Projects per year
The component drugs in the widely used antimalarial artemisinin combination therapy artemether–lumefantrine are lipophilic, with the possibility that recommended fixed doses in adults may lead to subtherapeutic concentrations and consequent treatment failure in overweight/obese individuals with malaria. The aim of this study was to investigate the pharmacokinetic properties of artemether, lumefantrine and their active metabolites dihydroartemisinin and desbutyl-lumefantrine in 16 normal-weight, overweight and obese healthy male volunteers [body mass index (BMI) categories ≤25 kg/m², >25–≤30 kg/m² and >30 kg/m², respectively; absolute range 19.3–37.2 kg/m²]. Participants received the conventional six doses of artemether–lumefantrine over 3 days, each dose comprising 80 mg artemether plus 480 mg lumefantrine administered with 6.7 g fat, and blood samples were collected at pre-specified time-points over 14 days. Plasma drug/metabolite concentrations were measured using liquid chromatography-mass spectrometry and included in multi-compartmental population pharmacokinetic models. There was a non-significant trend to a lower area under the plasma concentration–time curve with a higher body weight or BMI for dihydroartemisinin and especially artemether which was attenuated when normalized for mg/kg dose, but this relationship was not evident in the case of the more lipophilic lumefantrine and its metabolite desbutyl-lumefantrine. Simulated Day 7 plasma lumefantrine concentrations were >200 µg/L (the threshold at which Plasmodium falciparum recrudescences are minimized) in all participants. These results indicate that there is no need for artemether–lumefantrine dose modification in overweight and obese patients with malaria.
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- 2 Finished
Enhancing clinical management of paediatric malaria in endemic areas with transmission of multiple Plasmodium species
1/01/17 → 30/06/21
A study of artemisinin combination therapy given at delivery to prevent postpartum malaria and to young infants to treat uncomplicated malaria
1/01/17 → 30/06/21
- 1 Citations
- 1 Doctoral Thesis
A study of pharmacokinetic properties of artemisinin combination therapy for malaria in specific populationsSugiarto, S. R., 2023, (Unpublished)
Research output: Thesis › Doctoral ThesisFile96 Downloads (Pure)