JPS6284014A - Hair tonic - Google Patents
Hair tonicInfo
- Publication number
- JPS6284014A JPS6284014A JP22320185A JP22320185A JPS6284014A JP S6284014 A JPS6284014 A JP S6284014A JP 22320185 A JP22320185 A JP 22320185A JP 22320185 A JP22320185 A JP 22320185A JP S6284014 A JPS6284014 A JP S6284014A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- dione
- estrene
- skin
- agent
- 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
- 210000004209 hair Anatomy 0.000 title claims abstract description 45
- 230000001256 tonic effect Effects 0.000 title abstract description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000005977 Ethylene Substances 0.000 claims abstract description 18
- 239000000810 peripheral vasodilating agent Substances 0.000 claims description 9
- 229960002116 peripheral vasodilator Drugs 0.000 claims description 9
- 230000000694 effects Effects 0.000 abstract description 29
- 239000003795 chemical substances by application Substances 0.000 abstract description 13
- 230000002195 synergetic effect Effects 0.000 abstract description 3
- ZFMITUMMTDLWHR-UHFFFAOYSA-N Minoxidil Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 abstract description 2
- RZMKWKZIJJNSLQ-UHFFFAOYSA-M carpronium chloride Chemical compound [Cl-].COC(=O)CCC[N+](C)(C)C RZMKWKZIJJNSLQ-UHFFFAOYSA-M 0.000 abstract description 2
- 229950003631 carpronium chloride Drugs 0.000 abstract description 2
- 229960003632 minoxidil Drugs 0.000 abstract description 2
- 239000002674 ointment Substances 0.000 abstract description 2
- 210000005259 peripheral blood Anatomy 0.000 abstract description 2
- 239000011886 peripheral blood Substances 0.000 abstract description 2
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 abstract description 2
- 210000004761 scalp Anatomy 0.000 abstract description 2
- LXMSZDCAJNLERA-ZHYRCANASA-N spironolactone Chemical compound C([C@@H]1[C@]2(C)CC[C@@H]3[C@@]4(C)CCC(=O)C=C4C[C@H]([C@@H]13)SC(=O)C)C[C@@]21CCC(=O)O1 LXMSZDCAJNLERA-ZHYRCANASA-N 0.000 abstract description 2
- 229960002256 spironolactone Drugs 0.000 abstract description 2
- 239000004480 active ingredient Substances 0.000 abstract 1
- 210000004369 blood Anatomy 0.000 abstract 1
- 239000008280 blood Substances 0.000 abstract 1
- 230000000916 dilatatory effect Effects 0.000 abstract 1
- 239000006210 lotion Substances 0.000 abstract 1
- 230000001737 promoting effect Effects 0.000 abstract 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
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- 235000001815 DL-alpha-tocopherol Nutrition 0.000 description 7
- 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 7
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- -1 DL-α-tocopherol nicotinic acid ester Chemical class 0.000 description 6
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- FUWUEFKEXZQKKA-UHFFFAOYSA-N beta-thujaplicin Chemical compound CC(C)C=1C=CC=C(O)C(=O)C=1 FUWUEFKEXZQKKA-UHFFFAOYSA-N 0.000 description 6
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- 230000003779 hair growth Effects 0.000 description 5
- 238000005342 ion exchange Methods 0.000 description 5
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- NVKAWKQGWWIWPM-ABEVXSGRSA-N 17-β-hydroxy-5-α-Androstan-3-one Chemical compound C1C(=O)CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CC[C@H]21 NVKAWKQGWWIWPM-ABEVXSGRSA-N 0.000 description 4
- 201000004384 Alopecia Diseases 0.000 description 4
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- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 description 4
- KVYGGMBOZFWZBQ-UHFFFAOYSA-N benzyl nicotinate Chemical compound C=1C=CN=CC=1C(=O)OCC1=CC=CC=C1 KVYGGMBOZFWZBQ-UHFFFAOYSA-N 0.000 description 4
- 210000004027 cell Anatomy 0.000 description 4
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- 238000002156 mixing Methods 0.000 description 4
- 210000001732 sebaceous gland Anatomy 0.000 description 4
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- AOBORMOPSGHCAX-DGHZZKTQSA-N tocofersolan Chemical compound OCCOC(=O)CCC(=O)OC1=C(C)C(C)=C2O[C@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C AOBORMOPSGHCAX-DGHZZKTQSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 244000184734 Pyrus japonica Species 0.000 description 3
- 244000273928 Zingiber officinale Species 0.000 description 3
- 235000006886 Zingiber officinale Nutrition 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- TUFYVOCKVJOUIR-UHFFFAOYSA-N alpha-Thujaplicin Natural products CC(C)C=1C=CC=CC(=O)C=1O TUFYVOCKVJOUIR-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000008397 ginger Nutrition 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 229940057995 liquid paraffin Drugs 0.000 description 3
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 3
- 102000005962 receptors Human genes 0.000 description 3
- 108020003175 receptors Proteins 0.000 description 3
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 3
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 3
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 3
- 229930007845 β-thujaplicin Natural products 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 2
- 241000131283 Cantharis Species 0.000 description 2
- 235000002566 Capsicum Nutrition 0.000 description 2
- 240000008574 Capsicum frutescens Species 0.000 description 2
- 239000006000 Garlic extract Substances 0.000 description 2
- 235000010254 Jasminum officinale Nutrition 0.000 description 2
- 240000005385 Jasminum sambac Species 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 210000004100 adrenal gland Anatomy 0.000 description 2
- 206010068168 androgenetic alopecia Diseases 0.000 description 2
- 229950004580 benzyl nicotinate Drugs 0.000 description 2
- 239000001390 capsicum minimum Substances 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 229940082500 cetostearyl alcohol Drugs 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
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- 235000020706 garlic extract Nutrition 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 229940075507 glyceryl monostearate Drugs 0.000 description 2
- 208000024963 hair loss Diseases 0.000 description 2
- 230000003676 hair loss Effects 0.000 description 2
- UBHWBODXJBSFLH-UHFFFAOYSA-N hexadecan-1-ol;octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO.CCCCCCCCCCCCCCCCCCO UBHWBODXJBSFLH-UHFFFAOYSA-N 0.000 description 2
- 230000003054 hormonal effect Effects 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- YNBADRVTZLEFNH-UHFFFAOYSA-N methyl nicotinate Chemical compound COC(=O)C1=CC=CN=C1 YNBADRVTZLEFNH-UHFFFAOYSA-N 0.000 description 2
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 2
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 2
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- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 2
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- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
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- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
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- 239000011626 DL-alpha-tocopherylacetate Substances 0.000 description 1
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- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
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- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- JFIOVJDNOJYLKP-UHFFFAOYSA-N bithionol Chemical compound OC1=C(Cl)C=C(Cl)C=C1SC1=CC(Cl)=CC(Cl)=C1O JFIOVJDNOJYLKP-UHFFFAOYSA-N 0.000 description 1
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- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
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- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
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- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q7/00—Preparations for affecting hair growth
-
- 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
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Abstract
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は優れた養毛効果を持つ養毛料に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to a hair nourishing agent having excellent hair nourishing effects.
[従来の技術]
男性型の禿頭や脂漏などの生理学上の徴候は、男性ホル
モンの過剰蓄積に基づく男性ホルモン刺激の増大による
と言われているが、最近、毛根、皮脂線などの器官にお
けるこの男性ホルモン活性の本体は、これら標的器官に
おいてテストステロン(男性ホルモン)がテストステロ
ン−5α−レダクターゼという名の酵素(以下、レダク
ターゼと略す。)によって還元された5α−ジヒドロテ
ストステロン(以下、5α−DHTと略す。)であるこ
とが周知となってきている。即ち、畢丸や副腎で作られ
たテストステロンは血流に乗って皮脂線に行き、皮脂線
細胞の中にあるレダクターゼによって、より強力な男性
ホルモンである5α−DHTに変換される。この5α−
DHTは細胞内の受容体と結合し、核に働いて皮脂線細
胞の増殖を □促す一方、それ自体が皮脂腺細胞外に
出て血流に乗り、毛母の細胞に働き毛球部の毛母細胞の
分裂を抑制し、毛の成長を妨げ、抜毛、脱毛を促進する
ものとされている。[Prior Art] Physiological symptoms such as male-pattern baldness and seborrhea are said to be due to increased stimulation of male hormones due to excessive accumulation of male hormones. The main body of this male hormone activity is 5α-dihydrotestosterone (hereinafter referred to as 5α-DHT), which is produced by reducing testosterone (male hormone) in these target organs by an enzyme called testosterone-5α-reductase (hereinafter referred to as reductase). ) is becoming well known. In other words, testosterone produced by the adrenal glands and adrenal glands travels through the bloodstream to the sebaceous glands, where it is converted into 5α-DHT, a more powerful male hormone, by reductase in the sebaceous gland cells. This 5α-
DHT binds to intracellular receptors, acts on the nucleus, and promotes the proliferation of sebaceous gland cells, while DHT itself exits the sebaceous gland cells and enters the bloodstream, acting on hair matrix cells and stimulating the growth of hair in the hair bulb. It is said to suppress the division of mother cells, impede hair growth, and promote hair pulling and hair loss.
[発明が解決しようとする問題点]
従って、男性型の禿頭や脱毛などの徴候は、レダクター
ゼの活性を阻害すること、および5α−DHTと受容体
タンパクとの結合を阻害することにより低減または防止
することができると考えられ、この観点に基づいてこれ
までにクロルマジノンアセテート、オレイン酸、リノー
ル酸などの物質か見い出きれている。しかしながら、こ
れらの物質はレダクターゼ活性の阻害率は大きくても好
ましくない副作用があったり、5α−DHTと受容体タ
ンパクとの結合阻害率が非常に低かったりして、実質上
の養毛効果に劣るという欠点があった。[Problems to be Solved by the Invention] Therefore, symptoms such as male pattern baldness and hair loss can be reduced or prevented by inhibiting the activity of reductase and the binding of 5α-DHT to receptor proteins. Based on this viewpoint, substances such as chlormadinone acetate, oleic acid, and linoleic acid have been discovered so far. However, even though these substances have a high inhibition rate of reductase activity, they have undesirable side effects, and their inhibition rate of binding between 5α-DHT and receptor protein is very low, so they are inferior to the actual hair growth effect. There was a drawback.
[問題点を解決するための手段]
本発明者らは、上記事情に鑑み、ホルモン作用などの好
ましくない副作用を持たず、安全で、かつレダクターゼ
活性の阻害と、5α−D HTと受容体タンパクとの結
合阻害の両方の効果を併せ持つ物質を探究し、これを配
合することにより養毛効果の優れた養毛材を得るべく鋭
意研究を重ねた結果、4−エストレン−3,17−ジオ
ン−17−サイクリックエチレンケタールを配合するこ
とにより上記目的が達成できることを見い出した(特開
昭6O−67411)。今回、更に研究を進めた結果、
4−エストレン−3,17−ジオン−17−サイクリッ
クエチレンケタールと皮膚末梢血管拡張剤の一種または
二種以上とを配合することにより、その効果が相乗的に
増大することを見い出し本発明を完成するに至った。[Means for Solving the Problems] In view of the above circumstances, the present inventors have developed a method that does not have undesirable side effects such as hormonal effects, is safe, inhibits reductase activity, and inhibits 5α-D HT and receptor protein. As a result of intensive research in search of a substance that has both the effect of inhibiting the binding of 4-estrene-3,17-dione- It has been found that the above object can be achieved by blending 17-cyclic ethylene ketal (Japanese Patent Application Laid-Open No. 60-67411). This time, as a result of further research,
The present invention has been completed by discovering that by combining 4-estrene-3,17-dione-17-cyclic ethylene ketal with one or more skin peripheral vasodilators, the effects can be synergistically increased. I ended up doing it.
すなわち、本発明は4−エストレン−3,17−ジオン
−17−サイクリックエチレンケタールと、皮膚末梢血
管拡張剤の一種または二種以上とを含有することを特徴
とする養毛材である。That is, the present invention is a hair nourishing material containing 4-estrene-3,17-dione-17-cyclic ethylene ketal and one or more skin peripheral vasodilators.
以下、本発明の構成について詳述する。Hereinafter, the configuration of the present invention will be explained in detail.
4−゛ニストレンー3,17−ジオン−17−サイクリ
ックエチレンケタールの配合量は、本発明の養毛材中0
.0001〜2重量%が好ましい。特に好ましくは、0
.0001〜0.2重量%である。0.0001重量%
未満では、養毛効果が発揮できない場合がある。また配
合量が多い程養毛効果は大きいが、多量に用いられた時
の予期せぬ副作用の発現などを考えると、2重量%以下
が好ましい。The blending amount of 4-yenistrene-3,17-dione-17-cyclic ethylene ketal is 0 in the hair nourishing material of the present invention.
.. 0001 to 2% by weight is preferred. Particularly preferably, 0
.. 0001 to 0.2% by weight. 0.0001% by weight
If the amount is less than that, the hair nourishing effect may not be exhibited. The higher the amount, the greater the hair-nourishing effect, but in view of the possibility of unexpected side effects occurring when a large amount is used, the amount is preferably 2% by weight or less.
本発明において相乗的に養毛効果を増大させる物質であ
る皮膚末梢血管拡張剤は塩化カルプロニウム、ミノキシ
ジル、スピロノラクトン、ビタミンB6塩酸塩、セファ
ランチン(タマサキッヅラフジエキス)、D−カンフル
、DL−カンフル、DL−α−トコフェロール、ヨウ化
ニンニクエキス、DL−α−トコフエロールリルイン酸
エステル、センブリエキス、イノシトールヘキサニコチ
ン酸エステル、ビタミンE1デキストラン硫酸ナトリウ
ム、ニコチン酸、DL−α−トコフェロールニコチン酸
エステル、ニコチン酸ブトキシエチル、γ−オリプノー
ル、ニコチン酸ベンジル、ニコチン酸メチル、ノナン酸
バニリルアミド、コハク酸DL−α−トコフヱロール、
酢酸DL−α−トコフェロール、トウガラシチンキ、カ
ンタリスチンキ、ショウキョウチンキなどであり、セフ
ァランチン(タマサキッヅラフジエキス)、DL−α−
トコフェロール、ヨウ化ニンニクエキス、センブリエキ
ス、DL−α−トコフェロールニコチン酸エステル、ニ
コチン酸ペンシル、ノナン酸パニリルアミド、酢酸DL
−α−トコフェロール、トウガラシチンキ、カンタリス
チンキ、ショウキョウチンキなどが好ましい。In the present invention, the skin peripheral vasodilators, which are substances that synergistically increase the hair-nurturing effect, include carpronium chloride, minoxidil, spironolactone, vitamin B6 hydrochloride, cephalanthine (Tamasa Kidzurafji extract), D-camphor, DL-camphor, DL-α-tocopherol, iodized garlic extract, DL-α-tocopherol lyric acid ester, Jasmine japonica extract, inositol hexanicotinic acid ester, vitamin E1 dextran sodium sulfate, nicotinic acid, DL-α-tocopherol nicotinic acid ester, nicotine Butoxyethyl acid, γ-olipnol, benzyl nicotinate, methyl nicotinate, vanillylamide nonanoate, DL-α-tocopherol succinate,
These include DL-α-tocopherol acetate, capsicum tincture, cantharis tincture, and ginger tincture, as well as cephalanthine (Tamasakidzurafuji extract), DL-α-
Tocopherol, iodized garlic extract, Jasmine japonica extract, DL-α-tocopherol nicotinic acid ester, nicotinic acid pencil, nonanoic acid panillylamide, acetic acid DL
-α-tocopherol, capsicum tincture, cantharis tincture, ginger tincture, etc. are preferred.
皮膚末梢血管拡張剤の配合量は0.0001〜5重量%
が好ましく、特に好ましくは0.01〜3.0重量%で
ある。0.0001重量%未満では、養毛効果が発揮で
きない場合があり、5重量%を越えても、それ以上の養
毛効果を期待できない場合がある。The compounding amount of the skin peripheral vasodilator is 0.0001 to 5% by weight.
is preferred, particularly preferably 0.01 to 3.0% by weight. If it is less than 0.0001% by weight, the hair nourishing effect may not be exhibited, and even if it exceeds 5% by weight, no further hair nourishing effect may be expected.
本発明に係る養毛材には上記の4−エストレン−3,1
7−ジオン−17−サイクリックエチレンケタールと皮
膚末梢血管拡張剤のほか、通常養毛材に用いられる添加
剤、例えば、ヒノキチオール、ヘキサクロロフェン、フ
ェノール、ベンザルコニウムクロリド、セチルピリジニ
ウムクロリド、ウンデシレン酸、トリクロロカルバニリ
ドおよびビチオノールなどの抗菌剤、メントールなどの
清涼剤、サリチル酸、亜鉛及びその誘導体、乳酸及びそ
のアルキルエステルなどの薬剤、オリーブ油、スクワラ
ン、流動パラフィン、イソプロピルミリステート、高級
脂肪酸、高級アルコールなどの油分、その低界面活性剤
、香料、酸化防止剤、紫外線吸収剤、色素、エタノール
、水、保湿剤、増粘剤などが本発明の効果を損なわない
範囲で適宜配合することができる。The hair nourishing material according to the present invention includes the above-mentioned 4-estrene-3,1
In addition to 7-dione-17-cyclic ethylene ketal and a skin peripheral vasodilator, additives commonly used in hair care products, such as hinokitiol, hexachlorophene, phenol, benzalkonium chloride, cetylpyridinium chloride, undecylenic acid, Antibacterial agents such as trichlorocarbanilide and bithionol, cooling agents such as menthol, drugs such as salicylic acid, zinc and its derivatives, lactic acid and its alkyl esters, olive oil, squalane, liquid paraffin, isopropyl myristate, higher fatty acids, higher alcohols, etc. The oil component, its low surfactant, fragrance, antioxidant, ultraviolet absorber, pigment, ethanol, water, humectant, thickener, etc. can be appropriately blended within the range that does not impair the effects of the present invention.
本発明の養毛材の性状は、液状、乳液、軟膏など外皮に
適用できる性状のものであればいずれでもよい。The hair growth material of the present invention may be in any form as long as it can be applied to the outer skin, such as liquid, emulsion, or ointment.
本発明に係る養毛剤は4−エストレン−3,17−ジオ
ン−17−サイクリックエチレンケタールと頭皮の末梢
血管を拡張し血流量の増加を促す皮膚末梢血管拡張剤と
が効果的に作用し、相乗的な養毛効果を発揮するもので
ある。The hair growth agent according to the present invention has a synergistic effect in which 4-estrene-3,17-dione-17-cyclic ethylene ketal and a skin peripheral vasodilator that dilates peripheral blood vessels in the scalp and promotes an increase in blood flow. It has a hair-nourishing effect.
[実施例]
次に実施例をあげて本発明をさらに詳細に説明する。本
発明はこれにより限定されるものではない。配合量は重
量%である。[Example] Next, the present invention will be explained in more detail by giving examples. The present invention is not limited thereby. The blending amount is in weight%.
実施例に先たち試験法を説明する。The test method will be explained in Examples below.
l至万来土主抜
試料使用前後の洗髪時脱毛本数の変化で判定した。被験
者は実施例1〜6及び比較例1の計7種類の各々の郡ご
とに10名とした。測定期間は4力月間とし、前半の2
力月間は試料無塗布の期間、後半の2力月間を試料塗布
の期間とした。この間、2日おきに洗髪して抜毛を回収
し、1週間分をまとめて、その本数を数えた。各期間の
抜毛本数の表示は、試料無塗布の2力月間、計8回の抜
毛本数のデータと養毛剤塗布の2力月間、計8回の抜毛
本数のデータをそれぞれの期間ごとにまとめ、平均値±
αの形で1回当りの抜毛本数として表示した。単位は本
である。効果の判定は、それぞれの期間の平均値の差か
ら次のように表示した。Judgment was made based on the change in the number of strands of hair removed during hair washing before and after using the Shimanrai Dosu sample. There were 10 subjects in each of the seven groups of Examples 1 to 6 and Comparative Example 1. The measurement period is 4 months, and the first two
The first month was the period when no sample was applied, and the second half of the second month was the period when the sample was applied. During this period, the hair was washed every two days and the pulled hair was collected, and the number of hairs for one week was counted. To display the number of hairs pulled out for each period, data on the number of hairs pulled out 8 times in 2 months without sample application and data on the number of hairs pulled out 8 times in 2 months with hair tonic applied are summarized for each period, and the average is calculated. Value±
The number of hairs pulled per session was expressed in the form of α. The unit is a book. The effectiveness was determined based on the difference between the average values for each period as shown below.
++:抜毛本数が70本以上減っており著しい効果を認
めた。++: The number of hairs pulled was reduced by 70 or more, indicating a significant effect.
+ :抜毛本数が40本以上減っておりかなりの効果を
認めた。+: The number of hairs pulled was reduced by 40 or more, indicating a considerable effect.
± :抜毛本数が10本以上減っておりやや効果ありと
いえた。±: The number of hairs pulled was reduced by 10 or more, indicating that it was somewhat effective.
−:抜毛本数の減少が10本未満であり効果ありとはい
えない。-: The reduction in the number of hairs pulled is less than 10, and it cannot be said that there is an effect.
実施例1.2、比較例1
(以下余白)
(製造法)
95%エタノールに4−エストレン−3,17−ジオン
−17−サイクリックエチレンケタール、ニコチン酸ベ
ンジル、および硬化ヒマシ油E O(40モル)イ寸加
物を添加し、撹拌溶解させ、次も)でイオン交換水を添
加、混合して実施例1の透明液状の養毛剤を得た。実施
例2、比較例1も実施例1と同様心こして得た。Example 1.2, Comparative Example 1 (blank below) (Production method) 95% ethanol, 4-estrene-3,17-dione-17-cyclic ethylene ketal, benzyl nicotinate, and hydrogenated castor oil EO (40 A transparent liquid hair growth agent of Example 1 was obtained by adding mol) and stirring to dissolve ion-exchanged water and mixing. Example 2 and Comparative Example 1 were also obtained in the same manner as in Example 1.
(以下余白)
(結果)
前述した結果はすべて、4−エストレン−3,17−ジ
オン−17−サイクリックエチレンケタールと皮膚末梢
血管拡張剤配合の本発明に係る養毛材が従来公知の4−
エストレン−3,17−ジオン−17−サイクリックエ
チレンケタールを配合した養毛材に比して、相乗的にそ
の養毛効果が優れていることを示している。(Margins below) (Results) All of the above results indicate that the hair nourishing material of the present invention containing 4-estrene-3,17-dione-17-cyclic ethylene ketal and a skin peripheral vasodilator was better than the conventionally known 4-estrene-3,17-dione-17-cyclic ethylene ketal and skin peripheral vasodilator.
This shows that the hair-nurturing effect is synergistically superior to the hair-nurturing material containing estrene-3,17-dione-17-cyclic ethylene ketal.
実施例3
(A 相)
4−エストレン−3,17−ジオン
−17−サイクリックエチレンケタール 2.0セン
ブリエキス 3.0ポリオキシエ
チレン(60(ル)
硬化ヒマシ油 2.0
グリセリン 7.0ジプロピ
レングリコール 8.41.3−ブチレ
ングリコール 5.0ポリエチレングリコ
ール1500 5.0(B 相)
セチルイソオクタネート 10.0スクワ
ラン 5.0ワセリン
2.0プロピルパラベン
2.0(C相)
カルボキシビニルポリマー1χ水溶?& 30.0へ
キサメタリン酸ソーダ 0,03イオン
交換水 8.95(D 相)
イオン交換水 4.5(E 相
)
カセイカリ 0.12イオ
ン交換水 5.0(製造法)
A相、B相をそれぞれ60℃で加P8溶解し、混合して
ホモミキサー処理しゲルを作る。これにD相を徐々に添
加しホモミキサーで分散する。Example 3 (Phase A) 4-Estrene-3,17-dione-17-cyclic ethylene ketal 2.0 Japonica extract 3.0 Polyoxyethylene (60 L) Hydrogenated castor oil 2.0 Glycerin 7.0 Di Propylene glycol 8.4 1.3-Butylene glycol 5.0 Polyethylene glycol 1500 5.0 (Phase B) Cetyl isooctanate 10.0 Squalane 5.0 Vaseline
2.0 Propylparaben
2.0 (C phase) Carboxyvinyl polymer 1χ water soluble? & 30.0 Sodium hexametaphosphate 0.03 Ion exchange water 8.95 (D phase) Ion exchange water 4.5 (E phase) Caustic potash 0.12 Ion exchange water 5.0 (Production method) A phase, B phase P8 was dissolved in each at 60°C, mixed and treated with a homomixer to form a gel. Phase D is gradually added to this and dispersed using a homomixer.
次にこれに溶解したC相を加え、最後に溶解したE相を
添加しホモミキサーで乳化してO/W乳液型の養毛材を
得た。 −
この養毛材を実施例1.2と同様に実使用テストを行っ
たところ、その養毛効果が優れていることが確認きれた
。Next, the dissolved phase C was added thereto, and finally the dissolved phase E was added and emulsified with a homomixer to obtain an O/W emulsion type hair nourishing material. - When this hair nourishing material was subjected to a practical use test in the same manner as in Example 1.2, it was confirmed that its hair nourishing effect was excellent.
実施例4
(A 相)
4−エストレン−3,17−ジオン
−17−サイクリックエチレンケタール 0.24−
エストレン−3−オン−
17β−カルボン酸ペンチルエステル 0.1セフア
ランチン 5.0流動パラフイン
5.0セトステアリルアルコール
5.1グリセリルモノステアレート
3.0EO(20モル)−2−オクチルドデシルエー
テル 3.0
プロピルパラベン 0.3香料
0.1(B 相)
グリセリン 8.0ジプロピレ
ングリコール 20.0ポリエチレングリコ
ール4000 5.0へキサメタリン酸ソーダ
0.005イオン交換水
45.295(製造法)
A相、B相をそれぞれ加熱溶解して混合し、ホモミキサ
ーで乳化して軟膏状養毛料を得た。Example 4 (Phase A) 4-estrene-3,17-dione-17-cyclic ethylene ketal 0.24-
Estren-3-one-17β-carboxylic acid pentyl ester 0.1 Cephalanthine 5.0 Liquid paraffin
5.0 Cetostearyl alcohol 5.1 Glyceryl monostearate
3.0 EO (20 mol)-2-octyldodecyl ether 3.0 Propylparaben 0.3 Fragrance
0.1 (Phase B) Glycerin 8.0 Dipropylene glycol 20.0 Polyethylene glycol 4000 5.0 Sodium hexametaphosphate
0.005 ion exchange water
45.295 (Manufacturing method) Phase A and phase B were respectively heated and dissolved, mixed, and emulsified with a homomixer to obtain an ointment-like hair nourishing agent.
この養毛料を実施例3と同様に実使用テストを実施例5
エタノール 55.04−エ
ストレン−3,17−ジオン−17−サイクリックエチ
レンケタール 0.0001DL−α−トコフェ
ロールニコチン酸
エステル 0.01
EO(8モル)オレイルアルコール
エーテル 2.0
ヒノキチオール 0,05香料
0.1染料
0.0899イオン交換水
42゜75(製造法)
エタノールにEO(8モル)オレイルアルコールエーテ
ル、4−エストレン−3,17−ジオン−17−サイク
リックエチレンケタール、DL−α−トコフェロールニ
コチン酸エステル、ヒノキチオールを加え、これに香料
、染料を加えて溶解した後、イオン交換水を加えて可溶
化し養毛料を得た。This hair nourishing agent was tested in the same manner as in Example 3. Example 5: Ethanol 55.04-estrene-3,17-dione-17-cyclic ethylene ketal 0.0001DL-α-tocopherol nicotinic acid ester 0.01 EO (8 moles) Oleyl alcohol ether 2.0 Hinokitiol 0.05 Fragrance
0.1 dye
0.0899 ion exchange water
42゜75 (Production method) Add EO (8 mol) oleyl alcohol ether, 4-estrene-3,17-dione-17-cyclic ethylene ketal, DL-α-tocopherol nicotinic acid ester, and hinokitiol to ethanol; After adding and dissolving perfume and dye, ion-exchanged water was added to solubilize to obtain a hair nourishing agent.
実施例6
4−エストレン−3,17−ジオン−1フーサイクリツ
クエチレンケタール0.2g、ショウキョウチンキ0.
0001g 、流動パラフィン5.0 g−、セトステ
アリルアルコール5.5g、ワセリン5.5g、グリセ
リルモノステアレート3.0g、 EO(20モル)−
2−オクチルドデシルエーテル3.0 g Nプロピル
パラベン0.2g、および香料0.1gを加熱溶解、混
合する。これに、グリセリン7.0g、ジプロピレング
リコール20.Og、 5.0gのポリエチレングリコ
ール4000、ヘキサメタリン酸ソーダ0.005gお
よびイオン交換水45.4949gの熱溶解混合物を添
加し、ホモミキサーにて乳化してクリーム状養毛料を得
た。得られた養毛料は優れた養毛効果を示した。Example 6 0.2 g of 4-estrene-3,17-dione-1 fucylic ethylene ketal, 0.2 g of ginger tincture.
0001 g, liquid paraffin 5.0 g, cetostearyl alcohol 5.5 g, petrolatum 5.5 g, glyceryl monostearate 3.0 g, EO (20 mol)
3.0 g of 2-octyldodecyl ether, 0.2 g of N-propylparaben, and 0.1 g of fragrance are heated and dissolved and mixed. To this, 7.0 g of glycerin and 20 g of dipropylene glycol. A hot melt mixture of Og, 5.0 g of polyethylene glycol 4000, 0.005 g of sodium hexametaphosphate, and 45.4949 g of ion-exchanged water was added and emulsified with a homomixer to obtain a cream-like hair nourishing agent. The obtained hair nourishing agent showed an excellent hair nourishing effect.
[発明の効果]
本発明の養毛料は、優れた養毛効果を有し、かつ、局所
的に有効で、全身的には副作用がなく、皮膚刺激性の少
ない、安全性の高い養毛料である。[Effects of the Invention] The hair nourishing agent of the present invention has an excellent hair nourishing effect, is locally effective, has no systemic side effects, and has little skin irritation, and is a highly safe hair nourishing agent. be.
Claims (1)
クエチレンケタールと、皮膚末梢血管拡張剤の一種また
は二種以上とを含有することを特徴とする養毛料。A hair nourishment containing 4-estrene-3,17-dione-17-cyclic ethylene ketal and one or more skin peripheral vasodilators.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22320185A JPS6284014A (en) | 1985-10-07 | 1985-10-07 | Hair tonic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22320185A JPS6284014A (en) | 1985-10-07 | 1985-10-07 | Hair tonic |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6284014A true JPS6284014A (en) | 1987-04-17 |
Family
ID=16794373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22320185A Pending JPS6284014A (en) | 1985-10-07 | 1985-10-07 | Hair tonic |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6284014A (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6067411A (en) * | 1983-09-26 | 1985-04-17 | Shiseido Co Ltd | Cosmetic |
-
1985
- 1985-10-07 JP JP22320185A patent/JPS6284014A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6067411A (en) * | 1983-09-26 | 1985-04-17 | Shiseido Co Ltd | Cosmetic |
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