Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector

Detalhes bibliográficos
Autor(a) principal: Abad,Fernanda C.
Data de Publicação: 2010
Outros Autores: Winck,Priscila R., Silva,Juliana M. da, Caramão,Elina B., Zini,Cláudia A.
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=S0103-50532010000300010
Resumo: In this study, 14 pesticides (captan, chlorothalonil, deltamethrin, dicloran, fenthion, folpet, iprodione, linuron, malathion, prometryn, prochloraz, procymidone, trichlorphon and trifluralin) were employed for developing a multiresidue method (MRM) using pressurized liquid extraction (PLE). In situ clean-up was achieved using matrix solid phase dispersion (MSPD), where Florisil, XAD-4, XAD-7 and C18 were tested as dispersing material for carrot samples. Dichloromethane, ethyl acetate and acetone were used as solvents in a PLE unit at 75 ºC and 1,500 psi. Recovery was in the range of 70 to 133 %. Results obtained with wet carrots were not satisfactory, since most of the recovery values were below 70%. Determination coefficients of the analytical curves presented values between 0.9821 and 0.9970. Limits of detection (LOD) and quantification (LOQ) for the various components varied from 0.0024 to 0.1968 mg kg-1, and 0.0072 to 0.5963 mg kg-1, respectively.
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spelling Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detectormultiresidue methodPLEMSPDcarrotsGC/MSIn this study, 14 pesticides (captan, chlorothalonil, deltamethrin, dicloran, fenthion, folpet, iprodione, linuron, malathion, prometryn, prochloraz, procymidone, trichlorphon and trifluralin) were employed for developing a multiresidue method (MRM) using pressurized liquid extraction (PLE). In situ clean-up was achieved using matrix solid phase dispersion (MSPD), where Florisil, XAD-4, XAD-7 and C18 were tested as dispersing material for carrot samples. Dichloromethane, ethyl acetate and acetone were used as solvents in a PLE unit at 75 ºC and 1,500 psi. Recovery was in the range of 70 to 133 %. Results obtained with wet carrots were not satisfactory, since most of the recovery values were below 70%. Determination coefficients of the analytical curves presented values between 0.9821 and 0.9970. Limits of detection (LOD) and quantification (LOQ) for the various components varied from 0.0024 to 0.1968 mg kg-1, and 0.0072 to 0.5963 mg kg-1, respectively.Sociedade Brasileira de Química2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000300010Journal of the Brazilian Chemical Society v.21 n.3 2010reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532010000300010info:eu-repo/semantics/openAccessAbad,Fernanda C.Winck,Priscila R.Silva,Juliana M. daCaramão,Elina B.Zini,Cláudia A.eng2010-04-30T00:00:00Zoai:scielo:S0103-50532010000300010Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2010-04-30T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector
title Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector
spellingShingle Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector
Abad,Fernanda C.
multiresidue method
PLE
MSPD
carrots
GC/MS
title_short Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector
title_full Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector
title_fullStr Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector
title_full_unstemmed Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector
title_sort Multiresidue determination of pesticides in carrots using pressurized liquid extraction and gas chromatography with mass spectrometry detector
author Abad,Fernanda C.
author_facet Abad,Fernanda C.
Winck,Priscila R.
Silva,Juliana M. da
Caramão,Elina B.
Zini,Cláudia A.
author_role author
author2 Winck,Priscila R.
Silva,Juliana M. da
Caramão,Elina B.
Zini,Cláudia A.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Abad,Fernanda C.
Winck,Priscila R.
Silva,Juliana M. da
Caramão,Elina B.
Zini,Cláudia A.
dc.subject.por.fl_str_mv multiresidue method
PLE
MSPD
carrots
GC/MS
topic multiresidue method
PLE
MSPD
carrots
GC/MS
description In this study, 14 pesticides (captan, chlorothalonil, deltamethrin, dicloran, fenthion, folpet, iprodione, linuron, malathion, prometryn, prochloraz, procymidone, trichlorphon and trifluralin) were employed for developing a multiresidue method (MRM) using pressurized liquid extraction (PLE). In situ clean-up was achieved using matrix solid phase dispersion (MSPD), where Florisil, XAD-4, XAD-7 and C18 were tested as dispersing material for carrot samples. Dichloromethane, ethyl acetate and acetone were used as solvents in a PLE unit at 75 ºC and 1,500 psi. Recovery was in the range of 70 to 133 %. Results obtained with wet carrots were not satisfactory, since most of the recovery values were below 70%. Determination coefficients of the analytical curves presented values between 0.9821 and 0.9970. Limits of detection (LOD) and quantification (LOQ) for the various components varied from 0.0024 to 0.1968 mg kg-1, and 0.0072 to 0.5963 mg kg-1, respectively.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01
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=S0103-50532010000300010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000300010
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532010000300010
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.21 n.3 2010
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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