Ji Jian, Barbosa M A, Feng Linxian, Shen Jiacong
Department of Polymer Science, Zhejiang University, HangZhou, 310027, China.
J Mater Sci Mater Med. 2002 Jul;13(7):677-84. doi: 10.1023/a:1015789726455.
Surface modification to develop a biomolecules-presenting surface is of interest, both from a scientific and an industrial point of view. In this research, a penta-block-coupling polymer of warfarin-PEO-MDI-PEO-warfarin was specially designed as the surface modifying additive (SMA). The warfarin-modified polyurethane surfaces were then prepared by dip-coating method. Attenuated total reflection fourier transform infra-red (ATR-FTIR) spectra revealed that the urethane segments in the SMA could penetrate into the hard block of segmented polyurethane (SPU) via intermolecular hydrogen bonds. The X-ray photoelectron spectroscopy (XPS) results indicated that the intermolecular hydrogen bonds were strong enough to form stable warfarin-PEO composite surfaces in an aqueous environment. Fibrinogen and albumin adsorption onto unmodified and SMA-modified SPU was investigated by the (125)I-labeled method. The surface for attracting and reversibly binding albumin, which was proved to suppress the platelet adhesion and prolong the clotting time, has been developed by the simple coating of the novel SMA in SPU.
从科学和工业的角度来看,开发一种能呈现生物分子的表面进行表面改性都备受关注。在本研究中,一种华法林-聚环氧乙烷-二苯基甲烷二异氰酸酯-聚环氧乙烷-华法林的五嵌段偶联聚合物被专门设计为表面改性添加剂(SMA)。然后通过浸涂法制备了华法林改性的聚氨酯表面。衰减全反射傅里叶变换红外(ATR-FTIR)光谱表明,SMA中的聚氨酯链段可通过分子间氢键渗透到嵌段聚氨酯(SPU)的硬段中。X射线光电子能谱(XPS)结果表明,分子间氢键足够强,能够在水环境中形成稳定的华法林-聚环氧乙烷复合表面。采用¹²⁵I标记法研究了纤维蛋白原和白蛋白在未改性和SMA改性的SPU上的吸附情况。通过在SPU中简单涂覆新型SMA,已开发出一种能吸引并可逆结合白蛋白的表面,事实证明该表面可抑制血小板粘附并延长凝血时间。