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基于天然深共晶溶剂的食用油脂中总 3-氯-1,2-丙二醇的空气辅助液-液微萃取及其气相色谱-质谱法测定。

Air-assisted liquid-liquid microextraction of total 3-monochloropropane-1,2-diol from refined edible oils based on a natural deep eutectic solvent and its determination by gas chromatography-mass spectrometry.

机构信息

Food and Drug Safety Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Pharmaceutics and Food Control, Faculty of Pharmacy, Tabriz University of Medical Science, Tabriz, Iran.

Sivas Cumhuriyet University, Department of Chemistry, Sivas, Turkey.

出版信息

J Chromatogr A. 2021 Oct 25;1656:462559. doi: 10.1016/j.chroma.2021.462559. Epub 2021 Sep 15.

DOI:10.1016/j.chroma.2021.462559
PMID:34571280
Abstract

In this paper, a fast, sensitive, and selective sample preparation procedure was presented for the determination of 3-monochloropropane-1,2-diol (3-MCPD) in refined edible oils using gas chromatography-mass spectrometry. In this method, firstly, the sample lipids and analyte fatty esters are saponified by sodium hydroxide under sonication. After that the analyte was derivatized using phenylboronic acid (as the derivatization agent) and the obtained derivative was extracted during an air-assisted liquid-liquid microextraction procedure (AALLME). Six different deep eutectic solvents (DESs) were prepared as the extraction solvents and the most effective extraction for 3-MCPD was obtained in the presence of a natural DES (NDES) consisting of choline chloride (ChCl)-acetic acid (AcOH). Important variables such as sodium hydroxide concentration and volume, sonication time, temperature, extraction solvent type and volume, and phenylboronic acid concentration and volume have been optimized. Using the optimum conditions, broad linear range (0.88-1000 ng g), suitable coefficient of determination (0.995), and low limits of detection (0.26 ng g) and quantification (0.88 ng g) were obtained. Relative standard deviations for intra- (n=8) and inter-day (n=6) precisions at a concentration of 5 ng g were 2.6 and 3.2%, respectively. The developed method has been successfully applied to 3-MCPD determination in refined edible oil samples including sunflower, corn, and canola oils.

摘要

本文提出了一种快速、灵敏、选择性的样品前处理方法,用于气相色谱-质谱法测定精炼食用油中的 3-氯-1,2-丙二醇(3-MCPD)。在该方法中,首先,样品脂质和分析物脂肪酸酯在超声波作用下用氢氧化钠皂化。然后,使用苯硼酸(作为衍生化试剂)对分析物进行衍生化,所得衍生物在空气辅助液-液微萃取(AALLME)过程中进行提取。制备了六种不同的深共晶溶剂(DESs)作为萃取溶剂,在含有胆碱氯化物(ChCl)-乙酸(AcOH)的天然 DES(NDES)存在下,获得了对 3-MCPD 的最有效萃取。优化了重要变量,如氢氧化钠浓度和体积、超声时间、温度、萃取溶剂类型和体积以及苯硼酸浓度和体积。在最佳条件下,获得了宽线性范围(0.88-1000ngg)、合适的决定系数(0.995)和低检测限(0.26ngg)和定量限(0.88ngg)。在 5ngg 浓度下,日内(n=8)和日间(n=6)精密度的相对标准偏差分别为 2.6%和 3.2%。该方法已成功应用于葵花籽油、玉米油和菜籽油等精炼食用油中 3-MCPD 的测定。

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