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Figure 4 | Malaria Journal

Figure 4

From: A novel live-dead staining methodology to study malaria parasite viability

Figure 4

IC 50 determination using JC-1 and/or pLDH in parallel on drug treated P. falciparum cultures. Culture P. falciparum-infected erythrocyte were incubated for 48 h in the presence of the indicated drug concentration at haematocrit of 5% and 1% parasitaemia. Panel A - shows that the inter-experiment variability between 2 separate JC-1 determinations is low (red and violet lines) and that the methodology is more accurate (IC50 is consistently lower) than the IC50 determination obtained with the pLDH methodology; Panel B - shows typical curves obtained by splitting parasites derived from a same mother culture into plates, in which they were cultured in parallel under the same environmental conditions in the presence of rising artemisinin concentrations and IC50 curves where either determined using the pLDH (violet line) or the JC-1 (blue line) methodology; Panel C – shows typical curves obtained by splitting parasites derived from a same mother culture into plates, in which they were cultured in parallel under the same environmental conditions in the presence of rising atovaquone concentrations and IC50 curves where either determined using the pLDH (violet line) or the JC-1 (blue line) methodology.

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