首页 | 本学科首页   官方微博 | 高级检索  
     

新型凝血酶抑制剂阿加曲班
引用本文:袁莉娟,刘爱民,刘蕾. 新型凝血酶抑制剂阿加曲班[J]. 中国新药杂志, 2005, 14(2): 230-234
作者姓名:袁莉娟  刘爱民  刘蕾
作者单位:卫生部北京医院药学部,北京,100730
摘    要:阿加曲班(argatroban)是一种凝血酶抑制剂,可直接与凝血酶的催化位点结合,迅速可逆的与凝血块结合并溶解凝血酶,其半衰期为39~51min,停止治疗后迅速恢复凝血功能,通过监测抗凝血参数调整其使用剂量.现介绍阿加曲班的药理学、药效学、药动学及不良反应、相互作用等方面的研究进展.

关 键 词:阿加曲班  凝血酶抑制剂  药效学  药动学  临床评价
文章编号:1003-3734(2005)02-0230-05

Argatroban, a new direct thrombin inhibitor
YUAN Li-juan,LIU Ai-Min,LIU Lei. Argatroban, a new direct thrombin inhibitor[J]. Chinese Journal of New Drugs, 2005, 14(2): 230-234
Authors:YUAN Li-juan  LIU Ai-Min  LIU Lei
Abstract:Argatroban is the only direct thrombin inhibitor, binding to the catalytic site of the thrombin molecule. It is able to rapidly and reversibly bind to both clot-bound and soluble thrombin, reducing extension of existing thromboses. Its short half-life (39 to 51 minutes) and binding reversibility allow rapid onset of action and rapid restoration of normal haemostasis upon cessation of therapy. As an ideal anticoagulant for both the prophylaxis and treatment of heparin-induced thrombocytopenia (HIT) and associated thrombotic complications, argatroban offers a predictable dose response that is well correlated with changes in anticoagulant parameters and is minimally monitored. This paper reviews pharmacology, pharmacodynamics, pharmacokinetics, safety and drug interactions of argatroban.
Keywords:argatroban  thrombin inhibitor  pharmacodynamics   pharmacokinetics   clinical evaluation
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号