Role of mechanical stress in crystallization and relaxation behavior of amorphous Indomethacin

被引:54
作者
Bhugra, Chandan [1 ,2 ]
Shmeis, Rama [2 ]
Pikal, Michael J. [1 ]
机构
[1] Univ Connecticut, Sch Pharm, Dept Pharmaceut Sci, Storrs, CT 06269 USA
[2] Boehringer Ingelheim Pharmaceut Inc, Pharmaceut R&D, Ridgefield, CT 06877 USA
关键词
amorphous state; physical stability; crystallization; Indomethacin; molecular mobility; calorimetry (TAM); mechanical stress; thermally stimulated depolarization current spectroscopy (TSDC); polymorphs; induction time;
D O I
10.1002/jps.21291
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Even within an amorphous state, high energy sites can be generated due to sample handling and variations in preparation techniques can result in variation in these high energy sites. Such small handling variations may result in changes in physical properties and physical stability. The aim of this work is to characterize the differences in crystallization tendencies of amorphous Indomethacin arising from minor variations in sample handling. Amorphous Indomethacin was prepared by three variations on melt quenching using liquid nitrogen. Crystallization was studied by annealing the samples at various temperatures above T-g and then using DSC to observe the melt of the polymorph crystallized during annealing. The "No stress" samples showed only T-g whereas other samples showed three events: T-g crystallization and melting. Even at high temperatures (90 degrees C), crystallization was not reproducible in the "No Stress" sample. However, crystallization at 90 degrees C was reproducible and immediate in samples with mechanical stress. At lower temperatures, differences were observed in extent of crystallization and in polymorph formed, which demonstrated the introduction of nuclei due to sample handling. Differences were also observed in relaxation kinetics of the different sample preparations. However, at 35 degrees C the relaxation kinetics were similar but with crystallization behavior being different. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:4446 / 4458
页数:13
相关论文
共 24 条
[1]   Dielectric study of the molecular mobility and the isothermal crystallization kinetics of an amorphous pharmaceutical drug substance [J].
Alie, J ;
Menegotto, J ;
Cardon, P ;
Duplaa, H ;
Caron, A ;
Lacabanne, C ;
Bauer, M .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (01) :218-233
[2]   Crystal nucleation and growth of indomethacin polymorphs from the amorphous state [J].
Andronis, V ;
Zografi, G .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 2000, 271 (03) :236-248
[3]   Molecular mobility-based estimation of the crystallization rates of amorphous nifedipine and phenobarbital in poly(vinylpyrrolidone) solid dispersions [J].
Aso, Y ;
Yoshioka, S ;
Kojima, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (02) :384-391
[4]   Feasibility of using isothermal microcalorimetry to evaluate the physical stability of amorphous nifedipine and phenobarbital [J].
Aso, Y ;
Yoshioka, S ;
Kojima, S .
THERMOCHIMICA ACTA, 2001, 380 (02) :199-204
[5]   Explanation of the crystallization rate of amorphous nifedipine and phenobarbital from their molecular mobility as measured by 13C nuclear magnetic resonance relaxation time and the relaxation time obtained from the heating rate dependence of the glass transition temperature [J].
Aso, Y ;
Yoshioka, S ;
Kojima, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (06) :798-806
[6]   Prediction of the onset of crystallization of amorphous sucrose below the calorimetric glass transition temperature from correlations with mobility [J].
Bhugra, Chandan ;
Rambhatla, Shailaja ;
Bakri, Aziz ;
Duddu, Sarma P. ;
Miller, Danforth P. ;
Pikal, Michael J. ;
Lechuga-Ballesteros, David .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (05) :1258-1269
[7]   Predictions of onset of crystallization from experimental relaxation times I-correlation of molecular mobility from temperatures above the glass transition to temperatures below the glass transition [J].
Bhugra, Chandan ;
Shmeis, Rama ;
Krill, Steven L. ;
Pikal, Michael J. .
PHARMACEUTICAL RESEARCH, 2006, 23 (10) :2277-2290
[8]   Molecular mobility and fragility in indomethacin: A thermally stimulated depolarization current study [J].
Correia, NT ;
Ramos, JJM ;
Descamps, M ;
Collins, G .
PHARMACEUTICAL RESEARCH, 2001, 18 (12) :1767-1774
[9]   Cryogenic grinding of indomethacin polymorphs and solvates: Assessment of amorphous phase formation and amorphous phase physical stability [J].
Crowley, KJ ;
Zografi, G .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (02) :492-507
[10]  
FUKUOKA E, 1986, CHEM PHARM BULL, V34, P4314