Publication: Pharmacokinetics of artemether and dihydroartemisinin in healthy Pakistani male volunteers treated with artemether-lumefantrine
Issued Date
2010-10-13
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ISSN
14752875
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2-s2.0-77957656312
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Mahidol University
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SCOPUS
Bibliographic Citation
Malaria Journal. Vol.9, No.1 (2010)
Suggested Citation
Shabana Ali, Muzammil H. Najmi, Joel Tarning, Niklas Lindegardh Pharmacokinetics of artemether and dihydroartemisinin in healthy Pakistani male volunteers treated with artemether-lumefantrine. Malaria Journal. Vol.9, No.1 (2010). doi:10.1186/1475-2875-9-275 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/29185
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Title
Pharmacokinetics of artemether and dihydroartemisinin in healthy Pakistani male volunteers treated with artemether-lumefantrine
Abstract
Background. Artemether-lumefantrine is one of the most widely used anti-malarial drug combinations in the world with excellent tolerability and cure rates in adult and paediatric patients with uncomplicated falciparum malaria. The aim of this study was to evaluate the pharmacokinetics of artemether and its active metabolite, dihydroartemisinin, in healthy Pakistani volunteers. Methods. Twelve healthy male Pakistani subjects, aged 20 to 50, were recruited into the study. A fixed oral combination of artemether-lumefantrine (80-480 mg) was given as a single oral dose. Frequent blood samples were collected and artemether and dihydroartemisinin were quantified in human plasma using solid-phase extraction and liquid chromatography coupled with tandem mass spectrometry. Drug concentration-time data were evaluated with non-compartmental analysis. Results. Observed maximum concentrations (mean SD) of artemether and dihydroartemisinin were 184 100 ng/mL and 126 46 ng/mL, respectively. These concentrations were reached at 1.56 0.68 hr and 1.69 0.59 hr, respectively, after drug intake. The terminal elimination half-life of artemether and dihydroartemisinin were 2.00 0.71 hr and 1.80 0.31 hr, respectively. Apparent volume of distribution and oral clearance for artemether were estimated to 666 220 L and 257 140 L/hr. The same parameters were estimated to 702 220 L and 269 57 L/hr for dihydroartemisinin. Conclusions. The overall pharmacokinetic properties of artemether and dihydroartemisinin in healthy Pakistani subjects are comparable to healthy subjects and patients from other populations. © 2010 Ali et al; licensee BioMed Central Ltd.