JPH0669945B2 - Hair dyeing composition - Google Patents
Hair dyeing compositionInfo
- Publication number
- JPH0669945B2 JPH0669945B2 JP1183637A JP18363789A JPH0669945B2 JP H0669945 B2 JPH0669945 B2 JP H0669945B2 JP 1183637 A JP1183637 A JP 1183637A JP 18363789 A JP18363789 A JP 18363789A JP H0669945 B2 JPH0669945 B2 JP H0669945B2
- Authority
- JP
- Japan
- Prior art keywords
- hair
- agent
- dyeing
- melanin
- pyrocatechol
- 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.)
- Expired - Fee Related
Links
- 238000004043 dyeing Methods 0.000 title claims description 30
- 239000000203 mixture Substances 0.000 title claims description 8
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 claims description 40
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 30
- 239000003795 chemical substances by application Substances 0.000 claims description 30
- MTCFGRXMJLQNBG-UHFFFAOYSA-N serine Chemical compound OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims description 17
- 239000000243 solution Substances 0.000 claims description 12
- 108091000100 Tyrosine Phenol-Lyase Proteins 0.000 claims description 10
- 239000002243 precursor Substances 0.000 claims description 10
- 235000001674 Agaricus brunnescens Nutrition 0.000 claims description 9
- 150000004982 aromatic amines Chemical class 0.000 claims description 8
- DAEPDZWVDSPTHF-UHFFFAOYSA-M sodium pyruvate Chemical compound [Na+].CC(=O)C([O-])=O DAEPDZWVDSPTHF-UHFFFAOYSA-M 0.000 claims description 8
- 238000004513 sizing Methods 0.000 claims description 5
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 claims description 4
- 239000005695 Ammonium acetate Substances 0.000 claims description 4
- 229940043376 ammonium acetate Drugs 0.000 claims description 4
- 235000019257 ammonium acetate Nutrition 0.000 claims description 4
- 229940054269 sodium pyruvate Drugs 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 9
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 8
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 8
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 8
- 239000001099 ammonium carbonate Substances 0.000 description 8
- 239000008363 phosphate buffer Substances 0.000 description 8
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 7
- 239000008213 purified water Substances 0.000 description 7
- 229960001755 resorcinol Drugs 0.000 description 7
- 239000000118 hair dye Substances 0.000 description 6
- 239000002453 shampoo Substances 0.000 description 6
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 4
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 4
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 230000037308 hair color Effects 0.000 description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 4
- CWLKGDAVCFYWJK-UHFFFAOYSA-N m-Aminophenol Natural products NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 229960001153 serine Drugs 0.000 description 4
- 239000000661 sodium alginate Substances 0.000 description 4
- 235000010413 sodium alginate Nutrition 0.000 description 4
- 229940005550 sodium alginate Drugs 0.000 description 4
- 210000004243 sweat Anatomy 0.000 description 4
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- 206010020751 Hypersensitivity Diseases 0.000 description 3
- 230000007815 allergy Effects 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 239000003797 essential amino acid Substances 0.000 description 2
- 235000020776 essential amino acid Nutrition 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- 230000003020 moisturizing effect Effects 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N ortho-hydroxyaniline Natural products NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 210000004761 scalp Anatomy 0.000 description 2
- 229940075142 2,5-diaminotoluene Drugs 0.000 description 1
- JHKKTXXMAQLGJB-UHFFFAOYSA-N 2-(methylamino)phenol Chemical compound CNC1=CC=CC=C1O JHKKTXXMAQLGJB-UHFFFAOYSA-N 0.000 description 1
- 229940018563 3-aminophenol Drugs 0.000 description 1
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241001380536 Argna Species 0.000 description 1
- 206010012434 Dermatitis allergic Diseases 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 102000003425 Tyrosinase Human genes 0.000 description 1
- 108060008724 Tyrosinase Proteins 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 201000008937 atopic dermatitis Diseases 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 230000000035 biogenic effect Effects 0.000 description 1
- 239000001049 brown dye Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229960003067 cystine Drugs 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- VHJLVAABSRFDPM-QWWZWVQMSA-N dithiothreitol Chemical compound SC[C@@H](O)[C@H](O)CS VHJLVAABSRFDPM-QWWZWVQMSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002696 manganese Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000008099 melanin synthesis Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、染毛用組成物、特にメラニンを利用して毛髪
を温和な条件下に自然な黒褐色に染色するための組成物
に関する。Description: TECHNICAL FIELD The present invention relates to a hair dyeing composition, and more particularly to a composition for dyeing hair to a natural black brown color under mild conditions using melanin.
毛髪、殊に中高年者の白髪を黒髪に染めることを目的と
した永久酸化染毛剤として現在市場に出ているものは、
ほとんど、パラフェニレンジアミンを含む芳香族アミン
を、中性からアルカリ性領域で過酸化水素により重合さ
せ、生成する黒褐色の染料ポリマーを毛髪に染着させる
システムをとっている。しかし、出発物質として多用さ
れるパラフェニレンジアミンは頻度は大きくないが、ア
レルギー性皮フ炎を惹起する可能性を持っている。そこ
で、アレルギー発症の危険を少なくすることを目的と
し、また近年天然志向が強まっていることも相俟って、
生体の持つメラニン生成機構を利用し、生成するメラニ
ン色素を毛髪に染着させるメラニン系染毛剤について研
究開発が行なわれており、既にいくつかの提案がなされ
ている。Hair, especially those currently on the market as permanent oxidative hair dyes for the purpose of dyeing the gray hair of middle-aged and elderly people to black hair,
Mostly, aromatic amines including para-phenylenediamine are polymerized with hydrogen peroxide in the neutral to alkaline region, and the resulting black-brown dye polymer is dyed on the hair. However, paraphenylenediamine, which is frequently used as a starting material, has a possibility of causing allergic dermatitis, although the frequency is not so high. Therefore, with the aim of reducing the risk of developing allergies, and with the recent increase in natural orientation,
Research and development have been carried out on melanin-based hair dyes that dye the resulting melanin pigment on hair by utilizing the melanin-producing mechanism of the living body, and some proposals have already been made.
しかしながら、これらの染毛剤での一番の問題点は、生
成するメラニンを如何に毛髪に染着させるかであり、こ
の点について種々の試みがなされている。特開昭53−13
3641には、メラニン前駆物質に触媒として第1鉄塩、鉛
塩、マンガン塩およびコバルト塩などを添加して染着効
果を向上させ、酵素や過酸化水素を用いることなく、2
週間から1ケ月で自然な黒色に染毛する方法が示されて
いる。特開昭53−32132には、染着性向上のために、毛
髪を亜硫酸塩などの還元剤で前処理し、更に金属塩で処
理した後、メラニン前駆物質と過酸化水素の混合溶液に
より染毛する方法が提案されている。また、特開昭50−
88240には、毛髪を非常に強い還元剤であるジチオスレ
イトールで還元処理してシスチン結合を切断し、毛髪へ
の浸透性を向上させた上で、前駆物質溶液とチロシナー
ゼ混合液を塗布して、80分かけ染毛する方法が示されて
いる。しかしながら、これらは、いずれも、操作が繁雑
で染着に時間がかかること、重金属塩の使用や強い還元
剤の使用など毛髪に対する損傷が懸念されるなどの問題
を残している。However, the biggest problem with these hair dyes is how to dye the melanin formed on the hair, and various attempts have been made in this regard. JP53-13
3641 is a melanin precursor to which a ferrous salt, a lead salt, a manganese salt, a cobalt salt, or the like is added to improve the dyeing effect, and without using an enzyme or hydrogen peroxide,
A method of dyeing a natural black hair in one week to one month is shown. In JP-A-53-32132, in order to improve the dyeing property, the hair is pretreated with a reducing agent such as sulfite, further treated with a metal salt, and then dyed with a mixed solution of a melanin precursor and hydrogen peroxide. A method of hairing has been proposed. In addition, JP-A-50-
For 88240, reduce the cystine bond by reducing the hair with dithiothreitol, which is a very strong reducing agent, to improve the permeability to hair, and then apply the precursor solution and tyrosinase mixture solution. , A method of dyeing hair over 80 minutes is shown. However, these all have problems that the operation is complicated and it takes a long time for dyeing, and there is a fear of damage to hair such as the use of heavy metal salts and the use of strong reducing agents.
本発明は、重金属塩や還元剤あるいは過酸化水素などを
用いることなく、迅速で簡便かつ強固な染着性を与え、
しかも頭皮および毛髪に対してマイルドな条件下で染毛
ができる染毛剤を提供しようとするものである。The present invention provides fast, simple and strong dyeability without using heavy metal salts, reducing agents or hydrogen peroxide,
Moreover, it is an object of the present invention to provide a hair dye capable of dyeing hair on the scalp and hair under mild conditions.
本発明によれば、L−もしくはDL−セリンとピロカテコ
ールまたはピルビン酸ナトリウムとピロカテコールと酢
酸アンモニウムからなるメラニン前駆物質、芳香族アミ
ンからなる染着向上剤および糊剤を含む水溶液からなる
第1剤と、β−チロシナーゼ酵素液およびマッシュルー
ム抽出液から選ばれる少なくとも1種を含む第2剤とか
らなる、毛髪を染色するための組成物が提供される。According to the present invention, a melanin precursor consisting of L- or DL-serine and pyrocatechol or sodium pyruvate and pyrocatechol and ammonium acetate, a dyeing improving agent consisting of an aromatic amine and an aqueous solution containing a sizing agent are used. There is provided a composition for dyeing hair, which comprises an agent and a second agent containing at least one selected from a β-tyrosinase enzyme solution and a mushroom extract.
本発明者らは、鋭意検討の結果、上述の課題を解決する
ものとして、上記システムを完成するに至ったものであ
る。即ち、このシステムは、第1剤のメラニン前駆物質
と染着向上剤(メラニンキャリヤー)および糊剤(保護
コロイド膜生成物質)を含む溶液を充分毛髪内に浸透さ
せた後、β−チロシナーゼ酵素液および/またはマッシ
ュルーム抽出液を塗布し、空気との接触を充分行なうこ
とにより短時間で毛髪内部にメラニンを生成させかつ強
固に染着させるシステムである。As a result of intensive studies, the present inventors have completed the above system as a solution to the above problems. That is, this system is a β-tyrosinase enzyme solution after a solution containing a melanin precursor as a first agent, a dyeing enhancer (melanin carrier) and a paste (protective colloid film-forming substance) is sufficiently penetrated into the hair. And / or a system for applying melanin in the hair in a short time and strongly dyeing it by applying mushroom extract and contacting with air sufficiently.
メラニン前駆物質としては、生体必須アミノ酸であり、
保湿効果を有し、水に溶け易いL−セリンとピロカテコ
ールの系を用いるのが特に望ましい。The melanin precursor is a biogenic essential amino acid,
It is particularly desirable to use a system of L-serine and pyrocatechol, which has a moisturizing effect and is easily soluble in water.
とりわけ、本発明の最大の特徴は、染着性向上のために
芳香族アミンから選ばれるメラニンキャリヤーを添加し
たことである。メラニンはそれ自体では毛髪にほとんど
染着しないが、メラニンキャリヤーとしての芳香族アミ
ン、望ましくはパラフェニレンジアミン、を微量添加す
ることにより、染着性が急激に向上する。これは、メラ
ニン生成過程中にとり込まれたアミンが毛髪タンパクの
カルボキシル基と結合を形成することにより染着するた
めであろうと推定される。さらに、レゾルシンの微量添
加も染着性向上に寄与する。また、糊剤として添加され
たポリマーは、染着されたメラニンをコロイド膜で包み
込み、毛髪への固着をより強固にする働きをする。In particular, the greatest feature of the present invention is the addition of a melanin carrier selected from aromatic amines for improving the dyeing property. Although melanin hardly dyes hair by itself, dyeing property is drastically improved by adding a trace amount of aromatic amine as a melanin carrier, preferably paraphenylenediamine. It is presumed that this is because the amine taken in during the melanin production process is dyed by forming a bond with the carboxyl group of the hair protein. Further, the addition of a small amount of resorcin also contributes to the improvement of the dyeing property. Further, the polymer added as a sizing agent has a function of wrapping the dyed melanin in a colloid film, and further strengthening the fixation to the hair.
本発明の組成物において、染着向上剤として添加する芳
香族アミンの量は、従来の酸化染毛剤に含まれる量に比
べて1/10以下であるので、アレルギー発症の危険は極め
て少ないといえる。また、前駆物質として用いられるセ
リン等は生体必須アミノ酸でありNMF(天然保湿因子)
の重要な成分でもあるから、安全性は極めて高いといえ
る。また、本発明ではメラニン化のために過酸化水素を
使用せず、酵素を用いるため、施術pHは中性領域が最適
であり、かつ施術温度も室温から40℃位までが最もよい
活性を示すことからも、温和な条件で反応が進行するた
め、頭皮や毛髪への刺激や損傷は極めて少ないといえ
る。In the composition of the present invention, the amount of the aromatic amine added as a dyeing improver is 1/10 or less compared to the amount contained in the conventional oxidative hair dye, so that the risk of developing allergies is extremely small. I can say. Serine, which is used as a precursor, is an essential amino acid in the body and is NMF (natural moisturizing factor).
Since it is also an important ingredient of, the safety can be said to be extremely high. Further, in the present invention, since hydrogen peroxide is not used for melanization and an enzyme is used, the treatment pH is optimal in the neutral region, and the treatment temperature shows the best activity from room temperature to 40 ° C. Therefore, it can be said that since the reaction proceeds under mild conditions, irritation and damage to the scalp and hair are extremely small.
次に、本発明の組成物の好ましい構成とその使用につい
て説明する。メラニン前駆物質としてL−またはDL−セ
リンとピロカテコールおよびピルビン酸ナトリウムとピ
ロカテコールと酢酸アンモニウムの系から選んだ系、望
ましくはL−またはDL−セリンとピロカテコールの系を
溶解した液(好ましくは、0.2〜5%)に、o−,m−ま
たはp−アミノフェノール(それぞれOAP,MAP,PAPと略
記)、p−フェニレンジアミン(PPDA)、4,4′−ジア
ミノジフェニルアミン(DADPA)、p−メチルアミノフ
ェノール(PMAP)、2,5−ジアミノトルエン(DAT)など
の芳香族アミンの1種または2種(望ましくはp−フェ
ニレンジアミンを含む)を、好ましくは0.05〜0.2重量
%の量で添加し、さらにレゾルシンを微量加え、重炭酸
水素アンモニウムまたはアンモニア水でpHを、好ましく
は6〜8、さらに好ましくは7.5に調整する。さらに、
ヒドロキシエチルセルロース(HEC)、カルボキシメチ
ルセルロース(CMC)、アルギン酸ソーダ(ArgNa)ある
いはポリエチレングリコール(PEG)などの糊剤ポリマ
ーを、好ましくは0.2〜5.0重量%の量で添加することに
より、200〜300cpに粘度調整した液(第1剤)に毛髪を
15分間浸漬させる。その後、好ましくはpH6〜8、さら
に好ましくはpH7.5のリン酸緩衝液に使用直前に溶かし
たβ−チロシナーゼ酵素液(0.05〜0.1%溶液)あるい
はマッシュルーム抽出液(第2剤)を振りかけ、できる
だけ空気との接触を良くするように毛髪をもみほぐし、
15〜45分間染着させた後、シャンプーを用いず湯洗いす
る。酵素の徐効性から、翌日シャンプー洗浄することに
より、より良い染着性が得られる。Next, the preferable constitution of the composition of the present invention and its use will be explained. A system selected from the system of L- or DL-serine and pyrocatechol and the system of sodium pyruvate, pyrocatechol and ammonium acetate as the melanin precursor, preferably a solution in which the system of L- or DL-serine and pyrocatechol is dissolved (preferably , 0.2-5%), o-, m- or p-aminophenol (abbreviated as OAP, MAP, PAP, respectively), p-phenylenediamine (PPDA), 4,4'-diaminodiphenylamine (DADPA), p- Addition of one or two aromatic amines such as methylaminophenol (PMAP) and 2,5-diaminotoluene (DAT) (desirably including p-phenylenediamine), preferably in an amount of 0.05 to 0.2% by weight. Then, a small amount of resorcin is added, and the pH is adjusted to preferably 6 to 8, more preferably 7.5 with ammonium hydrogencarbonate or aqueous ammonia. further,
By adding a sizing agent polymer such as hydroxyethyl cellulose (HEC), carboxymethyl cellulose (CMC), sodium alginate (ArgNa) or polyethylene glycol (PEG), preferably in an amount of 0.2 to 5.0% by weight, a viscosity of 200 to 300 cp is obtained. Apply hair to the adjusted liquid (1st agent)
Soak for 15 minutes. Then, sprinkle with β-tyrosinase enzyme solution (0.05-0.1% solution) or mushroom extract (second agent) dissolved immediately before use in a phosphate buffer of pH 6 to 8, more preferably pH 7.5, and sprinkle as much as possible. Brush the hair to improve the contact with the air,
After dyeing for 15 to 45 minutes, wash in hot water without using shampoo. Due to the gradual effect of the enzyme, better dyeability can be obtained by washing with shampoo the next day.
尚、マッシュルーム抽出液は、例えば、マッシュルーム
を粉砕後、水を加えてよく振とうすることにより、得る
ことができる。The mushroom extract can be obtained, for example, by crushing mushrooms, adding water and shaking well.
次に、実施例をあげ、本発明をさらに説明する。 Next, the present invention will be further described with reference to examples.
実施例1 第1剤 L−セリン 2g ピロカテコール 2g パラフェニレンジアミン 0.2g レジルシン 0.2g 重炭酸水素アンモニウム 0.4g ヒドロキシエチルセルロース 0.5g 精製水を加えて100ml(pH7.5)とする。Example 1 1st agent L-serine 2g Pyrocatechol 2g Paraphenylenediamine 0.2g Resinicin 0.2g Ammonium hydrogencarbonate 0.4g Hydroxyethyl cellulose 0.5g Purified water is added to make 100 ml (pH 7.5).
第2剤 β−チロシナーゼ 0.1g リン酸緩衝液(pH7.5) 100ml (使用直前に溶解) 毛髪に第1剤50〜80mlを塗布し、室温で15分間放置して
充分毛髪内に浸透させた後、第2剤の酵素液20〜30mlを
頭髪全体に振りかけ、全体をもみほぐすようにして空気
との接触を充分に行ない、15〜45分間放置した後温湯で
洗い流す。直後にシャンプー洗浄を行なうことなく、翌
日シャンプー洗浄をすることによって、よりよい染着性
が得られる。Second agent β-tyrosinase 0.1 g Phosphate buffer (pH 7.5) 100 ml (dissolved immediately before use) 50 to 80 ml of the first agent was applied to the hair and left at room temperature for 15 minutes to allow it to fully penetrate into the hair. After that, 20 to 30 ml of the enzyme solution of the second agent is sprinkled on the whole hair, and the whole hair is loosened to make sufficient contact with air, left for 15 to 45 minutes, and then rinsed with warm water. By performing shampoo washing the next day without immediately performing shampoo washing, better dyeing property can be obtained.
上記の方法によって染毛することにより、白髪をカバー
し、耐久性のある自然な黒褐色の髪色が得られる。さら
に、試験用の毛束を用い、上記の方法で染毛したもの
を、シャンプー液(10%)中、および酸性人工汗(pH4.
5)、アルカリ性人工汗(pH7.9)中に、各3回液を入れ
替えながら、45℃の恒温槽中で、合計50時間浸漬して
も、色落ちが少なく、特にアルカリ性汗に対する耐久性
が大きかった。By dyeing hair by the above-mentioned method, white hair is covered and a durable natural brown hair color is obtained. Furthermore, using a test hair bundle, the hair dyed by the above method was put into a shampoo solution (10%) and an acidic artificial sweat (pH 4.
5) Even when immersed in alkaline artificial sweat (pH 7.9) three times each in a constant temperature bath at 45 ° C for a total of 50 hours, there is little discoloration and durability especially against alkaline sweat. It was great.
実施例2 第1剤 L−セリン 2g ピロカテコール 1g パラフェニレンジアミン 0.2g レゾルシン 0.2g 重炭酸水素アンモニウム 0.4g カルボキシメチルセルロース 1.0g 精製水を加えて100ml(pH7.5)とする。Example 2 First agent L-serine 2g Pyrocatechol 1g Paraphenylenediamine 0.2g Resorcin 0.2g Ammonium hydrogencarbonate 0.4g Carboxymethylcellulose 1.0g Purified water is added to make 100 ml (pH 7.5).
第2剤 β−チロシナーゼ 0.1g リン酸緩衝液(pH7.5) 100ml (使用直前に溶解) 染毛は実施例1と同じ方法で行った。耐久性のある自然
な黒褐色の髪色が得られる。Second agent β-tyrosinase 0.1 g Phosphate buffer (pH 7.5) 100 ml (dissolved immediately before use) Hair dyeing was performed in the same manner as in Example 1. A durable, natural dark brown hair color is obtained.
実施例3 第1剤 ピルビン酸ナトリウム 2g ピロカテコール 2g 酢酸アンモニウム 1g パラフェニレンジアミン 0.2g レゾルシン 0.1g 重炭酸水素アンモニウム 0.4g アルギン酸ナトリウム 1g 精製水を加えて100ml(pH7.2)とする。Example 3 First agent Sodium pyruvate 2g Pyrocatechol 2g Ammonium acetate 1g Paraphenylenediamine 0.2g Resorcinol 0.1g Ammonium bicarbonate 0.4g Sodium alginate 1g Purified water is added to make 100 ml (pH 7.2).
第2剤 β−チロシナーゼ 0.1g リン酸緩衝液(pH6.8) 100ml (使用直前に溶解) 染毛の方法は実施例1と同じである。耐久性のある自然
な焦茶色に染まる。Second agent β-tyrosinase 0.1 g Phosphate buffer (pH 6.8) 100 ml (dissolved immediately before use) The method for dyeing hair is the same as in Example 1. Dyes in a durable natural dark brown color.
実施例4 第1剤 DL−セリン 2g ピロカテコール 1g p−メチルアミノフェノール 0.1g 4,4′−ジアミノジフェニルアミン 0.1g 重炭酸水素アンモニウム 0.4g アルギン酸ソーダ 1g 精製水を加えて100ml(pH7.0)とする。Example 4 1st agent DL-serine 2g Pyrocatechol 1g p-methylaminophenol 0.1g 4,4'-diaminodiphenylamine 0.1g Ammonium hydrogencarbonate 0.4g Sodium alginate 1g Purified water was added to 100 ml (pH 7.0). To do.
第2剤 β−チロシナーゼ 0.1g リン酸緩衝液(pH6.8) 100ml (使用直前に溶解) 染毛の方法は実施例1と同じである。自然なグレーに染
毛される。Second agent β-tyrosinase 0.1 g Phosphate buffer (pH 6.8) 100 ml (dissolved immediately before use) The method for dyeing hair is the same as in Example 1. Hair is dyed in natural gray.
実施例5 第1剤 DL−セリン 2g ピロカテコール 2g pまたはm−アミノフェノール 0.1g p−フェニレンジアミン 0.1g 重炭酸水素アンモニウム 0.4g レゾルシン 0.1g ヒドロキシエチルセルロース 1g 精製水を加えて100ml(pH7.2)とする。Example 5 First agent DL-serine 2g Pyrocatechol 2g p- or m-aminophenol 0.1g p-Phenylenediamine 0.1g Ammonium hydrogencarbonate 0.4g Resorcinol 0.1g Hydroxyethylcellulose 1g Purified water added 100ml (pH 7.2) And
第2剤 β−チロシナーゼ 0.1g リン酸緩衝液(pH6.8) 100ml (使用直前に溶解) 染毛の方法は実施例1と同じである。やゝグレーがかっ
た自然な黒褐色に染毛される。Second agent β-tyrosinase 0.1 g Phosphate buffer (pH 6.8) 100 ml (dissolved immediately before use) The method for dyeing hair is the same as in Example 1. It is dyed in a natural blackish brown with a slight gray tinge.
実施例6 第1剤 DL−セリン 3g ピロカテコール 1.5g 4,4′−ジアミノジフェニルアミン 0.1g パラフェニレンジアミン 0.2g レゾルシン 0.2g 重炭酸水素アンモニウム 0.4g アルギン酸ナトリウム 0.5g 精製水を加えて100ml(pH7.3)とする。Example 6 First agent DL-serine 3 g Pyrocatechol 1.5 g 4,4'-Diaminodiphenylamine 0.1 g Paraphenylenediamine 0.2 g Resorcin 0.2 g Ammonium hydrogencarbonate 0.4 g Sodium alginate 0.5 g Purified water was added to 100 ml (pH 7. 3)
第2剤 β−チロシナーゼ 0.1g リン酸緩衝液(pH6.8) 100ml (使用直前に溶解) 実施例1と同じ方法で染毛する。やゝグレーがかった自
然な黒褐色に染毛され、長期に亘り色落ちや褪色が極め
て少なかった。Second agent β-tyrosinase 0.1 g Phosphate buffer (pH 6.8) 100 ml (dissolved immediately before use) Hair is dyed by the same method as in Example 1. It was dyed in a natural blackish brown with a slight grey, and there was very little discoloration or fading over a long period of time.
実施例7 第1剤 DL−セリン 2g ピロカテコール 2g パラフェニレンジアミン 0.2g レゾルシン 0.2g 重炭酸水素アンモニウム 0.4g カルボキシメチルセルロース 1.0g 精製水を加えて100ml(pH6.8)とする。Example 7 First agent DL-serine 2 g Pyrocatechol 2 g Paraphenylenediamine 0.2 g Resorcin 0.2 g Ammonium bicarbonate 0.4 g Carboxymethyl cellulose 1.0 g Purified water is added to make 100 ml (pH 6.8).
第2剤 マッシュルーム抽出液 (使用直前に溶解) 染毛は実施例1と同じ方法で行った。耐久性のある自然
な黒褐色の髪色が得られる。Second agent mushroom extract (dissolved immediately before use) Hair dyeing was performed in the same manner as in Example 1. A durable, natural dark brown hair color is obtained.
尚、上記で使用したマッシュルーム抽出液は、次のよう
なものである。The mushroom extract used above is as follows.
マッシュルーム100gをミキサーで粉砕した後、蒸溜水10
0mlを注ぎ入れ、よく振とうした後、グラスフィルター
で濾過し、濾液を凍結乾燥して粉末とする。この粉末を
pH7のリン酸緩衝液に溶解して1%の濃度としたものを
用いる。After crushing 100 g of mushrooms with a mixer, distilled water 10
Pour 0 ml, shake well, filter with a glass filter, and lyophilize the filtrate to give a powder. This powder
It is used by dissolving it in a pH 7 phosphate buffer to a concentration of 1%.
以上の実施例を含むいくつかの系についての染毛条件、
染着性などについて表1にまとめた。比較例についても
挙げた。Hair dyeing conditions for several systems, including the above examples,
The dyeability and the like are summarized in Table 1. A comparative example is also given.
〔発明の効果〕 上述のようにメラニン前駆物質に、メラニンキャリヤー
として芳香族アミンおよび糊剤としてコロイド膜生成ポ
リマーを微量添加したことにより、従来に比較して、非
常に簡便で迅速かつ強固な染毛が可能になった。この方
法で染めた毛髪は汗やシャンプーにも強く、色落ちや褪
色の少ない自然な黒褐色ないし栗色の髪色を保っていく
ことが可能となる。また、現在市場に出ている酸化染毛
剤に比べ、アレルギー発症の可能性は極めて低いことが
予測される。 [Advantages of the Invention] As described above, by adding a trace amount of an aromatic amine as a melanin carrier and a colloid film-forming polymer as a sizing agent to a melanin precursor, as compared with the conventional method, it is very simple, quick and strong dyeing. Hair became possible. Hair dyed by this method is resistant to sweat and shampoo, and it is possible to maintain a natural black-brown or maroon hair color with little discoloration or fading. Further, it is predicted that the possibility of developing allergies is extremely low as compared with the oxidative hair dye currently on the market.
Claims (1)
またはピルビン酸ナトリウムとピロカテコールと酢酸ア
ンモニウムからなるメラニン前駆物質、芳香族アミンか
らなる染着向上剤および糊剤を含む水溶液からなる第1
剤と、β−チロシナーゼ酵素液およびマッシュルーム抽
出液から選ばれる少なくとも1種を含む第2剤とからな
る、毛髪を染色するための組成物。1. A melanin precursor comprising L- or DL-serine and pyrocatechol or sodium pyruvate and pyrocatechol and ammonium acetate, a dyeing improving agent comprising an aromatic amine and an aqueous solution containing a sizing agent.
A composition for dyeing hair, which comprises an agent and a second agent containing at least one selected from a β-tyrosinase enzyme solution and a mushroom extract.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1183637A JPH0669945B2 (en) | 1989-07-18 | 1989-07-18 | Hair dyeing composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1183637A JPH0669945B2 (en) | 1989-07-18 | 1989-07-18 | Hair dyeing composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0348612A JPH0348612A (en) | 1991-03-01 |
| JPH0669945B2 true JPH0669945B2 (en) | 1994-09-07 |
Family
ID=16139268
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1183637A Expired - Fee Related JPH0669945B2 (en) | 1989-07-18 | 1989-07-18 | Hair dyeing composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0669945B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2228957T3 (en) | 2000-10-09 | 2005-04-16 | L'oreal | COLOR COMPOSITION, PROCEDURE FOR OBTAINING AND USING FOR COLORING SKIN AND / OR KERATIN MATERIALS. |
| KR100989724B1 (en) * | 2007-12-21 | 2010-10-26 | 주식회사 셀루스 | Hair dye composition containing nanonized chaga and preparation method thereof |
| JP6735535B2 (en) * | 2015-01-22 | 2020-08-05 | ホーユー株式会社 | Oxidative hair dye first agent and method for stabilizing color tone of oxidative hair dye composition |
| CN114159350A (en) * | 2021-12-16 | 2022-03-11 | 四川大学 | Hair dye using tyrosinase to catalyze the polymerization of artificial melanin and its preparation method |
| KR20250090660A (en) * | 2023-12-13 | 2025-06-20 | (주) 이지씨 테라퓨틱스 | Method for preparing mushroom melanin solution and mushroom melanin solution prepared thereby |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54110337A (en) * | 1978-02-14 | 1979-08-29 | Nonogawa Shoji Yk | Hair dyeing agent |
| JPS55115814A (en) * | 1979-02-28 | 1980-09-06 | Lion Corp | Hair-dye composition |
| JPS6212714A (en) * | 1985-07-10 | 1987-01-21 | Daicel Chem Ind Ltd | Hair dye |
| JPS62185008A (en) * | 1986-02-10 | 1987-08-13 | Nikka Chem Ind Co Ltd | Acidic permanently oxidizing hairdye |
-
1989
- 1989-07-18 JP JP1183637A patent/JPH0669945B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0348612A (en) | 1991-03-01 |
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