生物样品中多氯联苯分析中的绿色脂肪去除

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2023-08-01 DOI:10.1016/j.sampre.2023.100081
J. Bintanel-Cenis, L. Herrero, B. Gómara, L. Ramos
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引用次数: 1

摘要

在生物样品中多氯联苯(PCBs)的分析中,提出了一种基于深度共晶溶剂(DES)的绿色分析方法来去除脂肪。使用优先多氯联苯同系物作为模型化合物,开发了一种完全避免使用矿物酸的新样品制备方法。一旦优化,该程序可以通过在60°C下用[氯化氯]:[草酸二水合物]1:1摩尔比处理30min来完成脂肪去除,每5min涡旋3s以促进浆液的均匀化。然后,用4mL正己烷萃取20min,从浆料中回收目标多氯联苯。这种基于DES的方法与气相色谱-四极杆质谱法(GC-qMS)相结合,用于最终的PCB测定。完整的分析方法提供了令人满意的目标化合物回收率(所有分析物的回收率都在87%以上),使用0.150g的少量样品。用相对标准偏差表示的完整程序的重复性小于5%,中间精密度优于14%。拟议方法的最终验证包括将脂质含量低于18%(w/w鲜重,fw)的选定脂肪食品中内源性多氯联苯的计算浓度与通过更传统和可接受的参考程序分析相同样品时发现的浓度进行令人满意的比较。在所有情况下,检测限均低于30pg/g fw(根据真实样品计算),证明了所提出的准确测定生物样品中目标化合物的方法的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Green fat removal in the analysis of polychlorinated biphenyls in biotic samples

A green analytical method based on the use of a deep eutectic solvent (DES) has been proposed for fat removal in the analysis of polychlorinated biphenyl (PCBs) in biotic samples. Using priority PCB congeners as model compounds, a novel sample preparation approach fully avoiding the use of mineral acids has been developed. Once optimized, the procedure allowed fat removal to be accomplished by 30min treatment with [chlorine chloride]:[oxalic acid dihydrated] 1:1 molar ratio at 60°C, with 3s vortexing every 5min to facilitate the homogenization of the slurry. Then, the target PCBs were recovered from the slurry by 20min extraction with 4mL of n-hexane. This DES-based method was combined with gas chromatography-quadrupole mass spectrometry (GC-qMS) for final PCB determination. The complete analytical method provided satisfactory recoveries of the target compounds (above 87% for all analytes), using as a small amount of sample as 0.150g. The repeatability of the complete procedure, expressed as relative standard deviation, was less than 5%, and the intermediate precision better than 14%. Final validation of the proposed methodology included the satisfactory comparison of the concentrations calculated for the endogenous PCBs in selected fatty foodstuffs with lipid contents under 18% (w/w fresh weight, fw) with those found when the same samples were analyzed by a more conventional and accepted reference procedure. The limits of detection were in all cases lower than 30 pg/g fw (as calculated for real samples), demonstrating the feasibility of the proposed procedure for accurate determination of the target compounds in biotic samples.

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