Formulation and Evaluation of Indapamide Hemihydrate Sustained Release Tablets
DOI:
https://doi.org/10.21276/apjhs.2022.9.1.08Keywords:
Indapamide, Sustained release, Hypertension, In vitro dissolution, Wet granulationAbstract
The aim of the study is to formulate and to evaluate the indapamide SR tablet for the treatment of hypertension. Literature survey shows that indapamide is an anti-hypertensive and diuretic drug. The drug has been released up to 6–15 h, after taken orally. These tablets are absorbed into the systemic circulation and blood level shows the considerable peak of drug. It has been formulated as sustained release form for the betterment of therapeutic index and for maintaining constant blood levels. From the study, it has been concluded that HPMC shows the best results for the extending the release of drug. Wet granulation method is used for the preparation of these tablets. The compatibility study for optimized formulation shows satisfactory results. The evaluation of tablets was done for the hardness, friability, weight variation, thickness, drug content, in vitro buoyancy study, swelling index, in vitro dissolution studies, and stability study.
Downloads
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2022 Ayush Garg, Amul Mishra
This work is licensed under a Creative Commons Attribution 4.0 International License.
Asian Pacific Journal of Health Sciences applies the Creative Commons Attribution (CC-BY) license to published articles. Under this license, authors retain ownership of the copyright for their content, but they allow anyone to download, reuse, reprint, modify, distribute and/or copy the content as long as the original authors and source are cited. Appropriate attribution can be provided by simply citing the original article.