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一种新型微萃取纤维与在线样品堆积毛细管电泳紫外检测联用用于实际水样中酸性药物测定的方法的开发。

Development of a New Microextraction Fiber Combined to On-Line Sample Stacking Capillary Electrophoresis UV Detection for Acidic Drugs Determination in Real Water Samples.

作者信息

Espina-Benitez Maria, Araujo Lilia, Prieto Avismelsi, Navalón Alberto, Vílchez José Luis, Valera Paola, Zambrano Ana, Dugas Vincent

机构信息

Laboratory of Analytical Chemistry and Electrochemistry, Faculty of Engineering, University of Zulia, P.O. Box 4011-A-526, Maracaibo 4005, Venezuela.

Université de Lyon, CNRS, Université Claude Bernard Lyon 1, ENS de Lyon, Institut des Sciences Analytiques, UMR 5280, 5 rue de la Doua, F-69100 VILLEURBANNE, France.

出版信息

Int J Environ Res Public Health. 2017 Jul 7;14(7):739. doi: 10.3390/ijerph14070739.

Abstract

A new analytical method coupling a (off-line) solid-phase microextraction with an on-line capillary electrophoresis (CE) sample enrichment technique was developed for the analysis of ketoprofen, naproxen and clofibric acid from water samples, which are known as contaminants of emerging concern in aquatic environments. New solid-phase microextraction fibers based on physical coupling of chromatographic supports onto epoxy glue coated needle were studied for the off-line preconcentration of these micropollutants. Identification and quantification of such acidic drugs were done by capillary zone electrophoresis (CZE) using ultraviolet diode array detection (DAD). Further enhancement of concentration sensitivity detection was achieved by on-line CE "acetonitrile stacking" preconcentration technique. Among the eight chromatographic supports investigated, Porapak Q sorbent showed higher extraction and preconcentration capacities. The screening of parameters that influence the microextraction process was carried out using a two-level fractional factorial. Optimization of the most relevant parameters was then done through a surface response three-factor Box-Behnken design. The limits of detection and limits of quantification for the three drugs ranged between 0.96 and 1.27 µg∙L and 2.91 and 3.86 µg∙L, respectively. Recovery yields of approximately 95 to 104% were measured. The developed method is simple, precise, accurate, and allows quantification of residues of these micropollutants in Genil River water samples using inexpensive fibers.

摘要

开发了一种新的分析方法,该方法将(离线)固相微萃取与在线毛细管电泳(CE)样品富集技术相结合,用于分析水样中的酮洛芬、萘普生和氯贝酸,这些物质是水生环境中新兴的污染物。研究了基于将色谱载体物理偶联到涂有环氧胶的针上的新型固相微萃取纤维,用于这些微污染物的离线预富集。通过使用紫外二极管阵列检测(DAD)的毛细管区带电泳(CZE)对这些酸性药物进行鉴定和定量。通过在线CE“乙腈堆积”预富集技术进一步提高了浓度灵敏度检测。在所研究的八种色谱载体中,Porapak Q吸附剂表现出更高的萃取和预富集能力。使用二级分数因子设计对影响微萃取过程的参数进行筛选。然后通过表面响应三因子Box-Behnken设计对最相关的参数进行优化。三种药物的检测限和定量限分别在0.96至1.27μg∙L和2.91至3.86μg∙L之间。测得的回收率约为95%至104%。所开发的方法简单、精确、准确,并且使用廉价的纤维能够对赫尼尔河水样中的这些微污染物残留进行定量分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4276/5551177/8a3f0d7daa77/ijerph-14-00739-g001.jpg

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