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Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry

dc.contributor.authorVirgilio, Alex
dc.contributor.authorAmais, Renata Stabile
dc.contributor.authorSchiavo, Daniela
dc.contributor.authorGomes Neto, José Anchieta [UNESP]
dc.contributor.authorNóbrega, Joaquim de Araújo
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionBarueri
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:11:16Z
dc.date.available2018-12-11T17:11:16Z
dc.date.issued2017-03-24
dc.description.abstractA procedure for the determination of As, Cd, Cr, Ni, Pb, and V in phytotherapy medicines by inductively coupled plasma–tandem mass spectrometry is reported. The use of tandem mass spectrometry with oxygen into an octopole reaction system at various gas flow rates and the combination of on-mass and mass-shift modes was evaluated. Cadmium, Cr, Ni, and Pb were determined as free atomic ions while As and V were determined as the oxides AsO+ and VO+ in the same run. Samples were prepared by microwave-assisted digestion with dilute nitric acid and hydrogen peroxide. Two plant-certified reference materials (apple leaves and tomato leaves) were used to check the accuracy. For tandem mass spectrometry with 0.5 mL min−1 O2, recoveries in the 85–113% were typically obtained and no statistical differences were observed at the 95% confidence level (t-test) in comparison with the certified values. Using these conditions, the limits of detection for the method were 0.01, 0.0002, 0.008, 0.008, 0.003, and 0.002 µg g−1 for As, Cd, Cr, Ni, Pb, and V, respectively. The procedure was used for the analysis of four phytotherapic drugs and the determined concentrations were up to 0.168 µg g−1 As, 0.03 µg g−1 Cd, 0.82 µg g−1 Cr, 1.18 µg g−1 Ni, 0.52 µg g−1 Pb, and 2.4 µg g−1 V with average precision values of 8% as the relative standard deviation. The found concentrations were compared with limits proposed in official guidelines and, in most cases, the values were below the maximum limits allowed.en
dc.description.affiliationGroup for Applied Instrumental Analysis Department of Chemistry Federal University of São Carlos
dc.description.affiliationCenter for Nuclear Energy in Agriculture University of São Paulo
dc.description.affiliationAgilent Technologies Brazil Barueri
dc.description.affiliationDepartment of Analytical Chemistry Institute of Chemistry São Paulo State University - UNESP
dc.description.affiliationUnespDepartment of Analytical Chemistry Institute of Chemistry São Paulo State University - UNESP
dc.format.extent842-852
dc.identifierhttp://dx.doi.org/10.1080/00032719.2016.1195839
dc.identifier.citationAnalytical Letters, v. 50, n. 5, p. 842-852, 2017.
dc.identifier.doi10.1080/00032719.2016.1195839
dc.identifier.file2-s2.0-85017546906.pdf
dc.identifier.issn1532-236X
dc.identifier.issn0003-2719
dc.identifier.scopus2-s2.0-85017546906
dc.identifier.urihttp://hdl.handle.net/11449/174473
dc.language.isoeng
dc.relation.ispartofAnalytical Letters
dc.relation.ispartofsjr0,344
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectContaminants, elemental impurity determination
dc.subjectICP-MS/MS
dc.subjectinductively coupled plasma–tandem mass spectrometry
dc.subjectphytotherapy medicines
dc.subjectspectral interferences
dc.subjecttrace analysis
dc.titleElemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometryen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Analítica - IQARpt

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