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Journal :   Research Journal of Pharmacy and Technology

Volume No. :   4

Issue No. :  8

Year :  2011

Pages :   1197-1200

ISSN Print :  0974-3618

ISSN Online :  0974-360X


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Extrusion Process for High Active Pharmaceutical Ingredient Loading That Exhibit Controlled Release: Formulations and Evaluation Thereof



Address:   Shaik Parveen Begum1, R.K. Mohamed Mutahar1,2, B.M. Dinesh3, C.S.R. Lakshmi1 and L.V.G. Nargund1
1Dept. of Pharmaceutics, Nargund College of Pharmacy, Bangalore, Karnataka, India.
2Research Scholar, Dept. of Pharmaceutics, Karpagam University, Coimbatore, Tamil Nadu, India.
3Dept. of Pharmaceutics, K.L.E.S. College of Pharmacy, Bangalore, Karnataka, India.
*Corresponding Author
DOI No: Not Available

ABSTRACT:
Drugs required in a large dose size are difficult to design into a matrix based controlled release drug delivery system (CRDDS) because of the requirement of high amounts of polymers or other matrix formers, along with general excipients. In order to overcome this limitation, preparation of matrix based CRDDS containing high dose of active pharmaceutical ingredient (API) using extrusion as a process were formulated and evaluated which forms the backbone of the present research. Tablets extruded directly from the calibrated modified tablets extruder die exhibited extended release properties, excellent content uniformity; exceptional tablet hardness and friability results over control samples produced via direct compression and showed compliance with pharmacopoeial standards. The in vitro drug release data justifies the release process is diffusion-controlled as all the formulations best fitted into first order release kinetics and Higuchi’s equation. To confirm diffusion mechanism results, the data were fit into Korsmeyer- Peppas model, which revealed anomalous transport kinetics. The accelerated stability studies of optimized formulations TEM.2 made it clear that only negligible amount of drug content degraded. Release pattern was almost unaffected and could be claimed to be stable at the end of six months. It can be concluded that, apart from direct compression method of preparation of controlled release matrix tablets of nicotinic acid, extrusion process can also be successfully used as an effective method for the preparation tablets requiring high dose of API.
KEYWORDS:
Extrusion, Matrix tablets, Nicotinic acid, Stability studies.
Cite:
Shaik Parveen Begum, R.K. Mohamed Mutahar, B.M. Dinesh, C.S.R. Lakshmi, L.V.G. Nargund. Extrusion Process for High Active Pharmaceutical Ingredient Loading That Exhibit Controlled Release: Formulations and Evaluation Thereof. Research J. Pharm. and Tech. 4(8): August 2011; Page 1197-1200.
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