Determination of ecstasy components in human urine by gas chromatography using a dispersive liquid-liquid microextraction procedure
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | |
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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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 |
_version_ |
1750318174343004160 |