JPH0873323A - Method for modifying cuticle fiber - Google Patents

Method for modifying cuticle fiber

Info

Publication number
JPH0873323A
JPH0873323A JP20991694A JP20991694A JPH0873323A JP H0873323 A JPH0873323 A JP H0873323A JP 20991694 A JP20991694 A JP 20991694A JP 20991694 A JP20991694 A JP 20991694A JP H0873323 A JPH0873323 A JP H0873323A
Authority
JP
Japan
Prior art keywords
drug
shape
keratinous fibers
temperature
fiber
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
Application number
JP20991694A
Other languages
Japanese (ja)
Inventor
Naoki Sato
直紀 佐藤
Shinobu Nagase
忍 長瀬
Masato Oshika
正人 大鹿
Shinya Ueda
晋也 上田
Kaoru Tsujii
薫 辻井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Corp
Original Assignee
Kao Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kao Corp filed Critical Kao Corp
Priority to JP20991694A priority Critical patent/JPH0873323A/en
Publication of JPH0873323A publication Critical patent/JPH0873323A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: To enable the continuons and more effective development of a modifying effect on a cuticle fiber by selectively impregnating a chemical into a target part in the cuticle fiber. CONSTITUTION: A chemical is impregnated into a cuticle fiber by impregnating the chemical at a specific fixing temperature and varying the temperature. The fixing temperatur is defined by the temperature to keep >=25% of the shape by fixing cuticle fiber to a definite shape for 1hr and immersing the fiber in a water/ethanol mixture at -15 deg.C to release the fixation of the fiber, the temperature to keep >=15% and <25% of the shape or the temperature to keep <15% of the shape.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は毛髪に代表される角質繊
維の改質方法、更に詳細には角質繊維改質のための薬
剤、例えば染料、ハリコシ付与剤、柔軟化剤、還元剤、
酸化剤、損傷防止剤等の角質繊維内部への浸透を促進さ
せ、かつ当該薬剤の効果を充分に発揮させる方法に関す
る。
FIELD OF THE INVENTION The present invention relates to a method for modifying keratinous fibers represented by hair, and more specifically, agents for modifying keratinous fibers, such as dyes, elasticity-imparting agents, softening agents, reducing agents,
The present invention relates to a method of promoting the penetration of an oxidant, an anti-damage agent and the like into the inside of keratinous fibers, and sufficiently exerting the effect of the agent.

【0002】[0002]

【従来の技術】毛髪に代表される角質繊維の機械的性質
を変化させたり、その色を変化させたりする目的で染
料、ハリコシ付与剤、柔軟化剤、還元剤、酸化剤、損傷
防止剤等の各種薬剤を、角質繊維へ浸透させるため、例
えば角質繊維を単に水、温水などにて膨潤させた状態で
薬剤を繊維中に拡散させる最も単純な方法、或いはまた
ベンジルアルコール、或いはベンジルオキシエタノール
などの浸透促進剤とともに浸透させ、物質浸透の速度を
速める方法などが採られてきた。
2. Description of the Related Art Dyes, elasticity-imparting agents, softening agents, reducing agents, oxidizing agents, damage-preventing agents, etc. for the purpose of changing the mechanical properties of keratin fibers typified by hair and changing the color thereof. In order to permeate keratinous fibers of various drugs, for example, the simplest method of diffusing the drug into the fibers while swelling the keratinous fibers with water, warm water, etc., or benzyl alcohol, benzyloxyethanol, etc. In order to accelerate the rate of substance penetration, a method has been adopted in which the substance is permeated with the permeation enhancer.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、これら
従来の手段では適用された薬剤が角質繊維のどの部位
に、どれだけの量浸透しているかなどについては全く考
慮されていなかった。すなわち、角質繊維に損傷を与え
ずに、目的とする部位により効果的に薬剤を浸透させる
ための技術、更に浸透させた薬剤を長期間角質繊維内に
残留させ、効果を持続させるための技術は全く存在しな
かった。
However, in these conventional means, no consideration has been given to which part of the keratinous fibers the applied drug permeates, and to what extent. That is, a technique for more effectively penetrating the drug to a target site without damaging the keratinous fibers, and a technique for allowing the penetrated drug to remain in the keratinous fibers for a long period of time and maintaining the effect are It didn't exist at all.

【0004】従って、本発明の目的は、角質繊維の改質
効果を発現させるために、角質繊維の必要とする部位に
必要量の薬剤を浸透させることにより、薬剤の効果をよ
り高め、かつ持続的にその効果を発現させる方法を提供
することにある。
Therefore, an object of the present invention is to enhance the effect of a drug and to maintain the effect by allowing a necessary amount of the drug to penetrate into a region where the keratin fiber is needed in order to exert a modifying effect on the keratin fiber. To provide a method of expressing the effect.

【0005】[0005]

【課題を解決するための手段】かかる実情に鑑み、本発
明者は角質繊維の物質浸透性、浸透部位、角質繊維内部
の化学的変化、角質繊維の形状の変形能等の相互関係に
つき種々研究してきたところ、角質繊維はその形状の変
形能を指標とする2種類の温度を境にして薬剤の浸透性
等が極めてドラスチックに変化すること、また当該2種
類の温度は制御することもできること、更には当該2種
類の温度変化による角質繊維の性質の変化を利用すれ
ば、角質繊維への薬剤の浸透性を制御できることを見出
し、本発明を完成するに至った。
In view of the above situation, the present inventor has conducted various researches on the interrelationship of the substance permeability of keratinous fibers, the permeation site, the chemical change inside keratinous fibers, the deformability of the shape of keratinous fibers, and the like. As a result, the keratinous fibers have drastic changes in the drug permeability and the like at the boundaries of the two types of temperature with the shape deformability as an index, and the two types of temperatures can be controlled. Furthermore, they have found that the permeability of a drug into keratinous fibers can be controlled by utilizing changes in the properties of keratinous fibers due to the two types of temperature changes, and have completed the present invention.

【0006】すなわち、本発明は、角質繊維を1時間一
定の形状に固定した後−15℃の水/エタノール混合溶
媒に浸漬して当該固定を解除したときその形状が25%
以上保持される当該固定温度において、薬剤を当該角質
繊維に接触させることを特徴とする角質繊維内部への薬
剤の浸透方法を提供するものである。
That is, according to the present invention, when keratinous fibers are fixed in a constant shape for 1 hour and then immersed in a water / ethanol mixed solvent at -15 ° C to release the fixation, the shape is 25%.
Provided is a method for permeating a drug into the inside of keratinous fibers, which is characterized in that the drug is brought into contact with the keratinous fibers at the fixing temperature maintained as above.

【0007】また、本発明は、角質繊維を1時間一定の
形状に固定した後−15℃の水/エタノール混合溶媒に
浸漬して当該固定を解除したときその形状が25%以上
保持される当該固定温度において、当該角質繊維に薬剤
を接触せしめた後、その形状が15%以上25%未満保
持される当該固定温度又はその形状が15%未満保持さ
れる当該固定温度まで温度を低下させることを特徴とす
る角質繊維内部への薬剤の浸透方法を提供するものであ
る。
Further, according to the present invention, when the keratinous fibers are fixed in a constant shape for 1 hour and then immersed in a water / ethanol mixed solvent at -15 ° C. to release the fixation, the shape is maintained at 25% or more. After bringing the drug into contact with the keratinous fibers at a fixed temperature, lowering the temperature to the fixed temperature at which the shape is maintained at 15% or more and less than 25% or the fixed temperature at which the shape is maintained at less than 15%. It is intended to provide a method for penetrating a drug into the inside of the characteristic keratinous fibers.

【0008】更にまた、本発明は角質繊維を1時間一定
の形状に固定した後−15℃の水/エタノール混合溶媒
に浸漬して当該固定を解除したときその形状が15%以
上25%未満保持される当該固定温度において、当該角
質繊維に薬剤を接触せしめた後、その形状が15%未満
保持される当該固定温度まで温度を低下させることを特
徴とする角質繊維内部への薬剤の浸透方法を提供するも
のである。
Furthermore, according to the present invention, when keratinous fibers are fixed in a constant shape for 1 hour and then immersed in a water / ethanol mixed solvent at -15 ° C. to release the fixation, the shape is maintained at 15% or more and less than 25%. A method for permeating a drug into keratinous fibers, which comprises: bringing the drug into contact with the keratinous fibers at the fixed temperature, and then lowering the temperature to the fixed temperature where the shape is maintained at less than 15%. It is provided.

【0009】本発明における角質繊維を1時間一定の形
状に固定した後−15℃の水/エタノール混合溶媒に浸
漬して当該固定を解除したときその形状が25%以上保
持される当該固定温度の下限温度(以下「Th」とい
う)及び角質繊維を1時間一定の形状に固定した後−1
5℃の水/エタノール混合溶媒に浸漬して当該固定を解
除したときその形状が15%未満保持される当該固定温
度の上限温度(以下「Tl」という)は、ある温度で角
質繊維を1時間一定の形状に固定した後−15℃の水/
エタノール混合溶媒に浸漬して当該固定を解除し、その
形状の保持される割合(以下、「形状保持率」という)
を測定することにより判定できる。例えば、テフロン製
の円柱、例えば直径(D0)の円柱に毛髪繊維1本を巻
きつけ、ある一定の温度条件下(液体中でも、気体中で
もよい)で1時間固定したままとする。その後−15℃
に冷却した水/エタノール混合液(50%)に浸漬して
固定材をはずし、その状態で24時間放置した後のカー
ル径(D)を測定する。形状保持率はD0/D×100
により測定できる。その形状保持率からその固定条件温
度がTh以上、Tl以上Th未満又はTl未満のいずれ
であるかを判定すればよい。
After fixing the keratinous fibers in the present invention in a constant shape for 1 hour and then immersing them in a water / ethanol mixed solvent at -15 ° C to release the fixation, the shape is maintained at 25% or more. Lower limit temperature (hereinafter referred to as "Th") and after fixing the keratinous fiber in a constant shape for 1 hour -1
The shape is maintained at less than 15% when the fixation is released by immersing the mixture in a water / ethanol mixed solvent at 5 ° C. After fixing to a certain shape, water at -15 ° C /
The shape is retained by immersing it in an ethanol mixed solvent to release the fixation (hereinafter referred to as "shape retention rate").
Can be determined by measuring. For example, one hair fiber is wound around a column made of Teflon, for example, a column having a diameter (D 0 ), and is fixed for 1 hour under a certain constant temperature condition (either in liquid or gas). Then -15 ° C
The curling diameter (D) is measured after immersing in a water / ethanol mixed solution (50%) cooled to 1, removing the fixing material, and leaving it in that state for 24 hours. Shape retention rate is D 0 / D × 100
Can be measured by From the shape retention rate, it may be determined whether the fixed condition temperature is Th or higher, Tl or higher and lower than Th, or lower than Tl.

【0010】まず、Th以上、すなわち形状保持率が2
5%以上である固定温度においては、角質繊維の変形は
極めて容易であるが、角質繊維中への薬剤の浸透性は極
めて高く、種々の薬剤を含有する溶液で角質繊維を処理
することにより、容易に角質繊維内部に薬剤を浸透させ
ることができる。ただし、Th以上では、浸透した薬剤
を洗浄等の操作により除去することもまた容易である。
Th以上においては、薬剤は、角質繊維中のマクロフィ
ブリル及びマクロフィブリル間の両部位に浸透する。
First, Th or more, that is, the shape retention rate is 2
At a fixed temperature of 5% or more, the keratinous fibers are extremely easily deformed, but the permeability of the drug into the keratinous fibers is extremely high, and by treating the keratinous fibers with a solution containing various drugs, The drug can easily penetrate inside the keratinous fibers. However, above Th, it is also easy to remove the permeated drug by an operation such as washing.
Above Th, the drug penetrates both macrofibrils in the keratinous fibers and between macrofibrils.

【0011】次に、Tl以上Th未満、すなわち形状保
持率が15%以上25%未満である固定温度において
は、角質繊維の変形はやや良好であり、薬剤の浸透性は
やや良好であり、種々の薬剤を含有する溶液で角質繊維
を処理すれば当該薬剤を角質繊維内部に浸透させること
ができる。Tl以上Th未満においては、薬剤は角質繊
維中のマクロフィブリル間にのみ浸透する。またTh以
上の条件下で薬剤を角質繊維内に浸透させた後、この温
度範囲にすれば、薬剤がマクロフィブリル部にのみ保持
される。このようにTl以上Th未満においては、角質
繊維中のマクロフィブリル間にのみ選択的に薬剤を浸透
させることが可能である。
Next, at a fixed temperature of Tl or more and less than Th, that is, a shape retention rate of 15% or more and less than 25%, the deformation of the keratinous fibers is slightly good, and the drug permeability is slightly good, and various If the keratinous fiber is treated with a solution containing the drug, the drug can be permeated into the keratinous fiber. Above Tl and below Th, the drug penetrates only between macrofibrils in keratinous fibers. In addition, if the drug is permeated into the keratinous fibers under the condition of Th or more and then this temperature range is set, the drug is retained only in the macrofibril portion. As described above, when Tl or more and less than Th, it is possible to selectively permeate the drug only between the macrofibrils in the keratinous fibers.

【0012】また、Tl未満、すなわち形状保持率が1
5%未満である固定温度においては、角質繊維はほとん
ど塑性変形せず、薬剤はほとんど角質繊維内部に浸透し
ない。すなわち、Th以上の条件下で薬剤を浸透させた
角質繊維をTl未満の条件にすれば、薬剤はマクロフィ
ブリル部及びマクロフィブリル間の両部位に保持され
る。また、Tl以上Th未満の範囲で薬剤を浸透させた
角質繊維をTl未満にすると、マクロフィブリル間にの
み薬剤が保持される。
Further, it is less than Tl, that is, the shape retention rate is 1
At a fixed temperature of less than 5%, the keratinous fibers hardly plastically deform and the drug hardly penetrates inside the keratinous fibers. That is, when the keratinous fibers infiltrated with the drug under the condition of Th or more are set to the condition of less than Tl, the drug is retained at both the macrofibril portion and the site between the macrofibrils. When the keratinous fibers in which the drug has penetrated in the range of Tl or more and less than Th are set to less than Tl, the drug is retained only between the macrofibrils.

【0013】本発明におけるThは、純水中では約70
℃であるが、還元剤(添加により低下)、アルコール
(添加により低下)、アミン(添加により低下)などの
添加、溶媒のpHの変化(pH8以下で低下)により制御す
ることができる。
Th in the present invention is about 70 in pure water.
Although it is at 0 ° C, it can be controlled by addition of a reducing agent (decreased by addition), alcohol (decreased by addition), amine (decreased by addition), etc., and change in pH of the solvent (decreased at pH 8 or lower).

【0014】また、Tlは純水中では約0℃であるが、
アルコール(添加により上昇)、ホルムアミド(添加に
より低下)等の添加により制御することができる。
Although Tl is about 0 ° C. in pure water,
It can be controlled by addition of alcohol (increased by addition), formamide (decreased by addition) and the like.

【0015】このようにTh、Tlは制御可能であるの
で、角質繊維への薬剤の浸透を行う場合、これらの転移
点を制御して行うのが好ましい。
Since Th and Tl can be controlled as described above, it is preferable to control the transition points of these agents when the drug penetrates into the keratinous fibers.

【0016】本発明において、角質繊維としては毛髪、
ウール等が挙げられるが、毛髪が特に好ましい。
In the present invention, hair is used as the keratinous fiber,
Wool and the like can be mentioned, but hair is particularly preferable.

【0017】本発明において使用し得る薬剤としては、
角質繊維に適用できる溶媒に溶解するものであれば特に
制限されないが、例えばナフタレンスルホン酸、ナフト
エ酸等のハリコシ付与剤;染料;グリコール酸、乳酸等
の柔軟化剤;エチルカルビトール、UV遮閉剤等の損傷
防止剤;還元剤、酸化剤等が挙げられる。
The agents that can be used in the present invention include:
It is not particularly limited as long as it dissolves in a solvent applicable to keratinous fibers, for example, a syrup imparting agent such as naphthalenesulfonic acid and naphthoic acid; a dye; a softening agent such as glycolic acid and lactic acid; ethyl carbitol, UV shielding Anti-damage agents such as agents; reducing agents, oxidizing agents and the like.

【0018】薬剤の角質繊維への接触手段としては、薬
剤を溶媒に溶解した液に角質繊維を浸漬する方法、当該
液を角質繊維に塗布する方法等が挙げられる。
Means for contacting the keratin fibers with the drug include a method of immersing the keratin fibers in a liquid in which the drug is dissolved in a solvent, and a method of applying the liquid to the keratin fibers.

【0019】また、薬剤を角質繊維内の所望の部位に保
持するためには、例えばTh以上において角質繊維に薬
剤を接触させた後Tl以上Th未満に温度を低下させ、
当該角質繊維を洗浄すれば、薬剤はマクロフィブリル部
に保持される。他の部位に選択的に保持させる場合も同
様である。
In order to retain the drug at a desired site in the keratinous fiber, for example, after contacting the keratinous fiber with the drug at Th or more, the temperature is lowered to Tl or more and less than Th,
When the keratinous fibers are washed, the drug is retained in the macrofibril part. The same applies to the case where it is selectively held at another site.

【0020】[0020]

【実施例】次に実施例を挙げて本発明を更に詳細に説明
するが、本発明はこれらに限定されるものではない。
The present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.

【0021】実施例1 (1)未化学処理の日本人毛髪を直径3mmのテフロンロ
ッドに巻きつけ、種々の温度の水に1時間浸漬した。そ
の後−15℃の水/エタノール混合液(50%)中でテ
フロンロッドをはずし、24時間放置した。毛髪のカー
ル径(D)を測定し、形状保持率(3/D×100)を
求めた。得られた形状保持率を固定温度に対してプロッ
トしたところ、0℃と70℃に急な折れまがり点(変曲
点)が表われ、Tl及びThはそれぞれ0℃及び70℃
であることがわかった。
Example 1 (1) Unchemically treated Japanese hair was wrapped around a Teflon rod having a diameter of 3 mm and immersed in water at various temperatures for 1 hour. After that, the Teflon rod was removed in a water / ethanol mixed solution (50%) at −15 ° C. and left for 24 hours. The curl diameter (D) of the hair was measured to obtain the shape retention rate (3 / D × 100). When the obtained shape retention rate was plotted against the fixed temperature, a sharp bending point (inflection point) appeared at 0 ° C and 70 ° C, and Tl and Th were 0 ° C and 70 ° C, respectively.
It turned out to be.

【0022】(2)1時間固定する溶媒を水から30mM
亜硫酸ナトリウム水溶液に変更したところ、Tl及びT
hはそれぞれ0℃及び25℃であった。一方、1時間固
定する溶媒を95%プロパノール溶液に変更したとこ
ろ、Tl及びThはそれぞれ60℃及び70℃であっ
た。この事実より、Th及びTlはそれぞれ独立に制御
可能であることが判明した。
(2) Solvent fixed for 1 hour from water to 30 mM
When changed to an aqueous solution of sodium sulfite, Tl and T
h was 0 ° C. and 25 ° C., respectively. On the other hand, when the solvent fixed for 1 hour was changed to a 95% propanol solution, Tl and Th were 60 ° C and 70 ° C, respectively. From this fact, it was found that Th and Tl can be controlled independently.

【0023】実施例2 未化学処理の日本人毛髪(黒色)を水溶性染料、赤色1
06号(1mM水溶液)で染色する際に次のような異なる
3つの温度において浸透処理を行い、その浸透量、見え
方を目視により比較した。水中でのTl(0℃)より低
い−3℃にて浸透させた場合、毛髪は24時間の浸透時
間で全く染色されなかったが(試料1)、Tl以上Th
未満である50℃において染料の浸透を行ったところ2
0分の浸透時間で染料は充分認知可能な程度まで浸透し
た(試料2)。また染色された毛髪は髪の黒さを失うこ
となくわずかに赤い色が着色されていた。更にThより
高い温度90℃において20分染色したところ、髪の色
は濃く染まっており、また髪色は黒色から赤黒い色に大
きく変化していた(試料3)。従って、Th、Tl以上
の浸透によって浸透の促進が起きていることが分かっ
た。
Example 2 Unchemically treated Japanese hair (black) was treated with a water-soluble dye, red 1
When dyeing with No. 06 (1 mM aqueous solution), permeation treatment was performed at the following three different temperatures, and the permeation amount and appearance were visually compared. When permeated at −3 ° C., which is lower than Tl (0 ° C.) in water, the hair was not dyed at all in the permeation time of 24 hours (Sample 1).
When the dye is permeated at 50 ° C, which is less than 2
The dye penetrated to a perceptible extent with a penetration time of 0 minutes (Sample 2). In addition, the dyed hair had a slight red coloration without losing the blackness of the hair. Further, when the hair was dyed for 20 minutes at a temperature higher than Th at 90 ° C., the hair color was deeply dyed, and the hair color was greatly changed from black to reddish black (Sample 3). Therefore, it was found that the permeation of Th or Tl or more promotes the permeation.

【0024】実施例3 実施例2の処理の後、試料2、試料3の毛髪を50℃の
温水中に浸漬し、30分間洗浄した。その結果、試料2
の毛髪の色は元の黒い色に戻り赤い色味はほぼ完全に消
失した(試料4)。また試料3の毛髪を同じように洗浄
したところ(試料5)、染色の程度は試料3よりだいぶ
小さくなったが色合いは赤黒いままであり、実施例3−
試料2、3の色合いとは全く異なるものが得られた。透
過型電子顕微鏡で観察可能な重元素を含む染料を実施例
2と3の5種類の試料と同じ処理により、毛髪内に浸透
させ、その毛髪の断面を透過型電子顕微鏡にて観察し、
染料の浸透部位を観察した。その結果、試料1、試料4
では毛髪内に染料の存在が確認できないこと、試料2で
はマロクフィブリル間に選択的に浸透していること、試
料3では毛髪全体に浸透していること、試料5ではマク
ロフィブリルにのみ選択的に浸透していることがわか
り、これら処理毛髪の色の違いが浸透部位の違いによる
ことがわかった。従ってこれらの結果、選択的な薬剤浸
透により異なる効果が得られることがわかる。
Example 3 After the treatment of Example 2, the hairs of Sample 2 and Sample 3 were immersed in warm water at 50 ° C. and washed for 30 minutes. As a result, sample 2
The hair color of the product returned to the original black color and the reddish color disappeared almost completely (Sample 4). When the hair of Sample 3 was washed in the same manner (Sample 5), the degree of dyeing was considerably smaller than that of Sample 3, but the shade remained reddish black.
Colors completely different from those of Samples 2 and 3 were obtained. A dye containing a heavy element observable with a transmission electron microscope was permeated into the hair by the same treatment as the five kinds of samples of Examples 2 and 3, and the cross section of the hair was observed with the transmission electron microscope.
The penetration site of the dye was observed. As a result, sample 1 and sample 4
The presence of the dye in the hair cannot be confirmed in the sample, the sample 2 selectively penetrates between the maloc fibrils, the sample 3 penetrates the entire hair, and the sample 5 selectively selects only the macrofibrils. It was found that the difference in the color of these treated hairs was due to the difference in the permeation site. Therefore, as a result of these, it can be seen that different effects can be obtained by selective drug penetration.

【0025】実施例4 実施例2で作成した試料2、試料3を日常の洗髪処理を
想定して、40℃の温水で10分間洗浄する処理を繰り
返した。その結果、表1に示すように試料3は30回洗
浄後(1カ月後に対応)の観察時にも染色量はほとんど
変化しなかったが試料2については、染色量は漸次減少
し15回後にはほとんど着色しているか否か、判別でき
なかった。以上の結果から、Th以上での浸透処理によ
って、浸透物質の効果が長期間にわたり持続的に継続す
ることが分かった。
Example 4 Samples 2 and 3 prepared in Example 2 were repeatedly washed with warm water of 40 ° C. for 10 minutes, assuming daily hair washing treatment. As a result, as shown in Table 1, Sample 3 showed almost no change in the amount of staining even after the observation after washing 30 times (corresponding to one month later), but for Sample 2, the amount of staining gradually decreased and after 15 times, It was not possible to determine whether or not it was almost colored. From the above results, it was found that the effect of the permeative substance is continuously maintained for a long period of time by the permeation treatment at Th or more.

【0026】[0026]

【表1】 [Table 1]

【0027】実施例5 毛髪を直径10mmのテフロンロッドに巻き付け、その状
態で20%t−ブチルアルコール水溶液に浸漬し、様々
な温度で30分間加熱処理した。その後、その毛髪を2
5℃50%RH環境下で12時間乾燥させ、固定から外
してカール径を測定し、セットの良否を判定した。T
h、Tl両温度よりも低い0℃において浸漬処理した場
合、毛髪は全くセットすることはできなかったが、両温
度の間の35℃で浸漬処理した場合、セットは可能であ
った。更にTh、Tl両温度より高い70℃で浸漬処理
した場合、セットはより効果的であった。更に、日常の
洗髪処理を想定して、40℃の温水で10分間、これら
の処理毛髪を洗浄する操作を繰り返した。その結果、表
2に示すように35℃で処理した毛髪は1回の洗浄で形
状は元の形に戻ったが、70℃で処理した毛髪に関して
は30回の水洗い後も形状が保持され永久セットがなさ
れた。
Example 5 Hair was wrapped around a Teflon rod having a diameter of 10 mm, immersed in a 20% t-butyl alcohol aqueous solution in that state, and heat-treated at various temperatures for 30 minutes. After that, the hair 2
It was dried in an environment of 5 ° C. and 50% RH for 12 hours, removed from the fixing and the curl diameter was measured, and the quality of the set was judged. T
When the dipping treatment was performed at 0 ° C., which is lower than both the h and Tl temperatures, the hair could not be set at all, but when the dipping treatment was performed at 35 ° C. between the both temperatures, setting was possible. Furthermore, when the immersion treatment was performed at 70 ° C., which is higher than both the Th and Tl temperatures, the set was more effective. Furthermore, assuming daily hair washing treatment, the operation of washing these treated hair with warm water at 40 ° C. for 10 minutes was repeated. As a result, as shown in Table 2, the hair treated at 35 ° C returned to its original shape with one washing, but the hair treated at 70 ° C retained its shape after being washed 30 times with water. The set was made.

【0028】[0028]

【表2】 [Table 2]

【0029】実施例6 毛髪を柔軟化させる効果のあるグリコール酸を実施例2
と同様に3種類の温度で浸透させその柔軟化効果を判定
した。Tl(0℃)よりも低い−3℃において浸透処理
した場合、毛髪は全く柔軟化することはできなかった
が、Th、Tl両温度の間の35℃で浸透処理した場
合、柔軟化効果が認められた。更に、Th(70℃)、
Tl(0℃)両温度より高い80℃で処理した場合、柔
軟化効果は更に向上した。更に、日常の洗髪処理を想定
して、40℃の温水で10分間、これらの処理毛髪を洗
浄する操作を繰り返した。その結果表3に示すように、
35℃で処理した毛髪は5回の洗浄で毛髪の弾性は元の
値に戻ったが、80℃で処理した毛髪に関しては30回
の水洗い後も柔軟化効果が維持され永久的な柔軟化がな
された。
Example 6 Glycolic acid, which has the effect of softening the hair, was used in Example 2.
In the same manner as above, it was permeated at three different temperatures and its softening effect was evaluated. When the hair was permeabilized at -3 ° C, which is lower than Tl (0 ° C), the hair could not be softened at all. However, when the hair was permeated at 35 ° C between both Th and Tl temperatures, the softening effect was not achieved. Admitted. In addition, Th (70 ℃),
When treated at 80 ° C, which is higher than both Tl (0 ° C), the softening effect was further improved. Furthermore, assuming daily hair washing treatment, the operation of washing these treated hair with warm water at 40 ° C. for 10 minutes was repeated. As a result, as shown in Table 3,
The elasticity of the hair treated at 35 ° C returned to the original value after washing 5 times, but the hair treated at 80 ° C maintained its softening effect even after 30 times of washing with water, and the hair was permanently softened. Made

【0030】[0030]

【表3】 [Table 3]

【0031】[0031]

【発明の効果】本発明方法によれば角質繊維内の目的と
する部位に選択的に薬剤を浸透させ、それぞれの改質効
果をより効果的に持続的に発現させることができる。
EFFECTS OF THE INVENTION According to the method of the present invention, a drug can be selectively permeated into a target site in keratinous fibers to more effectively and continuously exhibit their respective modifying effects.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 上田 晋也 千葉県千葉市花見川区朝日ケ丘1−3 花 王検見川寮205 (72)発明者 辻井 薫 栃木県宇都宮市陽東1−11−23 直井ハイ ツ405 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Shinya Ueda Shinya Ueda 1-3 Asahioka, Hanamigawa-ku, Chiba, Chiba 205 Kao Kemigawa Dormitory (72) Inventor Kaoru Tsujii 1-11-23 Yohito, Utsunomiya-shi, Tochigi 405 Naoi Heights 405

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 角質繊維を1時間一定の形状に固定した
後−15℃の水/エタノール混合溶媒に浸漬して当該固
定を解除したときその形状が25%以上保持される当該
固定温度において、薬剤を当該角質繊維に接触させるこ
とを特徴とする角質繊維内部への薬剤の浸透方法。
1. At the fixing temperature at which the shape is maintained at 25% or more when the keratinous fibers are fixed in a constant shape for 1 hour and then immersed in a water / ethanol mixed solvent at -15 ° C. to release the fixation. A method for permeating a drug into the inside of keratinous fibers, which comprises contacting the drug with the keratinous fibers.
【請求項2】 角質繊維を1時間一定の形状に固定した
後−15℃の水/エタノール混合溶媒に浸漬して当該固
定を解除したときその形状が25%以上保持される当該
固定温度において、当該角質繊維に薬剤を接触せしめた
後、その形状が15%以上25%未満保持される当該固
定温度又はその形状が15%未満保持される当該固定温
度まで温度を低下させることを特徴とする角質繊維内部
への薬剤の浸透方法。
2. The fixing temperature at which the shape is maintained at 25% or more when the keratinous fibers are fixed in a constant shape for 1 hour and then immersed in a water / ethanol mixed solvent at −15 ° C. to release the fixation, After contacting a drug with the keratinous fibers, the temperature is lowered to the fixing temperature at which the shape is maintained at 15% or more and less than 25% or the fixing temperature at which the shape is maintained at less than 15%. Method of penetrating the drug into the fiber.
【請求項3】 角質繊維を1時間一定の形状に固定した
後−15℃の水/エタノール混合溶媒に浸漬して当該固
定を解除したときその形状が15%以上25%未満保持
される当該固定温度において、当該角質繊維に薬剤を接
触せしめた後、その形状が15%未満保持される当該固
定温度まで温度を低下させることを特徴とする角質繊維
内部への薬剤の浸透方法。
3. The immobilization in which the shape is maintained at 15% or more and less than 25% when the keratinous fibers are fixed in a constant shape for 1 hour and then immersed in a water / ethanol mixed solvent at −15 ° C. to release the fixation. A method for permeating a drug into keratinous fibers, which comprises contacting the drug with the keratinous fibers at a temperature and then lowering the temperature to the fixed temperature at which the shape is maintained at less than 15%.
【請求項4】 薬剤が、染料、ハリコシ付与剤、柔軟化
剤、還元剤、酸化剤、損傷防止剤、セット剤及びくせ矯
正剤(形状制御剤)から選ばれるものである請求項1〜
3のいずれかの項記載の角質繊維内部への薬剤の浸透方
法。
4. The drug is selected from a dye, a tension imparting agent, a softening agent, a reducing agent, an oxidizing agent, a damage preventing agent, a setting agent and a habit straightening agent (shape controlling agent).
4. The method for permeating a drug into the inside of keratinous fibers according to any one of 3 above.
JP20991694A 1994-09-02 1994-09-02 Method for modifying cuticle fiber Pending JPH0873323A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20991694A JPH0873323A (en) 1994-09-02 1994-09-02 Method for modifying cuticle fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20991694A JPH0873323A (en) 1994-09-02 1994-09-02 Method for modifying cuticle fiber

Publications (1)

Publication Number Publication Date
JPH0873323A true JPH0873323A (en) 1996-03-19

Family

ID=16580789

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20991694A Pending JPH0873323A (en) 1994-09-02 1994-09-02 Method for modifying cuticle fiber

Country Status (1)

Country Link
JP (1) JPH0873323A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE47520E1 (en) 2000-04-10 2019-07-16 Celgard, Llc Separator for a high energy rechargeable lithium battery

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE47520E1 (en) 2000-04-10 2019-07-16 Celgard, Llc Separator for a high energy rechargeable lithium battery

Similar Documents

Publication Publication Date Title
Harrison et al. Hair colouring, permanent styling and hair structure
AU595370B2 (en) A process for simultaneously waving and coloring hair
EP0226860B1 (en) Simultaneous method of dyeing and permanent waving of the hair
EP0114414B1 (en) Process for the permanent waving of newly grown hair and composition for performing it
US3973574A (en) Waving and straightening hair by producing metal chelates in the keratin of the hair
JP2567889B2 (en) Drug for oxidative dyeing of hair, method for preparing and using the same
KR890000189B1 (en) Hain dyeing process and compositions package
US5188639A (en) Product for improved permanent waving of hair and simultaneously coloring and permanently waving hair and method therefor
DE3629240C2 (en) Perm solution
US5599531A (en) Hair care, hydrating, coloring, and perming compositions and methods
DE2603175C3 (en) Method for treating human hair and scalp
DE3628398A1 (en) AGENT FOR OXIDATIVE COLORING OF HAIR, METHOD FOR THE PRODUCTION THEREOF AND USE OF THE AGENT
US2962031A (en) Apparatus for treating hair
US2540980A (en) Process and composition for treating keratinous material
JPH0465046B2 (en)
US4504466A (en) Permanent hair-waving
Cole Studies on hematoxylin stains
JPH0873323A (en) Method for modifying cuticle fiber
US4982749A (en) Method of recurling tightly curled hair
US5993794A (en) Perming agent and method of treating hair with the same
EP0257256A2 (en) Method and composition for permanent waving and straightening of hair
US4600028A (en) Saturated end wrap construction and composition
US4275748A (en) Method and composition for modifying filamentous keratins
DE1617904C3 (en) Process for waving, straightening and / or coloring hair and a hair treatment agent in the form of a solution or cream for carrying out the process
NO169752B (en) PORTFOLIOUS PREPARATION AND ITS USE FOR PERMANENTIZING HER