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Development of mouth dissolving tablets of clozapine using two different techniques. | LitMetric

Development of mouth dissolving tablets of clozapine using two different techniques.

Indian J Pharm Sci

Department of Pharmaceutics, K. L. E. S's College of Pharmacy, Nehrunagar, Belgaum-590 010, India.

Published: July 2011

AI Article Synopsis

  • Mouth dissolving tablets are a new type of medication that are easy to take and work quickly, particularly for clozapine, a medication used for mental health.
  • Researchers created four different tablet formulations using two methods—direct compression and sublimation—and tested their physical and chemical properties.
  • The direct compression method showed superior results, with faster disintegration times (25 to 35 seconds) and a higher drug release percentage (99.79%) compared to the sublimation method (93.58%) in 12 minutes.

Article Abstract

Mouth dissolving tablets constitute an innovative dosage form that overcomes the problems of swallowing and provides a quick onset of action. In view of enhancing bioavailability an attempt has been made to study two different methods direct compression and sublimation in formulation of mouth dissolving tablets of clozapine. Total four formulations using various superdisintegrants and subliming agents were prepared. All prepared formulations were evaluated for physico-chemical parameters. The formulations exhibited good disintegration properties with total disintegration time in the range of 25 to 35 s. Comparative evaluation of two methods showed direct compression method is a better alternative to sublimation method as its formulations rapidly disintegrate in oral cavity. In vitro cumulative percentage drug release for formulations prepared by direct compression with explotab superdisintegrants shows 99.79 while sublimation method using camphor 93.58 release in 12 min. Kinetic studies indicated that all the formulations followed first order release with diffusion mechanism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792538PMC
http://dx.doi.org/10.4103/0250-474X.44611DOI Listing

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