Predicting Crystallization of Amorphous Drugs with Terahertz Spectroscopy

被引:101
作者
Sibik, Juraj [1 ]
Lobmann, Korbinian [2 ]
Rades, Thomas [2 ]
Zeitler, J. Axel [1 ]
机构
[1] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge CB2 3RA, England
[2] Univ Copenhagen, Dept Pharm, DK-2100 Copenhagen, Denmark
基金
英国工程与自然科学研究理事会;
关键词
terahertz spectroscopy; amorphous; glass; stability; crystallization; GLASS-TRANSITION; MOLECULAR MOBILITY; PHYSICAL STABILITY; DISSOLUTION RATE; FAST RELAXATION; DYNAMICS; STATE; INDOMETHACIN; PHARMACEUTICALS; PARACETAMOL;
D O I
10.1021/acs.molpharmaceut.5b00330
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
There is a controversy about the extent to which the primary and secondary dielectric relaxations influence the crystallization of amorphous organic compounds below the glass transition temperature. Recent studies also point to the importance of fast molecular dynamics on picosecond-to-nanosecond time scales with respect to the glass stability. In the present study we provide terahertz spectroscopy evidence on the crystallization of amorphous naproxen well below its glass transition temperature and confirm the direct role of Johari-Goldstein (JG) secondary relaxation as a facilitator of the crystallization. We determine the onset temperature T beta above which the JG relaxation contributes to the fast molecular dynamics and analytically quantify the level of this contribution. We then show there is a strong correlation between the increase in the fast molecular dynamics and onset of crystallization in several chosen amorphous drugs. We believe that this technique has immediate applications to quantify the stability of amorphous drug materials.
引用
收藏
页码:3062 / 3068
页数:7
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