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通过与流动性的相关性预测低于量热玻璃化转变温度的无定形蔗糖结晶的起始。

Prediction of the onset of crystallization of amorphous sucrose below the calorimetric glass transition temperature from correlations with mobility.

作者信息

Bhugra Chandan, Rambhatla Shailaja, Bakri Aziz, Duddu Sarma P, Miller Danforth P, Pikal Michael J, Lechuga-Ballesteros David

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy, U-3092, University of Connecticut, 69 North Eagleville Road, Storrs, Connecticut 06269, USA.

出版信息

J Pharm Sci. 2007 May;96(5):1258-69. doi: 10.1002/jps.20918.

DOI:10.1002/jps.20918
PMID:17455303
Abstract

The objective of the present work is to determine if crystallization onset observed for an amorphous solid correlate with relaxation time at temperatures above and below the calorimetric glass transition (T(g)). Crystallization onset of spray-dried and freeze-dried amorphous sucrose were measured calorimetrically. Relaxation times measured in two temperature ranges by different techniques (isothermal calorimetry, dielectric spectroscopy) followed the expected modified Vogel-Tammann-Fulcher (VTF) behavior when extrapolated to a temperature near T(g). However, the change in slope was more conspicuous for freeze-dried sucrose, indicating that amorphous materials generated using different techniques differ in their mobilities for temperatures below T(g). Dielectric relaxation time values obtained above T(g) were well correlated to onset of crystallization. The model predicted 21 days for crystallization onset for spray-dried samples stored 7 K below T(g), compared to the experimentally observed crystallization onset of 17 days. Onset times versus temperature for freeze-dried sucrose, however, show a change in slope on approaching T(g), with the onsets somewhat decoupling from measured mobility for temperatures below T(g). Molecular mobility in amorphous materials at temperatures both above and below T(g) can be correlated to macroscopic physical change such as crystallization, but prediction of crystallization onset from relaxation time is only qualitatively correct at temperatures well below T(g).

摘要

本研究的目的是确定在量热玻璃化转变温度(T(g))以上和以下温度下,非晶态固体的结晶起始是否与弛豫时间相关。采用量热法测量喷雾干燥和冷冻干燥的非晶态蔗糖的结晶起始。当外推至接近T(g)的温度时,通过不同技术(等温量热法、介电谱法)在两个温度范围内测量的弛豫时间遵循预期的修正Vogel-Tammann-Fulcher(VTF)行为。然而,冷冻干燥蔗糖的斜率变化更为明显,这表明使用不同技术制备的非晶态材料在T(g)以下温度时的迁移率不同。在T(g)以上获得的介电弛豫时间值与结晶起始密切相关。该模型预测,在比T(g)低7 K的温度下储存的喷雾干燥样品的结晶起始时间为21天,而实验观察到的结晶起始时间为17天。然而,冷冻干燥蔗糖的起始时间与温度的关系在接近T(g)时显示出斜率变化,对于T(g)以下的温度,起始时间与测量的迁移率有些解耦。在T(g)以上和以下温度下,非晶态材料中的分子迁移率都可以与宏观物理变化(如结晶)相关,但从弛豫时间预测结晶起始仅在远低于T(g)的温度下在定性上是正确的。

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