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Magnetic particle spray mass spectrometry for the determination of beta-blockers in plasma samples

dc.contributor.authorde Castilho Alves Morais, Elizângela Maria
dc.contributor.authorMendes, Tássia Venga
dc.contributor.authorArnoni, Estela Domingos
dc.contributor.authorGorup, Luiz Fernando
dc.contributor.authorRosa, Mariana Azevedo
dc.contributor.authorMoreira, Ailton José [UNESP]
dc.contributor.authorFigueiredo, Eduardo Costa
dc.contributor.institutionFederal University of Alfenas
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionFederal University of Rio Grande
dc.contributor.institutionFederal University of Juiz de Fora
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T19:33:14Z
dc.date.issued2024-10-01
dc.description.abstractMagnetic particle spray mass spectrometry (MPS-MS), an innovative ambient ionization technique proposed by our research group, was employed to determine beta-blockers in human plasma samples. A dispersive solid phase extraction of atenolol, metoprolol, labetalol, propranolol, nadolol, and pindolol was carried out using magnetic molecularly imprinted polymer (M-MIP) particles that were attached to the tip of a metal probe, which was placed in the mass spectrometer inlet. A solvent (1% formic acid in methanol) was dispensed on the particles, and the Taylor cone was formed around them (in high voltage). The analytes were desorbed/ionized and determined by a triple quadrupole mass spectrometer. M-MIP was synthesized with oxprenolol as a pseudo-template, demonstrating good selectivity to beta-blockers compared with no-analog molecules, with an adsorption process occurring in monolayers, according to isotherm studies. Kinetic experiments indicated chemisorption as the predominant M-MIP/analyte interaction. The analytical curves were linear (R2 > 0.98), and the limit of quantification was 3 µg L−1 for all the analytes. Limits of detection ranged from 0.64 to 2.41 µg L−1. Precisions (relative standard deviation) and accuracies (relative error) ranged from 3.95 to 21.20% and -17.05 to 18.93%, respectively. MPS-MS proved to be a simple, sensitive, and advantageous technique compared with conventional approaches. The analyses were fast, requiring no chromatographic separation and without ionic suppression. The method is aligned with green chemistry principles, requiring minimal sample, solvent, and sorbent amounts. MPS-MS successfully integrates sample preparation and ambient ionization mass spectrometry and holds great potential for application with other sorbents, samples, and analytes. Graphical Abstract: (Figure presented.)en
dc.description.affiliationLaboratory of Toxicant and Drug Analyses Faculty of Pharmaceutical Sciences Federal University of Alfenas, MG
dc.description.affiliationInstitute of Chemistry Federal University of Alfenas, MG
dc.description.affiliationDepartment of Chemistry Interdiscipli5nary Laboratory of Electrochemistry and Ceramics (LIEC) Federal University of São Carlos, SP
dc.description.affiliationSchool of Chemistry and Food Science Federal University of Rio Grande, RS
dc.description.affiliationDepartment of Chemistry Federal University of Juiz de Fora, MG
dc.description.affiliationInstitute of Chemistry São Paulo State University (UNESP), SP
dc.description.affiliationUnespInstitute of Chemistry São Paulo State University (UNESP), SP
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.identifierhttp://dx.doi.org/10.1007/s00604-024-06698-2
dc.identifier.citationMicrochimica Acta, v. 191, n. 10, 2024.
dc.identifier.doi10.1007/s00604-024-06698-2
dc.identifier.issn1436-5073
dc.identifier.issn0026-3672
dc.identifier.scopus2-s2.0-85204872786
dc.identifier.urihttps://hdl.handle.net/11449/303855
dc.language.isoeng
dc.relation.ispartofMicrochimica Acta
dc.sourceScopus
dc.subjectAmbient ionization
dc.subjectDispersive solid phase extraction
dc.subjectMagnetic particle spray mass spectrometry
dc.subjectMagnetic sorbent
dc.subjectMolecularly imprinted polymers
dc.titleMagnetic particle spray mass spectrometry for the determination of beta-blockers in plasma samplesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.orcid0000-0002-7883-9717[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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