Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction

Detalhes bibliográficos
Autor(a) principal: Sabin,Guilherme P.
Data de Publicação: 2009
Outros Autores: Prestes,Osmar D., Adaime,Martha B., Zanella,Renato
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000500017
Resumo: In this work, a method using solid-phase extraction and gas chromatography coupled mass spectrometry in the selective ion monitoring (SIM) mode was developed and validated for the multi-class determination of 20 pesticides regulated by the Brazilian legislation for drinking water. Because these pesticides must be determined at low concentrations, a high preconcentration factor associated to the high sensitivity of chromatographic analysis was necessary. The method presented quantification limits between 0.003 and 0.093 µg L-1. Most of the compounds presented mean recoveries between 51 and 116%. Although the differing chemical nature of the pesticides analyzed difficult the attainment of good recovery for all of the compounds evaluated, the precision of the results was excellent. The selectivity of the method was evaluated through the relative intensity of quantification and qualification ions and was considered adequate. Analysis in real samples met criteria for instrumental qualification and the system suitability evaluation.
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spelling Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extractionsolid-phase extractionGC-MSpesticidemultiresiduewaterIn this work, a method using solid-phase extraction and gas chromatography coupled mass spectrometry in the selective ion monitoring (SIM) mode was developed and validated for the multi-class determination of 20 pesticides regulated by the Brazilian legislation for drinking water. Because these pesticides must be determined at low concentrations, a high preconcentration factor associated to the high sensitivity of chromatographic analysis was necessary. The method presented quantification limits between 0.003 and 0.093 µg L-1. Most of the compounds presented mean recoveries between 51 and 116%. Although the differing chemical nature of the pesticides analyzed difficult the attainment of good recovery for all of the compounds evaluated, the precision of the results was excellent. The selectivity of the method was evaluated through the relative intensity of quantification and qualification ions and was considered adequate. Analysis in real samples met criteria for instrumental qualification and the system suitability evaluation.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000500017Journal of the Brazilian Chemical Society v.20 n.5 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009000500017info:eu-repo/semantics/openAccessSabin,Guilherme P.Prestes,Osmar D.Adaime,Martha B.Zanella,Renatoeng2009-06-29T00:00:00Zoai:scielo:S0103-50532009000500017Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2009-06-29T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction
title Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction
spellingShingle Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction
Sabin,Guilherme P.
solid-phase extraction
GC-MS
pesticide
multiresidue
water
title_short Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction
title_full Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction
title_fullStr Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction
title_full_unstemmed Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction
title_sort Multiresidue determination of pesticides in drinking water by gas chromatography-mass spectrometry after solid-phase extraction
author Sabin,Guilherme P.
author_facet Sabin,Guilherme P.
Prestes,Osmar D.
Adaime,Martha B.
Zanella,Renato
author_role author
author2 Prestes,Osmar D.
Adaime,Martha B.
Zanella,Renato
author2_role author
author
author
dc.contributor.author.fl_str_mv Sabin,Guilherme P.
Prestes,Osmar D.
Adaime,Martha B.
Zanella,Renato
dc.subject.por.fl_str_mv solid-phase extraction
GC-MS
pesticide
multiresidue
water
topic solid-phase extraction
GC-MS
pesticide
multiresidue
water
description In this work, a method using solid-phase extraction and gas chromatography coupled mass spectrometry in the selective ion monitoring (SIM) mode was developed and validated for the multi-class determination of 20 pesticides regulated by the Brazilian legislation for drinking water. Because these pesticides must be determined at low concentrations, a high preconcentration factor associated to the high sensitivity of chromatographic analysis was necessary. The method presented quantification limits between 0.003 and 0.093 µg L-1. Most of the compounds presented mean recoveries between 51 and 116%. Although the differing chemical nature of the pesticides analyzed difficult the attainment of good recovery for all of the compounds evaluated, the precision of the results was excellent. The selectivity of the method was evaluated through the relative intensity of quantification and qualification ions and was considered adequate. Analysis in real samples met criteria for instrumental qualification and the system suitability evaluation.
publishDate 2009
dc.date.none.fl_str_mv 2009-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000500017
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000500017
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532009000500017
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.20 n.5 2009
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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