Please use this identifier to cite or link to this item: https://doi.org/10.3390/ijms22031141
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dc.titleArtemether-loaded zein nanoparticles: An innovative intravenous dosage form for the management of severe malaria
dc.contributor.authorBoateng-Marfo, Yaa
dc.contributor.authorDong, Yuancai
dc.contributor.authorNg, Wai Kiong
dc.contributor.authorLin, Hai-Shu
dc.date.accessioned2022-10-11T08:03:48Z
dc.date.available2022-10-11T08:03:48Z
dc.date.issued2021-01-24
dc.identifier.citationBoateng-Marfo, Yaa, Dong, Yuancai, Ng, Wai Kiong, Lin, Hai-Shu (2021-01-24). Artemether-loaded zein nanoparticles: An innovative intravenous dosage form for the management of severe malaria. International Journal of Molecular Sciences 22 (3) : 1-22. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms22031141
dc.identifier.issn1661-6596
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/232146
dc.description.abstractArtemether, an artemisinin derivative, is used in the management of life-threatening severe malaria. This study aimed to develop an intravenous dosage form of artemether using nanotechnology. Artemether-loaded zein nanoparticles were prepared by modified antisolvent precipitation using sodium caseinate as a stabilizer. Subsequently, the physicochemical properties of the nanoparticles were characterized; the in vitro hemolytic property was examined with red blood cells, while the pharmacokinetic profile was evaluated in Sprague–Dawley rats after intravenous administration. The artemether-loaded zein nanoparticles were found to display good encapsulation efficiency, excellent physical stability and offer an in vitro extended-release property. Interestingly, encapsulation of artemether into zein nanoparticles substantially suppressed hemolysis, a common clinical phenomenon occurring after artemisinin-based antimalarial therapy. Upon intravenous administration, artemether-loaded zein nanoparticles extended the mean residence time of artemether by ~80% in comparison to the free artemether formulation (82.9 ± 15.2 versus 45.6 ± 16.4 min, p < 0.01), suggesting that the nanoparticles may prolong the therapeutic duration and reduce the dosing frequency in a clinical setting. In conclusion, intravenous delivery of artemether by artemetherloaded zein nanoparticles appears to be a promising therapeutic option for severe malaria. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
dc.publisherMDPI AG
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.subjectArtemether
dc.subjectArtemisinin
dc.subjectExtended release
dc.subjectHemolysis
dc.subjectIntravenous
dc.subjectNanoparticles
dc.subjectPharmacokinetics
dc.subjectSevere malaria
dc.subjectSodium caseinate
dc.subjectZein
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.doi10.3390/ijms22031141
dc.description.sourcetitleInternational Journal of Molecular Sciences
dc.description.volume22
dc.description.issue3
dc.description.page1-22
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