Seo Ji-Hun, 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.
Biomaterials. 2008 Apr;29(10):1367-76. doi: 10.1016/j.biomaterials.2007.11.039. Epub 2007 Dec 26.
The surface modification of poly(dimethylsiloxane) (PDMS) substrates by using ABA-type block copolymers comprising poly(2-methacryloyloxyethyl phosphorylcholine (MPC)) (PMPC) and PDMS segments was investigated. The hydrophobic interaction between the swelling-deswelling nature of PDMS and PDMS segments in block copolymers was the main mechanism for surface modification. Block copolymers with various compositions were synthesized by using the atom transfer radical polymerization (ATRP) method. The kinetic plots revealed that polymerization could be initiated by PDMS macroinitiators and it proceeds in a well-controlled manner; therefore, the compositions of the block copolymers were controllable. The obtained block copolymers were dissolved in a chloroform/ethanol mixed solvent. The surface of the PDMS substrate was modified using block copolymers by the swelling-deswelling method. Static contact angle and X-ray photoelectron spectroscopy (XPS) measurements revealed that the hydrophobic surface of the PDMS substrate was converted to a hydrophilic surface because of modification by surface-tethered PMPC segments. Protein adsorption test and L929 cell adhesion test were carried out for evaluating the biocompatibility. As observed, the amount of adsorbed proteins and cell adhesion were drastically reduced as compared to those in the non-treated PDMS substrate. We conclude that this procedure is effective in fabricating biocompatible surfaces on PDMS substrates.
研究了使用包含聚(2-甲基丙烯酰氧基乙基磷酰胆碱)(MPC)和聚二甲基硅氧烷(PDMS)链段的ABA型嵌段共聚物对聚二甲基硅氧烷(PDMS)基底进行表面改性。PDMS在嵌段共聚物中的溶胀-去溶胀性质与PDMS链段之间的疏水相互作用是表面改性的主要机制。采用原子转移自由基聚合(ATRP)法合成了具有不同组成的嵌段共聚物。动力学曲线表明,聚合反应可由PDMS大分子引发剂引发,并以良好控制的方式进行;因此,嵌段共聚物的组成是可控的。将得到的嵌段共聚物溶解在氯仿/乙醇混合溶剂中。通过溶胀-去溶胀法使用嵌段共聚物对PDMS基底的表面进行改性。静态接触角和X射线光电子能谱(XPS)测量表明,由于表面连接的MPC链段的改性,PDMS基底的疏水表面转变为亲水表面。进行了蛋白质吸附试验和L929细胞粘附试验以评估生物相容性。如所观察到的,与未处理的PDMS基底相比,吸附的蛋白质量和细胞粘附量大幅降低。我们得出结论,该方法在制备PDMS基底上的生物相容性表面方面是有效的。