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A liquid chromatography/tandem mass spectrometric multi-mycotoxin method for the quantification of 87 analytes and its application to semi-quantitative screening of moldy food samples

机译:液相色谱/串联质谱多霉菌毒素法定量分析87种分析物及其在发霉食品样品的半定量筛选中的应用

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摘要

This paper describes the extension of a previously published method based on liquid chromatography/electrospray ionization tandem mass spectrometry (HPLC/ESI-MS/MS) from 39 to currently 87 analytes. Besides the mycotoxins for which regulated concentrations exist, the method now comprises not only almost all mycotoxins for which standards are commercially available, but also a number of other important metabolites produced by fungi involved in food spoilage. The method is based on a single extraction step using an acidified acetonitrile/water mixture followed by analysis of the diluted crude extract. Method performance characteristics were determined after spiking breadcrumbs as model matrix at multiple concentration levels. With very few exceptions, coefficients of variation of the whole procedure of <5% and repeatabilities at the highest spiking level of <7% were obtained. Limits of detection ranged between 0.02 and 225 μg kg?1. The quantitative determination of ergopeptides was disturbed by epimerization due to the acidic conditions. From the remaining 77 analytes, the apparent recoveries of nine substances deviated significantly from the CEN target range of 70–110% due to incomplete extraction and/or matrix effects. In principle, the latter can be compensated for by the application of matrix-matched calibration. The developed method was applied to 18 moldy samples (including bread, fruits, vegetables, jam, cheese, chestnuts and red wine) from private households. This study revealed the great value of the described method: 37 different fungal metabolites were identified at concentrations of up to 33 mg kg?1, and some of these have never been reported before in the context of moldy food products.
机译:本文介绍了基于液相色谱/电喷雾串联质谱法(HPLC / ESI-MS / MS)的先前发布方法的扩展,将其从39种分析物扩展到目前的87种分析物。除了存在浓度受控的霉菌毒素外,该方法现在不仅包括几乎所有市售标准品的霉菌毒素,还包括与食物腐败有关的真菌产生的许多其他重要代谢产物。该方法基于使用酸化的乙腈/水混合物的单一提取步骤,然后分析稀释的粗提物。在将面包屑加标为多个浓度水平的模型基质后,确定了方法的性能特征。除极少数例外外,整个过程的变异系数均<5%,最高加标水平的重复性<7%。检出限为0.02至225μgkg?1 。由于酸性条件,差向异构化干扰了麦角肽的定量测定。在剩余的77种分析物中,由于不完全提取和/或基质效应,九种物质的表观回收率明显偏离CEN目标范围70-110%。原则上,后者可以通过矩阵匹配校准来补偿。该方法适用于18个来自私人家庭的发霉样品(包括面包,水果,蔬菜,果酱,奶酪,栗子和红酒)。这项研究揭示了上述方法的巨大价值:鉴定出37种不同的真菌代谢物,其最高浓度为33 mg kg?1 ,其中一些在霉变食品中从未被报道过。

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  • 来源
    《Analytical and Bioanalytical Chemistry》 |2007年第5期|1505-1523|共19页
  • 作者单位

    Christian Doppler Laboratory for Mycotoxin Research Department IFA-Tulln University of Natural Resources and Applied Life Sciences Vienna Konrad Lorenzstr. 20 3430 Tulln Austria;

    Christian Doppler Laboratory for Mycotoxin Research Department IFA-Tulln University of Natural Resources and Applied Life Sciences Vienna Konrad Lorenzstr. 20 3430 Tulln Austria;

    Christian Doppler Laboratory for Mycotoxin Research Department IFA-Tulln University of Natural Resources and Applied Life Sciences Vienna Konrad Lorenzstr. 20 3430 Tulln Austria;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Liquid chromatography; Tandem mass spectrometry; Mycotoxins; Multi-target analysis; Food analysis; Molds;

    机译:液相色谱串联质谱霉菌毒素多目标分析食品分析霉菌;

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