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优化微QuEChERS萃取结合气相色谱-质谱法快速测定贻贝样品中的邻苯二甲酸酯。

Optimization of micro-QuEChERS extraction coupled with gas chromatography-mass spectrometry for the fast determination of phthalic acid esters in mussel samples.

作者信息

Carro N, Fernández R, Sóñora S, Cobas J, García I, Ignacio M, Mouteira A

机构信息

Instituto Tecnolóxico para o Control do Medio Mariño de Galicia (INTECMAR), Consellería do mar, Xunta de Galicia, Peirao de Vilaxoán s/n, 36611 Vilagarcía de Arousa, Spain.

出版信息

Anal Methods. 2023 Apr 6;15(14):1836-1845. doi: 10.1039/d3ay00042g.

DOI:10.1039/d3ay00042g
PMID:36974432
Abstract

In this study, a new miniaturized version of the analytical method based on the Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) technique using Florisil in the cleanup step for extracting six phthalic acid esters (PAEs) in mussel samples was developed by using a design of experiments. For this purpose, 1.5 mL of ultrapure water and later, 1.5 mL of acetonitrile were added to 0.1 g of the lyophilized sample, followed by 0.3 g of a commercial extraction salt packet (magnesium sulfate, sodium chloride, sodium citrate dihydrate, and sodium hydrogencitrate sesquihydrate). The recovered extract was purified using 0.1 g of Florisil. The final extract was evaporated and reconstituted in 1 mL of hexane. The six phthalates were determined by a GC-MS (SIM) system. The whole method was validated at two concentration levels. Recoveries ranged from 79% to 108%. Reproducibility in terms of coefficients of variation was between 4.9% and 12.1%. The limits of quantification of the whole method were between 0.53 and 38.0 μg per kg dry weight. Five mussel samples coming from the Galician Rías were analysed using this method. Except for three of the five samples where DOP (di--octyl phthalate) was below the limit of quantification, all PAEs were found in concentrations that ranged between 1.99 and 372.7 μg per kg dry weight.

摘要

在本研究中,采用实验设计方法,开发了一种基于快速、简便、廉价、高效、耐用和安全(QuEChERS)技术的新型小型化分析方法,该方法在净化步骤中使用弗罗里硅土来提取贻贝样品中的六种邻苯二甲酸酯(PAEs)。为此,向0.1 g冻干样品中加入1.5 mL超纯水,随后加入1.5 mL乙腈,再加入0.3 g市售萃取盐包(硫酸镁、氯化钠、二水合柠檬酸钠和倍半水合柠檬酸氢钠)。用0.1 g弗罗里硅土对回收的提取物进行净化。将最终提取物蒸发,并用1 mL己烷复溶。通过气相色谱-质谱联用(SIM)系统测定六种邻苯二甲酸酯。整个方法在两个浓度水平上进行了验证。回收率在79%至108%之间。变异系数方面的重现性在4.9%至12.1%之间。整个方法的定量限为每千克干重0.53至38.0 μg。使用该方法分析了来自加利西亚里亚斯的五个贻贝样品。除了五个样品中有三个样品的邻苯二甲酸二辛酯(DOP)低于定量限外,所有PAEs的浓度范围为每千克干重1.99至372.7 μg。

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