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由于L-抗坏血酸导致的聚碳酸酯上蛋白质吸附的变化。

Changes in protein adsorption on polycarbonate due to L-ascorbic acid.

作者信息

Chandy T, Sharma C P

出版信息

Biomaterials. 1985 Nov;6(6):416-20. doi: 10.1016/0142-9612(85)90103-6.

Abstract

When a synthetic material is introduced into blood, plasma proteins are rapidly adsorbed on to its surface, followed by the attachment of formed elements of blood, leading to thrombus formation. Previous research reported that vitamin C (L-ascorbic acid) prolongs the clotting time due to the formation of vitamin C-calcium complexes, which reduce the availability of Ca2+ ions for the clotting mechanism in in vitro conditions. Contact angle and platelet adhesion studies have indicated that vitamin C modifies the surface-protein interaction and surface-platelet binding at the interface. In this paper an increased thickness of protein layer deposited on the polycarbonate substrate has been observed in the presence of vitamin C (approximately 50 A) using ellipsometric measurements. Further polyacrylamide gel electrophoresis (PAG) and infrared attenuated total reflection spectroscopy (IR-ATR) techniques have provided a better understanding of the interfacial phenomena. It seems, that the adsorption of albumin is increased, relatively, in the presence of vitamin C, when compared with that of fibrinogen and gamma-globulin from an equal amount of protein mixture.

摘要

当一种合成材料被引入血液中时,血浆蛋白会迅速吸附在其表面,随后血液中的有形成分附着其上,导致血栓形成。先前的研究报道,维生素C(L-抗坏血酸)由于形成维生素C-钙复合物而延长凝血时间,该复合物在体外条件下会降低凝血机制中Ca2+离子的可用性。接触角和血小板黏附研究表明,维生素C会改变界面处的表面-蛋白质相互作用和表面-血小板结合。在本文中,使用椭圆偏振测量法观察到,在维生素C存在的情况下,沉积在聚碳酸酯基材上的蛋白质层厚度增加(约50埃)。此外,聚丙烯酰胺凝胶电泳(PAG)和红外衰减全反射光谱(IR-ATR)技术有助于更好地理解界面现象。与等量蛋白质混合物中的纤维蛋白原和γ-球蛋白相比,在维生素C存在的情况下,白蛋白的吸附相对增加。

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