Procházková A, Krivánková L, Bocek P
Institute of Analytical Chemistry, Academy of Sciences of the Czech Republic, Brno, Czech Republic.
J Chromatogr A. 1999 Apr 9;838(1-2):213-21. doi: 10.1016/s0021-9673(99)00114-4.
The techniques of the on-line combination of capillary isotachophoresis with zone electrophoresis in two coupled capillaries (ITP-CZE) and a single capillary zone electrophoresis (CZE) were used for the sensitive determination of orotic acid (OA) in human urine. The simple CZE system was successfully applied for fast and reliable analyses of urine of healthy adult volunteers (the detection limit 1.7.10(-6) M OA, the total time of analysis 6 min). However, this method failed in analyses of OA in urine of ill children due to more complex matrix of the samples. Here, the ITP preconcentration and preseparation step coupled on-line with CZE proved to serve well with an electrolyte system developed and optimized for this purpose. The maximum selectivity and resolution of OA from other sample constituents in ITP-CZE was achieved by use of an electrolyte system of very low pH 2.15 both for ITP and CZE stage. The sensitivity of detection and simplicity of OA identification were enhanced by use of an external UV scanning detector. High sensitivity of ITP-CZE combination (limit of detection 3.10(-7) M OA), low sample consumption (1 microliter), good reproducibility of migration times (inter-day RSD < 1.86%) and acceptable reproducibility of the determination of OA in urine samples (average RSD = 7.27%) make this technique suitable for routine determination of trace concentration of OA especially in urine of ill children under various pathological conditions and medication.
采用双毛细管在线联用毛细管等速电泳与区带电泳技术(ITP-CZE)以及单毛细管区带电泳(CZE)对人尿中的乳清酸(OA)进行灵敏测定。简单的CZE系统成功应用于健康成年志愿者尿液的快速可靠分析(检测限为1.7×10⁻⁶ M OA,总分析时间为6分钟)。然而,由于样品基质更为复杂,该方法在分析患病儿童尿液中的OA时失败。在此,ITP预浓缩和预分离步骤与CZE在线联用,结果证明对于为此开发和优化的电解质系统效果良好。通过在ITP和CZE阶段均使用极低pH值2.15的电解质系统,在ITP-CZE中实现了OA与其他样品成分之间的最大选择性和分辨率。通过使用外部紫外扫描检测器提高了检测灵敏度和OA鉴定的简便性。ITP-CZE联用具有高灵敏度(检测限为3×10⁻⁷ M OA)、低样品消耗(1微升)、迁移时间良好的重现性(日间相对标准偏差<1.86%)以及尿液样品中OA测定的可接受重现性(平均相对标准偏差=7.27%),使得该技术适用于常规测定痕量浓度的OA,特别是在各种病理状况和用药情况下患病儿童的尿液中。