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Standard [CURRENT]

DIN EN 16187:2015-09

Foodstuffs - Determination of fumonisin B1 and fumonisin B2 in processed maize containing foods for infants and young children - HPLC method with immunoaffinity column cleanup and fluorescence detection after pre-column derivatization; German version EN 16187:2015

German title
Lebensmittel - Bestimmung von Fumonisin B1 und Fumonisin B2 in Säuglings- und Kleinkindernahrung auf Maisbasis - HPLC-Verfahren mit Reinigung an einer Immunoaffinitätssäule und Fluoreszenzdetektion nach Vorsäulenderivatisierung; Deutsche Fassung EN 16187:2015
Publication date
2015-09
Original language
German
Pages
22
Note
The publisher recommends this document in lieu of the withdrawn document DIN EN 13585:2002-03 , for which no replacement is available.

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Publication date
2015-09
Original language
German
Pages
22
Note
The publisher recommends this document in lieu of the withdrawn document DIN EN 13585:2002-03 , for which no replacement is available.
DOI
https://dx.doi.org/10.31030/2283292

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Overview

Fumonisins are water-soluble mycotoxins which can be found worldwide and which are produced by certain plant pathogenic fungi of the genus fusarium, especially on maize. According to the Bibliography, maize flour and maize grits are most severely contaminated. The maximum levels for the fumonisins B1 and B2 have been specified for Germany in the Regulation amending the Ordinance on the maximum permissible quantities of mycotoxins in foodstuffs of 2004-02-04. This standard has been prepared by WG 5 "Biotoxins" of CEN/TC 275 "Food analysis - Horizontal methods" in order to be able to uniformly analyse these maximum levels throughout Europe. It specifies a method for the determination of fumonisin B1 (FB1) and fumonisin B2 (FB2) in processed maize-containing foods for infants and young children by high performance liquid chromatography (HPLC) with immunoaffinity cleanup and fluorescence detection (FLD). This method has been validated in an interlaboratory study via the analysis of both naturally contaminated and spiked samples ranging from 111,6 µg/kg to 458,0 µg/kg for FB1/FB2, 89,1 µg/kg to 384,4 µg/kg for FB1 and 22,5 µg/kg to 73,6 µg/kg for FB2. Fumonisins are extracted from the sample with a mixture of citrate-phosphate buffer-methanol-acetonitrile. The filtered extract is diluted with water and applied to an immunoaffinity column containing antibody specific to fumonisins. Fumonisins are eluted from the column with methanol and water and quantified by HPLC/FLD with pre-column derivatization with o-phthaldialdehyde (OPA) reagent.

Content
ICS
67.230
DOI
https://dx.doi.org/10.31030/2283292

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