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dc.contributor.authorKhaled, Abir
dc.contributor.authorGionfriddo, Emanuela
dc.contributor.authorAcquaro Jr, Vinicius
dc.contributor.authorSingh, Varoon
dc.contributor.authorPawliszyn, Janusz
dc.date.accessioned2020-01-06 15:11:37 (GMT)
dc.date.available2020-01-06 15:11:37 (GMT)
dc.date.issued2019-05-16
dc.identifier.urihttps://doi.org/10.1016/j.aca.2018.12.044
dc.identifier.urihttp://hdl.handle.net/10012/15401
dc.descriptionThe final publication is available at Elsevier via https://doi.org/10.1016/j.aca.2018.12.044. © 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.description.abstractThis paper presents the development and validation of a fully automated, high-throughput multiclass, multiresidue method for quantitative analysis of 77 veterinary drugs in chicken muscle via direct immersion solid phase microextraction (DI-SPME) and ultra-high pressure liquid chromatography-electrospray ionization - tandem mass spectrometry (UHPLC-ESI-MS/MS). The selected drugs represent more than 12 different classes of drugs characterized by varying physical and chemical properties. A Hydrophilic–lipophilic balance (HLB)/polyacrylonitrile (PAN) extraction phase, prepared using HLB particles synthesized in-house, yielded the best extraction/desorption performance among four different SPME extraction phases evaluated in the current work. The developed SPME method was optimized in terms of SPME coating and geometry, desorption solvent, extraction and rinsing conditions, and extraction and desorption times. Multivariate analysis was performed to determine the optimal desorption solvent for the proposed application. The developed method was validated according to the Food and Drug Administration (FDA) guidelines, taking into account Canadian maximum residue limits (MRLs) and US maximum tolerance levels for veterinary drugs in meat. Method accuracy ranged from 80 to 120% for at least 73 compounds, with relative standard deviation of 1–15%. Inter-day precision ranged from 4 to 15% for 70 compounds. Determination coefficients values were higher than 0.991 for all compounds under study with no significant lack of fit (p > 0.05) at the 5% level. In terms of limits of quantitation, the method was able to meet both Canadian and US regulatory levels for all compounds under study.en
dc.description.sponsorshipThe authors would like to acknowledge Perkin Elmer for the financial support and the staff at the University of Waterloo's Science Technical Services for their exceptional technical support and collaboration to improve the SPME brush of the high-throughput system. V.A.J.thanks FAPESP, process 2016/16180e6 for his scholarship.en
dc.language.isoenen
dc.publisherElsevieren
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectveterinary drugsen
dc.subjectmulti-class multi-residue analysisen
dc.subjectsolid phase microextractionen
dc.subjectmethod development and validationen
dc.subjectUHPLC-MS/MSen
dc.titleDevelopment and validation of a fully automated solid phase microextraction high throughput method for quantitative analysis of multiresidue veterinary drugs in chicken tissueen
dc.typeArticleen
dcterms.bibliographicCitationA. Khaled, E. Gionfriddo, V. Acquaro Jr., V. Singh, J. Pawliszyn, Development and Validation of a Fully Automated Solid-Phase Microextraction High Throughput Method for Quantitative Analysis of Multiresidue Veterinary Drugs in Chicken Tissue, Analytica Chimica Acta, https://doi.org/10.1016/j.aca.2018.12.044.en
uws.contributor.affiliation1Faculty of Scienceen
uws.contributor.affiliation2Chemistryen
uws.typeOfResourceTexten
uws.peerReviewStatusRevieweden
uws.scholarLevelFacultyen
uws.scholarLevelPost-Doctorateen


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