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 |
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.