Role of platelets in blood-biomaterial interactions

被引:17
|
作者
Rao, GHR [1 ]
Chandy, T [1 ]
机构
[1] Univ Minnesota, Acad Hlth Ctr, Inst Biomed Engn, Minneapolis, MN 55455 USA
关键词
platelet adhesion; protein adsorption; biomaterials; surface induced platelet activation; fibrinogen; platelet-surface receptors; antiplatelet drugs;
D O I
10.1007/BF02749979
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Over 2 million cardiovascular procedures are performed annually in the United States. Every one of these procedures requires some period of contact with blood with several different biomaterials used in the manufacture of assist devices or implant devices. In view of the increasing importance of the biomaterials in clinical practice, it would be timely to review briefly physicochemical characterization as well as biological evaluations. Blood compatibility encompasses a variety of events associated with blood interaction with the biomaterials used in various procedures. Two separate coagulation mechanisms are involved (arterial and venous) depending upon the flow characteristics. At least three Interacting factors modulate normal hemostasis and the pathogenesis of thromboembolic events. They are the state of activation of coagulation cascade, circulating levels of thrombin and fibrinogen and relative activity of platelets. In this overview we discuss the current concepts on the role of platelets in blood-biomaterial interactions. When blood contacts a biomaterial surface a variety of blood components interact with the surface. Some of the key players in platelet activation on biomaterial surface include fibrinogen and von Willebrand factor. Currently available antiplatelet drugs effectively block aggregation and secretion induced by physiological agonists such as epinephrine, adenosine diphosphate and thromboxane in suspension. However, they do not prevent platelet interaction on biomaterial surfaces. Mechanisms involved in platelet activation In suspension and on surfaces as well as the pharmacology of newer antiplatelet drugs will be discussed.
引用
收藏
页码:633 / 639
页数:7
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