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Simultaneous electrokinetic and hydrodynamic injection with on-line sample concentration via micelle to solvent stacking in micellar electrokinetic chromatography

机译:在胶束电动色谱中同时通过胶束对溶剂堆叠进行电动和流体动力学注射,同时在线进行样品浓缩

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摘要

Simultaneous electrokinetic and hydrodynamic injection (SEH1) of organic cations (tricyclic antidepressant and beta blocker drugs) with on-line sample concentration using micelle to solvent stacking (MSS) was studied in micellar electrokinetic chromatography. Compared to conventional injection, >300-fold improvements in signals were obtained by hydrodynamic injection. However, with SEHI the amount of sample ions introduced into the capillary was increased which afforded a higher gain of up to 4000-fold without compromise to separation efficiency. The electrokinetic injection at negative polarity (anode at the detector end) introduced the micelle bound analytes. The hydrodynamic injection also maintained the MSS boundary inside the capillary. The stability of the MSS boundary affected SEHI where mild conditions that were low voltage as well as pressure injection were desired. The limits of detection were in the range from 0.6-4.2 ng mL~(-1). A strategy for optimization was described and the method was applied to the ng mL~(-1) analysis of spiked wastewater after simple dilution and centrifugation.
机译:在胶束电动色谱中研究了使用胶束到溶剂堆叠(MSS)在线同时浓缩样品中有机阳离子(三环抗抑郁药和β受体阻滞剂)的同时进行电动和流体动力学注射(SEH1)。与常规注射相比,通过流体动力注射获得的信号改善> 300倍。但是,使用SEHI时,引入毛细管的样品离子数量增加了,从而获得了高达4000倍的更高增益,而不会影响分离效率。负极(在检测器末端为阳极)的电动注入引入了胶束结合的分析物。流体动力注射还保持了毛细管内部的MSS边界。 MSS边界的稳定性会影响SEHI,在这些环境中,希望有低电压和压力注入等温和条件。检测限在0.6-4.2 ng mL〜(-1)范围内。描述了一种优化策略,并将该方法应用于简单稀释和离心分离后加标废水的ng mL〜(-1)分析。

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