Goda Tatsuro, Matsuno Ryosuke, Konno Tomohiro, Takai Madoka, Ishihara Kazuhiko
Department of Materials Engineering, School of Engineering and Center for NanoBio Integration, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
Colloids Surf B Biointerfaces. 2008 May 1;63(1):64-72. doi: 10.1016/j.colsurfb.2007.11.014. Epub 2007 Nov 28.
The phosphorylcholine group functional methacrylate monomer, 2-methacryloyloxyethyl phosphorylcholine (MPC), was graft polymerized from the polydimethylsiloxane (PDMS) substrate using ultraviolet irradiation and using benzophenone as a photoinitiator. The varying monomer concentrations and irradiation times were investigated in order to verify the relationships between graft density and protein resistance under specific biological conditions. The ellipsometry analysis revealed that the layer thickness of the grafted polymer depended on the monomer concentrations after the irradiation for 1 min, however, it stabilized thereafter in all the specified conditions. The curve fitting of the C1s spectrum obtained by X-ray photoelectron spectroscopy analysis showed that the amount of grafted polymer increased with an increase in both monomer concentration and irradiation time. Atomic force microscopic images revealed that the terminations among the graft chains became dominant due to magnified chain mobility followed by growth of their length. In vitro albumin and fibrinogen adsorption results indicated that the resistance to protein adsorption was easily tuned by the specified conditions due to the controlled graft density. Lubrication was dramatically enhanced by the grafting and it was further promoted by an increase in the graft density in good solvents, indicating that the interactions between the graft chains and the solvents resulted in the lubrication system. These basic findings regarding the grafted PDMS surface are important for versatile applications, including its use as a biomaterial and microfluidic device.
采用紫外线辐照并以二苯甲酮作为光引发剂,使磷酰胆碱基团功能化的甲基丙烯酸酯单体2-甲基丙烯酰氧基乙基磷酰胆碱(MPC)从聚二甲基硅氧烷(PDMS)基底上接枝聚合。研究了不同的单体浓度和辐照时间,以验证在特定生物条件下接枝密度与蛋白质抗性之间的关系。椭偏仪分析表明,辐照1分钟后,接枝聚合物的层厚度取决于单体浓度,不过,在所有指定条件下此后其厚度趋于稳定。通过X射线光电子能谱分析获得的C1s光谱的曲线拟合表明,接枝聚合物的量随单体浓度和辐照时间的增加而增加。原子力显微镜图像显示,由于链迁移率放大及其长度增长,接枝链之间的末端变得占主导地位。体外白蛋白和纤维蛋白原吸附结果表明,由于接枝密度可控,特定条件下蛋白质吸附抗性易于调节。接枝显著增强了润滑作用,在良溶剂中,接枝密度的增加进一步促进了润滑作用,这表明接枝链与溶剂之间的相互作用导致了润滑体系。这些关于接枝PDMS表面的基本发现对于包括用作生物材料和微流体装置在内的多种应用而言非常重要。