Simultaneous in vivo visualization and localization of solid oral dosage forms in the rat gastrointestinal tract by magnetic resonance imaging (MRI)

被引:31
作者
Christmann, V
Rosenberg, J
Seega, J
Lehr, CM
机构
[1] KNOLL AG,RES & DEV,D-67008 LUDWIGSHAFEN,GERMANY
[2] UNIV SAARLAND,DEPT BIOPHARMACEUT & PHARMACEUT TECHNOL,D-66041 SAARBRUCKEN,GERMANY
关键词
gastrointestinal transit; magnetic resonance imaging; nuclear magnetic resonance; oral drug delivery; solid oral dosage forms;
D O I
10.1023/A:1012161630481
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. Bioavailability of orally administered drugs is much influenced by the behavior, performance and fate of the dosage form within the gastrointestinal (GI) tract. Therefore, MRI in vivo methods that allow for the simultaneous visualization of solid oral dosage forms and anatomical structures of the GI tract have been investigated. Methods. Oral contrast agents containing Gd-DTPA were used to depict the lumen of the digestive organs. Solid oral dosage forms were visualized in a wt model by a H-1-MRI double contrast technique (magnetite-labelled microtablets) and a combination of H-1- and F-19-MRI (fluorine-labelled minicapsules). Results. Simultaneous visualization of solid oral dosage forms and the Gi environment in the rat was possible using MRI. Microtablets could reproducibly be monitored in the rat stomach and in the intestines using a H-1-MRI double contrast technique. Fluorine-labelled minicapsules were detectable in the rat stomach by a combination of H-1- and F-19-MRI in vivo. Conclusions. The in vivo H-1-MRI double contrast technique described allows solid oral dosage forms in the rat GI tract to be depicted. Solid dosage forms can easily be labelled by incorporating trace amounts of non-toxic iron oxide (magnetite) particles. H-1-MRI is a promising tool for observing such pharmaceutical dosage forms in humans. Combined H-1- and F-19-MRI offer a means of unambiguously localizing solid oral dosage forms in more distal parts of the GI tract. Studies correlating MRI examinations with drug plasma levels could provide valuable information for the development of pharmaceutical dosage forms.
引用
收藏
页码:1066 / 1072
页数:7
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