结晶
热力学
多态性(计算机科学)
无定形固体
材料科学
动力学
Crystal(编程语言)
动能
工作(物理)
可预测性
化学物理
化学
结晶学
计算机科学
物理
基因型
基因
量子力学
生物化学
程序设计语言
作者
Daniel P. Otto,Melgardt M. de Villiers
标识
DOI:10.2174/1570163812666161201122452
摘要
During drug discovery and development the thermodynamics and kinetics of crystal form transitions must be studied and the fundamental properties of polymorphs must be identified. However, despite the accumulation of knowledge and experimental evidence that support the understanding of crystallization, its predictability still presents significant challenges. With the continuous development of new drug delivery technologies, even more complex situations arise such as difficult cases of polymorph selection, co-crystallization of different molecules, and manipulation of the crystallization environment for example amorphous solids. This review covers some fundamental thermodynamics and kinetics of simple system, before the discussions consider at these special cases and how the manipulation of thermodynamic and kinetic processes has increased our knowledge, understanding and application of crystallization science during the drug development process.
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