Baumann J M, Affolter B, Brenneisen J, Siegrist H P
Division of Urology, Regional Hospital, Biel, Switzerland.
Urol Int. 1997;59(4):214-20. doi: 10.1159/000283066.
Nucleation, growth and aggregation are thought to be the most important crystallization processes in stone formation. Since crystallization properties change with urinary dilution, centrifugation and filtration, crystallization should always be studied in freshly voided and not pretreated urine. Recently we developed an automated method where calcium oxalate crystallization is induced in native urine by an exogenous oxalate load and nucleation and growth are monitored by an ion-selective calcium electrode. The method has now been supplemented with the spectrophotometric measurement of crystal aggregation. Repeated experiments in the same urine with different oxalate loads enable the determination of the critical oxalate additionable to induce crystallization (metastable limit) and the calculation of an oxalate load-independent growth rate constant. Preliminary results obtained in the native urine of healthy controls showed an extremely high limit of metastability and a complete absence of crystal aggregation. These findings may explain why, despite frequent urinary calcium oxalate supersaturation, healthy people do not form stones.
成核、生长和聚集被认为是结石形成过程中最重要的结晶过程。由于结晶特性会随尿液稀释、离心和过滤而变化,因此结晶研究应始终使用刚排出的未经过预处理的尿液。最近我们开发了一种自动化方法,通过外源性草酸盐负荷在天然尿液中诱导草酸钙结晶,并通过离子选择性钙电极监测成核和生长过程。该方法现已补充了晶体聚集的分光光度测量。在同一尿液中使用不同草酸盐负荷进行重复实验,能够确定诱导结晶所需添加的临界草酸盐量(亚稳极限),并计算出与草酸盐负荷无关的生长速率常数。在健康对照者的天然尿液中获得的初步结果显示,亚稳极限极高,且完全没有晶体聚集。这些发现或许可以解释为什么尽管健康人的尿液中草酸钙经常处于过饱和状态,但他们却不会形成结石。