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Alternate Injections Coupled with Flow-Gated Capillary Electrophoresis for Rapid and Accurate Quantitative Analysis of Urine Samples

机译:交替进样与流控毛细管电泳联用可快速准确地定量分析尿液样品

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摘要

Capillary electrophoresis (CE) is a powerful separation technique with advantages over HPLC in terms of separation efficiency, speed, and cost. However, CE suffers in poor reproducibility in quantitative chemical analysis, which is one of major drawbacks preventing its widespread use in routine analytical laboratories. Here we report a novel strategy to enhance the quantitative capability of flow-gated CE. The platform integrated dual flow branches to respectively supply a sample and its standard additions that were then alternately injected into a single capillary for rapid separations (typically 20–90 s). A micro-fabricated switch was used to enable the alternate injections. It was assumed that the analytical system maintained constant conditions during neighboring injections that served as external self-standards for quantitation. This strategy was expected to reduce uncertainties caused by the fluctuation in capillary conditions and the drift of detection systems. Experimental results demonstrated that the dual-branch flow-gated CE coupled with alternate injections significantly improved the reproducibility with respect to peak height ratios under deliberate variations in injection volumes, separation voltages, optical focusing, and laser power; and thus the interday precision was ensured. To demonstrate its applicability, cyanide and amino acids in human urine were quantified rapidly with the one-point standard addition method after fluorogenic derivatization with naphthalene-2,3-dicarboxaldehyde (NDA), and the measurement accuracy was validated by determining the recovery of standard cyanide added to a urinary matrix. This strategy would be valuable to enable the quantitative capability of flow-gated CE in the measurements of a broad range of analytes, especially those lacking suited internal standards.
机译:毛细管电泳(CE)是一种强大的分离技术,在分离效率,速度和成本方面均优于HPLC。但是,CE在定量化学分析中的再现性很差,这是阻止其在常规分析实验室中广泛使用的主要缺点之一。在这里,我们报告了一种新的策略,以增强流动门控CE的定量能力。该平台集成了双流分支,分别提供样品及其标准添加物,然后将其交替注入单个毛细管中以快速分离(通常为20-90 s)。使用微型开关来进行交替注射。假定分析系统在相邻进样过程中保持恒定的条件,可以用作定量的外部自标。预期该策略将减少由毛细管条件的波动和检测系统的漂移引起的不确定性。实验结果表明,在有意改变注射量,分离电压,光学聚焦和激光功率的情况下,双分支流控CE与交替进样相结合可显着提高峰高比的重现性。从而确保了日间精度。为了证明其适用性,在萘-2,3-二甲苯甲醛(NDA)荧光衍生化后,通过单点标准加入法快速定量测定人尿中的氰化物和氨基酸,并通过测定标准品的回收率来验证测量准确性。氰化物添加到尿液基质中。该策略对于在多种分析物(特别是缺乏合适的内标物)的测量中实现流控CE的定量能力具有重要意义。

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