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Development and In-Vitro Evaluation of Plantago ovata Based Rapid Disintegrating Tablets of Labetalol Hydrochloride.

Authors :
Dubey, Abhay Kumar
Archana
Source :
Journal of Drug Delivery & Therapeutics; Jul/Aug2022, Vol. 12 Issue 4, p36-42, 7p
Publication Year :
2022

Abstract

Objectives: To avoid swallowing problems of conventional tablets and improved patient compliance Plantago Ovata based Labetalol HCl Rapid disintegrating tablets have been prepared. Methods: Six different (F1 to F6) batches of Labetalol HCl Rapid disintegrating tablets were developed by 'direct compression method' using Plantago ovata as a natural super-disintegrating agent. The formulated RDT were tested for angle of repose', densities like tapped and bulk density, Hausner's ratio, Carr's index like pre-compression parameters and for thickness, weight variation or weight uniformity, tablet hardness, % drug content or content uniformity, water absorption ratio', time require for wetting of tablets' means wetting time, in-vitro drug disintegration time and in-vitro drug dissolution studies under post-compression parameters of evaluation. Results: It was found that the all the results of these pre-compression and post-compression parameters comply with official standards. The drug release was determined using dissolution media of pH 6.8 phosphate buffer through in-vitro dissolution of drug. This study showed that a rapid drug release by prepared tablets. The optimized formulation F6 showed higher water absorption ratio, lower wetting time, minimum in-vitro disintegration time' and higher drug release amongst all the formulations. The F6 formulation was considered the best among all formulations. Conclusion: The prepared rapid disintegrating tablets shows rapid onset of action by quick drug release, minimize side effects and enhanced patient compliance. These prepared tablets containing selective alpha-1 and non-selective beta adrenergic antagonist' drug candidate Labetalol HCl, will be very useful in the treatment of high blood pressure with enhanced bioavailability. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22501177
Volume :
12
Issue :
4
Database :
Complementary Index
Journal :
Journal of Drug Delivery & Therapeutics
Publication Type :
Academic Journal
Accession number :
158134776
Full Text :
https://doi.org/10.22270/jddt.v12i4.5430