FORMULATION AND EVALUATION OF SUSTAINED RELEASE MATRIX TABLET OF IMDOMETHACIN BY WET GRANULATION METHOD
Dr. Amit B. Patil*, Dr. Vikas Jain, Dr. D. V. Gowda and Shweta Betala
Abstract
The main aim of the study was to develop sustained release matrix
tablet of Indomethacin by wet granulation technique. Indomethacin is a
non- steroidal anti-inflammatory drug and COX inhibitor. By wet
granulation method, all the ingredients were taken and passed through
sieve no. 40 and granulated by passing through sieve no. 25, the matrix
tablet were compressed by using 10 station Rimek mini press. The
preparation was evaluated for micromeritics properties such as bulk
density was achieved on an average 0.424 gm/ml, tapped density was
0.494 gm/ml, average Carrs’s index 1.214, and angle of repose
28.136º. Followed by physicochemical properties i.e. hardness test
4.93 kg/cm3, weight variation 199.44 mg, friability 0.256%. The
percentage drug liberated was found between 83.02% to 98.19% due to the various
concentration of HPMC K100M. The stability study, shows that percentage drug content
determined periodically at a temperature of 400C at 75% RH evaluated at different time
intervals, the control sample and test sample are kept at different storage condition at
different RH. The granules show good flow properties and test performed are within standard
limits. The stability study show that preparation was found to be stable. Drug release studied
was carried out in 0.1N for 1.5 hours and till 12th hour in 7.4 pH Phosphate buffer. The
release suggested that the formulations FA to FE showed a relationship as decrease in drug
release as increase in concentration of HPMC K 100, where FA had the lowest concentration
and FE having the highest concentration.
Keywords: Indomethacin, Sustained release, Wet Granulation, HPMC K100, Gaur Gum.
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