JPH04187623A - Hair cosmetics - Google Patents
Hair cosmeticsInfo
- Publication number
- JPH04187623A JPH04187623A JP2316116A JP31611690A JPH04187623A JP H04187623 A JPH04187623 A JP H04187623A JP 2316116 A JP2316116 A JP 2316116A JP 31611690 A JP31611690 A JP 31611690A JP H04187623 A JPH04187623 A JP H04187623A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- extract
- hair cosmetic
- preventing
- present
- 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
- 239000003676 hair preparation Substances 0.000 title description 4
- 210000004209 hair Anatomy 0.000 claims abstract description 82
- 239000002537 cosmetic Substances 0.000 claims abstract description 21
- 239000000284 extract Substances 0.000 claims abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000004615 ingredient Substances 0.000 claims abstract description 9
- 238000000605 extraction Methods 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 238000013329 compounding Methods 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 22
- 230000000694 effects Effects 0.000 abstract description 20
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract description 6
- 210000004761 scalp Anatomy 0.000 abstract description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract description 4
- 206010040880 Skin irritation Diseases 0.000 abstract description 3
- 239000003814 drug Substances 0.000 abstract description 3
- 231100000475 skin irritation Toxicity 0.000 abstract description 3
- 230000036556 skin irritation Effects 0.000 abstract description 3
- 208000008930 Low Back Pain Diseases 0.000 abstract description 2
- 230000000202 analgesic effect Effects 0.000 abstract description 2
- 206010003246 arthritis Diseases 0.000 abstract description 2
- 230000001747 exhibiting effect Effects 0.000 abstract 3
- 241000208689 Eucommia ulmoides Species 0.000 abstract 2
- 208000008035 Back Pain Diseases 0.000 abstract 1
- 230000000172 allergic effect Effects 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 12
- 235000015961 tonic Nutrition 0.000 description 12
- 230000001256 tonic effect Effects 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 10
- 230000002265 prevention Effects 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- 241001465754 Metazoa Species 0.000 description 6
- 210000003491 skin Anatomy 0.000 description 6
- 241000699670 Mus sp. Species 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000469 ethanolic extract Substances 0.000 description 4
- 210000002752 melanocyte Anatomy 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 206010015150 Erythema Diseases 0.000 description 3
- 241000208688 Eucommia Species 0.000 description 3
- 241000282412 Homo Species 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 230000007815 allergy Effects 0.000 description 3
- 239000006071 cream Substances 0.000 description 3
- 231100000321 erythema Toxicity 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 230000007794 irritation Effects 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 238000011076 safety test Methods 0.000 description 3
- 229960000716 tonics Drugs 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 201000004624 Dermatitis Diseases 0.000 description 2
- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- -1 Polyoxyethylene Polymers 0.000 description 2
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 2
- MHUWZNTUIIFHAS-CLFAGFIQSA-N dioleoyl phosphatidic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(COP(O)(O)=O)OC(=O)CCCCCCC\C=C/CCCCCCCC MHUWZNTUIIFHAS-CLFAGFIQSA-N 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000118 hair dye Substances 0.000 description 2
- 241000411851 herbal medicine Species 0.000 description 2
- 229960004502 levodopa Drugs 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000008164 mustard oil Substances 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000011746 C57BL/6J (JAX™ mouse strain) Methods 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 238000000692 Student's t-test Methods 0.000 description 1
- 206010047486 Virilism Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000012745 brilliant blue FCF Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 210000000245 forearm Anatomy 0.000 description 1
- 210000002721 hair follicle melanocyte Anatomy 0.000 description 1
- 230000003662 hair growth rate Effects 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 231100000794 masculinization Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000012353 t test Methods 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、毛髪化粧料に関するものであり、更に詳しく
は杜仲の抽出物を配合成分として含有することを特徴と
する毛髪用化粧料に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a hair cosmetic, and more particularly to a hair cosmetic containing an extract of Mori zhong as a compounding ingredient. It is.
[背景技術]
従来、白髪を改善する手段の一つとして、物理化学的染
色による染毛剤が用いられている。[Background Art] Hair dyes based on physicochemical dyeing have conventionally been used as one of the means for improving gray hair.
しかしなから、染毛剤はその使用上の操作の煩−さ、頭
皮に対する刺激性、感作性等安全性の面で開題があり、
ン・すしも使用者のニーズを満足する手段とはなってい
ない。また、白髪そのものの発生を、薬剤を用いて予防
ないしは改善する方法に関する提案もされている(例え
ば、特開昭58−99417号、特開昭62−6350
9号、特開昭f32’−63510号、特開昭62−4
55275号、特開昭63−183518号、特開昭6
4−25712号、特開平o1−207225号公報な
ど参照)。しかしながら、これらの方法も白髪の予防、
改善の目的に対しては実用的な効果は得られず、また、
安全性の面でも、必すしも満足すべき効果は得られてい
ない。However, hair dyes have been problematic in terms of safety, such as their cumbersome operation, irritation to the scalp, and sensitization.
Japanese sushi is also not a means to satisfy the needs of users. In addition, there have been proposals regarding methods for preventing or improving the occurrence of gray hair itself using drugs (for example, JP-A-58-99417, JP-A-62-6350).
No. 9, Japanese Patent Publication No. Sho f32'-63510, Japanese Patent Publication No. Sho 62-4
No. 55275, JP-A-63-183518, JP-A-6
4-25712, JP-A-1-207225, etc.). However, these methods also prevent gray hair,
It has no practical effect on the purpose of improvement, and
In terms of safety, satisfactory effects have not necessarily been obtained.
[発明の目的]
本発明は、頭皮に外用することによって、優れた白髪予
防、改善効果を発揮し、しかも、皮膚に対する安全性か
高い毛髪用化粧料を提供することを目自勺とするもので
ある。[Object of the invention] The purpose of the present invention is to provide a hair cosmetic that exhibits excellent gray hair prevention and improvement effects when applied externally to the scalp, and is highly safe for the skin. It is.
[発明の開示]
本発明者らは、実用的な効果を有する白髪予防・改善剤
を開発すべく、長年に渡って研究を重ねてきた結果、漢
方薬として知られている杜仲の抽出物を外用すると、白
髪予防、改善効果がもたらされることを見出した。本発
明は、かかる知見に基ついてなされたものである。[Disclosure of the Invention] As a result of many years of research in order to develop an agent for preventing and improving gray hair that has practical effects, the present inventors have developed an extract of Du Zhong, which is known as a Chinese herbal medicine, for external use. It has been found that this results in the prevention and improvement of gray hair. The present invention has been made based on this knowledge.
杜仲は、中国大陸の中部に分布しているトチュウ属トチ
ュウと呼ばれるM物の幹皮を乾燥したものである。この
も9は、従来漢方薬として強壮剤、腰痛、関節炎やリウ
マチの鎮痛薬として使用されてきた。また、近年、高血
圧の薬としての開発も進められてきているが、化粧品の
分野においては全く用いられていない。Eucommia is the dried trunk bark of Eucommia, a species of Eucommia that is distributed in central China. Konomo9 has traditionally been used as a tonic and analgesic for lower back pain, arthritis, and rheumatism as a Chinese herbal medicine. Furthermore, in recent years, development as a drug for hypertension has progressed, but it has not been used at all in the field of cosmetics.
本発明者らは、この杜仲の生理活性の強さに着目し、白
髪予防・酸1!F剤としての可能性に関し、種々研究を
行った。すなわち、杜仲を水又は低級アルコールで抽出
して得られるその抽出物に関し鋭意検討し、その抽出物
が動物の毛のメラノサイトを活性化すること、そしてマ
ウスの老化によって生じた白毛を黒化すること、更には
、人の白髪の予防、改善に対し効果を示すことを見出し
た。本発明はかかる知見に基づいてなされたらめである
。The present inventors focused on the strength of the physiological activity of this mori, and found that it is the best acid for preventing gray hair! Various studies were conducted regarding its potential as an F agent. In other words, we conducted extensive research on the extract obtained by extracting Mori Zhong with water or lower alcohols, and found that the extract activates melanocytes in animal hair and darkens gray hair that occurs due to aging in mice. Moreover, it has been found to be effective in preventing and improving gray hair in humans. The present invention was made based on this knowledge.
本発明は、杜仲を抽出用溶媒で抽出して得られる抽出物
を配合成分として含有することを特徴とする毛髪化粧料
を提供するもめである6以下に、本発明の詳細な説明す
る。The present invention is directed to providing a hair cosmetic that is characterized by containing as a compounding ingredient an extract obtained by extracting Mori annua with an extraction solvent.The present invention will be described in detail below.
本発明に係る毛髪化粧料に適用される杜仲はユーコミア
ウルモイデスEucoIlnia ulrQoide
s。The mori applied to the hair cosmetic according to the present invention is Eucomia ulrmoides EucoIlnia ulrQoid.
s.
トチュウ属に属する植物の幹皮を乾燥したものである0
本発明に係る毛髪化粧料に用いる杜仲は、この幹友を適
当な抽出用溶媒、例えば、水あるいは低級アルコール例
えば、メタノール、エタノール及びブタノール、好まし
くはエタノールによって冷浸抽出又は温浸抽出すること
により得られる抽出物を用いるものである。Dried stem bark of a plant belonging to the genus Eucommia0
The benzonia used in the hair cosmetics according to the present invention can be obtained by cold-extracting or hot-extracting the benzonia with a suitable extraction solvent, such as water or a lower alcohol such as methanol, ethanol, and butanol, preferably ethanol. The resulting extract is used.
本発明の毛髪化粧料に使用される杜仲抽出物の製造例を
以下に示す。An example of manufacturing the Mori extract used in the hair cosmetic of the present invention is shown below.
く製造例1〉
杜仲2 k+rを各20jのエタノールで3日間ずつ3
回に渡って冷浸抽出する。得られた抽出液を合わせてエ
バポレーターを用いてエタノールを留去し、約0.3b
zの抽出物を得る。Production Example 1〉 Mori 2 k+r was mixed with 20j of ethanol for 3 days each.
Cold immersion extraction is carried out several times. The obtained extracts were combined and ethanol was distilled off using an evaporator to obtain approximately 0.3b
Obtain the extract of z.
〈製造例2〉
杜仲2 kgを各20.flの水で3日間ずつ3回に渡
って温浸抽出する。得られた抽出液を合わせてエバポレ
ーターを用いて水を留去し、約0.1bzの抽出物を得
る。<Manufacturing Example 2> 2 kg of Mori Zhong, 20. Digestion extraction is carried out three times for three days each with fl water. The obtained extracts are combined and water is distilled off using an evaporator to obtain an extract of about 0.1 bz.
この2つの製造例で得られた抽出!P!l!lめ色は、
いずれも茶褐色の色調をしているが、エタノール抽出物
は、水抽出物に比し色調は濃い。両者をそれぞれ、40
゛Cにて約1カ月間放置し性状の変化を検討したが、色
調の変化、変臭等は起こらず安定なものであった。本発
明に係る毛髪化粧料における、杜仲の抽出物の使用量は
、通常毛髪化粧料全重量あたり0.05−20.0重量
%である6
本発明に係る毛髪化粧料は、これを頭友に外用すること
によって優れた白髪予防、改善効果を発揮するものであ
り、皮膚に対する安全性も高い0本発明に係る毛髪用化
粧料の剤形とじては、毛髪に適用するためぬ種々の剤形
、例えば、ヘアトニック、ヘアクリーム、ヘアローショ
ン、乳液、軟膏、ヘアトリートメント、ヘアコンディシ
ョナー等の外用できる各種剤形を幅広くとることかでき
る。Extraction obtained in these two production examples! P! l! The lth color is
Both have a brownish color, but the ethanol extract is darker than the water extract. 40 each for both
The product was left for about 1 month at C and examined for changes in properties, but it was found to be stable with no change in color tone or odor. In the hair cosmetic according to the present invention, the amount of the extract of Mori Zhong used is usually 0.05-20.0% by weight based on the total weight of the hair cosmetic. When applied externally, it exhibits excellent gray hair prevention and improvement effects, and is highly safe for the skin.The dosage form of the hair cosmetic according to the present invention includes various agents that are not intended for application to hair. A wide variety of externally applicable dosage forms can be taken, for example, hair tonics, hair creams, hair lotions, milky lotions, ointments, hair treatments, hair conditioners, and the like.
本発明に係る毛髪化粧料に使用される成分としては、通
常、この種の外用剤に使用される各材料物質、例えば、
基荊としては、水、エタノール、各種炭化水素類、高級
アルコール類、エステル類、高級脂肪酸類、各種の界面
活性剤等を、また、添加成分としては、香料、色素、防
腐剤、抗酸化剤及び各種の薬効成分等が挙げられる。Ingredients used in the hair cosmetic according to the present invention include various materials usually used in this type of external preparation, for example,
The base ingredients include water, ethanol, various hydrocarbons, higher alcohols, esters, higher fatty acids, various surfactants, etc., and the additive ingredients include fragrances, pigments, preservatives, and antioxidants. and various medicinal ingredients.
本発明に係る毛髪化粧料においては、配合成分として白
髪予防・改善物質として知られている他の物質を併用し
て含有させることができる。In the hair cosmetic according to the present invention, other substances known as substances for preventing and improving gray hair may be included in combination.
以下に、実施例と比較例を掲げ、本発明を説明する。な
お、例中の配合量は重量部で示されている。The present invention will be described below with reference to Examples and Comparative Examples. In addition, the blending amounts in the examples are shown in parts by weight.
実施例、比較例 ヘアトニック
〈処方〉
表 1
エタノール 79.89 79.89 8
0.89ポリオキシエ
チレン硬化し
マシ油f40E、o、) 0.5 0.5
0.5杜仲−エタノ
ール抽出物
(製造例1) 1.0 0゜00.0杜仲−
水抽出
物(製造例2> 0.0 1.0 0.0
精製水 18.5 18.5 18.
5香料 0.1 0.1 0.1
く製造法〉
各側とも、それぞれ、エタノールに杜仲抽出物(比較例
では不使用)、ポリオキシエチレン硬化しマシ油(40
E、O9)、香料及び色素を加えて、撹拌溶解し、次い
で精製水を加えて撹拌して、ローションを調製する。Examples, Comparative Examples Hair Tonic (Formulation) Table 1 Ethanol 79.89 79.89 8
0.89 Polyoxyethylene hardened mustard oil f40E, o,) 0.5 0.5
0.5 Mori Zhong - Ethanol Extract (Production Example 1) 1.0 0゜00.0 Mori Zhong -
Water extract (Production example 2> 0.0 1.0 0.0
Purified water 18.5 18.5 18.
5 Fragrance 0.1 0.1 0.1 Production method> For each side, ethanol, Morizhong extract (not used in the comparative example), polyoxyethylene hardened mustard oil (40%
E, O9), fragrance and coloring matter are added, stirred and dissolved, then purified water is added and stirred to prepare a lotion.
次に、本発明に隔る毛髪化粧料について行った動物によ
る白毛予防・改善試験、安全性試験及び人による白髪予
防・改善試験について述べる。Next, a description will be given of gray hair prevention/improvement tests in animals, safety tests, and gray hair prevention/improvement tests in humans conducted on hair cosmetics different from the present invention.
〈動物による白毛予防・改善実験〉
上記各実施例のヘアトニック及びその実験対照としての
比較例のヘアトニックに関して、それぞれを動物の老化
によって生じた毛に直#:適用することにより、白毛の
進行の予防及び改善の状態が観察された。<Grey hair prevention/improvement experiment using animals> By applying each of the hair tonics of the above examples and the hair tonic of the comparative example as an experimental control directly to the hair caused by aging of animals, it was possible to reduce gray hair. Progress prevention and improvement were observed.
隨1基月 実施例1及び実施例2の各ヘアトニック、比
較例1のヘアトニック
に鼠方韮
動物は、C57BL/6Jマウスの1.5年令で黒色の
毛に老化による白色の毛が混在したマウスを用いた。各
試料毎にC57BLマウス10匹を1群とし各試料毎に
計3群を設けた。Each of the hair tonics of Examples 1 and 2 and the hair tonic of Comparative Example 1 showed that the hair tonic of Example 1 and Comparative Example 1 had white hair due to aging in the black hair of C57BL/6J mice at 1.5 years of age. A mixed set of mice was used. A total of 3 groups were established for each sample, with 10 C57BL mice per group.
本島0.05tpe/■2を一日2回動物の頭皮の毛の
根元の皮膚に充分に塗擦し、3力月の間継続塗布した。0.05 tpe/■2 of Honjima was sufficiently rubbed twice a day on the skin at the root of the hair on the scalp of the animal, and the application was continued for 3 months.
Li亙羞
途中観察経過から、塗布期間内では白毛全体か完全に黒
毛に置き換わることはなく、毛先は白いが、毛の根元か
ら毛の途中まで黒くなったものか観察された。そこで、
評価方法として、マウスの頭部の毛先め白い毛を無作為
に抜毛し、その抜毛した毛の数及び根元から少しでも黒
くなっている毛の数を計数し、後者を前者で除した値を
黒毛の発生頻度とした。From the observation progress during the application period, it was observed that the white hairs were not completely replaced by black hairs during the application period, and although the tips of the hairs were white, it was observed that the hairs turned black from the roots to the middle of the hairs. Therefore,
As an evaluation method, white hairs from the tips of the mice's heads are randomly pulled out, and the number of hairs that are pulled out and the number of hairs that are even slightly black from the roots are counted, and the value is calculated by dividing the latter by the former. was taken as the frequency of occurrence of black hair.
その結果をt検定(群間比較)して、試料の白毛黒化効
果の有意性を評価した。The results were subjected to a t-test (comparison between groups) to evaluate the significance of the graying effect of the samples.
表2から明らかなように、実施例1及び実施例2の各ヘ
アトニyりは、比較例1のヘアトニ・ツクに比し、白色
の毛メ男化を惹起し、その効果か示された。なお、エタ
ノール抽出物を含む実施例1と水抽出物を含む実施例2
の結果は、水抽出物に比しエタノール抽出物を使用した
場合の方か効果か高い結果か得られた。As is clear from Table 2, each of the hair toning treatments of Examples 1 and 2 caused white hair masculinization compared to the hair toning treatment of Comparative Example 1, demonstrating its effectiveness. In addition, Example 1 containing ethanol extract and Example 2 containing water extract
The results showed that the ethanol extract was more effective than the water extract.
また、マウスの組織を採取し、ドーパ染色を施して、毛
包メラノサイトの活性化に関する検討を行なった。実施
例1及び実施例2の製品は、比較例1の製品に比し、メ
ラノサイトの存在する毛根部は明らかにより強く、黒く
ドーパによって染色され、毛根部のメラノサイトが活性
化されていることが認められた。In addition, tissue from mice was collected and stained with DOPA to examine the activation of hair follicle melanocytes. In the products of Examples 1 and 2, compared to the product of Comparative Example 1, the hair roots where melanocytes are present were clearly more strongly stained by DOPA, and it was observed that the melanocytes in the hair roots were activated. It was done.
従って、このことは、毛根部のメラノサイトを活性化す
ることによって、白毛を黒毛に変えているものと考えら
れる。Therefore, it is thought that this changes white hair into black hair by activating melanocytes in the hair root.
く安全性テスト〉
人での効果評価を行なう前に、皮膚に対する本発明に係
る毛髪化粧料の刺激性についての検討を行なうなめ、以
下の通り人体パッチテストを行なった。Safety Test> Before evaluating the effects on humans, a human patch test was conducted as follows in order to examine the irritation of the hair cosmetic according to the present invention to the skin.
試料として実施例1及び実施例2の各ヘアトニックを用
いた。Each hair tonic of Example 1 and Example 2 was used as a sample.
被験者としては、1試料につき成人女子45名を1群と
し、24時間、人体前腕クローズドパッチテストを行な
った。The test subjects were 45 adult females per group, and a human forearm closed patch test was conducted for 24 hours.
判定基準は次記の基準に従った。Judgment criteria were based on the following criteria.
強紅斑 ++
紅斑 十
微かな紅斑 士
陰性 −
表 3 人バッチテストの結果
表3から明らかなように、本発明に係る毛髪化粧料につ
いてはいずれも刺激性か低いことが認められた。その他
、安全性テストとして動物による皮膚−次刺激性試験及
びアレルギー試験を行なったが、皮膚刺激性及びアレル
ギー性とも全く認められず、皮膚に対する安全性は極め
て高いものであった。Strong erythema ++ Erythema Slight erythema Negative - Table 3 Human batch test results As is clear from Table 3, all of the hair cosmetics according to the present invention were found to be irritating. In addition, a skin secondary irritation test and an allergy test using animals were conducted as safety tests, and no skin irritation or allergy was observed, indicating that the product was extremely safe for the skin.
く人による白髪予防・改善試験〉
上記結果を受けて、本発明に係る毛髪化粧料を人の白髪
に適用し、その白髪予防、改善効果を検討するため次の
試験を行なった。Human Gray Hair Prevention/Improvement Test> Based on the above results, the following test was conducted in order to apply the hair cosmetic according to the present invention to human gray hair and examine its effect on gray hair prevention and improvement.
駁肱藍1 実施例1及び実施例2の各ヘアトニック、比
較例1のヘアトニック
m 被験者として各試料ごとに白髪を有する40〜6
0才の男女30名を3群に分け、試料各1 rsllを
一日2回頭皮に塗擦し、5力月間継続使用した。Pierre Blue 1 Each hair tonic of Example 1 and Example 2, hair tonic of Comparative Example 1 40 to 6 with gray hair for each sample as a test subject
Thirty men and women aged 0 years were divided into 3 groups, and 1 rsll of each sample was rubbed onto the scalp twice a day for 5 months of continuous use.
L毀立韮 塗擦部位の状態を試料使用前と後とで、写真
撮影して比較し、白髪予防、改善効果を評価した。なお
、判定基準はいずれの場合も下記のような基準に従って
行なった。L-Kitate-Nira The condition of the rubbed area was photographed and compared before and after using the sample, and the effect of preventing and improving gray hair was evaluated. In addition, the evaluation criteria were as follows in each case.
著しい効果 十十
かなりめ効果 十
やや効果あり ±
効果なし 〜
表 4 人での効果試験
表4から明らかなように、実施例1のヘアトニック及び
実施例2のヘアトニックのいずれの場合も白髪の増加を
きなさず、優れた白髪予防、改善効果を示すことか認め
られた。一方、比較例1は、効果があまり認められなが
った。Significant effect 10% effect 10% moderately effective ± no effect ~ Table 4 Human effect test As is clear from Table 4, both the hair tonic of Example 1 and the hair tonic of Example 2 have no effect on gray hair. It was confirmed that the hair growth rate did not increase and showed excellent effects on preventing and improving gray hair. On the other hand, in Comparative Example 1, little effect was observed.
実施例3 ヘアクリーム
く処方〉
く製造法〉
処方原料A及び同Bをそれぞれ加熱溶解し、80″Cに
保つ。温度調整器付きホモミキサーの容器にAをとり、
Bを加えて混合乳化する。撹拌しながら常温まで冷却し
てクリームタイプの白髪予防、改善剤を得た。Example 3 Hair cream formulation〉 Production method〉 Prescription raw materials A and B are respectively heated and dissolved and kept at 80''C. Place A in a container of a homomixer equipped with a temperature controller,
Add B and mix and emulsify. The mixture was cooled to room temperature while stirring to obtain a cream type agent for preventing and improving gray hair.
し発明の効果J
以上のように本発明に係る毛髪化粧料は、白髪予防、改
善効果として優れた効果を有し、しかも皮膚刺激性、ア
レルギー性は認められない。Effects of the Invention J As described above, the hair cosmetic according to the present invention has an excellent effect of preventing and improving gray hair, and has no skin irritation or allergy.
Claims (1)
成分として含有することを特徴とする毛髪化粧料。 2)前記の抽出溶媒が、水または低級アルコールから選
ばれたものである請求項1)記載の毛髪化粧料。[Scope of Claims] 1) A hair cosmetic comprising, as a compounding ingredient, an extract obtained by extracting Mori annua with an extraction solvent. 2) The hair cosmetic according to claim 1, wherein the extraction solvent is selected from water and lower alcohols.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2316116A JPH04187623A (en) | 1990-11-22 | 1990-11-22 | Hair cosmetics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2316116A JPH04187623A (en) | 1990-11-22 | 1990-11-22 | Hair cosmetics |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04187623A true JPH04187623A (en) | 1992-07-06 |
Family
ID=18073427
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2316116A Pending JPH04187623A (en) | 1990-11-22 | 1990-11-22 | Hair cosmetics |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04187623A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001002575A (en) * | 1999-06-21 | 2001-01-09 | Sunstar Inc | Accelerator for accelerating production of melanine |
JP2001302437A (en) * | 2000-04-24 | 2001-10-31 | Fancl Corp | Irritation mitigating composition |
US6905714B2 (en) * | 2000-02-29 | 2005-06-14 | National University Of Singapore | Method for modulating steroidogenic activity |
KR100787640B1 (en) * | 2007-02-08 | 2007-12-21 | 이태희 | Natural hair growth promoter composition |
KR100787641B1 (en) * | 2007-02-08 | 2007-12-21 | 이태희 | Natural hair growth promoter composition |
KR100787639B1 (en) * | 2005-11-16 | 2007-12-21 | 이태희 | Natural hair growth promoter composition |
JP2008127305A (en) * | 2006-11-20 | 2008-06-05 | Pola Chem Ind Inc | Orally administrable composition for arthritis or arthropathia |
CN107095990A (en) * | 2017-06-13 | 2017-08-29 | 刘向源 | A kind of Chinese medicine composition for treating pain in waist and lower extremities |
-
1990
- 1990-11-22 JP JP2316116A patent/JPH04187623A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001002575A (en) * | 1999-06-21 | 2001-01-09 | Sunstar Inc | Accelerator for accelerating production of melanine |
US6905714B2 (en) * | 2000-02-29 | 2005-06-14 | National University Of Singapore | Method for modulating steroidogenic activity |
JP2001302437A (en) * | 2000-04-24 | 2001-10-31 | Fancl Corp | Irritation mitigating composition |
KR100787639B1 (en) * | 2005-11-16 | 2007-12-21 | 이태희 | Natural hair growth promoter composition |
JP2008127305A (en) * | 2006-11-20 | 2008-06-05 | Pola Chem Ind Inc | Orally administrable composition for arthritis or arthropathia |
KR100787640B1 (en) * | 2007-02-08 | 2007-12-21 | 이태희 | Natural hair growth promoter composition |
KR100787641B1 (en) * | 2007-02-08 | 2007-12-21 | 이태희 | Natural hair growth promoter composition |
CN107095990A (en) * | 2017-06-13 | 2017-08-29 | 刘向源 | A kind of Chinese medicine composition for treating pain in waist and lower extremities |
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