首页 | 本学科首页   官方微博 | 高级检索  
     

伊曲康唑影响的药代动力学相互作用研究进展
引用本文:苗彩云,陈漪,陈江飞. 伊曲康唑影响的药代动力学相互作用研究进展[J]. 中国临床药理学与治疗学, 2009, 14(10): 1183-1192
作者姓名:苗彩云  陈漪  陈江飞
作者单位:1. 宁波市妇女儿童医院药剂科,宁波,315012,浙江
2. 宁波市第一医院药剂科,宁波,315010,浙江
摘    要:伊曲康唑为三唑类广谱抗真菌药,临床应用广泛,具有CYP3A4和P-糖蛋白抑制作用。由于临床CYP3A4和P-糖蛋白底物广泛,它们在口服药物吸收的主要部位胃肠道均有高表达,同时两者的底物具有显著的重叠性,由此导致的受伊曲康唑影响的药代动力学相互作用广泛产生,甚至引起显著的临床意义。本文综述并讨论了受其影响的药代动力学相互作用研究,以促进临床的安全用药。

关 键 词:伊曲康唑  抗真菌药  药代动力学  药物相互作用

Progress and research in the effect of itraconazole on pharmacokinetic drug-drug interactions
MIAO Cai-yun,CHEN Yi,CHEN Jiang-fei. Progress and research in the effect of itraconazole on pharmacokinetic drug-drug interactions[J]. Chinese Journal of Clinical Pharmacology and Therapeutics, 2009, 14(10): 1183-1192
Authors:MIAO Cai-yun  CHEN Yi  CHEN Jiang-fei
Affiliation:1Department of Pharmacy, Ningbo Women and Children ' s Hospital, Ningbo 315012, Zhejiang , China ; 2Department of Pharmacy, Ningbo NO. 1 Hospital, Ningbo 315010, Zhejiang, China)
Abstract:Itraconazole,as one of the broad-spectrum antifungal drags,is an inhibitor of CYP3A4 and P-glycoprotein and was widely used in clinic.CYP3A4 and P-glycoprotein with extensive substrate have present at high levels in gastrointestinal tract,the primary site of absorption for orally administrated drugs,and share a significant overlap in substrate specificity,thus resuhing in widely phannaeokinetie interaction by itraconazole,part of which has clinical importance.In this article,the effect of itraconazole on phannaeokinetie drug-drug interactions is reviewed and discussed in order to promote its safe usage.
Keywords:itraconazole  antifugal drug  pharmacokinetics  drug-drug interaction
本文献已被 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