Relative bioavailability of artesunate and dihydroartemisinin: Investigations in the isolated perfused rat liver and in healthy Caucasian volunteers

被引:29
作者
Batty, KT
Ilett, KF
Powell, SM
Martin, J
Davis, TME
机构
[1] Univ Western Australia, Dept Pharmacol, Nedlands, WA 6907, Australia
[2] Univ Western Australia, Fremantle Hosp, Dept Med, Fremantle, WA 6959, Australia
[3] Curtin Univ Technol, Sch Pharm, Western Australian Ctr Pathol & Med Res, Clin Pharmacol & Toxicol Lab, Bentley, WA 6102, Australia
关键词
D O I
10.4269/ajtmh.2002.66.130
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The aim of this study was to evaluate the bioavailability of artesunate (ARTS) and dihydroartemisinin (DHA). When the single-pass isolated perfused rat liver model Was used, the hepatic bioavailability of ARTS (39 muM) was 0.20 and the bioavailability of DHA in ARTS and DHA (35 muM) perfusions was 0.12 and 0.11. respectively. Thus, the combined bioavailability of ARTS and DHA in the ARTS perfusions (0,32) was three-fold higher than the bioavailability of DHA. In the human study, eight healthy volunteers were randomised to receive oral ARTS (135 mg 352 mumol) or oral DHA (120 mg: 422 mumol). The area under the curve (AUC(0-6 hr)) of DHA following ARTS (2.9 mumol.hr/L) was higher than the AUC(0-6) (hr) of DHA following DHA administration ( 1,2 P 0,005). The dose-corrected relative oral bioavailability of DHA for DHA compared with ARTS was 43%. Thus, the use of conventional oral dosage regimens of ARTS appears preferable to oral administration of DHA.
引用
收藏
页码:130 / 136
页数:7
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