Author(s): Asija Rajesh, Kaur Manmeet, Asija Sangeeta

Email(s): asijar@gmail.com

DOI: Not Available

Address: Asija Rajesh*, Kaur Manmeet, Asija Sangeeta
Department of Pharmaceutics, Maharishi Arvind Institute of Pharmacy, Jaipur, Rajasthan, India.
*Corresponding Author

Published In:   Volume - 5,      Issue - 6,     Year - 2012


ABSTRACT:
In the present work, fast dissolving tablets of pioglitazone were prepared by direct compression method with a view to enhance patient compliance. Two superdisintegrants viz, crospovidone and croscarmellose sodium with different concentration were used. The prepared batches of tablets were evaluated for hardness, friability, weight variation, disintegration, wetting time, drug content and in vitro dissolution studies. Based on evaluating parameters, formulation prepared by using croscarmellose sodium and crospovidone were selected as optimized formulation. Finally, the optimized formulation was compared with marketed conventional formulation. Pioglitazone is a prescription drug of the class thiazolidinedione with hypoglycemic (antihyperglycemic, anti diabetic) action. Pioglitazone reduces insulin resistance in the liver and peripheral tissues; increases the expense of insulin-dependent glucose; decreases withdrawal of glucose from the liver; reduces quantity of glucose, insulin and glycated haemoglobin in the bloodstream. Following oral administration, in the fasting state, pioglitazone is first measurable in serum within 30 minutes, with peak concentrations observed within 2 hours. Food slightly delays the time to peak serum concentration to 3 to 4 hours, but does not alter the extent of absorption.


Cite this article:
Asija Rajesh, Kaur Manmeet, Asija Sangeeta. Formulation and evaluation of fast dissolving tablet of Pioglitazone. Research J. Pharm. and Tech. 5(6): June 2012; Page 817-821.

Cite(Electronic):
Asija Rajesh, Kaur Manmeet, Asija Sangeeta. Formulation and evaluation of fast dissolving tablet of Pioglitazone. Research J. Pharm. and Tech. 5(6): June 2012; Page 817-821.   Available on: https://rjptonline.org/AbstractView.aspx?PID=2012-5-6-11


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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

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