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. 2007 Apr 16;51(6):2280–2281. doi: 10.1128/AAC.01532-06

TABLE 1.

In vitro drug susceptibility profiles of the day 0 and day 49 parasitesa

Sample Date of collection Parasitemia IC50 (nmol/liter) for drug
Chloroquine Quinine Mefloquine Halofantrine b-Artemether Atovaquone
Day 0 14 February 2005 2 116 83 14.2 8.7 1.3 1.6
Day 49 04 April 2005 1 111 364 21 3.4 2.7 20.5
a

Drug assays were performed at a 1% hematocrit over a 48-h culture period using the 3H-hypoxanthine incorporation microtest (6). Each isolate was tested once in duplicate against serial twofold dilutions of antimalarials over the following concentration ranges: 5,120 to 5 nM for chloroquine (chloroquine diphosphate; Sigma; catalog no. C6628), 6,400 to 6.2 nM for quinine (quinine sulfate; Sigma; catalog no. Q1878), 1,024 to 1 nM for mefloquine (Hoffman-La Roche, Inc.), 25.6 to 0.025 nM for halofantrine (GlaxoSmithKline, Inc.), and 200 to 0.19 nM for artemether (Novartis Pharma, Inc.) and atovaquone (GlaxoSmithKline, Inc.). The IC50 was calculated using probit/log regression of the percent growth inhibition for each drug.