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Determination of Ochratoxin A in Rye and Rye-Based Products by Fluorescence Polarization Immunoassay
A rapid fluorescence polarization immunoassay (FPIA) was optimized and validated for the determination of ochratoxin A (OTA) in rye and rye crispbread. Samples were extracted with a mixture of acetonitrile/water (60:40, v/v) and purified by SPE-aminopropyl column clean-up before performing the FPIA....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666352/ https://www.ncbi.nlm.nih.gov/pubmed/28954398 http://dx.doi.org/10.3390/toxins9100305 |
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author | Lippolis, Vincenzo Porricelli, Anna C. R. Cortese, Marina Suman, Michele Zanardi, Sandro Pascale, Michelangelo |
author_facet | Lippolis, Vincenzo Porricelli, Anna C. R. Cortese, Marina Suman, Michele Zanardi, Sandro Pascale, Michelangelo |
author_sort | Lippolis, Vincenzo |
collection | PubMed |
description | A rapid fluorescence polarization immunoassay (FPIA) was optimized and validated for the determination of ochratoxin A (OTA) in rye and rye crispbread. Samples were extracted with a mixture of acetonitrile/water (60:40, v/v) and purified by SPE-aminopropyl column clean-up before performing the FPIA. Overall mean recoveries were 86 and 95% for spiked rye and rye crispbread with relative standard deviations lower than 6%. Limits of detection (LOD) of the optimized FPIA was 0.6 μg/kg for rye and rye crispbread, respectively. Good correlations (r > 0.977) were observed between OTA contents in contaminated samples obtained by FPIA and high-performance liquid chromatography (HPLC) with immunoaffinity cleanup used as reference method. Furthermore, single laboratory validation and small-scale collaborative trials were carried out for the determination of OTA in rye according to Regulation 519/2014/EU laying down procedures for the validation of screening methods. The precision profile of the method, cut-off level and rate of false suspect results confirm the satisfactory analytical performances of assay as a screening method. These findings show that the optimized FPIA is suitable for high-throughput screening, and permits reliable quantitative determination of OTA in rye and rye crispbread at levels that fall below the EU regulatory limits. |
format | Online Article Text |
id | pubmed-5666352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56663522017-11-09 Determination of Ochratoxin A in Rye and Rye-Based Products by Fluorescence Polarization Immunoassay Lippolis, Vincenzo Porricelli, Anna C. R. Cortese, Marina Suman, Michele Zanardi, Sandro Pascale, Michelangelo Toxins (Basel) Article A rapid fluorescence polarization immunoassay (FPIA) was optimized and validated for the determination of ochratoxin A (OTA) in rye and rye crispbread. Samples were extracted with a mixture of acetonitrile/water (60:40, v/v) and purified by SPE-aminopropyl column clean-up before performing the FPIA. Overall mean recoveries were 86 and 95% for spiked rye and rye crispbread with relative standard deviations lower than 6%. Limits of detection (LOD) of the optimized FPIA was 0.6 μg/kg for rye and rye crispbread, respectively. Good correlations (r > 0.977) were observed between OTA contents in contaminated samples obtained by FPIA and high-performance liquid chromatography (HPLC) with immunoaffinity cleanup used as reference method. Furthermore, single laboratory validation and small-scale collaborative trials were carried out for the determination of OTA in rye according to Regulation 519/2014/EU laying down procedures for the validation of screening methods. The precision profile of the method, cut-off level and rate of false suspect results confirm the satisfactory analytical performances of assay as a screening method. These findings show that the optimized FPIA is suitable for high-throughput screening, and permits reliable quantitative determination of OTA in rye and rye crispbread at levels that fall below the EU regulatory limits. MDPI 2017-09-26 /pmc/articles/PMC5666352/ /pubmed/28954398 http://dx.doi.org/10.3390/toxins9100305 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lippolis, Vincenzo Porricelli, Anna C. R. Cortese, Marina Suman, Michele Zanardi, Sandro Pascale, Michelangelo Determination of Ochratoxin A in Rye and Rye-Based Products by Fluorescence Polarization Immunoassay |
title | Determination of Ochratoxin A in Rye and Rye-Based Products by Fluorescence Polarization Immunoassay |
title_full | Determination of Ochratoxin A in Rye and Rye-Based Products by Fluorescence Polarization Immunoassay |
title_fullStr | Determination of Ochratoxin A in Rye and Rye-Based Products by Fluorescence Polarization Immunoassay |
title_full_unstemmed | Determination of Ochratoxin A in Rye and Rye-Based Products by Fluorescence Polarization Immunoassay |
title_short | Determination of Ochratoxin A in Rye and Rye-Based Products by Fluorescence Polarization Immunoassay |
title_sort | determination of ochratoxin a in rye and rye-based products by fluorescence polarization immunoassay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666352/ https://www.ncbi.nlm.nih.gov/pubmed/28954398 http://dx.doi.org/10.3390/toxins9100305 |
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