Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1080/00032719.2016.1195839 http://hdl.handle.net/11449/174473 |
Resumo: | A 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. |
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Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass SpectrometryContaminants, elemental impurity determinationICP-MS/MSinductively coupled plasma–tandem mass spectrometryphytotherapy medicinesspectral interferencestrace analysisA 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.Group for Applied Instrumental Analysis Department of Chemistry Federal University of São CarlosCenter for Nuclear Energy in Agriculture University of São PauloAgilent Technologies Brazil BarueriDepartment of Analytical Chemistry Institute of Chemistry São Paulo State University - UNESPDepartment of Analytical Chemistry Institute of Chemistry São Paulo State University - UNESPUniversidade Federal de São Carlos (UFSCar)Universidade de São Paulo (USP)BarueriUniversidade Estadual Paulista (Unesp)Virgilio, AlexAmais, Renata StabileSchiavo, DanielaGomes Neto, José Anchieta [UNESP]Nóbrega, Joaquim de Araújo2018-12-11T17:11:16Z2018-12-11T17:11:16Z2017-03-24info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article842-852application/pdfhttp://dx.doi.org/10.1080/00032719.2016.1195839Analytical Letters, v. 50, n. 5, p. 842-852, 2017.1532-236X0003-2719http://hdl.handle.net/11449/17447310.1080/00032719.2016.11958392-s2.0-850175469062-s2.0-85017546906.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAnalytical Letters0,344info:eu-repo/semantics/openAccess2023-11-21T06:15:37Zoai:repositorio.unesp.br:11449/174473Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:21:40.687797Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry |
title |
Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry |
spellingShingle |
Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry Virgilio, Alex Contaminants, elemental impurity determination ICP-MS/MS inductively coupled plasma–tandem mass spectrometry phytotherapy medicines spectral interferences trace analysis |
title_short |
Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry |
title_full |
Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry |
title_fullStr |
Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry |
title_full_unstemmed |
Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry |
title_sort |
Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry |
author |
Virgilio, Alex |
author_facet |
Virgilio, Alex Amais, Renata Stabile Schiavo, Daniela Gomes Neto, José Anchieta [UNESP] Nóbrega, Joaquim de Araújo |
author_role |
author |
author2 |
Amais, Renata Stabile Schiavo, Daniela Gomes Neto, José Anchieta [UNESP] Nóbrega, Joaquim de Araújo |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Carlos (UFSCar) Universidade de São Paulo (USP) Barueri Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Virgilio, Alex Amais, Renata Stabile Schiavo, Daniela Gomes Neto, José Anchieta [UNESP] Nóbrega, Joaquim de Araújo |
dc.subject.por.fl_str_mv |
Contaminants, elemental impurity determination ICP-MS/MS inductively coupled plasma–tandem mass spectrometry phytotherapy medicines spectral interferences trace analysis |
topic |
Contaminants, elemental impurity determination ICP-MS/MS inductively coupled plasma–tandem mass spectrometry phytotherapy medicines spectral interferences trace analysis |
description |
A 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. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-03-24 2018-12-11T17:11:16Z 2018-12-11T17:11:16Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1080/00032719.2016.1195839 Analytical Letters, v. 50, n. 5, p. 842-852, 2017. 1532-236X 0003-2719 http://hdl.handle.net/11449/174473 10.1080/00032719.2016.1195839 2-s2.0-85017546906 2-s2.0-85017546906.pdf |
url |
http://dx.doi.org/10.1080/00032719.2016.1195839 http://hdl.handle.net/11449/174473 |
identifier_str_mv |
Analytical Letters, v. 50, n. 5, p. 842-852, 2017. 1532-236X 0003-2719 10.1080/00032719.2016.1195839 2-s2.0-85017546906 2-s2.0-85017546906.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Analytical Letters 0,344 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
842-852 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128925186916352 |