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采用离线等速电泳样品预处理的硝基酚毛细管区带电泳法。

Capillary zone electrophoresis of nitrophenols with off-line isotachophoretic sample pretreatment.

作者信息

Kaniansky D, Masár M

机构信息

Department of Analytical Chemistry, Faculty of Natural Sciences, Comenius University, Bratislava, Slovak Republic.

出版信息

Electrophoresis. 1997 Feb;18(2):260-7. doi: 10.1002/elps.1150180214.

Abstract

Preparative capillary isotachophoresis (ITP) operating in a discontinuous fractionation mode was studied as a sample pretreatment technique for capillary zone electrophoresis (CZE) trace analysis of a group of ten nitrophenols. Different separation mechanisms employed by these capillary electrophoresis techniques made possible a group isolation of the studied analytes by ITP while their CZE resolutions based on differences in the interactions with polyvinylpyrrolidone (PVP) provided suitable conditions for a final analytical evaluation. Experiments with model and practical water samples revealed high and reproducible recovery rates of the ITP pretreatment of nitrophenols when sample loadability limits of the preparative ITP equipment were met. A main disadvantage of the studied ITP-CZE combination was an inefficient use of the pretreated sample as only 0.5% of the fraction containing nitrophenols was used in the final CZE step. Despite these limitations associated with the CZE sample injection, the concentration limit of detection (LOD) for nitrophenols in practical water samples could be reduced to 2-8 ppb concentrations (photometric absorbance detector operating at a 254 nm wavelength) when 200 microL sample volumes were taken for the ITP pretreatment. This was accompanied by an efficient sample clean-up as no other trace ionic constituents originating from the samples were detected on CZE.

摘要

研究了以不连续分级模式运行的制备型毛细管等速电泳(ITP)作为一组十种硝基酚毛细管区带电泳(CZE)痕量分析的样品预处理技术。这些毛细管电泳技术采用的不同分离机制使得通过ITP对所研究的分析物进行组分离成为可能,而基于它们与聚乙烯吡咯烷酮(PVP)相互作用差异的CZE分辨率为最终的分析评估提供了合适的条件。对模型水样和实际水样进行的实验表明,当达到制备型ITP设备的样品负载能力极限时,ITP对硝基酚的预处理具有高且可重复的回收率。所研究的ITP-CZE组合的一个主要缺点是预处理样品的利用效率低下,因为在最终的CZE步骤中仅使用了含硝基酚馏分的0.5%。尽管存在与CZE进样相关的这些限制,但当取200微升样品体积进行ITP预处理时,实际水样中硝基酚的浓度检测限(LOD)可降至2 - 8 ppb浓度(在254 nm波长下运行的光度吸收检测器)。这伴随着有效的样品净化,因为在CZE上未检测到来自样品的其他痕量离子成分。

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