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蛋白质/血小板与人工表面的相互作用:维生素和血小板抑制剂的作用

Protein/platelet interaction with an artificial surface: effect of vitamins and platelet inhibitors.

作者信息

Chandy T, Sharma C P

出版信息

Thromb Res. 1986 Jan 1;41(1):9-22. doi: 10.1016/0049-3848(86)90275-6.

Abstract

Protein adsorption and platelet adhesion are two important biological processes arising at the blood-prosthetic interface. The effect of Vitamins and antiplatelet drugs to modulate the surface induced platelet adhesion to polycarbonate was investigated using washed calf platelets in presence and absence of fibrinogen. This study also demonstrated the effects of Vitamins and antiplatelet drugs towards protein adsorption to an artificial surface. It seems Vitamin B6, Vitamin E, combinations of Aspirin-Persantine, Aspirin-Vitamin C, a synthetic Polyelectrolyte and Galactosamine reduced the fibrinogen (fg) surface concentration from a mixture of proteins. These antiplatelet agents also enhanced the albumin surface concentration. This itself may be one of the parameters to reduce the platelet adhesion towards an artificial surface. A combination of Aspirin-Vitamin C-Vitamin B6-Vitamin E inhibited the fibrinogen surface binding, which might be beneficial to improve the blood compatibility of an artificial surface.

摘要

蛋白质吸附和血小板黏附是在血液与人工假体界面发生的两个重要生物学过程。在有和没有纤维蛋白原的情况下,使用洗涤过的小牛血小板研究了维生素和抗血小板药物对调节表面诱导的血小板与聚碳酸酯黏附的作用。本研究还证明了维生素和抗血小板药物对蛋白质吸附到人工表面的影响。似乎维生素B6、维生素E、阿司匹林-潘生丁组合、阿司匹林-维生素C组合、一种合成聚电解质和半乳糖胺降低了蛋白质混合物中纤维蛋白原(fg)的表面浓度。这些抗血小板药物还提高了白蛋白的表面浓度。这本身可能是降低血小板对人工表面黏附的参数之一。阿司匹林-维生素C-维生素B6-维生素E组合抑制了纤维蛋白原的表面结合,这可能有利于改善人工表面的血液相容性。

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