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采用固相萃取与气相色谱-串联质谱法分析食品基质中的呋喃及其衍生物。

Analysis of Furan and Its Derivatives in Food Matrices Using Solid Phase Extraction Coupled with Gas Chromatography-Tandem Mass Spectrometry.

机构信息

Department of Food Science, Fu Jen Catholic University, New Taipei City 242, Taiwan.

National Institute of Environmental Health Sciences, Miaoli 350, Taiwan.

出版信息

Molecules. 2023 Feb 8;28(4):1639. doi: 10.3390/molecules28041639.

DOI:10.3390/molecules28041639
PMID:36838626
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9963530/
Abstract

The objective of this study was to develop a simultaneous analysis method of furan and its 10 derivatives in different food commodities. The results indicated that furan and its 10 derivatives could be separated within 9.5 min by using a HP-5MS column and gas chromatography-tandem mass spectrometry (GC-MS/MS) with multiple reaction monitoring mode for detection. Furthermore, this method could resolve several furan isomers, such as 2-methyl furan and 3-methyl furan, as well as 2,3-dimethyl furan and 2,5-dimethyl furan. The most optimal extraction conditions were: 5 g of the fruit or juice sample mixed with 5 mL of the saturated NaCl solution, separately, or 1 g of the canned oily fish sample mixed with 9 mL of the saturated NaCl solution, followed by the equilibration of each sample at 35 °C for 15 min, using a carboxen-polydimethylsiloxane SPME arrow to adsorb the analytes for 15 min at 35 °C for subsequent analysis by GC-MS/MS. For method validation of all the analytes in the different food matrices, the recovery was 76-117% and the limit of the quantitation was 0.003-0.675 ng/g, while the relative standard deviation (RSD%) of the intra-day variability range from 1-16%, and that of the inter-day variability was from 4-20%. The method validation data further demonstrated that a reliable method was established for the analysis of furan and its 10 derivatives in commercial foods.

摘要

本研究旨在开发一种同时分析不同食品中呋喃及其 10 种衍生物的方法。结果表明,采用 HP-5MS 柱和气相色谱-串联质谱(GC-MS/MS)多反应监测模式,可在 9.5 分钟内分离呋喃及其 10 种衍生物。此外,该方法还可分辨几种呋喃异构体,如 2-甲基呋喃和 3-甲基呋喃,以及 2,3-二甲基呋喃和 2,5-二甲基呋喃。最佳提取条件为:将 5 g 水果或果汁样品与 5 mL 饱和 NaCl 溶液混合,或 1 g 罐装油性鱼样品与 9 mL 饱和 NaCl 溶液混合,然后将每个样品在 35°C 下平衡 15 min,使用羧基-聚二甲基硅氧烷 SPME 箭头在 35°C 下吸附分析物 15 min,随后进行 GC-MS/MS 分析。对不同食品基质中所有分析物的方法验证,回收率为 76-117%,定量限为 0.003-0.675ng/g,日内变异度的相对标准偏差(RSD%)为 1-16%,日间变异度的 RSD%为 4-20%。方法验证数据进一步表明,已建立了一种可靠的方法,可用于分析商业食品中的呋喃及其 10 种衍生物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d18/9963530/348000646ed2/molecules-28-01639-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d18/9963530/95af63188865/molecules-28-01639-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d18/9963530/45b3ddfa25fc/molecules-28-01639-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d18/9963530/348000646ed2/molecules-28-01639-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d18/9963530/95af63188865/molecules-28-01639-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d18/9963530/45b3ddfa25fc/molecules-28-01639-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d18/9963530/348000646ed2/molecules-28-01639-g003.jpg

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