AN INVITRO MICROTECHNIQUE FOR DETERMINATION OF THE ANTIMALARIAL ACTIVITY OF DRUGS
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Abstract
An invitro microtechnique was developed for the deter mination of antimalarial activity of drugs on Plasmodium falciparium strain FCC1. Plastic plates each with 40 wells were used. Each well (6.7 mm in diameter and 10 mm in depth) held 180 μl of RPMI 1640 culture medium containing 2.5% RBC (infEction rate about 1%) and 20 μl of glucose saline containing drugs to be tested. The cultures were incubated at 36~37℃ in candle-jar for 48 hrs., according to Trager & Jensen's method, without changing the medium during the incubation period. In the control, the parasites multiplied with a rate increasing from 1.05±0.10% to 3.75±0.89%. Using Finney's method the ED50 of the tested drug was calculated as a dose which causes 50% reduction of the parasite as compared with control. As shown in Table 3 the mean ED50 of chloroquine was 4.40±0.82ng/ml(5.59~3.36ng/ml). This method is considered to be useful and reproducible for testing antimalarials directly with human malaria parasites.
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