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- DocumentoIn this work, the purpose of the study was to formulate and optimize azilsartan nanoparticles by employing factorial design. The nanoparticles were prepared successfully with a modified emulsification method by using biodegradable and biocompatible polymer poly (L-lactide) (PLA). Various process parameters were manipulated to investigate their effects on particle size, polydispersity index, entrapment efficiency and percentage of cumulative drug release after 12 hours of formulated nanoparticles. In addition, morphology and compatibility between the drug and polymer of nanoparticles were studied with scanning electron microscope (SEM) and FTIR studies. The optimized formulation had a particle size range of 267.14 - 280.01 nm, PDI range of 0.101-0.361, entrapment efficiency range of 69.14 - 84.72% and % CDR after 12 hours 56.11 - 67.01%. The nanoparticles were confirmed to be spherical in shape by SEM results while FTIR results established the compatibility of components of the formulatenviado porRAPPORTS DE PHARMACIE
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