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Comparison of manual and automatic sampling for monitoring ochratoxin A in barley grain

Automatic and manual sampling for ochratoxin A (OTA) in barley grain was compared under industrial conditions considering sampling uncertainty as well as practical and technical aspects. Ten tonnes of barley inoculated with Penicillium verrucosum were incubated until the OTA concentration reached ap...

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Autores principales: Andersson, M.G., Reiter, E.V., Lindqvist, P.-A., Razzazi-Fazeli, E., Häggblom, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357967/
https://www.ncbi.nlm.nih.gov/pubmed/21598140
http://dx.doi.org/10.1080/19440049.2011.576438
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author Andersson, M.G.
Reiter, E.V.
Lindqvist, P.-A.
Razzazi-Fazeli, E.
Häggblom, P.
author_facet Andersson, M.G.
Reiter, E.V.
Lindqvist, P.-A.
Razzazi-Fazeli, E.
Häggblom, P.
author_sort Andersson, M.G.
collection PubMed
description Automatic and manual sampling for ochratoxin A (OTA) in barley grain was compared under industrial conditions considering sampling uncertainty as well as practical and technical aspects. Ten tonnes of barley inoculated with Penicillium verrucosum were incubated until the OTA concentration reached approximately 15 μg kg(−1) and sampled with manual and automatic sampling. A nested experimental design and ANOVA was used to estimate variance components from sampling, sample reduction, sample preparation and analysis. Manual sampling resulted in a high sampling uncertainty and OTA concentrations in aggregate samples ranged from 2 to 80 μg kg(−1). When aggregate samples were formed by automatic sampling the uncertainty arising from nugget effects and spatial distribution was practically eliminated. Results from this study show that an automatic sampler mounted after a mixer or conveyer can provide representative samples of OTA from a moving stream of barley. Automatic sampling might present a practical and economical alternative to manual sampling for feed mill operators when monitoring low levels of mycotoxins in grain or other commodities. Despite careful precautions, sample preparation and analysis resulted in a relative uncertainty of ±40% (p = 0.95), which was attributed to the sub-sampling following the two grinding steps. Size fractionation of the coarsely ground barley showed that 40% of the total amount of OTA was present in a small fraction of fine particles with a strong tendency to aggregate or stick to equipment and containers. Thus, in order to take advantage of the automatic sampling, it is crucial to apply an appropriate sub-sampling to prevent segregation of particles which may affect the OTA measurements.
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spelling pubmed-33579672012-05-23 Comparison of manual and automatic sampling for monitoring ochratoxin A in barley grain Andersson, M.G. Reiter, E.V. Lindqvist, P.-A. Razzazi-Fazeli, E. Häggblom, P. Food Addit Contam Part A Chem Anal Control Expo Risk Assess Research Article Automatic and manual sampling for ochratoxin A (OTA) in barley grain was compared under industrial conditions considering sampling uncertainty as well as practical and technical aspects. Ten tonnes of barley inoculated with Penicillium verrucosum were incubated until the OTA concentration reached approximately 15 μg kg(−1) and sampled with manual and automatic sampling. A nested experimental design and ANOVA was used to estimate variance components from sampling, sample reduction, sample preparation and analysis. Manual sampling resulted in a high sampling uncertainty and OTA concentrations in aggregate samples ranged from 2 to 80 μg kg(−1). When aggregate samples were formed by automatic sampling the uncertainty arising from nugget effects and spatial distribution was practically eliminated. Results from this study show that an automatic sampler mounted after a mixer or conveyer can provide representative samples of OTA from a moving stream of barley. Automatic sampling might present a practical and economical alternative to manual sampling for feed mill operators when monitoring low levels of mycotoxins in grain or other commodities. Despite careful precautions, sample preparation and analysis resulted in a relative uncertainty of ±40% (p = 0.95), which was attributed to the sub-sampling following the two grinding steps. Size fractionation of the coarsely ground barley showed that 40% of the total amount of OTA was present in a small fraction of fine particles with a strong tendency to aggregate or stick to equipment and containers. Thus, in order to take advantage of the automatic sampling, it is crucial to apply an appropriate sub-sampling to prevent segregation of particles which may affect the OTA measurements. Taylor & Francis 2011-11-27 2011-08 /pmc/articles/PMC3357967/ /pubmed/21598140 http://dx.doi.org/10.1080/19440049.2011.576438 Text en © 2011 Taylor & Francis http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Taylor & Francis journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Andersson, M.G.
Reiter, E.V.
Lindqvist, P.-A.
Razzazi-Fazeli, E.
Häggblom, P.
Comparison of manual and automatic sampling for monitoring ochratoxin A in barley grain
title Comparison of manual and automatic sampling for monitoring ochratoxin A in barley grain
title_full Comparison of manual and automatic sampling for monitoring ochratoxin A in barley grain
title_fullStr Comparison of manual and automatic sampling for monitoring ochratoxin A in barley grain
title_full_unstemmed Comparison of manual and automatic sampling for monitoring ochratoxin A in barley grain
title_short Comparison of manual and automatic sampling for monitoring ochratoxin A in barley grain
title_sort comparison of manual and automatic sampling for monitoring ochratoxin a in barley grain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357967/
https://www.ncbi.nlm.nih.gov/pubmed/21598140
http://dx.doi.org/10.1080/19440049.2011.576438
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