| Literature DB >> 28067090 |
Henry Nettey1, Grace Lovia Allotey-Babington1,2, Isaac Somuah1, N'guessan Benoit Banga1, Barima Afrane1, Seth Kwabena Amponsah1, Henrietta Annor1, Henry Darko1, Kwame Hanson1, Anoa Aidoo1, Marisa Nyarkoa Broni1, Clement Sasu1, Alexander Nyarko1.
Abstract
The aim of this study was to formulate, characterise and evaluate the activity of amodiaquine microparticles against Leishmania donovani. Microparticles were formulated by encapsulating the drug in bovine serum albumin using the spray-dryer method. The microparticles were evaluated for size, zeta potential, drug content, encapsulation efficiency and in vitro release profile. The size range of the microparticles formulated was between 1.9 and 10 μm with an average zeta potential of -25.5 mV. Of the expected 20% drug loading, an average of 18.27% was obtained giving an encapsulation efficiency of 91.35%. Pharmacokinetic profile of amodiaquine improved with microencapsulation of the drug with Cmax, AUC0→48 and t1//2 all significantly higher than amodiaquine solution. Amodiaquine microparticles showed an overall higher bioavailability and hence were more effective in eliminating intra-tissue parasites than the drug solution. It would therefore be expected that the formulated microparticles will be more effective in treating visceral leishmaniasis.Entities:
Keywords: Amodiaquine; Leishmania donovani; albumin; microparticles; pharmacokinetics
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Year: 2017 PMID: 28067090 DOI: 10.1080/02652048.2017.1280094
Source DB: PubMed Journal: J Microencapsul ISSN: 0265-2048 Impact factor: 3.142