JPH0713007B2 - Pre-hair rinse type hair treatment composition - Google Patents
Pre-hair rinse type hair treatment compositionInfo
- Publication number
- JPH0713007B2 JPH0713007B2 JP30103386A JP30103386A JPH0713007B2 JP H0713007 B2 JPH0713007 B2 JP H0713007B2 JP 30103386 A JP30103386 A JP 30103386A JP 30103386 A JP30103386 A JP 30103386A JP H0713007 B2 JPH0713007 B2 JP H0713007B2
- Authority
- JP
- Japan
- Prior art keywords
- hair
- treatment composition
- rinse
- hair treatment
- composition according
- 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 - Lifetime
Links
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- 235000021120 animal protein Nutrition 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 235000009582 asparagine Nutrition 0.000 description 1
- 229960001230 asparagine Drugs 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- YSMODUONRAFBET-UHFFFAOYSA-N delta-DL-hydroxylysine Natural products NCC(O)CCC(N)C(O)=O YSMODUONRAFBET-UHFFFAOYSA-N 0.000 description 1
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- YSMODUONRAFBET-UHNVWZDZSA-N erythro-5-hydroxy-L-lysine Chemical compound NC[C@H](O)CC[C@H](N)C(O)=O YSMODUONRAFBET-UHNVWZDZSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000002523 gelfiltration Methods 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 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 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- QJHBJHUKURJDLG-UHFFFAOYSA-N hydroxy-L-lysine Natural products NCCCCC(NO)C(O)=O QJHBJHUKURJDLG-UHFFFAOYSA-N 0.000 description 1
- 229960002591 hydroxyproline Drugs 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Natural products ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 239000004474 valine Substances 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、ヘアリンス前に毛髪に塗布して用いるプレヘ
アリンス型毛髪処理剤組成物に関する。更に詳しくは、
少なくとも一種以上の陰イオン性高分子を含み、毛髪に
なめらかさ、しなやかさを与えながら、張り、こしをも
付与することを特徴とするプレヘアリンス型毛髪処理剤
組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial field of use] The present invention relates to a pre-hair rinse type hair treatment composition used by applying to hair before hair rinsing. For more details,
The present invention relates to a pre-hair rinse type hair treatment composition, which comprises at least one or more anionic polymer and imparts smoothness and suppleness to the hair while imparting tension and firmness.
[従来の技術] 従来シャンプーは、地肌や毛髪についた汚れを洗浄し清
潔にする機能を有するが、その反面幾つかの欠点が指摘
されてきているそれは、頭皮から分泌される皮脂成分を
過剰に除去するため毛髪の手触り感触、ブラシもしくは
櫛の通り、光沢、まとまりやすさ等が劣ることである。[Prior Art] Conventional shampoo has a function to clean and clean dirt on the skin and hair, but on the other hand, some drawbacks have been pointed out that excessive sebum components secreted from the scalp are excessive. Since the hair is removed, the feel of the hair, the brush, the comb, the gloss, and the easiness of cohesion are inferior.
そのためシャンプー後の毛髪に、なめらかさ、しなやか
さ、光沢を回復させ櫛通りを良くする事を目的とした毛
髪化粧料としては、ヘアリンス、ヘアートリートメン
ト、ヘアーコンデショナー等の名称(以下、ヘアリンス
剤として総称する)のものが市販されている。これら毛
髪化粧料には、主に、第4級アンモニウム塩が配合さ
れ、更になめらかさ、しっとりさ、光沢を向上させる目
的で、油分やタンパク質等が添加されてきた。Therefore, as hair cosmetics for the purpose of restoring smoothness, suppleness, and luster to hair after shampoo to improve combability, names of hair rinses, hair treatments, hair conditioners, etc. (hereinafter collectively referred to as hair rinse agents Are available on the market. A quaternary ammonium salt is mainly added to these hair cosmetics, and oil, protein, etc. have been added for the purpose of improving smoothness, moisturizing and gloss.
[発明が解決しようとする問題点] しかしながら、シャンプー後に従来のヘアリンス剤を使
用することにより、髪のしなやかさ、なめらかさ、光沢
を回復させ櫛通りをよくすることはできるが、その反
面、油っぽさ、べたつき等が現れ、更には仕上り感の重
さから髪に張り、こしがなくなり自然な感じでのまとま
りやすさに難点があることが指摘されてきた。[Problems to be Solved by the Invention] However, by using a conventional hair rinse agent after shampooing, it is possible to restore the suppleness, smoothness and luster of hair and improve combability, but on the other hand, the oil It has been pointed out that the softness, stickiness, etc. appear, and that the hair has a feeling of finishing and sticks to the hair, and there is a lack of stiffness and a natural feeling of cohesion.
本発明者らは、こうした事情にかんがみ、上記の欠点を
解決すべく鋭意研究を重ねた結果、シャンプー後ヘアリ
ンス剤を使用する前に、特定の陰イオン性高分子を有効
成分として配合したプレヘアリンス型毛髪処理剤組成物
を毛髪に塗布し、その後ヘアリンス剤で処理すれば、シ
ャンプー後の髪に、しなやかさ、なめらかさ、光沢を与
え、更には櫛通りを回復させ、尚且つ、油っぽさ、べた
つき感がなく髪にはり、こしを与え、自然な感じでのま
とまりやすさが得られることを見いだしこの知見にもと
ずいて本発明を完成するに至った。In view of these circumstances, the present inventors have conducted intensive studies to solve the above-mentioned drawbacks, and as a result, before using the hair rinse agent after shampoo, pre-hair rinse containing a specific anionic polymer as an active ingredient. When the hair treatment composition is applied to hair and then treated with a hair rinse agent, the hair after shampoo is given suppleness, smoothness and luster, and further, combing is restored, and yet it is oily. Based on this finding, the present invention has been completed based on the finding that it gives the hair a feeling of stickiness and firmness without stickiness and gives a natural feeling of cohesion.
[問題点を解決するための手段および作用] すなわち、本発明は、少なくとも一種以上の陰イオン性
高分子を含有することを特徴とするプレヘアリンス型毛
髪処理剤組成物を提供するものである。[Means and Actions for Solving Problems] That is, the present invention provides a prehair rinse-type hair treatment composition containing at least one or more anionic polymers.
以下、本発明の構成について詳述する。本発明に用いら
れる陰イオン性高分子は、キサンタンガム、グルコマン
ナン、クインスシードガム、ローカストビーンガム、ア
ラビアガム、グアーガム、アルギン酸ソーダ、カラギー
ナン(カッパー,ラムダ,アイオタ)、ペクチン、ヒア
ルロン酸、コンドロイチン4硫酸、コンドロイチン8硫
酸、デルマタン硫酸、コンドロイチン4,8ジ硫酸、デル
マタン4,8ジ硫酸、ケラタン硫酸、又はヘパラン硫酸と
いった天然多糖類又はポリアクリル酸ソーダ、カルボキ
シメチルセルロース、メチルビニールエーテル/無水マ
イレン酸共重合物、アクリル酸エステル/メタアクリル
酸エステル/ダイアセトンアクリルアマイド/アクリル
酸/メタアクリル酸共重合物又は架橋化カルボキシビニ
ールポリマーなどの合成高分子であり、これらのうち一
種又は二種以上が任意に選択されて用いられる。Hereinafter, the configuration of the present invention will be described in detail. The anionic polymer used in the present invention is xanthan gum, glucomannan, quince seed gum, locust bean gum, gum arabic, guar gum, sodium alginate, carrageenan (copper, lambda, iota), pectin, hyaluronic acid, chondroitin tetrasulfate. , Polysaccharides such as chondroitin octasulfate, dermatan sulfate, chondroitin 4,8 disulfate, dermatan 4,8 disulfate, keratan sulfate, or heparan sulfate, or sodium polyacrylate, carboxymethyl cellulose, methyl vinyl ether / maleic anhydride copolymerization A synthetic polymer such as an acrylic acid ester / methacrylic acid ester / diacetone acrylic amide / acrylic acid / methacrylic acid copolymer or a crosslinked carboxyvinyl polymer. Above species is selected and used arbitrarily.
陰イオン性高分子の配合量はプレヘアリンス型毛髪処理
剤組成物全量中の0.01〜5重量%(以下、単に%と略
す)、好ましくは0.1〜3%である。0.01未満では、本
プレヘアリンス型毛髪処理剤組成物を塗布後、ヘアリン
ス剤で処理してもしなやかさ、なめらかさ、光沢が発現
しにくく、毛髪の、はり、こしも満足されるものではな
い。また5%を越えると毛髪がべたついたり乾いた後で
ごわついたりして好ましくない。The amount of the anionic polymer compounded is 0.01 to 5% by weight (hereinafter simply abbreviated as%), preferably 0.1 to 3%, based on the total amount of the pre-hair rinse hair treatment composition. If it is less than 0.01, suppleness, smoothness, and gloss are less likely to be exhibited even after treatment with the hair rinse agent after application of the present pre-hair rinse type hair treatment composition, and the firmness and firmness of the hair are not satisfactory. If it exceeds 5%, the hair becomes sticky or stiff after drying, which is not preferable.
本発明に係る陰イオン性高分子を含有してなるプレヘア
リンス型毛髪処理剤組成物は、更に下記一般式[1]で
示される第4級トリメチルアンモニウム誘導ポリペプタ
イドの一種又は二種以上を併用することによって、毛髪
への効果が更に改善される。The pre-hair rinse type hair treatment composition containing the anionic polymer according to the present invention further comprises one or more quaternary trimethylammonium-derived polypeptide represented by the following general formula [1] in combination. By doing so, the effect on the hair is further improved.
(式中、R1はコラーゲンより誘導されるポリペプタイド
を構成するアミノ酸であり、nは3〜20である。) 以下に、第4級トリメチルアンモニウム誘導ポリペプタ
イドについて説明する。 (In the formula, R 1 is an amino acid that constitutes a polypeptide derived from collagen, and n is 3 to 20.) The quaternary trimethylammonium-derived polypeptide is described below.
上記一般式(I)におけるポリペプタイド部分はコラー
ゲンを構成する蛋白質(絹蛋白質)より誘導されるもの
であり、R1で示される側鎖はコラーゲンを構成する蛋白
質の側鎖アミノ酸を示す。一般的には、アラニン、グリ
シン、バリン、ロイシン、イソロイシン、プロリン、フ
ェニルアラニン、チロシン、セリン、トレオニン、アル
ギニン、リジン、アスパラギン酸、アスパラギン、グル
タミン酸、ヒスチジン、メチオニン、ヒドロキシプロリ
ン、ヒドロキシリジンなどの混合物であり、その一例を
挙げれば表1のような組成である。The polypeptide moiety in the above general formula (I) is derived from a protein (silk protein) that constitutes collagen, and the side chain represented by R 1 is a side chain amino acid of the protein that constitutes collagen. Generally, it is a mixture of alanine, glycine, valine, leucine, isoleucine, proline, phenylalanine, tyrosine, serine, threonine, arginine, lysine, aspartic acid, asparagine, glutamic acid, histidine, methionine, hydroxyproline, hydroxylysine, etc. The composition is shown in Table 1 as an example.
このような一般式(I)で示される第4級トリメチルア
ンモニウム誘導ポリペプタイドは、一般的には3−クロ
ロ−2−ヒドロキシプロピルトリメチルアンモニウムク
ロライドとコラーゲン誘導ポリペプタイドとの反応によ
って得られる。 Such a quaternary trimethylammonium-derived polypeptide represented by the general formula (I) is generally obtained by reacting 3-chloro-2-hydroxypropyltrimethylammonium chloride with a collagen-derived polypeptide.
上記反応に使用される3−クロロ−2−ヒドロキシプロ
ピルトリメチルアンモニウムクロライド(以下、CTAと
いう)は、既存化学物質(2)−181として公知のもの
であり、濃度50%(重量%、以下同様)程度の水溶液が
市販されていて容易に入手可能である。一方、コラーゲ
ン誘導ポリペプタイドは一般的には、コラーゲンの変性
物であるゼラチンを酸、アルカリあるいは蛋白質分解酵
素などを用いて加水分解することによって得られる。3-Chloro-2-hydroxypropyltrimethylammonium chloride (hereinafter referred to as CTA) used in the above reaction is known as existing chemical substance (2) -181, and has a concentration of 50% (wt%, the same applies hereinafter). Aqueous solutions are commercially available and are easily available. On the other hand, collagen-derived polypeptides are generally obtained by hydrolyzing gelatin, which is a modified product of collagen, with an acid, an alkali, or a protease.
加水分解に際して、添加する酸、アルカリあるいは酵素
の量、反応温度、反応時間を適宜選択することによっ
て、得られる動物性蛋白質誘導ポリペプタイドの重合度
{一般式(I)のnの値}を3〜20すなわち分子量で約
300〜焼結体2000の範囲に適宜調製できる。Upon hydrolysis, the amount of acid, alkali or enzyme to be added, the reaction temperature, and the reaction time are appropriately selected so that the degree of polymerization of the animal protein-derived polypeptide obtained (value of n in the general formula (I)} is 3 ~ 20 or about by molecular weight
It can be appropriately adjusted within the range of 300 to 2000 sintered bodies.
なお、このような分子量範囲のコラーゲン誘導ポリペプ
タイドは、従来より天然物誘導の安全な化粧品原料とし
て多方面に使用されている。そして一般式(I)で示さ
れる第4級トリメチルアンモニウム誘導ポリペプタイド
においてnが3未満では毛髪への吸着が充分でなく、ま
たnが20を超えると毛髪への吸着が弱くなり、かつゲル
化することなどにより取り扱いが困難になるからであ
る。It should be noted that collagen-derived polypeptides having such a molecular weight range have hitherto been used in various fields as a natural cosmetic material-derived safe cosmetic raw material. In the quaternary trimethylammonium-derived polypeptide represented by the general formula (I), when n is less than 3, adsorption to hair is insufficient, and when n exceeds 20, adsorption to hair is weak and gelation occurs. It is difficult to handle because of
そして、反応はコラーゲン誘導ポリペプタイドの水溶液
を滴下し、コラーゲン誘導ポリペプタイドとCTAを水中
で接触させることによって行なわれる。反応に際して反
応系内のpHを8〜12、とくに9〜11に保つことが望まし
く、そのため水酸化ナトリウム、水酸化カリウムなどの
アルカリ水溶液を必要に応じて反応液中に滴下すること
が行なわれる。Then, the reaction is carried out by dropping an aqueous solution of collagen-derived polypeptide and bringing the collagen-derived polypeptide and CTA into contact with each other in water. During the reaction, it is desirable to keep the pH in the reaction system at 8 to 12, particularly 9 to 11, and therefore, an alkaline aqueous solution such as sodium hydroxide or potassium hydroxide is added dropwise into the reaction solution as needed.
反応時、反応系内のpHを前記のごとき範囲に維持するの
は、コラーゲン誘導ポリペプタイドのアミノ基がCTAと
反応するにはpH8以上のアルカリであることが望まし
く、またpHが12を超えるとCTAやコラーゲン誘導ポリペ
プタイドが加水分解を起こすからである。During the reaction, the pH in the reaction system is maintained within the above range, in order for the amino group of the collagen-derived polypeptide to react with CTA, it is desirable that the pH is 8 or more alkali, and if the pH exceeds 12, This is because CTA and collagen-derived polypeptide cause hydrolysis.
反応は常温でも進行するが温度が高いほど反応がはやく
なる。しかし、pHが高い状態では温度が高くなるとコラ
ーゲン誘導ポリペプタイドやCTAの加水分解が促進さ
れ、低分子のものしか得られなくなるので、高くても60
℃以下にするのが好ましい。反応に際してコラーゲン誘
導ポリペプタイドは、濃度が高いと粘度が高くなり均一
な反応が難しくなるので、濃度30〜50%程度の水溶液に
するのが好ましく、CTAは市販の濃度約50%の水溶液を
そのまま使用すればよい。The reaction proceeds even at room temperature, but the higher the temperature, the faster the reaction. However, when the temperature is high at high pH, the hydrolysis of collagen-derived polypeptide and CTA is accelerated, and only low molecular weight compounds can be obtained.
It is preferable that the temperature is not higher than ° C. At the time of reaction, collagen-derived polypeptide has a high viscosity at high concentration and a uniform reaction becomes difficult, so it is preferable to use an aqueous solution with a concentration of about 30 to 50% .For CTA, a commercially available aqueous solution with a concentration of about 50% is used as it is. You can use it.
コラーゲン誘導ポリペプタイドへのCTAの滴下は30分〜
6時間で終わるのが好ましい。CTAを滴下すると、下記
の式に示すような反応が進行し、 塩化水素が生成して反応液のpHが低下するので、アルカ
リをCTAの滴下と同時に滴下し、撹拌して液中のpHを反
応に適するpHに維持するのが好ましく、そのため滴下に
少なくとも30分間程度の時間をかけるのが好ましい。CT
Aの滴下後、約2〜6時間撹拌を続け、かつpHを9〜11
に保ち、さらに1昼夜放置するか、あるいは約60℃まで
加温して反応を完了させるのが好ましい。そして、反応
の進行と終了は、Van Slake法によりポリペプタイド中
のアミノ態チッ素を測定することによって確認される。Drip of CTA to collagen-derived polypeptide is 30 minutes ~
It is preferably finished in 6 hours. When CTA is dropped, the reaction shown in the following formula proceeds, Since hydrogen chloride is generated and the pH of the reaction solution decreases, it is preferable to add an alkali at the same time as the addition of CTA and stir to maintain the pH in the solution at a pH suitable for the reaction, and thus at least 30 minutes for the addition. It is preferable to take some time. CT
After dropping A, continue stirring for about 2 to 6 hours and adjust the pH to 9 to 11
It is preferable that the reaction is completed by keeping the temperature at room temperature and then leaving it for one day or night or by heating to about 60 ° C. Then, the progress and completion of the reaction are confirmed by measuring amino nitrogen in the polypeptide by the Van Slake method.
第4級トリメチルアンモニウム誘導ポリペプタイドの配
合量は、プレヘアリンス型毛髪処理剤組成物全量中の0.
001〜5重量%、好ましくは0.01〜3重量%である。こ
れ未満では頭髪に対する親和性が不足して吸着性に劣
り、この範囲を越えると使用感触がべたつき気味とな
り、好ましくない。The amount of the quaternary trimethylammonium-derived polypeptide used is 0,0 based on the total amount of the pre-hair rinse type hair treatment composition.
It is 001 to 5% by weight, preferably 0.01 to 3% by weight. If it is less than this range, the affinity for hair is insufficient and the adsorptivity is poor, and if it exceeds this range, the feeling of use tends to be sticky, which is not preferable.
本発明において使用される陰イオン性高分子を仮にカチ
オン性界面活性剤を主成分とするヘアリンス剤組成物中
に併用配合しても本発明の様な優れた効果は得られない
ばかりか、組成物中で凝集物が生じたり、又経日で分
離、沈澱が起こり安定性はきわめて悪いものであった。Even if the anionic polymer used in the present invention is used together in a hair rinse composition containing a cationic surfactant as a main component, not only the excellent effect as in the present invention cannot be obtained, but also the composition The stability was extremely poor because agglomerates were formed in the product, and separation and precipitation occurred over time.
本発明のプレヘアリンス型毛髪処理剤組成物には、上記
の必須成分に加えて配合組成物を完成させるための水を
要する他、毛髪化粧料に常用される成分や添加剤を配合
することも可能である。即ち、高級アルコール、シリコ
ーン油、流動パラフィン等の油分、プロピレングリコー
ル、グリセリン等の保湿剤、POE(ポリオキシエチレ
ン;以下同じ)硬化ヒマシ油、POEアルキルエーテル等
の非イオン性界面活性剤、クエン酸、乳酸等の有機酸、
塩化ナトリウム、塩化カリウム等の無機塩、香料、色
剤、防腐剤、キレート剤、紫外線吸収剤等を本発明の効
果を損なわない範囲で適宜配合できる。The pre-hair rinse hair treatment composition of the present invention requires water for completing the composition composition in addition to the above-mentioned essential components, and may also be compounded with components and additives commonly used in hair cosmetics. It is possible. That is, higher alcohols, oils such as silicone oil and liquid paraffin, humectants such as propylene glycol and glycerin, POE (polyoxyethylene; hereinafter the same) hydrogenated castor oil, nonionic surfactants such as POE alkyl ethers, citric acid , Organic acids such as lactic acid,
Inorganic salts such as sodium chloride and potassium chloride, fragrances, coloring agents, preservatives, chelating agents, ultraviolet absorbers and the like can be appropriately added within a range that does not impair the effects of the present invention.
[実施例] 次に実施例によって本発明を更に詳細に説明する。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。尚、プレヘアリンス型毛髪処理剤組成物の性
能評価は以下の方法によった。EXAMPLES Next, the present invention will be described in more detail with reference to examples. The present invention is not limited to this. The blending amount is% by weight. The performance of the pre-hair rinse hair treatment composition was evaluated by the following methods.
洗髪後の髪の感触 女性パネル20名によるHalf−Head(半頭比較法)にて比
較判定した。すなわち、市販シャンプー10gで1回洗髪
し軽くすすいだ後、同じシャンプー5gで2回目の洗髪を
した。軽くすすいだ後、頭髪の半分に本発明のプレヘア
リンス型毛髪処理剤組成物10gを塗布し、もう半分は何
もつけない。2分後に、市販ヘアリンス剤を頭髪全部に
塗布し2分後、お湯で全てを洗い流す。その後、風乾し
官能によって評価した。Feeling of Hair after Washing 20 female panels were compared and evaluated by Half-Head (half-head comparison method). That is, the hair was washed once with 10 g of commercial shampoo and rinsed lightly, and then the second shampoo was washed with 5 g of the same shampoo. After light rinsing, 10 g of the pre-hair rinse type hair treatment composition of the present invention is applied to one half of the hair, and nothing is applied to the other half. After 2 minutes, apply a commercial hair rinse to all the hair, and after 2 minutes, wash it off with hot water. Then, it air-dried and evaluated by sensory.
評価は、「なめらかさ」「しなやかさ」「光沢」「毛髪
のはり、こし」「髪のまとまり易さ」の5項目について
実施した。The evaluation was carried out on five items of "smoothness", "suppleness", "gloss", "hair and firmness of hair", and "easiness of cohesion of hair".
官能評価は、本発明のプレヘアリンス型毛髪処理剤組成
物を塗布しない方を基準として一対比較によって以下の
4段階評価でおこなった。The sensory evaluation was carried out by the following four-level evaluation by paired comparison with the one not coated with the pre-hair rinse type hair treatment composition of the present invention.
著しく良好であれば◎、良好であれば○、普通であれば
△、劣っていれば×と評価した。Remarkably good, ⊚, good, ◯, normal, and poor.
実施例1〜3 表2に示す毛髪処理剤組成物を以下の方法にて調整し
た。Examples 1 to 3 The hair treatment composition shown in Table 2 was prepared by the following method.
(製法) 比較例1、2は、イオン交換水にジプロピレングリコー
ル又はグリセリンを添加溶解し、更に、加熱溶解したPO
E(20)オレイルエーテルを添加し順次防腐剤、色剤、
香料を添加し試料を得た。(Production method) In Comparative Examples 1 and 2, PO was prepared by adding and dissolving dipropylene glycol or glycerin in ion-exchanged water, and further dissolving by heating.
E (20) oleyl ether was added to the preservative, coloring agent,
A fragrance was added to obtain a sample.
比較例3は、イオン交換水に、ジプロピレングリコー
ル、カセイカリを添加し、加熱溶解し70℃に保つ。(A
部)他の成分を混合し加熱溶解して70℃に保つ。(B
部)A部にB部を添加し、攪拌混合した後、ホモミキサ
ーにて乳化した。乳化後かきまぜながら30℃まで冷却し
て、乳液状のヘアクリームを得た。In Comparative Example 3, dipropylene glycol and causticari were added to ion-exchanged water, and the mixture was heated and dissolved and kept at 70 ° C. (A
Part) Other ingredients are mixed, dissolved by heating and kept at 70 ° C. (B
Part) Part B was added to Part A, and the mixture was mixed with stirring and then emulsified with a homomixer. After emulsification, the mixture was stirred and cooled to 30 ° C. to obtain a milky hair cream.
実施例1〜3はイオン交換水に各種陰イオン性高分子を
攪拌溶解し、その後加熱溶解したPOE(20)オレイルエ
ーテル防腐剤、香料、色剤を順次添加しゲル状の試料を
得た。In Examples 1 to 3, various anionic polymers were dissolved in ion-exchanged water with stirring, and then POE (20) oleyl ether preservative, which was heated and dissolved, a fragrance, and a coloring agent were sequentially added to obtain gel-like samples.
(効果) 表2からわかるように本発明例では、なめらかさ、しな
やかさ、光沢、毛髪のはり、こし髪のまとまりやすさの
全ての項目において、比較例の保湿剤水溶液やヘアクリ
ームに比べ非常に優れていることがわかる。(Effects) As can be seen from Table 2, in all of the items of the present invention, smoothness, suppleness, gloss, hair elasticity, and hair easiness of cohesion, it is much more effective than the moisturizer aqueous solutions and hair creams of Comparative Examples. It turns out that it is excellent.
実施例4〜9 表3に示す毛髪処理剤組成物を以下の方法にて調整し
た。 Examples 4 to 9 The hair treatment composition shown in Table 3 was prepared by the following method.
(製法) 表3に示す各種高分子をジプロピレングリコールに湿潤
分散させ、イオン交換水に添加し攪拌溶解し、その後、
加熱溶解したPOE(20)オレイルエーテル、防腐剤、香
料、色剤を順次溶解し試料を得た。(Production method) Various polymers shown in Table 3 were wet-dispersed in dipropylene glycol, added to ion-exchanged water and dissolved by stirring, and then,
A sample was obtained by sequentially dissolving the heat-dissolved POE (20) oleyl ether, the preservative, the fragrance, and the coloring agent.
(効果) 表3からわかるように、陰イオン性高分子を含有してい
ない毛髪処理剤を用いた場合、なめらかさが著しく劣
り、しなやかさ、光沢も好ましくなく、又、毛髪のは
り、こしも適切でなくかえってごわつく傾向にあった。
陰イオン性高分子を含有した系が非常に優れたなめらか
さ、しなやかさと、セットのしやすい毛髪へのはり、こ
しを付与する理由は定かでないがシャンプー後、陰イオ
ン性高分子が毛髪に静電的に吸着しコートした状態とな
り、その後ヘアリンス剤で処理すると、ヘアリンス剤中
の陽イオン性界面活性剤との親和性が増して複合体を形
成し更に、ヘアリンス剤中の油分が、陽イオン界面活性
剤の親油基に物理的に吸着することにより、洗い流した
後も、複合体ならびに油分が毛髪に残存することによ
り、優れた使用性が現れるためと考えられる。(Effect) As can be seen from Table 3, when a hair treatment agent containing no anionic polymer is used, the smoothness is remarkably inferior, and the suppleness and gloss are also unfavorable. It was not appropriate and tended to be stiff.
The system containing the anionic polymer is very excellent in smoothness, suppleness, and easy-to-set hair. When it is electrically adsorbed and coated, and then treated with a hair rinse agent, the affinity with the cationic surfactant in the hair rinse agent increases to form a complex, and the oil content in the hair rinse agent becomes cations. It is considered that excellent usability appears because the complex and the oil component remain on the hair even after washing by physically adsorbing to the lipophilic group of the surfactant.
実施例10〜11 表4に示す毛髪処理剤組成物を実施例1〜9と同様にし
て調整し効果を調べた。 Examples 10 to 11 The hair treatment compositions shown in Table 4 were prepared in the same manner as in Examples 1 to 9 and the effects were examined.
尚、比較例9、実施例11に配合された第4級トリメチル
アンモニウム誘導コラーゲンポリペプタイドは次の参考
例1で示された方法により得られた。The quaternary trimethylammonium-derived collagen polypeptide blended in Comparative Example 9 and Example 11 was obtained by the method shown in Reference Example 1 below.
参考例 濃度40.5%のコラーゲン誘導ポリペプタイド838g(コラ
ーゲン誘導ポリペプタイドの平均分子量1500、アミノ態
チッ素の総量216ミリモル)を反応容器に入れ、撹拌し
ながら濃度49%のCTA水溶液71g(コラーゲン誘導ポリペ
プタイドのアミノ態チッ素の0.85当量)を30分間かけて
滴下し、かつその間20%水酸化ナトリウム水溶液を適宜
滴下して反応後のPHを11.0に維持しながら2時間撹拌を
続け、ついで24時間放置した後、アミノ態チッ素を測定
したところ、アミノ態チッ素の総量は39ミリモルであ
り、アミノ態チッ素の82%が反応していた。Reference Example 838 g of collagen-derived polypeptide with a concentration of 40.5% (average molecular weight of collagen-derived polypeptide of 1500, total amount of amino-nitride 216 mmol) was placed in a reaction vessel, and 71 g of CTA aqueous solution with a concentration of 49% was added with stirring (71 g (collagen-derived polypeptide)). Amino acid nitrogen of peptide (0.85 equivalent) was added dropwise over 30 minutes, and 20% aqueous sodium hydroxide solution was added dropwise during that period to continue stirring for 2 hours while maintaining the PH after the reaction at 11.0, and then for 24 hours. After the standing, the amino nitrogen was measured and the total amount of amino nitrogen was 39 mmol, indicating that 82% of the amino nitrogen had reacted.
つぎに弱酸型陽イオン交換樹脂アンバーライトIRC−50
(商品名、オルガノ(株))120mlを加え、pH6.7に中和
し、反応液中のナトリウムイオンとわずかに残存してい
る未反応のCTAをイオン交換樹脂に吸着させ、ついでイ
オン交換樹脂を除去して乾燥残分30%の水溶液を得た。Next, weak acid cation exchange resin Amberlite IRC-50
(Trade name: Organo Co., Ltd.) 120 ml was added to neutralize to pH 6.7, sodium ions in the reaction solution and a little remaining unreacted CTA were adsorbed on the ion exchange resin, and then ion exchange resin Was removed to obtain an aqueous solution having a dry residue of 30%.
得られた水溶液について第4級アンモニウム塩の呈性反
応を行なったところ、テトラフェニルホウ素ナトリウム
により白色の沈澱を生じ、またドラーゲンドルフ試薬に
より赤色の沈澱を生じ、陽性を示した。When the resulting aqueous solution was subjected to a quaternary ammonium salt exhibiting reaction, sodium tetraphenylboron caused a white precipitate and a Dragendorff reagent caused a red precipitate, which was positive.
さらに、コラーゲン誘導ポリペプタイドとCTAとが結合
していることを確認するために、得られ水溶液を用い、
ゲル濾過(G-25、ファルマシア社製)を行ない、各分子
量フラクションについて、上記の呈性反応を行なったと
ころ、各フラクションはいずれも第4級アンモニウム塩
の呈性反応が陽性であり、コラーゲン誘導ポリペプタイ
ドとCTAとが結合していることが確認された。Furthermore, in order to confirm that the collagen-derived polypeptide and CTA are bound, the obtained aqueous solution was used,
Gel filtration (G-25, manufactured by Pharmacia) was carried out, and the above-mentioned oxidative reaction was carried out for each molecular weight fraction. As a result, each quaternary ammonium salt was positive for the oxidative reaction and collagen induction was observed. It was confirmed that the polypeptide and CTA were bound.
(効果) 表4からわかるように、第4級トリメチルアンモニウム
誘導コラーゲンポリペプタイド配合だけでは、髪への効
果は決して満足されるものではなかった。しかし、本発
明の陰イオン性高分子と組合せ配合した試料は、全ての
項目において優れており、特に、毛髪のはり、こし又、
髪のまとまりやすさにおいて、一段と優れた効果を示し
た。 (Effect) As can be seen from Table 4, the effect on hair was never satisfied only by the incorporation of the quaternary trimethylammonium-derived collagen polypeptide. However, the sample compounded with the anionic polymer of the present invention is excellent in all the items, and particularly, it is particularly effective for the hair beam, the strain, and the
The effect was much more excellent in terms of hair cohesion.
[発明の効果] 本発明のプレヘアリンス型の毛髪処理剤組成物は従来の
シャンプーとヘアリンスの間に使用する。而して、髪に
しなやかさ、なめらかさ、光沢を与え、櫛通りをよく
し、且つべたつき、油っぽさがなく、髪に張り、こしを
与えて自然な感じで髪をまとめることができる。EFFECT OF THE INVENTION The pre-hair rinse type hair treatment composition of the present invention is used between conventional shampoo and hair rinse. Thus, you can give your hair a suppleness, smoothness, and luster, make it easier to comb, and have no stickiness or oiliness. .
Claims (6)
含有することを特徴とするプレヘアリンス型毛髪処理剤
組成物。1. A pre-hair rinse type hair treatment composition comprising at least one anionic polymer.
請求の範囲第(1)項記載のプレヘアリンス型毛髪処理
剤組成物。2. The pre-hair rinse type hair treatment composition according to claim 1, wherein the anionic polymer is a natural polysaccharide.
ナン、クインスシードガム、ローカストビーンガム、ア
ラビアガム、グアーガム、アルギン酸ソーダ、カラギー
ナン(カッパー,ラムダ,アイオタ)、ペクチン、ヒア
ルロン酸、コンドロイチン4硫酸、コンドロイチン8硫
酸、デルマタン硫酸、コンドロイチン4,8ジ硫酸、デル
マタン4,8ジ硫酸、ケラタン硫酸又はヘパラン硫酸であ
る特許請求の範囲第(2)項記載のプレヘアリンス型毛
髪処理剤組成物。3. Natural polysaccharides are xanthan gum, glucomannan, quince seed gum, locust bean gum, gum arabic, guar gum, sodium alginate, carrageenan (copper, lambda, iota), pectin, hyaluronic acid, chondroitin 4 sulfate, chondroitin 8 The pre-hair rinse hair treatment composition according to claim (2), which is sulfuric acid, dermatan sulfate, chondroitin 4,8 disulfate, dermatan 4,8 disulfate, keratan sulfate or heparan sulfate.
請求の範囲第(1)項記載のプレヘアリンス型毛髪処理
剤組成物。4. The prehair rinse-type hair treatment composition according to claim 1, wherein the anionic polymer is a synthetic polymer.
ボキシメチルセルロース、メチルビニールエーテル/無
水マレイン酸共重合物、アクリル酸エステル/メタアク
リル酸エステル/ダイアセトンアクリルアマイド/アク
リル酸/メタアクリル酸共重合物又は架橋化カルボキシ
ビニールポリマーである特許請求の範囲第(4)項記載
のプレヘアリンス型毛髪処理剤組成物。5. Synthetic polymer is sodium polyacrylate, carboxymethyl cellulose, methyl vinyl ether / maleic anhydride copolymer, acrylic ester / methacrylic ester / diacetone acrylate / acrylic acid / methacrylic acid copolymer. A pre-hair rinse hair treatment composition according to claim (4), which is a substance or a cross-linked carboxyvinyl polymer.
級トリメチルアンモニウム誘導ポリペプタイドの一種又
は二種以上を含有することを特徴とする特許請求の範囲
第(1)項乃至第(5)のいずれかに記載のプレヘアリ
ンス型毛髪処理剤組成物。 (式中、R1はコラーゲンより誘導されるポリペプタイド
を構成するアミノ酸であり、nは3〜20である。)6. A fourth structure represented by the following general formula [1]:
The prehair rinse-type hair treatment composition according to any one of claims (1) to (5), characterized in that it contains one or more kinds of secondary trimethylammonium-derived polypeptides. (In the formula, R 1 is an amino acid constituting a polypeptide derived from collagen, and n is 3 to 20.)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP30103386A JPH0713007B2 (en) | 1986-12-17 | 1986-12-17 | Pre-hair rinse type hair treatment composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP30103386A JPH0713007B2 (en) | 1986-12-17 | 1986-12-17 | Pre-hair rinse type hair treatment composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63154610A JPS63154610A (en) | 1988-06-27 |
| JPH0713007B2 true JPH0713007B2 (en) | 1995-02-15 |
Family
ID=17892042
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP30103386A Expired - Lifetime JPH0713007B2 (en) | 1986-12-17 | 1986-12-17 | Pre-hair rinse type hair treatment composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0713007B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01175924A (en) * | 1987-12-28 | 1989-07-12 | Hoou Kk | Hair treatment agent |
-
1986
- 1986-12-17 JP JP30103386A patent/JPH0713007B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63154610A (en) | 1988-06-27 |
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