理することにより、豚皮中に浸透した評価物質(アピゲニン又はナイルレッド)を抽出して定量した。評価物質を定量するためのHPLC条件は下記の通りである。
(Evaluation method)
(1) Permeability:
(i) After washing the pork skin (Landlace candy) with a face wash (Sofina Beaute milk face wash, manufactured by Kao), wipe off the water and leave the skin surface in a mixture of acetone / ether (1/1) for 3 minutes. Soaked.
(ii) Pork skin is sandwiched between Franz diffusion cells, and each cosmetic material containing an evaluation substance (apigenin or Nile red) on the surface side is applied to 0.4 mL / cm 2 , in an environment of 30 ° C. For 16 hours.
(iii) The surface of the pig skin is washed away with a facial cleanser (Sofina Beaute milk facial cleanser, manufactured by Kao Corporation) to remove cosmetics, the skin is cut out with a biopsy punch (8 mmΦ), soaked in 1.5 mL of extraction solvent, and subjected to ultrasound. The test substance (Apigenin or Nile Red) that permeated into the pig skin was extracted and quantified. The HPLC conditions for quantifying the evaluation substance are as follows.
(アピゲニン分析条件)
抽出溶媒:60%1,3−ブチレングリコール
カラム:GLサイエンス inertsil ODS3(5μm:3.0×150mm)
溶離液:25mMリン酸水素カリウム水溶液/メタノール(=1/1)
流速:0.5mL/min
温度:40℃
検出:UV340nm
分析時間:20min
インジェクション量:10μL
なお、アピゲニンの浸透量は、比較例1の値を1とし、その相対値を結果として記載した。
(Apigenin analysis conditions)
Extraction solvent: 60% 1,3-butylene glycol Column: GL Science insertsil ODS3 (5 μm: 3.0 × 150 mm)
Eluent: 25 mM aqueous potassium hydrogen phosphate / methanol (= 1/1)
Flow rate: 0.5mL / min
Temperature: 40 ° C
Detection: UV340nm
Analysis time: 20min
Injection volume: 10μL
In addition, the penetration amount of apigenin was described with the value of Comparative Example 1 as 1, and the relative value as a result.
(ナイルレッド分析条件)
抽出溶媒:55%エタノール
カラム:GLサイエンス inertsil ODS3(5μm:4.0×150mm)
溶離液:アセトニトリル/メタノール(=9/1)
流速:1.0mL/min
温度:40℃
検出:Ex:550nm Em:650nm
分析時間:10min
インジェクション量:10μL
なお、ナイルレッドの浸透量は、比較例5の値を1とし、その相対値を結果として記載した。
(Nile Red analysis conditions)
Extraction solvent: 55% ethanol column: GL Science insertsil ODS3 (5 μm: 4.0 × 150 mm)
Eluent: acetonitrile / methanol (= 9/1)
Flow rate: 1.0 mL / min
Temperature: 40 ° C
Detection: Ex: 550 nm Em: 650 nm
Analysis time: 10min
Injection volume: 10μL
In addition, the penetration amount of Nile Red was described with the value of Comparative Example 5 as 1, and the relative value as a result.
(2)保存安定性:
各化粧料をガラス瓶に充填し、室温で1ヶ月保存した後、外観を目視により観察し、分離の有無を評価した。均一で分離のないものを「○」、分離しているものを「×」で示した。
(2) Storage stability:
Each cosmetic was filled in a glass bottle and stored at room temperature for 1 month, and then the appearance was visually observed to evaluate the presence or absence of separation. Uniform and non-separated samples are indicated by “◯”, and separated samples are indicated by “x”.
(3)使用感:
専門パネラー10名により、各化粧料0.3gを顔に塗布し、手で顔全体に塗り広げた。このとき、塗布時の広がり、ぬるぬるしない、べたつかない、塗布時のなめらかさを官能評価した。更に、塗布3分後に、塗布後の肌のなめらかさを官能評価した。結果を、評価が良いとする人数で示した。
(3) Usability:
Ten professional panelists applied 0.3 g of each cosmetic on the face and spread it over the entire face by hand. At this time, sensory evaluation was performed on the spread at the time of application, not slimy, not sticky, and the smoothness at the time of application. Furthermore, 3 minutes after application | coating, sensory evaluation was carried out about the smoothness of the skin after application | coating. The results are shown in terms of the number of people with good evaluation.
Claims (6)
(A)次の一般式(1)
で表されるカチオン界面活性剤 0.1〜1質量%、
(B)HLB12.5〜15の非イオン界面活性剤、
(C)SP値が15.5〜18.5であり、25℃で液状のエステル油及びエーテル油から選ばれる油剤 1〜10質量%、
(D)高級アルコール 0.7〜2質量%、
(E)SP値が23〜30である美白剤 0.0001〜0.1質量%、
(F)水
を含有し、成分(A)と成分(B)の質量比(A)/(B)が、0.5〜5である皮膚化粧料。 The following components (A), (B), (C), (D), (E) and (F):
(A) The following general formula (1)
0.1 to 1% by mass of a cationic surfactant represented by
(B) HLB 12.5-15 nonionic surfactant,
(C) 1 to 10% by mass of an oil agent having an SP value of 15.5 to 18.5 and selected from ester oil and ether oil which are liquid at 25 ° C.
(D) 0.7-2 mass% higher alcohol,
(E) Whitening agent having an SP value of 23 to 30 0.0001 to 0.1% by mass,
(F) A skin cosmetic containing water and having a mass ratio (A) / (B) of the component (A) to the component (B) of 0.5 to 5.
工程1:成分(A)〜(D)を混合し、各成分の融点以上に加熱し、均一にする工程(混合物(3))。
工程2:成分(F)及び、その他水溶性成分を混合し、混合物(3)とほぼ同温に加熱し、混合物(3)と混合する工程(混合物(4))。
工程3:混合物(4)を室温まで冷却し、成分(E)を混合し、均一にする工程。
The manufacturing method of the skin cosmetics of any one of Claims 1-4 provided with the following processes.
Step 1: A step of mixing components (A) to (D) and heating to a temperature equal to or higher than the melting point of each component (mixture (3)).
Process 2: A process (mixture (4)) which mixes a component (F) and another water-soluble component, is heated to substantially the same temperature as the mixture (3), and mixes with the mixture (3).
Process 3: The process of cooling a mixture (4) to room temperature, mixing a component (E), and making it uniform.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012263591A JP6139867B2 (en) | 2012-11-30 | 2012-11-30 | Skin cosmetics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012263591A JP6139867B2 (en) | 2012-11-30 | 2012-11-30 | Skin cosmetics |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2017089920A Division JP6385517B2 (en) | 2017-04-28 | 2017-04-28 | Skin cosmetics |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2014108935A JP2014108935A (en) | 2014-06-12 |
JP6139867B2 true JP6139867B2 (en) | 2017-05-31 |
Family
ID=51029776
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012263591A Active JP6139867B2 (en) | 2012-11-30 | 2012-11-30 | Skin cosmetics |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP6139867B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7266975B2 (en) * | 2018-07-20 | 2023-05-01 | 株式会社 資生堂 | Skin gel formulation for external use |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0714283B1 (en) * | 1993-07-03 | 1999-05-12 | The Procter & Gamble Company | Personal cleansing compositions |
JP3113844B2 (en) * | 1996-11-15 | 2000-12-04 | 花王株式会社 | Cosmetics |
JPH10204001A (en) * | 1996-11-15 | 1998-08-04 | Kao Corp | Percutaneous absorption accelerator |
JP2004346046A (en) * | 2003-05-26 | 2004-12-09 | Shin Etsu Chem Co Ltd | Cosmetic |
JP2006219423A (en) * | 2005-02-10 | 2006-08-24 | Kao Corp | Skin cosmetic |
JP2010163363A (en) * | 2009-01-13 | 2010-07-29 | Kao Corp | Method for producing extract containing apigenin in high concentration |
US8318222B2 (en) * | 2010-02-19 | 2012-11-27 | Mary Kay, Inc. | Topical skin care formulation |
JP5227467B2 (en) * | 2011-02-28 | 2013-07-03 | 株式会社 資生堂 | Transparent or translucent oil-in-water emulsified cosmetics |
-
2012
- 2012-11-30 JP JP2012263591A patent/JP6139867B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
JP2014108935A (en) | 2014-06-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2008247756A (en) | Oil-in-water type emulsion composition | |
JP2006111620A (en) | Oil-in-water type liquid composition | |
JP2009126791A (en) | Oil-in-polyhydric alcohol type emulsified cosmetic | |
JP4731301B2 (en) | Moisturizer and cosmetics containing the same | |
JP4215918B2 (en) | Cosmetics | |
JP6796949B2 (en) | Manufacturing method of oil-in-water emulsified cosmetics | |
JP2007014866A (en) | Method for preparing oil in water microemulsion composition | |
KR20160065658A (en) | Emulsifier-Free Washable Cleansing Cosmetic Composition | |
JP6139867B2 (en) | Skin cosmetics | |
TW570809B (en) | External application composition | |
JP5132800B1 (en) | Oil-in-water topical skin preparation | |
JP6385517B2 (en) | Skin cosmetics | |
JP2013189429A (en) | Water-in-oil-in-water type emulsified cosmetic | |
JP2001002521A (en) | Water-in-oil type emulsion cosmetic having excellent phase inversion feeling having high inner water phase ratio | |
WO2019245024A1 (en) | Aerosol cosmetic | |
JP4553607B2 (en) | Oil-in-water emulsified fragrance composition and method for producing the same | |
JP6341766B2 (en) | Skin cosmetics | |
JP2008094811A (en) | O/w type emulsified composition and its preparing method | |
JP2005089366A (en) | Emulsified composition for hair | |
JP2009191017A (en) | Emulsified hair cosmetic | |
JP2010001260A (en) | Water-in-oil type emulsion cosmetic | |
JP7352713B2 (en) | emulsifying composition | |
JPS63154606A (en) | Transparent skin cosmetic | |
JP5562674B2 (en) | Emulsion composition for hairdressing | |
JP2003055141A (en) | W/o-type emulsion cosmetic |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20150925 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20160728 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20160809 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20161007 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20161208 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20170314 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20170327 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20170404 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20170428 |
|
R151 | Written notification of patent or utility model registration |
Ref document number: 6139867 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R151 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |