JPS6113953A - Blood conduit - Google Patents
Blood conduitInfo
- Publication number
- JPS6113953A JPS6113953A JP59133954A JP13395484A JPS6113953A JP S6113953 A JPS6113953 A JP S6113953A JP 59133954 A JP59133954 A JP 59133954A JP 13395484 A JP13395484 A JP 13395484A JP S6113953 A JPS6113953 A JP S6113953A
- Authority
- JP
- Japan
- Prior art keywords
- leucine
- film
- amino acid
- blood
- 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
Links
Landscapes
- Materials For Medical Uses (AREA)
- Prostheses (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、ロイシンを含むアミノ酸重合体を内表面に有
することにより、細胞が付着しにくいことを特徴とする
血液導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 blood conduit that is characterized by having an amino acid polymer containing leucine on its inner surface, thereby making it difficult for cells to adhere to it.
血液専管とは人工血管、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、
成型人工肺、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 vessels include artificial blood vessels, catheters, shunts (used to lead blood out of the body), dialysis-type artificial kidneys,
It includes tubular blood flow channels used in molded 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、ポリウレタン、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細胞の付
着しない材料が求められている。(b') Description of Prior Art Conventionally, blood conduits have been made using synthetic polymer materials such as silicone rubber, polyurethane, and tetrafluoroethylene. Cells attach to the bloodstream, forming a blood clot, which obstructs blood flow. Therefore, there is a need for materials that do not allow cells to adhere to them in blood conduits.
(C)発明の目的
本発明は上記の問題を、ロイシンを含むアミノ酸重合体
を用いることにより、細胞付着性の少ない血液導管を提
供することを目的どする。(C) Object of the Invention The present invention aims to solve the above problem by providing a blood conduit with less cell adhesion by using an amino acid polymer containing leucine.
(d)発明の構成
本発明者は細胞の付着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、ロイシンを含むアミノ酸重
合体は、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 make it difficult for cells to adhere to them, and has found that amino acid polymers containing leucine have properties that do not allow cells to adhere to a large extent.
They found that it is suitable as a blood conduit and completed the present invention.
即ち、本発明の血液導管は、ロイシンを含むアミノ酸重
合体を目的とする管状に成型して得るか、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
にロイシンを含むアミノ酸重合体を塗布して得る。That is, the blood conduit of the present invention can be obtained by molding a leucine-containing amino acid polymer into a desired tube shape, or it can be obtained by molding an amino acid polymer containing leucine into a tube shape in advance, or it can be obtained by molding an amino acid polymer containing leucine into a tube shape in advance, and then molding the leucine-containing amino acid polymer onto the inner surface of the tube. Obtained by applying coalescence.
本発明のアミノ酸重合体構成素材としてのロイシン及び
その共重合成分としてのアミノ酸は、0体、L体、ラセ
ミ体でもよく、他のアミノ酸として、アラニン、グリシ
ン、メチオニン、バリン、グルタミン酸誘導体、アスパ
ラギン酸誘導体、リジン誘導体、オルニヂン誘導体など
が用いられる。Leucine as the constituent material of the amino acid polymer of the present invention and the amino acid as its copolymerization component may be 0-form, L-form, or racemic form, and other amino acids include alanine, glycine, methionine, valine, glutamic acid derivatives, and aspartic acid. Derivatives, lysine derivatives, ornidine derivatives, etc. are used.
アミノ酸重合体の分子量はその皮膜が形成される程度で
あればよく、また重合体中のロイシン含量はアミノ酸の
種類によって変わるが、30モル%以上が好ましい。The molecular weight of the amino acid polymer is sufficient as long as it forms a film, and the leucine content in the polymer varies depending on the type of amino acid, but is preferably 30 mol% or more.
(e)発明の実施例 次に本発明を実施例によりざらに詳細に説明する。(e) Examples of the invention Next, the present invention will be roughly explained in detail with reference to Examples.
実施例1
L−ロイシンとL−グルタミン酸ベンジルとの共重合体
(ロイシンとグルタミン酸ベンジルとのモル比−7=3
)のベンゼンとジオキサン(7:3)との混合溶液をガ
ラス板上に流延し、風乾して皮膜(膜厚的0.05mm
)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、乾燥した。Example 1 Copolymer of L-leucine and benzyl L-glutamate (molar ratio of leucine to benzyl glutamate -7 = 3
) A mixed solution of benzene and dioxane (7:3) was cast on a glass plate and air-dried to form a film (0.05 mm thick).
) was obtained. This film was subjected to Soxhlet extraction with ethanol and then dried.
この皮膜上で、人由来の上皮性細胞を含む培養液(約1
0万個/mΩ)を接触させたまま、炭酸ガス濃麿5%、
湿度100%、37℃の部屋に静置した。On this film, a culture solution containing human-derived epithelial cells (approximately 1
00,000 pieces/mΩ) in contact with 5% carbon dioxide gas,
It was left standing in a room with a humidity of 100% and a temperature of 37°C.
17時間後、皮膜をリン酸緩衝液で軽く洗浄し、皮膜上
に付着している細胞の量を核染色法により定量した。比
較のため、グルタミン酸ベンジル単独重合体皮膜及び血
液導管に使用されているシリコーンゴム、標準試料とし
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量を、標準試料に付着
した細胞の量で割ることにより、細胞付着率を求めた。After 17 hours, the film was lightly washed with phosphate buffer, and the amount of cells adhering to the film was quantified by nuclear staining. For comparison, a similar cell adhesion test was conducted using a benzyl glutamate homopolymer film, silicone rubber used for blood conduits, and a commercially available cell culture sheet as a standard sample. The cell attachment rate was determined by dividing the amount of cells attached to the film by the amount of cells attached to the standard sample.
その結果を第1表に示す。The results are shown in Table 1.
第1表
実施例2
L−ロイシンとL−グルタミン酸ベンジルとの共重合体
のかわりに、L−ロイシンとし一カルボベンゾキシリジ
ンとの共重合体(ロイシンとカルボベンゾキシリジンと
のモル比−7:3)を用いた以外は実施例1と同様にし
て、皮膜を成型し、細胞付着実験を行った。結果を第2
表に示す。Table 1 Example 2 Instead of the copolymer of L-leucine and benzyl L-glutamate, a copolymer of L-leucine and monocarbobenzoxylidine (molar ratio of leucine to carbobenzoxylidine -7) was used. :3) A film was molded in the same manner as in Example 1, except that 3) was used, and a cell adhesion experiment was conducted. Second result
Shown in the table.
第2表
実施例3
ガラス管の内表面にロイシン含有アミノ酸重合体を塗布
し、乾燥後ガラス管からはずし、管状物を1qた。Table 2 Example 3 A leucine-containing amino acid polymer was applied to the inner surface of a glass tube, and after drying, it was removed from the glass tube, and the tube was weighed 1 q.
実施例4
L−ロイシンとL−グルタミン酸ベンジルとの共重合体
において、それぞれのモル比が85 : 15.50
: 50.30 : 70のものを実施例1と同様の方
法で皮膜を得た。Example 4 In a copolymer of L-leucine and benzyl L-glutamate, the molar ratio of each is 85:15.50
: 50.30 : A film of 70 was obtained in the same manner as in Example 1.
実施例5
L−ロイシンとL−カルボベンゾキシリジンとの共重合
体において、それぞれのモル比が85:15.50 :
50.30 : 70のものを実施例1と同様の方法
で皮膜を得た。Example 5 In a copolymer of L-leucine and L-carbobenzoxylidine, the molar ratio of each is 85:15.50:
A film of 50.30:70 was obtained in the same manner as in Example 1.
実施例6
ポリーL−ロイシンを熱ベンゼンに溶解し、実施例1と
同様にして皮膜を得た。Example 6 Poly L-leucine was dissolved in hot benzene and a film was obtained in the same manner as in Example 1.
実施例7
L−ロイシンとL−グルタミン酸ベンジルとから成るブ
ロック共重合体を、N−カルボキシアミノ酸無水物法に
より合成した(このブロック共重合体の組成は、(グル
タミン酸ベンジル(18%))−ベロイシン(64%)
トーヘグルタミン酸ベンジル(18%))であった。)
。この共重合体を熱ベンゼンに溶解し、実施例1と同様
にして皮膜を得た。Example 7 A block copolymer consisting of L-leucine and benzyl L-glutamate was synthesized by the N-carboxyamino acid anhydride method (the composition of this block copolymer was (benzyl glutamate (18%))-veleucine (64%)
benzyl toheglutamate (18%)). )
. This copolymer was dissolved in hot benzene, and a film was obtained in the same manner as in Example 1.
実施例8
L−グルタミン酸ベンジルの代わりにL−カルボベンゾ
キシリジンを用い、以下実施例7と同様にして、ブロッ
ク共重合体皮膜を得た。Example 8 A block copolymer film was obtained in the same manner as in Example 7 except that L-carbobenzoxylidine was used instead of benzyl L-glutamate.
(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、ロイシンを含むアミノ
酸重合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 suppresses cell adhesion by molding an amino acid polymer containing leucine on the inner surface of a blood conduit that requires low cell adhesion. , it is possible 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 高橋救司 一9λ3−designated agent Director, Product Science Research Institute, Agency of Industrial Science and Technology Keiji Takahashi 19λ3-
Claims (1)
血液導管(1) Blood conduit with an amino acid polymer containing leucine on its inner surface
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59133954A JPS6113953A (en) | 1984-06-28 | 1984-06-28 | Blood conduit |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59133954A JPS6113953A (en) | 1984-06-28 | 1984-06-28 | Blood conduit |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6113953A true JPS6113953A (en) | 1986-01-22 |
JPS644470B2 JPS644470B2 (en) | 1989-01-25 |
Family
ID=15116958
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59133954A Granted JPS6113953A (en) | 1984-06-28 | 1984-06-28 | Blood conduit |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6113953A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH037462U (en) * | 1989-06-08 | 1991-01-24 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59133953A (en) * | 1983-01-18 | 1984-08-01 | Kobe Steel Ltd | Connecting method of feed nozzle and tundish in horizontal continuous casting device |
-
1984
- 1984-06-28 JP JP59133954A patent/JPS6113953A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59133953A (en) * | 1983-01-18 | 1984-08-01 | Kobe Steel Ltd | Connecting method of feed nozzle and tundish in horizontal continuous casting device |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH037462U (en) * | 1989-06-08 | 1991-01-24 |
Also Published As
Publication number | Publication date |
---|---|
JPS644470B2 (en) | 1989-01-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |