In vitro activity of new artemisinin derivatives against Plasmodium falciparum clinical isolates from Gabon

被引:8
作者
Held, Jana [1 ,2 ]
Soomro, Shahid A. [3 ]
Kremsner, Peter G. [1 ,2 ]
Jansen, F. Herwig [3 ]
Mordmueller, Benjamin [1 ,2 ]
机构
[1] Univ Tubingen, Inst Trop Med, D-72074 Tubingen, Germany
[2] Albert Schweitzer Hosp, Med Res Unit, Lambarene, Gabon
[3] Dafra Pharma R&D, Turnhout, Belgium
关键词
Malaria; Artemisinin; Plasmodium falciparum; MALARIA; SENSITIVITY; ARTESUNATE; RESISTANCE; DRUG;
D O I
10.1016/j.ijantimicag.2010.12.022
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Nowadays, artemisinins are the mainstay of malaria treatment, but initial indications of resistance against clinically used derivatives are present. In this study, ten new artemisinin derivatives were tested in vitro against Plasmodium falciparum laboratory strains as well as clinical isolates from Gabon. All derivatives were highly active, with 50% inhibitory concentrations (IC50 values) < 13nM in the clinical isolates. The activity of one fluoro-containing derivative did not correlate with that of the parent compound, suggesting a different activity profile. New artemisinin derivatives with different activity profiles are of special interest as they represent an important class of candidates for pre-clinical testing in clinical parasite isolates adapted to currently used artemisinins, since derivatisation is one possible strategy to prolong the clinical usefulness of this important class of antimalarials. (C) 2011 Elsevier B. V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:485 / 488
页数:4
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