Fast Surface Crystallization of Amorphous Griseofulvin Below T g

被引:94
作者
Zhu, Lei [2 ]
Jona, Janan [1 ]
Nagapudi, Karthik [1 ]
Wu, Tian [1 ]
机构
[1] Small Mol Proc & Prod Dev Amgen Inc, Thousand Oaks, CA 91320 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
关键词
amorphous solids; coating; crystallization kinetic; griseofulvin; surface-enhanced crystallization; MOLECULAR MOBILITY; GLASS-TRANSITION; PHARMACEUTICAL SOLIDS; INDOMETHACIN; KINETICS; THERMODYNAMICS; STATE;
D O I
10.1007/s11095-010-0140-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To study crystal growth rates of amorphous griseofulvin (GSF) below its glass transition temperature (T (g)) and the effect of surface crystallization on the overall crystallization kinetics of amorphous GSF. Amorphous GSF was generated by melt quenching. Surface and bulk crystal growth rates were determined using polarized light microscope. X-ray powder diffraction (XRPD) and Raman microscopy were used to identify the polymorph of the crystals. Crystallization kinetics of amorphous GSF powder stored at 40A degrees C (T (g)-48A degrees C) and room temperature (T (g)-66A degrees C) was monitored using XRPD. Crystal growth at the surface of amorphous GSF is 10- to 100-fold faster than that in the bulk. The surface crystal growth can be suppressed by an ultrathin gold coating. Below T (g), the crystallization of amorphous GSF powder was biphasic with a rapid initial crystallization stage dominated by the surface crystallization and a slow or suspended late stage controlled by the bulk crystallization. GSF exhibits the fastest surface crystallization kinetics among the known amorphous pharmaceutical solids. Well below T (g), surface crystallization dominated the overall crystallization kinetics of amorphous GSF powder. Thus, surface crystallization should be distinguished from bulk crystallization in studying, modeling and controlling the crystallization of amorphous solids.
引用
收藏
页码:1558 / 1567
页数:10
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