JPS6150562A - Blood conduit - Google Patents

Blood conduit

Info

Publication number
JPS6150562A
JPS6150562A JP59172072A JP17207284A JPS6150562A JP S6150562 A JPS6150562 A JP S6150562A JP 59172072 A JP59172072 A JP 59172072A JP 17207284 A JP17207284 A JP 17207284A JP S6150562 A JPS6150562 A JP S6150562A
Authority
JP
Japan
Prior art keywords
blood
film
treated
acid derivative
blood conduit
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
JP59172072A
Other languages
Japanese (ja)
Other versions
JPS6317463B2 (en
Inventor
憲彦 箕浦
誠一 相羽
冨士原 行彦
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.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
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 Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP59172072A priority Critical patent/JPS6150562A/en
Publication of JPS6150562A publication Critical patent/JPS6150562A/en
Publication of JPS6317463B2 publication Critical patent/JPS6317463B2/ja
Granted legal-status Critical Current

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  • Materials For Medical Uses (AREA)

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】 (a)発明の技術分野 本発明は、アミノアルコールで表面処理されたポリグル
タミン酸誘導体を内表面に有することにより、細胞が付
着しにくいことを特徴とする血液専管に関するものであ
る。
Detailed Description of the Invention (a) Technical Field of the Invention The present invention relates to a specialized blood tube that is characterized by having a polyglutamic acid derivative surface-treated with amino alcohol on its inner surface to prevent cells from adhering to it. It is.

血液導管とは人工血管、カテーテル、シャント(血液を
体外に導き出すために用いるもの)、透析型人工腎臓、
模型人工肺、人工心臓などに用いられている管状の血液
の流路を包含するものである。
Blood conduits include artificial blood vessels, catheters, shunts (used to lead blood out of the body), dialysis-type artificial kidneys,
It includes the tubular blood flow path used in model artificial lungs, artificial hearts, etc.

(b)従来技術の説明 従来、血液導管は、シリコーンゴム、ポリ「フレタン、
ポリテトラフルオロエチレン等の合成高分子材料を用い
て作製されているが、これらの材料を用いた血液導管で
は、その材料表面に細胞が付着し、すなわち血栓が生じ
、血流を阻害する。したがって、血液導管においては1
1胞の付着しない材料が求められている。
(b) Description of the Prior Art Conventionally, blood conduits are made of silicone rubber, polyurethane,
Blood conduits are made using synthetic polymer materials such as polytetrafluoroethylene, but in blood conduits made of these materials, cells adhere to the surface of the material, that is, thrombus forms, which obstructs blood flow. Therefore, in the blood conduit, 1
There is a need for materials that do not have single cells attached to them.

(C)発明の目的 本発明は上記の問題を、アミノアルコールで表面処理さ
れたポリグルタミン酸誘導体を用いることにより、細胞
付着性の少ない血液々9管を提供することを目的とする
(C) Object of the Invention The object of the present invention is to solve the above-mentioned problem by providing a blood tube with less cell adhesion by using a polyglutamic acid derivative surface-treated with amino alcohol.

(d)発明の構成 本発明者は細胞の角希しにくい性質を有する材料につい
て種々研究を重ねたところ、アミノアルコールで表面処
理されたポリグルタミンLg 19体は、細胞を著しく
付着させない性質を有しており血液導管として好適であ
ることを見い出し、本発明を完成するに到った。
(d) Structure of the Invention The present inventor has repeatedly conducted various studies on materials that have properties that prevent cells from being easily damaged, and has found that polyglutamine Lg 19, whose surface has been treated with amino alcohol, has properties that do not significantly allow cells to adhere to it. The present inventors have discovered that this material is suitable for use as a blood conduit, and have completed the present invention.

゛ 即ち、本発明の血液導管は、ポリグルタミン酸誘導
体を目的とする管状に成型した後、その管状物をアミノ
アルコールで表面処理してIGるか、あるいはあらかじ
め他の高分子材料で管状に成型した後、その内表面にポ
リグルタミン酸誘導体を塗布した後、アミノアルコール
で表面処理して(qる。
゛ That is, the blood conduit of the present invention is made by molding a polyglutamic acid derivative into a desired tube shape, and then surface-treating the tube with amino alcohol and using IG, or by pre-shaping it into a tube shape with other polymeric materials. After that, a polyglutamic acid derivative is applied to the inner surface, and then the surface is treated with amino alcohol (q).

本発明のポリグルタミン酸誘導体は、0体、L体、ラセ
ミ体でもよく、ポリグルタミン酸誘導体として、ポリグ
ルタミン醒メチル、ポリグルタミン酸ベンジルなどの脂
肪族炭化水素及び芳香族炭化水素のエステルなどが用い
られる。ポリグルタミンIH導体の分子mはその皮膜が
形成される程度であればよい。
The polyglutamic acid derivative of the present invention may be 0-form, L-form, or racemic form. As the polyglutamic acid derivative, esters of aliphatic hydrocarbons and aromatic hydrocarbons such as methyl polyglutamine and benzyl polyglutamate are used. The number of molecules m of the polyglutamine IH conductor may be such that a film thereof is formed.

アミンアルコールとして、エタノールアミン、アミノプ
ロパツールなどの他、Hz NC2H40C2HaOH
などのアルキレングリコール誘導体などが用いられる。
As amine alcohol, in addition to ethanolamine, aminopropanol, etc., Hz NC2H40C2HaOH
Alkylene glycol derivatives such as these are used.

表面処理時間はアミノアルコールの種類・濃度及びポリ
グルタミン酸誘導体の種類に応じて適宜選択するが、い
ずれにしても表面処理により、管状物の内表面の水に対
する接触角が45゛以下になるのが望ましい。
The surface treatment time is appropriately selected depending on the type and concentration of the amino alcohol and the type of polyglutamic acid derivative, but in any case, the surface treatment should reduce the contact angle of the inner surface of the tube to water to 45 degrees or less. desirable.

(e)発明の実施例 次に本発明を実施例によりさらに詳細に説明する。(e) Examples of the invention Next, the present invention will be explained in more detail with reference to Examples.

実施例1 グルタミン酸ベンジル単独重合体のジオキサン溶液をガ
ラス板上に流延し、風乾して皮I15!(膜厚的0.0
5 mm>を得た。この皮膜をエタノールでソックスレ
ー抽出を行った後、92燥した。
Example 1 A solution of benzyl glutamate homopolymer in dioxane was cast on a glass plate, air-dried, and the result was a peel I15! (film thickness 0.0
5 mm> was obtained. This film was subjected to Soxhlet extraction with ethanol and then dried for 92 hours.

この皮膜を3−アミノ−1−プロパツール中55℃で4
時間アミツリシス反応させた。反応後エタノールで皮膜
を洗浄した。この皮膜を80℃以上の熱水中に8時間以
上浸漬し、乾燥して表面処理皮膜を(qた。この表面処
理皮膜の水に対する接触角を第1表に示す。
This film was heated at 55°C in 3-amino-1-propanol for 4 hours.
The amithrisis reaction was allowed to take some time. After the reaction, the film was washed with ethanol. This film was immersed in hot water of 80° C. or higher for 8 hours or more and dried to form a surface-treated film. Table 1 shows the contact angle of this surface-treated film with water.

第1表 実施例2 グルタミン酸ベンジル単独重合体のジオキサン溶液のか
わりにグルタミン酸メチル単独重合体のジクロルエタン
溶液を用いた以外は実施例1と同様にして表面処理皮膜
を得た。
Table 1 Example 2 A surface treated film was obtained in the same manner as in Example 1 except that a dichloroethane solution of methyl glutamate homopolymer was used instead of the dioxane solution of benzyl glutamate homopolymer.

実施例3 実施例1で得た皮膜上で、人由来の上皮性細胞を含む培
養液(約10万個/mQ)を接触させたまま、炭酸ガス
濃ff15%、湿度100%、37℃の部屋に静置した
。11時間後、皮膜をリン酸緩衝液でかるく洗浄し、皮
膜上に付着している細胞の釘を核染色法により定量した
。比較のため、血液導管に使用されているシリコーンゴ
ム、8X準試料として市販の細胞培養シートを用いて、
同様の細胞付着試験を行った。皮膜に付着した細胞のm
を、標準試料に(=J着した細胞のmで割ることにより
、細胞付着率を求め、その結果を第2表に示ず。
Example 3 A culture solution containing human-derived epithelial cells (approximately 100,000 cells/mQ) was placed on the film obtained in Example 1 at 15% carbon dioxide concentration, 100% humidity, and 37°C. I left it in the room. After 11 hours, the film was gently washed with phosphate buffer, and the number of cell nails adhering to the film was quantified by nuclear staining. For comparison, we used silicone rubber used for blood conduits and a commercially available cell culture sheet as an 8X quasi-sample.
A similar cell adhesion test was conducted. m of cells attached to the membrane
The cell adhesion rate was determined by dividing (=J) by m of cells attached to the standard sample, and the results are not shown in Table 2.

第2表 実施例4 3−アミノ−1−プロパツール中55°Cで4時間の処
理のかわりにH2NC2H40C2Ha OH中60℃
で4時間の処理を行った以外は実施例1と同様にして表
面処理皮膜を得た。
Table 2 Example 4 H2NC2H40C2Ha instead of 4 hours treatment at 55°C in 3-amino-1-propatur 60°C in OH
A surface treated film was obtained in the same manner as in Example 1 except that the treatment was carried out for 4 hours.

実施例5 ガラス管の内表面にポリグルタミン酸誘)9体を塗布し
、乾燥させたのら、3−アミノ−1−プロパツール中5
5℃で4時間処理し、エタノールで洗浄したのら、さら
に80°C以上の熱水中に8時間以上浸漬させ、乾燥後
ガラス管からはずし、管状物を得た。
Example 5 After applying polyglutamic acid derivative (9) to the inner surface of a glass tube and drying,
After being treated at 5°C for 4 hours and washed with ethanol, it was further immersed in hot water at 80°C or higher for 8 hours or more, and after drying, it was removed from the glass tube to obtain a tubular product.

(f)発明の効果 本発明は以上説明したように、細胞付着性の少ないこと
を必要とする血液導管において、アミノアルコールで表
面処理されたポリグルタミンlLiう9体を内表面に成
型することにより細胞の付着を抑え、かつ、この血液導
管を任意の形状で得ることが可能である。
(f) Effects of the Invention As explained above, the present invention is made by molding polyglutamine lLi, which has been surface-treated with amino alcohol, on the inner surface of a blood conduit that requires low cell adhesion. It is possible to suppress the adhesion of cells and to obtain this blood conduit in any shape.

指定代理人 工業技術院製品科学研究所長 高橋教司designated agent Director, Product Science Research Institute, Agency of Industrial Science and Technology Kyouji Takahashi

Claims (1)

【特許請求の範囲】[Claims] (1)アミノアルコールで表面処理されたポリグルタミ
ン酸誘導体を内表面に有する血液導管
(1) Blood conduit with polyglutamic acid derivative surface treated with amino alcohol on the inner surface
JP59172072A 1984-08-17 1984-08-17 Blood conduit Granted JPS6150562A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59172072A JPS6150562A (en) 1984-08-17 1984-08-17 Blood conduit

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59172072A JPS6150562A (en) 1984-08-17 1984-08-17 Blood conduit

Publications (2)

Publication Number Publication Date
JPS6150562A true JPS6150562A (en) 1986-03-12
JPS6317463B2 JPS6317463B2 (en) 1988-04-13

Family

ID=15935019

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59172072A Granted JPS6150562A (en) 1984-08-17 1984-08-17 Blood conduit

Country Status (1)

Country Link
JP (1) JPS6150562A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0458159A (en) * 1990-06-27 1992-02-25 Sharp Corp Multiprober

Also Published As

Publication number Publication date
JPS6317463B2 (en) 1988-04-13

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