Department of Pharmacology, University of Gothenburg, Gothenburg, Sweden.
Antimicrob Agents Chemother. 2010 Nov;54(11):4780-8. doi: 10.1128/AAC.00252-10. Epub 2010 Aug 16.
The combination of artemether (ARM) and lumefantrine is currently the first-line treatment of uncomplicated falciparum malaria in mainland Tanzania. While the exposure to lumefantrine has been associated with the probability of adequate clinical and parasitological cure, increasing exposure to artemether and the active metabolite dihydroartemisinin (DHA) has been shown to decrease the parasite clearance time. The aim of this analysis was to describe the pharmacokinetics and pharmacodynamics of artemether, dihydroartemisinin, and lumefantrine in African children with uncomplicated malaria. In addition to drug concentrations and parasitemias from 50 Tanzanian children with falciparum malaria, peripheral parasite densities from 11 asymptomatic children were included in the model of the parasite dynamics. The population pharmacokinetics and pharmacodynamics of artemether, dihydroartemisinin, and lumefantrine were modeled in NONMEM. The distribution of artemether was described by a two-compartment model with a rapid absorption and elimination through metabolism to dihydroartemisinin. Dihydroartemisinin concentrations were adequately illustrated by a one-compartment model. The pharmacokinetics of artemether was time dependent, with typical oral clearance increasing from 2.6 liters/h/kg on day 1 to 10 liters/h/kg on day 3. The pharmacokinetics of lumefantrine was sufficiently described by a one-compartment model with an absorption lag time. The typical value of oral clearance was estimated to 77 ml/h/kg. The proposed semimechanistic model of parasite dynamics, while a rough approximation of the complex interplay between malaria parasite and the human host, adequately described the early effect of ARM and DHA concentrations on the parasite density in malaria patients. However, the poor precision in some parameters illustrates the need for further data to support and refine this model.
青蒿琥酯(ART)和咯萘啶的联合用药目前是坦桑尼亚大陆治疗无并发症恶性疟的一线治疗药物。尽管咯萘啶的暴露与充分的临床和寄生虫学治愈率有关,但增加青蒿琥酯和其活性代谢物双氢青蒿素(DHA)的暴露已被证明可缩短寄生虫清除时间。本分析的目的是描述青蒿琥酯、双氢青蒿素和咯萘啶在坦桑尼亚无并发症疟疾儿童中的药代动力学和药效动力学。除了 50 名患有恶性疟的坦桑尼亚儿童的药物浓度和寄生虫血症外,还将 11 名无症状儿童的外周寄生虫密度纳入寄生虫动力学模型中。在 NONMEM 中对青蒿琥酯、双氢青蒿素和咯萘啶的群体药代动力学和药效动力学进行建模。青蒿琥酯的分布通过一个两室模型来描述,该模型通过代谢快速吸收和消除至双氢青蒿素。双氢青蒿素浓度通过一个一室模型得到充分说明。青蒿琥酯的药代动力学具有时间依赖性,典型的口服清除率从第 1 天的 2.6 升/小时/千克增加到第 3 天的 10 升/小时/千克。咯萘啶的药代动力学通过一个具有吸收滞后时间的一室模型得到充分说明。口服清除率的典型值估计为 77 毫升/小时/千克。所提出的寄生虫动力学半机械模型虽然是对疟原虫与人体宿主之间复杂相互作用的粗略近似,但充分描述了 ARM 和 DHA 浓度对疟疾患者寄生虫密度的早期影响。然而,一些参数的精度较差表明需要进一步的数据来支持和完善该模型。