Solid Lipid Nanoparticles As Drug Carriers For Atovaquone
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Date
2013-03
Authors
Mohtar, Noratiqah
Journal Title
Journal ISSN
Volume Title
Publisher
Universiti Sains Malaysia
Abstract
Solid lipid nanoparticles of atovaquone (ATQ-SLNs) were prepared by high shear
homogenization method using tripalmitin, trilaurin, and Compritol 888 ATO as the
lipid matrix and hydrogenated soy lecithin, Tween 80 and, poloxamer 188 as the
surfactants. Optimization of the formulations was conducted using 6 sets of 24
factorial design study based on four independent variables which were homogenizing
cycle, concentration of lipid, concentration of main surfactant, and concentration of
co-surfactant. The dependent variables were particle size and polydistribution index.
The effect of the four independent variables towards the responses was analyzed
using ANOVA and response surface plots. Finally, the best formulations with the
highest entrapment efficiency were chosen from each lipid system which were TPT 8
and TLT 16 for tripalmitin and trilaurin system, respectively, while Compritol 888
ATO was excluded for further study. Lyophilization process
by using trehalose as the cryoprotectant was done to improve stability of both
formulations. Incorporation of trehalose during homogenization process showed an
improvement in the particle size and entrapment efficiency when compared to the
incorporation after homogenization in both formulations. TLT 16 DH was selected as
the final formulation with an average diameter of 84.63 ± 1.51nm before and 217.9 ±
8.42nm after lyophilization, and entrapment efficiency of 93.57 ± 3.07% before and
66.04 ± 1.74% after lyophilization process.
Description
Keywords
Solid Lipid Nanoparticles , Drug Carriers For Atovaquone