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A Bioanalytical Platform for Simultaneous Detection and Quantification of Biological Toxins

Prevalent incidents support the notion that toxins, produced by bacteria, fungi, plants or animals are increasingly responsible for food poisoning or intoxication. Owing to their high toxicity some toxins are also regarded as potential biological warfare agents. Accordingly, control, detection and n...

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Autores principales: Weingart, Oliver G., Gao, Hui, Crevoisier, François, Heitger, Friedrich, Avondet, Marc-André, Sigrist, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304168/
https://www.ncbi.nlm.nih.gov/pubmed/22438766
http://dx.doi.org/10.3390/s120202324
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author Weingart, Oliver G.
Gao, Hui
Crevoisier, François
Heitger, Friedrich
Avondet, Marc-André
Sigrist, Hans
author_facet Weingart, Oliver G.
Gao, Hui
Crevoisier, François
Heitger, Friedrich
Avondet, Marc-André
Sigrist, Hans
author_sort Weingart, Oliver G.
collection PubMed
description Prevalent incidents support the notion that toxins, produced by bacteria, fungi, plants or animals are increasingly responsible for food poisoning or intoxication. Owing to their high toxicity some toxins are also regarded as potential biological warfare agents. Accordingly, control, detection and neutralization of toxic substances are a considerable economic burden to food safety, health care and military biodefense. The present contribution describes a new versatile instrument and related procedures for array-based simultaneous detection of bacterial and plant toxins using a bioanalytical platform which combines the specificity of covalently immobilized capture probes with a dedicated instrumentation and immuno-based microarray analytics. The bioanalytical platform consists of a microstructured polymer slide serving both as support of printed arrays and as incubation chamber. The platform further includes an easy-to-operate instrument for simultaneous slide processing at selectable assay temperature. Cy5 coupled streptavidin is used as unifying fluorescent tracer. Fluorescence image analysis and signal quantitation allow determination of the toxin’s identity and concentration. The system’s performance has been investigated by immunological detection of Botulinum Neurotoxin type A (BoNT/A), Staphylococcal enterotoxin B (SEB), and the plant toxin ricin. Toxins were detectable at levels as low as 0.5–1 ng·mL(−1) in buffer or in raw milk.
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spelling pubmed-33041682012-03-21 A Bioanalytical Platform for Simultaneous Detection and Quantification of Biological Toxins Weingart, Oliver G. Gao, Hui Crevoisier, François Heitger, Friedrich Avondet, Marc-André Sigrist, Hans Sensors (Basel) Article Prevalent incidents support the notion that toxins, produced by bacteria, fungi, plants or animals are increasingly responsible for food poisoning or intoxication. Owing to their high toxicity some toxins are also regarded as potential biological warfare agents. Accordingly, control, detection and neutralization of toxic substances are a considerable economic burden to food safety, health care and military biodefense. The present contribution describes a new versatile instrument and related procedures for array-based simultaneous detection of bacterial and plant toxins using a bioanalytical platform which combines the specificity of covalently immobilized capture probes with a dedicated instrumentation and immuno-based microarray analytics. The bioanalytical platform consists of a microstructured polymer slide serving both as support of printed arrays and as incubation chamber. The platform further includes an easy-to-operate instrument for simultaneous slide processing at selectable assay temperature. Cy5 coupled streptavidin is used as unifying fluorescent tracer. Fluorescence image analysis and signal quantitation allow determination of the toxin’s identity and concentration. The system’s performance has been investigated by immunological detection of Botulinum Neurotoxin type A (BoNT/A), Staphylococcal enterotoxin B (SEB), and the plant toxin ricin. Toxins were detectable at levels as low as 0.5–1 ng·mL(−1) in buffer or in raw milk. Molecular Diversity Preservation International (MDPI) 2012-02-21 /pmc/articles/PMC3304168/ /pubmed/22438766 http://dx.doi.org/10.3390/s120202324 Text en © 2012 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Weingart, Oliver G.
Gao, Hui
Crevoisier, François
Heitger, Friedrich
Avondet, Marc-André
Sigrist, Hans
A Bioanalytical Platform for Simultaneous Detection and Quantification of Biological Toxins
title A Bioanalytical Platform for Simultaneous Detection and Quantification of Biological Toxins
title_full A Bioanalytical Platform for Simultaneous Detection and Quantification of Biological Toxins
title_fullStr A Bioanalytical Platform for Simultaneous Detection and Quantification of Biological Toxins
title_full_unstemmed A Bioanalytical Platform for Simultaneous Detection and Quantification of Biological Toxins
title_short A Bioanalytical Platform for Simultaneous Detection and Quantification of Biological Toxins
title_sort bioanalytical platform for simultaneous detection and quantification of biological toxins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304168/
https://www.ncbi.nlm.nih.gov/pubmed/22438766
http://dx.doi.org/10.3390/s120202324
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