Department of Pharmaceutics, Babaria Institute of Pharmacy, BITS Edu Campus, Vadodara-Mumbai NH-8, Varnama, Vadodara-391240, Gujarat, India
*Corresponding Author E-mail: apmcashok@gmail.com
Online published on 3 June, 2021.
The objective of present investigation was comparison of porous carriers to increase the dissolution properties of BCS class II drug Ziprasidone. Solvent evaporation method was used for the adsorption of ziprasidone on various porous carriers. Three different porous carriers namely Florite, Neusilin US2, Sylysia 350 were used in the study. Prepared microparticles were characterised for invitro drug release, SEM, XRD and DSC. The optimized formulation containing ziprasidone: florite microparticles had high drug release (94.88% in 45 min) than plain ziprasidone tablets (21.13% in 45 min) which is due to increase in surface area and decrease in crystallinity of drug after adsorption onto porous carrier
Ziprasidone, Porous carrier, Florite, Dissolution, Microparticles
