Author(s): Deepak Khobragade, Sunil Kumar, Arun Kotha, Richa Gupta, K. Ravalika

Email(s): ksdeepak31@gmail.com

DOI: 10.5958/0975-4377.2016.00024.0   

Address: Deepak Khobragade, Sunil Kumar, Arun Kotha, Richa Gupta, K. Ravalika
Vijaya College of Pharmacy, Hyderabad-501 511, Telangana, India
*Corresponding Author

Published In:   Volume - 8,      Issue - 3,     Year - 2016


ABSTRACT:
Most of the ayurvedic medicines are in the form of powder and they may have some kind of unacceptable or bitter taste and have problem of patient compliance. Medicines in powder form have problem of administration of accurate dose with ease. Furthermore it needs water or honey for administration and chances of spoilage and waste are more. Formulation of Oro-dispersible tablets which rapidly disintegrate in mouth will be the best remedy for efficient use of ayurvedic powders. The aim of this study was to formulate oro-dispersible tablets of ayurvedic polyherbal powder Sitopaladi and Talisadi using various excipients like super-disintegrants and sweeteners and compare the efficacy in vivo using rats. The cough suppressing activities of powder and tablets was evaluated by counting bouts of cough in control group and treated group rats with powders and ODT. Codeine was taken as standard anti-tussive drug for our research. The cough bouts were produced in rats by exposure to SO2 generated by reaction of Na2SO3 and water in a Desiccator. The test results show that there is very little change in the activity of formulated tablets and pure ayurvedic powder. Thus it can be concluded from the study that that formulation of oro-dispersible tablets of ayurvedic powder preparation not only results in improving acceptability, ease and accuracy of administration without affecting efficiency of powder ayurvedic preparations like Talisadi and Sitopaladi.


Cite this article:
Deepak Khobragade, Sunil Kumar, Arun Kotha, Richa Gupta, K. Ravalika. Formulation and in vivo evaluation of oro-dispersible tablets of ayurvedic powders Sitopaladi and Talisadi. Res. J. Pharm. Dosage Form. & Tech. 2016; 8(3): 177-180. doi: 10.5958/0975-4377.2016.00024.0


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