Development and in vitro evaluation of floating rosiglitazone maleate microspheres.

BACKGROUND: Various approaches have been used to retain the dosage form in stomach as a way of increasing the gastric residence time, including floatation systems; high-density systems; mucoadhesive systems; magnetic systems; unfoldable, extensible, or swellable systems; and superporous hydrogel systems. AIM: The objective of this study was to prepare and evaluate floating microspheres of rosiglitazone maleate for the prolongation of gastric residence time. METHOD: The microspheres were prepared by solvent diffusion-evaporation method using ethyl cellulose and hydroxypropylmethylcellulose. A full factorial design was applied to optimize the formulation. RESULTS: Preliminary studies revealed that the polymer:drug ratio, concentration of polymer, and stirring speed significantly affected the characteristics of microspheres. The optimum batch exhibited a prolonged drug release, remained buoyant for >12 hours, high entrapment efficiency, and particle size in the order of 350 microm. CONCLUSION: The results of 32 full factorial design revealed that the concentration of ethylcellulose 7 cps (X(1)) and stirring speed (X(2)) significantly affected drug entrapment efficiency, percentage release after 8 h and particle size of microspheres.