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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/14125
Title: THEOPHYLLINE LOADED GASTRORETENTIVE FLOATING TABLETS BASED ON HYDROPHILIC POLYMERS: PREPARATION AND IN VITRO EVALUATION
Authors: KHAN, FERDOUS
MILLAT IBN RAZZAK, MD. SHAIKHUL
RAHMAN KHAN, MD. ZIAUR
ABUL KALAM AZAD, MOHAMMAD
AHMED CHOWDHURY, JAKIR
REZA, MD. SELIM
Keywords: Gastroretentive dosage form
floating tablet
theophylline
absorption window
hydrophilic polymer
Issue Date: 7-Apr-2009
Publisher: Karachi: Faculty of Pharmacy & Pharmaceutical Sciences, Karachi
Citation: Khan, F., Razzak, S. M. I., Khan, Z. R., Azad, M. A. K., Chowdhury, J. A., & Reza, S. (2009). Theophylline loaded gastroretentive floating tablets based on hydrophilic polymers: preparation and in vitro evaluation. Pakistan journal of pharmaceutical sciences, 22(2).
Abstract: This investigation describes the preparation and in vitro evaluation of gastroretentive floating tablet of theophylline. Two hydrophilic cellulose derivatives, Methocel K100M and Methocel K15MCR were evaluated for their gel forming and release controlling properties. Sodium bicarbonate and citric acid were incorporated as gas generating agents. The effects of soluble components (sodium bicarbonate and citric acid), gel forming agents and amount variation of theophylline on drug release profile and floating properties were investigated. Tablets were prepared by direct compression technique. Formulations were evaluated for in vitro buoyancy and drug release study was evaluated for eight hours using USP XXII paddle-type dissolution apparatus using 0.1N HCl as dissolution medium. The release mechanisms were explored and explained with zero order, first order, Higuchi and Korsmeyer equations. The release rate, extent and mechanisms were found to be governed by polymer and floating agent content. The content of active ingredient was also a vital factor in controlling drug release pattern. It was found that polymer content and amount of floating agent significantly affected the mean dissolution time, percentage drug release after 8 hours, release rate constant and diffusion exponent.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/14125
ISSN: 1011-601X
Appears in Collections:Issue 02

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