Miller J D, Randolph A D, Drach G W
J Urol. 1977 Mar;117(3):342-5. doi: 10.1016/s0022-5347(17)58453-0.
Two major etiologic theories of urinary stones are excessive saturation of urine with crystallizable substances or defects in inhibitors that allow relative supersaturation to occur. To date, it has been difficult to confirm the supersaturation theory in experiments using diffusion-limited crystallization systems because direct measurements of the nucleation process of crystallization could not be performed. We used well developed, continuous crystallizer techniques and adapted them from industrial use to the study of stone disease. Data derived from the experiments allow the absolute measurement of crystal growth rate and determination of nucleation rate. These methods were applied to study the calcium oxalate dihydrate (weddellite) system in artificial urine that lacked only proteinaceous components. Based on these experiments it was not possible to grow crystals large enough within 5 to 20 minutes to obstruct the collecting ducts of the kidney. Therefore, it appears that other processes, such as aggregation or stasis within tissues, may well be related to initiation of stone disease. Under the experimental conditions of this study nucleation rate exceeded growth rate. Therefore, multiple small particles are created at the expense of allowing larger particles to grow. Inhibitors can be tested rapidly in this system by adding them in concentrations compatible with those found in urine.
尿路结石的两大主要病因学理论是,可结晶物质在尿液中过度饱和,或抑制物存在缺陷,从而导致相对过饱和状态的出现。迄今为止,在使用扩散受限结晶系统的实验中,很难证实过饱和理论,因为无法对结晶的成核过程进行直接测量。我们采用了成熟的连续结晶器技术,并将其从工业应用领域改编用于结石病研究。实验所得数据能够对晶体生长速率进行绝对测量,并确定成核速率。这些方法被应用于研究仅缺少蛋白质成分的人工尿液中的二水合草酸钙(水草酸钙)系统。基于这些实验,在5至20分钟内无法生长出足够大的晶体以阻塞肾集合管。因此,似乎其他过程,如组织内的聚集或淤积,很可能与结石病的起始有关。在本研究的实验条件下,成核速率超过生长速率。因此,是以牺牲让较大颗粒生长为代价来生成多个小颗粒。通过以与尿液中发现的浓度相匹配的浓度添加抑制剂,可在该系统中快速对其进行测试。