Author(s):
Hamid Khan, Javed Ali
Email(s):
khanhamid770@gmail.com
DOI:
10.5958/0975-4377.2017.00004.0 
Address:
Hamid Khan1*, Javed Ali2
1Associate Professor, JK College of Pharmacy, Bilaspur, CG, India-495001
2Department of Pharmaceutics, Faculty of Pharmacy, Hamdard University, New Delhi, India-110062
*Corresponding Author
Published In:
Volume - 9,
Issue - 1,
Year - 2017
ABSTRACT:
The formulation and in-vitro evaluation of matrix tablets containing telmisartan as sustained release using low viscosity grade HPMC as the matrix forming hydrophilic polymer by wet granulation method. The tablets were subjected to in-vitro drug release study in hydrochloric acid buffer of pH 1.2 (0.1N) with 1% w/v SLS using USP paddle apparatus. The drug released at various time intervals were determined by validated UPLC-PDA method. The prepared tablets showed better sustained release effect when compared with marketed tablets. The drug release mechanism from hydrophilic polymer was proposed. The formulated tablets provided sustained release of telmisartan over a period of 24 h.
Cite this article:
Hamid Khan, Javed Ali. Formulation and In-Vitro Evaluation of a Sustained Release Matrix Tablet of Telmisatan. Res. J. Pharm. Dosage Form. & Tech. 9(1): Jan.-Mar. 2017; Page 19-23. doi: 10.5958/0975-4377.2017.00004.0
Cite(Electronic):
Hamid Khan, Javed Ali. Formulation and In-Vitro Evaluation of a Sustained Release Matrix Tablet of Telmisatan. Res. J. Pharm. Dosage Form. & Tech. 9(1): Jan.-Mar. 2017; Page 19-23. doi: 10.5958/0975-4377.2017.00004.0 Available on: https://rjpdft.com/AbstractView.aspx?PID=2017-9-1-4