Formulation and evaluation of sustained release matrix tablet of captopril

Authors

  • SIMRAN SHIVDAS PAWAR SPPU
  • Prashant S. Malpure
  • Santosh S Surana
  • Jayashri S Bhadane

Abstract

The objective of the present study was to study the effect of polymers on sustained release of Captopril from tablets. Compatibility was studied by Fourier transform infrared spectroscopy and DSC. The tablets were prepared by direct compression technique using Xanthan gum and Ethyl Cellulose. The prepared matrix tablets were evaluated for their physicochemical parameters such as weight variation, hardness, friability, content uniformity and in-vitro dissolution. Pre and post compression parameters were evaluated and all the parameters were found within the limit. The drug release data were subjected to different models in order to evaluate release kinetics and mechanism of drug release. Formulation F4 was selected as best formulation. The dissolution of formulation F4 can be Shows Non-fickian drug release mechanism.

DOI

https://doi.org/10.22270/jddt.v9i4-A.3406

Published

2019-09-07
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How to Cite

1.
PAWAR SS, Malpure PS, Surana SS, Bhadane JS. Formulation and evaluation of sustained release matrix tablet of captopril. J. Drug Delivery Ther. [Internet]. 2019 Sep. 7 [cited 2025 Dec. 5];9(4-A):260-8. Available from: https://jddtonline.info/index.php/jddt/article/view/3406

How to Cite

1.
PAWAR SS, Malpure PS, Surana SS, Bhadane JS. Formulation and evaluation of sustained release matrix tablet of captopril. J. Drug Delivery Ther. [Internet]. 2019 Sep. 7 [cited 2025 Dec. 5];9(4-A):260-8. Available from: https://jddtonline.info/index.php/jddt/article/view/3406