Department of Chemistry, East China Normal University, Shanghai, P. R. China.
Electrophoresis. 2010 Sep;31(17):2989-96. doi: 10.1002/elps.201000191.
A novel method of CE coupled with dual electrochemical detection has been developed for the determination of pathological metabolites of phenylalanine in urine samples. Factors influencing the separation and detection were examined and optimized. Five aromatic acid metabolites and a major coexisting interfering compound uric acid could be well separated within 23 min at a separation voltage of 16 kV using a 35 mmol/L SDS/60 mmol/L H(3)BO(3)-Na(2)B(4)O(7) running buffer (pH 8.2). Highly linear response was obtained for these five biomarker compounds over three orders of magnitude with detection limits ranging from 6.6 to 0.064 μg/mL (S/N=3). The average recovery and RSD were within the range of 92.6-121.0 and 1.0-12.0%, respectively. The proposed method has been used to detect the unconjugated aromatic acids simultaneously in urine samples with the advantages of obtaining more information about target analytes and avoiding redundant measurements and high assay cost, thus could find potential applications involving assays of biomarker compounds for the purpose of fast diagnose of some metabolic diseases including phenylketonuria.
一种新颖的 CE 与双电化学检测相结合的方法已被开发出来,用于测定尿液样品中苯丙氨酸的病理代谢物。考察并优化了影响分离和检测的因素。在分离电压为 16 kV 时,使用 35 mmol/L SDS/60 mmol/L H(3)BO(3)-Na(2)B(4)O(7)运行缓冲液(pH 8.2),可在 23 分钟内将 5 种芳香酸代谢物和一种主要共存的干扰化合物尿酸很好地分离。这些五种生物标志物化合物在三个数量级范围内具有高度线性响应,检测限范围为 6.6 至 0.064 μg/mL(S/N=3)。平均回收率和 RSD 在 92.6-121.0 和 1.0-12.0%范围内。该方法已用于同时检测尿液样品中的未结合芳香酸,具有获得更多目标分析物信息、避免冗余测量和高测定成本的优点,因此可用于涉及生物标志物化合物测定的快速诊断某些代谢疾病,包括苯丙酮尿症。