The goal of the present study was to develop a gastric floating drug delivery system (GFDDS) of Zidovudine (AZT), an antiretroviral drug. The tablets of AZT were prepared by direct compression technique using HPMC K15M as a polymer with other standard excipients. The mixture of sodium bicarbonate and citric acid was used as gas generating agent. Preliminary studies demonstrated that the, tablets remained buoyant for over 15 hr in the release medium(pH 1.2). 32 factorial design was applied to systematically optimize the drug release profile. The proportion of retardant material HPMC K15 M (X1) and gas generating agent (X2) were selected as independent variables. The time required for 50% drug release t50% (Y1) was selected as dependent variable. The optimization was carried out using 50% 1 softwares like statplus. The derived polynomial equations for t were verified by two check point formulations, which showed that factor X1 and X2 significantly affects the studied dependent variable. The non Fickian diffusion release 1 2 transport was confirmed as the release mechanism for the optimized formulation. The predicated values agreed well with the experimental values and the results demonstrated feasibility of the model in the development of GFDDS.
Key words: 32 factorial design, Zidovudine, HPMC, floating system, Non Fickians diffusion.