Background
The spread of
Plasmodium falciparum
resistance in common antimalarial drugs, including artemisinin-based combination therapies, has necessitated the discovery of new drugs with novel mechanisms of action. In the present study, the in vitro antimalarial and toxicological activities of acetone, methanol, ethanol and aqueous extracts of
Quercus infectoria
(
Q. infectoria
) galls were investigated.
Methods
The extracts were assessed for the antimalarial potential using a malarial SYBR Green I fluorescence-based (MSF) assay, while the toxicity was screened by using brine shrimp lethality test (BSLT), haemolytic assay, and cytotoxicity assay against normal embryo fibroblast cell line (NIH/3T3) and normal kidney epithelial cell line (Vero).
Results
The acetone extract showed the highest antimalarial activity (50% inhibitory concentration, IC
50
= 5.85 ± 1.64 μg/mL), followed by the methanol extract (IC
50
= 10.31 ± 1.90 μg/mL). Meanwhile, the ethanol and aqueous extracts displayed low antimalarial activity with IC
50
values of 20.00 ± 1.57 and 30.95 μg/mL ± 1.27 μg/mL, respectively. The significant antimalarial activity was demonstrated in all extracts and artemisinin (
P
< 0.05). All extracts were non-toxic to brine shrimps (50% lethality concentration, LC
50
> 1000 ppm). Furthermore, no occurrence of haemolysis (< 5%) was observed in normal erythrocytes when treated with all extracts compared to Triton X-100 that caused 100% haemolysis (
P
< 0.05). The acetone and methanol extracts were non-toxic to the normal cell lines and statistically significant to artemisinin (
P
< 0.05).
Conclusion
Taken together with satisfactory selectivity index (SI) values, the acetone and methanol extracts of
Q. infectoria
galls could serve as an alternative, promising and safe antimalarial agents.