JPS62120311A - Hair nourishing cosmetic - Google Patents

Hair nourishing cosmetic

Info

Publication number
JPS62120311A
JPS62120311A JP25911585A JP25911585A JPS62120311A JP S62120311 A JPS62120311 A JP S62120311A JP 25911585 A JP25911585 A JP 25911585A JP 25911585 A JP25911585 A JP 25911585A JP S62120311 A JPS62120311 A JP S62120311A
Authority
JP
Japan
Prior art keywords
cosmetic
hair
hair nourishing
oxide
effect
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP25911585A
Other languages
Japanese (ja)
Other versions
JPH0566927B2 (en
Inventor
Takeo Kinji
金児 猛夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP25911585A priority Critical patent/JPS62120311A/en
Publication of JPS62120311A publication Critical patent/JPS62120311A/en
Publication of JPH0566927B2 publication Critical patent/JPH0566927B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/63Steroids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A61K8/4953Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q7/00Preparations for affecting hair growth

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:A hair nourishing cosmetic showing effective and efficient growth promoting action on hair, obtained by combining three compounds such as an antiandrogen agent, etc. CONSTITUTION:A cosmetic base is blended with 0.25-2.5wt% antiandrogen agent (e.g., 16beta-ethyl-17beta-hydroxy-4-estren-3-one, etc.,), 0.1-1wt% 2,4-diamino-6- piperidinopyrimidin-3-oxide and 1-10wt% 1-dodecylazacycloheptan-2-one to give a hair nourishing cosmetic. Since the antiandrogen agent which is slightly soluble in a solvent is dissolved in 1-dodecylazacycloheptan-2-one, a cosmetic having more improved hair nourishing effect than a cosmetic obtained by blending only both the antiandrogen agent and 2,4-diamino-6-piperidino-pyrimidin-3- oxide can be obtained.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、公知の化合物3種類を組み合わせることによ
って、結果的に有効な毛髪の成長促進作用を示す養毛化
粧品に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a hair nourishing cosmetic product that exhibits an effective hair growth promoting effect by combining three types of known compounds.

従来技術及び問題点 本発明者は、先に抗アンドロジエン剤(antiand
rogen)と2.4−ノアミノ−6−ビペリクノビリ
ミシンー3−オキサイド(2,4−diamino −
6−piperidinopyrimidine −3
−oxide)との組み合わせによる有効な毛髪の成長
促進作用を見出だし、特Ill 60−4625にこれ
らの化合物を有効成分として含む養毛化粧料をIll示
した0本発明者は、上記養毛化粧料の改善を志し、様々
な検討を試みていたが、通常の溶媒に溶けにくい抗アン
ドロノヱン剤が1−ドデシルアザシクロヘプタン−2−
オン(1−dodecylazacyclohepta
n −2−one)に溶解することを見出だし、本発明
を完成するに至った。
PRIOR ART AND PROBLEMS The present inventor has previously developed an anti-androgien agent.
rogen) and 2,4-noamino-6-bipericnobilimicin-3-oxide (2,4-diamino-
6-piperidinopyrimidine-3
The present inventors have discovered an effective hair growth promoting effect in combination with the above-mentioned hair growth cosmetics (-oxides), and have specifically proposed a hair-growth cosmetic containing these compounds as active ingredients in Patent No. 60-4625. However, the anti-andronodine agent, which is difficult to dissolve in ordinary solvents, was found to be 1-dodecyl azacycloheptane-2-
On (1-dodecylazacyclohepta
n-2-one), and completed the present invention.

解決手段 本発明の要旨は抗アンドロジェン剤(anti−and
rogen)を1−ドデシルアザシクロヘプタン−2−
オンに溶解せしめて、2.4−ジアミノ−6−ピベリノ
/ピリミジン−3−オキサイドとともに有効成分として
化粧品基剤中に配合することにより、抗アンドロジェン
剤と2.4−:)アミ/−6−ビベリジノビリミシンー
3−オキサイドの両者のみを配合した化粧品に比べて、
さらに養毛効果にすぐれた化粧品を得ることが出来るこ
とにある。以下詳細に説明する。
Solution The gist of the present invention is to provide an anti-androgen agent.
rogen) to 1-dodecyl azacycloheptane-2-
By dissolving the 2.4-diamino-6-piberino/pyrimidine-3-oxide in a cosmetic base as an active ingredient, the anti-androgen agent and 2.4-:)ami/-6 can be combined. - Compared to cosmetics containing only biverizinobilimicin and 3-oxide,
Furthermore, it is possible to obtain cosmetics with excellent hair-nourishing effects. This will be explained in detail below.

化粧品基剤中への抗アンドロジエン剤の配合量は、凡そ
、化粧品基剤の0.25〜2.5重量%、2.4−ノア
ミノ−6−ビベリジノビリミシンー3−オキサイドのそ
れは、0.1〜1%、1−ドデシルアザシクロヘプタン
−2−オンは、1〜10%の範囲で夫々用いることによ
り十分に目的を達成することができる。抗アンドaツエ
ン剤としては、16β−エチル−17β−ヒドロキシ−
4−ニストレン−3−オンなどを挙げることができる。
The amount of anti-androgien agent added to the cosmetic base is approximately 0.25 to 2.5% by weight of the cosmetic base, and that of 2.4-noamino-6-biveridinobilimicin-3-oxide is: The purpose can be sufficiently achieved by using 0.1 to 1% and 1-dodecyl azacycloheptan-2-one in the range of 1 to 10%, respectively. As an anti-and-a-thiene agent, 16β-ethyl-17β-hydroxy-
Examples include 4-nystren-3-one.

以下に本願化粧品の養毛効果を示す試験例と製造実施例
とを掲げる。
Test examples and manufacturing examples showing the hair-nurturing effect of the cosmetics of the present invention are listed below.

[試験例] 本願化粧品の養毛効果の検定の為、下記のようなA、8
2種の供試液を準備し、これらの供試液使用前後の洗髪
時の抜毛本数の変化で、効果の判定をした。被試験者は
、総じて男性で、供試液の各について5名ずつ2群に分
けて、1週間に1度の割合で、4ケ月間計16回抜毛を
回収した、最初の2ケ月間は自然抜毛回収期間とし、後
半の2ケ月間を後記供試液A、Bの塗布による効果を見
る期間とした。効果は、供試液使用前の期間(無塗布期
間)と該液使用中の期間(塗布期間)のそれぞれ8回の
平均で比較した。尚、1回の洗髪間隔は2日とした。
[Test Example] In order to test the hair growth effect of the cosmetics of this application, the following A and 8 were tested.
Two types of test liquids were prepared, and the effectiveness was determined based on the change in the number of hairs removed during hair washing before and after using these test liquids. The test subjects were generally male, and they were divided into two groups of 5 people for each test solution, and hair was collected once a week for a total of 16 times over 4 months. The hair removal period was used as a collection period, and the latter two months were used as a period to observe the effects of applying test solutions A and B described later. The effects were compared using the average of eight times each during the period before the test solution was used (non-application period) and during the period during which the test solution was used (application period). The interval between each hair wash was 2 days.

供試液A: 16β−エチル−17β−ヒドロキシ −4−ニストレン−3−オン・・・・・・0.5g2.
4−ジアミノ−6−ビベリノ/ピ リミジン−3−オキサイド・・・・・・0.5g95%
エタノール     ・・・・・・50g蒸留水   
      ・・・・・・49゜供試液B: 16β−エチル−17β−ヒトaキシ −4−ニストレン−3−オン・・・0.5g1−トチ°
シル7ザシクひへブタン−2−オン         
・・・・・・5.0゜2.4−ノアミノ−6−ビベリノ
/ピ リミジン−3−オキサイド ・・・O,5g95%エタ
/−ル    ・・・・・・50g蒸留水      
   ・・・・・・44g結果 下表に示すように、供試液Aでは、5名中者しい効果(
+十+)1名、かなりの効果(十十)2名、やや効果(
+)2名という結果であったが、供試液Bでは、者しい
効果3名かなりの効果2名という結果を得た。
Test solution A: 16β-ethyl-17β-hydroxy-4-nystren-3-one...0.5g2.
4-diamino-6-viverino/pyrimidine-3-oxide...0.5g95%
Ethanol: 50g distilled water
...49゜Test solution B: 16β-ethyl-17β-human axy-4-nystren-3-one...0.5g 1-horse chestnut
Sil7zasikhihebutan-2-one
・・・・・・5.0゜2.4-Noamino-6-biverino/pyrimidine-3-oxide ・・・O, 5g 95% ethyl alcohol ・・・・・・50g Distilled water
・・・・・・44g Results As shown in the table below, sample solution A showed a moderate effect (
+10 +) 1 person, significant effect (10) 2 people, moderate effect (
+) 2 people, but with sample solution B, 3 people had a significant effect and 2 people had a significant effect.

A群 パネルNO無塗布期間 塗布期間 効果1261±34
  233±42+ 2313±52  222±38 −)++3    
 196 ±26    138  ±51   ++
4296±41264±25+ 5     352 ±53    309  ±33
   ←B群 パネルNO無塗布期間 塗布期間 効果1397二43
   336±27 −i+2184±27   10
1+:56  →3    224+39    xz
s: 53  +++4    324 + 44  
 212 ”: 48  →5    289”28 
  22.6±31  ++−尚ヒ表において、判定基
準は次の通りである。
Group A panel NO No application period Application period Effect 1261±34
233±42+ 2313±52 222±38 -)++3
196 ±26 138 ±51 ++
4296±41264±25+ 5 352 ±53 309 ±33
←Group B Panel No. No application period Application period Effect 1397243
336±27 -i+2184±27 10
1+:56 →3 224+39 xz
s: 53 +++4 324 + 44
212”: 48 →5 289”28
22.6±31 ++-In addition, in the table below, the criteria for judgment are as follows.

抜毛本数の減少数     効果小僧170本以上  
   者しV1効果+ 40〜69    かなりの効果廿 11〜39    やや効果あり + 10本以下    効果なし   − 上記から明らかなように、16β−エチル−17β−ヒ
ドロキシ−4−ニストレン−3−オンと2.4−ノアミ
ツ−6−ビベリノノビリミノン−3−オキサイドの併用
よりも、この二者に、更に1−ドデシルアザシクロヘプ
タン−2−オンを添加することによる相乗効果がみられ
る、 1実施例1  ヘアローションの製造 16β−エチル−17β−ヒドロキシ−4−ニストレン
−3−オン0.5gを、1−ドデシルアザシクロヘプタ
ン−2−オン5gに溶解せしめる。一方、2.4−ジア
ミノ−6一ビベリノノビリミシン−3−オキサイド0.
5gヲ、95%エタ/−ル50…1に溶解せしめ、得ら
れた両液を混合後、香料、養毛料を適量加え、さらに精
製水を加えて全体を100gとして、へ7117−シ3
ンを得る。
Reduction in the number of hairs pulled: 170 or more effective hairs
V1 effect + 40-69 Considerable effect 11-39 Somewhat effective + 10 or less No effect - As is clear from the above, 16β-ethyl-17β-hydroxy-4-nystrene-3-one and 2. 1 Example 1 A synergistic effect is seen by adding 1-dodecyl azacycloheptan-2-one to these two rather than using 4-noamitsu-6-biberinonobiriminone-3-oxide in combination. Preparation of hair lotion 1. 0.5 g of 6β-ethyl-17β-hydroxy-4-nystren-3-one is dissolved in 5 g of 1-dodecyl azacycloheptan-2-one. On the other hand, 2,4-diamino-6-bivelinonobilimicin-3-oxide 0.
Dissolve 5 g in 95% ethanol 50...1, mix the obtained two solutions, add appropriate amounts of fragrance and hair nourishing agent, and further add purified water to make a total of 100 g, and mix into 7117-3.
get the results.

Claims (1)

【特許請求の範囲】[Claims] 抗アンドロジェン剤と1−ドデシルアザシクロヘプタン
−2−オンとおよび2,4−ジアミノ−6−ピペリジノ
ピリミジン−3−オキサイドとを養毛成分として含有す
る養毛化粧品
A hair nourishing cosmetic containing an antiandrogen, 1-dodecyl azacycloheptan-2-one, and 2,4-diamino-6-piperidinopyrimidine-3-oxide as hair nourishing ingredients.
JP25911585A 1985-11-19 1985-11-19 Hair nourishing cosmetic Granted JPS62120311A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25911585A JPS62120311A (en) 1985-11-19 1985-11-19 Hair nourishing cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25911585A JPS62120311A (en) 1985-11-19 1985-11-19 Hair nourishing cosmetic

Publications (2)

Publication Number Publication Date
JPS62120311A true JPS62120311A (en) 1987-06-01
JPH0566927B2 JPH0566927B2 (en) 1993-09-22

Family

ID=17329522

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25911585A Granted JPS62120311A (en) 1985-11-19 1985-11-19 Hair nourishing cosmetic

Country Status (1)

Country Link
JP (1) JPS62120311A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62230710A (en) * 1986-03-31 1987-10-09 Nitto Electric Ind Co Ltd Hair tonic composition
JPS63290814A (en) * 1987-05-25 1988-11-28 Kayoko Kaneko Hair-nourishing and hair-dressing agent
JP2006015140A (en) * 2004-06-30 2006-01-19 General Electric Co <Ge> System and method for magnetizing block on magnet assembly of mri device

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62230710A (en) * 1986-03-31 1987-10-09 Nitto Electric Ind Co Ltd Hair tonic composition
JPS63290814A (en) * 1987-05-25 1988-11-28 Kayoko Kaneko Hair-nourishing and hair-dressing agent
JP2006015140A (en) * 2004-06-30 2006-01-19 General Electric Co <Ge> System and method for magnetizing block on magnet assembly of mri device

Also Published As

Publication number Publication date
JPH0566927B2 (en) 1993-09-22

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