preparation and characterization of dexamethasone microemulsion based on pseudoternary phase diagram

results the results showed that the maximum oil was incorporated in microemulsion system that contained surfactant to cosurfactant ratio of 4:1. the mean droplet size range of microemulsion formulation was in the range of 5.09 to 159 nm, and its refractory index (ri) and ph were 1.44 and 7, respectively. viscosity range was 57-226 cps. drug release profile showed that 48.18% of the drug released in the 24 hours of experiment. also, hexagonal, cubic and lamellar structures were seen in the sem photograph and xrd peak of microemulsions. materials and methods the prepared microemulsions were evaluated regarding their particle size, zeta potential, x-ray scattering, conductivity, stability, viscosity, differential scanning calorimetry (dsc), scanning electron microscopy (sem), refractory index (ri), ph, and x-ray diffraction (xrd). conclusions this study demonstrated that physicochemical properties and in vitro release were dependent upon the contents of s/c, water, and oil percentage in formulations. saxs technique and sem obtained important information about microstructure of microemulsions. w/o and bicontinuous microemulsion with different microstructures were found in formulations. background the increased incidence of inflammatory diseases has necessitated the need to search for new topical dosage form of dexamethasone. objectives the purpose of the present study was the preparation and evaluation of novel microemulsion as a topical delivery system for dexamethasone by mixing appropriate amount of surfactant including tween 80 and labrasol, cosurfactant such as capryol 90 and oil phase including labrafac lipophile wl-transcutol p (10:1 ratio).