Determination of fumonisins B1 and B2 in beer
A total of 20 Slovak beers produced from the 2003 barley harvest by different companies were analysed for fumonisin B1 and B2 contamination. A method based on immunoaffinity column extraction and clean-up, coupled with HPLC analysis with fluorescence detection after derivatisation with a mixture of...
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Published in | Czech Journal of Food Sciences Vol. 23; no. 1 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Abstract | A total of 20 Slovak beers produced from the 2003 barley harvest by different companies were analysed for fumonisin B1 and B2 contamination. A method based on immunoaffinity column extraction and clean-up, coupled with HPLC analysis with fluorescence detection after derivatisation with a mixture of o-phthaldialdehyde and 2-mercaptoethanol, was used. The detection limit for both fumonisins was 1 microg/mL, the recovery was 93% for fumonisin B1 and 78% for fumonisin B2. Phosphate buffer usually applied resulted in a poor separation of derivatised fumonisins. Peak splitting depended on the pH of the eluent. The pH value of 2.6 was found suitable for the peak splitting elimination. A convenient gradient elution metod was suggested to avoid possible interference in the determination of fumonisin concentrations. Fumonisins concentrations were under the limit of detection in all the beer samples tested. |
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AbstractList | A total of 20 Slovak beers produced from the 2003 barley harvest by different companies were analysed for fumonisin B1 and B2 contamination. A method based on immunoaffinity column extraction and clean-up, coupled with HPLC analysis with fluorescence detection after derivatisation with a mixture of o-phthaldialdehyde and 2-mercaptoethanol, was used. The detection limit for both fumonisins was 1 microg/mL, the recovery was 93% for fumonisin B1 and 78% for fumonisin B2. Phosphate buffer usually applied resulted in a poor separation of derivatised fumonisins. Peak splitting depended on the pH of the eluent. The pH value of 2.6 was found suitable for the peak splitting elimination. A convenient gradient elution metod was suggested to avoid possible interference in the determination of fumonisin concentrations. Fumonisins concentrations were under the limit of detection in all the beer samples tested. |
Author | Rauova, D Dasko, L.(Vyskumny Ustav Potravinarsky, Bratislava (Slovak Republic))E-mail:dasko@vup.sk Belajova, E Kovac, M |
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SubjectTerms | BEERS BIERE BIOLOGICAL CONTAMINATION CERVEZAS CONTAMINACION BIOLOGICA CONTAMINATION BIOLOGIQUE FLUORESCENCE FLUORESCENCIA FUMONISINAS FUMONISINE FUMONISINS HPLC METHODE METHODS METODOS SEPARACION SEPARATING SEPARATION |
Title | Determination of fumonisins B1 and B2 in beer |
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