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Non-targeted analysis of unexpected food contaminants using LC-HRMS

A non-target analysis method for unexpected contaminants in food is described. Many current methods referred to as “non-target” are capable of detecting hundreds or even thousands of contaminants. However, they will typically still miss all other possible contaminants. Instead, a metabolomics approa...

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Autores principales: Kunzelmann, Marco, Winter, Martin, Åberg, Magnus, Hellenäs, Karl-Erik, Rosén, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096699/
https://www.ncbi.nlm.nih.gov/pubmed/29594430
http://dx.doi.org/10.1007/s00216-018-1028-4
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author Kunzelmann, Marco
Winter, Martin
Åberg, Magnus
Hellenäs, Karl-Erik
Rosén, Johan
author_facet Kunzelmann, Marco
Winter, Martin
Åberg, Magnus
Hellenäs, Karl-Erik
Rosén, Johan
author_sort Kunzelmann, Marco
collection PubMed
description A non-target analysis method for unexpected contaminants in food is described. Many current methods referred to as “non-target” are capable of detecting hundreds or even thousands of contaminants. However, they will typically still miss all other possible contaminants. Instead, a metabolomics approach might be used to obtain “true non-target” analysis. In the present work, such a method was optimized for improved detection capability at low concentrations. The method was evaluated using 19 chemically diverse model compounds spiked into milk samples to mimic unknown contamination. Other milk samples were used as reference samples. All samples were analyzed with UHPLC-TOF-MS (ultra-high-performance liquid chromatography time-of-flight mass spectrometry), using reversed-phase chromatography and electrospray ionization in positive mode. Data evaluation was performed by the software TracMass 2. No target lists of specific compounds were used to search for the contaminants. Instead, the software was used to sort out all features only occurring in the spiked sample data, i.e., the workflow resembled a metabolomics approach. Procedures for chemical identification of peaks were outside the scope of the study. Method, study design, and settings in the software were optimized to minimize manual evaluation and faulty or irrelevant hits and to maximize hit rate of the spiked compounds. A practical detection limit was established at 25 μg/kg. At this concentration, most compounds (17 out of 19) were detected as intact precursor ions, as fragments or as adducts. Only 2 irrelevant hits, probably natural compounds, were obtained. Limitations and possible practical use of the approach are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-018-1028-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-60966992018-08-24 Non-targeted analysis of unexpected food contaminants using LC-HRMS Kunzelmann, Marco Winter, Martin Åberg, Magnus Hellenäs, Karl-Erik Rosén, Johan Anal Bioanal Chem Research Paper A non-target analysis method for unexpected contaminants in food is described. Many current methods referred to as “non-target” are capable of detecting hundreds or even thousands of contaminants. However, they will typically still miss all other possible contaminants. Instead, a metabolomics approach might be used to obtain “true non-target” analysis. In the present work, such a method was optimized for improved detection capability at low concentrations. The method was evaluated using 19 chemically diverse model compounds spiked into milk samples to mimic unknown contamination. Other milk samples were used as reference samples. All samples were analyzed with UHPLC-TOF-MS (ultra-high-performance liquid chromatography time-of-flight mass spectrometry), using reversed-phase chromatography and electrospray ionization in positive mode. Data evaluation was performed by the software TracMass 2. No target lists of specific compounds were used to search for the contaminants. Instead, the software was used to sort out all features only occurring in the spiked sample data, i.e., the workflow resembled a metabolomics approach. Procedures for chemical identification of peaks were outside the scope of the study. Method, study design, and settings in the software were optimized to minimize manual evaluation and faulty or irrelevant hits and to maximize hit rate of the spiked compounds. A practical detection limit was established at 25 μg/kg. At this concentration, most compounds (17 out of 19) were detected as intact precursor ions, as fragments or as adducts. Only 2 irrelevant hits, probably natural compounds, were obtained. Limitations and possible practical use of the approach are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-018-1028-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-03-29 2018 /pmc/articles/PMC6096699/ /pubmed/29594430 http://dx.doi.org/10.1007/s00216-018-1028-4 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Paper
Kunzelmann, Marco
Winter, Martin
Åberg, Magnus
Hellenäs, Karl-Erik
Rosén, Johan
Non-targeted analysis of unexpected food contaminants using LC-HRMS
title Non-targeted analysis of unexpected food contaminants using LC-HRMS
title_full Non-targeted analysis of unexpected food contaminants using LC-HRMS
title_fullStr Non-targeted analysis of unexpected food contaminants using LC-HRMS
title_full_unstemmed Non-targeted analysis of unexpected food contaminants using LC-HRMS
title_short Non-targeted analysis of unexpected food contaminants using LC-HRMS
title_sort non-targeted analysis of unexpected food contaminants using lc-hrms
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096699/
https://www.ncbi.nlm.nih.gov/pubmed/29594430
http://dx.doi.org/10.1007/s00216-018-1028-4
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