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多壁碳纳米管涂覆的棒状吸附微萃取 - 痕量分析环境水样中药物的应用。

Bar adsorptive microextraction coated with multi-walled carbon nanotube phases - Application for trace analysis of pharmaceuticals in environmental waters.

机构信息

Environmental Sciences Institute (ICAM), Department of Analytical Chemistry and Food Technology, University of Castilla-La Mancha, Avda. Carlos III s/n, 45071 Toledo, Spain.

Centro de Química e Bioquímica e Centro de Química Estrutural, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, Campo Grande, 1749-016 Lisboa, Portugal.

出版信息

J Chromatogr A. 2019 Aug 30;1600:17-22. doi: 10.1016/j.chroma.2019.04.035. Epub 2019 Apr 13.

DOI:10.1016/j.chroma.2019.04.035
PMID:31005293
Abstract

Bar adsorptive microextraction devices were modified with multi-walled carbon nanotubes for the first time. A bar adsorptive microextraction method followed by microliquid desorption and high-performance liquid chromatography with diode array detection was developed for the determination of trace levels of ketoprofen, diclofenac, gemfibrozil and mefenamic acid in water samples. The mean parameters affecting the bar adsorptive microextraction and microliquid desorption efficiency were studied and optimized using a univariate optimization strategy. The methodology was validated in terms of linearity, limits of detection and quantification, recovery, intra- and inter-day precision, accuracy, and matrix effect. The developed method showed lower limits of quantification of 0.35 μg L, calibration curves from 0.35 up to 1000.0 μg L and determination coefficients higher than 0.9917. Recoveries in tap, surface, sea and waste water samples at three spiking levels were between 70.2 and 117.3% for all the pharmaceuticals. The coefficients of variation values for intra- (n = 6) and inter-day precisions (n = 18) were below 9.7%. The proposed analytical methodology allowed preconcentration factors up to 250 and proved to be cost-effective, easy to operate and environmentally friendly.

摘要

首次采用多壁碳纳米管对棒状吸附微萃取装置进行了修饰。建立了一种棒状吸附微萃取方法,随后采用微液相解吸和高效液相色谱-二极管阵列检测法,用于测定水样中痕量的酮洛芬、双氯芬酸、吉非罗齐和甲芬那酸。采用单因素优化策略研究并优化了影响棒状吸附微萃取和微液相解吸效率的平均参数。该方法在线性、检测限和定量限、回收率、日内和日间精密度、准确度和基质效应等方面进行了验证。所建立的方法具有较低的检出限(0.35μg/L)、从 0.35 至 1000.0μg/L 的校准曲线和大于 0.9917 的测定系数。在三种加标水平下,在自来水、地表水、海水和废水中的所有药物的回收率均在 70.2%至 117.3%之间。日内(n=6)和日间精密度(n=18)的变异系数值均低于 9.7%。该分析方法允许浓缩因子高达 250 倍,且具有成本效益高、易于操作和环境友好等优点。

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