Comparison of beta-artemether and beta-arteether against malaria parasites in vitro and in vivo

Am J Trop Med Hyg. 1993 Mar;48(3):377-84. doi: 10.4269/ajtmh.1993.48.377.

Abstract

The antimalarial activity of beta-artemether and beta-arteether was compared in three test systems: in vitro against chloroquine-resistant and chloroquine-sensitive Plasmodium falciparum parasites, in mice infected with P. berghei, and in Aotus monkeys infected with chloroquine-resistant P. falciparum. In vitro, the mean 50% inhibitory concentration (IC50) for beta-artemether was 1.74 nM (range 1.34-1.81 nM), and this value for beta-arteether was 1.61 nM (range 1.57-1.92 nM). They were approximately 2.5-fold more potent than artemisinin, which had a mean IC50 of 4.11 nM (range 3.36-4.60 nM). In the mouse model, the 50% curative doses (CD50) of beta-artemether and beta-arteether had a mean value of 55 mg/kg (32-78 mg/kg). The 50% effective curative doses (ED50) in the Aotus monkey were 7.1 mg/kg (95% confidence interval [CI] = 3.7-13.5) for beta-artemether and 11.8 mg/kg (95% CI = 6.5-21.3) for beta-arteether. Overall, the activities of the two drugs were comparable.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Antimalarials / pharmacology*
  • Antimalarials / therapeutic use
  • Aotus trivirgatus
  • Artemether
  • Artemisinins*
  • Chloroquine / pharmacology
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Female
  • Malaria / drug therapy
  • Malaria, Falciparum / drug therapy*
  • Male
  • Mefloquine / pharmacology
  • Mice
  • Plasmodium berghei / drug effects
  • Plasmodium falciparum / drug effects*
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / pharmacology*
  • Sesquiterpenes / therapeutic use
  • Structure-Activity Relationship

Substances

  • Antimalarials
  • Artemisinins
  • Sesquiterpenes
  • Chloroquine
  • Artemether
  • Mefloquine
  • artemotil