The Formulation and Evaluation of Gastro-Retentive Floating Tablets of Verapamil Hydrochloride
Abstract
Background: Verapamil Hydrochloride has a short biological half-life and undergoes extensive first-pass metabolism, necessitating frequent dosing. Gastro-retentive floating drug delivery systems offer prolonged gastric residence and sustained drug release, thereby improving therapeutic efficacy and patient compliance.
Objective: The present study aimed to formulate and evaluate gastro-retentive floating matrix tablets of Verapamil Hydrochloride using HPMC K4M and Xanthan Gum.
Methods: Tablets were prepared by the direct compression method using a 3² full factorial design. The formulations were evaluated for drug–polymer compatibility, pre-compression and post-compression characteristics, buoyancy, swelling index, in vitro drug release, drug release kinetics, and stability.
Results: FTIR and DSC studies confirmed drug–polymer compatibility. All formulations exhibited satisfactory physical properties and remained buoyant for 12 h. Floating lag time ranged from 62 ± 0.595 to 128 ± 0.598 s, while cumulative drug release after 12 h ranged from 85.1 ± 0.42% to 94.0 ± 0.23%. Drug release followed the Korsmeyer–Peppas model for most formulations, whereas a few exhibited Zero-order kinetics. Formulation F3 showed the shortest floating lag time (62 ± 0.595 s), highest drug release (94.0 ± 0.23%), and satisfactory stability under different storage conditions.
Conclusion: The optimized formulation (F3) demonstrated excellent buoyancy, sustained drug release, and stability, indicating its potential as a gastro-retentive floating drug delivery system for Verapamil Hydrochloride.
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Copyright (c) 2026 Shraddha P. Malpani, Dr. Nishan N. Bobade, Dr. Shrikant D. Pande

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