JPH1036246A - Suppressant for melanogenesis and preparation for external use for skin - Google Patents
Suppressant for melanogenesis and preparation for external use for skinInfo
- Publication number
- JPH1036246A JPH1036246A JP19472096A JP19472096A JPH1036246A JP H1036246 A JPH1036246 A JP H1036246A JP 19472096 A JP19472096 A JP 19472096A JP 19472096 A JP19472096 A JP 19472096A JP H1036246 A JPH1036246 A JP H1036246A
- Authority
- JP
- Japan
- Prior art keywords
- skin
- cedrol
- preparation
- melanin production
- melanogenesis
- 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.)
- Pending
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 36
- 230000003061 melanogenesis Effects 0.000 title abstract 4
- SVURIXNDRWRAFU-OGMFBOKVSA-N cedrol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](O)(C)CC2 SVURIXNDRWRAFU-OGMFBOKVSA-N 0.000 claims abstract description 30
- 229940026455 cedrol Drugs 0.000 claims abstract description 30
- PCROEXHGMUJCDB-UHFFFAOYSA-N cedrol Natural products CC1CCC2C(C)(C)C3CC(C)(O)CC12C3 PCROEXHGMUJCDB-UHFFFAOYSA-N 0.000 claims abstract description 30
- SVURIXNDRWRAFU-UHFFFAOYSA-N juniperanol Natural products C1C23C(C)CCC3C(C)(C)C1C(O)(C)CC2 SVURIXNDRWRAFU-UHFFFAOYSA-N 0.000 claims abstract description 30
- 239000004480 active ingredient Substances 0.000 claims abstract description 7
- 230000008099 melanin synthesis Effects 0.000 claims description 38
- 239000003112 inhibitor Substances 0.000 claims description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 11
- 241000196324 Embryophyta Species 0.000 abstract description 6
- 208000012641 Pigmentation disease Diseases 0.000 abstract description 5
- 239000006210 lotion Substances 0.000 abstract description 5
- 239000000243 solution Substances 0.000 abstract description 5
- 239000003814 drug Substances 0.000 abstract description 4
- 239000003921 oil Substances 0.000 abstract description 4
- 206010014970 Ephelides Diseases 0.000 abstract description 3
- 208000003351 Melanosis Diseases 0.000 abstract description 3
- 206010042496 Sunburn Diseases 0.000 abstract description 3
- 239000010627 cedar oil Substances 0.000 abstract description 3
- 239000002537 cosmetic Substances 0.000 abstract description 3
- 239000006071 cream Substances 0.000 abstract description 3
- 230000019612 pigmentation Effects 0.000 abstract description 3
- 239000002552 dosage form Substances 0.000 abstract description 2
- 230000002500 effect on skin Effects 0.000 abstract description 2
- 238000000605 extraction Methods 0.000 abstract description 2
- 239000002674 ointment Substances 0.000 abstract description 2
- 229930004725 sesquiterpene Natural products 0.000 abstract description 2
- 150000004354 sesquiterpene derivatives Chemical class 0.000 abstract description 2
- 241000218691 Cupressaceae Species 0.000 abstract 2
- 241000021559 Dicerandra Species 0.000 abstract 1
- 235000010654 Melissa officinalis Nutrition 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000000865 liniment Substances 0.000 abstract 1
- 231100000989 no adverse effect Toxicity 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 9
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 8
- 230000002401 inhibitory effect Effects 0.000 description 8
- 210000004027 cell Anatomy 0.000 description 7
- -1 tannin and glycoside Natural products 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 6
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 5
- 239000008309 hydrophilic cream Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 4
- BJRNKVDFDLYUGJ-RMPHRYRLSA-N hydroquinone O-beta-D-glucopyranoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=C(O)C=C1 BJRNKVDFDLYUGJ-RMPHRYRLSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 3
- RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Natural products OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 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
- 230000000052 comparative effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 239000002953 phosphate buffered saline Substances 0.000 description 3
- 210000004694 pigment cell Anatomy 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- 108010024636 Glutathione Proteins 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 229930003268 Vitamin C Natural products 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000002260 anti-inflammatory agent Substances 0.000 description 2
- 229940121363 anti-inflammatory agent Drugs 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 229960000271 arbutin Drugs 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000000174 gluconic acid Substances 0.000 description 2
- 235000012208 gluconic acid Nutrition 0.000 description 2
- 229960003180 glutathione Drugs 0.000 description 2
- 239000003906 humectant Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229940074358 magnesium ascorbate Drugs 0.000 description 2
- AIOKQVJVNPDJKA-ZZMNMWMASA-L magnesium;(2r)-2-[(1s)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2h-furan-3-olate Chemical compound [Mg+2].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] AIOKQVJVNPDJKA-ZZMNMWMASA-L 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- BJRNKVDFDLYUGJ-UHFFFAOYSA-N p-hydroxyphenyl beta-D-alloside Natural products OC1C(O)C(O)C(CO)OC1OC1=CC=C(O)C=C1 BJRNKVDFDLYUGJ-UHFFFAOYSA-N 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 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 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 235000018553 tannin Nutrition 0.000 description 2
- 229920001864 tannin Polymers 0.000 description 2
- 239000001648 tannin Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 235000019154 vitamin C Nutrition 0.000 description 2
- 239000011718 vitamin C Substances 0.000 description 2
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 description 1
- WTVHAMTYZJGJLJ-UHFFFAOYSA-N (+)-(4S,8R)-8-epi-beta-bisabolol Natural products CC(C)=CCCC(C)C1(O)CCC(C)=CC1 WTVHAMTYZJGJLJ-UHFFFAOYSA-N 0.000 description 1
- RGZSQWQPBWRIAQ-CABCVRRESA-N (-)-alpha-Bisabolol Chemical compound CC(C)=CCC[C@](C)(O)[C@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-CABCVRRESA-N 0.000 description 1
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (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-carboxylic acid Chemical compound 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 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- SGTNSNPWRIOYBX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 description 1
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- MUZDXNQOSGWMJJ-UHFFFAOYSA-N 2-methylprop-2-enoic acid;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(=C)C(O)=O MUZDXNQOSGWMJJ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- MOMKYJPSVWEWPM-UHFFFAOYSA-N 4-(chloromethyl)-2-(4-methylphenyl)-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=NC(CCl)=CS1 MOMKYJPSVWEWPM-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
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- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
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- QZKRHPLGUJDVAR-UHFFFAOYSA-K EDTA trisodium salt Chemical compound [Na+].[Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O QZKRHPLGUJDVAR-UHFFFAOYSA-K 0.000 description 1
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- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical compound [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000000481 effect on pigmentation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012894 fetal calf serum Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- LBQIJVLKGVZRIW-UHFFFAOYSA-N glabridine Natural products C1OC2=C3C=CC(C)(C)OC3=CC=C2CC1C1=CC=C(O)C=C1O LBQIJVLKGVZRIW-UHFFFAOYSA-N 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 235000011187 glycerol Nutrition 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
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 1
- 239000001685 glycyrrhizic acid Substances 0.000 description 1
- 229960004949 glycyrrhizic acid Drugs 0.000 description 1
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 1
- 235000019410 glycyrrhizin Nutrition 0.000 description 1
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 1
- TWVJWDMOZJXUID-QJPTWQEYSA-N guaiol Natural products OC(C)(C)[C@H]1CC=2[C@H](C)CCC=2[C@@H](C)CC1 TWVJWDMOZJXUID-QJPTWQEYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 229920002674 hyaluronan Polymers 0.000 description 1
- 229960003160 hyaluronic acid Drugs 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- BEJNERDRQOWKJM-UHFFFAOYSA-N kojic acid Chemical compound OCC1=CC(=O)C(O)=CO1 BEJNERDRQOWKJM-UHFFFAOYSA-N 0.000 description 1
- WZNJWVWKTVETCG-UHFFFAOYSA-N kojic acid Natural products OC(=O)C(N)CN1C=CC(=O)C(O)=C1 WZNJWVWKTVETCG-UHFFFAOYSA-N 0.000 description 1
- 229960004705 kojic acid Drugs 0.000 description 1
- 229940069445 licorice extract Drugs 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 201000001441 melanoma Diseases 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- CZMAXQOXGAWNDO-UHFFFAOYSA-N propane-1,1,2-triol Chemical compound CC(O)C(O)O CZMAXQOXGAWNDO-UHFFFAOYSA-N 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229960001790 sodium citrate Drugs 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 235000019983 sodium metaphosphate Nutrition 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- GYDJEQRTZSCIOI-LJGSYFOKSA-N tranexamic acid Chemical compound NC[C@H]1CC[C@H](C(O)=O)CC1 GYDJEQRTZSCIOI-LJGSYFOKSA-N 0.000 description 1
- 229960000401 tranexamic acid Drugs 0.000 description 1
- 150000003625 trehaloses Chemical class 0.000 description 1
- 229960005066 trisodium edetate Drugs 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 229960001722 verapamil Drugs 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 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 1
Landscapes
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、メラニン産生抑制
剤及び皮膚外用剤に関し、詳しくは、日焼け後の色素沈
着、しみ・そばかす等の予防または改善効果を有するメ
ラニン産生抑制剤及び皮膚外用剤に関する。The present invention relates to a melanin production inhibitor and an external preparation for the skin, and more particularly to a melanin production inhibitor and an external preparation for the skin having an effect of preventing or improving pigmentation after sunburn, spots and freckles, etc. .
【0002】[0002]
【従来の技術】日光からの紫外線が皮膚に照射される
と、皮膚内のチロシナーゼ活性作用によりメラニンが著
しく生成して皮膚が黒化しやすい傾向がある。これを回
復または予防する皮膚外用剤に対する要望は非常に強
い。日焼け等による皮膚の黒化の防止を目的とする皮膚
外用剤として、ビタミンCやその誘導体、グルタチオン
やその誘導体、過酸化水素、ハイドロキノンやその誘導
体、コロイド硫黄など或いは例えば桂皮などの植物から
の抽出エキスであるタンニンや配糖体などの各種の天然
物を配合したものが知られている。2. Description of the Related Art When ultraviolet rays from sunlight are irradiated on the skin, melanin is remarkably generated due to the tyrosinase activity in the skin, and the skin tends to be darkened. There is a strong demand for an external preparation for the skin to recover or prevent this. As an external preparation for the purpose of preventing skin darkening due to sunburn etc., extraction from plants such as vitamin C and its derivatives, glutathione and its derivatives, hydrogen peroxide, hydroquinone and its derivatives, colloidal sulfur, and for example, cinnamon What blended various natural products, such as tannin and glycoside, which are extracts, is known.
【0003】ところが、アスコルビン酸類は湿性皮膚外
用剤の如き水分を多く含む系において酸化されやすく不
安定であり、変色、変臭の原因となり、過酸化水素は保
存上、安定性ならびに安全上の問題があり、グルタチオ
ンや硫黄は著しい異臭を放つため皮膚外用剤へ使用する
ことは不適当である。また、従来知られている植物から
の抽出エキスなどの天然物においては、作用が緩慢であ
るため皮膚の黒化を充分効果的に防止できないことがあ
る。また、ハイドロキノンは、効果は一応認められてい
るが、皮膚刺激性があるので一般には使用が制限されて
いる。[0003] However, ascorbic acids are easily oxidized and unstable in a system containing a large amount of water, such as an external preparation for moist skin, causing discoloration and odor. Hydrogen peroxide is a problem in storage, stability and safety. Glutathione and sulfur emit a remarkable off-flavor and are not suitable for use in external preparations for skin. In addition, in the case of a conventionally known natural product such as an extract from a plant, its action is slow, so that blackening of the skin may not be sufficiently effectively prevented. Although hydroquinone has been recognized as having some effect, its use is generally restricted because of its skin irritation.
【0004】一方、セドロールが香料成分としてセダー
ウッド油等の香油中に含まれる事は既に知られていた
が、かかるメラニン産生抑制効果を持つことは今まで知
られていない。[0004] On the other hand, it has been known that cedrol is contained as a flavor component in perfume oils such as Cedarwood oil, but it has not been known to have such an effect of inhibiting melanin production.
【0005】[0005]
【発明が解決しようとする課題】本発明は斯る実情に鑑
みてなされたものであって、皮膚の黒化をきわめて効果
的に防止することができるばかりか、皮膚に対する弊害
がなく安全に使用することのできるメラニン産生抑制剤
及び皮膚外用剤を提供することを課題とする。SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and not only can it prevent blackening of the skin very effectively, but also can be used safely without any harm to the skin. An object of the present invention is to provide a melanin production inhibitor and a skin external preparation that can be used.
【0006】[0006]
【課題を解決するための手段】本発明者らは、これらの
課題を解決するために、培養細胞を用いてメラニン産生
抑制効果について広く種々の物質をスクリーニングした
結果、香料の一成分として知られるセドロールにメラニ
ン産生抑制活性があることを見い出し、この知見に基づ
いて本発明を完成するに至った。Means for Solving the Problems In order to solve these problems, the present inventors have screened a wide variety of substances for their melanin production inhibitory effect using cultured cells, and as a result, they are known as one component of perfume. It has been found that cedrol has a melanin production inhibitory activity, and the present invention has been completed based on this finding.
【0007】すなわち本発明は、セドロールを有効成分
とするメラニン産生抑制剤及びこれを含有する皮膚外用
剤である。本発明の皮膚外用剤中のメラニン産生抑制剤
の含有量は、セドロールに換算して0.01〜10重量
%であることが好ましい。That is, the present invention relates to a melanin production inhibitor containing cedrol as an active ingredient and an external preparation for skin containing the same. The content of the melanin production inhibitor in the external preparation for skin of the present invention is preferably 0.01 to 10% by weight in terms of cedrol.
【0008】[0008]
【発明の実施の形態】以下、本発明について詳述する。
まず、本発明のメラニン産生抑制剤について説明する。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail.
First, the melanin production inhibitor of the present invention will be described.
【0009】<1>本発明のメラニン産生抑制剤 本発明のメラニン産生抑制剤は、セドロールを有効成分
とすることを特徴とする。本発明に用いられるセドロー
ルは、ヒノキ科植物やスギ科植物等に含まれるセスキテ
ルペンアルコールの一種で、セダーウッド油等の香油の
香料成分として知られており、式(1)で示される化合
物である。セドロールには光学異性体があり、式(1)
は(+)体のセドロールを示す。本発明のメラニン産生
抑制剤の有効成分であるセドロールは、光学異性体の
(+)体または(−)体のいずれの形態であってもよ
い。<1> Melanin production inhibitor of the present invention The melanin production inhibitor of the present invention comprises cedrol as an active ingredient. Cedrol used in the present invention is a kind of sesquiterpene alcohol contained in cypress plants and cedar plants, and is known as a flavor component of perfume oils such as Cedarwood oil, and is a compound represented by the formula (1). . Cedrol has optical isomers and has the formula (1)
Indicates a (+)-form cedrol. Cedrol, which is an active ingredient of the melanin production inhibitor of the present invention, may be in the form of (+) or (−) optical isomer.
【0010】[0010]
【化1】 Embedded image
【0011】本発明のメラニン産生抑制剤の有効成分で
あるセドロールは、上記植物から抽出したものでもよい
し、また合成品でもよい。セドロールは市販されてお
り、市販品を用いてもよい。Cedrol, which is an active ingredient of the melanin production inhibitor of the present invention, may be extracted from the above plants or may be a synthetic product. Cedrol is commercially available, and a commercially available product may be used.
【0012】本発明のメラニン産生抑制剤にはセドロー
ルの他、各種基剤等を配合してもよく、基剤としてはエ
タノール、1,3−ブチレングリコール、オリーブ油等
が挙げられる。メラニン産生抑制剤中のセドロールの含
有量や基剤の種類は特に限定されるものではなく、用途
などに応じて適宜設定してよい。The melanin production inhibitor of the present invention may contain various bases in addition to cedrol. Examples of the base include ethanol, 1,3-butylene glycol, olive oil and the like. The content of cedrol and the type of base in the melanin production inhibitor are not particularly limited, and may be appropriately set according to the use and the like.
【0013】セドロールを含む植物等からの抽出物はそ
のまま本発明のメラニン産生抑制剤とすることができる
が、抽出物中にメラニン産生抑制効果を発現する量のセ
ドロールが含まれていると、抽出物中の他成分の香りが
強くなりすぎて使用するにあたって好ましくないことが
ある。An extract from a plant or the like containing cedrol can be used as the melanin production inhibitor of the present invention as it is. However, if the extract contains cedrol in an amount capable of exhibiting a melanin production inhibitory effect, it will not be extracted. In some cases, the scent of other components in the product becomes too strong, which is not preferable for use.
【0014】本発明のメラニン産生抑制剤は、必要に応
じて他のメラニン産生抑制物質と併用してもよい。他の
メラニン産生抑制物質としては、アスコルビン酸リン酸
マグネシウム、アルブチン、グアイオール等が挙げられ
る。The melanin production inhibitor of the present invention may be used in combination with another melanin production inhibitor, if necessary. Other melanin production inhibitors include magnesium ascorbate phosphate, arbutin, guaiaol and the like.
【0015】<2>本発明の皮膚外用剤 本発明の皮膚外用剤は、上記メラニン産生抑制剤を含有
することを特徴とする。<2> External preparation for skin of the present invention The external preparation for skin of the present invention is characterized by containing the above-mentioned melanin production inhibitor.
【0016】皮膚外用剤中での上記メラニン産生抑制剤
の含有量は特に限定されるものではないが、好ましくは
皮膚外用剤の全量に対してセドロールの含有量が0.0
1〜10重量%となるようにメラニン産生抑制剤を配合
することが好適であり、特に好ましくは0.05〜5重
量%が好適である。0.01重量%以上の含有量であれ
ばメラニン産生抑制効果を十分に発揮できる一方、10
重量%を越えて含有しても効果の増強はほとんど頭打ち
となる。The content of the melanin production inhibitor in the external preparation for skin is not particularly limited, but preferably, the content of cedrol is 0.0 to the total amount of the external preparation for skin.
It is preferable to mix the melanin production inhibitor so as to be 1 to 10% by weight, and particularly preferably 0.05 to 5% by weight. When the content is 0.01% by weight or more, the melanin production inhibitory effect can be sufficiently exerted.
Even if the content exceeds about 10% by weight, the enhancement of the effect is almost leveled off.
【0017】本発明の皮膚外用剤には、ビタミンC、ア
スコルビン酸リン酸マグネシウム、アスコルビン酸グル
コシド、アルブチン、グアイオール、コウジ酸、イソフ
ェルラ酸ナトリウム等のメラニン産生抑制剤または美白
剤を必要に応じて配合してもよい。The skin preparation for external use of the present invention may optionally contain a melanin production inhibitor such as vitamin C, magnesium ascorbate phosphate, glucoside ascorbate, arbutin, guaiol, kojic acid, sodium isoferrate, or a whitening agent. May be.
【0018】本発明の皮膚外用剤には、これらの他にも
通常皮膚外用剤に用いられる成分、例えば、水性成分、
水、油性成分、アルコール類、炭化水素類、高級脂肪酸
類、ロウ類、保湿剤、抗酸化剤、紫外線吸収剤、界面活
性剤、増粘剤、粉末成分、防腐剤、抗炎症剤、pH調整
剤、金属封鎖剤、糖類、香料、着色剤、各種皮膚栄養剤
等を必要に応じて適宜配合することができる。The external preparation for skin of the present invention includes, in addition to these, other components usually used in external preparations for skin, such as aqueous components,
Water, oily components, alcohols, hydrocarbons, higher fatty acids, waxes, humectants, antioxidants, ultraviolet absorbers, surfactants, thickeners, powder components, preservatives, anti-inflammatory agents, pH adjustment Agents, sequestering agents, sugars, fragrances, coloring agents, various skin nutrients, and the like can be appropriately added as necessary.
【0019】具体的には、アルコール類としてエタノー
ル、プロパノール、セタノール、ステアリルアルコー
ル、グリセリン、プロピレングリコール、ブチレングリ
コール等、炭化水素類としてワセリン、スクワラン、流
動パラフィン等、高級脂肪酸類としてステアリン酸、オ
レイン酸等、ロウ類としてゲイロウ等、保湿剤としてヒ
アルロン酸等、抗酸化剤としてトコフェロール、酢酸ト
コフェロール、ブチルヒドロキシルトルエン(BHT)
等、紫外線吸収剤としてベンゾフェノン誘導体等、界面
活性剤として、ポリオキシエチレンセチルエーテル、モ
ノステアリン酸ポリエチレングリコール、モノステアリ
ン酸グリセリン、ポリオキシエチレンソルビタンモノラ
ウリン酸エステル、ポリオキシエチレンラウリルエーテ
ル、ポリオキシエチレンポリオキシプロピレングリコー
ル、脂肪酸モノグリセライド、ポリオキシエチレン硬化
ヒマシ油、ラウリル酸ナトリウム、アルキルスルホコハ
ク酸エステル、4級アルキルアミン、アルキルベタイン
等、増粘剤としてアラビアゴム、カルボキシビニルポリ
マー、キサンタンガム、ポリビニルアルコール等、粉末
成分としてタルク、シリカゲル、酸化チタン、アクリル
酸−メタクリル酸強重合体等の粉末、防腐剤としてパラ
ベン、グルコン酸クロルヘキシジン等、抗炎症剤として
グリチル酸ジカリウム、トラネキサム酸およびその誘導
体等、pH調整剤としてクエン酸塩、酢酸塩等、金属封
鎖剤として、エデト酸二ナトリウム、エデト酸三ナトリ
ウム、クエン酸ナトリウム、ポリリン酸ナトリウム、メ
タリン酸ナトリウム、グルコン酸等、糖類としてグルコ
ース、フルクトース、マンノース、ショ糖、トレハロー
ス、硫酸化トレハロース等が挙げられる。また、これら
のほかにはカフェイン、タンニン、ベラパミル、甘草抽
出物、グラブリジン、各種生薬、グリチルリチン酸およ
びその誘導体またはその塩、4−(1,1−ジメチルエ
チル)−4’−メトキシ−ジベンゾイルメタン、水酸化
カリウム、ビサボロール等が挙げられる。Specifically, alcohols such as ethanol, propanol, cetanol, stearyl alcohol, glycerin, propylene glycol and butylene glycol, hydrocarbons such as petrolatum, squalane and liquid paraffin, and higher fatty acids such as stearic acid and oleic acid And waxes, such as gay wax, humectants such as hyaluronic acid, antioxidants tocopherol, tocopherol acetate, butylhydroxyl toluene (BHT)
Benzophenone derivatives, etc. as ultraviolet absorbers; polyoxyethylene cetyl ether, polyethylene glycol monostearate, glyceryl monostearate, polyoxyethylene sorbitan monolaurate, polyoxyethylene lauryl ether, polyoxyethylene poly as surfactants Oxypropylene glycol, fatty acid monoglyceride, polyoxyethylene hydrogenated castor oil, sodium laurate, alkylsulfosuccinate, quaternary alkylamine, alkylbetaine, etc., gum arabic, carboxyvinyl polymer, xanthan gum, polyvinyl alcohol, etc. as thickeners, powder Ingredients such as talc, silica gel, titanium oxide, powders of acrylic acid-methacrylic acid strong polymer, and parabens and gluconic acid as preservatives Lolhexidine, dipotassium glycylate, tranexamic acid and derivatives thereof as anti-inflammatory agents, citrate, acetate, etc. as pH adjusters, disodium edetate, trisodium edetate, sodium citrate, polyphosphoric acid as sequestering agents Examples of sugars such as sodium acid, sodium metaphosphate and gluconic acid include glucose, fructose, mannose, sucrose, trehalose, sulfated trehalose and the like. In addition to these, caffeine, tannin, verapamil, licorice extract, glabridine, various crude drugs, glycyrrhizic acid and its derivatives or salts thereof, 4- (1,1-dimethylethyl) -4′-methoxy-dibenzoyl Methane, potassium hydroxide, bisabolol and the like can be mentioned.
【0020】本発明の皮膚外用剤は、メラニン産生を抑
制することにより皮膚の色素沈着の予防、改善に用いる
ことができ、そのような目的であれば、医薬品、医薬部
外品または化粧料等の用途は特に限定されない。The topical skin preparation of the present invention can be used for preventing and improving pigmentation of the skin by suppressing melanin production. For such purposes, pharmaceuticals, quasi-drugs, cosmetics and the like can be used. Is not particularly limited.
【0021】本発明の皮膚外用剤の剤型は皮膚外用剤と
して用いることができれば特に制限されず、例えば、溶
液、軟膏、クリーム、乳液、ローション、パック、水性
ゲル、オイルゲル等が挙げられる。また、本発明の皮膚
外用剤を化粧料として用いる際には、ファンデーショ
ン、コントロールカラー等の仕上げ料の形態でも用いる
ことができる。The dosage form of the external preparation for skin of the present invention is not particularly limited as long as it can be used as an external preparation for skin, and examples thereof include solutions, ointments, creams, emulsions, lotions, packs, aqueous gels, oil gels and the like. When the external preparation for skin of the present invention is used as a cosmetic, it can be used in the form of a finish such as a foundation or a control color.
【0022】本発明の皮膚外用剤は、上記メラニン産生
抑制剤を配合する以外は、通常の皮膚外用剤と同様の方
法で製造することができる。The external preparation for skin of the present invention can be produced by the same method as that for a normal external preparation for skin, except that the above-mentioned melanin production inhibitor is added.
【0023】[0023]
【実施例】以下、本発明の実施例を示すが、本発明はこ
れら実施例に制限されるものではない。まず、本発明の
メラニン産生抑制剤及びその効果の評価について説明す
る。EXAMPLES Examples of the present invention will be described below, but the present invention is not limited to these examples. First, the melanin production inhibitor of the present invention and the evaluation of its effect will be described.
【0024】[0024]
【実施例1】 メラニン産生抑制効果の評価 (1)メラニン産生抑制剤の調製 市販セドロール(フルカ社製、試薬特級)をエタノール
に1重量%の濃度となるよう溶かし、この溶液を希釈し
て濃度を調整し、これを用いて以下の実験を行った。Example 1 Evaluation of melanin production inhibitory effect (1) Preparation of melanin production inhibitor Commercially available cedrol (manufactured by Fluka, reagent grade) was dissolved in ethanol to a concentration of 1% by weight, and this solution was diluted to give a concentration. Was adjusted, and the following experiment was performed using this.
【0025】(2)色素細胞に対するメラニン産生抑制
効果の評価 (試験方法)プラスチック培養フラスコ(75cm2)
内の10%牛胎児血清を含むイーグルMEM培地に、3
×104個のマウスメラノーマ由来細胞B−16を播種
し、5%二酸化炭素、37℃の条件下にて培養した。2
日後、上記セドロールの1重量%溶液を、セドロールが
培地中の濃度で5〜20μMとなるように添加し、さら
に4日間培養した。培養終了後、培地を取り出し、平衡
リン酸緩衝塩溶液(PBS)で洗浄後、トリプシン及び
EDTA含有溶液を使用して細胞を剥離させ、遠心分離
機により細胞を回収した。(2) Evaluation of melanin production inhibitory effect on pigment cells (Test method) Plastic culture flask (75 cm 2 )
Eagle's MEM medium containing 10% fetal calf serum
× 10 4 mouse melanoma-derived cells B-16 were seeded and cultured under the conditions of 5% carbon dioxide and 37 ° C. 2
One day later, a 1% by weight solution of cedrol was added so that the concentration of cedrol was 5 to 20 μM in the medium, and the cells were further cultured for 4 days. After completion of the culture, the medium was taken out, washed with an equilibrated phosphate buffered saline (PBS), the cells were detached using a solution containing trypsin and EDTA, and the cells were collected by a centrifuge.
【0026】細胞をPBSで洗浄した後、沈渣に1N水
酸化ナトリウムを加え加熱溶解した。冷却後クロロホル
ムを加えて攪拌し、再び遠心分離した。これによって得
られた上清を400nmの吸光度で測定し、予め合成メ
ラニンを用いて作成した検量線よりメラニン量を求め
た。その結果を表1に示す。尚、細胞数は、セドロール
を添加しないコントロールを100%として求めた。ま
たメラニン量は、106個の細胞当たりの量に換算し、
セドロールを添加しないコントロールを100%として
求めた。After washing the cells with PBS, 1N sodium hydroxide was added to the precipitate and dissolved by heating. After cooling, chloroform was added, the mixture was stirred, and centrifuged again. The supernatant thus obtained was measured at an absorbance of 400 nm, and the amount of melanin was determined from a calibration curve previously prepared using synthetic melanin. Table 1 shows the results. In addition, the number of cells was determined assuming that a control without adding cedrol was 100%. In addition, the amount of melanin is converted to the amount per 10 6 cells,
The control without adding cedrol was determined as 100%.
【0027】[0027]
【表1】 [Table 1]
【0028】表1の結果から明らかなように、セドロー
ルは色素細胞に対するメラニン産生抑制効果を有し、少
量であってもこの効果が顕著なものであることが明らか
となった。尚、この時、色素細胞に対する毒性は全く認
められなかった。As is clear from the results in Table 1, it was found that cedrol has a melanin production inhibitory effect on pigment cells, and this effect is remarkable even in a small amount. At this time, no toxicity to the pigment cells was observed.
【0029】[0029]
【実施例2】 水中油型クリーム (製法)表2の(A)の各成分を混合して、80℃に加
熱した。(A)とは別に(B)の各成分を混合して80
℃に加熱した。(A)の成分に(B)の成分を加えて撹
拌乳化し、その後35℃まで冷却して水中油型クリーム
を得た。Example 2 Oil-in-water cream (Preparation method) Each component of (A) in Table 2 was mixed and heated to 80 ° C. The components of (B) are mixed separately from (A) to 80
Heated to ° C. The component (B) was added to the component (A), and the mixture was emulsified with stirring, and then cooled to 35 ° C. to obtain an oil-in-water cream.
【0030】[0030]
【表2】 [Table 2]
【0031】[0031]
【実施例3】 実使用テスト 次に、本発明の皮膚外用剤が如何に皮膚色素沈着症の予
防及び改善効果の点で優れているかを実証するため、実
施例2に示した水中油型クリームを用いて、長期連続使
用による実使用テストを行いその効力を確認した。比較
品としては、実施例2におけるセドロールを精製水に置
き換えて調製した水中油型クリームを用いた。Example 3 Actual use test Next, in order to demonstrate how the external preparation for skin of the present invention is superior in the effect of preventing and improving skin pigmentation, the oil-in-water cream shown in Example 2 was used. Was used to conduct a long-term continuous use test to confirm its efficacy. As a comparative product, an oil-in-water cream prepared by replacing cedrol in Example 2 with purified water was used.
【0032】(試験方法)色黒、シミ、ソバカスに悩む
女性ボランティア40名を、統計的に同等な2群に分
け、A群の顔面には、本発明品である実施例2の水中油
型クリームを、B群の顔面には比較品の水中油型クリー
ムをそれぞれ3ヶ月間使用してもらった。3ヶ月後の色
素沈着に対する改善効果を肉眼観察により評価し、群間
比較を行なった。その結果を表3に示す。尚、有効率は
やや改善以上の効果が認められた場合を有効とした。(Test Method) Forty female volunteers suffering from black-and-white, spots and freckles were divided into two statistically equivalent groups, and the face of Group A was covered with the oil-in-water type of Example 2 of the present invention. The cream was used, and a comparative oil-in-water cream was used on the face of Group B for 3 months. The improvement effect on pigmentation three months later was evaluated by visual observation, and comparison between groups was performed. Table 3 shows the results. In addition, the effective rate was considered to be effective when an effect more than slightly improved was recognized.
【0033】[0033]
【表3】 [Table 3]
【0034】表3の結果に示されるように、本発明の皮
膚外用剤は比較品に比し、格段に有効な皮膚色素沈着症
の予防及び改善効果を有することが証明された。尚、本
発明の皮膚外用剤塗布部位において、皮膚に好ましくな
い反応は観察されず、本発明の皮膚外用剤は、安全性の
高いことも併せて確認された。As shown in the results in Table 3, it was proved that the external preparation for skin of the present invention had a significantly more effective preventive and ameliorating effect on skin pigmentation than the comparative product. In addition, no undesired reaction on the skin was observed at the site where the external preparation for skin of the present invention was applied, and it was also confirmed that the external preparation for skin of the present invention had high safety.
【0035】[0035]
【実施例4】 乳液 (製法)表4の(A)成分及び(B)成分を70℃で各
々撹拌しながら溶解した。(B)成分に(A)成分を加
え予備乳化を行った後、ホモミキサーで均一に乳化し
た。乳化後かき混ぜながら30℃まで冷却し、乳液を得
た。Example 4 Emulsion (Production method) The components (A) and (B) in Table 4 were dissolved at 70 ° C. while stirring. After the component (A) was added to the component (B) and pre-emulsification was performed, the mixture was uniformly emulsified with a homomixer. After emulsification, the mixture was cooled to 30 ° C. with stirring to obtain an emulsion.
【0036】[0036]
【表4】 [Table 4]
【0037】[0037]
【実施例5】 化粧水 (製法)表5の(A)の各成分を混合し室温下にて溶解
し、また(B)の各成分も混合し室温下に溶解した。
(B)成分を(A)成分に加えて可溶化し、化粧水を得
た。Example 5 Lotion (Production method) Each component of (A) in Table 5 was mixed and dissolved at room temperature, and each component of (B) was also mixed and dissolved at room temperature.
The component (B) was added to the component (A) and solubilized to obtain a lotion.
【0038】[0038]
【表5】 [Table 5]
【0039】[0039]
【実施例6】 パック料 (製法)表6の(A)を室温にて分散溶解し、これに
(B)成分を加えて均一に溶解してパック料を得た。Example 6 Packing Charge (Production Method) (A) in Table 6 was dispersed and dissolved at room temperature, and the component (B) was added thereto and uniformly dissolved to obtain a packing charge.
【0040】[0040]
【表6】 [Table 6]
【0041】[0041]
【発明の効果】本発明のメラニン産生抑制剤によれば、
効果的にメラニン産生を抑制することができる。また、
このメラニン産生抑制剤を含有する皮膚外用剤は、皮膚
沈着症を効果的に予防、改善し、皮膚の黒化を防止する
ことができ、しかも皮膚に対する弊害がなく安全に使用
することができる。According to the melanin production inhibitor of the present invention,
It can effectively suppress melanin production. Also,
The external preparation for skin containing this melanin production inhibitor can effectively prevent and improve skin deposition and prevent blackening of the skin, and can be used safely without any harm to the skin.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A61K 31/045 ADA A61K 31/045 ADA ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code Agency reference number FI Technical display location A61K 31/045 ADA A61K 31/045 ADA
Claims (3)
とするメラニン産生抑制剤。1. A melanin production inhibitor comprising cedrol as an active ingredient.
含有することを特徴とする皮膚外用剤。2. An external preparation for skin, comprising the melanin production inhibitor according to claim 1.
ールに換算して0.01〜10重量%である請求項2に
記載の皮膚外用剤。3. The external preparation for skin according to claim 2, wherein the content of the melanin production inhibitor is 0.01 to 10% by weight in terms of cedrol.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19472096A JPH1036246A (en) | 1996-07-24 | 1996-07-24 | Suppressant for melanogenesis and preparation for external use for skin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19472096A JPH1036246A (en) | 1996-07-24 | 1996-07-24 | Suppressant for melanogenesis and preparation for external use for skin |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH1036246A true JPH1036246A (en) | 1998-02-10 |
Family
ID=16329131
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19472096A Pending JPH1036246A (en) | 1996-07-24 | 1996-07-24 | Suppressant for melanogenesis and preparation for external use for skin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH1036246A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001013881A1 (en) * | 1999-08-24 | 2001-03-01 | Kao Corporation | Cosmetics |
| EP1031348A3 (en) * | 1999-02-22 | 2001-03-21 | Kao Corporation | Interleukin-4 production inhibitors |
| WO2003028673A1 (en) * | 2001-09-11 | 2003-04-10 | Kao Corporation | Cosmetic preparation |
| US7125911B2 (en) | 2000-02-10 | 2006-10-24 | Kao Corporation | Autonomic nerve regulating agent |
| KR101142009B1 (en) | 2009-07-20 | 2012-05-17 | 주식회사 코리아나화장품 | Cosmetic Composition Comprising Extract of Glyptostrobus pensilis as Active Ingredient |
| KR101145814B1 (en) | 2008-10-09 | 2012-07-09 | 주식회사 엘지생활건강 | Composition for improving skin wrinkle |
| KR101240816B1 (en) | 2010-12-17 | 2013-03-07 | 서울대학교산학협력단 | Cryptomeria japonica extracts having whitening effect and anti-oxydation activity |
| CN107920983A (en) * | 2015-08-10 | 2018-04-17 | 高砂香料工业株式会社 | Melanogenesis inhibitor |
| WO2024246279A1 (en) * | 2023-05-31 | 2024-12-05 | Chemcom S.A. | Lightening compositions and use of compounds as depigmenting agents |
-
1996
- 1996-07-24 JP JP19472096A patent/JPH1036246A/en active Pending
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6974596B2 (en) | 1999-02-22 | 2005-12-13 | Kao Corporation | Interleukin-4 production inhibitors |
| EP1031348A3 (en) * | 1999-02-22 | 2001-03-21 | Kao Corporation | Interleukin-4 production inhibitors |
| US6960359B2 (en) | 1999-02-22 | 2005-11-01 | Kao Corporation | Interleukin-4 production inhibitors |
| WO2001013881A1 (en) * | 1999-08-24 | 2001-03-01 | Kao Corporation | Cosmetics |
| JP2009051835A (en) * | 2000-02-10 | 2009-03-12 | Kao Corp | Autonomic nerve regulator |
| US7125911B2 (en) | 2000-02-10 | 2006-10-24 | Kao Corporation | Autonomic nerve regulating agent |
| WO2003028673A1 (en) * | 2001-09-11 | 2003-04-10 | Kao Corporation | Cosmetic preparation |
| KR101145814B1 (en) | 2008-10-09 | 2012-07-09 | 주식회사 엘지생활건강 | Composition for improving skin wrinkle |
| KR101142009B1 (en) | 2009-07-20 | 2012-05-17 | 주식회사 코리아나화장품 | Cosmetic Composition Comprising Extract of Glyptostrobus pensilis as Active Ingredient |
| KR101240816B1 (en) | 2010-12-17 | 2013-03-07 | 서울대학교산학협력단 | Cryptomeria japonica extracts having whitening effect and anti-oxydation activity |
| CN107920983A (en) * | 2015-08-10 | 2018-04-17 | 高砂香料工业株式会社 | Melanogenesis inhibitor |
| US20180228720A1 (en) * | 2015-08-10 | 2018-08-16 | Takasago International Corporation | Melanogenesis inhibitor |
| EP3335694B1 (en) * | 2015-08-10 | 2023-09-27 | Takasago International Corporation | Melanogenesis inhibitor |
| WO2024246279A1 (en) * | 2023-05-31 | 2024-12-05 | Chemcom S.A. | Lightening compositions and use of compounds as depigmenting agents |
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