Solid-state 13C NMR study of indomethacin polymorphism

被引:47
|
作者
Masuda, Katsuhiko
Tabata, Sachio
Kono, Hiroyuki
Sakata, Yasuyuki
Hayase, Tetsuo
Yonemochi, Etsuo
Terada, Katsuhide
机构
[1] Toho Univ, Sch Pharmaceut Sci, Dept Pharmaceut, Chiba 2748510, Japan
[2] Mitsubishi Pharma Corp, Discovery Technol Lab 2, Aoba Ku, Yokohama, Kanagawa 2270033, Japan
[3] Mitsubishi Chem Grp Sci & Technol Res Ctr Inc, Yokohama Lab, Aoba Ku, Yokohama, Kanagawa 2270033, Japan
[4] Bruker Biospin Co Ltd, Tsukuba, Ibaraki 3050051, Japan
[5] Mitsubishi Chem Grp Sci & Technol Res Ctr Inc, Yokkaichi Lab, Yokaichi, Mie 5108530, Japan
[6] Mitsubishi Pharma Corp, Pharmaceut Technol Coordinat Dept, Ibaraki 3140255, Japan
关键词
solid-state C-13 NMR; indomethacin; polymorphism;
D O I
10.1016/j.ijpharm.2006.03.029
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to analyze the difference in the molecular conformation packed in the crystal lattice between the meta-stable alpha-form and stable gamma-form of indomethacin on, the basis of solid-state C-13 NMR spectral patterns. The chemical shifts of each resonance of the alpha-form were distinctly different from the gamma-form. Each carbon nucleus of the gamma-form showed a single signal with no splitting. In contrast, carbon nuclei of the alpha-form showed a complicated set of resonances for each carbon. For some carbons of the alpha-form, four signals assigned to one carbon were observed at 203 K. Two of these four signals were merged between the temperature range from 203 to 343 K without a transformation in the crystal structure. It was found that solid-state 13 C NMR can be a powerful tool to estimate the number of molecular conformations as well as configurational differences in the packing of molecules in a unit cell. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 153
页数:8
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