Pharmacokinetics and ex vivo pharmacodynamic antimalarial activity of dihydroartemisinin-piperaquine in patients with uncomplicated falciparum malaria in Vietnam

Antimicrob Agents Chemother. 2009 Aug;53(8):3534-7. doi: 10.1128/AAC.01717-08. Epub 2009 Jun 15.

Abstract

Compared to healthy subjects, malaria patients show a reduction in the mean oral clearance (1.19 versus 5.87 liters/h/kg of body weight) and apparent volume of distribution (1.47 versus 8.02 liters/kg) of dihydroartemisinin in Vietnamese patients following treatment with dihydroartemisinin-piperaquine (Artekin) for uncomplicated Plasmodium falciparum. Dihydroartemisinin is responsible for most of the ex vivo antimalarial activity of dihydroartemisinin-piperaquine.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Antimalarials / pharmacokinetics*
  • Antimalarials / therapeutic use*
  • Artemisinins / pharmacokinetics*
  • Artemisinins / therapeutic use*
  • Humans
  • Malaria, Falciparum / drug therapy*
  • Male
  • Middle Aged
  • Quinolines / pharmacokinetics*
  • Quinolines / therapeutic use*
  • Vietnam
  • Young Adult

Substances

  • Antimalarials
  • Artemisinins
  • Quinolines
  • artenimol
  • piperaquine