Catalysis Research Center, Hokkaido University , Sapporo 001-0021, Japan.
Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University , Tokyo 101-0062, Japan.
ACS Appl Mater Interfaces. 2015 Oct 14;7(40):22709-18. doi: 10.1021/acsami.5b07760. Epub 2015 Oct 2.
Polyrotaxanes, such as supramolecular assemblies with methylated α-cyclodextrins (α-CDs) as host molecules noncovalently threaded on the linear polymer backbone, are promising materials for biomedical applications because they allow adsorbed proteins possessing a high surface flexibility as well as control of the cellular morphology and adhesion. To provide a general design principle for biomedical materials, we examined the surface reorganization behaviors and adsorption conformations of fibrinogen on the polyrotaxane surfaces with comparison to several random copolymers by sum frequency generation (SFG) vibrational spectroscopy. We showed that the polyrotaxane (OMe-PRX-PMB) with methylated α-CDs as the host molecule exhibited unique surface structures in an aqueous environment. The hydrophobic interaction between the methoxy groups of the methylated α-CD molecules and methyl groups of the n-butyl methacrylate (BMA) side chains may dominate the surface restructuring behavior of the OMe-PRX-PMB. The orientation analysis revealed that the orientation of the fibrinogen adsorbed on the OMe-PRX-PMB surface is close to a single distribution, which is different from the adsorption behaviors of fibrinogen on other polyrotaxane or random copolymer surfaces.
聚轮烷,如超分子组装物,其中甲基化的α-环糊精(α-CDs)作为主分子非共价地穿在线性聚合物主链上,是用于生物医学应用的有前途的材料,因为它们允许吸附具有高表面柔韧性的蛋白质以及控制细胞形态和粘附。为了为生物医学材料提供通用的设计原理,我们通过和几种随机共聚物进行比较,通过和频发生(SFG)振动光谱研究了纤维蛋白原在聚轮烷表面上的表面重排行为和吸附构象。我们表明,作为主分子的甲基化α-CDs 的聚轮烷(OMe-PRX-PMB)在水相环境中表现出独特的表面结构。甲氧基基团的疏水性相互作用和甲基化α-CD 分子的甲基基团与正丁基甲基丙烯酸酯(BMA)侧链之间可能主导 OMe-PRX-PMB 的表面重排行为。取向分析表明,吸附在 OMe-PRX-PMB 表面上的纤维蛋白原的取向接近于单一分布,这与纤维蛋白原在其他聚轮烷或随机共聚物表面上的吸附行为不同。