Design and Development, In vitro Characterization of Gastro Retentive Floating Tablets of Anti-Ulcer Drug
Research Article
Keywords:
Famotidine, Floating System, Antiulcer Activity, HPMC K4M, HPMC K15MAbstract
The objective of this study was to design a delayed release formulation of Famotidine, aimed at sustaining therapeutic drug concentrations for an extended period exceeding 12 hours. Famotidine was administered at a fixed dose of 40 mg, and the total tablet weight was set at 250 mg. Hydroxypropyl methylcellulose (HPMC) derivatives, specifically HPMC K4M and HPMC K15M, were employed as polymer matrices at concentrations of 20, 40, and 80 mg. All formulations successfully met established physicochemical criteria, falling within predetermined limits. Dissolution studies revealed that formulation F6 exhibited superior and desired drug release characteristics, achieving a release rate of 96.33% within the 12-hour timeframe. Furthermore, the release mechanism of this formulation was found to conform to the Higuchi release kinetics model
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