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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2012
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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. |
format | Online Article Text |
id | pubmed-3304168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
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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