| Literature DB >> 16892206 |
Jaakko Aaltonen1, Paula Heinänen, Leena Peltonen, Hanna Kortejärvi, Veli Pekka Tanninen, Leena Christiansen, Jouni Hirvonen, Jouko Yliruusi, Jukka Rantanen.
Abstract
In this study, solvent-mediated phase transformations of theophylline (TP) and nitrofurantoin (NF) were measured in a channel flow intrinsic dissolution test system. The test set-up comprised simultaneous measurement of drug concentration in the dissolution medium (with UV-Vis spectrophotometry) and measurement of the solid-state form of the dissolving solid (in situ with Raman spectroscopy). The solid phase transformations were also investigated off-line with scanning electron microscopy. TP anhydrate underwent a transformation to TP monohydrate, and NF anhydrate (form beta) to NF monohydrate (form II). Transformation of TP anhydrate to TP monohydrate resulted in a clear decrease in the dissolution rate, while the transformation of NF anhydrate (form beta) to NF monohydrate (form II) could not be linked as clearly to changes in the dissolution rate. The transformation of TP was an order of magnitude faster than that of NF. The presence of a water absorbing excipient, microcrystalline cellulose, was found to delay the onset of the transformation of TP anhydrate. Combining the measurement of drug concentration in the dissolution medium with the solid phase measurement offers a deeper understanding of the solvent-mediated phase transformation phenomena during dissolution. (c) 2006 Wiley-Liss, Inc. and the American Pharmacists AssociationEntities:
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Year: 2006 PMID: 16892206 DOI: 10.1002/jps.20725
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534