Cho Woo Kyung, Kong Bokyung, Choi Insung S
Department of Chemistry and School of Molecular Science (BK21), Center for Molecular Design and Synthesis, KAIST, Daejeon 305-701, Korea.
Langmuir. 2007 May 8;23(10):5678-82. doi: 10.1021/la063737w. Epub 2007 Apr 14.
This work describes the formation of highly efficient non-biofouling polymeric thin films of poly((3-(methacryloylamino)propyl)-dimethyl(3-sulfopropyl)ammonium hydroxide), (poly(MPDSAH)). The poly(MPDSAH) films were generated from the self-assembled monolayers terminating in an initiator of atom transfer radical polymerization (ATRP) by the surface-initiated ATRP of MPDSAH. The poly(MPDSAH) films on a gold surface were characterized by ellipsometry, FT-IR spectroscopy, contact angle goniometery, and X-ray photoelectron spectroscopy. The copper complexes and unpolymerized monomers trapped inside the polymer brushes were completely washed out by soaking the poly(MPDSAH)-coated substrate in water at 40 degrees C for 4 days. The amount of proteins nonspecifically adsorbed onto the poly(MPDSAH) films was evaluated by surface plasmon resonance spectroscopy: the adsorption of proteins was <0.6 ng/cm(2) on the surfaces for all the model proteins. The ability of the poly(MPDSAH) films to resist the nonspecific adsorption of proteins was comparable to that of the best known systems.
这项工作描述了聚((3 - (甲基丙烯酰氨基)丙基) - 二甲基(3 - 磺丙基)氢氧化铵)(聚(MPDSAH))高效抗生物污染聚合物薄膜的形成。聚(MPDSAH)薄膜是通过MPDSAH的表面引发原子转移自由基聚合(ATRP),由以原子转移自由基聚合引发剂(ATRP)终止的自组装单分子层生成的。通过椭偏仪、傅里叶变换红外光谱、接触角测角仪和X射线光电子能谱对金表面的聚(MPDSAH)薄膜进行了表征。将涂有聚(MPDSAH)的基底在40℃的水中浸泡4天,可将捕获在聚合物刷内的铜配合物和未聚合的单体完全洗出。通过表面等离子体共振光谱评估非特异性吸附在聚(MPDSAH)薄膜上的蛋白质的量:对于所有模型蛋白质,蛋白质在表面上的吸附量<0.6 ng/cm²。聚(MPDSAH)薄膜抵抗蛋白质非特异性吸附的能力与最知名的系统相当。