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药用玻璃中分子流动性与物理稳定性之间的相关性

Correlation between Molecular Mobility and Physical Stability in Pharmaceutical Glasses.

作者信息

Mehta Mehak, Ragoonanan Vishard, McKenna Gregory B, Suryanarayanan Raj

机构信息

Department of Pharmaceutics, University of Minnesota , Minneapolis, Minnesota 55455, United States.

Department of Chemical Engineering, Texas Tech University , Lubbock, Texas 79409, United States.

出版信息

Mol Pharm. 2016 Apr 4;13(4):1267-77. doi: 10.1021/acs.molpharmaceut.5b00853. Epub 2016 Mar 4.

Abstract

We investigated a possible correlation between molecular mobility and physical stability in glassy celecoxib and indomethacin and identified the specific mobility mode responsible for physical instability (crystallization). In the glassy state, because the structural relaxation times are very long, the measurement was enabled by time domain dielectric spectroscopy. However, the local motions in the glassy state were characterized by frequency domain dielectric spectroscopy. Isothermal crystallization was monitored by powder X-ray diffractometry using either a laboratory source (supercooled state) or synchrotron source (glassy state). Structural (α) relaxation time correlated well with characteristic crystallization time in the supercooled state. On the other hand, a stronger correlation was observed between the Johari-Goldstein (β) relaxation time and physical instability in the glassy state but not with structural relaxation time. These results suggest that Johari-Goldstein relaxation is a potential predictor of physical instability in the glassy state of these model systems.

摘要

我们研究了玻璃态塞来昔布和吲哚美辛中分子流动性与物理稳定性之间的可能相关性,并确定了导致物理不稳定(结晶)的特定流动性模式。在玻璃态下,由于结构弛豫时间非常长,通过时域介电谱进行测量。然而,玻璃态下的局部运动通过频域介电谱进行表征。使用实验室光源(过冷状态)或同步辐射光源(玻璃态)通过粉末X射线衍射法监测等温结晶。在过冷状态下,结构(α)弛豫时间与特征结晶时间具有良好的相关性。另一方面,在玻璃态下,观察到乔哈里-戈尔茨坦(β)弛豫时间与物理不稳定性之间存在更强的相关性,但与结构弛豫时间无关。这些结果表明,乔哈里-戈尔茨坦弛豫是这些模型系统玻璃态下物理不稳定性的潜在预测指标。

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