Department of Materials Engineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
ACS Appl Mater Interfaces. 2013 Aug 14;5(15):6832-6. doi: 10.1021/am402051e. Epub 2013 Aug 5.
We synthesized photoreactive phospholipid polymers for use in the versatile surface modification of various materials. The photoreactive methacrylate derivative 2-methacryloyloxyethyl-4-azidobenzoate (MPAz) was synthesized. MPAz was copolymerized with 2-methacryloyloxyethyl phosphorylcholine (MPC) to obtain poly(MPC-co-MPAz) (PMPAz) and with both MPC and n-butyl methacrylate (BMA) to obtain poly(MPC-co-BMA-co-MPAz) (PMBPAz). PMPAz and PMBPAz were bound to the surfaces of various materials, including polymers, glass, and metals, by exposure to ultraviolet irradiation. The azide groups in the MPAz units played a role in the surface anchoring; the polymer was bound covalently to the substrate. After the photoreaction, the surfaces were converted from hydrophobic to superhydrophilic, and their cell adhesion was effectively suppressed.
我们合成了光反应性磷脂聚合物,用于各种材料的多功能表面修饰。合成了光反应性甲基丙烯酸酯衍生物 2-甲基丙烯酰氧基乙基-4-叠氮苯甲酸酯(MPAz)。MPAz 与 2-甲基丙烯酰氧基乙基磷酸胆碱(MPC)共聚得到聚(MPC-co-MPAz)(PMPAz),与 MPC 和正丁基甲基丙烯酸酯(BMA)共聚得到聚(MPC-co-BMA-co-MPAz)(PMBPAz)。通过暴露于紫外光照射,PMPAz 和 PMBPAz 结合到各种材料的表面上,包括聚合物、玻璃和金属。MPAz 单元中的叠氮基团在表面锚定中起作用;聚合物通过共价键结合到基底上。光反应后,表面从疏水性转变为超亲水性,其细胞黏附被有效抑制。