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The International Journal of Gastroenterology and Hepatology Diseases

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Research Article

Development and In vitro Evaluation of Pantoprazole-Sustained Release Effervescent Floating Tablets for Effective Management of Ulcer

Author(s): Onyishi Ikechuchukwu Virgilus, Chime Salome Amarachi*, Ike-Onyishi Ugochi Elizabeth, Ndukauba Ijeoma, Akpa Paul Achile*, Ezeudoh Clara Chigozie and Ogbonna Emmanuella Tochuchukwu

Volume 3, 2024

Published on: 25 June, 2024

Article ID: e250624231309 Pages: 9

DOI: 10.2174/0126662906296242240603104029

Price: $65

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Abstract

Introduction: Pantoprazole is a very suitable drug for the treatment of numerous acid-related conditions in humans and mammals. Owing to its short half-life (0.9 - 1.9 h), it is ideal for sustained release formulation.

Methods: This study was aimed at developing pantoprazole gastroretentive (GR) controlledrelease tablets and to determine the effects of this formulation and processing parameters on drug release and other critical quality attributes of directly compressed tablets produced using different matrix-forming polymers, namely, Hydroxypropyl methylcellulose (HPMC), chitosan, sodium alginate, maize starch, kappa- carrageenan, and propyl vinyl pyrrolidine PVP K- 30 when formulated into effervescent Floating Drug Delivery Systems (FDDS).

Results: The buoyancy lag time of less than 5 seconds and a total floating time of more than 12 hours for all batches is a good indication of achieved floatation for FDDS.

Conclusion: Validation processes initiated with the five batches indicated that the polymer blends had the potential for the formulation of pantoprazole FDDS and, hence, could enhance patient compliance and better treatment outcomes due to their sustained release potentials.

Keywords: Buoyancy lag time, controlled release tablets, gastro-retentive drug delivery- effervescence tablets, floating tablets, k-carrageenan, ulcer, proton pump inhibitors, pantoprazole.

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