Holmes R P
Department of Urology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 27157, USA.
Clin Chem. 1995 Sep;41(9):1297-301.
We describe a method for measuring urinary oxalate and citrate with capillary electrophoresis (CE) and indirect ultraviolet absorbance detection. Sample preparation is minimal, requiring an acidification, brief centrifugation, and dilution. The method is rapid, with oxalate and citrate having mean migration times of 4.02 and 4.50 min, respectively. The minimal detectable concentration (signal-to-noise ratio of 7) of both oxalate and citrate in urine was 7 mg/L. Total imprecisions (CV) were 1.2-5.6% for three urine samples with oxalate and citrate concentrations of 8-60 mg/L and 80-860 mg/L, respectively. The recovery of added oxalate ranged from 94% to 101%. Results of CE analyses agreed well with enzymatic determinations of oxalate and citrate. Rapid analysis time, accuracy, and reproducibility make this procedure well suited for routine urinary oxalate and citrate determinations.
我们描述了一种采用毛细管电泳(CE)和间接紫外吸收检测法测量尿草酸和柠檬酸的方法。样品制备工作极少,只需进行酸化、短暂离心和稀释。该方法速度快,草酸和柠檬酸的平均迁移时间分别为4.02分钟和4.50分钟。尿中草酸和柠檬酸的最低可检测浓度(信噪比为7)均为7毫克/升。对于三个草酸和柠檬酸浓度分别为8 - 60毫克/升和80 - 860毫克/升的尿样,总不精密度(CV)分别为1.2 - 5.6%。添加草酸的回收率在94%至101%之间。CE分析结果与草酸和柠檬酸的酶法测定结果高度一致。快速的分析时间、准确性和重现性使得该方法非常适合用于尿草酸和柠檬酸的常规测定。