چكيده لاتين :
The purpose of this study was to prepare and characterize nimodipine loaded
microspheres using ethyl cellulose (EC) as a carrier polymer through an emulsion
solvent evaporation method. These evaluations characterized the pattern of drug
release from prepared microspheres. Nimodipin loaded microspheres were prepared
using an emulsification solvent evaporation method. The effect of process variables
such as stirring rate, drug polymer ratio in the organic phase, the viscosity of the
dispersed phase and the emulsifier concentration, on the morphology of microspheres,
particle size distribution, drug content and in vitro release profile of nimodipine were
investigated. The prepared microspheres were spherical with smooth surface. The
mean diameter of microspheres decreased with increasing the concentration of the
emulsifier in the continuous phase and stirring rate of the medium. However,
increasing the viscosity of the dispersed organic phase increased the particle size
of microspheres. Both the drug and polymer concentration in the organic phase
increased the entrapment of nimodipine in ethyl cellulose microspheres. Drug
content of the microspheres was lowered by increasing the viscosity of the dispersed
phase and increasing the concentration of poly vinyl alcohol. The rate of drug
release from microspheres was directly influenced by the drug to polymer ratio, as
any increase in this ratio allowed the higher release rates from microspheres. The
higher the polymer concentration the lower was the rate of drug release from
microspheres.
