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Optimization of Aflatoxin B(1)-Lysine Analysis for Public Health Exposure Studies
Aflatoxin B(1) is a potent human carcinogen produced by several species of Aspergillus mainly found on nuts and maize. Exposures in parts of Africa, Latin America and Asia can be at multiples, sometimes orders of magnitude above tolerable daily levels. Although human exposure to aflatoxin can be est...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606987/ https://www.ncbi.nlm.nih.gov/pubmed/36287941 http://dx.doi.org/10.3390/toxins14100672 |
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author | Renaud, Justin B Walsh, Jacob P Sumarah, Mark W |
author_facet | Renaud, Justin B Walsh, Jacob P Sumarah, Mark W |
author_sort | Renaud, Justin B |
collection | PubMed |
description | Aflatoxin B(1) is a potent human carcinogen produced by several species of Aspergillus mainly found on nuts and maize. Exposures in parts of Africa, Latin America and Asia can be at multiples, sometimes orders of magnitude above tolerable daily levels. Although human exposure to aflatoxin can be estimated by analysis of the diet, only determination of the serum albumin aflatoxin adduct provides a health-relevant exposure measure. The lack of a reference serum limits interlaboratory method validation and data comparisons. In this study, we synthetically produced AFB(1)-dialdehyde and covalently coupled it to serum albumin in human serum. This synthetic produced aflatoxin-serum reference material was used in conjunction with isotopically labelled internal standards to evaluate sample digestion methods. This showed using sufficient Pronase in the digestion step was critical to ensure complete proteolytic digestion, which occurs within 4 h. Increasing the digestion temperature from 37 °C to 50 °C also provided a benefit to the overall analysis. In addition, the use of dried blood spots and Volumetric Absorptive Microsampling (VAMS) were investigated showing samples stored with VAMS produced equivalent results to serum samples. |
format | Online Article Text |
id | pubmed-9606987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96069872022-10-28 Optimization of Aflatoxin B(1)-Lysine Analysis for Public Health Exposure Studies Renaud, Justin B Walsh, Jacob P Sumarah, Mark W Toxins (Basel) Article Aflatoxin B(1) is a potent human carcinogen produced by several species of Aspergillus mainly found on nuts and maize. Exposures in parts of Africa, Latin America and Asia can be at multiples, sometimes orders of magnitude above tolerable daily levels. Although human exposure to aflatoxin can be estimated by analysis of the diet, only determination of the serum albumin aflatoxin adduct provides a health-relevant exposure measure. The lack of a reference serum limits interlaboratory method validation and data comparisons. In this study, we synthetically produced AFB(1)-dialdehyde and covalently coupled it to serum albumin in human serum. This synthetic produced aflatoxin-serum reference material was used in conjunction with isotopically labelled internal standards to evaluate sample digestion methods. This showed using sufficient Pronase in the digestion step was critical to ensure complete proteolytic digestion, which occurs within 4 h. Increasing the digestion temperature from 37 °C to 50 °C also provided a benefit to the overall analysis. In addition, the use of dried blood spots and Volumetric Absorptive Microsampling (VAMS) were investigated showing samples stored with VAMS produced equivalent results to serum samples. MDPI 2022-09-28 /pmc/articles/PMC9606987/ /pubmed/36287941 http://dx.doi.org/10.3390/toxins14100672 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 Renaud, Justin B Walsh, Jacob P Sumarah, Mark W Optimization of Aflatoxin B(1)-Lysine Analysis for Public Health Exposure Studies |
title | Optimization of Aflatoxin B(1)-Lysine Analysis for Public Health Exposure Studies |
title_full | Optimization of Aflatoxin B(1)-Lysine Analysis for Public Health Exposure Studies |
title_fullStr | Optimization of Aflatoxin B(1)-Lysine Analysis for Public Health Exposure Studies |
title_full_unstemmed | Optimization of Aflatoxin B(1)-Lysine Analysis for Public Health Exposure Studies |
title_short | Optimization of Aflatoxin B(1)-Lysine Analysis for Public Health Exposure Studies |
title_sort | optimization of aflatoxin b(1)-lysine analysis for public health exposure studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606987/ https://www.ncbi.nlm.nih.gov/pubmed/36287941 http://dx.doi.org/10.3390/toxins14100672 |
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