Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: Lippolis, Vincenzo, Porricelli, Anna C. R., Cortese, Marina, Suman, Michele, Zanardi, Sandro, Pascale, Michelangelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
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
_version_ 1783275293101785088
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
work_keys_str_mv AT lippolisvincenzo determinationofochratoxinainryeandryebasedproductsbyfluorescencepolarizationimmunoassay
AT porricelliannacr determinationofochratoxinainryeandryebasedproductsbyfluorescencepolarizationimmunoassay
AT cortesemarina determinationofochratoxinainryeandryebasedproductsbyfluorescencepolarizationimmunoassay
AT sumanmichele determinationofochratoxinainryeandryebasedproductsbyfluorescencepolarizationimmunoassay
AT zanardisandro determinationofochratoxinainryeandryebasedproductsbyfluorescencepolarizationimmunoassay
AT pascalemichelangelo determinationofochratoxinainryeandryebasedproductsbyfluorescencepolarizationimmunoassay