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dc.contributor.authorÁlvarez-Romero, María
dc.contributor.authorMarín Sáez, Jesús
dc.contributor.authorGarcía Campaña, Ana María 
dc.contributor.authorHernández Mesa, Maykel 
dc.contributor.authorGámiz Gracia, Laura 
dc.date.accessioned2025-06-25T11:31:54Z
dc.date.available2025-06-25T11:31:54Z
dc.date.issued2025-06-17
dc.identifier.citationÁlvarez-Romero, María et al. Food Control, Vol. 178 (2025) 111504. https://doi.org/10.1016/j.foodcont.2025.111504es_ES
dc.identifier.urihttps://hdl.handle.net/10481/104854
dc.descriptionThis work was supported by Project PID2021-127804OB-I00 funded by MCIN/AEI/10.13039/501100011033 ‘A way to make Europe’ and the Andalousian Government (Project ref. PROYEXCEL_00195). MAR gratefully acknowledges the contract from the project PROYEXCEL_00195, funded by Consejería de Universidad, Investigación e Innovación, Junta de Andalucía. JMS thanks the University of Almería for his “Convocatoria de Recualificación del Sistema Universitario Español-Margarita Salas” postdoc grant under the “Plan de Recuperación Transformación” program funded by the Spanish Ministry of Universities with European Union's NextGenerationEU funds. MHM gratefully acknowledges the grant RYC2023-044255-I funded by MCIU/AEI/10.13039/501100011033 and FSE+. Funding for open access charge: Universidad de Granada / CBUA.es_ES
dc.description.abstractThis work presents an ultrasound assisted extraction (UAE) combined with a QuEChERS approach, followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis, for the determination of 20 mycotoxins and 10 pesticides in bee pollen and honey samples. The method was validated according to SANTE/11312/2021 guideline. Linearity was satisfactory (r > 0.99), with LODs ranging from 0.03 to 13.3 μg kg−1 and LOQs from 0.11 to 44.4 μg kg−1, except for five analytes in pollen. Trueness, expressed as apparent recoveries and evaluated at three concentration levels, was between 70 and 120 %, except for three compounds in honey and eight in pollen. RSDs for precisions were below 20 %. The method was applied to 28 honey and six pollen samples. Acetamiprid and azoxystrobin were detected in 29 % and 32 % of the honey samples, with concentration ranges of 1.26–16.2 μg kg−1 and 1.31–1.56 μg kg−1, respectively. No contaminants were found in any of the pollen samples.es_ES
dc.description.sponsorshipMCIN/AEI/10.13039/501100011033 PID2021-127804OB-I00, RYC2023-044255-Ies_ES
dc.description.sponsorshipAndalousian Government PROYEXCEL_00195es_ES
dc.description.sponsorshipUniversity of Almeríaes_ES
dc.description.sponsorshipSpanish Ministry of Universitieses_ES
dc.description.sponsorshipEuropean Union's NextGenerationEU fundses_ES
dc.description.sponsorshipFSE+es_ES
dc.description.sponsorshipUniversidad de Granada / CBUAes_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nd/4.0/*
dc.subjectMycotoxins es_ES
dc.subjectPesticides es_ES
dc.subjectBeekeeping productses_ES
dc.subjectUltrasound-assisted extractiones_ES
dc.subjectQuEChERSes_ES
dc.subjectLiquid chromatography-tandem mass spectrometryes_ES
dc.titleAddressing chemical risks in beekeeping products: development of a combined ultrasound-assisted extraction and QuEChERS-based method for the simultaneous determination of mycotoxins and pesticides in bee pollen and honeyes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.foodcont.2025.111504
dc.type.hasVersionVoRes_ES


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