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dc.contributorIRTA. Recerca i Tecnologia Agroalimentàries
dc.contributor.authorGarcía-Altares, María
dc.contributor.authorDiogène Fadini, Jorge
dc.contributor.authorDe la Iglesia González, Pablo de la
dc.contributor.otherProducció Animalcat
dc.date.accessioned2013-02-07T15:38:03Z
dc.date.accessioned2025-05-09T11:15:58Z
dc.date.available2013-02-07T15:38:03Z
dc.date.available2025-05-09T11:15:58Z
dc.date.created2012
dc.date.issued2013
dc.identifier.citationGarcía-Altares, M., et al. (2013) The implementation of liquid chromatography tandem mass spectrometry for the official control of lipophilic toxins in seafood: Single-laboratory validation under four chromatographic conditions. Journal of Chromatrography A, 1275: 48-60cat
dc.identifier.urihttp://hdl.handle.net/20.500.12327/4491
dc.description.abstractWe performed a comprehensive study to assess the fit for purpose of four chromatographic conditions for the determination of six groups of marine lipophilic toxins (okadaic acid and dinophysistoxins, pectenotoxins, azaspiracids, yessotoxins, gymnodimine and spirolides) by LC-MS/MS to select the most suitable conditions as stated by the European Union Reference Laboratory for Marine Biotoxins (EURLMB). For every case, the elution gradient has been optimized to achieve a total run-time cycle of 12 min. We performed a single-laboratory validation for the analysis of three relevant matrices for the seafood aquaculture industry (mussels, pacific oysters and clams), and for sea urchins for which no data about lipophilic toxins have been reported before. Moreover, we have compared the method performance under alkaline conditions using two quantification strategies: the external standard calibration (EXS) and the matrix-matched standard calibration (MMS). Alkaline conditions were the only scenario that allowed detection windows with polarity switching in a 3200 QTrap mass spectrometer, thus the analysis of all toxins can be accomplished in a single run, increasing sample throughput. The limits of quantification under alkaline conditions met the validation requirements established by the EURLMB for all toxins and matrices, while the remaining conditions failed in some cases. The accuracy of the method and the matrix effects where generally dependent on the mobile phases and the seafood species. The MMS had a moderate positive impact on method accuracy for crude extracts, but it showed poor trueness for seafood species other than mussels when analyzing hydrolyzed extracts. Alkaline conditions with EXS and recovery correction for OA were selected as the most proper conditions in the context of our laboratory. This comparative study can help other laboratories to choose the best conditions for the implementation of LC-MS/MS according to their own necessities.eng
dc.format.extent29 p.
dc.language.isoengcat
dc.publisherElseviercat
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAttribution-NonCommercial-NoDerivatives 3.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subject.otherToxines marinescat
dc.subject.otherEspectrometria de massescat
dc.subject.otherCromatografia líquidacat
dc.titleThe implementation of liquid chromatography tandem mass spectrometry for the official control of lipophilic toxins in seafood: Single-laboratory validation under four chromatographic conditionscat
dc.typeinfo:eu-repo/semantics/articlecat
dc.typeinfo:eu-repo/semantics/acceptedVersioncat
dc.embargo.termscapcat
dc.contributor.groupAqüiculturacat
dc.contributor.groupAigües Marines i Continentalscat


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Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by-nc-nd/3.0/
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