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dc.contributor.authorBUTTINGER Gerharden_GB
dc.contributor.authorKARASEK LUBOMIRen_GB
dc.contributor.authorVERLINDE PHILIPPEen_GB
dc.contributor.authorWENZL Thomasen_GB
dc.date.accessioned2014-01-23T01:02:52Z-
dc.date.available2014-01-22en_GB
dc.date.available2014-01-23T01:02:52Z-
dc.date.created2014-01-16en_GB
dc.date.issued2014en_GB
dc.date.submitted2014-01-10en_GB
dc.identifier.isbn978-92-79-35417-5en_GB
dc.identifier.issn1831-9424en_GB
dc.identifier.otherEUR 26491en_GB
dc.identifier.otherOPOCE LA-NA-26491-EN-Nen_GB
dc.identifier.urihttp://publications.jrc.ec.europa.eu/repository/handle/JRC88197-
dc.description.abstractMeat from male pigs may develop an off-flavour, commonly known as boar taint. For that reason male piglets are surgically castrated at young age to avoid the potential off-flavour formation. Animal welfare concerns have triggered research into alternatives to surgical castration of male piglets with the long-term goal of abandoning it by 1 January 2018. The ALCASDE study has shown that the agreement of testing results for androstenone and skatole in pig fat produced in several laboratories was not satisfactory and one of the conclusions of this project was that in a follow-on project a standardised reference method should be elaborated to rectify this shortcoming. In the suggested reference method, the 3 marker compounds (skatole, andostrenone and indole), for boar taint are quantified in pork fat by isotope dilution liquid chromatography tandem mass spectrometry (LC MS/MS). The fat is separated from the ground pork fat tissue sample via melting and centrifugation thereafter. The fat is spiked with isotopically labelled standards and prepared for size exclusion chromatography (SEC). The SEC purified sample is evaporated nearly to dryness and after addition of an injection standard analysed by LC-MS/MS in selected reaction monitoring mode. This method has been validated to obtain the method performance characteristics. When summarising the method performance characteristics and comparing them to requirements for official food control methods in the area of food contaminants it can be concluded that the method is fit for its intended purpose. The recovery rates are between 106 % and 115% and are therefore within the range of 60 % to 120 %. The repeatability standard deviation ranges from 7 % to 18 % and the intermediate precision between 9 % and 18 %, all below the set limit of 20 %. The measurement uncertainty (U) is below 30 % for all analytes. The method has proven to be robust and free from matrix interferences. The method is sensitive enough to determine the off-flavour compounds at the sensory threshold values.en_GB
dc.description.sponsorshipJRC.D.5-Standards for Food Bioscienceen_GB
dc.format.mediumOnlineen_GB
dc.languageENGen_GB
dc.publisherPublications Office of the European Unionen_GB
dc.relation.ispartofseriesJRC88197en_GB
dc.titleIn house validation of a reference method for the determination of boar taint compounds by LC-MSMSen_GB
dc.typeEUR - Scientific and Technical Research Reportsen_GB
dc.identifier.doi10.2787/88600en_GB
JRC Directorate:Health, Consumers and Reference Materials

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