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Antimicrobial Agents and Chemotherapy, September 1998, p. 2347-2351, Vol. 42, No. 9
Institut Français de Recherche
Scientifique pour le Développement en Coopération
(ORSTOM)
Received 4 May 1998/Returned for modification 20 May 1998/Accepted 29 June 1998
The in vitro antimalarial activity of the new Chinese synthetic
drug, lumefantrine, also known as benflumetol (a fluorene derivative
belonging to the aminoalcohol class), was determined by an isotopic
microtest against 61 fresh clinical isolates of Plasmodium
falciparum and compared with that of other established antimalarial agents. The geometric mean 50% inhibitory concentration of lumefantrine was 11.9 nmol/liter (95% confidence intervals, 10.4 to
13.6 nmol/liter; range, 3.3 to 25.6 nmol/liter). The in vitro
activities of lumefantrine against the chloroquine-sensitive and the
chloroquine-resistant isolates did not differ (P > 0.05). There was a significant positive correlation of responses
between lumefantrine and two other aminoalcohols studied, mefloquine
(r = 0.688) and halofantrine (r = 0.677), and between lumefantrine and artesunate (r = 0.420), suggesting a potential for in vitro cross-resistance. Our data
suggest high in vitro activity of lumefantrine, comparable to that of
mefloquine, and are in agreement with the promising results of
preliminary clinical trials.
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
In Vitro Activity of Lumefantrine (Benflumetol)
against Clinical Isolates of Plasmodium falciparum in
Yaoundé, Cameroon
Laboratoire de Recherche sur le Paludisme, Laboratoire
Associé Francophone 302, Organisation de Coordination pour la
lutte contre les Endémies en Afrique Centrale (OCEAC),
Yaoundé, Cameroon
*
Corresponding author. Mailing address: ORSTOM/OCEAC, BP
288, Yaoundé, Cameroon. Phone: 237 232 232. Fax: 237 230 061. E-mail: oceac@camnet.cm.
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