CLINICAL PHARMACOKINETICS AND PHARMACODYNAMICS OF ARTEMISININ AND DERIVATIVES

被引:88
作者
WHITE, NJ
机构
[1] CHO QUAN HOSP, CTR TROP DIS, WELLCOME TRUST CLIN RES UNIT, HO CHI MINH CITY, VIETNAM
[2] JOHN RADCLIFFE HOSP, NUFFIELD DEPT CLIN MED, OXFORD OX3 9DU, ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0035-9203(94)90471-5
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Reliable and reproducible methods for the measurement of artemisinin and its derivatives in body fluids have proved difficult to develop. The available evidence suggests that all compounds are hydrolysed to a biologically active metabolite, dihydroartemisinin, which is eliminated rapidly. The role of other (hydroxylated) metabolites in humans requires further study. The hydrolysis of artesunate is so rapid that it may be considered a pro-drug for dihydroartemisinin. All the artemisinin compounds induce more rapid reduction of parasitaemia than other antimalarial drugs, indicating a direct effect on ring forms. This pharmacodynamic measure can be used in drug comparisons, and allows estimations of the number of parasites removed before sequestration.
引用
收藏
页码:41 / 43
页数:3
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