Holzbach R T
Gastrointestinal Research Unit, Cleveland Clinic Foundation, Ohio 44195-5218.
Hepatology. 1990 Sep;12(3 Pt 2):155S-159S; discussion 159S-161S.
Any substance capable of ultimately forming itself into a solid crystal must undergo an initial step of forming crystal nuclei. The nucleation step in crystallization for all such systems has been a difficult process to describe. Even the definition of what constitutes a "nucleus" remains elusive because one is dealing with a conceptual construct that is found only in the submicroscopic domain and therefore is inaccessible to direct measurement. Based on these considerations, the so-called nucleation time assay can at best only be taken as an empirical parameter. Nucleation (operationally defined) and growth of cholesterol monohydrate crystals in both model and native biles occurs rapidly after aggregation of supersaturated vesicles. Cholesterol made available for crystal growth also originates from the vesicular pathway and not directly from biliary micelles. The exact mechanism(s) governing this linked "precursor-product" relationship remains undefined.
任何最终能够形成固体晶体的物质都必须经历形成晶核的初始步骤。对于所有此类系统,结晶过程中的成核步骤一直是一个难以描述的过程。甚至“晶核”的构成定义也仍然难以捉摸,因为人们处理的是一种仅存在于亚微观领域的概念性结构,因此无法直接测量。基于这些考虑,所谓的成核时间测定充其量只能被视为一个经验参数。在模型胆汁和天然胆汁中,过饱和囊泡聚集后,一水合胆固醇晶体的成核(按操作定义)和生长迅速发生。可用于晶体生长的胆固醇也源自囊泡途径,而非直接来自胆汁微胶粒。控制这种相关“前体 - 产物”关系的确切机制仍不明确。