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血浆稀释对纤维蛋白原吸附到固体表面的影响。

Effect of plasma dilution on adsorption of fibrinogen to solid surfaces.

作者信息

Brash J L, ten Hove P

出版信息

Thromb Haemost. 1984 Jul 29;51(3):326-30.

PMID:6495253
Abstract

The adsorption of various plasma proteins to three solid surfaces has been studied as a function of plasma concentration. Albumin adsorption on glass showed no dependence on plasma concentration and increased to a plateau value on both polyethylene and siliconized glass. Immunoglobulin G (IgG) adsorption showed no dependence on plasma concentration on any surface. Fibrinogen adsorption increased with plasma concentration and then decreased, the maximum occurring at about 1% normal plasma concentration and varying somewhat with the surface. On glass the kinetics of fibrinogen adsorption was dependent on plasma concentration: at concentrations less than the adsorption maximum, the kinetics was conventional, with adsorption increasing onto a plateau; at concentrations greater than the adsorption maximum, kinetics curves also showed maxima the position of which shifted to longer times as plasma concentration decreased. These data are interpreted in terms of competitive adsorption between fibrinogen and other, as yet unidentified species in plasma. The data reported are in general agreement with the model of Vroman (12) for plasma-surface interactions which holds that initially adsorbed fibrinogen is later replaced by high molecular weight kininogen (HMWK), the rate of replacement depending on the relative activity of the surface in promoting coagulation.

摘要

研究了不同血浆蛋白在三种固体表面上的吸附情况与血浆浓度的关系。白蛋白在玻璃上的吸附不依赖于血浆浓度,而在聚乙烯和硅化玻璃上均增加至平稳值。免疫球蛋白G(IgG)在任何表面上的吸附均不依赖于血浆浓度。纤维蛋白原的吸附随血浆浓度增加,然后下降,最大值出现在约1%正常血浆浓度时,且随表面不同略有变化。在玻璃上,纤维蛋白原吸附动力学依赖于血浆浓度:在浓度低于吸附最大值时,动力学是常规的,吸附增加至平稳状态;在浓度高于吸附最大值时,动力学曲线也显示出最大值,其位置随着血浆浓度降低而向更长时间偏移。这些数据根据纤维蛋白原与血浆中其他尚未明确的物质之间的竞争性吸附来解释。所报道的数据总体上与Vroman(12)的血浆-表面相互作用模型一致,该模型认为最初吸附的纤维蛋白原随后被高分子量激肽原(HMWK)取代,取代速率取决于表面促进凝血的相对活性。

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