Ashton M, Hai T N, Sy N D, Huong D X, Van Huong N, Niêu N T, Công L D
Division of Biopharmaceutics & Pharmacokinetics, Department of Pharmacy, Uppsala University, Uppsala, Sweden.
Drug Metab Dispos. 1998 Jan;26(1):25-7.
The pharmacokinetics of the antimalarial artemisinin exhibited an unusual time dependency during a 7-day oral daily regimen of 500 mg in 10 healthy, male Vietnamese adults. Artemisinin areas under the plasma concentration-time curve (AUC) decreased to 34% (median) by day 4 with a further decrease by day 7 to only 24% of values obtained after the first day of administration. In seven subjects restudied after a 2-week washout period, artemisinin AUCs had almost normalized, demonstrating the reversibility of the time-dependent drug disposition. The results suggest artemisinin exhibits an auto-inductive effect on drug metabolism of an unusual magnitude. This may partly explain why some patients on standard doses, due to subparasiticidal drug levels toward the end of a standard regimen, do not completely clear parasites. Further, the possibility of drug-drug metabolic interactions during combination regimens is implicated.
在10名健康的越南成年男性中进行了一项为期7天、每日口服500毫克抗疟药物青蒿素的研究,结果显示其药代动力学呈现出不同寻常的时间依赖性。血浆浓度-时间曲线下的青蒿素面积(AUC)在第4天时降至34%(中位数),到第7天时进一步降至仅为给药第一天后所测值的24%。在经过2周洗脱期后重新研究的7名受试者中,青蒿素的AUC几乎恢复正常,表明这种时间依赖性药物处置具有可逆性。结果表明,青蒿素对药物代谢具有不同寻常程度的自身诱导作用。这可能部分解释了为什么一些接受标准剂量治疗的患者,由于在标准疗程接近尾声时药物水平低于杀寄生虫水平,未能完全清除寄生虫。此外,联合用药方案中药物-药物代谢相互作用的可能性也被涉及。