Pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometry

Residues of four pesticides in groundwaters were surveyed during one year in an agricultural area in southern Brazil. The methods for separation, identification and quantification of the compounds included high-performance liquid chromatography with diode array detection (HPLC-DAD) and liquid chromatography with electrospray interface tandem mass spectrometry (LC-ESI-MS/MS). A pre-concentration step based on solid-phase extraction with 200 mg C18 cartridges was applied. All the analytical parameters were within the limits suggested for the validation of chromatographic methods. The LOQs for the methods, considering the 250-fold pre-concentration step, were 0.2 μg L-1 for all pesticides by HPLC-DAD, 4.0 ng L-1 for clomazone, carbofuran and tebuconazole and 40.0 ng L-1 for 2,4-D by LC-ESI-MS/MS. In groundwater samples, 2,4-D was not detected, and carbofuran, clomazone and tebuconazole were detected in concentrations ranging from 0.25 to 10.40 μg L-1, from 0.20 to 0.82 μg L-1 and from 0.20 to 4.16 μg L-1, respectively. The methods proved to be adequate for the analysis of pesticides in groundwaters.

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Main Authors: Caldas,Sergiane S., Demoliner,Adriana, Costa,Fabiane P., D'Oca,Marcelo G. M., Primel,Ednei G.
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2010
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000400009
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spelling oai:scielo:S0103-505320100004000092010-05-21Pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometryCaldas,Sergiane S.Demoliner,AdrianaCosta,Fabiane P.D'Oca,Marcelo G. M.Primel,Ednei G. groundwaters pesticides HPLC-DAD SPE LC-MS/MS Residues of four pesticides in groundwaters were surveyed during one year in an agricultural area in southern Brazil. The methods for separation, identification and quantification of the compounds included high-performance liquid chromatography with diode array detection (HPLC-DAD) and liquid chromatography with electrospray interface tandem mass spectrometry (LC-ESI-MS/MS). A pre-concentration step based on solid-phase extraction with 200 mg C18 cartridges was applied. All the analytical parameters were within the limits suggested for the validation of chromatographic methods. The LOQs for the methods, considering the 250-fold pre-concentration step, were 0.2 μg L-1 for all pesticides by HPLC-DAD, 4.0 ng L-1 for clomazone, carbofuran and tebuconazole and 40.0 ng L-1 for 2,4-D by LC-ESI-MS/MS. In groundwater samples, 2,4-D was not detected, and carbofuran, clomazone and tebuconazole were detected in concentrations ranging from 0.25 to 10.40 μg L-1, from 0.20 to 0.82 μg L-1 and from 0.20 to 4.16 μg L-1, respectively. The methods proved to be adequate for the analysis of pesticides in groundwaters.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society v.21 n.4 20102010-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000400009en10.1590/S0103-50532010000400009
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Caldas,Sergiane S.
Demoliner,Adriana
Costa,Fabiane P.
D'Oca,Marcelo G. M.
Primel,Ednei G.
spellingShingle Caldas,Sergiane S.
Demoliner,Adriana
Costa,Fabiane P.
D'Oca,Marcelo G. M.
Primel,Ednei G.
Pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometry
author_facet Caldas,Sergiane S.
Demoliner,Adriana
Costa,Fabiane P.
D'Oca,Marcelo G. M.
Primel,Ednei G.
author_sort Caldas,Sergiane S.
title Pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometry
title_short Pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometry
title_full Pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometry
title_fullStr Pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometry
title_full_unstemmed Pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometry
title_sort pesticide residue determination in groundwater using solid-phase extraction and high-performance liquid chromatography with diode array detector and liquid chromatography-tandem mass spectrometry
description Residues of four pesticides in groundwaters were surveyed during one year in an agricultural area in southern Brazil. The methods for separation, identification and quantification of the compounds included high-performance liquid chromatography with diode array detection (HPLC-DAD) and liquid chromatography with electrospray interface tandem mass spectrometry (LC-ESI-MS/MS). A pre-concentration step based on solid-phase extraction with 200 mg C18 cartridges was applied. All the analytical parameters were within the limits suggested for the validation of chromatographic methods. The LOQs for the methods, considering the 250-fold pre-concentration step, were 0.2 μg L-1 for all pesticides by HPLC-DAD, 4.0 ng L-1 for clomazone, carbofuran and tebuconazole and 40.0 ng L-1 for 2,4-D by LC-ESI-MS/MS. In groundwater samples, 2,4-D was not detected, and carbofuran, clomazone and tebuconazole were detected in concentrations ranging from 0.25 to 10.40 μg L-1, from 0.20 to 0.82 μg L-1 and from 0.20 to 4.16 μg L-1, respectively. The methods proved to be adequate for the analysis of pesticides in groundwaters.
publisher Sociedade Brasileira de Química
publishDate 2010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000400009
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