Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection

Food and crop contaminations with mycotoxins are a severe health risk for consumers and cause high economic losses worldwide. Currently, different chromatographic- and immuno-based methods are used to detect mycotoxins within different sample matrices. There is a need for novel, highly sensitive det...

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Main Authors: Jan Pietschmann, Holger Spiegel, Hans-Joachim Krause, Stefan Schillberg, Florian Schröper
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/12/5/337
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author Jan Pietschmann
Holger Spiegel
Hans-Joachim Krause
Stefan Schillberg
Florian Schröper
author_facet Jan Pietschmann
Holger Spiegel
Hans-Joachim Krause
Stefan Schillberg
Florian Schröper
author_sort Jan Pietschmann
collection DOAJ
description Food and crop contaminations with mycotoxins are a severe health risk for consumers and cause high economic losses worldwide. Currently, different chromatographic- and immuno-based methods are used to detect mycotoxins within different sample matrices. There is a need for novel, highly sensitive detection technologies that avoid time-consuming procedures and expensive laboratory equipment but still provide sufficient sensitivity to achieve the mandated detection limit for mycotoxin content. Here we describe a novel, highly sensitive, and portable aflatoxin B1 detection approach using competitive magnetic immunodetection (cMID). As a reference method, a competitive ELISA optimized by checkerboard titration was established. For the novel cMID procedure, immunofiltration columns, coated with aflatoxin B1-BSA conjugate were used for competitive enrichment of biotinylated aflatoxin B1-specific antibodies. Subsequently, magnetic particles functionalized with streptavidin can be applied to magnetically label retained antibodies. By means of frequency mixing technology, particles were detected and quantified corresponding to the aflatoxin content in the sample. After the optimization of assay conditions, we successfully demonstrated the new competitive magnetic detection approach with a comparable detection limit of 1.1 ng aflatoxin B1 per mL sample to the cELISA reference method. Our results indicate that the cMID is a promising method reducing the risks of processing contaminated commodities.
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spelling doaj.art-da2ca4c95e794780b53e34f6e4e7faf52023-11-20T01:10:24ZengMDPI AGToxins2072-66512020-05-0112533710.3390/toxins12050337Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic ImmunodetectionJan Pietschmann0Holger Spiegel1Hans-Joachim Krause2Stefan Schillberg3Florian Schröper4Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074 Aachen, GermanyFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074 Aachen, GermanyInstitute of Biological Information Processing, Bioelectronics IBI-3, Forschungszentrum Jülich, 52428 Jülich, GermanyFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074 Aachen, GermanyFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074 Aachen, GermanyFood and crop contaminations with mycotoxins are a severe health risk for consumers and cause high economic losses worldwide. Currently, different chromatographic- and immuno-based methods are used to detect mycotoxins within different sample matrices. There is a need for novel, highly sensitive detection technologies that avoid time-consuming procedures and expensive laboratory equipment but still provide sufficient sensitivity to achieve the mandated detection limit for mycotoxin content. Here we describe a novel, highly sensitive, and portable aflatoxin B1 detection approach using competitive magnetic immunodetection (cMID). As a reference method, a competitive ELISA optimized by checkerboard titration was established. For the novel cMID procedure, immunofiltration columns, coated with aflatoxin B1-BSA conjugate were used for competitive enrichment of biotinylated aflatoxin B1-specific antibodies. Subsequently, magnetic particles functionalized with streptavidin can be applied to magnetically label retained antibodies. By means of frequency mixing technology, particles were detected and quantified corresponding to the aflatoxin content in the sample. After the optimization of assay conditions, we successfully demonstrated the new competitive magnetic detection approach with a comparable detection limit of 1.1 ng aflatoxin B1 per mL sample to the cELISA reference method. Our results indicate that the cMID is a promising method reducing the risks of processing contaminated commodities.https://www.mdpi.com/2072-6651/12/5/337frequency mixing technologyimmunofiltrationmagnetic beadsmycotoxin
spellingShingle Jan Pietschmann
Holger Spiegel
Hans-Joachim Krause
Stefan Schillberg
Florian Schröper
Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection
Toxins
frequency mixing technology
immunofiltration
magnetic beads
mycotoxin
title Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection
title_full Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection
title_fullStr Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection
title_full_unstemmed Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection
title_short Sensitive Aflatoxin B1 Detection Using Nanoparticle-Based Competitive Magnetic Immunodetection
title_sort sensitive aflatoxin b1 detection using nanoparticle based competitive magnetic immunodetection
topic frequency mixing technology
immunofiltration
magnetic beads
mycotoxin
url https://www.mdpi.com/2072-6651/12/5/337
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AT stefanschillberg sensitiveaflatoxinb1detectionusingnanoparticlebasedcompetitivemagneticimmunodetection
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