<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>817</id><JournalTitle>FORMULATION AND EVALUATION OF NANOSUSPENSION BY EMULSIFICATION METHOD</JournalTitle><Abstract>Olmesartan medoxomil (OLM), an anti-hypertensive agent administered orally has absolute bioavailability of
only 26% due to the poor aqueous solubility. The present investigation aimed at enhancing the oral bioavailability of OLM
by improving its solubility and dissolution rate by preparing nanosuspensions. The nanosuspensions of OLM were
prepared using emulsification solvent evaporation method. Various formulation as well as process parameters were
optimized in order to achieve desirable size and saturation solubility. Characterization of the prepared nanosuspension was
done with respect to particle size, zeta potential, saturation solubility, dissolution rate, morphology study (SEM), in-vitro
dissolution study. The results indicated that Increase in the stabilizer concentration of PVP K90 shows 98.65% of drug
release, so the formulations prepared by using PVP K90 releases more drug release at the end of 30mins than the other
stabilizers and follows first order kinetics. Nanosuspension seems to be a promising approach for bioavailability
enhancement because of the simple method of its preparation and its universal applicability.</Abstract><Email>jyoshnagolkonda@gmail.com</Email><articletype>Research</articletype><volume>10</volume><issue>2</issue><year>2019</year><keyword>Olmesartan medoxomil, PVP K90, Poloxamer 184, SEM.</keyword><AUTHORS>Jayasree G,Praveen Kumar J,Umasankar K,Jayachandra Reddy P</AUTHORS><afflication>Jayasree G,Praveen Kumar J,Umasankar K,Jayachandra Reddy P</afflication></Article></Articles>