JPH01290613A - Remedy for dermatosis and cosmetic - Google Patents
Remedy for dermatosis and cosmeticInfo
- Publication number
- JPH01290613A JPH01290613A JP12066688A JP12066688A JPH01290613A JP H01290613 A JPH01290613 A JP H01290613A JP 12066688 A JP12066688 A JP 12066688A JP 12066688 A JP12066688 A JP 12066688A JP H01290613 A JPH01290613 A JP H01290613A
- Authority
- JP
- Japan
- Prior art keywords
- squalene
- results
- skin
- dermatosis
- remedy
- 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
- 239000002537 cosmetic Substances 0.000 title claims abstract description 12
- 208000017520 skin disease Diseases 0.000 title claims abstract description 12
- 206010048768 Dermatosis Diseases 0.000 title abstract 3
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 claims abstract description 13
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 claims abstract description 13
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229940031439 squalene Drugs 0.000 claims abstract description 13
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 claims abstract description 13
- FODTZLFLDFKIQH-FSVGXZBPSA-N gamma-Oryzanol (TN) Chemical compound C1=C(O)C(OC)=CC(\C=C\C(=O)O[C@@H]2C([C@@H]3CC[C@H]4[C@]5(C)CC[C@@H]([C@@]5(C)CC[C@@]54C[C@@]53CC2)[C@H](C)CCC=C(C)C)(C)C)=C1 FODTZLFLDFKIQH-FSVGXZBPSA-N 0.000 claims abstract description 8
- MPDGHEJMBKOTSU-YKLVYJNSSA-N 18beta-glycyrrhetic acid Chemical compound C([C@H]1C2=CC(=O)[C@H]34)[C@@](C)(C(O)=O)CC[C@]1(C)CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@H](O)C1(C)C MPDGHEJMBKOTSU-YKLVYJNSSA-N 0.000 claims abstract description 7
- 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 claims abstract description 7
- 229940042585 tocopherol acetate Drugs 0.000 claims abstract description 7
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims abstract description 5
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000003814 drug Substances 0.000 claims description 8
- 229940124597 therapeutic agent Drugs 0.000 claims description 6
- 230000000694 effects Effects 0.000 abstract description 14
- 239000000203 mixture Substances 0.000 abstract description 4
- 239000004744 fabric Substances 0.000 abstract description 2
- 238000001914 filtration Methods 0.000 abstract description 2
- 239000004615 ingredient Substances 0.000 abstract description 2
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 208000002874 Acne Vulgaris Diseases 0.000 description 4
- 206010027627 Miliaria Diseases 0.000 description 4
- 206010034972 Photosensitivity reaction Diseases 0.000 description 4
- 206010000496 acne Diseases 0.000 description 4
- WNIFXKPDILJURQ-JKPOUOEOSA-N octadecyl (2s,4as,6ar,6as,6br,8ar,10s,12as,14br)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1h-picene-2-carboxylate Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C)CC[C@@](C(=O)OCCCCCCCCCCCCCCCCCC)(C)C[C@H]5C4=CC(=O)[C@@H]3[C@]21C WNIFXKPDILJURQ-JKPOUOEOSA-N 0.000 description 4
- 208000007578 phototoxic dermatitis Diseases 0.000 description 4
- WNIFXKPDILJURQ-UHFFFAOYSA-N stearyl glycyrrhizinate Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C)CCC(C(=O)OCCCCCCCCCCCCCCCCCC)(C)CC5C4=CC(=O)C3C21C WNIFXKPDILJURQ-UHFFFAOYSA-N 0.000 description 4
- 208000010445 Chilblains Diseases 0.000 description 3
- 206010015150 Erythema Diseases 0.000 description 3
- 231100000321 erythema Toxicity 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 206010008528 Chillblains Diseases 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 208000030961 allergic reaction Diseases 0.000 description 2
- 238000003287 bathing Methods 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 230000003203 everyday effect Effects 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 208000002440 photoallergic dermatitis Diseases 0.000 description 2
- 231100000018 phototoxicity Toxicity 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- -1 stearyl phosphate Chemical compound 0.000 description 2
- 230000008685 targeting Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 241000251730 Chondrichthyes Species 0.000 description 1
- 206010012442 Dermatitis contact Diseases 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- MPDGHEJMBKOTSU-UHFFFAOYSA-N Glycyrrhetinsaeure Natural products C12C(=O)C=C3C4CC(C)(C(O)=O)CCC4(C)CCC3(C)C1(C)CCC1C2(C)CCC(O)C1(C)C MPDGHEJMBKOTSU-UHFFFAOYSA-N 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 206010033733 Papule Diseases 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 206010040849 Skin fissures Diseases 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003470 adrenal cortex hormone Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 208000010247 contact dermatitis Diseases 0.000 description 1
- 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
- 229960003720 enoxolone Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003163 gonadal steroid hormone Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 244000000010 microbial pathogen Species 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 231100001085 no phototoxicity Toxicity 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 235000013594 poultry meat Nutrition 0.000 description 1
- 210000001732 sebaceous gland Anatomy 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 206010040882 skin lesion Diseases 0.000 description 1
- 231100000444 skin lesion Toxicity 0.000 description 1
- 230000005808 skin problem Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 210000000106 sweat gland Anatomy 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 210000003371 toe Anatomy 0.000 description 1
- 210000000689 upper leg Anatomy 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 235000005282 vitamin D3 Nutrition 0.000 description 1
- 239000011647 vitamin D3 Substances 0.000 description 1
- 229940021056 vitamin d3 Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/63—Steroids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/67—Vitamins
- A61K8/678—Tocopherol, i.e. vitamin E
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は新規な皮膚疾患治療剤および化粧品に関し、更
に詳しくは、従来より各種の皮膚疾患治療剤或いは化粧
品に用いられている酢酸トコフェロール・グリチルレチ
ン酸ステアリン、γ−オリザノールのほか医薬品または
化粧品の材料としては全く新規な天然抽出物スクアレン
を加えることによりなる皮膚疾9.治療剤および化粧品
に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to novel skin disease therapeutic agents and cosmetics, and more specifically, tocopherol acetate and glycyrrhetinic acid, which have been conventionally used in various skin disease therapeutic agents and cosmetics. 9. Skin diseases caused by adding squalene, a completely new natural extract as a material for pharmaceuticals or cosmetics, in addition to acid stearin and γ-oryzanol.9. Regarding therapeutic agents and cosmetics.
スクアレンはオリーブ油その他の植物成分、獣肉、鳥肉
々どに微ながら存在し、最も多くは1000メートル前
後の深海に棲むアイ鮫の肝!1AVctまれる。Squalene exists in small amounts in olive oil and other plant ingredients, meat, and poultry meat, and is most commonly found in the liver of the eye shark, which lives in the deep sea around 1000 meters! 1AVct is applied.
ヒト生体内圧おいてもスクアレンの生合成が行われ、全
身臓器に分布が見られる。皮脂腺から上孔を通って皮膚
表面に分泌されたスクアレンは汗腺からの水分と混合乳
化して、保湿作用、病原微生物の排除など、皮膚表面を
保護する作用を有する。Squalene is biosynthesized even under human internal pressure, and is distributed throughout the body's organs. Squalene secreted from the sebaceous glands to the skin surface through the upper pores is mixed with water from the sweat glands and emulsified, and has the effect of protecting the skin surface, such as moisturizing and eliminating pathogenic microorganisms.
また、スクアレンはヒト生体において若干の中間体を経
てビタミンD3、各種性ホルモン°および各種副腎皮質
ホルモンなどの重要な物質に生合成される。In addition, squalene is biosynthesized into important substances such as vitamin D3, various sex hormones, and various adrenal cortical hormones through some intermediates in the human body.
従来、医薬品または化粧品の単味剤としても或いは配合
剤としても用いられることのなかったスクアレンを配合
することにより、−ノーすぐれた効果を示し、かつ安全
性の高い皮膚疾患治療剤および化粧品を得たことに本発
明の意義がある。By incorporating squalene, which has not previously been used as a single agent or as a compounding agent in pharmaceuticals or cosmetics, we are able to obtain skin disease treatment agents and cosmetics that exhibit excellent efficacy and are highly safe. This is particularly the significance of the present invention.
本発明の皮膚疾患治療剤および化粧品は酢酸トコフェロ
ール0.3グラムないし0.08グラム、グリチルレチ
ン酸ステアリン0.03グラムないし0.08グラム、
γ−オリザノール0.03グラムないし0.08グラム
およびスクアレン99グラムないし99.7グラムを加
え60℃に加温し。The skin disease therapeutic agent and cosmetics of the present invention include tocopherol acetate from 0.3 to 0.08 g, stearic glycyrrhetinate from 0.03 to 0.08 g,
0.03 g to 0.08 g of γ-oryzanol and 99 g to 99.7 g of squalene were added and heated to 60°C.
15分間攪拌する。これを−夜呈渦にて静置したのち、
布でろ過して得られる。Stir for 15 minutes. After leaving this still in the night vortex,
Obtained by filtering through cloth.
本則は従来用いられている皮膚疾患治療剤または化粧品
よりも治療効果においても、さらに予防効果においても
著しいものがあり、しかも副作用は全く認められない。This principle has more significant therapeutic and preventive effects than conventional skin disease treatment agents or cosmetics, and no side effects are observed.
以下本発明の実施例によって、その有効性と安全性を示
すつ
実施例 1゜
16オから23才°までの難治性のにきび患者を対象K
、本則と既存のにきび治療剤をそれぞれ異なる患者の患
部に1日朝、昼、夕および就寝前の各洗顔後針4回10
日間塗布したところ本則に著しい効果をみた。The following examples demonstrate the effectiveness and safety of the present invention.
Apply the basic and existing acne treatment agents to the affected areas of different patients 4 times 10 times a day after washing your face in the morning, noon, evening, and before bedtime.
When applied for several days, a remarkable effect was seen on the main rules.
その成Mを表1)に示す。Its composition M is shown in Table 1).
実施例 2゜
乳児および成人のあせも患者を対象に、本則と既存のあ
せも治療剤を、それぞれ異なる患者の患部に、入浴後1
回を含む1日3回、15日間塗布して著しい効果をみた
。Example 2゜ Targeting infants and adult heat rash patients, administer the standard and existing heat rash treatment agents to the affected areas of different patients one day after bathing.
It was applied three times a day for 15 days, including once, and showed remarkable effects.
その成績を表2)に示す。The results are shown in Table 2).
表 2) あせも治療成績
実施例 3゜
しもやけを有する5才から1)才までの児童を対象に、
本則と既存のしもやけ治療剤をそれぞれ異なる患者の患
部に1缶入浴後1回を含む1日5回、7日間塗布したと
ころ、本則に著しい効果をみた。Table 2) Examples of heat rash treatment results 3゜For children aged 5 to 1) with chilblains,
When Honjoku and an existing chilblain treatment were applied to the affected areas of different patients five times a day, including once after taking a bath, for seven days, Honjoku had a significant effect.
その成績を表3)に示す。The results are shown in Table 3).
表3)シもやけ治療成績
実施例 4゜
手指にひび、あかぎれを有する主婦および食堂等の食器
洗担当の女性を対象に本則と既存のひび、あかぎれ治療
剤をそれぞれ異なる患者の患部に1日5回、15日間塗
布したところ本則に著しい効果をみた。Table 3) Practical results of skin irritation treatment 4゜ Targeted at housewives with cracked and chapped hands and women who wash dishes in cafeterias, etc., the main treatment and existing crack and chapped treatment were applied to the affected areas of different patients for one day. When applied 5 times for 15 days, significant effects were seen on the main principle.
その成績を表4)に示す。The results are shown in Table 4).
実施例 &
肌あれ、あれ性を有する35才から58才までの女性患
者を対象に、本則および既存の肌あれ、あれ性治療剤を
それぞれ異なる患者の患部に1日5回、lO日間塗布し
たところ本則に著しい効果をみた。Example & Targeting female patients between the ages of 35 and 58 who have rough skin, regular and existing treatment agents for rough skin and rough skin were applied to the affected areas of different patients 5 times a day for 10 days. However, we saw a significant effect on the main rules.
表 5) 肌あれ、あれ性治療成績
実施例 6゜
例年春から初夏ににきびの多発をみる16オから22才
の女性を対象に、にきび予防の目的で本則を毎夜洗顔後
に1回30日間顔面途布したところ、ましい効果を得た
。Table 5) Examples of treatment results for rough skin and rough skin 6゜Targeting women aged 16 to 22 who usually experience frequent acne from spring to early summer, we applied the basic rule to the face once every night after washing for 30 days to prevent acne. When it was discontinued, it had a wonderful effect.
表6) にきび予防成績
実施例 7゜
乳児および例年夏にあせもを発症する女性を対象に、そ
の予肪ヲ目的に、本則を毎日入浴後、発症が予想される
躯幹部、大腿部内に20日間塗布させたところ著しい効
果をみた。Table 6) Acne prevention results example 7゜Targeting infants and women who usually develop heat rash in the summer, for the purpose of fattening, the main rule was applied every day after bathing and on the trunk and thighs where the onset is expected for 20 days. When applied, a remarkable effect was observed.
その成績を表7)に示す。The results are shown in Table 7).
実施例 8゜
例年冬季手指、足指にしもやけの発症をみ!
る児童を対象にその予防の目的で、毎日入浴後1回20
日間塗布したところ、著しい効果をみた。Example 8゜I see the onset of chilblains on my fingers and toes every winter! For the purpose of prevention, 20 days after taking a bath every day.
When I applied it for a day, I saw a remarkable effect.
その成績を表8)に示す。The results are shown in Table 8).
実施例 9゜
例年冬季、手指にひび、あかぎれの発症をみる女性にそ
の予防の目的で、1日3回、30日間手指に本則を塗布
させたところ著しい効果をみた。Example 9゜In order to prevent cracks and chapped hands and fingers during the winter season, a woman applied this product to her hands and fingers three times a day for 30 days, and found that it had a remarkable effect.
その成績を表9)に示す。The results are shown in Table 9).
表9) ひび、あかぎれ予防成績
実施例 10゜
例年状から冬にかけ、肌あれ、あれ性をみる女性を対象
として、その予防の目的で、毎朝1回と夜入浴後の1回
計1日2回、30日間顔面と手掌の背部および手指に1
本剤をマツサージするように塗布させたところ著しい成
果を得た。Table 9) Example of results for prevention of cracks and chapped skin once on the face, back of the palms, and fingers for 30 days.
When this agent was applied as a pine surge, remarkable results were obtained.
その成績を表10)に示す。The results are shown in Table 10).
表10) 肌あれ、あれ性の予防成績実施例 1)゜
本則の副作用の有無、副作用を生じた場合のその程度に
ついても検討した。Table 10) Examples of preventive results for rough skin and rough skin 1) The presence or absence of side effects of the main rule and the extent of side effects when they occur were also examined.
すでに接触皮膚炎その他何らかの皮膚疾患を有し、皮膚
におけるトラブルを生ずる可能性が高いと考えられる患
者16例を対象として以下の方法による実験を行なった
。Experiments were conducted using the following method on 16 patients who already had contact dermatitis or some other skin disease and were thought to have a high possibility of developing skin problems.
本則を大正製薬のパッチPK厚くつけ、これを各患者の
患部を避け、背面に貼布した。48時間後に貼布したサ
メミロンエー激性)を観察して記録、引き続きデルマレ
イ(エーザイ)のUV−860tsZ分、すなわち通常
何らの反応も示さない光エネルギー量の光線をこの部位
に照射、その48時間および72時間後に対照と比較し
て炎症反応惹起の有無を詳細に観察、光毒性ないし光ア
レルギー反応を検索した。Taisho Pharmaceutical's patch PK was applied thickly and applied to the back of each patient, avoiding the affected area. After 48 hours, the area was observed and recorded, and the area was then irradiated with UV-860tsZ of Delmarray (Eisai), that is, an amount of light energy that normally does not cause any reaction, for 48 hours. And 72 hours later, the presence or absence of induction of inflammatory reactions was observed in detail in comparison with the control, and phototoxicity or photoallergic reactions were searched.
その結果は次のとおりである。The results are as follows.
1)−次刺激性反応
紅斑以上の反応を示したものは皆無で、−次刺激反応F
i認められなかった。1) - None showed a reaction worse than erythema, - secondary irritation reaction F
i was not recognized.
2)接触アレルギー性反応
本反応はpo l)rmorphism 多型性といわ
れるように紅斑、丘疹、小水痕などの様々な皮疹が一局
面に混在する反応であり、同時に貼布部位以外にもはみ
出した形で反応が出現すること、さらに48時間以降に
反応のピークを示すので遅延型アレルギー反応といわれ
るが如き反応を以て特徴とする。2) Contact allergic reaction This reaction is called polymorphism, which is a reaction in which various skin lesions such as erythema, papules, and small vesicles are mixed together in one area, and at the same time, it protrudes beyond the area where the patch was applied. It is characterized by a reaction that appears in a delayed form, and a reaction that peaks after 48 hours, so it is called a delayed allergic reaction.
今回実施した16例に於てサメミロン エースにより陽性反応を示したものは皆無であった。Samemilon was used in 16 cases conducted this time. None of the cases tested positive by Ace.
3)光過敏反応
本来、皮膚に何らの反応も示さない光エネルギーの照射
によシ、貼布部位に紅斑その他の反応を示すとき、光過
敏反応−光毒性及び光アレルギーと判定する。3) Photosensitivity reaction When erythema or other reactions occur at the application site due to irradiation with light energy, which normally does not cause any reaction on the skin, it is determined to be a photosensitivity reaction - phototoxicity and photoallergy.
基剤貼布部位は16例中全例が陰性であり、光毒性、光
アレルギー性は間められなかった。All of the 16 cases tested negative at the site where the base was applied, and no phototoxicity or photoallergy was detected.
なお念のため、72時間後も観察した12例も引き続い
て陰性であった。As a precaution, 12 cases that were observed 72 hours later also remained negative.
以上の実験結果を表1))に示す。The above experimental results are shown in Table 1)).
表1)) サメミロンエースフォトバッチテスト手続
補正書(勿
昭和すう年グ1)2ダ日
特許守旧“C小川邦夫殿
3、補正をする者
事件との関係 特 許出願人
日各或マソンエー業上(2’; 棋
4、代理人
5、補正命令の日付 昭和 年 月 日ろ
補 正 内 容
1不断の「%許請求の範囲」を以下のように訂正する。Table 1)) Samemilon Ace Photobatch Test Procedures Amendment (No. 1, 2013) 2nd Day Patent Guardian Former “Mr. C. Ogawa Kunio 3, Relationship with the Person Who Makes the Amendment Case” Patent Applicant Date Each or Mason A Business (2'; Ki 4, Agent 5, Date of amendment order: 1925, month, day, date, date, date, date) Amendment Contents 1. The perennial "% claim scope" is corrected as follows.
r(1) 酢酸トコフェロール、グリチルレチン酸ス
テアリル、γ−オリザノールおよびスクアレンからなる
皮膚疾患治療剤。r(1) A therapeutic agent for skin diseases comprising tocopherol acetate, stearyl glycyrrhetinate, γ-oryzanol and squalene.
(21ff[トコフェロール、グリチルレチン酸ステア
リル、γ−オリザノールおよびスクアレンからなる化粧
品。」
二本願明超書中第1貞16行目冒頭に「ン酸ステアリン
、」とあるを「ン酸ステアリル、」と訂正する。(21ff [Cosmetic product consisting of tocopherol, stearyl glycyrrhetinate, γ-oryzanol, and squalene.) At the beginning of line 16 of the second application, the words "stearyl phosphate" are corrected to "stearyl phosphate." do.
3、回書第3頁5行目冒頭に「グリチルレチン酸ステア
リル」とあるを「グリチルレチン酸ステアリル」と訂正
する。3. At the beginning of page 3, line 5 of the circular, the words "stearyl glycyrrhetinate" are corrected to "stearyl glycyrrhetinate."
Claims (2)
ン、γ−オリザノールおよび スクアレンからなる皮膚疾患治療剤。(1) A therapeutic agent for skin diseases consisting of tocopherol acetate, stearin glycyrrhetinate, γ-oryzanol and squalene.
ン、γ−オリザノールおよび スクアレンからなる化粧品。(2) A cosmetic product comprising tocopherol acetate, stearin glycyrrhetinate, γ-oryzanol and squalene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12066688A JPH01290613A (en) | 1988-05-19 | 1988-05-19 | Remedy for dermatosis and cosmetic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12066688A JPH01290613A (en) | 1988-05-19 | 1988-05-19 | Remedy for dermatosis and cosmetic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01290613A true JPH01290613A (en) | 1989-11-22 |
Family
ID=14791905
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12066688A Pending JPH01290613A (en) | 1988-05-19 | 1988-05-19 | Remedy for dermatosis and cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01290613A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0766960A1 (en) * | 1995-04-21 | 1997-04-09 | Sekisui Kagaku Kogyo Kabushiki Kaisha | External preparations for treating dermatoses |
JPH09169637A (en) * | 1995-10-18 | 1997-06-30 | Sekisui Chem Co Ltd | External preparation for treating dermatosis |
JPH09169640A (en) * | 1995-10-18 | 1997-06-30 | Sekisui Chem Co Ltd | External preparation for treating dermatosis |
JP2005053785A (en) * | 2003-05-20 | 2005-03-03 | Nippon Menaade Keshohin Kk | External preparation |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5334912A (en) * | 1976-09-10 | 1978-03-31 | Yasuhisa Kitamura | Skin ointment of extract from deep sea shark |
JPS5616409A (en) * | 1979-07-19 | 1981-02-17 | Ikeda Mohandou:Kk | Gamma-oryzanol pharmaceutical preparation |
JPS5885808A (en) * | 1981-11-16 | 1983-05-23 | Shiseido Co Ltd | Cosmetic |
JPS59225107A (en) * | 1983-06-03 | 1984-12-18 | Katsuhiro Nakaoka | Medical cosmetic for skin and muscle |
-
1988
- 1988-05-19 JP JP12066688A patent/JPH01290613A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5334912A (en) * | 1976-09-10 | 1978-03-31 | Yasuhisa Kitamura | Skin ointment of extract from deep sea shark |
JPS5616409A (en) * | 1979-07-19 | 1981-02-17 | Ikeda Mohandou:Kk | Gamma-oryzanol pharmaceutical preparation |
JPS5885808A (en) * | 1981-11-16 | 1983-05-23 | Shiseido Co Ltd | Cosmetic |
JPS59225107A (en) * | 1983-06-03 | 1984-12-18 | Katsuhiro Nakaoka | Medical cosmetic for skin and muscle |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0766960A1 (en) * | 1995-04-21 | 1997-04-09 | Sekisui Kagaku Kogyo Kabushiki Kaisha | External preparations for treating dermatoses |
EP0766960A4 (en) * | 1995-04-21 | 2000-07-12 | Seikisui Chemical Co Ltd | External preparations for treating dermatoses |
US6248779B1 (en) | 1995-04-21 | 2001-06-19 | Sekisui Kagaku Kogyo Kabushiki Kaisha | External preparations for treating dermatoses |
EP1374861A1 (en) * | 1995-04-21 | 2004-01-02 | Sekisui Kagaku Kogyo Kabushiki Kaisha | External preparations for treating dermatoses |
JPH09169637A (en) * | 1995-10-18 | 1997-06-30 | Sekisui Chem Co Ltd | External preparation for treating dermatosis |
JPH09169640A (en) * | 1995-10-18 | 1997-06-30 | Sekisui Chem Co Ltd | External preparation for treating dermatosis |
JP2005053785A (en) * | 2003-05-20 | 2005-03-03 | Nippon Menaade Keshohin Kk | External preparation |
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