JPS63264512A - Aqueous cosmetic - Google Patents
Aqueous cosmeticInfo
- Publication number
- JPS63264512A JPS63264512A JP9448987A JP9448987A JPS63264512A JP S63264512 A JPS63264512 A JP S63264512A JP 9448987 A JP9448987 A JP 9448987A JP 9448987 A JP9448987 A JP 9448987A JP S63264512 A JPS63264512 A JP S63264512A
- Authority
- JP
- Japan
- Prior art keywords
- component
- phospholipid
- hydrogenated
- aqueous cosmetic
- weight
- 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.)
- Granted
Links
- 239000002537 cosmetic Substances 0.000 title claims abstract description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 32
- 150000003904 phospholipids Chemical class 0.000 claims abstract description 27
- 239000007788 liquid Substances 0.000 claims abstract description 15
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 13
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 13
- 239000004094 surface-active agent Substances 0.000 claims abstract description 13
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 12
- 239000003945 anionic surfactant Substances 0.000 claims description 5
- 239000002736 nonionic surfactant Substances 0.000 claims description 5
- 238000002156 mixing Methods 0.000 abstract description 9
- 238000001556 precipitation Methods 0.000 abstract description 5
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 239000013078 crystal Substances 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 3
- 230000003647 oxidation Effects 0.000 abstract description 3
- 238000007254 oxidation reaction Methods 0.000 abstract description 3
- 238000000926 separation method Methods 0.000 abstract description 2
- 230000003213 activating effect Effects 0.000 abstract 1
- 125000000129 anionic group Chemical group 0.000 abstract 1
- 230000008030 elimination Effects 0.000 abstract 1
- 238000003379 elimination reaction Methods 0.000 abstract 1
- 230000002633 protecting effect Effects 0.000 abstract 1
- 238000004062 sedimentation Methods 0.000 abstract 1
- -1 fatty acid salts Chemical class 0.000 description 31
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 15
- 239000006210 lotion Substances 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 13
- 235000014113 dietary fatty acids Nutrition 0.000 description 11
- 229930195729 fatty acid Natural products 0.000 description 11
- 239000000194 fatty acid Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000008213 purified water Substances 0.000 description 6
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 239000003205 fragrance Substances 0.000 description 5
- 230000001953 sensory effect Effects 0.000 description 5
- 238000002834 transmittance Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000003755 preservative agent Substances 0.000 description 4
- XOJVVFBFDXDTEG-UHFFFAOYSA-N pristane Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- 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 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
- 229910019142 PO4 Inorganic materials 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000005037 alkyl phenyl group Chemical group 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 235000016709 nutrition Nutrition 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 239000004166 Lanolin Substances 0.000 description 2
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 230000003796 beauty Effects 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 230000008034 disappearance Effects 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Natural products O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229940039717 lanolin Drugs 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000011734 sodium Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229940083466 soybean lecithin Drugs 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 2
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-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
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical class 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 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 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
- BIVBRWYINDPWKA-VLQRKCJKSA-L Glycyrrhizinate dipotassium Chemical compound [K+].[K+].O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@H]1CC[C@]2(C)[C@H]3C(=O)C=C4[C@@H]5C[C@](C)(CC[C@@]5(CC[C@@]4(C)[C@]3(C)CC[C@H]2C1(C)C)C)C(O)=O)C([O-])=O)[C@@H]1O[C@H](C([O-])=O)[C@@H](O)[C@H](O)[C@H]1O BIVBRWYINDPWKA-VLQRKCJKSA-L 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002385 Sodium hyaluronate Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N Taurine Natural products NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 229940087168 alpha tocopherol Drugs 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000003613 bile acid Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 108700041286 delta Proteins 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 229940101029 dipotassium glycyrrhizinate Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 239000008350 hydrogenated phosphatidyl choline Substances 0.000 description 1
- 229940099578 hydrogenated soybean lecithin Drugs 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- HXGWMCJZLNWEBC-UHFFFAOYSA-K lithium citrate tetrahydrate Chemical compound [Li+].[Li+].[Li+].O.O.O.O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HXGWMCJZLNWEBC-UHFFFAOYSA-K 0.000 description 1
- 150000004701 malic acid derivatives Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 229940042880 natural phospholipid Drugs 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000008935 nutritious Nutrition 0.000 description 1
- 150000008105 phosphatidylcholines Chemical class 0.000 description 1
- 150000008104 phosphatidylethanolamines Chemical class 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229940010747 sodium hyaluronate Drugs 0.000 description 1
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(2s,3s,4s,5r,6r)-6-[(2s,3r,4r,5s,6r)-3-acetamido-2-[(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5s,6r)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2- Chemical compound [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000004835 α-tocopherol Nutrition 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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/31—Hydrocarbons
-
- 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
Abstract
Description
[産業上の利用分野]
本発明は新規な水性化粧料に関し、更に詳しくは、水素
添加リン脂質を安定に配合した水性化粧料に関するもの
である。
[従来の技術]
リン脂質は生体膜の構成成分であり、皮膚への安全性が
極めて高く、皮膚の保護効果、保湿効果、界面活性効果
を有することから化粧品原料として利用されている。
しかしながら、天然のリン脂質は不飽和脂肪酸を多く含
んでいるため、酸化や熱に対して不安定であって、化粧
料に安定に配合するのに問題があった。
水素添加リン脂質は、リン脂質に水素添加することによ
って得られるもので、酸化や熱に対しての安定性が非常
に向上している。
しかしながら、水素添加リン脂質は結晶性が強く、水性
化粧料に配合した場合は、その結晶化防とが困難であり
、しばしば結晶化が進行し、水性化粧料の外観がパール
様外観を呈することもあった0例えば、特開昭59−2
12418号では、水素添加レシチンの結晶性を利用し
て、香粧品用の真珠光沢付与剤を提案している。また、
水性化粧料に於いて、水素添加リン脂質の結晶化を防止
するために、界面活性剤の使用量を増加させること等も
試みられている。
[発明が解決しようとする問題点]
上記の如く、従来、水性化粧料にリン脂質を安定に配合
すべく種々検討されてきた。
しかしながら、リン脂質として安定な水素添加リン脂質
を利用したとしても、水性化粧料に配合した場合には、
その結晶化防止が困難であった。またその結晶化を防止
する為に多量の界面活性剤を配合した場合には、化粧料
としての官能性ならびに安全性の点で満足すべきものは
得られなかった。
[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、リン脂質を安定に配合し
、かつ使用感、安全性に優れた水性化粧料を得るべく鋭
意研究した結果、水素添加リン脂質に対して特定割合の
液状炭化水素ならびに特定割合の界面活性剤を配合する
ことにより、優れた安定性、使用感を有する水性化粧料
が得られることを見い出し、本発明を完成させた。
すなわち、本発明は、水素添加リン脂質(A成分) 0
.05〜5重量%と、液状炭化水素(B成分) 0.0
5〜5重量%と、アニオン界面活性剤およびノニオン界
面活性剤から選らばれるHLB値12以上の界面活性剤
(C成分) 0.05〜5重量%と、エタノール1〜4
0重量%とからなり、A成分/C成分の重量比が0.2
〜5であり、かつ(A成分子C成分)/B酸成分重量比
が0.2〜5であることを特徴とする水性化粧料である
。
本発明に使用する水素添加リン脂質は、ヨウ素価が30
以下のものが好ましく、大豆レシチン、卵黄レシチン等
の天然レシチンを常法に従って水素添加したものの他、
ホスファチジルコリン、ホスファチジルエタノールアミ
ン、ホスファチジルセリン等を水素添加したもの等が挙
げられ、これらの1種または2種以上を組み合せて用い
得る。
また1本発明に使用する液状炭化水素は、常温で液状の
ものであって、通常化粧品用原料として使われるもので
あれば良く、例えばスタンラン、プリスタン、流動パラ
フィン、低粘度ポリブテン(粘度5〜1000cst)
等が挙げられ、これらの1種または2種以上を組み合わ
せて用い得る。
本発明に使用するアニオン界面活性剤は、例えば、脂肪
酸塩、アルキルベンゼンスルホン酸塩、アルキルスルホ
ン酸塩、α−オレフィンスルホン酸塩、ジアルキルスル
ホコハク酸塩、α−スルホン化脂肪酸塩、ナトリウムN
−メチル−N−アルキルタウリン、ポリオキシエチレン
アルキルエーテル硫酸塩、ポリオキシエチレンアルキル
フェニルエーテル硫酸塩、アルキル燐酸塩、ポリオキシ
エチレンアルキルエーテル燐酸塩、ポリオキシエチレン
アルキルフェニルエーテル燐酸塩、N−アシルグルタミ
ン酸塩、N−アシル−N−アルキルアミノ酸塩、O−ア
ルキル置換リンゴ酸塩等であり、HLB値12以上のも
のが、1種もしくは2種以上の組み合わせで用い得る。
ノニオン界面活性剤は、例えば、デカグリセリン脂肪酸
エステル、ポリグリセリン脂肪酸エステル、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
ンソルビット脂肪酸エステル、ポリオキシエチレングリ
セリン脂肪酸エステル、ポリエチレングリコール脂肪酸
エステル、ポリオキシエチレンアルキルエーテル、ポリ
オキシエチレンフィトステロール、ポリオキシエチレン
フィトステロール、ポリオキシエチレンポリオキシプロ
ピレンアルキルエーテル、ポリオキシエチレンアルキル
フェニルエーテル、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ラノ
リン、ポリオキシエチレンラノリンアルコール、ポリオ
キシエチレンアルキルアミン、ポリオキシエチレン脂肪
酸アミド、ポリオキシエチレンアルキルフェニルホルム
アルデヒド縮合物、ショ糖脂肪酸エステル等であり、H
LB値12以上のものが、1種もしくは2種以上の組み
合わせで用い得る。
本発明に用いられる各成分は、特定量、特定割合で配合
される。すなわち、水素添加リン脂質(A成分)の配合
量は0.05〜5重量%であり、液状炭化水素(B成分
)の配合量は0.05〜5重量%であり、アニオン界面
活性剤およびノニオン界面活性剤から選ばれるHLB値
!2以上の界面活性剤(C成分)の配合量は0.05〜
5重量%であり、エタノールの配合量は1〜40重量%
である。かつまた、A成分/C成分の重量比が0.2〜
5であり、(A成分子C成分)/B酸成分重量比が0.
2〜5である。該範囲内であれば、広い温度領域に於い
て、白濁度の変化や、沈殿、分離、結晶の析出、白濁の
消滅等がなく、水素添加リン脂質を安定に配合した水性
化粧料が得られ、かつまた、その使用感、安全性も良好
である。
本発明の水性化粧料は外観が半透明〜白濁のものを指し
、分光光度計で透過率を測定した時、0〜95%のもの
である。
本発明でいう水性化粧料とは、精製水を主成分とした、
柔軟化粧水、栄養化粧水、収斂化粧水、洗詐用化粧水、
美容液、ヘアローション等である。
本発明の水性化粧料の製造方法は、水素添加リン脂質と
、液状炭化水素と、アニオン界面活性剤およびノニオン
界面活性剤から選ばれるHLB値12以上の界面活性剤
と、エタノールとからなるアルコール部を、精製水を主
成分とする木部に添加する方法であっても良いし、逆に
、木部をアルコール部に添加する方法であっても良い、
また、この時、アルコール部、木部を適宜加温もしくは
加熱してもよい。
更に本発明に於いては、上記必須成分のほか、本発明の
目的を妨げない範囲に於いて、通常の水性化粧料等に使
用される、香料、色素、防腐剤、殺菌剤、湿潤剤、紫外
線吸収剤、塩、塩基、キレート剤、増粘剤、パール剤、
界面活性剤、油剤、各種薬剤等を適宜配合し得る。
[実施例]
次に、本発明について実施例を挙げて更に説明する。こ
れらは本発明をなんら限定するものではない。
実施例H1〜[4] 、比較例 Hl 〜[8]実施例
[1]〜[4] につき、比較例 [11〜[Industrial Application Field] The present invention relates to a novel aqueous cosmetic composition, and more particularly, to an aqueous cosmetic composition stably containing a hydrogenated phospholipid. [Prior Art] Phospholipids are constituent components of biological membranes, are extremely safe to the skin, and have skin protective effects, moisturizing effects, and surfactant effects, and are therefore used as raw materials for cosmetics. However, since natural phospholipids contain a large amount of unsaturated fatty acids, they are unstable to oxidation and heat, making it difficult to stably incorporate them into cosmetics. Hydrogenated phospholipids are obtained by hydrogenating phospholipids, and have significantly improved stability against oxidation and heat. However, hydrogenated phospholipids are highly crystalline, and when added to aqueous cosmetics, it is difficult to prevent crystallization, and crystallization often progresses, giving the aqueous cosmetics a pearl-like appearance. For example, JP-A-59-2
No. 12418 proposes a pearlescent agent for cosmetics by utilizing the crystallinity of hydrogenated lecithin. Also,
In water-based cosmetics, attempts have been made to increase the amount of surfactants used in order to prevent crystallization of hydrogenated phospholipids. [Problems to be Solved by the Invention] As described above, various studies have been made to stably incorporate phospholipids into aqueous cosmetics. However, even if hydrogenated phospholipids, which are stable as phospholipids, are used, when added to aqueous cosmetics,
It was difficult to prevent its crystallization. Furthermore, when a large amount of surfactant is added to prevent crystallization, satisfactory cosmetics cannot be obtained in terms of functionality and safety. [Means for Solving the Problems] In view of the above-mentioned points, the present inventors conducted extensive research to obtain an aqueous cosmetic that stably contains phospholipids and has excellent usability and safety. The present invention was completed by discovering that an aqueous cosmetic with excellent stability and usability can be obtained by blending a specific proportion of liquid hydrocarbon and a specific proportion of surfactant with added phospholipid. . That is, the present invention provides hydrogenated phospholipids (component A) 0
.. 05 to 5% by weight and liquid hydrocarbon (component B) 0.0
5 to 5% by weight, 0.05 to 5% by weight of a surfactant with an HLB value of 12 or more selected from anionic surfactants and nonionic surfactants (component C), and 1 to 4% of ethanol.
0% by weight, and the weight ratio of component A/component C is 0.2.
5, and the weight ratio of (A component, C component)/B acid component is 0.2 to 5. The hydrogenated phospholipid used in the present invention has an iodine value of 30
The following are preferred, and in addition to natural lecithins such as soybean lecithin and egg yolk lecithin that are hydrogenated according to conventional methods,
Examples include hydrogenated phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, etc., and one or more of these may be used in combination. The liquid hydrocarbon used in the present invention may be one that is liquid at room temperature and is normally used as a raw material for cosmetics, such as stanlan, pristane, liquid paraffin, and low-viscosity polybutene (viscosity 5 to 1000 cst). )
etc., and these may be used alone or in combination of two or more. Examples of the anionic surfactants used in the present invention include fatty acid salts, alkylbenzene sulfonates, alkyl sulfonates, α-olefin sulfonates, dialkyl sulfosuccinates, α-sulfonated fatty acid salts, sodium N
-Methyl-N-alkyl taurine, polyoxyethylene alkyl ether sulfate, polyoxyethylene alkyl phenyl ether sulfate, alkyl phosphate, polyoxyethylene alkyl ether phosphate, polyoxyethylene alkyl phenyl ether phosphate, N-acyl glutamic acid salts, N-acyl-N-alkyl amino acid salts, O-alkyl substituted malates, etc., and those having an HLB value of 12 or more can be used singly or in combination of two or more. Nonionic surfactants include, for example, decaglycerin fatty acid ester, polyglycerin fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene glycerin fatty acid ester, polyethylene glycol fatty acid ester, polyoxyethylene alkyl ether, Polyoxyethylene phytosterol, polyoxyethylene phytosterol, polyoxyethylene polyoxypropylene alkyl ether, polyoxyethylene alkyl phenyl ether, polyoxyethylene castor oil, polyoxyethylene hydrogenated castor oil, polyoxyethylene lanolin, polyoxyethylene lanolin alcohol, Polyoxyethylene alkylamine, polyoxyethylene fatty acid amide, polyoxyethylene alkylphenyl formaldehyde condensate, sucrose fatty acid ester, etc.
Those having an LB value of 12 or more can be used alone or in combination of two or more. Each component used in the present invention is blended in a specific amount and in a specific ratio. That is, the amount of hydrogenated phospholipid (component A) is 0.05 to 5% by weight, the amount of liquid hydrocarbon (component B) is 0.05 to 5% by weight, and the amount of anionic surfactant and HLB value selected from nonionic surfactants! The blending amount of two or more surfactants (component C) is 0.05~
5% by weight, and the blending amount of ethanol is 1 to 40% by weight.
It is. Moreover, the weight ratio of component A/component C is 0.2 to
5, and the weight ratio of (A component, C component)/B acid component is 0.
It is 2-5. Within this range, there will be no change in white turbidity, precipitation, separation, precipitation of crystals, disappearance of white turbidity, etc. over a wide temperature range, and an aqueous cosmetic containing a stable combination of hydrogenated phospholipids can be obtained. Moreover, the usability and safety are also good. The aqueous cosmetic composition of the present invention has a translucent to cloudy appearance, and has a transmittance of 0 to 95% when measured with a spectrophotometer. The aqueous cosmetics referred to in the present invention are those containing purified water as a main component.
Soft lotion, nutritional lotion, astringent lotion, cleansing lotion,
These include beauty serums and hair lotions. The method for producing an aqueous cosmetic of the present invention includes an alcohol component comprising a hydrogenated phospholipid, a liquid hydrocarbon, a surfactant with an HLB value of 12 or more selected from anionic surfactants and nonionic surfactants, and ethanol. may be added to the xylem whose main component is purified water, or conversely, the xylem may be added to the alcoholic part.
Moreover, at this time, the alcohol part and the wood part may be warmed or heated as appropriate. Furthermore, in the present invention, in addition to the above-mentioned essential ingredients, fragrances, pigments, preservatives, bactericidal agents, humectants, UV absorbers, salts, bases, chelating agents, thickeners, pearling agents,
Surfactants, oil agents, various drugs, etc. may be appropriately blended. [Example] Next, the present invention will be further described with reference to Examples. These do not limit the invention in any way. Examples H1 to [4], Comparative Examples Hl to [8] Examples [1] to [4], Comparative Examples [11 to
【61と共
に1表1に処方を示す6表中配合量は重量%である。各
実施例ならびに比較例につき、製造当日に透過率の測定
を行なうと共に、3ケ月後の経時安定性のチェックを行
なった。結果は同じく表1に示す。
(透過率の測定)
■島津製作所分光光度計υV−180を用いた。測定条
件は500n腸、lc■である0表中測定値は%であり
、 100は完全透明を、0は完全白濁を示すものであ
る。
(経時安定性のチェック)
経時安定性は、5℃、室温、40℃の各温度にそれぞれ
セットしたものを3ケ月後にその外観をチェックするこ
とにより行なった。なお、安定なものについては、更に
透過率の測定をも行なった。
表 1
表 1(つづき)
(製法)
A(1)〜(7)を60℃にて加温混合する。
B (8)、(9)を60℃にて加温溶解する。
CBにAを加えて乳化をする。
DCを35℃まで冷却して完了とする。
表1の結果から明らかな如く、本発明の実施例 【11
〜口1に於いては、半透明〜白濁の種々の水性化粧料が
得られ、また、広い温度領域にて経時安定性に優れ、か
つその濁度の変化もほとんどない水性化粧料が得られた
。
一方、液状炭化水素を配合しないもの(比較例[1]、
[2])は水素添加リン脂質が結晶として析出し安定性
が悪い、また、液状炭化水素以外の液状油を配合したも
の(比較例[3])は分離してしまっている。液状炭化
水素の配合比が少ないもの(比較例[41)は高温での
安定性が悪い、さらに、HLB値12以上の界面活性剤
の配合比が多いもの(比較例【51)も、配合比が少な
いもの(比較例〔81)も、安定性が悪い。
実施例 [5]〜[81、比較例 [7]、 [8]実
施例[51〜【8]につき、比較例 [7]、 [8]
と共に1表2に処方を示す0表中配合量は重量%である
。製法は実施例【11に準する。各実施例ならびに比較
例につき、透過率の測定ならびに官能評価を行なった。
結果は同じく表2に示す。
(官能評価)
官能評価は1女性lO名からなる専門パネルを対象とし
た使用テストを行ない、3項目につき5点評価を行なっ
た。
評価項目:(1)使用中のみずみずしさく2)使用後の
さっばり感
(3)使用後のしっとり感
5点評価: 2 非常に感じる
1 感じる
0 どちらともいえない
−1感じない
−2まったく感じられない
官能評価=10名の専門パネルの平均値をもって、次の
ように示した。
0 1〜2
o O〜1
Δ −1〜O
X −2〜−1
(以下余白)
表2
表2の結果より明らかな如く、本発明の実施例 [51
〜【8] に於いては、半透明〜白濁の種々の水性化粧
料が得られ、また、使用中にはみずみずしさが感じられ
、使用後にはさっばり感が感じられると共にしっとり感
も感じられるという官能に優れた水性化粧料が得られた
。
一方、各必須成分の配合量が少ないもの(比較例[71
)は、使用後のしっとり感がない、また液状炭化水素の
配合量が多いもの(比較例【81]は使用中のみずみず
しさ並びに使用後のさっばり感が感じられない。
実施例 【8】 栄養化粧水
(処方) (重量%)(1)
水素添加卵黄レシチン 0.6(2)
スタンラン 1.0(3)
デカグリセリルモノラウレート 0.4(HLB値1
5.5)
(4) 香料 0.1(5
) 防腐剤 0.1(〔エタ
ノール 10.0(7) 1.3
−ブチレングリコール 6.0(8)色素
適量(9)精製水
残量(製法)
A(1)〜(6)を60℃にて加温混合する。
B(7)〜(8)を60℃にて加温溶解する。
CBにAを加えて乳化をする。
DCを35℃まで冷却して、栄養化粧水を得る。
以上のようにして得られた栄養化粧水は、白濁の美しい
外観を有し、さっばりした使用感を有しながらも、使用
後の肌をしっとりと潤わせた。また安定性も良好であっ
た。
実施例[101収斂化粧水
(処方) (電縫%)(1)
水素添加大豆レシチン 0.6(渇 プ
リスタン 0,3(3) グリ
チルリチン酸ジカリウム 0.2(アニオン)
(4酢酸di−α−ミーα−トコフェロール、05(5
)香料 0.1((へ)
防腐剤 0.1(2) エタ
ノール 20.0(8) 加水分
解コラーゲン 0.1(9) 色素
適量60) 精製水
残量(製法)
A (1)〜(7)を60℃にて加温混合する。
B(8)〜(lO)を60℃にて加温溶解する。
CBにAを加えて乳化する。
DCを35℃まで冷却して、収斂化粧水を得る。
以上のようにして得られた収斂化粧水は、半透明の外観
を有し、のびや肌へのなじみが良く、みずみずしい使用
感を有していた。半透明性も変化なく経時安定性が良好
であった。
実施例【111 ヘアローション
(処方) (重量%)(1)
水素添加卵黄レシチン i、。
(り 流動パラフィン 2.0(3)
ショ糖脂肪酸エステル(HLB 1.5値18
.0)
(4) 香料 0.2(5
) 殺菌剤 0.1(@ 見
−メントール 0.01(7) エタ
ノール 35.0(8) プロ
ピレングリコール 3.0(匂 カチオン化
セルロース 0.05(10) 精製水
残量(製法)
A(1)〜(7)を60℃にて加温混合する。
B(8)〜(lO)を60℃にて加温溶解する。
CAにBを加えて乳化する。
DCを35℃まで冷却して、ヘアローションを得る。
以上のようにして得られたヘアロージオンは、白濁の美
しい外観を示し、べたつきのない、しっとりとした使用
感を有していた。また経時安定性も良好であった。
実施例[12] 美容液
(処方) (重量%)(1)
水索榛加大豆レシチン 1.5(渇 ス
タワラン 0.8(3) 胆汁
酸ナトリウム(アニオン)0.8(4) ホホバオイル
0.1(5) 香料
0.1(6) 防腐剤
0.1(7) エタノール
5.0(8)グリセリン
6.0(9) ヒアルロン酸ナトリウム
0.1(10) カルボキシビニルポリマー
0.15(1リ 水酸化ナトリウム
0.03(12)精製水 残
量(製法)
A(1)〜(7)を80℃にて加温混合する。
B(8)〜(12)を80℃にて加温溶解する。
CBにAを加えて乳化をする。
DCを35℃まで冷却して、美容液を得る。
以上のようにして得られた美容液は、半透明の外観を有
し、コクを有しながらもみずみずしい使用感を有すると
共に、あと肌はべたつきもなくしっとりするものであっ
た。半透明性も変化なく経時安定性も良好であった。
[発明の効果]
本発明の水性化粧料は、以上詳述した如く、リン脂質を
安定に配合した半透明〜白濁の水性化粧料であって、広
い温度領域に於いて、白濁度の変化や、沈殿1分離、結
晶の析出、白濁の消滅等がない、また、水素添加リン脂
質、液状炭化水素、エタノールを効果的に配合している
ので、しっとり感を有しながらも、べたつき感を感じさ
せず、みずみずしい使用感を有する水性化粧料を提供す
ることが可能になった。
以 上The formulations are shown in Table 1 along with [61] and the amounts in Table 6 are weight %. For each Example and Comparative Example, the transmittance was measured on the day of manufacture, and the stability over time was checked after 3 months. The results are also shown in Table 1. (Measurement of transmittance) ■A Shimadzu spectrophotometer υV-180 was used. The measurement conditions were 500n intestine and lc■0 The measured values in the table are in %, where 100 indicates complete transparency and 0 indicates complete cloudiness. (Checking stability over time) Stability over time was determined by checking the appearance of the samples set at 5°C, room temperature, and 40°C after 3 months. Furthermore, for stable materials, transmittance measurements were also performed. Table 1 Table 1 (Continued) (Manufacturing method) A(1) to (7) are heated and mixed at 60°C. B Dissolve (8) and (9) by heating at 60°C. Add A to CB and emulsify. Finish by cooling the DC to 35°C. As is clear from the results in Table 1, Examples of the present invention [11
- In the case of 1, various water-based cosmetics can be obtained that are translucent to cloudy, and also have excellent stability over time in a wide temperature range and have almost no change in turbidity. Ta. On the other hand, those containing no liquid hydrocarbon (Comparative Example [1],
[2]) has poor stability because hydrogenated phospholipids precipitate as crystals, and the product containing liquid oil other than liquid hydrocarbon (Comparative Example [3]) separates. The one with a small blending ratio of liquid hydrocarbon (Comparative Example [41]) has poor stability at high temperatures, and the one with a large blending ratio of a surfactant with an HLB value of 12 or more (Comparative Example [51]) also has a low blending ratio. The one with a small amount (Comparative Example [81)] also has poor stability. Examples [5] to [81] Comparative examples [7], [8] Examples [51 to [8], Comparative examples [7], [8]
The formulations are shown in Table 1 and Table 2. The blending amounts in Table 1 are weight %. The manufacturing method is based on Example [11]. Transmittance measurements and sensory evaluations were performed for each Example and Comparative Example. The results are also shown in Table 2. (Sensory Evaluation) For the sensory evaluation, a usage test was conducted with an expert panel consisting of 1 woman, and a 5-point evaluation was made for 3 items. Evaluation items: (1) Refreshing feeling during use 2) Refreshing feeling after use (3) Moist feeling after use 5 points rating: 2 Very felt 1 Feeling 0 Neutral - 1 Not feeling - 2 Not feeling at all Sensory evaluation that cannot be evaluated is the average value of a panel of 10 experts, and is shown as follows. 0 1~2 o O~1 Δ -1~O
~ [8] Various aqueous cosmetics that are translucent to cloudy are obtained, and also feel fresh during use, and feel light and moist after use. An aqueous cosmetic with excellent sensory properties was obtained. On the other hand, those containing a small amount of each essential component (comparative example [71
) does not give a moist feeling after use, and contains a large amount of liquid hydrocarbon (comparative example [81] does not give a fresh feeling during use and does not give a refreshing feeling after use. Example [8] Nutritional lotion (prescription) (weight%) (1)
Hydrogenated egg yolk lecithin 0.6 (2)
Stan Run 1.0 (3)
Decaglyceryl monolaurate 0.4 (HLB value 1
5.5) (4) Fragrance 0.1 (5
) Preservative 0.1 ([Ethanol 10.0 (7) 1.3
-Butylene glycol 6.0(8) Pigment
Appropriate amount (9) Purified water
Remaining amount (manufacturing method) A (1) to (6) are heated and mixed at 60°C. B(7) to (8) are heated and dissolved at 60°C. Add A to CB and emulsify. Cool the DC to 35°C to obtain a nutritional lotion. The nutritious lotion obtained as described above had a beautiful cloudy appearance, had a light feeling on use, and left the skin moist and moisturized after use. Moreover, the stability was also good. Example [101 Astringent lotion (prescription) (ERW%) (1)
Hydrogenated soybean lecithin 0.6 (thirsty) Pristane 0.3 (3) Dipotassium glycyrrhizinate 0.2 (anion) (di-α-me α-tocopherol 4acetate, 05 (5)
) Fragrance 0.1 ((to)
Preservative 0.1 (2) Ethanol 20.0 (8) Hydrolyzed collagen 0.1 (9) Pigment
Appropriate amount 60) Purified water
Remaining amount (manufacturing method) A (1) to (7) are heated and mixed at 60°C. B(8) to (lO) are dissolved by heating at 60°C. Add A to CB and emulsify. Cool the DC to 35°C to obtain an astringent lotion. The astringent lotion obtained as described above had a translucent appearance, spread well, blended well into the skin, and had a refreshing feeling on use. There was no change in translucency and the stability over time was good. Example [111 Hair lotion (formulation) (wt%) (1)
Hydrogenated egg yolk lecithin i. (li liquid paraffin 2.0 (3)
Sucrose fatty acid ester (HLB 1.5 value 18
.. 0) (4) Fragrance 0.2 (5
) Disinfectant 0.1 (@Mi-Menthol 0.01 (7) Ethanol 35.0 (8) Propylene glycol 3.0 (Odor Cationized cellulose 0.05 (10) Purified water
Remaining amount (manufacturing method) A (1) to (7) are heated and mixed at 60°C. B(8) to (lO) are dissolved by heating at 60°C. Add B to CA and emulsify. Cool the DC to 35°C to obtain hair lotion. The hair lotion obtained as described above had a beautiful white cloudy appearance, and had a non-sticky and moist feeling on use. The stability over time was also good. Example [12] Beauty serum (prescription) (weight%) (1)
Mizusaku Haruka Soybean Lecithin 1.5 (Tsugaran 0.8 (3) Sodium Bile Acid (Anion) 0.8 (4) Jojoba Oil 0.1 (5) Fragrance
0.1 (6) Preservative
0.1(7) Ethanol
5.0(8) Glycerin
6.0(9) Sodium hyaluronate
0.1 (10) carboxyvinyl polymer
0.15 (1 Li Sodium hydroxide
0.03 (12) Purified water Remaining amount (manufacturing method) A (1) to (7) are heated and mixed at 80°C. B(8) to (12) are dissolved by heating at 80°C. Add A to CB and emulsify. Cool the DC to 35°C to obtain a serum. The serum obtained in the above manner had a translucent appearance, had a rich yet refreshing feeling upon use, and left the skin moist without any stickiness. There was no change in translucency and stability over time was also good. [Effects of the Invention] As detailed above, the aqueous cosmetic of the present invention is a translucent to cloudy aqueous cosmetic that stably contains phospholipids, and exhibits no change in white turbidity over a wide temperature range. , no precipitation, no precipitation of crystals, no disappearance of cloudiness, etc.Also, since hydrogenated phospholipids, liquid hydrocarbons, and ethanol are effectively blended, it has a moist feeling but does not feel sticky. It has now become possible to provide an aqueous cosmetic that has a fresh feeling on use without causing any dryness. that's all
Claims (1)
と、液状炭化水素(B成分)0.05〜5重量%と、ア
ニオン界面活性剤およびノニオン界面活性剤から選ばれ
るHLB値12以上の界面活性剤(C成分)0.05〜
5重量%と、エタノール1〜40重量%とからなり、A
成分/C成分の重量比が0.2〜5であり、かつ(A成
分+C成分)/B成分の重量比が0.2〜5であること
を特徴とする水性化粧料。(1) Hydrogenated phospholipid (component A) 0.05-5% by weight
, 0.05 to 5% by weight of liquid hydrocarbon (component B), and 0.05 to 5% by weight of a surfactant with an HLB value of 12 or higher selected from anionic surfactants and nonionic surfactants (component C).
5% by weight and 1 to 40% by weight of ethanol, A
An aqueous cosmetic characterized in that the weight ratio of component/component C is 0.2 to 5, and the weight ratio of component (A component+component C)/component B is 0.2 to 5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62094489A JP2521467B2 (en) | 1987-04-17 | 1987-04-17 | Translucent lotion |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62094489A JP2521467B2 (en) | 1987-04-17 | 1987-04-17 | Translucent lotion |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63264512A true JPS63264512A (en) | 1988-11-01 |
JP2521467B2 JP2521467B2 (en) | 1996-08-07 |
Family
ID=14111709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62094489A Expired - Lifetime JP2521467B2 (en) | 1987-04-17 | 1987-04-17 | Translucent lotion |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2521467B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU616263B2 (en) * | 1988-06-15 | 1991-10-24 | Wella Aktiengesellschaft | Emulsion for care of the hair |
WO2000033798A1 (en) * | 1998-12-04 | 2000-06-15 | L'oreal | Compositions and methods for controlling deposition of water-insoluble ingredients |
JP2008189686A (en) * | 1997-06-09 | 2008-08-21 | L'oreal Sa | Aqueous carrier system for water-insoluble material |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5277011B2 (en) | 2008-02-13 | 2013-08-28 | 株式会社 資生堂 | Oil-in-water emulsified cloudy skin cosmetic |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5356315A (en) * | 1976-11-01 | 1978-05-22 | Eisai Co Ltd | Emulsified solution of fat soluble drugs |
JPS5910511A (en) * | 1982-07-07 | 1984-01-20 | Eisai Co Ltd | Aqueous solution containing fat-soluble substance |
JPS6094903A (en) * | 1983-10-28 | 1985-05-28 | Nisshin Oil Mills Ltd:The | Cosmetic |
JPS61167610A (en) * | 1985-01-19 | 1986-07-29 | Shiseido Co Ltd | Cosmetic |
-
1987
- 1987-04-17 JP JP62094489A patent/JP2521467B2/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5356315A (en) * | 1976-11-01 | 1978-05-22 | Eisai Co Ltd | Emulsified solution of fat soluble drugs |
JPS5910511A (en) * | 1982-07-07 | 1984-01-20 | Eisai Co Ltd | Aqueous solution containing fat-soluble substance |
JPS6094903A (en) * | 1983-10-28 | 1985-05-28 | Nisshin Oil Mills Ltd:The | Cosmetic |
JPS61167610A (en) * | 1985-01-19 | 1986-07-29 | Shiseido Co Ltd | Cosmetic |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU616263B2 (en) * | 1988-06-15 | 1991-10-24 | Wella Aktiengesellschaft | Emulsion for care of the hair |
JP2008189686A (en) * | 1997-06-09 | 2008-08-21 | L'oreal Sa | Aqueous carrier system for water-insoluble material |
WO2000033798A1 (en) * | 1998-12-04 | 2000-06-15 | L'oreal | Compositions and methods for controlling deposition of water-insoluble ingredients |
Also Published As
Publication number | Publication date |
---|---|
JP2521467B2 (en) | 1996-08-07 |
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