Study of dissolution hydrodynamic conditions versus drug release from hypromellose matrices: The influence of agitation sequence

Asare-Addo, Kofi, Levina, Marina, Rajabi-Siahboomi, Ali R. and Nokhodchi, Ali (2010) Study of dissolution hydrodynamic conditions versus drug release from hypromellose matrices: The influence of agitation sequence. Colloids and Surfaces B: Biointerfaces, 81 (2). pp. 452-460. ISSN 0927-7765

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Abstract

In this article, the influence of agitation in descending and ascending sequences as a systematic method development process for potentially discriminating fed and fasted states and evaluation of its effects on the drug release from swelling gel-forming hydrophilic matrix tablets were investigated. Theophylline extended release (ER) matrices containing hypromellose (hydroxypropyl methylcellulose (HPMC)) were evaluated in media with a pH range of 1.2-7.5, using an automated USP type III, Bio-Dis dissolution apparatus at 5, 10, 15, 20,25 and 30 dips per minute (dpm). Agitation had a profound effect on the drug release from the HPMC K100LV matrices. Drug release in pH 1.2 changed from about 40% at 5 dpm to about 80% at 30 dpm over a 60 min period alone. The matrices containing HPMC K4M, K15M and K100M however were not significantly affected by the agitation rate. The similarity factor f(2) was calculated using drug release at 10 dpm as a reference. The ascending agitations of 5-30 dpm and the descending order of agitation 30-5 dpm were also evaluated. Anomalous transport was the only kinetic of release for the K4M, K15M and K100M tablet matrices. The lower viscous polymer of K100LV had some matrices exhibiting Fickian diffusion as its kinetics of release. The use of systematic change of agitation method may indicate potential fed and fasted effects on drug release from hydrophilic matrices.

Item Type:	Article
Subjects:	Q Science > Q Science (General)
Schools:	School of Applied Sciences
Related URLs:	Author
Depositing User:	Kofi Asare-Addo
Date Deposited:	01 Jun 2012 09:32
Last Modified:	05 Apr 2018 16:15
URI:	http://eprints.hud.ac.uk/id/eprint/13604

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