4.7 Article

Artemether-Loaded Zein Nanoparticles: An Innovative Intravenous Dosage Form for the Management of Severe Malaria

Journal

Publisher

MDPI
DOI: 10.3390/ijms22031141

Keywords

artemether; artemisinin; extended release; hemolysis; intravenous; nanoparticles; pharmacokinetics; severe malaria; sodium caseinate; zein

Funding

  1. Academic Research Fund Tier 1 grant from the Ministry of Education, Singapore [R-148-000-215-112]
  2. Singapore International Graduate Award

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The study demonstrated that intravenous delivery of artemether using nanotechnology could extend the drug's residence time in the body and reduce dosing frequency. This method exhibits good stability, excellent sustained-release properties, and may offer a promising therapeutic option for severe malaria.
Artemether, 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 similar to 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 artemether-loaded zein nanoparticles appears to be a promising therapeutic option for severe malaria.

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