In vitro susceptibility of Gabonese wild isolates of Plasmodium falciparumto artemether, and comparison with chloroquine, quinine, halofantrine and amodiaquine
B. Pradines et al., In vitro susceptibility of Gabonese wild isolates of Plasmodium falciparumto artemether, and comparison with chloroquine, quinine, halofantrine and amodiaquine, PARASITOL, 117, 1998, pp. 541-545
The in vitro activity of artemether against 63 African isolates of Plasmodi
um falciparum from Libreville, Gabon was evaluated using an isotopic drug s
usceptibility semi-microtest. The 50 % inhibitory concentration (IC50) valu
es for artemether were in a narrow range from 0.8 to 34.8 nM (mean IC50 5.0
nM) and the 95 % confidence interval (CI95 %) was 3.6-6.3 nM. In vitro dec
reased susceptibility or resistance were observed with artemether (14 %), t
o chloroquine (90 %), to quinine (32 %). Isolate susceptibility to amodiaqu
ine and halofantrine was high i.e. 100 % and 98 %, respectively. There was
a significant positive correlation between responses to artemether and amod
iaquine (r(2) = 0.45, P < 0.001), artemether and chloroquine (r(2) = 0.36,
P < 0.001), artemether and quinine (r(2) = 0.31, P < 0.001), and artemether
and halofantrine (r(2) = 0.19, P < 0.01). Positive correlation between the
se drugs suggests in vitro cross-resistance or at least common features in
drug uptake and/or mode of action or resistance.