JP2003113031A - Skin care preparation - Google Patents
Skin care preparationInfo
- Publication number
- JP2003113031A JP2003113031A JP2001337078A JP2001337078A JP2003113031A JP 2003113031 A JP2003113031 A JP 2003113031A JP 2001337078 A JP2001337078 A JP 2001337078A JP 2001337078 A JP2001337078 A JP 2001337078A JP 2003113031 A JP2003113031 A JP 2003113031A
- Authority
- JP
- Japan
- Prior art keywords
- production example
- skin
- replaced
- effect
- schindl
- 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 23
- 239000004927 clay Substances 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 14
- 239000000284 extract Substances 0.000 abstract description 6
- 230000037303 wrinkles Effects 0.000 abstract description 5
- 239000002537 cosmetic Substances 0.000 abstract description 4
- 241000249490 Anthyllis Species 0.000 abstract description 2
- 244000285094 Flemingia macrophylla Species 0.000 abstract description 2
- 244000212114 Lathyrus maritimus Species 0.000 abstract description 2
- 235000007300 Lathyrus maritimus Nutrition 0.000 abstract description 2
- 241000750617 Lotus tenuis Species 0.000 abstract description 2
- 241000522226 Campylotropis Species 0.000 abstract 3
- 206010040849 Skin fissures Diseases 0.000 abstract 2
- 238000004061 bleaching Methods 0.000 abstract 2
- 244000144706 Aeschynomene indica Species 0.000 abstract 1
- 235000004051 Aeschynomene indica Nutrition 0.000 abstract 1
- 240000004500 Alysicarpus vaginalis Species 0.000 abstract 1
- 241000565319 Butea monosperma Species 0.000 abstract 1
- 241001279229 Campylotropis delavayi Species 0.000 abstract 1
- 240000005099 Cercis occidentalis Species 0.000 abstract 1
- 235000006228 Cercis occidentalis Nutrition 0.000 abstract 1
- 241001127579 Flemingia philippinensis Species 0.000 abstract 1
- 244000169660 Flemingia strobilifera Species 0.000 abstract 1
- 241000913796 Fordia cauliflora Species 0.000 abstract 1
- 241001258488 Lathyrus quinquenervius Species 0.000 abstract 1
- 241000215452 Lotus corniculatus Species 0.000 abstract 1
- 241000350318 Lysidice rhodostegia Species 0.000 abstract 1
- 241001423217 Ormosia henryi Species 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 description 123
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 49
- 239000000203 mixture Substances 0.000 description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 32
- 239000008213 purified water Substances 0.000 description 28
- 238000000034 method Methods 0.000 description 25
- 239000000706 filtrate Substances 0.000 description 21
- 238000003756 stirring Methods 0.000 description 19
- 241000196324 Embryophyta Species 0.000 description 15
- 238000005520 cutting process Methods 0.000 description 14
- 238000001914 filtration Methods 0.000 description 8
- 208000034656 Contusions Diseases 0.000 description 7
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 241001480167 Lotus japonicus Species 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 229940058015 1,3-butylene glycol Drugs 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 235000019437 butane-1,3-diol Nutrition 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000002087 whitening effect Effects 0.000 description 3
- 235000003932 Betula Nutrition 0.000 description 2
- 241000219429 Betula Species 0.000 description 2
- 244000280842 Corchorus trilocularis Species 0.000 description 2
- 206010011224 Cough Diseases 0.000 description 2
- 240000002853 Nelumbo nucifera Species 0.000 description 2
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 208000004880 Polyuria Diseases 0.000 description 2
- 206010037660 Pyrexia Diseases 0.000 description 2
- 206010040880 Skin irritation Diseases 0.000 description 2
- 206010053262 Skin swelling Diseases 0.000 description 2
- 244000300264 Spinacia oleracea Species 0.000 description 2
- 235000009337 Spinacia oleracea Nutrition 0.000 description 2
- 206010052428 Wound Diseases 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 230000035619 diuresis Effects 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 206010039073 rheumatoid arthritis Diseases 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 102220240796 rs553605556 Human genes 0.000 description 2
- 230000036556 skin irritation Effects 0.000 description 2
- 231100000475 skin irritation Toxicity 0.000 description 2
- KEEKMOIRJUWKNK-CABZTGNLSA-N (2S)-2-[[2-[(4R)-4-(difluoromethyl)-2-oxo-1,3-thiazolidin-3-yl]-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepin-9-yl]amino]propanamide Chemical compound FC([C@H]1N(C(SC1)=O)C=1N=C2N(CCOC3=C2C=CC(=C3)N[C@H](C(=O)N)C)C=1)F KEEKMOIRJUWKNK-CABZTGNLSA-N 0.000 description 1
- BIIBYWQGRFWQKM-JVVROLKMSA-N (2S)-N-[4-(cyclopropylamino)-3,4-dioxo-1-[(3S)-2-oxopyrrolidin-3-yl]butan-2-yl]-2-[[(E)-3-(2,4-dichlorophenyl)prop-2-enoyl]amino]-4,4-dimethylpentanamide Chemical compound CC(C)(C)C[C@@H](C(NC(C[C@H](CCN1)C1=O)C(C(NC1CC1)=O)=O)=O)NC(/C=C/C(C=CC(Cl)=C1)=C1Cl)=O BIIBYWQGRFWQKM-JVVROLKMSA-N 0.000 description 1
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
- UXHQLGLGLZKHTC-CUNXSJBXSA-N 4-[(3s,3ar)-3-cyclopentyl-7-(4-hydroxypiperidine-1-carbonyl)-3,3a,4,5-tetrahydropyrazolo[3,4-f]quinolin-2-yl]-2-chlorobenzonitrile Chemical compound C1CC(O)CCN1C(=O)C1=CC=C(C=2[C@@H]([C@H](C3CCCC3)N(N=2)C=2C=C(Cl)C(C#N)=CC=2)CC2)C2=N1 UXHQLGLGLZKHTC-CUNXSJBXSA-N 0.000 description 1
- RSIWALKZYXPAGW-NSHDSACASA-N 6-(3-fluorophenyl)-3-methyl-7-[(1s)-1-(7h-purin-6-ylamino)ethyl]-[1,3]thiazolo[3,2-a]pyrimidin-5-one Chemical compound C=1([C@@H](NC=2C=3N=CNC=3N=CN=2)C)N=C2SC=C(C)N2C(=O)C=1C1=CC=CC(F)=C1 RSIWALKZYXPAGW-NSHDSACASA-N 0.000 description 1
- BWJHJLINOYAPEG-HOTGVXAUSA-N 8-chloro-6-[(6-chloropyridin-3-yl)methyl]-3-[(1S,2S)-2-hydroxycyclopentyl]-7-methyl-2H-1,3-benzoxazin-4-one Chemical compound ClC1=C(C(=CC=2C(N(COC=21)[C@@H]1[C@H](CCC1)O)=O)CC=1C=NC(=CC=1)Cl)C BWJHJLINOYAPEG-HOTGVXAUSA-N 0.000 description 1
- 206010063409 Acarodermatitis Diseases 0.000 description 1
- 241000838706 Alysicarpus Species 0.000 description 1
- 241000217377 Amblema plicata Species 0.000 description 1
- 241000282817 Bovidae Species 0.000 description 1
- 241000726739 Butea Species 0.000 description 1
- 241000334161 Cercis chinensis Species 0.000 description 1
- 241001137251 Corvidae Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- LRULVYSBRWUVGR-FCHUYYIVSA-N GSK2879552 Chemical compound C1=CC(C(=O)O)=CC=C1CN1CCC(CN[C@H]2[C@@H](C2)C=2C=CC=CC=2)CC1 LRULVYSBRWUVGR-FCHUYYIVSA-N 0.000 description 1
- 241000928943 Hirtella <Actinopterygii> Species 0.000 description 1
- 241000134253 Lanka Species 0.000 description 1
- 241000219729 Lathyrus Species 0.000 description 1
- 241000219734 Lathyrus ochrus Species 0.000 description 1
- 241001127702 Lysidice <polychaete> Species 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- UQONAEXHTGDOIH-AWEZNQCLSA-N O=C(N1CC[C@@H](C1)N1CCCC1=O)C1=CC2=C(NC3(CC3)CCO2)N=C1 Chemical compound O=C(N1CC[C@@H](C1)N1CCCC1=O)C1=CC2=C(NC3(CC3)CCO2)N=C1 UQONAEXHTGDOIH-AWEZNQCLSA-N 0.000 description 1
- 241000337007 Oceania Species 0.000 description 1
- 241000522652 Ormosia <angiosperm> Species 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 1
- 241000447727 Scabies Species 0.000 description 1
- 244000292071 Scorzonera hispanica Species 0.000 description 1
- 235000018704 Scorzonera hispanica Nutrition 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 208000006981 Skin Abnormalities Diseases 0.000 description 1
- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- MCRWZBYTLVCCJJ-DKALBXGISA-N [(1s,3r)-3-[[(3s,4s)-3-methoxyoxan-4-yl]amino]-1-propan-2-ylcyclopentyl]-[(1s,4s)-5-[6-(trifluoromethyl)pyrimidin-4-yl]-2,5-diazabicyclo[2.2.1]heptan-2-yl]methanone Chemical compound C([C@]1(N(C[C@]2([H])C1)C(=O)[C@@]1(C[C@@H](CC1)N[C@@H]1[C@@H](COCC1)OC)C(C)C)[H])N2C1=CC(C(F)(F)F)=NC=N1 MCRWZBYTLVCCJJ-DKALBXGISA-N 0.000 description 1
- ODUIXUGXPFKQLG-QWRGUYRKSA-N [2-(4-chloro-2-fluoroanilino)-5-methyl-1,3-thiazol-4-yl]-[(2s,3s)-2,3-dimethylpiperidin-1-yl]methanone Chemical compound C[C@H]1[C@@H](C)CCCN1C(=O)C1=C(C)SC(NC=2C(=CC(Cl)=CC=2)F)=N1 ODUIXUGXPFKQLG-QWRGUYRKSA-N 0.000 description 1
- LPQOADBMXVRBNX-UHFFFAOYSA-N ac1ldcw0 Chemical compound Cl.C1CN(C)CCN1C1=C(F)C=C2C(=O)C(C(O)=O)=CN3CCSC1=C32 LPQOADBMXVRBNX-UHFFFAOYSA-N 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000020411 cell activation Effects 0.000 description 1
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- 239000003795 chemical substances by application Substances 0.000 description 1
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- 230000001186 cumulative effect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 201000006549 dyspepsia Diseases 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003172 expectorant agent Substances 0.000 description 1
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- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 201000006747 infectious mononucleosis Diseases 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- AYOOGWWGECJQPI-NSHDSACASA-N n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-3-(3-propan-2-yloxy-1h-pyrazol-5-yl)imidazo[4,5-b]pyridin-5-amine Chemical compound N1C(OC(C)C)=CC(N2C3=NC(N[C@@H](C)C=4N=CC(F)=CN=4)=CC=C3N=C2)=N1 AYOOGWWGECJQPI-NSHDSACASA-N 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 238000011076 safety test Methods 0.000 description 1
- 208000005687 scabies Diseases 0.000 description 1
- OEBIHOVSAMBXIB-SJKOYZFVSA-N selitrectinib Chemical compound C[C@@H]1CCC2=NC=C(F)C=C2[C@H]2CCCN2C2=NC3=C(C=NN3C=C2)C(=O)N1 OEBIHOVSAMBXIB-SJKOYZFVSA-N 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
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- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- KMIOJWCYOHBUJS-HAKPAVFJSA-N vorolanib Chemical compound C1N(C(=O)N(C)C)CC[C@@H]1NC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C KMIOJWCYOHBUJS-HAKPAVFJSA-N 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
Description
【発明の詳細な説明】
【0001】
【発明の属する技術分野】本発明は医薬品、医薬部外品
や化粧品などの皮膚外用剤に関するものである。さらに
詳しくはクサネム、ササハギ、ウンド.クレー、ジュケ
ツ、ハナズオウ、サンリョウシコウシショウ、ギショウ
コウシショウ、セイナンコウシショウ、ケコウシショ
ウ、カンカトウ、ジンホア、ミヤコグサ、ワタリミヤコ
グサ、レンリソウ、ハマエンドウ、ダイヨウセンキンバ
ツ、ツルセンキンバツ、マルホバナセンキンバツ、カリ
ンボクの抽出物の1種以上を配合することを特徴とした
安全で有効な皮膚外用剤に関するものである。
【0002】
【従来の技術】クサネム(学名=Aeschynome
ne indica L.)は温帯から熱帯に分布し、
日本では広く田や川辺などの湿地に見られる一年草であ
る。全草を利尿約として用いられる。
ササハギ(学名=Alysicarpus vagin
alis)は東半球の熱帯地方に広く分布し、空き地や
草地に多く生える多年草で種子を消化不良や咳止め薬と
して応用されている。
ウンド.クレー(学名=Anthyllis vule
neraria L.)はヨーロッパの芝生、森林、道
端に広く見られる。全草を打ち身や傷の治療に用いられ
る。
【0003】ジュケツ(学名=Butea monos
perma)はインド、スリランカ、ミヤンマーの森林
に分布する、高さ10〜30mの高木で、葉は利尿、収
斂などに用いられる。
ハナズオウ(学名=Cercis chinensi
s)、別称=紫荊は中国の華北、華南、中南、西南地方
の山の斜面や渓流沿い、低木の茂みに分布する低木で打
撲症などに樹皮(紫荊皮)が応用されている。
サンリョウシコウシショウ(三稜枝杭支梢)(学名=C
ampylotropis trigonoclada
Schindl)は中国の雲南、貴州、四川の各省の
山の斜面の林や低木の茂みなどに生える低木で発熱や打
撲症に枝葉や根を用いる。
ギショコウシショウ(宜昌杭支梢)(学名=Campy
lotropis ichangensis Schi
ndl)は中国の四川、湖北、江西、安徽、江蘇の各省
の山地の草の斜面や谷間に生える低木でその枝葉や根を
下痢や打撲症に用いる。
セイナンコウシショウ(西南杭支梢)(学名=Camp
ylotropisdelavayi Schind
l)は中国の雲南、貴州、四川の各省の乾燥地帯の低木
の茂みや叢などに生える低木で発熱や打撲症に枝葉や根
を用いる。
ケコウシショウ(毛杭支梢)(学名=Campylot
ropis hirtella Schindl)は中
国の雲南、四川の各省の山渓辺や水田、叢、山地の低木
内などに生える低木でうっ血や解毒に枝葉や根を用い
る。
【0004】カンカトウ(幹花豆)(学名=Fordi
a cauliflora)は中国の広東省、広西自治
区の山の斜面、谷間の疎林、谷間周辺に生える低木でる
低木でその枝葉や根を関節リュウマチや打撲症に用い
る。
ジンホア(学名=Lysidice rhodoste
gia)は中国の雲南、貴州、広西、広東の各省や台湾
の川辺や雑木林の中などに生える高木でその枝葉や根を
うっ血や腫れ物に用いる。
ミヤコグサ(学名=Lotus corniculat
us L.)は日本、中国、台湾、朝鮮、ヒマラヤ、オ
セアニア、北アメリカ、アフリカ北部等の温帯から亜熱
帯の道端や叢、田の畦などの湿地に生える多年草で根を
吐瀉や解熱に用いる。
ワタリミヤコグサ(学名=Lotus tenuis
Kitag)は中国の甘粛、陜西、山西、貴州の各省や
新疆ウイグル自治区やヨーロッパの草地や水辺に生える
多年草でその枝葉を解熱、止血薬として用いる。
【0005】レンリソウ(学名=Lathyrus q
uinquenervius LitvまたはL.pa
lustris L.var.lineaifoli
u)は日本の本州、九州、朝鮮、中国、東シベリアの温
帯のやや湿気のある草原などに生える多年草で全草を解
毒、疥癬に用いる。
ハマエンドウ(学名=Lathyrus mariti
mus Bigel)は日本、アジア北部、ヨーロッパ
北部、北アメリカの温帯から暖帯の海岸の砂地に生える
多年草で全草を薬として用いる。
ダイヨウセンキンバツ(大葉千斤抜)エノキマメ(学名
=Moghaniamacrophylla)は中国の
江西、福建、四川、雲南、貴州、広西、広東の各省や台
湾の山の斜面や荒地や低木の茂みに生える低木で根を関
節リュウマチ、打撲症に用いる。
ツルセンキンバツ(蔓性千斤抜)(学名=Moghan
ia philippinensis)は中国の湖南、
湖北、貴州、広西、広東、福建の各省や台湾、フィリピ
ンの山地の草地に生える低木で根を結構促進、発汗に用
いる。
マルホバナセンキンバツ(球穂花千斤抜)(学名=Mo
ghania strobilifera)は中国の雲
南、広東の各省や台湾、フィリピン、インド、マレーシ
アの叢に生える低木で根を止咳、去痰などに用いる。
カリンボク(花梨木)(学名=Ormosia hen
ryi Prain)は中国の湖南、湖北、江西、福
建、四川、雲南、貴州、広東、安徽、浙江の各省やベト
ナムの雑木林に生える常緑の小高木で枝葉を風邪や解毒
に用いる。
【0006】
【発明が解決しようとする課題】化粧品をはじめとする
皮膚外用剤は長期間に渡って連用されることがあり、皮
膚という面積の多い臓器に適用されるため、安全性は最
重視される項目の1つでまた、皮膚外用剤にとって必要
な有効性は様々にあるが、特に、日本では肌が白いこと
が好まれるので美白作用は重要な皮膚外用剤の有効性の
1つである。また、肌荒れ改善効果、肌のはり、シワ改
善効果、化粧ののりの改善効果などが求められている。
【0007】
【発明が解決するための手段】安全性と皮膚との有効性
を考え、鋭意検討した結果、クサネム、ササハギ、ウン
ド.クレー、ジュケツ、ハナズオウ、サンリョウシコウ
シショウ、ギショウコウシショウ、セイナンコウシショ
ウ、ケコウシショウ、カンカトウ、ジンホア、ミヤコグ
サ、ワタリミヤコグサ、レンリソウ、ハマエンドウ、ダ
イヨウセンキンバツ、ツルセンキンバツ、マルホバナセ
ンキバツ、カリンボクの抽出物を配合することが本発明
の目的に最適なことが判明した。
【0008】クサネム、ササハギ、ウンド.クレー、ジ
ュケツ、ハナズオウ、サンリョウシコウシショウ、ギシ
ョウコウシショウ、セイナンコウシショウ、ケコウシシ
ョウ、カンカトウ、ジンホア、ミヤコグサ、ワタリミヤ
コグサ、レンリソウ、ハマエンドウ、ダイヨウセンキン
バツ、ツルセンキンバツ、マルホバナセンキバツ、カリ
ンボクの抽出物抽出物の利用方法は特に限定はないが、
抽出物として利用する場合は、抽出を容易にするため、
必要によりミキサーなどで裁断、粉砕する。これを水或
いは親水性有機溶媒で抽出する。用いる親水性有機溶媒
はメタノール、エタノール、アセトン、グリセリン、
1,3ブチレングリコール、プロピレングリコール等、
あるいはこれらの混合物、あるいは1種以上の親水性有
機溶媒と水混合物で抽出する。しかし、皮膚に適用する
製剤であるので水やエタノールやグリセリンなど皮膚外
用剤に用いても問題ない溶媒の方が、溶媒の留去の必要
性がなく利用範囲が広い。本発明者らの実験では熱水抽
出か低濃度の親水性有機溶媒水溶液が好ましい。抽出条
件は裁断の程度や目的、溶媒の種類によって変化するが
水のみの場合はかなり加温が可能であり、100℃まで
加温しても有効性の低下は有意に低下することはない。
溶媒の種類や皮膚外用剤の剤型によっては溶媒を1部あ
るいはすべてを留去する。これを皮膚外用剤に配合す
る。
【0009】クサネム、ササハギ、ウンド.クレー、ジ
ュケツ、ハナズオウ、サンリョウシコウシショウ、ギシ
ョウコウシショウ、セイナンコウシショウ、ケコウシシ
ョウ、カンカトウ、ジンホア、ミヤコグサ、ワタリミヤ
コグサ、レンリソウ、ハマエンドウ、ダイヨウセンキン
バツ、ツルセンキンバツ、マルホバナセンキバツ、カリ
ンボクの抽出物を皮膚外用剤に配合するが、抽出方法や
配合目的などによって変化するが、配合量は固形分とし
て0.0001〜5.0%が好ましい。また、他の配合
する原料は限定されることはないので、自由に選択すれ
ばよいが、本発明の安全で有効性のある皮膚外用剤とい
う趣旨に反しない原料を選択することは当然のことであ
る。このため、美白や抗酸化、細胞賦活(細胞老化防
止)、保湿、肌荒れ防止及びその改善等に効果のある各
種の薬剤と併用することは本発明の目的をさらに効果的
にする。また、用途等によって、クリーム、乳液、ロー
ション、パック、スプレー、ジェル等任意の剤型より選
択することはなんら問題はない。
【0010】以下に実際の抽出方法の例である製造例と
製造例を配合した実施例を記載するが当然これらに限定
されることはない。
【0011】製造例−1
クサネムの全草の乾燥物100gを細断した後、精製水
2kgを加えて、80℃まで加熱し、5時間後、放冷し
たのち、濾紙で濾過後、濾液を減圧濃縮した。
【0012】製造例−2
クサネムの全草の乾燥物100gを細断した後、精製水
1kgとエタノール1kgを加えて、攪拌しつつ10日
間放置したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0013】製造例−3
クサネムの全草の乾燥物100gを細断した後、精製水
1kgと1,3ブチレングリコール1kgを加えて、攪
拌しつつ10日間放置したのち、濾紙で濾過後、濾液を
減圧濃縮した。
【0014】製造例−4
ササハギの種子の乾燥物100gを細断した後、精製水
1kgとエタノール1kgを加えて、攪拌しつつ10日
間放置したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0015】製造例−5
ウンド.クレーの全草の乾燥物100gを細断した後、
精製水1kgとエタノール1kgを加えて、攪拌しつつ
10日間放置したのち、濾紙で濾過後、濾液を減圧濃縮
した。
【0016】製造例−6
ジュケツの葉の乾燥物100gを細断した後、精製水1
kgとエタノール1kgを加えて、攪拌しつつ10日間
放置したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0017】製造例−7
ハナズオウの樹皮の乾燥物100gを細断した後、精製
水2kgを加えて、80℃まで加熱し、5時間後、放冷
したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0018】製造例−8
ハナズオウの樹皮の乾燥物100gを細断した後、精製
水1kgとエタノール1kgを加えて、攪拌しつつ10
日間放置したのち、濾紙で濾過後、濾液を減圧濃縮し
た。
【0019】製造例−9
サンリョウシコウシショウの枝葉の乾燥物100gを細
断した後、精製水1kgとエタノール1kgを加えて、
攪拌しつつ10日間放置したのち、濾紙で濾過後、濾液
を減圧濃縮した。
【0020】製造例−10
サンリョウシコウシショウの根の乾燥物100gを細断
した後、精製水1kgとエタノール1kgを加えて、攪
拌しつつ10日間放置したのち、濾紙で濾過後、濾液を
減圧濃縮した。
【0021】製造例−11
セイナンコウシショウの枝葉の乾燥物100gを細断し
た後、精製水2kgを加えて、80℃まで加熱し、5時
間後、放冷したのち、濾紙で濾過後、濾液を減圧濃縮し
た。
【0022】製造例−12
セイナンコウシショウの根の乾燥物100gを細断した
後、精製水2kgを加えて、80℃まで加熱し、5時間
後、放冷したのち、濾紙で濾過後、濾液を減圧濃縮し
た。
【0023】製造例−13
ケコウシショウの枝葉の乾燥物100gを細断した後、
精製水1kgとエタノール1kgを加えて、攪拌しつつ
10日間放置したのち、濾紙で濾過後、濾液を減圧濃縮
した。
【0024】製造例−14
ケコウシショウの根の乾燥物100gを細断した後、精
製水1kgとエタノール1kgを加えて、攪拌しつつ1
0日間放置したのち、濾紙で濾過後、濾液を減圧濃縮し
た。
【0025】製造例−15
カンカトウの枝葉の乾燥物100gを細断した後、精製
水1kgとエタノール1kgを加えて、攪拌しつつ10
日間放置したのち、濾紙で濾過後、濾液を減圧濃縮し
た。
【0026】製造例−16
カンカトウの根の乾燥物100gを細断した後、精製水
1kgとエタノール1kgを加えて、攪拌しつつ10日
間放置したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0027】製造例−17
ジンホアの枝葉の乾燥物100gを細断した後、精製水
1kgとエタノール1kgを加えて、攪拌しつつ10日
間放置したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0028】製造例−18
ジンホアの根の乾燥物100gを細断した後、精製水1
kgとエタノール1kgを加えて、攪拌しつつ10日間
放置したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0029】製造例−19
ミヤコグサの根の乾燥物100gを細断した後、精製水
1kgとエタノール1kgを加えて、攪拌しつつ10日
間放置したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0030】製造例−20
ミヤコグサの根の乾燥物100gを細断した後、精製水
2kgを加えて、80℃まで加熱し、5時間後、放冷し
たのち、濾紙で濾過後、濾液を減圧濃縮した。
【0031】製造例−21
ワタリミヤコグサの葉の乾燥物100gを細断した後、
精製水1kgとエタノール1kgを加えて、攪拌しつつ
10日間放置したのち、濾紙で濾過後、濾液を減圧濃縮
した。
【0032】製造例−22
レンリソウの全草の乾燥物100gを細断した後、精製
水1kgとエタノール1kgを加えて、攪拌しつつ10
日間放置したのち、濾紙で濾過後、濾液を減圧濃縮し
た。
【0033】製造例−23
レンリソウの全草の乾燥物100gを細断した後、精製
水2kgを加えて、80℃まで加熱し、5時間後、放冷
したのち、濾紙で濾過後、濾液を減圧濃縮した。
【0034】製造例−24
ハマエンドウの全草の乾燥物100gを細断した後、精
製水1kgとエタノール1kgを加えて、攪拌しつつ1
0日間放置したのち、濾紙で濾過後、濾液を減圧濃縮し
た。
【0035】製造例−25
ダイヨウセンキンバツの根の乾燥物100gを細断した
後、精製水1kgとエタノール1kgを加えて、攪拌し
つつ10日間放置したのち、濾紙で濾過後、濾液を減圧
濃縮した。
【0036】製造例−26
マルホバナセンキンバツの根の乾燥物100gを細断し
た後、精製水1kgとエタノール1kgを加えて、攪拌
しつつ10日間放置したのち、濾紙で濾過後、濾液を減
圧濃縮した。
【0037】製造例−27
マルホバナセンキンバツの根の乾燥物100gを細断し
た後、精製水1kgと1,3ブチレングリコール1kg
を加えて、攪拌しつつ10日間放置したのち、濾紙で濾
過後、濾液を減圧濃縮した。
【0038】製造例−28
カリンボクの枝葉の乾燥物100gを細断した後、精製
水1kgとエタノール1kgを加えて、攪拌しつつ10
日間放置したのち、濾紙で濾過後、濾液を減圧濃縮し
た。
【0039】実施例は表1に示す処方で、A、Bともに
80℃で加温溶解し、BをAに撹拌しながら徐々に加え
乳化する。撹拌しながら冷却し35℃で撹拌を止め、放
置する方法でクリームを作成した。
【0040】
【表1】
【0041】実施例5
実施例1の製造例1を製造例4に置き換え、他は実施例
1と同様に作成した。
【0042】実施例6
実施例2の製造例2を製造例5に置き換え、他は実施例
2と同様に作成した。
【0043】実施例7
実施例3の製造例3を製造例6に置き換え、他は実施例
3と同様に作成した。
【0044】実施例8
実施例1の製造例1を製造例4に、製造例2を製造例5
に、製造例3を製造例6に置き換え、他は実施例4と同
様に作成した。
【0045】実施例9
実施例1の製造例1を製造例7に置き換え、他は実施例
1と同様に作成した。
【0046】実施例10
実施例2の製造例2を製造例8に置き換え、他は実施例
2と同様に作成した。
【0047】実施例11
実施例3の製造例3を製造例9に置き換え、他は実施例
3と同様に作成した。
【0048】実施例12
実施例1の製造例1を製造例7に、製造例2を製造例8
に、製造例3を製造例9に置き換え、他は実施例4と同
様に作成した。
【0049】実施例13
実施例1の製造例1を製造例10に置き換え、他は実施
例1と同様に作成した。
【0050】実施例14
実施例2の製造例2を製造例11に置き換え、他は実施
例2と同様に作成した。
【0051】実施例15
実施例3の製造例3を製造例12に置き換え、他は実施
例3と同様に作成した。
【0052】実施例16
実施例1の製造例1を製造例10に、製造例2を製造例
11に、製造例3を製造例12に置き換え、他は実施例
4と同様に作成した。
【0053】実施例17
実施例1の製造例1を製造例13に置き換え、他は実施
例1と同様に作成した。
【0054】実施例18
実施例2の製造例2を製造例14に置き換え、他は実施
例2と同様に作成した。
【0055】実施例19
実施例3の製造例3を製造例15に置き換え、他は実施
例3と同様に作成した。
【0056】実施例20
実施例1の製造例1を製造例12に、製造例2を製造例
13に、製造例3を製造例6に置き換え、他は実施例1
4と同様に作成した。
【0057】実施例21
実施例1の製造例1を製造例16に置き換え、他は実施
例1と同様に作成した。
【0058】実施例22
実施例2の製造例2を製造例17に置き換え、他は実施
例2と同様に作成した。
【0059】実施例23
実施例3の製造例3を製造例18に置き換え、他は実施
例3と同様に作成した。
【0060】実施例24
実施例1の製造例1を製造例16に、製造例2を製造例
17に、製造例3を製造例18に置き換え、他は実施例
4と同様に作成した。
【0061】実施例25
実施例1の製造例1を製造例19に置き換え、他は実施
例1と同様に作成した。
【0062】実施例26
実施例2の製造例2を製造例20に置き換え、他は実施
例2と同様に作成した。
【0063】実施例27
実施例3の製造例3を製造例21に置き換え、他は実施
例3と同様に作成した。
【0064】実施例28
実施例1の製造例1を製造例19に、製造例2を製造例
20に、製造例3を製造例21に置き換え、他は実施例
4と同様に作成した。
【0065】実施例29
実施例1の製造例1を製造例22に置き換え、他は実施
例1と同様に作成した。
【0066】実施例30
実施例2の製造例2を製造例23に置き換え、他は実施
例2と同様に作成した。
【0067】実施例31
実施例3の製造例3を製造例24に置き換え、他は実施
例3と同様に作成した。
【0068】実施例32
実施例1の製造例1を製造例22に、製造例2を製造例
23に、製造例3を製造例24に置き換え、他は実施例
4と同様に作成した。
【0069】実施例33
実施例1の製造例1を製造例25に置き換え、他は実施
例1と同様に作成した。
【0070】実施例34
実施例2の製造例2を製造例26に置き換え、他は実施
例2と同様に作成した。
【0071】実施例35
実施例3の製造例3を製造例27に置き換え、他は実施
例3と同様に作成した。
【0072】実施例36
実施例1の製造例1を製造例25に、製造例2を製造例
26に、製造例3を製造例27に置き換え、他は実施例
4と同様に作成した。
【0073】実施例37
実施例1の製造例1を製造例28に置き換え、他は実施
例1と同様に作成した。
【0074】効果を確認するため、以下の実験を行っ
た。
【0075】以下の基準で、1つの実験につき5名で6
ヶ月使用後に肌の白さ、肌荒れ改善効果、肌のはり、シ
ワ改善効果、化粧ののりについて聞き取りした。結果を
表2および表3に示す。数字は平均値を表す。(なお、
試験期間中に皮膚の異常を訴えた人はいなかった)
使用前に比較して非常に改善した 3
使用前に比較してに改善した 2
使用前に比較してややに改善した 1
使用前と変化なし 0
使用前に比較して悪化した −1
使用前に比較してに悪化した −2
使用前に比較して非常に悪化した −3
【0076】
【表2】【0077】
【表3】【0078】安全性試験に関しては、皮膚一次刺激性試
験、皮膚累積刺激性試験、感作性試験、ヒトパッチテス
トを行ったがいずれも問題なかった。
【0079】
【発明の効果】クサネム、ササハギ、ウンド.クレー、
ジュケツ、ハナズオウ、サンリョウシコウシショウ、ギ
ショウコウシショウ、セイナンコウシショウ、ケコウシ
ショウ、カンカトウ、ジンホア、ミヤコグサ、ワタリミ
ヤコグサ、レンリソウ、ハマエンドウ、ダイヨウセンキ
ンバツ、ツルセンキンバツ、マルホバナセンキバツ、カ
リンボクの抽出物の1種以上を配合することを特徴とす
る皮膚外用剤、美白効果、肌荒れ改善効果、肌のはり、
シワ改善効果、化粧ののりが改善し、皮膚外用剤として
有効性の高いことがわかった。また、古くより食用とさ
れており、また各種の試験を行った結果からも安全性も
全く問題ないことは言うまでもない。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an external preparation for skin such as pharmaceuticals, quasi-drugs and cosmetics. For more details, Kusanem, Sasahagi and Wound. Klee, Juketsu, Hanazu-oh, San-Yoshi-Ko-shi-shaw, Giant-faced-ki-shaw-shaw, Seinan-shi-ko-sha-shi, Skeweed-shaw-shaw, Kanka-tou, Jin-hoa, Miyakogusa, Watari-miyako-gusa, Ren-ri-so, Hama-endo, Daisen-kinbatsu, Tulsen-kin-batsu, Malhovana-Kin-batsu, Malhovana-Kin-batsu The present invention relates to a safe and effective skin external preparation characterized by incorporating at least one extract. 2. Description of the Related Art Xanem (scientific name: Aesynome)
ne indica L. ) Ranges from temperate to tropical,
In Japan, it is an annual plant widely found in wetlands such as rice fields and riversides. Whole grass is used as diuresis. Sasahagi (scientific name = Alysicarpus vagin)
alis) is a perennial plant that is widely distributed in the tropics of the eastern hemisphere and grows in vacant lots and grasslands, and its seed is used as an indigestion and cough medicine. Und. Clay (scientific name = Anthyllis vule
neraria L. ) Are widely found on lawns, forests and roadsides in Europe. Whole grass is used to treat bruises and wounds. [0003] Juketsu (scientific name = Butea monos)
perma) is a tall tree with a height of 10 to 30 m, which is distributed in forests of India, Sri Lanka and Myanmar, and its leaves are used for diuresis and convergence. Hanazou (scientific name = Cercis chinensi
s), also known as Shijing, is a shrub distributed along the mountain slopes and mountain streams in northern, southern, central and southwestern China and in shrub bushes, and its bark (purple thorn bark) is applied to bruises and the like. Sanryo Oshiwashi (Surrounded by three ridges) (scientific name = C
ampytropis trigonoclada
Schindl) is a shrub that grows on mountain slope forests and shrub bushes in Yunnan, Guizhou and Sichuan provinces of China, and uses foliage and roots for fever and bruises. Gishokushiyusha (Yichang pile branch) (scientific name = Campy)
lotropis ichangensis Schi
ndl) is a shrub that grows on grass slopes and valleys in the mountains of Sichuan, Hubei, Jiangxi, Anhui and Jiangsu provinces in China, and uses its branches and leaves for diarrhea and bruises. Seinanushi-shi (Southwest pile support) (scientific name = Camp)
ylotropicsdelavayi School
l) is a shrub that grows in bushes and plexus of shrubs in dry areas in Yunnan, Guizhou and Sichuan provinces of China, and uses foliage and roots for fever and bruises. Scarlet Shaw (hair pile support) (scientific name = Campylot)
(ropis hirtella Schindl) is a shrub that grows in mountain valleys, paddy fields, flora, and shrubs in mountainous areas of Yunnan and Sichuan provinces in China, and uses branches and leaves and roots for congestion and detoxification. [0004] Kankato (stem flower bean) (scientific name = Fordi)
a cauliflora is a shrub that grows on mountain slopes, in valleys, and in valleys in Guangxi Autonomous Region, Guangdong Province, China, and uses its branches and leaves and roots for rheumatoid arthritis and bruises. Jinhua (scientific name = Lysidice rhodoste)
Gia) is a tree that grows in Yunnan, Guizhou, Guangxi, and Guangdong provinces of China and in riversides and coppice forests in Taiwan, and uses its branches and leaves for congestion and swelling. Lotus japonicus (scientific name = Lotus corniculat
us L. ) Is a perennial plant that grows in temperate zones such as Japan, China, Taiwan, Korea, the Himalayas, Oceania, North America, and northern Africa, and in subtropical roadsides, plexuses, and rice fields. Cottonweed (scientific name = Lotus tenuis)
Kitag) is a perennial plant that grows in the provinces of Gansu, Shaanxi, Shanxi and Guizhou in China, Xinjiang Uygur Autonomous Region and grasslands and watersides in Europe. [0005] Lotus root (scientific name = Lathyrus q
uinquenervius Litv or L. pa
lustris L .; var. lineaifoli
u) is a perennial plant that grows in temperate and slightly humid grasslands in Honshu, Kyushu, Korea, China and East Siberia in Japan, and detoxifies the whole plant and uses it for scabies. Yellow pea (scientific name = Lathyrus mariti
mus Bigel) is a perennial plant that grows on the sandy shores of temperate to temperate shores in Japan, northern Asia, northern Europe, and North America, and uses whole plants as medicines. The enamel bean (Scientific name = Moghaniamacrophylla) is a shrub that grows on mountain slopes, wastelands and shrub bushes in the provinces of Jiangxi, Fujian, Sichuan, Yunnan, Guizhou, Guangxi, Guangdong and Taiwan. The root is used for rheumatoid arthritis and bruises. Tsursenkinbatu (vines 1000 buns) (scientific name = Moghan
ia philippinensis) is Hunan, China.
The roots of the shrubs in Hubei, Guizhou, Guangxi, Guangdong, Fujian provinces and mountains of Taiwan and the Philippines are used to promote and sweat the roots. Malhovana Senkinbats
Ghonia stabilifera is a shrub that grows in the provinces of Yunnan and Guangdong in China, and in the flora of Taiwan, the Philippines, India and Malaysia, and its roots are used for coughing and expectorant. Karinboku (Kariniki) (scientific name = Ormosia hen)
(ryi Plan) is an evergreen small tree that grows in the provinces of Hunan, Hubei, Jiangxi, Fujian, Sichuan, Yunnan, Guizhou, Guangdong, Anhui, Zhejiang and Vietnam. [0006] Skin external preparations such as cosmetics are often used continuously for a long period of time, and are applied to organs having a large area such as the skin. There is a variety of efficacy requirements for skin external preparations, but whitening is particularly important in Japan because white skin is preferred. is there. Further, there is a demand for an effect of improving rough skin, an effect of improving skin swelling, wrinkles, and an effect of improving makeup sizing. Means for Solving the Problems As a result of intensive studies in consideration of safety and effectiveness with the skin, Kusanem, Sasahagi, Undo. Clay, Juketsu, Hanazuo, Sansho-shikihoshi, Gyokushikihoshihashi, Seinanshihihashi, Kokeshishah, Kankatou, Jinhua, Miyakogusa, Watarimiyakogusa, Renrensou, Hamaendo, Daisenkinbatsu, Tsurusenkinbatsu, Marhobanasenbuki It has been found that compounding the product is optimal for the purpose of the present invention. [0008] Kusanem, Sasahagi, Undo. Clay, Juketsu, Hanazuo, Sansho-shikihoshi, Gyokushikihoshihashi, Seinanshihihashi, Kokeshishah, Kankatou, Jinhua, Miyakogusa, Watarimiyakogusa, Renrensou, Hamaendo, Daisenkinbatsu, Tsurusenkinbatsu, Marhobanasenbuki There is no particular limitation on how to use the product extract,
When used as an extract, to facilitate extraction,
If necessary, cut and crush with a mixer. This is extracted with water or a hydrophilic organic solvent. The hydrophilic organic solvent used is methanol, ethanol, acetone, glycerin,
1,3 butylene glycol, propylene glycol, etc.
Alternatively, the mixture is extracted with a mixture thereof, or a mixture of at least one hydrophilic organic solvent and water. However, since it is a preparation to be applied to the skin, a solvent having no problem even when used for an external preparation for skin, such as water, ethanol, and glycerin, has a wider range of use because there is no need to remove the solvent. In our experiments, hot water extraction or a low concentration aqueous solution of a hydrophilic organic solvent is preferred. The extraction conditions vary depending on the degree of cutting, the purpose, and the type of the solvent, but when only water is used, considerable heating is possible, and even when the temperature is increased to 100 ° C., the effectiveness does not decrease significantly.
Depending on the type of the solvent and the form of the external preparation for skin, one part or all of the solvent is distilled off. This is mixed with a skin external preparation. Kusanem, Sasahagi, Undo. Clay, Juketsu, Hanazuo, Sansho-shikihoshi, Gyokushikihoshihashi, Seinanshihihashi, Kokeshishah, Kankatou, Jinhua, Miyakogusa, Watarimiyakogusa, Renrensou, Hamaendo, Daisenkinbatsu, Tsurusenkinbatsu, Marhobanasenbuki The compound is mixed with the external preparation for skin, and it varies depending on the extraction method and the purpose of mixing, but the compounding amount is preferably 0.0001 to 5.0% as a solid content. In addition, since the other ingredients to be blended are not limited, they may be freely selected, but it is a matter of course that ingredients that do not contradict the purpose of the safe and effective skin external preparation of the present invention are selected. It is. For this reason, the use of various agents effective for whitening, antioxidation, cell activation (prevention of cell aging), moisturization, prevention of rough skin and improvement thereof makes the object of the present invention more effective. In addition, there is no problem in selecting an arbitrary dosage form such as a cream, an emulsion, a lotion, a pack, a spray, and a gel depending on the use and the like. [0010] In the following, a production example as an example of an actual extraction method and an example in which the production example is blended will be described. Production Example 1 After cutting 100 g of dried whole plant of Kusanem, 2 kg of purified water was added, heated to 80 ° C., and after 5 hours, allowed to cool, filtered with filter paper, and the filtrate was filtered. It was concentrated under reduced pressure. Production Example 2 After 100 g of dried whole plant of Kusanem was chopped, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was allowed to stand for 10 days with stirring. After filtration with filter paper, the filtrate was concentrated under reduced pressure. . Preparation Example 3 After cutting 100 g of dried whole plant of Kusanem, 1 kg of purified water and 1 kg of 1,3-butylene glycol were added, and the mixture was allowed to stand for 10 days with stirring. Was concentrated under reduced pressure. Production Example-4 After cutting 100 g of dried seeds of Sasahagi, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was allowed to stand for 10 days with stirring. After filtration with filter paper, the filtrate was concentrated under reduced pressure. Production Example-5 Wind. After shredding 100 g of the dried clay whole plant,
After adding 1 kg of purified water and 1 kg of ethanol, the mixture was allowed to stand with stirring for 10 days, filtered with a filter paper, and the filtrate was concentrated under reduced pressure. Production Example-6 After cutting 100 g of dried dried bean leaves, chopped purified water 1
After addition of 1 kg of ethanol and 1 kg of ethanol, the mixture was allowed to stand with stirring for 10 days, filtered through filter paper, and concentrated under reduced pressure. Preparation Example 7 After 100 g of dried bark of Hanazou were cut into small pieces, 2 kg of purified water was added, heated to 80 ° C., and after 5 hours, allowed to cool, filtered with filter paper, and the filtrate was decompressed. Concentrated. Production Example-8 After cutting 100 g of dried bark of the Japanese bark, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was stirred for 10 hours.
After standing for a day, the mixture was filtered with filter paper, and the filtrate was concentrated under reduced pressure. Production Example-9 After cutting 100 g of dried leaves of the leaves of Sanrius oxensis, 1 kg of purified water and 1 kg of ethanol were added.
After standing for 10 days while stirring, the mixture was filtered with filter paper, and the filtrate was concentrated under reduced pressure. Production Example-10 After cutting 100 g of the dried product of the root of the sorghum magpie, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was allowed to stand for 10 days with stirring. After filtration with filter paper, the filtrate was decompressed. Concentrated. Preparation Example 11 After cutting 100 g of the dried leaves of the leaves of Saenanthus oleracea, 2 kg of purified water was added, the mixture was heated to 80 ° C., after 5 hours, allowed to cool, filtered through filter paper, and filtered. Was concentrated under reduced pressure. Production Example-12 After 100 g of dried roots of S. antelope were chopped, 2 kg of purified water was added, the mixture was heated to 80.degree. C., after 5 hours, allowed to cool, filtered through filter paper, and filtered. Was concentrated under reduced pressure. Production Example-13 After cutting 100 g of the dried product of the branches and leaves of Betula lucidum,
After adding 1 kg of purified water and 1 kg of ethanol, the mixture was allowed to stand with stirring for 10 days, filtered with a filter paper, and the filtrate was concentrated under reduced pressure. Preparation Example 14 After cutting 100 g of dried root of Betula serrata, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was stirred for 1 hour.
After standing for 0 days, the mixture was filtered with filter paper, and the filtrate was concentrated under reduced pressure. Production Example-15 After 100 g of the dried leaves of Kankatou were cut into small pieces, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was stirred for 10 minutes.
After standing for a day, the mixture was filtered with filter paper, and the filtrate was concentrated under reduced pressure. Production Example 16 After 100 g of dried dried coconut root was cut into pieces, 1 kg of purified water and 1 kg of ethanol were added, the mixture was allowed to stand with stirring for 10 days, filtered through filter paper, and concentrated under reduced pressure. Production Example 17 After 100 g of the dried leaves of Jinhua were cut into small pieces, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was allowed to stand for 10 days with stirring. After filtration with filter paper, the filtrate was concentrated under reduced pressure. Production Example 18 After 100 g of the dried product of the root of Jinhua were chopped, purified water 1
After addition of 1 kg of ethanol and 1 kg of ethanol, the mixture was allowed to stand with stirring for 10 days, filtered through filter paper, and concentrated under reduced pressure. Production Example-19 After 100 g of dried root of Lotus japonicus was chopped, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was allowed to stand for 10 days with stirring. After filtration with filter paper, the filtrate was concentrated under reduced pressure. Preparation Example 20 After 100 g of dried root of Lotus japonicus was chopped, 2 kg of purified water was added, heated to 80 ° C., and after 5 hours, allowed to cool, filtered with filter paper, and the filtrate was decompressed. Concentrated. Production Example 21 After chopping 100 g of dried leaves of cottonweed leaves,
After adding 1 kg of purified water and 1 kg of ethanol, the mixture was allowed to stand with stirring for 10 days, filtered with a filter paper, and the filtrate was concentrated under reduced pressure. Production Example-22 After 100 g of dried whole plant of spinach was chopped, 1 kg of purified water and 1 kg of ethanol were added, and 10 g of the mixture was stirred.
After standing for a day, the mixture was filtered with filter paper, and the filtrate was concentrated under reduced pressure. Preparation Example 23 After 100 g of dried whole plant of spinach was chopped, 2 kg of purified water was added, the mixture was heated to 80 ° C., 5 hours later, allowed to cool, filtered through filter paper, and filtered. It was concentrated under reduced pressure. Production Example-24 After cutting 100 g of dried whole plant of cucumbers, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was stirred for 1 hour.
After standing for 0 days, the mixture was filtered with filter paper, and the filtrate was concentrated under reduced pressure. Production Example-25 After cutting 100 g of dried roots of radish, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was allowed to stand with stirring for 10 days. After filtration with filter paper, the filtrate was filtered. It was concentrated under reduced pressure. Production Example-26 100 g of dried roots of malhovana serrata were chopped, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was allowed to stand with stirring for 10 days. After filtration with filter paper, the filtrate was filtered. It was concentrated under reduced pressure. Production Example 27 After drying 100 g of dried roots of malhovana serrata, 1 kg of purified water and 1 kg of 1,3-butylene glycol were obtained.
Was added, and the mixture was allowed to stand for 10 days with stirring. After filtration with filter paper, the filtrate was concentrated under reduced pressure. Production Example-28 After cutting 100 g of dried Karinboku branches and leaves, 1 kg of purified water and 1 kg of ethanol were added, and the mixture was stirred for 10 minutes.
After standing for a day, the mixture was filtered with filter paper, and the filtrate was concentrated under reduced pressure. In the examples, the formulations shown in Table 1 are used. Both A and B are heated and dissolved at 80 ° C., and B is gradually added to A while stirring to emulsify. The mixture was cooled with stirring, the stirring was stopped at 35 ° C., and a cream was prepared by leaving the mixture. [Table 1] Example 5 The same procedure as in Example 1 was carried out except that Production Example 1 of Example 1 was replaced with Production Example 4. Example 6 The procedure of Example 2 was repeated except that Production Example 2 of Example 2 was replaced with Production Example 5. Example 7 The procedure of Example 3 was repeated except that Production Example 3 of Example 3 was replaced with Production Example 6. Example 8 Production Example 1 of Example 1 is Production Example 4 and Production Example 2 is Production Example 5.
Then, Production Example 3 was replaced with Production Example 6, and the other conditions were the same as in Example 4. Example 9 The procedure of Example 1 was repeated except that Production Example 1 of Example 1 was replaced with Production Example 7. Example 10 The same procedure as in Example 2 was repeated except that Production Example 2 of Example 2 was replaced with Production Example 8. Example 11 The procedure of Example 3 was repeated except that Production Example 3 of Example 3 was replaced with Production Example 9. Example 12 Manufacturing Example 1 of Example 1 is changed to Manufacturing Example 7, and Manufacturing Example 2 is changed to Manufacturing Example 8.
Then, Production Example 3 was replaced with Production Example 9, and the other conditions were the same as in Example 4. Example 13 The same procedure as in Example 1 was carried out except that Production Example 1 of Example 1 was replaced with Production Example 10. Example 14 The procedure of Example 2 was repeated except that Production Example 2 of Example 2 was replaced with Production Example 11. Example 15 The same procedure as in Example 3 was carried out except that Production Example 3 of Example 3 was replaced with Production Example 12. Example 16 Production Example 1 of Example 1 was replaced with Production Example 10, Production Example 2 was replaced with Production Example 11, and Production Example 3 was replaced with Production Example 12, except for Example 4. Example 17 The procedure of Example 1 was repeated except that Production Example 1 of Example 1 was replaced with Production Example 13. Example 18 The same procedure as in Example 2 was carried out except that Production Example 2 of Example 2 was replaced with Production Example 14. Example 19 The procedure of Example 3 was repeated, except that Production Example 3 of Example 3 was replaced with Production Example 15. Example 20 Production Example 1 of Example 1 was replaced with Production Example 12, Production Example 2 was replaced with Production Example 13, Production Example 3 was replaced with Production Example 6, and the rest of Example 1 was replaced with Production Example 6.
4 was prepared in the same manner. Example 21 The procedure of Example 1 was repeated except that Production Example 1 of Example 1 was replaced with Production Example 16. Example 22 The same procedure as in Example 2 was repeated except that Production Example 2 of Example 2 was replaced with Production Example 17 to produce the same. Example 23 The same procedure as in Example 3 was carried out except that Production Example 3 of Example 3 was replaced with Production Example 18. Example 24 Production Example 1 of Example 1 was replaced with Production Example 16, Production Example 2 was replaced with Production Example 17, and Production Example 3 was replaced with Production Example 18, except that Example 4 was prepared. Example 25 The same procedure as in Example 1 was carried out except that Production Example 1 of Example 1 was replaced by Production Example 19. Example 26 The same procedure as in Example 2 was carried out except that Production Example 2 of Example 2 was replaced with Production Example 20. Example 27 The same procedures as in Example 3 were carried out except that Production Example 3 of Example 3 was replaced with Production Example 21. Example 28 Production Example 1 was replaced with Production Example 19, Production Example 2 was replaced with Production Example 20, and Production Example 3 was replaced with Production Example 21. Example 29 A device was prepared in the same manner as in Example 1 except that Production Example 1 of Example 1 was replaced with Production Example 22. Example 30 A device was prepared in the same manner as in Example 2 except that Production Example 2 of Example 2 was replaced with Production Example 23. Example 31 The procedure of Example 3 was repeated except that Production Example 3 of Example 3 was replaced by Production Example 24. Example 32 The same procedure as in Example 4 was carried out except that Production Example 1 of Example 1 was replaced with Production Example 22, Production Example 2 was replaced with Production Example 23, and Production Example 3 was replaced with Production Example 24. Example 33 The procedure of Example 1 was repeated except that Production Example 1 of Example 1 was replaced with Production Example 25. Example 34 The same procedure as in Example 2 was carried out except that Production Example 2 of Example 2 was replaced with Production Example 26. Example 35 The same procedure as in Example 3 was carried out except that Production Example 3 of Example 3 was replaced with Production Example 27. Example 36 Production Example 1 of Example 1 was replaced with Production Example 25, Production Example 2 was replaced with Production Example 26, and Production Example 3 was replaced with Production Example 27, and the other processes were the same as in Example 4. Example 37 The procedure of Example 1 was repeated except that Production Example 1 of Example 1 was replaced with Production Example 28. The following experiment was conducted to confirm the effect. On the basis of the following criteria, 5 persons per experiment
After a month of use, we heard about the whiteness of the skin, the effect of improving the roughness of the skin, the effect of improving skin swelling, wrinkles, and the application of makeup. The results are shown in Tables 2 and 3. The numbers represent average values. (Note that
No one complained of skin abnormalities during the test period) Very improved compared to before use 3 Improved compared to before use 2 Slightly improved compared to before use 1 Change from before use None 0 Deteriorated compared to before use -1 Deteriorated compared to before use -2 Very deteriorated compared to before use -3 [Table 3] As for the safety test, a primary skin irritation test, a cumulative skin irritation test, a sensitization test, and a human patch test were performed, but no problem was found. According to the present invention, Xanem, Sasahagi, Undo. clay,
Juketsu, Hanazu-oh, San-Yoshi-Koushi-shaw, Giant-short-faced ox-shape, Seinan-shi-ko-sha-shi, Koke-shi-ko-sha, Kanka-tou, Jin-ho-a, Lotus japonicus, Watari-ya-kogusa, Renrensou, Hama-endo, Daisen-kin-batsu, Tsuru-sen-kin-batsu, Mar-ho-ka-ka-n-ba-k-in An external preparation for skin characterized by combining one or more kinds, a whitening effect, a skin roughness improving effect, a skin sticking,
It has been found that the effect of improving wrinkles and the application of makeup are improved, and that it is highly effective as an external preparation for skin. Needless to say, it has been considered edible since ancient times, and there is no problem in safety at all from the results of various tests.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A61K 35/78 A61K 35/78 J A61P 17/00 A61P 17/00 17/16 17/16 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) A61K 35/78 A61K 35/78 J A61P 17/00 A61P 17/00 17/16 17/16
Claims (1)
ュケツ、ハナズオウ、サンリョウシコウシショウ、ギシ
ョウコウシショウ、セイナンコウシショウ、ケコウシシ
ョウ、カンカトウ、ジンホア、ミヤコグサ、ワタリミヤ
コグサ、レンリソウ、ハマエンドウ、ダイヨウセンキン
バツ、ツルセンキンバツ、マルホバナセンキバツ、カリ
ンボクの抽出物の1種以上を配合することを特徴とする
皮膚外用剤[Claim 1] Kusanem, Sasahagi, Undo. Clay, Juketsu, Hanazuo, Sansho-shikihoshi, Gyokushikihoshihashi, Seinanshihihashi, Kokeshishah, Kankatou, Jinhua, Miyakogusa, Watarimiyakogusa, Renrensou, Hamaendo, Daisenkinbatsu, Tsurusenkinbatsu, Marhobanasenbuki External preparation for skin characterized by incorporating at least one kind of substance
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JP2001337078A JP2003113031A (en) | 2001-09-28 | 2001-09-28 | Skin care preparation |
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JP2001337078A JP2003113031A (en) | 2001-09-28 | 2001-09-28 | Skin care preparation |
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JP2003113031A true JP2003113031A (en) | 2003-04-18 |
Family
ID=19151794
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JP2001337078A Pending JP2003113031A (en) | 2001-09-28 | 2001-09-28 | Skin care preparation |
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EP1572223A4 (en) * | 2002-12-17 | 2007-03-21 | Avon Prod Inc | Use of active extracts to improve the appearance of skin, lips, hair and/or nails |
JP2009013128A (en) * | 2007-07-06 | 2009-01-22 | Sosin:Kk | Skin care preparation for external use and oral composition |
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JP2019112391A (en) * | 2017-12-21 | 2019-07-11 | シャネル パフュームズ ビューテ | Alcoholic extract of aerial parts of anthyllis vulneraria, methods for obtaining the same, and cosmetics or pharmaceutical compositions comprising the same |
JP7418151B2 (en) | 2017-12-21 | 2024-01-19 | シャネル パフュームズ ビューテ | Alcoholic extract of the aerial parts of Anthyllis vulneraria, methods for obtaining the same, and cosmetic or pharmaceutical compositions containing the same |
KR20210078833A (en) * | 2019-12-19 | 2021-06-29 | 재단법인 경기도경제과학진흥원 | Composition for Skin-lightening Using an Extract of Lotus corniculatus var. japonica |
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