Literature DB >> 25888797

Development of taste masked caffeine citrate formulations utilizing hot melt extrusion technology and in vitro-in vivo evaluations.

Manjeet B Pimparade1, Joseph T Morott1, Jun-Bom Park2, Vijay I Kulkarni1, Soumyajit Majumdar3, S N Murthy1, Zhuoyang Lian4, Elanor Pinto4, Vivian Bi4, Thomas Durig4, Reena Murthy5, H N Shivakumar5, K Vanaja6, P C Kumar6, Michael A Repka7.   

Abstract

The objective of this study was to develop caffeine citrate orally disintegrating tablet (ODT) formulations utilizing hot-melt extrusion technology and evaluate the ability of the formulation composition to mask the unpleasant bitter taste of the drug using in vitro and in vivo methods. Ethylcellulose, along with a suitable plasticizer, was used as a polymeric carrier. Pore forming agents were incorporated into the extruded matrix to enhance drug release. A modified screw configuration was applied to improve the extrusion processability and to preserve the crystallinity of the API. The milled extrudates were subjected to dissolution testing in an artificial salivary fluid and investigations using e-tongue, to assess the extent of masking of bitter taste of the API. There was an insignificant amount of drug released from the formulation in the salivary medium while over 80% of drug released within 30 min in 0.1N HCl. ODTs were also developed with the extrudate mixed with mannitol and crospovidone. The quality properties such as friability and disintegration time of the ODTs met the USP specifications. The lead extrudate formulations and the ODTs prepared using this formulation were subjected to human gustatory evaluation. The formulations were found to mask the unpleasant taste of caffeine citrate significantly.
Copyright © 2015. Published by Elsevier B.V.

Entities:  

Keywords:  Ethylcellulose (EC); Hot-melt extrusion; Modified screw design; Pediatric and geriatric; Taste-masking

Mesh:

Substances:

Year:  2015        PMID: 25888797      PMCID: PMC4543393          DOI: 10.1016/j.ijpharm.2015.04.030

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


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