Ex Vivo Activity of Endoperoxide Antimalarials, Including Artemisone and Arterolane, against Multidrug-Resistant Plasmodium falciparum Isolates from Cambodia

Abstract

Novel synthetic endoperoxides are being evaluated as new components of artemisinin combination therapies (ACTs) to treat artemisinin-resistant Plasmodium falciparum malaria. We conducted blinded ex vivo activity testing of fully synthetic (OZ78 and OZ277) and semisynthetic (artemisone, artemiside, artesunate, and dihydroartemisinin) endoperoxides in the histidine-rich protein 2 enzyme-linked immunosorbent assay against 200 P. falciparum isolates from areas of artemisinin-resistant malaria in western and northern Cambodia in 2009 and 2010. The order of potency and geometric mean (GM) 50% inhibitory concentrations (IC50s) were as follows: artemisone (2.40 nM)>artesunate (8.49 nM)>dihydroartemisinin (11.26 nM)>artemiside (15.28 nM)>OZ277 (31.25 nM)>OZ78 (755.27 nM). Ex vivo activities of test endoperoxides positively correlated with dihydroartemisinin and artesunate. The isolates were over 2-fold less susceptible to dihydroartemisinin than the artemisinin-sensitive P. falciparum W2 clone and showed sensitivity comparable to those with test endoperoxides and artesunate, with isolate/W2 IC50 susceptibility ratios of<2.0. All isolates had P. falciparum chloroquine resistance transporter mutations, with negative correlations in sensitivity to endoperoxides and chloroquine. The activities of endoperoxides (artesunate, dihydroartemisinin, OZ277, and artemisone) significantly correlated with that of the ACT partner drug, mefloquine. Isolates had mutations associated with clinical resistance to mefloquine, with 35% prevalence of P. falciparum multidrug resistance gene 1 (pfmdr1) amplification and 84.5% occurrence of the pfmdr1 Y184F mutation. GM IC50s for mefloquine, lumefantrine, and endoperoxides (artesunate, dihydroartemisinin, OZ277, OZ78, and artemisone) correlated with pfmdr1 copy number.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2014
Accession Number
ADA614568

Entities

People

  • Chanthap Lon
  • Charlotte A. Lanteri
  • David L. Saunders
  • Ian Bathurst
  • Kritsanai Yingyuen
  • Stuart D. Tyner
  • Suwanna Chaorattanakawee
  • Wiriya Rutvisuttinunt
  • Xavier C. Ding

Organizations

  • United States Army Institute of Surgical Research

Tags

DTIC Thesaurus Topics

  • Anti-Infective Agents
  • Antimalarials
  • Blood
  • Cambodia
  • Chemical Synthesis
  • Chemistry
  • Chemotherapy
  • Clinical Trials
  • Combination Therapy
  • Correlation Analysis
  • Data Analysis
  • Health Services
  • Malaria
  • Medical Personnel
  • Parasitic Diseases
  • Public Health
  • Southeast Asia

Fields of Study

  • Biology

Readers

  • Parasitology and Pharmacology of Malaria.