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Two-Dimensional Capillary Electrophoresis with On-Line Sample Preparation and Cyclodextrin Separation Environment for Direct Determination of Serotonin in Human Urine

机译:在线样品制备和环糊精分离环境的二维毛细管电泳直接测定人尿中的血清素

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摘要

An advanced two-dimensional capillary electrophoresis method, based on on-line combination of capillary isotachophoresis and capillary zone electrophoresis with cyclodextrin additive in background electrolyte, was developed for effective determination of serotonin in human urine. Hydrodynamically closed separation system and large bore capillaries (300–800 µm) were chosen for the possibility to enhance the sample load capacity, and, by that, to decrease limit of detection. Isotachophoresis served for the sample preseparation, defined elimination of sample matrix constituents (sample clean up), and preconcentration of the analyte. Cyclodextrin separation environment enhanced separation selectivity of capillary zone electrophoresis. In this way, serotonin could be successfully separated from the rest of the sample matrix constituents migrating in capillary zone electrophoresis step so that human urine could be directly (i.e., without any external sample preparation) injected into the analyzer. The proposed method was successfully validated, showing favorable parameters of sensitivity (limit of detection for serotonin was 2.32 ng·mL−1), linearity (regression coefficient higher than 0.99), precision (repeatability of the migration time and peak area were in the range of 0.02–1.17% and 5.25–7.88%, respectively), and recovery (ranging in the interval of 90.0–93.6%). The developed method was applied for the assay of the human urine samples obtained from healthy volunteers. The determined concentrations of serotonin in such samples were in the range of 12.4–491.2 ng·mL−1 that was in good agreement with literature data. This advanced method represents a highly effective, reliable, and low-cost alternative for the routine determination of serotonin as a biomarker in human urine.
机译:建立了一种先进的二维毛细管电泳方法,该方法基于毛细管等速电泳和毛细管区带电泳与环糊精添加剂在背景电解质中的在线结合,可有效测定人尿中的血清素。选择了流体动力学封闭的分离系统和大口径毛细管(300–800 µm),以增强样品的负载能力,从而降低检测限。等速电泳用于样品的预分离,确定的样品基体成分消除(样品净化)和分析物的预浓缩。环糊精分离环境提高了毛细管区带电泳的分离选择性。以这种方式,可以将5-羟色胺与在毛细管区带电泳步骤中迁移的其余样品基质成分成功分离,从而可以将人尿液直接(即,无需任何外部样品制备)注入分析仪中。该方法成功验证,显示出良好的灵敏度参数(5-羟色胺的检出限为2.32 ng·mL -1 ),线性(回归系数高于0.99),精度(迁移时间可重复)和峰面积分别在0.02–1.17%和5.25–7.88%之间,以及恢复(在90.0–93.6%之间)。所开发的方法用于从健康志愿者获得的人类尿液样品的分析。这些样品中血清素的测定浓度为12.4–491.2 ng·mL -1 ,与文献数据相吻合。这种先进的方法代表了常规测定5-羟色胺作为人类尿液中生物标志物的高效,可靠且低成本的替代方法。

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