JPS5928955A - Skin replica material - Google Patents

Skin replica material

Info

Publication number
JPS5928955A
JPS5928955A JP57137938A JP13793882A JPS5928955A JP S5928955 A JPS5928955 A JP S5928955A JP 57137938 A JP57137938 A JP 57137938A JP 13793882 A JP13793882 A JP 13793882A JP S5928955 A JPS5928955 A JP S5928955A
Authority
JP
Japan
Prior art keywords
skin
replica
water
replica material
present
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP57137938A
Other languages
Japanese (ja)
Other versions
JPS613331B2 (en
Inventor
清一 新井
平 竹本
隆 安部
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.)
Kanebo Ltd
Original Assignee
Kanebo Ltd
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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP57137938A priority Critical patent/JPS5928955A/en
Publication of JPS5928955A publication Critical patent/JPS5928955A/en
Publication of JPS613331B2 publication Critical patent/JPS613331B2/ja
Granted legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、皮膚のレプリカの観察に使用するレプリカ材
組成物Gこ関する。詳しくは、皮膚に刺激を与えること
なく、短時間で簡便心こ皮膚表面の微細構造の正確な観
察を可能にするレプリカ材に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a replica material composition G used for observing skin replicas. Specifically, the present invention relates to a replica material that allows accurate observation of the fine structure of the skin surface in a short time without irritating the skin.

従来、皮膚のレプリカを観察する方法としでは、(1)
  セルロイド板に酢酸ブチルを塗布して皮膚に押し付
けて乾燥した後、これをはく離して得られる皮膚レプリ
カを湾曲しないように台紙に接着後、光学顕微鏡で観察
する方法(スンプ法)。
Conventionally, methods for observing skin replicas include (1)
A method of applying butyl acetate to a celluloid plate, pressing it against the skin, drying it, peeling it off, and gluing the resulting skin replica onto a mount to prevent it from curving, which is then observed under an optical microscope (Sump method).

(2)  歯科用印象剤(シリコーン樹脂)を皮膚に塗
布して硬化後、さらにこの上に同様に印象剤を流し込ん
で硬化させた後はく離して、これを実体顕微鏡で観察す
る方法(二段レプリカ法)。
(2) A method in which dental impression material (silicone resin) is applied to the skin and cured, then another impression material is poured on top of this, cured, peeled off, and observed under a stereomicroscope (two-step method). replica method).

(3) セロイジン液にトロセルロースのア七トン・エ
ーテル溶液)を皮膚に塗布して乾燥した後、透明な接着
剤のついたセロファンを付着してはく離し、湾曲しない
ようにスライドグラスに固定した後、光学顕微鏡で観察
する方法(Wollf法)。
(3) Celloidin solution and trocellulose a7tone ether solution) were applied to the skin and allowed to dry, then cellophane with transparent adhesive was attached and peeled off, and fixed on a slide glass to prevent it from bending. Then, a method of observing with an optical microscope (Wollf method).

等がある。etc.

上記皮膚レプリカの観察方法のうち、二段レプリカ法は
、作業が繁雑で観察までに長時間を要することおよびか
なりの熟練を要する欠点がある。
Among the above methods for observing skin replicas, the two-stage replica method has the drawbacks of being complicated, requiring a long time for observation, and requiring considerable skill.

W01f法は作業は簡便であるが、皮膚に対する接着力
が強くてはく離時の刺激が大きく、顔面部への適用が不
可能である。
Although the W01f method is easy to work with, it has strong adhesion to the skin and causes great irritation when peeled off, making it impossible to apply to the face.

このため、一般にはスンプ法が採用されているが、この
方法においても、表面微細構造の優れたレプリカは得ら
れるものの、セルロイド板が熱お  。
For this reason, the Sumpp method is generally used, but although this method also provides an excellent replica of the surface microstructure, the celluloid plate becomes too hot.

よび光に対して分解しやすいために、その分解物による
皮膚障害が発生すること、あるいは作業にあたって使用
する酢酸ブチルの適量の決定に熟練を要するなどの欠点
がある。
Since it is easily decomposed by light and light, it has drawbacks such as skin damage caused by its decomposed products and the need for skill in determining the appropriate amount of butyl acetate to be used in the work.

本発明は、従来技術に付帯する上記欠点の改良された特
定の共重合ポリアミド、水混和性有機溶剤および水から
なる皮膚レプリカ材を提供することを目的とするもので
、本レプリカ材は安全性が高く)安定で保存性が良く、
シかも皮膚に刺激(痛み等)を与えることなく、簡便、
短時間に皮膚表面の微細構造に忠実なレプリカの作成を
可能にするものである。
The object of the present invention is to provide a skin replica material consisting of a specific copolymer polyamide, a water-miscible organic solvent, and water, which has improved the above-mentioned drawbacks associated with the prior art. is stable and has a good shelf life.
It is easy to use, does not cause irritation (pain, etc.) to the skin, and is easy to use.
This makes it possible to create a faithful replica of the fine structure of the skin surface in a short time.

本発明に使用する共重合ポリアミドは、α−(N、N−
ジメチルアミノ)−ε−カプロラクタムとε−カプロラ
クタムを公知の重合法(例えば、アニオン重合法等)で
共重合することによって得られ、かつ水混和性有機溶剤
および水に溶解し得るものである。
The copolyamide used in the present invention is α-(N, N-
It is obtained by copolymerizing dimethylamino)-ε-caprolactam and ε-caprolactam by a known polymerization method (for example, anionic polymerization method, etc.), and is soluble in a water-miscible organic solvent and water.

具体的には、下記式(I)で示される構造単位が33〜
74’%ル%、好ましくはll0〜70モル%と、下記
式(It)で示される構造単位が乙7〜2乙モル%、好
ましくは60〜30モル%とを含有し、かつ相対粘度が
/、9〜3/、好ましくは2.2〜21gのものである
Specifically, the structural unit represented by the following formula (I) is 33 to
74'%, preferably 10 to 70 mol%, and the structural unit represented by the following formula (It) contains 7 to 2 mol%, preferably 60 to 30 mol%, and has a relative viscosity of /, 9 to 3/, preferably 2.2 to 21 g.

−NH〜(CH2) 4 0 H−CO−−NH(CH
2) 4  (3H2−GO(II)本発明における相
対粘度とは、qr%硫酸を溶媒としてこれに上記共重合
ポリアミドを/g/100mtの濃度で溶解した溶液に
つき2 j ’Cで測定した相対粘度をいう。
-NH~(CH2) 4 0 H-CO--NH(CH
2) 4 (3H2-GO (II) Relative viscosity in the present invention is the relative viscosity measured at 2 j 'C for a solution prepared by dissolving the above copolyamide at a concentration of /g/100mt in qr% sulfuric acid as a solvent. Refers to viscosity.

本発明に使用するL記共重合ポリアミドは、α−(N、
N−ジメチルアミン)−ε−カプロラクタムとε−カプ
ロラクタムを、例えば通常のアニオン重合法を用いて容
易に得ることができる。この重合反応はアニオン重合触
媒(例えば、金属す) IJウム等のアルカリ金属)と
アニオン重合助触媒(例えば、N−アセチル−ε−カプ
ロラクタム等)をα−(N、 N−ジメチルアミノ〕−
ε−カプロラクタムおよびε−カプロラクタムにそれぞ
れ所定量添加して溶解させ、両者を混合した後、不活性
気流中で重合温度730〜−2!;O”Cに数分間以上
加熱することによって実施することができる。
The L copolyamide used in the present invention is α-(N,
N-dimethylamine)-ε-caprolactam and ε-caprolactam can be easily obtained using, for example, a conventional anionic polymerization method. This polymerization reaction involves combining an anionic polymerization catalyst (e.g., a metal or alkali metal such as aluminum) and an anionic polymerization promoter (e.g., N-acetyl-ε-caprolactam, etc.) with α-(N, N-dimethylamino)-
A predetermined amount of ε-caprolactam and ε-caprolactam are added and dissolved, and after mixing the two, polymerization is carried out at a temperature of 730 to -2! This can be carried out by heating to O''C for several minutes or more.

本発明に使用する共重合ポリアミドは、メチルアルコー
ル、エチルアルコール、n−プロピルアルコール、イソ
プロピルアルコール等の有機溶剤から水等の非有機溶剤
にわたる広い範囲の溶剤に可溶性で、しかもそれ自体柔
軟で、ひび割れや湾曲を起さず、かつ皮膚に対する親和
性も高い。
The copolyamide used in the present invention is soluble in a wide range of solvents, ranging from organic solvents such as methyl alcohol, ethyl alcohol, n-propyl alcohol, and isopropyl alcohol to inorganic solvents such as water, and is flexible and resistant to cracks. It does not cause bending or curvature, and has a high affinity for the skin.

本発明のレプリカ材に使用される共重合ポリアミド(含
有量)は組成成分の全量重量を基準として3〜70重量
%、好ましくは75〜35重量%である。この量が乙重
量%以下になるとレプリカ皮膜の厚みが不足して均一な
はく離が困難になる場合があり、逆に70重量%より多
くなるに従って乾燥時間が長くなって、短時間の観察が
困難になる。
The copolyamide (content) used in the replica material of the present invention is 3 to 70% by weight, preferably 75 to 35% by weight, based on the total weight of the composition components. If this amount is less than 70% by weight, the thickness of the replica film may be insufficient and it may be difficult to peel it off uniformly.On the other hand, if it exceeds 70% by weight, the drying time becomes longer, making short-term observation difficult. become.

本発明に使用する水混和性有機溶剤は、水と混和して上
記共重合ポリアミドと混溶可能な有機溶媒が好ましく、
例えば皮膚に対する安全性を考慮スルトエチルアルコー
ル、イソプロピルアルコール、アセトンを好ましいもの
として例示できる。
The water-miscible organic solvent used in the present invention is preferably an organic solvent that is miscible with water and is miscible with the copolyamide,
For example, preferable examples include sultoethyl alcohol, isopropyl alcohol, and acetone in view of skin safety.

水混和性有機溶剤は一種または二種以上を組合せて使用
することが可能で、その使用量(含有量)は組成成分の
全量重量を基準として30〜10重量%、好ましくは3
3〜乙5重量%である。この量が30重量%以下になる
と、乾燥時間が長くなるために短時間での観察が困難に
なり、逆にに0重量%以トになると粘度が適切でなくな
り、均一な皮膚レプリカ膜が得られ難くなる。
The water-miscible organic solvent can be used alone or in combination of two or more, and the amount used (content) is 30 to 10% by weight, preferably 3% by weight based on the total weight of the composition components.
3 to Otsu 5% by weight. If this amount is less than 30% by weight, the drying time will be longer, making it difficult to observe in a short time.On the other hand, if it is less than 0% by weight, the viscosity will not be appropriate and a uniform skin replica film will not be obtained. It becomes difficult to get caught.

本発明に使用する水の量は組成成分全量重量に対して1
0−30重量%、好ましくは15〜35重量%である。
The amount of water used in the present invention is 1% based on the total weight of the components.
0-30% by weight, preferably 15-35% by weight.

この量が70重量%以下になると、共重合ポリアミドの
溶解性が低下して組成物は不均一系を形成しやすくなり
、逆に50重量%以上になると乾燥時間が長くなって短
時間での観察が困難になる。
When this amount is less than 70% by weight, the solubility of the copolyamide decreases and the composition tends to form a heterogeneous system.On the other hand, when it is more than 50% by weight, the drying time becomes longer and the composition can be dried in a short time. Observation becomes difficult.

本発明の皮膚レプリカ材には、必要に応じて香料、染料
、防腐剤等を添加することも可能である。
It is also possible to add fragrances, dyes, preservatives, etc. to the skin replica material of the present invention, if necessary.

本発明の皮膚レプリカ材は、例えば上記共重合ポリアミ
ドを水に溶解し、これに水混和性有機溶剤および必要に
応じて香料、着色剤等の慣用添加物を攪拌下に添加混合
して製造される新規の組成物であって、上記構成成分が
均一に混溶した実質的に透明な液体である。この組成物
は皮膚表面に適量塗布すると数分間で乾燥して皮膚表面
に忠実なレプリカを形成するので正確な皮膚像の観察を
可能にする。さらに、このレプリカは皮膚との間に適切
な接着力を有するので安全性の面からも優れている。
The skin replica material of the present invention is produced by, for example, dissolving the above-mentioned copolyamide in water, and adding and mixing thereto a water-miscible organic solvent and, if necessary, conventional additives such as fragrances and colorants. The composition is a substantially transparent liquid in which the above-mentioned components are uniformly mixed. When an appropriate amount of this composition is applied to the skin surface, it dries in a few minutes and forms a faithful replica of the skin surface, allowing accurate observation of skin images. Furthermore, this replica has an appropriate adhesion force to the skin, so it is also excellent from a safety standpoint.

このように、本発明のレプリカ剤は、従来技術の有する
長所、すなわちWolf法の簡便性、スンプ法の忠実な
レプリカ及び二段レプリカ法の安全性等全てを具備し、
かつ従来法に付帯する欠点の全てを解消したレプリカ材
ということができる。
As described above, the replica agent of the present invention has all the advantages of the prior art, such as the simplicity of the Wolf method, the faithful replica of the Sumpp method, and the safety of the two-stage replica method.
Moreover, it can be said that this is a replica material that eliminates all of the drawbacks associated with conventional methods.

以下、実施例によって本発明を具体的に説明するが、実
施例中の部およびパーセントは全て重量単位による。
Hereinafter, the present invention will be specifically explained with reference to Examples, in which all parts and percentages are based on weight units.

実施例/ α−(N、N−ジメチルアミノ)−ε−カプロラクタム
(前記式(I))からなる構成単位を32モル%および
ε−カプロラクタム(前記式(If) )からなる構成
単位をグざモル%含有する共重合ポリアミド(相対粘度
2乙)20部を水30部に溶解した後、エチルアルコー
ル10部、アセトンll0部を加え、混合機にて30分
間攪拌して透明均一な本発明の皮膚レプリカ材を得た。
Example/ A structural unit consisting of α-(N,N-dimethylamino)-ε-caprolactam (formula (I) above) was 32 mol% and a structural unit consisting of ε-caprolactam (formula (If) above) was examined. After dissolving 20 parts of copolyamide containing mol% (relative viscosity 2 O) in 30 parts of water, 10 parts of ethyl alcohol and 0 parts of acetone were added, and the mixture was stirred for 30 minutes using a mixer to obtain a transparent and uniform product of the present invention. A skin replica material was obtained.

この本発明品と比較例としてセロイジン液〔5%ニトロ
セルロース/アセトン−エーテル(/ : /)溶液:
 Wolf法〕を用いて尋問技術者が男子パネラ−70
名に対して、前腕部にてレプリカを作成した。すなわち
、両レプリカ材を直径2鰭、長さ101EInのナイロ
ン毛束からなるはけを用いて皮膚面に直径約/am程度
の面積に均一に塗布しく塗布量は約10mg)、乾燥後
市販の透明な接着テープ(セロテープ)を用いて皮膚面
よりはく離した。この結果、本発明のレプリカ材に対し
てははぐり時の痛みを訴えたものはなかったが、セpイ
ジン液に対しては4名がびりつきを訴えた。この原因は
、第1図の両レプリカ面の走査電顕像に示されている如
く、角質に対する接着力の差によるものである。
This invention product and as a comparative example celloidin solution [5% nitrocellulose/acetone-ether (/:/) solution:
The interrogation technician uses the Wolf method to examine male panelists - 70.
A replica was created in the forearm for the name. That is, using a brush made of nylon hair bundles with a diameter of 2 fins and a length of 101 EIn, both replica materials were uniformly applied to the skin surface over an area of approximately 10 mm in diameter (approximately 10 mg), and after drying, commercially available It was removed from the skin using transparent adhesive tape (cellotape). As a result, none of the participants complained of pain when peeling off the replica material of the present invention, but four patients complained of stiffness when using the Sepidine solution. The reason for this is the difference in adhesive strength to the stratum corneum, as shown in the scanning electron microscope images of both replica surfaces in FIG.

すなわち、本発明品による皮膚レプリカの表面は、第1
図(AIに見られるように、表面に角質細胞が薄く付着
しているのみであるのに対して、Wolf法による皮膚
レプリカ表面は、第1図(B)に見られるように、角質
の大きな固りが点在しており、強い接着力によって数層
の角質がむしりとられている。このように、本発明品は
皮膚に対して適切な接着力を有するので、一般の女性顔
面部の肌の状態を調べる場合に危険性がなく利用価値が
高い。
That is, the surface of the skin replica made of the product of the present invention is
Figure (As seen in AI, there are only thin keratinocytes attached to the surface, whereas the skin replica surface created by the Wolf method has large keratin cells as seen in Figure 1 (B). There are scattered lumps, and several layers of dead skin have been peeled off due to the strong adhesive force.In this way, the product of the present invention has an appropriate adhesive force to the skin, so it is suitable for use on the general female facial area. It is not dangerous and has high utility value when examining the condition of the skin.

さらに、本発明品は110℃で3ケ月間保存しても何ら
変化を示さず、安定性に問題のないことも確認された0
得られたレプリカの透過光式光学顕微鏡像は、第2図に
示すように皮溝、皮丘の微細構造が明瞭に再現されてお
り、本発明の目的を十分満足するものであった。
Furthermore, the product of the present invention did not show any change even after being stored at 110°C for 3 months, confirming that there were no problems with stability.
As shown in FIG. 2, the transmitted-light optical microscope image of the obtained replica clearly reproduced the fine structure of the skin grooves and the skin mounds, and fully satisfied the purpose of the present invention.

実施例! α−(N 、 N−ジメチルアミノ)−ε−カプロラク
タムからなる構成単位の乙3モル%およびε−カプロラ
クタムからなるl 酸単位の37モル%を含有する共重
合ポリアミド(相対粘度2.3 )20部を水2部部に
溶解した後、イソプロピルアルコールS部、エチルアル
コ−/I/ !; 部、アセトング5部を加え、実施例
/と全く同様にして本発明の透明均一なレプリカ材を製
造した。この本発明品を尋問技術者3名が50名の女子
パネラ−の頬部の皮膚に実施例/と同様に塗布した。3
分後に、顕微鏡に直接セットできるように工夫した台紙
と接着テープとが一体となった補助具を用いてレプリカ
を皮膚からはく離した。この補助具は第3図に示すよう
に、(1)平面性を保つための台紙部、(2)レプリカ
を′はく離するための透明テープ部、および(3)接着
面を保護するための離型紙から構成されている。本発明
のレプリカを皮膚からはく離するには、レプリカが乾燥
した時点で離型紙(3)をはずし、接着剤面を押しつけ
てレプリカを透明テープに接着させ、次いで皮膚からは
く離する。これによってプレパラートが完成するので、
レプリカの観察はだれにでも簡単に行なえる。
Example! Copolyamide (relative viscosity 2.3) containing 3 mol % of the structural unit consisting of α-(N, N-dimethylamino)-ε-caprolactam and 37 mol % of the l acid unit consisting of ε-caprolactam (relative viscosity 2.3) 20 After dissolving 1 part in 2 parts of water, S part of isopropyl alcohol, ethyl alcohol/I/! A transparent and uniform replica material of the present invention was produced in exactly the same manner as in Example 1 by adding 5 parts of acetone and 5 parts of acetone. The product of the present invention was applied to the cheek skin of 50 female panelists by three interrogation technicians in the same manner as in Example. 3
After a few minutes, the replica was peeled off from the skin using an auxiliary tool that combined a mount and adhesive tape so that it could be placed directly on the microscope. As shown in Figure 3, this auxiliary tool consists of (1) a mount part to maintain flatness, (2) a transparent tape part to peel off the replica, and (3) a peeling part to protect the adhesive surface. It is made up of paper patterns. To peel off the replica of the present invention from the skin, once the replica is dry, remove the release paper (3), press the adhesive side to adhere the replica to the transparent tape, and then peel it off from the skin. This will complete the preparation, so
Anyone can easily observe replicas.

上記プレバレートを顕微鏡で観察した結果は、第7図に
代表例が示されているように、いずれのレプリカ像も皮
溝、皮丘、毛穴等の皮膚表面の微細構造が明瞭に示され
、顔面部の肌の状態を正確に写し取ることができた。す
なわち、本発明のレプリカ材を使用することによって、
肌のきめ、肌また/3;0名のパネラ−のうち刺激を訴
えたものはなく、さらにllo℃で3ケ月間の保存後も
レプリカ材には何らの変化は認められず、安定性にも問
題のないことが確認された。
As a result of observing the above-mentioned prevalates under a microscope, as shown in a typical example in Figure 7, all replica images clearly show the fine structure of the skin surface such as skin grooves, skin mounds, and pores, and the facial I was able to accurately capture the condition of the skin in the area. That is, by using the replica material of the present invention,
Skin texture, skin texture/3; None of the 0 panelists complained of irritation, and no changes were observed in the replica material after storage for 3 months at 10°C, indicating stability. It was confirmed that there were no problems.

実施例3 α−(N、N−ジメチルアミノ)〜ε−カプロラクタム
からなる構成単位の52モル%およびε−カプロラクタ
ムからなる構成単位のlIざモル%を含有する共重合ポ
リアミド(相対粘度22)22部を水23部に溶解した
後、エチルアルコール10部、アセトンl/−5部を加
え、実施例/と全く同様にして本発明の透明均一なレプ
リカ材を製造した。
Example 3 Copolymerized polyamide (relative viscosity 22) containing 52 mol% of structural units consisting of α-(N,N-dimethylamino) to ε-caprolactam and 11 mol% of structural units consisting of ε-caprolactam (relative viscosity 22) After dissolving 1 part in 23 parts of water, 10 parts of ethyl alcohol and 1/-5 parts of acetone were added, and a transparent and uniform replica material of the present invention was produced in exactly the same manner as in Example.

この発明品および比較例としてスンプ法によるレプリカ
材を、レプリカ作成の経験のない男女パネラ−30名を
施術者として、各施術者に各々70名の女性パネラ−の
頬部に対して塗布させた。
As a comparative example, this invention and a replica material made by the Sumpu method were applied to the cheeks of 70 female panelists by 30 male and female panelists who had no experience in creating replicas. .

すなわち、10名の女性パ・ネラーの頬左側には本発明
のレプリカ材を実施例2と同様にして塗布し、頬右側に
は スンプ板に酢酸ブチルを塗布した後に接着し、それ
ぞれ3分後にはく離して両者を顕微鏡で観察した。結果
は第S図に示すように、レプリカに泡の混入した例(第
5図(A))や乾燥の不完全な例(第5図(B))等の
不良な例が、スンプ法では27%にも達したのに、本発
明品ではわずかに2%であった。このように、本発明品
では、使用上熟練を必要とせず無経験者でも正確なレプ
リカの得られることが立証された。さらに、スンプ法で
は前述したように熱、光等によって生成する分解物の強
い刺激性による保存上の問題があるのに対して、本発明
品は110℃で3ケ月間保存しても何ら変化なく、安定
性の問題は発生しなかった。
That is, the replica material of the present invention was applied to the left side of the cheek of 10 female pa-ners in the same manner as in Example 2, and the replica material of the present invention was applied to the right side of the cheek after applying butyl acetate to the dump board, and after 3 minutes each They were peeled off and both were observed under a microscope. As shown in Figure S, the results show that there are some defective examples such as bubbles mixed into the replica (Figure 5 (A)) and incomplete drying (Figure 5 (B)), which are not found in the Sumpp method. Although it reached 27%, it was only 2% in the product of the present invention. In this way, it has been proven that the product of the present invention does not require any skill in use and even an inexperienced person can obtain an accurate replica. Furthermore, as mentioned above, with the SUMP method, there is a storage problem due to the strong irritation of decomposed products produced by heat, light, etc., whereas the product of the present invention shows no change even after being stored at 110°C for 3 months. There were no stability issues.

実施例を 構成成分を下記第1表に示す組成にする以外は、実施例
/と全く同様にして本発明のレプリカ材No。
Replica material No. of the present invention was prepared in exactly the same manner as in Example 1, except that the constituent components were changed to the compositions shown in Table 1 below.

/〜//を製造した。これらレプリカ材の乾燥性、安定
性、レプリカ画像、刺激性についても、検討結果を第1
表に示した。
/~// were manufactured. The drying properties, stability, replica images, and irritation properties of these replica materials were also examined in the first place.
Shown in the table.

第1表の結果は、本発明のレプリカ材は変性ポリアミド
乙〜35%、水混和性有機溶剤30〜70%、水70〜
jO%の場合に良好な結果を与えることを示している。
The results in Table 1 show that the replica material of the present invention contains 35% modified polyamide, 30% to 70% water-miscible organic solvent, and 70% to 70% water.
It is shown that good results are given when jO%.

乾燥性:3分以内にはく離可能の場合を良、3〜乙分の
場合をやや良、乙分以 上の場合を不良。
Drying property: Good if it can be peeled off within 3 minutes, Fairly good if it is between 3 and 3 minutes, Poor if it is more than 3 minutes.

安定性=lIO”C,3ケ月間の保存において、変化の
ない場合を良、変色、粘度 等に何らかの変化の認められる場 合を不良。
Stability = lIO"C, if there is no change after storage for 3 months, it is considered good; if there is any change in color, viscosity, etc., it is considered bad.

画 像:皮溝等が明瞭、例えば第1図のような場合を良
、均一にはく離でき ず不明瞭な場合を不良、部分的に 良好な場合をやや良。
Image: Good if the skin grooves are clear, for example as shown in Figure 1, Poor if the skin cannot be peeled off uniformly and is unclear, Fairly good if it is partially good.

刺激性:20名のパネラ−の上腕内側部位に、常法でオ
ープンバッチテスト を行なったが、本テストでは全品 紅斑等の異状は認められなかった。
Irritation: An open batch test was conducted in a conventional manner on the inner side of the upper arm of 20 panelists, and no abnormalities such as erythema were observed in any of the products.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は走査型電子顕微鏡によるレプリカ表面への角質
の付着状態を示し、(A)は本発明、(B)はWO1f
法による場合である。第2図は本発明による皮膚レプリ
カの透過光式光学顕微鏡像を示現第3図は顕微鏡観察用
補助具の一例を示す。第を図は顔面部の肌の状態を示す
顕微鏡写真で、(A)はきめの細い肌、(B)はきめの
荒い肌を示す。第5図は本発明およびスンプ法の不完全
なレプリカの一例で、(尋は気泡混入、(B)は乾燥不
完全を示す。 /、二台紙部    ノ、:透明テープ部3、:離型紙 特許出願人 鐘紡株式会社 第1図と△少 第1図(73) 第 2 図 第   3  図 第4図(〜 第4図CB) 第1図Cん 第(図(刀ジ
Figure 1 shows the state of adhesion of keratin to the replica surface by scanning electron microscopy, (A) is the present invention, (B) is WO1f.
This is a case according to law. FIG. 2 shows a transmitted light optical microscope image of a skin replica according to the present invention, and FIG. 3 shows an example of an auxiliary tool for microscopic observation. Figure 5 is a micrograph showing the condition of the skin on the face, where (A) shows fine-textured skin and (B) shows rough-textured skin. FIG. 5 is an example of an incomplete replica of the present invention and the Sumpu method (the bottom shows air bubbles mixed in and (B) shows incomplete drying. Patent applicant Kanebo Co., Ltd. Figure 1 and △ Figure 1 (73) Figure 2 Figure 3 Figure 4 (~ Figure 4 CB) Figure 1 C (Figure (Sword Jigs)

Claims (1)

【特許請求の範囲】 (1)  α−(N、N−ジメチルアミノ)−ε−(カ
プロラクタム)とε−力プロラクタムからなる共重合ポ
リアミドと、水混和性有機溶剤、と、水が混溶している
ことを特徴とする皮膚レプリカ材。 (2)  前記の共重合ポリアミドが、下記式(1)で
示される構造単位33〜74’モル%と、下記式(II
)で示される構造単位≦7〜2乙モル%を含有しており
、かつ相対粘度が7.9〜3.7のものである特許請求
の範囲第1項記載の皮膚レプリカ材。 −NH−(CH2)イーGH−CO− −NH−(CH2) 4−0H2−(10−(n)(3
)  前記の共重合アミドが組成物成分の全量重量を基
準として乙〜グ0重量%混溶している特許請求の範囲第
1項記載の皮膚レプリカ材。 (4)  前記の水混和性有機溶剤が、エチルアルコー
ル、イソプロピルアルコール、アセトンあるいはそれら
の組合せである特許請求の範囲第1項記載の皮膚レプリ
カ材。 (5)  前記の水混和性有機溶剤が、組成物成分の全
 ゛最重量を基準として30〜ざ0重量%混溶している
特許請求の範囲第1項記載の皮膚レプリカ材。 (6)  前記の水が、組成物成分の全量重量を基準と
して70〜50重量%混溶している特許請求の範囲第1
項記載の皮膚レプリカ材。
[Scope of Claims] (1) A copolyamide consisting of α-(N,N-dimethylamino)-ε-(caprolactam) and ε-prolactam, a water-miscible organic solvent, and water are mixedly dissolved. A skin replica material that is characterized by: (2) The above-mentioned copolyamide has 33 to 74' mol% of structural units represented by the following formula (1) and the following formula (II
The skin replica material according to claim 1, which contains structural units ≦7 to 2 mol % represented by ) and has a relative viscosity of 7.9 to 3.7. -NH-(CH2)eGH-CO- -NH-(CH2) 4-0H2-(10-(n)(3
) The skin replica material according to claim 1, wherein the copolymerized amide is mixed and dissolved in an amount of 0% to 0% by weight based on the total weight of the composition components. (4) The skin replica material according to claim 1, wherein the water-miscible organic solvent is ethyl alcohol, isopropyl alcohol, acetone, or a combination thereof. (5) The skin replica material according to claim 1, wherein the water-miscible organic solvent is mixed in an amount of 30 to 0% by weight based on the total weight of the composition components. (6) Claim 1, wherein the water is mixed in an amount of 70 to 50% by weight based on the total weight of the composition components.
Skin replica material described in Section 1.
JP57137938A 1982-08-10 1982-08-10 Skin replica material Granted JPS5928955A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57137938A JPS5928955A (en) 1982-08-10 1982-08-10 Skin replica material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57137938A JPS5928955A (en) 1982-08-10 1982-08-10 Skin replica material

Publications (2)

Publication Number Publication Date
JPS5928955A true JPS5928955A (en) 1984-02-15
JPS613331B2 JPS613331B2 (en) 1986-01-31

Family

ID=15210207

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57137938A Granted JPS5928955A (en) 1982-08-10 1982-08-10 Skin replica material

Country Status (1)

Country Link
JP (1) JPS5928955A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0346973U (en) * 1989-09-13 1991-04-30

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0346973U (en) * 1989-09-13 1991-04-30

Also Published As

Publication number Publication date
JPS613331B2 (en) 1986-01-31

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