Author(s): Mangukia Dhruv K., Asija Rajesh, Patel Chirag J., Yadav Alpesh, Isha Shah, Sojitra Ishita S.

Email(s): dhruvmangukia@gmail.com

DOI: Not Available

Address: Mangukia Dhruv K. 1*, Asija Rajesh1, Patel Chirag J.1, Yadav Alpesh1, Isha Shah1, Sojitra Ishita S.2
1Maharishi Arvind Institute of Pharmacy, Mansarovar, Jaipur, Rajasthan, India.
2Parul Institute of Pharmacy, Vadodra, Gujarat, India.
*Corresponding Author

Published In:   Volume - 5,      Issue - 8,     Year - 2012


ABSTRACT:
Ondansetron HCl melt in mouth tablets were prepared with an intention for quick disintegration of tablet with minimum quantity of water. Reduced quantity of water also has an advantage in antiemetic action. This dosage form was formulated to achieve quick onset of action and maximize oral bioavailability. The purpose of the present research work was to compare the efficiency of different superdisintegrants on the mouth dissolving property of Ondansetron HCl tablets. Melt in mouth tablets of Ondansetron HCl were prepared using croscarmellose sodium, sodium carboxy methyl cellulose, alginic acid, crospovidone and sodium starch glycollate as superdisintegrants by direct compression technique. Prepared tablets were evaluated for weight variation, hardness, friability, content uniformity, wetting time, in vitro dispersion time and dissolution studies. In vitro dispersion time for all the prepared formulations was found to be in following order : In vitro dispersion was found to be rapid in F5 formulation. Sodium starch glycollate (SSG) showed faster dispersion of tablets among all other superdisintegrants.


Cite this article:
Mangukia Dhruv K. , Asija Rajesh, Patel Chirag J., Yadav Alpesh, Isha Shah, Sojitra Ishita S. Formulation and evaluation of melt in mouth tablets of Ondansetron HCl. Research J. Pharm. and Tech. 5(8): August 2012; Page 1089-1092.


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

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