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首页> 外文期刊>Journal of biomaterials science >Non-fouling biomaterials based on blends of polyethylene oxide copolymers and polyurethane: simultaneous measurement of platelet adhesion and fibrinogen adsorption from flowing whole blood
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Non-fouling biomaterials based on blends of polyethylene oxide copolymers and polyurethane: simultaneous measurement of platelet adhesion and fibrinogen adsorption from flowing whole blood

机译:基于聚环氧乙烷共聚物和聚氨酯共混物的防污生物材料:同时测量流动的全血中的血小板粘附和纤维蛋白原吸附

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Measurements of platelet adhesion and fibrinogen adsorption from flowing whole blood to a series of polyethylene oxide (PEO)-based materials were carried out. A unique experimental design was used in which both quantities were measured in the same experiment. The materials consisted of a polyurethane (PU) as a matrix into which various triblock copolymers of general structure PEO-PU-PEO were blended; the PU block was the same in all materials but the PEO blocks ranged in molecular weight from 550 to 5000. Platelets were isolated from fresh human blood and labeled with ~(51)Cr; purified fibrinogen was labeled with ~(125)I. A whole blood preparation containing these labeled species was used for the adhesion/adsorption studies. The surfaces were exposed to the flowing blood in a cone and plate device at a wall shear rate of 300 s~(-1). It was found that both platelet adhesion and fibrinogen adsorption decreased with increasing copolymer content in the blends and with decreasing PEO block size for a given copolymer content. The block size effect was due probably to higher PEO surface coverage for the lower molecular weight blocks. Fibrinogen adsorption and platelet adhesion were linearly and strongly correlated. The best performing materials showed very low fibrinogen adsorption of the order of 25 ng/cm~2, and correspondingly low platelet densities around 10,000 per cm~2, i.e. fractional platelet coverage in the vicinity of 0.2%.
机译:测量了从全血流向一系列聚环氧乙烷(PEO)基材料的血小板粘附和纤维蛋白原的吸附。使用了独特的实验设计,其中在同一实验中测量了两个数量。该材料由聚氨酯(PU)作为基质,共混了各种结构为PEO-PU-PEO的三嵌段共聚物。在所有材料中,PU嵌段都是相同的,但PEO嵌段的分子量范围为550至5000。从新鲜的人血中分离血小板,并用〜(51)Cr标记。用〜(125)I标记纯化的纤维蛋白原。包含这些标记物质的全血制剂用于粘附/吸附研究。在锥形板装置中,以300 s〜(-1)的壁切速率将表面暴露于流动的血液中。发现在给定共聚物含量下,血小板粘附力和纤维蛋白原吸附均随着共混物中共聚物含量的增加和PEO嵌段尺寸的减小而降低。嵌段尺寸效应可能是由于较低分子量嵌段的较高的PEO表面覆盖率。纤维蛋白原的吸附与血小板的黏附呈线性相关。表现最好的材料显示出非常低的纤维蛋白原吸附量,约为25 ng / cm〜2,相应的血小板密度较低,大约为10,000 / cm〜2,即血小板覆盖率在0.2%附近。

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