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Development and Validation of LC-Q-TOF-MS Methodology to Determine Mycotoxin Biomarkers in Human Urine

Mycotoxin contamination of foodstuffs is a health concern worldwide and monitoring human exposure to mycotoxins is a key concern. Most mycotoxins and their metabolites are excreted in urine, but a reliable detection method is required, considering the low levels present in this biological sample. Th...

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Autores principales: Dasí-Navarro, Nuria, Lozano, Manuel, Llop, Sabrina, Esplugues, Ana, Cimbalo, Alessandra, Font, Guillermina, Manyes, Lara, Mañes, Jordi, Vila-Donat, Pilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612178/
https://www.ncbi.nlm.nih.gov/pubmed/36287920
http://dx.doi.org/10.3390/toxins14100651
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author Dasí-Navarro, Nuria
Lozano, Manuel
Llop, Sabrina
Esplugues, Ana
Cimbalo, Alessandra
Font, Guillermina
Manyes, Lara
Mañes, Jordi
Vila-Donat, Pilar
author_facet Dasí-Navarro, Nuria
Lozano, Manuel
Llop, Sabrina
Esplugues, Ana
Cimbalo, Alessandra
Font, Guillermina
Manyes, Lara
Mañes, Jordi
Vila-Donat, Pilar
author_sort Dasí-Navarro, Nuria
collection PubMed
description Mycotoxin contamination of foodstuffs is a health concern worldwide and monitoring human exposure to mycotoxins is a key concern. Most mycotoxins and their metabolites are excreted in urine, but a reliable detection method is required, considering the low levels present in this biological sample. The aim of this work is to validate a sensitive methodology capable of simultaneously determining ten targeted mycotoxins as well as detecting untargeted ones by using Liquid Chromatography coupled to Quadrupole Time of Flight Mass Spectrometry (LC-Q-TOF-MS). The targeted mycotoxins were: enniatin A, B, A1, and B1, beauvericine, aflatoxin B1, B2, G1 and G2, and ochratoxin A. Several extraction procedures such as liquid-liquid extraction, dilute and shoot, and QuEChERS were assessed. Finally, a modified simple QuEChERS extraction method was selected. Creatinine adjustment and matrix-matched calibration curves are required. The limit of detection and limit of quantification values ranged from 0.1 to 1.5 and from 0.3 to 5 ng/mL, respectively. Recoveries achieved were higher than 65% for all mycotoxins. Later, the method was applied to 100 samples of women’s urine to confirm the applicability and determine their internal exposure. The untargeted mycotoxins most found were trichothecenes, zearalenones, and ochratoxins.
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spelling pubmed-96121782022-10-28 Development and Validation of LC-Q-TOF-MS Methodology to Determine Mycotoxin Biomarkers in Human Urine Dasí-Navarro, Nuria Lozano, Manuel Llop, Sabrina Esplugues, Ana Cimbalo, Alessandra Font, Guillermina Manyes, Lara Mañes, Jordi Vila-Donat, Pilar Toxins (Basel) Article Mycotoxin contamination of foodstuffs is a health concern worldwide and monitoring human exposure to mycotoxins is a key concern. Most mycotoxins and their metabolites are excreted in urine, but a reliable detection method is required, considering the low levels present in this biological sample. The aim of this work is to validate a sensitive methodology capable of simultaneously determining ten targeted mycotoxins as well as detecting untargeted ones by using Liquid Chromatography coupled to Quadrupole Time of Flight Mass Spectrometry (LC-Q-TOF-MS). The targeted mycotoxins were: enniatin A, B, A1, and B1, beauvericine, aflatoxin B1, B2, G1 and G2, and ochratoxin A. Several extraction procedures such as liquid-liquid extraction, dilute and shoot, and QuEChERS were assessed. Finally, a modified simple QuEChERS extraction method was selected. Creatinine adjustment and matrix-matched calibration curves are required. The limit of detection and limit of quantification values ranged from 0.1 to 1.5 and from 0.3 to 5 ng/mL, respectively. Recoveries achieved were higher than 65% for all mycotoxins. Later, the method was applied to 100 samples of women’s urine to confirm the applicability and determine their internal exposure. The untargeted mycotoxins most found were trichothecenes, zearalenones, and ochratoxins. MDPI 2022-09-20 /pmc/articles/PMC9612178/ /pubmed/36287920 http://dx.doi.org/10.3390/toxins14100651 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dasí-Navarro, Nuria
Lozano, Manuel
Llop, Sabrina
Esplugues, Ana
Cimbalo, Alessandra
Font, Guillermina
Manyes, Lara
Mañes, Jordi
Vila-Donat, Pilar
Development and Validation of LC-Q-TOF-MS Methodology to Determine Mycotoxin Biomarkers in Human Urine
title Development and Validation of LC-Q-TOF-MS Methodology to Determine Mycotoxin Biomarkers in Human Urine
title_full Development and Validation of LC-Q-TOF-MS Methodology to Determine Mycotoxin Biomarkers in Human Urine
title_fullStr Development and Validation of LC-Q-TOF-MS Methodology to Determine Mycotoxin Biomarkers in Human Urine
title_full_unstemmed Development and Validation of LC-Q-TOF-MS Methodology to Determine Mycotoxin Biomarkers in Human Urine
title_short Development and Validation of LC-Q-TOF-MS Methodology to Determine Mycotoxin Biomarkers in Human Urine
title_sort development and validation of lc-q-tof-ms methodology to determine mycotoxin biomarkers in human urine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612178/
https://www.ncbi.nlm.nih.gov/pubmed/36287920
http://dx.doi.org/10.3390/toxins14100651
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