Formulation and in vitro evaluation of glucosamine hydrochloride modified release tablets

  • Sambasiva Rao Maram Department of Pharmaceutical Sciences, JNTUH Campus, Kukatpally, Hyderabad- 500085, India
  • Vidyadhara S Chebrolu Hanumaiah College of Pharmacy, Guntur-522002, Andhra Pradesh, India
  • Raju NSV Genovo Development Services Limited, Bangalore-560099, Karnataka, India

Abstract

The present study was aimed towards the formulation and evaluation of Glucosamine Hydrochloride modified release tablets of 1500mg tablets in aiming to control the release over 24hours with bi-phasic release model as immediate release followed by controlled release of the dosage form. Around 40% of Glucosamine Hydrochloride i.e., 600mg was aimed to release immediately and remaining 60% of Glucosamine Hydrochloride was aimed to release in a controlled manner. Different grades at different concentrations of hydroxy propyl methylcellulose were used to achieve controlled release. Blend parameters, Physical parameters and Dissolution profile were taken as the basis to optimize the controlled release tablet. It was observed that formulation F7 was able to control the release of Glucosamine till 24hrs.

Keywords: Accelerated stability, Bi-Phasic release, Glucosamine hydrochloride, HPMC K100M, HPMC K200M, In-vitro dissolution, Modified release

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Published
2012-01-25
Citations
How to Cite
Sambasiva Rao Maram, Vidyadhara S, & Raju NSV. (2012). Formulation and in vitro evaluation of glucosamine hydrochloride modified release tablets. International Journal of Research in Pharmaceutical Sciences, 3(1), 84-88. Retrieved from https://pharmascope.org/index.php/ijrps/article/view/1001
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Original Articles
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