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首页> 外文期刊>Journal of biomedical materials research, Part A >Nonfouling biomaterials based on polyethylene oxide-containing amphiphilic triblock copolymers as surface modifying additives: protein adsorption on PEO-copolymer/polyurethane blends.
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Nonfouling biomaterials based on polyethylene oxide-containing amphiphilic triblock copolymers as surface modifying additives: protein adsorption on PEO-copolymer/polyurethane blends.

机译:基于含聚环氧乙烷的两亲三嵌段共聚物作为表面改性添加剂的防污生物材料:在PEO共聚物/聚氨酯共混物中的蛋白质吸附。

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摘要

Surface modification of a segmented polyurethane was achieved by blending with novel PEO-containing amphiphilic triblock copolymers (PEO-polyurethane-PEO). Three copolymers having different PEO MW (550, 2000, 5000) were used as surface modification additives. The protein resistance of the blend surfaces was evaluated using radiolabeling methods. On the blends of copolymers with PEO blocks of MW 2000 and 5000, fibrinogen adsorption from physiologic buffer decreased with increasing copolymer content up to 20 wt%. On the blends with PEO blocks of MW 550, resistance to adsorption for a given copolymer content was much greater. For all three blend types at 20% copolymer content, reductions in adsorption compared to the unmodified PU matrix were greater than 95%. Reductions in adsorption were similar for the 20% blends and surfaces prepared by coating the copolymers directly on the matrix, suggesting that the 20% blend surfaces were completely covered by copolymer. At low copolymer content (< or =10 wt %), fibrinogen adsorption decreased with decreasing PEO block length. This was probably due to increasing surface coverage of the copolymers with decreasing block length. It is therefore concluded that surface density of PEO is more important than PEO MW for the protein resistance of these surfaces. Lysozyme, a much smaller protein, showed adsorption trends similar to fibrinogen. The adsorption of fibrinogen and lysozyme from binary solutions to blends of the copolymer with PEO blocks of 2000 MW was investigated to probe the effects of protein size on adsorption resistance. Fibrinogen and lysozyme showed similar fractional decreases in adsorption relative to the PU matrix independent of the surface density of PEO. However lysozyme was enriched in the surface relative to the solution, that is, it was adsorbed preferentially to fibrinogen.
机译:通过与新型的含PEO的两亲三嵌段共聚物(PEO-聚氨酯-PEO)共混可实现链段聚氨酯的表面改性。具有不同的PEO MW(550,2000,5000)的三种共聚物用作表面改性添加剂。共混物表面的蛋白质抗性使用放射标记法评估。在分子量为2000和5000的带有PEO嵌段的共聚物的共混物中,随着共聚物含量的增加,最多达20 wt%,从生理缓冲剂中吸收的纤维蛋白原减少了。在具有MW 550的PEO嵌段的共混物中,对于给定的共聚物含量,其吸附阻力要大得多。对于共聚物含量为20%的所有三种共混物类型,与未改性的PU基体相比,吸附量的减少幅度均大于95%。对于20%共混物和通过将共聚物直接涂覆在基质上制备的表面,吸附的减少是相似的,这表明20%共混物表面被共聚物完全覆盖。在低共聚物含量(<或= 10 wt%)下,纤维蛋白原吸附随PEO嵌段长度的减少而降低。这可能是由于嵌段长度减小而增加了共聚物的表面覆盖率。因此得出结论,对于这些表面的蛋白抗性,PEO的表面密度比PEO MW更重要。溶菌酶是一种较小的蛋白质,其吸附趋势与纤维蛋白原相似。研究了二元溶液中纤维蛋白原和溶菌酶对共聚物与2000 MW PEO嵌段的共混物的吸附作用,以研究蛋白质大小对吸附阻力的影响。相对于PU基质,纤维蛋白原和溶菌酶相对于PE基质的表面密度显示出相似的分数降低。但是,溶菌酶相对于溶液在表面富集,也就是说,其优先被纤维蛋白原吸附。

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