In situ measurement of solvent-mediated phase transformations during dissolution testing

被引:81
作者
Aaltonen, Jaakko
Heinanen, Paula
Peltonen, Leena
Kortejarvi, Hanna
Tanninen, Veli Pekka
Christiansen, Leena
Hirvonen, Jouni
Yliruusi, Jouko
Rantanen, Jukka
机构
[1] Univ Helsinki, Div Pharmaceut Technol, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Drug Discovery & Dev Technol Ctr, FIN-00014 Helsinki, Finland
[3] Danish Univ Pharmaceut Sci, Dept Pharmaceut & Analyt Chem, DK-2100 Copenhagen, Denmark
[4] Orion Pharma, Espoo 02101, Finland
基金
芬兰科学院;
关键词
dissolution; hydrates/solvates; dissolution rate; polymorphism; Raman spectroscopy; solid state;
D O I
10.1002/jps.20725
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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 II) 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.
引用
收藏
页码:2730 / 2737
页数:8
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