Ueda Tomoya, Murakami Daiki, Tanaka Masaru
Graduate School of Engineering, Kyushu University, Fukuoka, Japan.
Institute for Materials Chemistry and Engineering, Kyushu University, Fukuoka, Japan.
Front Chem. 2018 Nov 8;6:542. doi: 10.3389/fchem.2018.00542. eCollection 2018.
The correlation between the interfacial structure and protein adsorption at a polymer/water interface was investigated. Poly(2-methoxyethyl acrylate)(PMEA), which is one of the best blood compatible polymers available, was employed. Nanometer-scale structures generated through the phase separation of polymer and water were observed at the PMEA/phosphate buffered saline interface. The interaction between the interfacial structures and fibrinogen (FNG) was measured using atomic force microscopy. Attraction was observed in the polymer-rich domains as well as in the non-blood compatible polymer. In contrast, no attractive interactions were observed, and only a repulsion occurred in the water-rich domains. The non-adsorption of FNG into the water rich domains was also clarified through topographic and phase image analyses. Furthermore, the FNG molecules adsorbed on the surface of PMEA were easily desorbed, even in the polymer-rich domains. Water molecules in the water-rich domains are anticipated to be the dominant factor in preventing FNG adsorption and thrombogenesis on a PMEA interface.
研究了聚合物/水界面的界面结构与蛋白质吸附之间的相关性。使用了聚(丙烯酸2-甲氧基乙酯)(PMEA),它是目前最好的血液相容性聚合物之一。在PMEA/磷酸盐缓冲盐水界面观察到通过聚合物和水的相分离产生的纳米级结构。使用原子力显微镜测量界面结构与纤维蛋白原(FNG)之间的相互作用。在富含聚合物的区域以及非血液相容性聚合物中均观察到吸引力。相比之下,未观察到有吸引力的相互作用,在富含水的区域仅发生排斥作用。通过形貌和相位图像分析也阐明了FNG不会吸附到富含水的区域。此外,即使在富含聚合物的区域,吸附在PMEA表面的FNG分子也很容易解吸。预计富含水的区域中的水分子是防止FNG在PMEA界面上吸附和血栓形成的主要因素。