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dc.contributor.authorSteyn, Minette
dc.contributor.authorN'Da, David D.
dc.contributor.authorBreytenbach, Jaco C.
dc.contributor.authorBreytenbach, Wilma J.
dc.contributor.authorSmith, Peter J.
dc.contributor.authorMeredith, Sandra
dc.date.accessioned2012-10-29T11:08:32Z
dc.date.available2012-10-29T11:08:32Z
dc.date.issued2011
dc.identifier.citationSteyn, M. et al. 2011. Synthesis and antimalarial activity of ethylene glycol oligomeric ethers of artemisinin. Journal of pharmacy and pharmacology, 63(2):278-286. [https://doi.org/10.1111/j.2042-7158.2010.01205.x]en_US
dc.identifier.issn0022-3573
dc.identifier.issn2042-7158 (Online)
dc.identifier.urihttp://hdl.handle.net/10394/7659
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.2042-7158.2010.01205.x
dc.identifier.urihttps://doi.org/10.1111/j.2042-7158.2010.01205.x
dc.description.abstractObjectives The aim of this study was to synthesize a series of ethylene glycol ether derivatives of the antimalarial drug artemisinin, determine their values for selected physicochemical properties and evaluate their antimalarial activity in vitro against Plasmodium falciparum strains. Methods The ethers were synthesized in a one-step process by coupling ethylene glycol moieties of various chain lengths to carbon C-10 of artemisinin. The aqueous solubility and log D values were determined in phosphate buffered saline (pH 7.4). The derivatives were screened for antimalarial activity alongside artemether and chloroquine against chloroquinesensitive (D10) and moderately chloroquine-resistant (Dd2) strains of P. falciparum. Key findings The aqueous solubility within each series increased as the ethylene glycol chain lengthened. The IC50 values revealed that all the derivatives were active against both D10 and Dd2 strains. All were less potent than artemether irrespective of the strain. However, they proved to be more potent than chloroquine against the resistant strain. Compound 8, featuring three ethylene oxide units, was the most active of all the synthesized ethers. Conclusions The conjugation of dihydroartemisinin to ethylene glycol units of various chain lengths through etheral linkage led to water-soluble derivatives. The strategy did not result in an increase of antimalarial activity compared with artemether. It is nevertheless a promising approach to further investigate and synthesize water-soluble derivatives of artemisinin that may be more active than artemether by increasing the ethylene glycol chain length.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectArtemetheren_US
dc.subjectArtemisininen_US
dc.subjectChloroquineen_US
dc.subjectMalariaen_US
dc.subjectPlasmodium falciparumen_US
dc.titleSynthesis and antimalarial activity of ethylene glycol oligomeric ethers of artemisininen_US
dc.typeArticleen_US
dc.contributor.researchID10059768 - Breytenbach, Jaco Cornelius
dc.contributor.researchID20883072 - N'Da, David Dago
dc.contributor.researchID10187081 - Breytenbach, Johanna Wilhelmina


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