Structural characterization and aging of glassy pharmaceuticals made using acoustic levitation

被引:42
作者
Benmore, Chris J. [1 ,2 ]
Weber, J. K. R. [1 ]
Tailor, Amit N. [1 ]
Cherry, Brian R. [3 ,4 ]
Yarger, Jeffery L. [2 ,3 ,4 ]
Mou, Qiushi [2 ,3 ]
Weber, Warner [3 ,4 ]
Neuefeind, Joerg [5 ]
Byrn, Stephen R. [6 ]
机构
[1] Argonne Natl Lab, Adv Photon Source, Xray Sci Div, Argonne, IL 60439 USA
[2] Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA
[3] Arizona State Univ, Magnet Resonance Res Ctr, Tempe, AZ 85287 USA
[4] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[5] Oak Ridge Natl Lab, Spallat Neutron Source, Oak Ridge, TN 37922 USA
[6] Purdue Univ, Dept Ind & Phys Pharm, W Lafayette, IN 47907 USA
基金
美国国家科学基金会;
关键词
structure; X-ray powder diffractometry; NMR spectroscopy; glass; glass transition; materials science; CHOLESTEROL-LOWERING DRUG; X-RAY; DIFFRACTION PATTERN; NEUTRON-DIFFRACTION; CARBAMAZEPINE; POLYMORPHS; SCATTERING; CRYSTALLIZATION; DIHYDRATE; SYSTEM;
D O I
10.1002/jps.23464
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Here, we report the structural characterization of several amorphous drugs made using the method of quenching molten droplets suspended in an acoustic levitator. 13C NMR, X-ray, and neutron diffraction results are discussed for glassy cinnarizine, carbamazepine, miconazole nitrate, probucol, and clotrimazole. The 13C NMR results did not find any change in chemical bonding induced by the amorphization process. High-energy X-ray diffraction results were used to characterize the ratio of crystalline to amorphous material present in the glasses over a period of 8 months. All the glasses were stable for at least 6months except carbamazepine, which has a strong tendency to crystallize within a few months. Neutron and X-ray pair distribution function analyses were applied to the glassy materials, and the results were compared with their crystalline counterparts. The two diffraction techniques yielded similar results in most cases and identified distinct intramolecular and intermolecular correlations. The intramolecular scattering was calculated based on the crystal structure and fit to the measured X-ray structure factor. The resulting intermolecular pair distribution functions revealed broad-nearest and next-nearest neighbor moleculemolecule correlations. (c) 2013 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:12901300, 2013
引用
收藏
页码:1290 / 1300
页数:11
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