Effects of phospholipid adsorption on nonthrombogenicity of polymer with phospholipid polar group

✍ Scribed by Ishihara, Kazuhiko ;Oshida, Hiroko ;Endo, Yutaka ;Watanabe, Akihiko ;Ueda, Tomoko ;Nakabayashi, Nobuo

• Publisher: John Wiley and Sons
• Year: 1993
• Tongue: English
• Weight: 642 KB
• Volume: 27
• Category: Article
• ISSN: 0021-9304
• DOI: 10.1002/jbm.820271011

✦ Synopsis

Abstract

Polymers with phospholipid 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 phospholipids, 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. © 1993 John Wiley & Sons, Inc.