FORMULATION AND EVALUATION OF MOUTH DISSOLVING TABLET OF GLIPIZIDE BY SOLID DISPERSION
AbstractThe aim of the present research work was to enhance the solubility of Glipizide by solid dispersion method and to formulate a mouth dissolving tablet. Drugs are more frequently taken by oral administration. The solubility of Glipizide enhanced with different ratios of CCS by the kneading method .In-vitro release profile of solid dispersion obtained in Ph 6.8 phosphate buffer indicate that 100% drug release found within 20 min. These solid dispersions were directly compressed into tablets using sodium starch glycolate, crosspovidone and pregelatinised starch in different concentrations as a superdisintegrants. The prepared tablets containing the solid dispersion of Glipizide had sufficient strength of 1.5-2 kg/cm2. The disintegrated in the oral cavity within 21 sec. contain crosspovidone (5%) as superdisintegrant.
Article Information
54
4929-4937
977KB
1518
English
Ijpsr
Yogesh L. Jadhav* and Parashar Bharat
Department of Pharmaceutics, Manav Bharti University , Solan, Himachal Pradesh, India
jadhav.yogesh530@gmail.com
25 August, 2012
05 November, 2012
19 November, 2012
54. http://dx.doi.org/10.13040/IJPSR.0975-8232.3(12).4929-37
01 December, 2012
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