ABSTRACT
Sustained release Miglitol-loaded poly (d, l-lactide-co-glycolide) (PLGA) microparticles were prepared using high pressure homogenization-solvent evaporation method. 23 full factorial design was employed to study effect of independent variables (X1-Polymer amount; X2-Surfactant concentration and X3-Homogenization Pressure) on percent encapsulation efficiency (%EE) as response. The microparticles produced were characterized for particle size, morphology, % EE, drug polymer compatibility and in vitro drug release. An average particle size of Miglitol-loaded PLGA microparticles was 230.1 nm and found almost spherical with smooth surface. % EE ranged from 58.7% ± 2.11 to 86.5% ± 0.24 depending on the polymer amount, surfactant concentration and homogenization pressure. An absence of chemical interaction between drug-polymer and reduction in % crystallinity of drug was confirmed by FTIR and X-ray diffraction analysis respectively. In vitro release studies showed a sustained release of Miglitol from microparticles up to 12 hrs.
GRAPHICAL ABSTRACT
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Acknowledgement
Authors are very much thankful to Glenmark Pharmaceuticals, Nashik, India for providing gift sample of Miglitol (MGL) and PURAC biochem, Holland for providing gift sample of Poly (D, L-lactide-glycolide) −75:25 respectively.