The Application of Modeling and Prediction to the Formation and Stability of Amorphous Solid Dispersions

被引:80
作者
DeBoyace, Kevin [1 ]
Wildfong, Peter L. D. [1 ]
机构
[1] Duquesne Univ, Dept Pharmaceut Sci, 600 Forbes Av, Pittsburgh, PA 15282 USA
关键词
amorphous; solid dispersion; solid solutions; thermodynamics; kinetics; in silico modeling; molecular dynamics; molecular modeling; QSPR; physical stability; MOLECULAR-DYNAMICS SIMULATION; DRUG-POLYMER SOLUBILITY; FLORY-HUGGINS THEORY; HYDROGEN-BONDING INTERACTIONS; MELTING-POINT DEPRESSION; GLASS-FORMING ABILITY; IN-SILICO PREDICTION; CRYSTALLIZATION TENDENCY; PHASE-DIAGRAMS; PHYSICAL STABILITY;
D O I
10.1016/j.xphs.2017.03.029
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Amorphous solid dispersion (ASD) formulation development is frequently difficult owing to the inherent physical instability of the amorphous form, and limited understanding of the physical and chemical interactions that translate to initial dispersion formation and long-term physical stability. Formulation development for ASDs has been historically accomplished through trial and error or experience with extant systems; however, rational selection of appropriate excipients is preferred to reduce time to market and decrease costs associated with development. Current efforts to develop thermodynamic and computational models attempt to rationally direct formulation and show promise. This review compiles and evaluates important methods used to predict ASD formation and physical stability. Recent literature in which these methods are applied is also reviewed, and limitations of each method are discussed. (c) 2018 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:57 / 74
页数:18
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