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Fluorescence Polarization Immunoassay of Mycotoxins: A Review

Immunoassays are routinely used in the screening of commodities and foods for fungal toxins (mycotoxins). Demands to increase speed and lower costs have lead to continued improvements in such assays. Because many reported mycotoxins are low molecular weight (below 1 kDa), immunoassays for their dete...

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Autor principal: Maragos, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202780/
https://www.ncbi.nlm.nih.gov/pubmed/22069541
http://dx.doi.org/10.3390/toxins1020196
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author Maragos, Chris
author_facet Maragos, Chris
author_sort Maragos, Chris
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description Immunoassays are routinely used in the screening of commodities and foods for fungal toxins (mycotoxins). Demands to increase speed and lower costs have lead to continued improvements in such assays. Because many reported mycotoxins are low molecular weight (below 1 kDa), immunoassays for their detection have generally been constructed in competitive heterogeneous formats. An exception is fluorescence polarization immunoassay (FPIA), a homogeneous format that does not require the separation of bound and free labels (tracer). The potential for rapid, solution phase, immunoassays has been realized in the development of FPIA for many of the major groups of mycotoxins, including aflatoxins, fumonisins, group B trichothecenes (primarily deoxynivalenol), ochratoxin A, and zearalenone. This review describes the basic principles of FPIA and summarizes recent research in this area with regard to mycotoxins.
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spelling pubmed-32027802011-11-08 Fluorescence Polarization Immunoassay of Mycotoxins: A Review Maragos, Chris Toxins (Basel) Review Immunoassays are routinely used in the screening of commodities and foods for fungal toxins (mycotoxins). Demands to increase speed and lower costs have lead to continued improvements in such assays. Because many reported mycotoxins are low molecular weight (below 1 kDa), immunoassays for their detection have generally been constructed in competitive heterogeneous formats. An exception is fluorescence polarization immunoassay (FPIA), a homogeneous format that does not require the separation of bound and free labels (tracer). The potential for rapid, solution phase, immunoassays has been realized in the development of FPIA for many of the major groups of mycotoxins, including aflatoxins, fumonisins, group B trichothecenes (primarily deoxynivalenol), ochratoxin A, and zearalenone. This review describes the basic principles of FPIA and summarizes recent research in this area with regard to mycotoxins. Molecular Diversity Preservation International 2009-12-10 /pmc/articles/PMC3202780/ /pubmed/22069541 http://dx.doi.org/10.3390/toxins1020196 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Maragos, Chris
Fluorescence Polarization Immunoassay of Mycotoxins: A Review
title Fluorescence Polarization Immunoassay of Mycotoxins: A Review
title_full Fluorescence Polarization Immunoassay of Mycotoxins: A Review
title_fullStr Fluorescence Polarization Immunoassay of Mycotoxins: A Review
title_full_unstemmed Fluorescence Polarization Immunoassay of Mycotoxins: A Review
title_short Fluorescence Polarization Immunoassay of Mycotoxins: A Review
title_sort fluorescence polarization immunoassay of mycotoxins: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202780/
https://www.ncbi.nlm.nih.gov/pubmed/22069541
http://dx.doi.org/10.3390/toxins1020196
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