Far-Infrared Spectroscopy as a Probe for Polymorph Discrimination

被引:7
|
作者
Suresh, Kuthuru [1 ]
Ashe, Jeffrey S. [1 ]
Matzger, Adam J. [1 ,2 ]
机构
[1] Univ Michigan, Dept Chem, 930 North Univ Ave, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Macromol Sci & Engn, 930 North Univ Ave, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
pharmaceuticals; polymorph; amorphous; crystal packing; far-IR spectroscopy; TERAHERTZ PULSED SPECTROSCOPY; ANHYDROUS POLYMORPHS; FORM; DISCOVERY;
D O I
10.1016/j.xphs.2018.12.020
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pharmaceutical crystalline polymorph and amorphous form detection and quantification is a standard requirement in the pharmaceutical industry. Infrared (IR) spectroscopy provides an important probe for the characterization of polymorphs. Nonetheless, characterization and discrimination among poly morphs using mid-IR spectroscopy is not always possible in part because the technique mainly probes vibrational modes arising from functional groups in the sample. In the present work, far-IR spectroscopy is demonstrated for the discrimination of polymorphs. This region is influenced by delocalized lattice vibrational modes derived from intermolecular forces and packing arrangements in the crystal structure. A total of 10 polymorphic pharmaceuticals were prepared to conduct a critical evaluation of the question, does this far-IR region add value for polymorph differentiation? It is demonstrated that the far-IR region offers high discriminating power for polymorphs compared to the mid-IR spectral region. In addition, structural similarity and dissimilarity in polymorphic packing arrangements can be derived from this analysis. (C) 2019 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1915 / 1920
页数:6
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