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Standard [CURRENT]

DIN EN 16619:2015-06

Food analysis - Determination of benzo[a]pyrene, benz[a]anthracene, chrysene and benzo[b]fluoranthene in foodstuffs by gas chromatography mass spectrometry (GC-MS); German version EN 16619:2015

German title
Lebensmittelanalytik - Bestimmung von Benzo[a]pyren, Benz[a]anthracen, Chrysen und Benzo[b]fluoranthen in Lebensmitteln mit Gaschromatographie und Massenspektrometrie (GC-MS); Deutsche Fassung EN 16619:2015
Publication date
2015-06
Original language
German
Pages
40

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Publication date
2015-06
Original language
German
Pages
40
DOI
https://dx.doi.org/10.31030/2249431

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Overview

This European Standard specifies a method for the determination of 4 of the 16 EU priority polycyclic aromatic hydrocarbons (PAHs), identified as target PAHs. They are benz[a]anthracene (BaA), benzo[a]pyrene (BaP), benzo[b]fluoranthene (BbF) and chrysene (CHR). The method allows their quantification in the presence of the other 12 EU priority PAHs (benzo[j]fluoranthene (BjF), cyclopenta[cd]pyrene (CPP), benzo[k]fluoranthene (BkF), dibenz[a,h]anthracene (DhA), benzo[c]fluorene (BcL), dibenzo[a,e]pyrene (DeP), benzo[ghi]perylene (BgP), dibenzo[a,h]pyrene (DhP), dibenzo[a,i]pyrene (DiP), dibenzo[a,l]pyrene (DlP), indeno[1,2,3-cd]pyrene (IcP), 5-methylchrysene (5MC)) in extruded wheat flour, smoked fish, dry infant formula, sausage meat, freeze-dried mussels, edible oil and wheat flour, by gas-chromatography mass-spectrometry (GC-MS). The extraction of PAHs from solid samples is performed by pressurized liquid extraction (PLE). Soxhlet extraction was applied by some participants in the method validation study by collaborative trial as alternative to PLE. The sample clean-up is performed by applying the following techniques in the reported sequence: size exclusion chromatography (SEC), and solid phase extraction (SPE). This method complies with the performance characteristics specified in Commission Regulation (EU) No 836/2011 (see [1]). In particular the specifications for the limit of detection (LOD) and of the limit of quantification (LOQ) (0,30 μg/kg and 0,90 μg/kg respectively) were met. The method has been validated in an interlaboratory study via the analysis of both naturally contaminated and spiked samples, ranging from 0,5 μg/kg to 11,9 μg/kg. However, linearity of the instrument response was proven for the concentration range 0,5 μg/kg to 20 μg/kg. For the determination of PAHs in edible fats and oils, two other standards are also available, EN ISO 22959 and EN ISO 15753. This document (EN 16619:2015) has been prepared by Technical Committee CEN/TC 275 "Food analysis - Horizontal methods" the secretariat of which is held by DIN (Germany). The responsible national standardization committee is Working Committee NA 057-01-14 AA "Prozesskontaminanten" ("Process contaminants") at the DIN Standards Committee Food and Agricultural Products (NAL).

Content
ICS
67.050
DOI
https://dx.doi.org/10.31030/2249431

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