Skip to main content

Research Repository

Advanced Search

Drug repositioning as a route to anti-malarial drug discovery: preliminary investigation of the in vitro anti-malarial efficacy of emetine dihydrochloride hydrate

Matthews, H; Usman-Idris, M; Khan, F; Read, M; Nirmalan, NJ

Drug repositioning as a route to anti-malarial drug discovery: preliminary investigation of the in vitro anti-malarial efficacy of emetine dihydrochloride hydrate Thumbnail


Authors

H Matthews

M Usman-Idris

F Khan

M Read



Abstract

Background

Drug repurposing or repositioning refers to the usage of existing drugs in diseases other than those it was originally used for. For diseases like malaria, where there is an urgent need for active drug candidates, the strategy offers a route to significantly shorten the traditional drug development pipelines. Preliminary high-throughput screens on patent expired drug libraries have recently been carried out for Plasmodium falciparum. This study reports the systematic and objective further interrogation of selected compounds reported in these studies, to enable their repositioning as novel stand-alone anti-malarials or as combinatorial partners.
Methods

SYBR Green flow cytometry and micro-titre plate assays optimized in the laboratory were used to monitor drug susceptibility of in vitro cultures of P. falciparum K1 parasite strains. Previously described fixed-ratio methods were adopted to investigate drug interactions.
Results

Emetine dihydrochloride hydrate, an anti-protozoal drug previously used for intestinal and tissue amoebiasis was shown to have potent inhibitory properties (IC50 doses of ~ 47nM) in the multidrug resistant K1 strain of P. falciparum. The sum 50% fractional inhibitory concentration ([n-ary summation]FIC50, 90) of the interaction of emetine dihydrochloride hydrate and dihydroartemisinin against the KI strains of P. falciparum ranged from 0.88-1.48.
Conclusion

The results warrant further investigation of emetine dihydrochloride hydrate as a potential stand-alone anti-malarial option. The interaction between the drug and the current front line dihydroartemisinin ranged from additive to mildly antagonistic in the fixed drug ratios tested.

Citation

Matthews, H., Usman-Idris, M., Khan, F., Read, M., & Nirmalan, N. Drug repositioning as a route to anti-malarial drug discovery: preliminary investigation of the in vitro anti-malarial efficacy of emetine dihydrochloride hydrate. Malaria Journal, 12(1), 359. https://doi.org/10.1186/1475-2875-12-359

Journal Article Type Article
Deposit Date Oct 15, 2013
Publicly Available Date Apr 5, 2016
Journal Malaria Journal
Publisher Springer Verlag
Peer Reviewed Peer Reviewed
Volume 12
Issue 1
Pages 359
DOI https://doi.org/10.1186/1475-2875-12-359
Keywords Drug repositioning; Antimalarial chemotherapy; Emetine; Dihydroartemisinin; Drug susceptibility assays; Flow cytometry
Publisher URL http://dx.doi.org/10.1186/1475-2875-12-359
Related Public URLs http://www.malariajournal.com/

Files






You might also like



Downloadable Citations