The efficacy of antifolate antimalarial combinations in Africa: A predictive model based on pharmacodynamic and pharmacokinetic analyses

被引:130
作者
Watkins, WM
Mberu, EK
Winstanley, PA
Plowe, CV
机构
[1] WELLCOME TRUST RES LABS,NAIROBI,KENYA
[2] UNIV LIVERPOOL,DEPT PHARMACOL & THERAPEUT,LIVERPOOL L3 5QA,MERSEYSIDE,ENGLAND
[3] UNIV MARYLAND,SCH MED,DIV GEOG MED,MOL PARASITOL & MALARIA FIELD STUDIES UNIT,BALTIMORE,MD 21201
来源
PARASITOLOGY TODAY | 1997年 / 13卷 / 12期
基金
英国惠康基金;
关键词
D O I
10.1016/S0169-4758(97)01124-1
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
At present, effective treatment for non-severe malaria is the most important malaria control strategy in Africa. Pyrimethamine-sulfadoxine (PSD) is rapidly becoming the first-line treatment in areas of chloroquine resistance, although the parasite chemoresistance factors that dispose towards clinical failure with PSD are still unclear!ear. Here, Bill Watkins and colleagues analyse the relationship between the pharmacokinetic properties of two treatment combinations (PSD and chlorprouanil-dapsone) in vivo and the respective in vitro isobolograms for parasites with specific drug-resistance patterns. From this relationship, they develop a hypothesis that may explain clinical drug failure and differential efficacy between treatments. The deductions can be tested in field studies to validate or refute the model.
引用
收藏
页码:459 / 464
页数:6
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