Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure

Detalhes bibliográficos
Autor(a) principal: Mashayekhi,Hossein Ali
Data de Publicação: 2012
Outros Autores: Rezaee,Mohammad
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=S0103-50532012000900015
Resumo: A new method was developed for preconcentration and determination of ecstasy compounds, 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxymethylamphetamine (MDMA), 3,4-methylenedioxyethylamphetamine (MDEA) and 3,4-methylenedioxypropylamphetamine (MDPA), in urine samples using dispersive liquid-liquid microextraction (DLLME) and gas chromatography (GC) with flame ionization detection (GC-FID). The method was based on the formation of tiny droplets of an organic extractant in prepared sample solution using water, immiscible organic solvent (CS2) dissolved in water-miscible organic disperser solvent (acetone). The organic phase, which extracted MDA, MDEA, MDMA and MDPA from the prepared sample solution, was separated by centrifugation. Parameters affecting extraction efficiency were investigated and optimized. Under the optimum conditions, linearities of the method were 1.0-500 µg L-1 for MDEA and MDPA and 2.5-500 µg L-1 for MDA and MDMA. The limits of detection (LODs, S/N = 3, signal-to-noise ratio) were in the range from 0.3 to 0.8 µg L-1. The method was successfully applied to the determination of analytes in urine samples.
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spelling Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction proceduredispersive liquid-liquid microextractionecstasyamphetamineurine samplesgas chromatographyA new method was developed for preconcentration and determination of ecstasy compounds, 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxymethylamphetamine (MDMA), 3,4-methylenedioxyethylamphetamine (MDEA) and 3,4-methylenedioxypropylamphetamine (MDPA), in urine samples using dispersive liquid-liquid microextraction (DLLME) and gas chromatography (GC) with flame ionization detection (GC-FID). The method was based on the formation of tiny droplets of an organic extractant in prepared sample solution using water, immiscible organic solvent (CS2) dissolved in water-miscible organic disperser solvent (acetone). The organic phase, which extracted MDA, MDEA, MDMA and MDPA from the prepared sample solution, was separated by centrifugation. Parameters affecting extraction efficiency were investigated and optimized. Under the optimum conditions, linearities of the method were 1.0-500 µg L-1 for MDEA and MDPA and 2.5-500 µg L-1 for MDA and MDMA. The limits of detection (LODs, S/N = 3, signal-to-noise ratio) were in the range from 0.3 to 0.8 µg L-1. The method was successfully applied to the determination of analytes in urine samples.Sociedade Brasileira de Química2012-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000900015Journal of the Brazilian Chemical Society v.23 n.9 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012005000032info:eu-repo/semantics/openAccessMashayekhi,Hossein AliRezaee,Mohammadeng2012-10-15T00:00:00Zoai:scielo:S0103-50532012000900015Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-10-15T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
title Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
spellingShingle Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
Mashayekhi,Hossein Ali
dispersive liquid-liquid microextraction
ecstasy
amphetamine
urine samples
gas chromatography
title_short Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
title_full Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
title_fullStr Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
title_full_unstemmed Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
title_sort Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
author Mashayekhi,Hossein Ali
author_facet Mashayekhi,Hossein Ali
Rezaee,Mohammad
author_role author
author2 Rezaee,Mohammad
author2_role author
dc.contributor.author.fl_str_mv Mashayekhi,Hossein Ali
Rezaee,Mohammad
dc.subject.por.fl_str_mv dispersive liquid-liquid microextraction
ecstasy
amphetamine
urine samples
gas chromatography
topic dispersive liquid-liquid microextraction
ecstasy
amphetamine
urine samples
gas chromatography
description A new method was developed for preconcentration and determination of ecstasy compounds, 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxymethylamphetamine (MDMA), 3,4-methylenedioxyethylamphetamine (MDEA) and 3,4-methylenedioxypropylamphetamine (MDPA), in urine samples using dispersive liquid-liquid microextraction (DLLME) and gas chromatography (GC) with flame ionization detection (GC-FID). The method was based on the formation of tiny droplets of an organic extractant in prepared sample solution using water, immiscible organic solvent (CS2) dissolved in water-miscible organic disperser solvent (acetone). The organic phase, which extracted MDA, MDEA, MDMA and MDPA from the prepared sample solution, was separated by centrifugation. Parameters affecting extraction efficiency were investigated and optimized. Under the optimum conditions, linearities of the method were 1.0-500 µg L-1 for MDEA and MDPA and 2.5-500 µg L-1 for MDA and MDMA. The limits of detection (LODs, S/N = 3, signal-to-noise ratio) were in the range from 0.3 to 0.8 µg L-1. The method was successfully applied to the determination of analytes in urine samples.
publishDate 2012
dc.date.none.fl_str_mv 2012-09-01
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=S0103-50532012000900015
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000900015
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532012005000032
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.23 n.9 2012
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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