Kitamoto Y, Tomita M, Kiyama S, Inoue T, Yabushita Y, Sato T, Ryoda H, Sato T
Third Department of Internal Medicine, Kumamoto University Medical School, Japan.
Thromb Haemost. 1991 Jan 23;65(1):73-6.
Urokinase immobilized polymer is highly antithrombotic, which cannot be explained only by fibrinolysis. We immobilized 10 IU/cm2 of urokinase to polyurethane by using maleic anhydride methylvinyl ether copolymer as a carrier. Then we incubated blood in circular tubes made of this material, measured the clotting factors and observed the surface of the tubes after incubation by scanning electronmicroscopy and immunofluorescence microscopy. After 5 min incubation, the relative activities of factors V, VIII, IX, X and XII, fibrinogen, plasminogen and alpha 2 plasmin inhibitor decreased, but the activity of factor VII increased. No platelet adhesion to the surface of the urokinase immobilized polyurethane was observed and there was no significant adsorption of serum proteins, including fibrinogen, fibronectin and vWF antigen, on the surface. Urokinase-immobilized polyurethane catalyzed the digestion of clotting factors as well as fibrinolysis and also inhibited platelet adhesion on its surface probably by inhibiting protein adsorption and its clinical application including vessel prosthesis should be developed further.
固定化尿激酶聚合物具有高度抗血栓形成作用,这不能仅用纤维蛋白溶解来解释。我们以马来酸酐甲基乙烯基醚共聚物为载体,将10国际单位/平方厘米的尿激酶固定在聚氨酯上。然后,我们在由这种材料制成的圆形管中孵育血液,测量凝血因子,并通过扫描电子显微镜和免疫荧光显微镜观察孵育后管的表面。孵育5分钟后,因子V、VIII、IX、X和XII、纤维蛋白原、纤溶酶原和α2纤溶酶抑制剂的相对活性降低,但因子VII的活性增加。未观察到血小板黏附在固定化尿激酶的聚氨酯表面,且表面未观察到包括纤维蛋白原、纤连蛋白和vWF抗原在内的血清蛋白的显著吸附。固定化尿激酶的聚氨酯催化凝血因子的消化以及纤维蛋白溶解,并且可能通过抑制蛋白质吸附来抑制血小板在其表面的黏附,其包括血管假体在内的临床应用应进一步开发。