Abstract
Background: Floating tablets extend drug residence time, enhance bioavailability and
promote the delivery of local drugs to the stomach. With this objective, floating tablets were
prepared for the treatment of gastric ulcers containing aqueous extract of liquorice and Isabgol.
Methods: Tablets containing HPMC K100M (hydrophilic polymer), liquorice extract, sodium
bicarbonate (gas generating agent), talc, and magnesium stearate were prepared using direct
compression method. Physical parameters of formulations such as diameter, thickness, hardness,
friability, weight uniformity, drug content, buoyancy time, dissolution, and the mechanism for drug
release, were assessed. The formulations have been optimized based on buoyancy time and invitro
drug release.
Results: The diameter of all formulations was in the range 11.310-11.833 mm; thickness was in the
range 4.02-4.071 mm. The hardness ranged from 3.1 to 3.4 kg/cm. All the formulations passed the
USP requirements for friability and uniformity of weight. All tablet formulations had a buoyancy
period of less than 5 min and throughout the research, the tablet stayed in floating condition. All
tablet formulations were accompanied in drug discharge by zero-order kinetics and Korsmeyer-
Peppas model.
Conclusion: It was discovered that the optimized formulation was F7, which released 98.5 percent
of the drug in 8 hr. in-vitro, while the buoyancy time was 3.5 min. For gastroretentive drug
delivery systems, formulations containing Isabgol, sodium bicarbonate and HPMC K100 M in
combination may be promising.
Keywords:
Nutraceutical, floating tablets, isabgol, liquorice extract, gastric ulcer, floating drug delivery system.
Graphical Abstract
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