Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, People's Republic of China.
Acta Biomater. 2010 Aug;6(8):2898-902. doi: 10.1016/j.actbio.2010.02.025. Epub 2010 Feb 20.
Poly(dimethylsiloxane) (PDMS) is the choice of material for a wide range of biological and non-biological applications because of its chemical inertness, non-toxicity, ease of handling and commercial availability. However, PDMS exhibits uncontrolled protein adsorption and cell adhesion and it has proved difficult to functionalize to present bioactive ligands. We present a facile strategy for functional surface modification of PDMS using commercial reagents to engineer polymer brushes of oligo(ethylene glycol) methacrylate that prevent cell adhesion and can be functionalized to display bioadhesive ligands. The polymer brushes resist biofouling and prevent cell adhesion and bioadhesive peptides can be tethered either uniformly or constrained to micropatterned domains using standard peptide chemistry approaches. This approach is relevant to various biomedical and biotechnological applications.
聚二甲基硅氧烷(PDMS)因其化学惰性、无毒、易于处理和商业可用性,成为广泛的生物和非生物应用的材料选择。然而,PDMS 表现出不可控的蛋白质吸附和细胞黏附,并且已经证明难以功能化以呈现生物活性配体。我们提出了一种使用商业试剂对 PDMS 进行功能表面修饰的简便策略,以工程化聚甲基丙烯酸乙二醇酯的聚合物刷,防止细胞黏附,并可进行功能化以展示生物黏附配体。聚合物刷具有抗生物污染和防止细胞黏附的功能,并且可以使用标准的肽化学方法将生物黏附肽均匀地或约束地固定在微图案化区域上。这种方法与各种生物医学和生物技术应用相关。