The rationale of this research was to formulate and evaluate a gastro-retentive floating drug delivery system of Baclofen. Sustained
release gastro-retentive dosage forms enable prolonged and continuous input of the drug to the upper parts of gastrointestinal
tract and improve the bioavailability of the drug that is characterized by narrow absorption window and short half-life. Floating
tablets of Baclofen were prepared by effervescent approach by using sodium bicarbonate as the gas forming agent and hydrophilic
matrix forming polymers like HPMC K4M, HPMC K15M, HPMC K100M, Polyethylene oxide WSR-301,Polyethylene oxide WSR- 303
and Xanthan, guar gum. Direct compression technique was employed for the preparation of tablets. The prepared tablets were evaluated in terms of their pre-compression parameters (before compression), physical appearance, hardness, friability, weight
variation, content uniformity, in-vitro buoyancy and in-vitro drug release. The optimized formulation (F12) containing xanthan gum40% and sodium bicarbonate-12.5% sustained the drug release (98.47±0.71%) upto 24 h and remained buoyant for 24 h with a
floating lag time of 20.33±6.03 seconds. The optimized formulation (F12) was subjected to various kinetic release investigations and
it was found that the mechanism of drug release was predominantly non-fickian (anomalous) diffusion. Optimized formulation (F12)
showed no significant change in physical appearance, drug content, floating properties and drug release after storage at 40°C/75%
RH for three months. Finally the formulation was found to be economical and may overcome the draw backs associated with the
drug during its absorption
Keywords: Salbutamol, disintegrants, Pleurotus tuber-regium, FDTs