Formulation and Evaluation of Metformin HCL Gastroretentive Floating Sustained Released Tablet

The Metformin HCl Gastroretentive Floating Sustained Release Tablet was formulated using the Wet Granulation method. This tablet incorporates an effervescent system, where Hydroxypropyl Methylcellulose (HPMC) K 100, a swellable polymer, facilitates the floating mechanism. Sodium bicarbonate is employed to create the effervescent system. A synergistic combination of HPMC K 100 and Xanthan Gum enhances the sustained release profile of the formulation. The prepared gastroretentive floating tablets were evaluated for various pharmaceutical parameters, including bulk density, tapped density, angle of repose, Carr’s index, weight variation, friability, and in vitro dissolution studies, along with the total floating time. The results from the optimized batch were satisfactory, indicating favorable flow properties. Both weight variation and friability were within the pharmacopoeial limits. In vitro dissolution testing revealed a maximum drug release of 99.10% within 8 hours.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-05-31
DOI
https://doi.org/10.5281/zenodo.15566054
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
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article

Formulation and Evaluation of Metformin HCL Gastroretentive Floating Sustained Released Tablet

Zenodo (CERN European Organization for Nuclear Research)
Drug Solubulity and Delivery Systems
article

Formulation and Evaluation of Metformin HCL Gastroretentive Floating Sustained Released Tablet

article en

Abstract

The Metformin HCl Gastroretentive Floating Sustained Release Tablet was formulated using the Wet Granulation method. This tablet incorporates an effervescent system, where Hydroxypropyl Methylcellulose (HPMC) K 100, a swellable polymer, facilitates the floating mechanism. Sodium bicarbonate is employed to create the effervescent system. A synergistic combination of HPMC K 100 and Xanthan Gum enhances the sustained release profile of the formulation. The prepared gastroretentive floating tablets were evaluated for various pharmaceutical parameters, including bulk density, tapped density, angle of repose, Carr’s index, weight variation, friability, and in vitro dissolution studies, along with the total floating time. The results from the optimized batch were satisfactory, indicating favorable flow properties. Both weight variation and friability were within the pharmacopoeial limits. In vitro dissolution testing revealed a maximum drug release of 99.10% within 8 hours.

Zenodo (CERN European Organization for Nuclear Research)
Clean water and sanitation
Openalex Percentile: Top 61%
Drug Solubulity and Delivery Systems
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