JPH0525535B2 - - Google Patents
Info
- Publication number
- JPH0525535B2 JPH0525535B2 JP59177248A JP17724884A JPH0525535B2 JP H0525535 B2 JPH0525535 B2 JP H0525535B2 JP 59177248 A JP59177248 A JP 59177248A JP 17724884 A JP17724884 A JP 17724884A JP H0525535 B2 JPH0525535 B2 JP H0525535B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- water
- alcohol
- polyhydric alcohol
- emulsion composition
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 claims description 44
- 150000005846 sugar alcohols Polymers 0.000 claims description 21
- 150000003904 phospholipids Chemical class 0.000 claims description 17
- 239000000839 emulsion Substances 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 14
- 125000004442 acylamino group Chemical group 0.000 claims description 14
- 239000000344 soap Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 239000007764 o/w emulsion Substances 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000003921 oil Substances 0.000 description 11
- 235000019198 oils Nutrition 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 239000006071 cream Substances 0.000 description 7
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 7
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 6
- 239000003814 drug Substances 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 229960000541 cetyl alcohol Drugs 0.000 description 4
- 239000002537 cosmetic Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- -1 phosphatidyl monomethylethanolamine Chemical compound 0.000 description 4
- 239000008213 purified water Substances 0.000 description 4
- 229940058015 1,3-butylene glycol Drugs 0.000 description 3
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 235000001014 amino acid Nutrition 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 235000019437 butane-1,3-diol Nutrition 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229960000735 docosanol Drugs 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000003349 gelling agent Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 235000015110 jellies Nutrition 0.000 description 3
- 239000008274 jelly Substances 0.000 description 3
- 235000010445 lecithin Nutrition 0.000 description 3
- 239000000787 lecithin Substances 0.000 description 3
- 229940067606 lecithin Drugs 0.000 description 3
- 229940057995 liquid paraffin Drugs 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 3
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 3
- 229940083466 soybean lecithin Drugs 0.000 description 3
- 229940032094 squalane Drugs 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- 239000004475 Arginine Substances 0.000 description 2
- 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 2
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 2
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 2
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 2
- 239000004472 Lysine Substances 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 2
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 2
- 230000003796 beauty Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 2
- 229960003104 ornithine Drugs 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- ZNYIJXQYUNSKDX-NTISSMGPSA-M sodium;hydron;(2s)-2-(tetradecanoylamino)pentanedioate Chemical compound [Na+].CCCCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CCC(O)=O ZNYIJXQYUNSKDX-NTISSMGPSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 229940012831 stearyl alcohol Drugs 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- JQWAHKMIYCERGA-UHFFFAOYSA-N (2-nonanoyloxy-3-octadeca-9,12-dienoyloxypropoxy)-[2-(trimethylazaniumyl)ethyl]phosphinate Chemical compound CCCCCCCCC(=O)OC(COP([O-])(=O)CC[N+](C)(C)C)COC(=O)CCCCCCCC=CCC=CCCCCC JQWAHKMIYCERGA-UHFFFAOYSA-N 0.000 description 1
- ZYJZBFYRVKLOAA-KRWDZBQOSA-N (2s)-2-(hexadecanoylamino)butanedioic acid Chemical compound CCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CC(O)=O ZYJZBFYRVKLOAA-KRWDZBQOSA-N 0.000 description 1
- XWECHXDFKBPXQY-IBGZPJMESA-N (2s)-2-(octadecanoylamino)butanedioic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CC(O)=O XWECHXDFKBPXQY-IBGZPJMESA-N 0.000 description 1
- MTJZWYHTZFVEGI-INIZCTEOSA-N (2s)-2-(tetradecanoylamino)pentanedioic acid Chemical compound CCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O MTJZWYHTZFVEGI-INIZCTEOSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 description 1
- MLOYYKYQLFOZOE-UHFFFAOYSA-N 2-(tetradecanoylamino)butanedioic acid Chemical compound CCCCCCCCCCCCCC(=O)NC(C(O)=O)CC(O)=O MLOYYKYQLFOZOE-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- MFGOFGRYDNHJTA-UHFFFAOYSA-N 2-amino-1-(2-fluorophenyl)ethanol Chemical compound NCC(O)C1=CC=CC=C1F MFGOFGRYDNHJTA-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 1
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- KMAOMYOPEIRFLB-SFHVURJKSA-N N-Palmitoyl glutamic acid Chemical compound CCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O KMAOMYOPEIRFLB-SFHVURJKSA-N 0.000 description 1
- ATFFFUXLAJBBDE-FQEVSTJZSA-N N-Stearoyl glutamic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O ATFFFUXLAJBBDE-FQEVSTJZSA-N 0.000 description 1
- 102000015636 Oligopeptides Human genes 0.000 description 1
- 108010038807 Oligopeptides Proteins 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940092738 beeswax Drugs 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 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
- ZGSPNIOCEDOHGS-UHFFFAOYSA-L disodium [3-[2,3-di(octadeca-9,12-dienoyloxy)propoxy-oxidophosphoryl]oxy-2-hydroxypropyl] 2,3-di(octadeca-9,12-dienoyloxy)propyl phosphate Chemical compound [Na+].[Na+].CCCCCC=CCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCC=CCCCCC)COP([O-])(=O)OCC(O)COP([O-])(=O)OCC(OC(=O)CCCCCCCC=CCC=CCCCCC)COC(=O)CCCCCCCC=CCC=CCCCCC ZGSPNIOCEDOHGS-UHFFFAOYSA-L 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000013345 egg yolk Nutrition 0.000 description 1
- 210000002969 egg yolk Anatomy 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 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 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002327 glycerophospholipids Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 1
- 150000008104 phosphatidylethanolamines Chemical class 0.000 description 1
- 150000003905 phosphatidylinositols Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229940045845 sodium myristate Drugs 0.000 description 1
- QKHBMQWPOUUMQZ-BDQAORGHSA-M sodium;hydron;(2s)-2-(octadecanoylamino)pentanedioate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC([O-])=O QKHBMQWPOUUMQZ-BDQAORGHSA-M 0.000 description 1
- JUQGWKYSEXPRGL-UHFFFAOYSA-M sodium;tetradecanoate Chemical compound [Na+].CCCCCCCCCCCCCC([O-])=O JUQGWKYSEXPRGL-UHFFFAOYSA-M 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000002023 wood 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- A61K8/553—Phospholipids, e.g. lecithin
-
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Colloid Chemistry (AREA)
Description
[産業上の利用分野]
本発明は天然に存在する安全性の高い界面活性
剤として知られているリン脂質を油の増粘・ゲル
化剤および乳化剤として、化粧品および医薬品な
どに有効に活用することを目的として、安定な乳
化組成物を提供するものであり、さらにこの乳化
組成物に水を加えて得られる水中油型乳化組成物
を提供するものである。
[従来の技術]
従来、リン脂質を油の増粘・ゲル化剤および乳
化剤として使用する試みがなされており、例えば
レシチンと分子内に2個以上の水酸基を有する水
溶性多価アルコールと油相成分とからなる多価ア
ルコール中油型乳化組成物が知られている(特開
昭56−70826号公報)。
[発明が解決しようとする問題点]
しかしながら、レシチンのHLB値が低すぎる
ために得られた乳化組成物の安定性が不十分であ
り、安定性の向上が望まれていた。
[問題点を解決するための手段]
本発明者等は係る点に鑑み、リン脂質を利用し
た乳化組成物につき、特に安定化方法について鋭
意研究の結果、リン脂質を多価アルコール中に溶
解し、これに油相成分を添加して、微細な粒子径
をもつ乳化組成物を得るに際し、リン脂質に特定
の石けんおよび高級アルコールを併用することに
より、安定性が向上することを見い出し、本発明
を完成させた。
すなわち本発明は、リン脂質および/またはそ
の塩と、N−長鎖アシルアミノ酸石ケンと、高級
アルコールと、分子内に2個以上の水酸基を有す
る水溶性多価アルコールと、油相成分とを含有す
ることを特徴とする多価アルコール中油型乳化組
成物、および、この多価アルコール中油型乳化組
成物にさらに水を含有することを特徴とする水中
油型乳化組成物である。
以下に本発明の構成について述べる。
本発明に使用するリン脂質は、大豆・トウモロ
コシ・落花生・ナタネ・麦等の植物、卵黄・牛等
の動物、大腸菌等の微生物から抽出されるリン脂
質であり、ホスフアチジン酸・ホスフアチジルグ
リセリン・ホスフアチジルイノシトール・ホスフ
アチジルエタノールアミン・ホスフアチジルモノ
メチルエタノールアミン・ホスフアチジルメチル
エタノールアミン・ホスフアチジルコリン(レシ
チン)・ホスフアチジルセリン・ビスホスフアチ
ジン酸・ジホスフアチジルグリセリン(カルジオ
リピン)等のグリセロリン脂質、スフインゴミエ
リン等のスフインゴリン脂質を挙げることがで
き、さらに、これらを水素添加処理したものも挙
げることができる。これらは単独で用いてもよ
く、あるいは複数の組み合わせで用いてもよい。
リン脂質を塩として利用する場合、塩を形成す
る物質としては、水酸化リチウム・水酸化ナトリ
ウム・水酸化カリウム・水酸化セシウム・水酸化
アンモニウム等の無機塩基、アルギニン・リジ
ン・ヒスチジン・オルニチン等の塩基性アミノ
酸、塩基性アミノ酸を残基として有する塩基性オ
リゴペプチド、モノエタノールアミン・ジエタノ
ールアミン・トリエタノールアミン等の塩基性ア
ミンを挙げることができる。リン脂質の塩は単独
で用いてもよく、あるいは複数の組み合わせで用
いてもよい。
本発明に使用するN−長鎖アシルアミノ酸石ケ
ンはN−長鎖アシルアミノ酸と塩基と反応させる
ことにより得られる反応生成物である。そして、
このN−長鎖アシルアミノ酸石ケンを合成させる
のに使用されるN−長鎖アシルアミノ酸は、脂肪
酸の炭素数が12〜26のものである。特に好ましく
は、N−ステアロイルグルタミン酸・N−パルミ
トイルグルタミン酸・N−ミリストイルグルタミ
ン酸・N−ステアロイルアスパラギン酸・N−パ
ルミトイルアスパラギン酸・N−ミリストイルア
スパラギン酸等を挙げることができる。また、こ
れらのN−長鎖アシルアミノ酸は、D−体・L−
体・DL−体の別を問わず使用できる。しかも、
これらは単独で用いてもよく、あるいは複数の組
み合わせで用いてもよい。
上記N−長鎖アシルアミノ酸石ケンを合成する
のに使用される塩基は、例えば、トリエタノール
アミン・水酸化ナトリウム・水酸化カリウム・ア
ルギニン・リジン・ヒスチジン・オルニチン・オ
キシリジン等を挙げることができる。また、この
うちで塩基性アミノ酸は、D−体・L−体・DL
−体の別を問わず使用できる。しかも、これらは
単独で用いてもよく、あるいは複数の組み合わせ
で用いてもよい。
また、高級アルコールは、炭素数8〜40の長鎖
の飽和アルコール、側鎖を有する飽和アルコー
ル、直鎖の不飽和アルコール、側鎖を有する不飽
和アルコールである。特に好ましくは、ラウリル
アルコール・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・オレイルアルコ
ール・イソステアリルアルコール・ベヘニルアル
コール等を挙げることができる。また、これらは
単独で用いてもよく、あるいは複数の組み合わせ
で用いてもよい。
本発明に使用する分子内に2個以上の水酸基を
有する水溶性多価アルコールは、例えば、プロピ
レングリコール・1,3−ブチレングリコール・
ジプロピレングリコール等のグリコール類、グリ
セリン・ジグリセリン等のグリセロール類、ソル
ビトール・マルチトール等の糖類、ペンタエリス
リトール等を挙げることができる。これらは単独
で用いてもよく、あるいは複数の組み合わせで用
いてもよい。
次に油相成分としては、通常、化粧品・医薬
品・食品等の分野で使用され、人体に対して安全
とされているものが用い得る。例えば、オリーブ
油・ヒマシ油等の植物油ミツロウ・ラノリン・キ
ヤンデリラワツクス・木ロウ等のワツクス類、流
動パラフイン・スクワラン・ワセリン・パラフイ
ンワツクス等の炭化水素、セタノール・ステアリ
ルアルコール・ベヘニルアルコール等の高級アル
コール、その他のエステル油、シリコン油等を挙
げることができる。
リン脂質および/またはその塩と、N−長鎖ア
シルアミノ酸石ケンの配合量は、重量比1:9〜
9:1の範囲であり、該範囲内であれば適正な
HLBとなり、良好な乳化組成物が得られる。
N−長鎖アシルアミノ酸石ケンと、高級アルコ
ールの配合量は、重量比1:9〜9:1の範囲で
あり、該範囲内であれば長期間良好な安定性を示
す。
分子内に2個以上の水酸基を有する水溶性多価
アルコールの配合量は、リン脂質および/または
その塩、N−長鎖アシルアミノ酸石ケン、高級ア
ルコールの合計量の1〜100重量倍の範囲であり、
該範囲内であれば、リン脂質・石ケン・高級アル
コール等の溶解性が良好であり、乳化安定性も良
好である。
油性成分の配合量は、リン脂質および/または
その塩、N−長鎖アシルアミノ酸石ケン、水溶性
多価アルコールの合計量の5重量倍以下の範囲で
あり、該範囲内であれば、安定な乳化組成物が得
られる。
本発明は、上記成分を必須に配合することを特
徴とする多価アルコール中油型乳化組成物であ
り、また、本発明に係る他の水中油型乳化組成物
は、本発明の多価アルコール中油型乳化組成物と
水とを必須に配合することを特徴とするものであ
る。本発明の乳化組成物には、前期必須成分に加
えてさらに、化粧品・医薬品に一般に使用される
薬剤・粉体・界面活性剤・色素・香料・アルコー
ル・保湿剤・防腐剤・美容剤・酸化防止剤・紫外
線吸収剤・水溶性高分子等を適宜配合することが
できる。
本発明で得られる多価アルコール中油型乳化組
成物は、均一で半透明もしくは白色のペーストで
あるので、このままで、例えば、美容液・マツサ
ージゼリー・クレンジングゼリー・薬用ゼリー・
サンオイル等に使用することができる。
また、本発明で得られる他の水中油型乳化組成
物は、一般の水中油型乳化組成物と同じ形態であ
るので、化粧品・医薬品として巾広く利用するこ
とができる。
[実施例]
次に本発明について実施例をあげてさらに説明
する。これらは本発明を何ら限定するものではな
い。
実施例1〜2、比較例1〜3
レシチン、石ケン、高級アルコール、多価アル
コール、油相成分を、表1および表2に示す配合
量にて、70℃にてホモミクサー処理して、実施例
1、比較例1および2の多価アルコール中油型乳
化組成物を得た。またさらに、表1および表2に
示すように、一旦多価アルコール中油型乳化組成
物をつくり、それに70℃の水を加えて、実施例
2、比較例3の水中油型乳化組成物を得た。
[Industrial Application Field] The present invention effectively utilizes phospholipids, which are known as naturally occurring and highly safe surfactants, as oil thickening/gelling agents and emulsifiers in cosmetics, pharmaceuticals, etc. For this purpose, the present invention provides a stable emulsified composition, and further provides an oil-in-water emulsified composition obtained by adding water to this emulsified composition. [Prior Art] Previously, attempts have been made to use phospholipids as oil thickeners, gelling agents, and emulsifiers. For example, phospholipids have been used as oil thickeners, gelling agents, and emulsifiers. An oil-in-polyhydric alcohol emulsion composition is known (Japanese Unexamined Patent Publication No. 70826/1982). [Problems to be Solved by the Invention] However, because the HLB value of lecithin is too low, the stability of the obtained emulsion composition is insufficient, and improvement in stability has been desired. [Means for Solving the Problems] In view of the above points, the present inventors conducted extensive research on emulsion compositions using phospholipids, particularly on stabilization methods, and as a result, they solved the problem by dissolving phospholipids in polyhydric alcohol. discovered that when adding an oil phase component to this to obtain an emulsified composition with a fine particle size, the stability was improved by using a specific soap and a higher alcohol in combination with the phospholipid, and the present invention completed. That is, the present invention comprises a phospholipid and/or a salt thereof, an N-long chain acylamino acid soap, a higher alcohol, a water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule, and an oil phase component. and an oil-in-water emulsion composition characterized in that the polyhydric alcohol-in-oil emulsion composition further contains water. The configuration of the present invention will be described below. The phospholipids used in the present invention are phospholipids extracted from plants such as soybeans, corn, peanuts, rapeseed, and wheat, animals such as egg yolks and cows, and microorganisms such as Escherichia coli. Phosphatidylinositol, phosphatidylethanolamine, phosphatidyl monomethylethanolamine, phosphatidylmethylethanolamine, phosphatidylcholine (lecithin), phosphatidylserine, bisphosphatidic acid, diphosphatidylglycerin ( Examples include glycerophospholipids such as cardiolipin, sphingophospholipids such as sphingomyelin, and hydrogenated products of these. These may be used alone or in combination. When using phospholipids as salts, salt-forming substances include inorganic bases such as lithium hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide, and ammonium hydroxide, and arginine, lysine, histidine, ornithine, etc. Examples include basic amino acids, basic oligopeptides having basic amino acids as residues, and basic amines such as monoethanolamine, diethanolamine, and triethanolamine. Phospholipid salts may be used alone or in combination. The N-long chain acylamino acid soap used in the present invention is a reaction product obtained by reacting an N-long chain acylamino acid with a base. and,
The N-long chain acylamino acid used to synthesize this N-long chain acylamino acid soap has a fatty acid having 12 to 26 carbon atoms. Particularly preferred examples include N-stearoylglutamic acid, N-palmitoylglutamic acid, N-myristoylglutamic acid, N-stearoyl aspartic acid, N-palmitoyl aspartic acid, and N-myristoyl aspartic acid. In addition, these N-long chain acylamino acids are D-form, L-
Body/DL - Can be used regardless of body type. Moreover,
These may be used alone or in combination. Examples of the base used to synthesize the N-long chain acylamino acid soap include triethanolamine, sodium hydroxide, potassium hydroxide, arginine, lysine, histidine, ornithine, and oxylysine. Among these, basic amino acids include D-form, L-form, and DL-form.
- Can be used regardless of body type. Furthermore, these may be used alone or in combination. Further, higher alcohols include long chain saturated alcohols having 8 to 40 carbon atoms, saturated alcohols having side chains, straight chain unsaturated alcohols, and unsaturated alcohols having side chains. Particularly preferred examples include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, isostearyl alcohol, and behenyl alcohol. Further, these may be used alone or in combination. Water-soluble polyhydric alcohols having two or more hydroxyl groups in the molecule used in the present invention include, for example, propylene glycol, 1,3-butylene glycol,
Examples include glycols such as dipropylene glycol, glycerols such as glycerin and diglycerin, saccharides such as sorbitol and maltitol, and pentaerythritol. These may be used alone or in combination. Next, as the oil phase component, those that are normally used in the fields of cosmetics, medicine, food, etc. and are considered safe for the human body can be used. For example, vegetable oils such as olive oil and castor oil, waxes such as beeswax, lanolin, candelilla wax, and wood wax, hydrocarbons such as liquid paraffin, squalane, petrolatum, paraffin wax, and higher alcohols such as cetanol, stearyl alcohol, and behenyl alcohol. , other ester oils, silicone oils, etc. The blending amount of phospholipid and/or its salt and N-long chain acylamino acid soap is 1:9 to 1:9 by weight.
The range is 9:1, and if it is within this range, it is appropriate.
HLB and a good emulsified composition can be obtained. The blending amount of the N-long chain acylamino acid soap and the higher alcohol is in a weight ratio of 1:9 to 9:1, and within this range, good long-term stability is exhibited. The amount of water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule is 1 to 100 times the total weight of the phospholipid and/or its salt, N-long chain acylamino acid soap, and higher alcohol. and
Within this range, the solubility of phospholipids, soaps, higher alcohols, etc. is good, and the emulsion stability is also good. The blending amount of the oily component is within the range of 5 times the total weight of the phospholipid and/or its salt, N-long chain acylamino acid soap, and water-soluble polyhydric alcohol, and within this range, it is stable. An emulsified composition is obtained. The present invention is an oil-in-polyhydric alcohol emulsion composition characterized in that the above components are essentially blended, and another oil-in-water emulsion composition according to the present invention is an oil-in-polyhydric alcohol emulsion composition according to the present invention. It is characterized in that it essentially contains a type emulsion composition and water. In addition to the above essential ingredients, the emulsified composition of the present invention further contains drugs, powders, surfactants, pigments, fragrances, alcohol, humectants, preservatives, beauty agents, and oxidants commonly used in cosmetics and pharmaceuticals. Inhibitors, ultraviolet absorbers, water-soluble polymers, etc. can be added as appropriate. The oil-in-polyhydric alcohol emulsion composition obtained in the present invention is a homogeneous, translucent or white paste, so it can be used as it is, for example, in beauty serums, pine surge jelly, cleansing jelly, medicated jelly, etc.
Can be used as sun oil etc. Further, since the other oil-in-water emulsion composition obtained by the present invention has the same form as a general oil-in-water emulsion composition, it can be widely used as cosmetics and pharmaceuticals. [Example] Next, the present invention will be further explained by giving examples. These do not limit the present invention in any way. Examples 1 to 2, Comparative Examples 1 to 3 Lecithin, soap, higher alcohol, polyhydric alcohol, and oil phase components were treated in a homomixer at 70°C in the amounts shown in Tables 1 and 2. Oil-in-polyhydric alcohol emulsion compositions of Example 1 and Comparative Examples 1 and 2 were obtained. Furthermore, as shown in Tables 1 and 2, oil-in-water emulsion compositions of polyhydric alcohol were once prepared, and water at 70°C was added thereto to obtain oil-in-water emulsion compositions of Example 2 and Comparative Example 3. Ta.
【表】
配合量は重量%で示す
[Table] Ingredients are shown in weight%
【表】
配合量は重量%で示す
本発明の乳化組成物の安定性の良さを確認する
ために、実施例1〜2につき、比較例1〜2とと
もに、40℃に於ける1ケ月後の状態を観察した。
実施例1〜2のものは、それぞれ均一で製造時と
何ら変わることなく、良好な安定性を示した。一
方、比較例1および2のものは、分離しており、
また、比較例3のものは、脂肪酸と思われる固体
の析出が見られ、安定性に劣るものであつた。
実施例 3
クリーム
(処方) (重量%)
(1) 大豆レシチン 2.0
(2) N−ミリストイル−L−グルタミン酸モノナ
トリウム 1.0
(3) グリセリン 10.0
(4) パラオキシ安息香酸メチル 0.1
(5) セチルアルコール 1.0
(6) スクワラン 50.0
(7) 1,3−ブチレングリコール 5.0
(8) カルボキシビニルポリマー 0.3
(9) 水酸化ナトリウム 0.04
(10) 精製水 残量
(製法)
A (1)〜(4)を70℃にて混合溶解する。
B Aに(5)〜(6)を70℃にて加え、均一に混合して
多価アルコール中油型乳化組成物とする。
C (7)〜(10)を70℃にて混合溶解する。
D BにCを加えて乳化し、冷却をしてクリーム
を得る。
以上の如くして得られた実施例3のクリーム
は、きめの細かなクリームであり、皮膚安全性が
高く、経時安定性にも優れたものであつた。
比較例 4
クリーム
(処方) (重量%)
(1) 大豆レシチン 2.0
(2) N−ミリストイル−L−グルタミン酸モノナ
トリウム 1.0
(3) パラオキシ安息香酸メチル 0.1
(4) セチルアルコール 1.0
(5) スクワラン 50.0
(6) 1,3−ブチレングリコール 5.0
(7) グリセリン 10.0
(8) カルボキシビニルポリマー 0.3
(9) 水酸化ナトリウム 0.04
(10) 精製水 残量
(製法)
A (1)〜(3)を70℃にて混合溶解する。
B Aに(4)〜(5)を70℃にて加え均一に混合する。
C (6)〜(10)を70℃にて混合溶解する。
D BにCを加えて乳化し、冷却してクリームを
得る。
以上の如くして得られた実施例4のクリーム
は、非常にきめが悪く、一部固体の析出が見られ
るものであつた。
実施例 4
乳液
(処方) (重量%)
(1) 卵黄レシチン 1.0
(2) ミリスチン酸ナトリウム 0.5
(3) ソルビトール 10.0
(4) パラオキシ安息香酸ブチル 0.1
(5) N−ステアロイル−L−グルタミン酸モノナ
トリウム 0.1
(6) ステアリルアルコール 0.5
(7) 流動パラフイン 5.0
(8) 硬化油 2.0
(9) ジペンタエリトリツト脂肪酸エステル 1.0
(10) ジプロプレングリコール 10.0
(11) メチルセルロース 0.1
(12) 精製水 残量
(製法)
A (1)〜(6)を70℃にて混合溶解する。
B Aに(7)〜(9)を70℃にて加え、均一に混合して
多価アルコール中油型乳化組成物とする。
C (10)〜(12)を70℃にて混合溶解する。
D BにCを加えて乳化し、冷却をして、乳液を
得る。
実施例 5
白濁ローシヨン
(処方) (重量%)
(1) 大豆レシチン 0.5
(2) N−ココイル−L−グルタミン酸モノナトリ
ウム 0.2
(3) グリセリン 5.0
(4) パラオキシ安息香酸メチル 0.1
(5) ベヘニルアルコール 0.2
(6) 流動パラフイン 1.0
(7) ポリオキシエチレン(20)ソルビタンモノオレエ
ート 0.5
(8) エタノール 10.0
(9) 精製水 残量
(製法)
A (1)〜(4)を70℃にて混合溶解する。
B Aに(5)〜(6)を70℃にて加え、均一に混合して
多価アルコール中油型乳化組成物とする。
C (7)〜(9)を60℃にて混合溶解する。
D Bを60℃に冷却し、Cを加えて乳化をし、冷
却をして、白濁ローシヨンを得る。
[発明の効果]
以上詳述した如く、本発明は、リン脂質と分子
内に2個以上の水酸基を有する水溶性多価アルコ
ールと油相成分とを含有する乳化組成物におい
て、乳化剤として、リン脂質と共にN−長鎖アシ
ルアミノ酸石ケン及び高級アルコールを併用する
ことにより、安定性の顕著に向上した多価アルコ
ール中油型乳化組成物、及びこれと水とを含有す
る水中油型乳化組成物を提供することができたも
のである。[Table] Ingredients are shown in weight%
In order to confirm the stability of the emulsified composition of the present invention, the conditions of Examples 1 and 2 and Comparative Examples 1 and 2 after one month at 40°C were observed.
Examples 1 and 2 were uniform and showed good stability, with no change from the time of manufacture. On the other hand, those of Comparative Examples 1 and 2 are separated,
Furthermore, in Comparative Example 3, precipitation of solids thought to be fatty acids was observed, and the stability was poor. Example 3 Cream (formulation) (wt%) (1) Soybean lecithin 2.0 (2) Monosodium N-myristoyl-L-glutamate 1.0 (3) Glycerin 10.0 (4) Methyl paraoxybenzoate 0.1 (5) Cetyl alcohol 1.0 ( 6) Squalane 50.0 (7) 1,3-butylene glycol 5.0 (8) Carboxyvinyl polymer 0.3 (9) Sodium hydroxide 0.04 (10) Purified water Remaining amount (manufacturing method) A Heat (1) to (4) to 70℃ Mix and dissolve. B Add (5) to (6) to A at 70°C and mix uniformly to obtain an oil-in-polyhydric alcohol emulsion composition. Mix and dissolve C (7) to (10) at 70°C. Add C to D B, emulsify it, and cool it to obtain cream. The cream of Example 3 obtained as described above was a fine-textured cream with high skin safety and excellent stability over time. Comparative Example 4 Cream (formulation) (wt%) (1) Soybean lecithin 2.0 (2) Monosodium N-myristoyl-L-glutamate 1.0 (3) Methyl paraoxybenzoate 0.1 (4) Cetyl alcohol 1.0 (5) Squalane 50.0 ( 6) 1,3-butylene glycol 5.0 (7) Glycerin 10.0 (8) Carboxyvinyl polymer 0.3 (9) Sodium hydroxide 0.04 (10) Purified water Remaining amount (manufacturing method) A Heat (1) to (3) to 70℃ Mix and dissolve. B Add (4) to (5) to A at 70°C and mix uniformly. Mix and dissolve C (6) to (10) at 70°C. D Add C to B, emulsify it, and cool it to obtain cream. The cream of Example 4 obtained as described above had a very poor texture and some solid precipitation was observed. Example 4 Emulsion (formulation) (wt%) (1) Egg yolk lecithin 1.0 (2) Sodium myristate 0.5 (3) Sorbitol 10.0 (4) Butyl paraoxybenzoate 0.1 (5) Monosodium N-stearoyl-L-glutamate 0.1 (6) Stearyl alcohol 0.5 (7) Liquid paraffin 5.0 (8) Hydrogenated oil 2.0 (9) Dipentaerythritol fatty acid ester 1.0 (10) Dipropylene glycol 10.0 (11) Methyl cellulose 0.1 (12) Purified water Remaining amount (manufacturing method) A Mix and dissolve (1) to (6) at 70°C. B Add (7) to (9) to A at 70°C and mix uniformly to obtain an oil-in-polyhydric alcohol emulsion composition. Mix and dissolve C (10) to (12) at 70°C. Add C to D B, emulsify it, and cool it to obtain a milky lotion. Example 5 Cloudy lotion (formulation) (wt%) (1) Soybean lecithin 0.5 (2) Monosodium N-cocoyl-L-glutamate 0.2 (3) Glycerin 5.0 (4) Methyl paraoxybenzoate 0.1 (5) Behenyl alcohol 0.2 ( 6) Liquid paraffin 1.0 (7) Polyoxyethylene (20) sorbitan monooleate 0.5 (8) Ethanol 10.0 (9) Purified water Remaining amount (manufacturing method) A Mix and dissolve (1) to (4) at 70℃. . B Add (5) to (6) to A at 70°C and mix uniformly to obtain an oil-in-polyhydric alcohol emulsion composition. Mix and dissolve C (7) to (9) at 60°C. D Cool B to 60°C, add C to emulsify, and cool to obtain a cloudy lotion. [Effects of the Invention] As detailed above, the present invention provides an emulsifying composition containing a phospholipid, a water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule, and an oil phase component. By using an N-long chain acylamino acid soap and a higher alcohol in combination with a lipid, an oil-in-water emulsion composition containing polyhydric alcohol and water, which has significantly improved stability, and an oil-in-water emulsion composition containing this and water are produced. This is what we were able to provide.
Claims (1)
アシルアミノ酸石ケンと、高級アルコールと、分
子内に2個以上の水酸基を有する水溶性多価アル
コールと、油相成分とを含有することを特徴とす
る多価アルコール中油型乳化組成物。 2 リン脂質および/またはその塩と、N−長鎖
アシルアミノ酸石ケンと、高級アルコールと、分
子内に2個以上の水酸基を有する水溶性多価アル
コールと、油相成分とを含む多価アルコール中油
型乳化組成物と、水とを含有することを特徴とす
る水中油型乳化組成物。[Claims] 1. A phospholipid and/or a salt thereof, an N-long chain acylamino acid soap, a higher alcohol, a water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule, and an oil phase component. An oil-in-polyhydric alcohol emulsion composition comprising: 2. A polyhydric alcohol containing a phospholipid and/or a salt thereof, an N-long chain acylamino acid soap, a higher alcohol, a water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule, and an oil phase component. An oil-in-water emulsion composition comprising a medium oil-in-water emulsion composition and water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59177248A JPS6154231A (en) | 1984-08-24 | 1984-08-24 | Emulsified composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59177248A JPS6154231A (en) | 1984-08-24 | 1984-08-24 | Emulsified composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6154231A JPS6154231A (en) | 1986-03-18 |
JPH0525535B2 true JPH0525535B2 (en) | 1993-04-13 |
Family
ID=16027744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59177248A Granted JPS6154231A (en) | 1984-08-24 | 1984-08-24 | Emulsified composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6154231A (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3535583B2 (en) * | 1994-09-20 | 2004-06-07 | 株式会社資生堂 | Clear lotion |
JP2003104864A (en) * | 2001-09-28 | 2003-04-09 | Kose Corp | Cosmetic for whitening |
JP4495941B2 (en) * | 2003-02-19 | 2010-07-07 | 株式会社コーセー | Oil-in-water emulsified cosmetic |
JP5495543B2 (en) * | 2008-12-15 | 2014-05-21 | ポーラ化成工業株式会社 | Oil droplet-dispersed aqueous carrier and composite emulsion composition comprising the same |
WO2013149853A2 (en) | 2012-04-03 | 2013-10-10 | Basf Se | Hair cosmetic composition which comprises a plant lecithin |
BR112018008361A2 (en) * | 2015-10-29 | 2018-10-23 | Glaxosmithkline Consumer Healthcare Holdings | composition, and method for moistening, and protecting, repairing or restoring the skin's lipid barrier. |
JP6728930B2 (en) * | 2016-04-20 | 2020-07-22 | 日油株式会社 | Oil gel composition |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58121209A (en) * | 1982-01-11 | 1983-07-19 | Eisai Co Ltd | Emulsion type composition for external use |
-
1984
- 1984-08-24 JP JP59177248A patent/JPS6154231A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58121209A (en) * | 1982-01-11 | 1983-07-19 | Eisai Co Ltd | Emulsion type composition for external use |
Also Published As
Publication number | Publication date |
---|---|
JPS6154231A (en) | 1986-03-18 |
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