Evaluation of amorphous solid dispersion properties using thermal analysis techniques

被引:384
作者
Baird, Jared A. [1 ,2 ]
Taylor, Lynne S. [1 ]
机构
[1] Purdue Univ, Coll Pharm, Dept Ind & Phys Pharm, W Lafayette, IN 47907 USA
[2] Allergan Pharmaceut Inc, Irvine, CA 92612 USA
基金
美国国家科学基金会;
关键词
Calorimetry; Mobility; Glass transition; Miscibility; Crystallization; GLASS-TRANSITION TEMPERATURE; DRUG-POLYMER MISCIBILITY; DSC HYPER-DSC; MOLECULAR MOBILITY; PHYSICAL STABILITY; ENTHALPY RELAXATION; DIELECTRIC-RELAXATION; PHASE-BEHAVIOR; PHARMACEUTICAL SOLIDS; STRUCTURAL RELAXATION;
D O I
10.1016/j.addr.2011.07.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Amorphous solid dispersions are an increasingly important formulation approach to improve the dissolution rate and apparent solubility of poorly water soluble compounds. Due to their complex physicochemical properties, there is a need for multi-faceted analytical methods to enable comprehensive characterization, and thermal techniques are widely employed for this purpose. Key parameters of interest that can influence product performance include the glass transition temperature (T-g), molecular mobility of the drug, miscibility between the drug and excipients, and the rate and extent of drug crystallization. It is important to evaluate the type of information pertaining to the aforementioned properties that can be extracted from thermal analytical measurements, in addition to considering any inherent assumptions or limitations of the various analytical approaches. Although differential scanning calorimetry (DSC) is the most widely used thermal analytical technique applied to the characterization of amorphous solid dispersions, there are many established and emerging techniques which have been shown to provide useful information. Comprehensive characterization of fundamental material descriptors will ultimately lead to the formulation of more robust solid dispersion products. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:396 / 421
页数:26
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