EFFECTS OF PHOSPHOLIPID ADSORPTION ON NONTHROMBOGENICITY OF POLYMER WITH PHOSPHOLIPID POLAR GROUP

被引:68
作者
ISHIHARA, K
OSHIDA, H
ENDO, Y
WATANABE, A
UEDA, T
NAKABAYASHI, N
机构
[1] Institute for Medical and Dental Engineering, Tokyo Medical and Dental University, Tokyo, 101, 2-3-10, Kanda-Surugadai Chiyoda-ku
来源
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH | 1993年 / 27卷 / 10期
关键词
D O I
10.1002/jbm.820271011
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Polymers with phosphohpid polar groups, 2-methacryloyloxyethyl phosphorylcholine (MPC) polymers, have excellent nonthrombogenic properties. The effects of adsorption of phospholipids on platelet adhesion and activation on the MPC copolymer with n-butyl methacrylate (BMA) were investigated with particular attention to the structure of the phospholipids adsorbed onto the polymer surface. The electrical nature of the phospholipids adsorbed on the polymer surface affected the thrombogenicity of the polymer. On the MPC polymer surface treated with an aqueous liposomal solution of acidic phosphohpids, phosphatidylserine, platelet adhesion and activation occurred to a greater extent when compared to a poly(MPC-co-BMA) surface. However, on the MPC polymer surface treated with electrically neutral phosphatidylcholines, reduced thrombogenicity could be observed. Therefore, the adsorption of the phosphatidylcholines was an important factor in reducing the thrombogenicity on the polymers. Moreover, by comparison of the poly(MPC-co-BMA) to a poly(BMA), platelet adhesion and activation on these polymer surfaces depended on the adsorption state of the phosphatidylcholines. The amount of phosphatidylcholine adsorbed on the poly(MPC-co-BMA) increased with an increase in the MPC mole fraction of the copolymer. This indicates that the MPC moieties have affinity for the phosphatidylcholines. We conclude that the poly(MPC-co-BMA) can adsorb large amounts of phosphatidylcholines and that these phospholipids organize themselves. The organized adsorption layer of the phosphatidylcholines on the surface, which construct biomembrane-like surfaces, can reduce platelet adhesion and activation effectively. (C) 1993 John Wiley & Sons, Inc.
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收藏
页码:1309 / 1314
页数:6
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