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通过自引发接枝聚合用甲基丙烯酰基官能化磷脂聚合物对聚醚醚酮进行表面改性。

Surface modification of poly(ether ether ketone) with methacryloyl-functionalized phospholipid polymers via self-initiation graft polymerization.

作者信息

Kawasaki Yoshihiro, Iwasaki Yasuhiko

机构信息

a Faculty of Chemistry, Materials and Bioengineering, Department of Chemistry and Materials Engineering , Kansai University , 3-3-35 Yamate-cho, Suita-shi , Osaka 564-8680 , Japan.

出版信息

J Biomater Sci Polym Ed. 2014;25(9):895-906. doi: 10.1080/09205063.2014.911570. Epub 2014 Apr 25.

DOI:10.1080/09205063.2014.911570
PMID:24766535
Abstract

To improve blood compatibility of poly(ether ether ketone) (PEEK), surface modification with methacryloyl-functionalized phospholipid polymers was performed through self-initiation graft polymerization. The copolymers (PMA) of 2-methacryloyloxyethyl phosphorylcholine (MPC) and 2-aminoethyl methacrylate hydrochloride were synthesized by conventional free radical polymerization. The PMA was then immobilized with pentafluorophenyl methacrylate to obtain methacryloyl-functionalized MPC polymers (PMAMA). The degree of substitution of the methacryloyl group into the copolymer was nearly completed. The PMAMA was dissolved in 1-butanol and the solution was dropped on PEEK. UV light (350±50 nm) was subsequently irradiated on PEEK for various periods. Elemental analysis of the PEEK surface was performed by X-ray photoelectron spectroscopy and phosphorus and nitrogen signals due to the MPC units on PEEK were observed. The surface wettability of PEEK was also improved by immobilization of PMAMA. Plasma protein adsorption was effectively reduced on the PMAMA-immobilized surface regardless of the type of protein. Furthermore, PMAMA immobilization was also useful in reducing platelet adhesion on PEEK. In conclusion, methacryloyl-functionalized MPC polymers could be immobilized on PEEK by simple photo-irradiation, resulting in significant improvement in blood compatibility.

摘要

为提高聚醚醚酮(PEEK)的血液相容性,通过自引发接枝聚合对其进行了甲基丙烯酰基功能化磷脂聚合物的表面改性。通过常规自由基聚合合成了2-甲基丙烯酰氧基乙基磷酰胆碱(MPC)与甲基丙烯酸盐酸氨基乙酯的共聚物(PMA)。然后用甲基丙烯酸五氟苯酯将PMA固定化,得到甲基丙烯酰基功能化的MPC聚合物(PMAMA)。甲基丙烯酰基在共聚物中的取代度几乎达到完全。将PMAMA溶解在正丁醇中,然后将溶液滴加到PEEK上。随后用紫外光(350±50 nm)对PEEK照射不同时间。通过X射线光电子能谱对PEEK表面进行元素分析,观察到了PEEK上由于MPC单元产生的磷和氮信号。通过固定PMAMA,PEEK的表面润湿性也得到了改善。无论蛋白质类型如何,在固定有PMAMA的表面上血浆蛋白吸附都能有效降低。此外,固定PMAMA对减少PEEK上的血小板黏附也很有用。总之,通过简单的光照射可将甲基丙烯酰基功能化的MPC聚合物固定在PEEK上,从而显著提高血液相容性。

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