Alibeik Sara, Sheardown Heather, Rizkalla Amin S, Mequanint Kibret
Biomedical Engineering Graduate Program, University of Western Ontario, London, ON, Canada N6A 5B9.
J Biomater Sci Polym Ed. 2007;18(9):1195-210. doi: 10.1163/156856207781554055.
Protein adsorption and platelet adhesion properties of polyurethane biomaterials are important considerations for blood-contacting applications. Although the presence of ionic groups on the surface of biomaterials is believed to influence their blood response, their exact role is not known. The objective of this work was to study the protein adsorption and platelet adhesion properties of ion-containing polyurethane biomaterials. Thus, we prepared polyurethanes that contained ions either on the soft segment or hard segment and investigated their in vitro protein adsorption and platelet adhesion. The presence of ions increased the amount of adsorbed proteins and adhered platelets on the synthesized polyurethanes. Whereas albumin and lysozyme adsorption were independent of the location of the ions (soft vs. hard segments), fibrinogen adsorption was strongly dependent on the location of the ions. Platelet adhesion, on the other hand, was found to be less dependent on the location of the ions within the polyurethane structure. This is the first evidence to unequivocally demonstrate the exact role of ions on protein adsorption and platelet adhesion. Taken together, our study suggests that in the absence of known biocompatible chains such as polyethyleneoxide, ion-containing polyurethanes do not demonstrate improved blood compatibility. Therefore, we conclude that ion incorporation into polyurethanes may not be a viable approach to design polyurethane biomaterials for blood-contacting applications.
聚氨酯生物材料的蛋白质吸附和血小板黏附特性是血液接触应用中的重要考量因素。尽管人们认为生物材料表面离子基团的存在会影响其血液反应,但其确切作用尚不清楚。本研究的目的是研究含离子聚氨酯生物材料的蛋白质吸附和血小板黏附特性。因此,我们制备了在软段或硬段含有离子的聚氨酯,并研究了它们的体外蛋白质吸附和血小板黏附情况。离子的存在增加了合成聚氨酯上吸附的蛋白质和黏附的血小板数量。白蛋白和溶菌酶的吸附与离子位置(软段与硬段)无关,而纤维蛋白原的吸附则强烈依赖于离子位置。另一方面,发现血小板黏附对聚氨酯结构中离子位置的依赖性较小。这是明确证明离子对蛋白质吸附和血小板黏附确切作用的首个证据。综上所述,我们的研究表明,在缺乏已知生物相容性链(如聚环氧乙烷)的情况下,含离子聚氨酯并未表现出更好的血液相容性。因此,我们得出结论,将离子引入聚氨酯可能不是设计用于血液接触应用的聚氨酯生物材料的可行方法。