首页> 外文期刊>Journal of biomedical materials research, Part A >Fibrinogen adsorption and platelet lysis characterization of fluorinated surface-modified polyetherurethanes.
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Fibrinogen adsorption and platelet lysis characterization of fluorinated surface-modified polyetherurethanes.

机译:氟化的表面改性聚醚氨基甲酸酯的纤维蛋白原吸附和血小板裂解特性。

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A polyetherurethane (PU) was modified using fluorinated surface-modifying macromolecules (SMMs). A double radiolabel method was used simultaneously to measure the number of adhered platelets ((51)Cr) and the quantity of adsorbed Fg ((125)I), in a cone-and-plate instrument. The objectives were to determine if adsorbed Fg levels correlated to platelet adhesion on the surfaces, and to assess if any reductions in platelet adhesion for the SMM-treated surfaces resulted from surface-induced platelet lysis, rather than changes directly related to lower platelet activation and attachment on the novel surfaces. Platelet lysis was determined from lactate dehydrogenase (LDH) and unbound (51)Cr released into plasma isolated from whole blood exposed to test materials. The corresponding Fg adsorption, evaluated under the same platelet adhesion conditions, did not account for the reduced platelet adhesion on the treated surfaces. LDH and (51)Cr platelet release were very low and indicated no statistically significantdifferences between the materials. It was therefore concluded that platelet lysis did not contribute to the reduction in platelet adhesion characteristic observed on the SMM-treated surfaces. More importantly, the work emphasizes that the platelet activation cannot be inferred to by assessing the quantity of fibrinogen as is commonly done in the literature. The finding suggests a much more complex mechanism of action for the SMM surface modifiers. On-going work is investigating other Fg parameters such as protein binding affinity and protein conformational state in order to establish the mechanism by which the fluorinated surface modifiers may be reducing platelet adhesion via intermediary changes in initial protein adsorption.
机译:使用氟化的表面改性大分子(SMM)改性聚醚氨基甲酸酯(PU)。在锥板仪器中,同时使用双重放射标记法测量粘附的血小板数量((51)Cr)和吸附的Fg数量((125)I)。目的是确定吸附的Fg水平是否与表面上的血小板粘附相关,并评估表面诱导的血小板裂解是否导致SMM处理过的表面的血小板粘附减少,而不是与较低的血小板活化和降低直接相关的变化。附着在新颖的表面上。从乳酸脱氢酶(LDH)测定血小板裂解,未结合的(51)Cr释放到血浆中,血浆从暴露于测试材料的全血中分离出来。在相同的血小板粘附条件下评估的相应Fg吸附量并未说明在处理过的表面上血小板粘附的减少。 LDH和(51)Cr血小板释放非常低,表明材料之间没有统计学上的显着差异。因此,得出的结论是,血小板溶解不会导致在SMM处理过的表面观察到的血小板粘附特性降低。更重要的是,这项工作强调不能通过评估纤维蛋白原的量来推断血小板活化,正如文献中通常所做的那样。该发现表明SMM表面改性剂的作用机理要复杂得多。正在进行的工作是研究其他Fg参数,例如蛋白质结合亲和力和蛋白质构象状态,以建立一种机制,通过该机制,氟化表面改性剂可通过初始蛋白质吸附中的中间变化降低血小板粘附。

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