Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2486356 | Journal of Pharmaceutical Sciences | 2011 | 6 Pages |
Abstract
Dissolution critically affects the bioavailability of Biopharmaceutics Classification System class 2 compounds. When unexpected dissolution behaviour occurs, detailed studies using high information content technologies are warranted. In the present study, an evaluation of realâtime ultraviolet (UV) imaging for conducting singleâcrystal dissolution studies was performed. Using lidocaine as a model compound, the aim was to develop a setup capable of monitoring and quantifying the dissolution of lidocaine into a phosphate buffer, pH 7.4, under stagnant conditions. A single crystal of lidocaine was placed in the quartz dissolution cell and UV imaging was performed at 254Â nm. Spatially and temporally resolved mapping of lidocaine concentration during the dissolution process was achieved from the recorded images. UV imaging facilitated the monitoring of lidocaine concentrations in the dissolution media adjacent to the single crystals. The concentration maps revealed the effects of natural convection due to density gradients on the dissolution process of lidocaine. UV imaging has great potential for in vitro drug dissolution testing. © 2011 WileyâLiss, Inc. and the American Pharmacists Association J Pharm Sci 100:3405-3410, 2011
Keywords
Related Topics
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Pharmacology, Toxicology and Pharmaceutical Science
Drug Discovery
Authors
Jesper Ãstergaard, Fengbin Ye, Jukka Rantanen, Anan Yaghmur, Susan Weng Larsen, Claus Larsen, Henrik Jensen,