Population Pharmacokinetics and Pharmacodynamics of Artemether and Lumefantrine during Combination Treatment in Children with Uncomplicated Falciparum Malaria in Tanzania

被引:48
|
作者
Hietala, Sofia Friberg [1 ]
Martensson, Andreas [2 ,3 ]
Ngasala, Billy [4 ]
Dahlstrom, Sabina [2 ]
Lindegardh, Niklas [5 ,6 ]
Annerberg, Anna [5 ]
Premji, Zul [4 ]
Farnert, Anna [2 ]
Gil, Pedro [2 ,7 ]
Bjorkman, Anders [2 ]
Ashton, Michael [1 ]
机构
[1] Univ Gothenburg, Dept Pharmacol, Unit Pharmacokinet & Drug Metab, Sahlgrenska Acad, SE-40530 Gothenburg, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Dept Med, Infect Dis Unit, Solna, Sweden
[3] Karolinska Inst, Div Global Hlth, Dept Publ Hlth Sci, Solna, Sweden
[4] Muhimbili Univ Hlth & Allied Sci, Dept Parasitol, Dar Es Salaam, Tanzania
[5] Mahidol Univ, Fac Trop Med, Bangkok, Thailand
[6] Univ Oxford, Nuffield Dept Clin Med, Ctr Trop Med, Oxford, England
[7] Univ Algarve, Ctr Mol & Struct Biomed, Inst Biotechnol & Bioengn, Faro, Portugal
基金
英国惠康基金;
关键词
PLASMODIUM-FALCIPARUM; HEALTHY-SUBJECTS; DOSE PHARMACOKINETICS; ASYMPTOMATIC CHILDREN; DYNAMICS; TRIAL; ARTEMISININ; BENFLUMETOL; EFFICACY; PLASMA;
D O I
10.1128/AAC.00252-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:4780 / 4788
页数:9
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