Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry
Autor(a) principal: | |
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Data de Publicação: | 2008 |
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=S0103-50532008000300006 |
Resumo: | A reliable, highly selective and sensitive procedure is presented for simultaneous determination of captopril and thioguanine based on cathodic adsorptive stripping of Cu(I)-captopril and Cu(I)-thioguanine complexes on a hanging mercury drop electrode. Captopril and thioguanine were preconcentrated onto the surface of hanging mercury drop electrode using Cu(II) as a suitable probe, with accumulation time of 90 s. Then the preconcentrated complexes were analyzed by cathodic stripping differential pulse voltammetry. The effect of various parameters such as pH, concentration of copper, accumulation potential, accumulation time and scan rate on the sensitivity were studied. The optimum conditions for simultaneous determination of captopril and thioguanine include pH=3.5, 45.0 ng mL-1 copper(II) concentration, accumulation potential of -0.10 V and scan rate of 60 mV s-1. Under the optimum conditions and for an accumulation time of 90 s, the measured peak currents at about -0.15 V and -0.40 V (vs. Ag/AgCl) are proportional to the concentrations of thioguanine and captopril over the ranges of 0.15-180 and 0.5-100 nmol L-1, respectively. The limits of detection are 0.08 and 0.3 nmol L-1 for thioguanine and captopril, respectively. The relative standard deviations for five replicate analyses of 20.0 nmol L-1 captopril and thioguanine are 2.5% and 2.1%, respectively. The method was applied to the determination of captopril and thioguanine in synthetic mixed samples, pharmaceutical samples and human serum with satisfactory results. |
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Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetrycaptoprilthioguaninecopper(II)adsorptive cathodic stripping voltammetryA reliable, highly selective and sensitive procedure is presented for simultaneous determination of captopril and thioguanine based on cathodic adsorptive stripping of Cu(I)-captopril and Cu(I)-thioguanine complexes on a hanging mercury drop electrode. Captopril and thioguanine were preconcentrated onto the surface of hanging mercury drop electrode using Cu(II) as a suitable probe, with accumulation time of 90 s. Then the preconcentrated complexes were analyzed by cathodic stripping differential pulse voltammetry. The effect of various parameters such as pH, concentration of copper, accumulation potential, accumulation time and scan rate on the sensitivity were studied. The optimum conditions for simultaneous determination of captopril and thioguanine include pH=3.5, 45.0 ng mL-1 copper(II) concentration, accumulation potential of -0.10 V and scan rate of 60 mV s-1. Under the optimum conditions and for an accumulation time of 90 s, the measured peak currents at about -0.15 V and -0.40 V (vs. Ag/AgCl) are proportional to the concentrations of thioguanine and captopril over the ranges of 0.15-180 and 0.5-100 nmol L-1, respectively. The limits of detection are 0.08 and 0.3 nmol L-1 for thioguanine and captopril, respectively. The relative standard deviations for five replicate analyses of 20.0 nmol L-1 captopril and thioguanine are 2.5% and 2.1%, respectively. The method was applied to the determination of captopril and thioguanine in synthetic mixed samples, pharmaceutical samples and human serum with satisfactory results.Sociedade Brasileira de Química2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000300006Journal of the Brazilian Chemical Society v.19 n.3 2008reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532008000300006info:eu-repo/semantics/openAccessEnsafi,Ali AsgharHajian,Rezaeng2008-05-27T00:00:00Zoai:scielo:S0103-50532008000300006Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2008-05-27T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry |
title |
Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry |
spellingShingle |
Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry Ensafi,Ali Asghar captopril thioguanine copper(II) adsorptive cathodic stripping voltammetry |
title_short |
Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry |
title_full |
Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry |
title_fullStr |
Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry |
title_full_unstemmed |
Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry |
title_sort |
Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry |
author |
Ensafi,Ali Asghar |
author_facet |
Ensafi,Ali Asghar Hajian,Reza |
author_role |
author |
author2 |
Hajian,Reza |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Ensafi,Ali Asghar Hajian,Reza |
dc.subject.por.fl_str_mv |
captopril thioguanine copper(II) adsorptive cathodic stripping voltammetry |
topic |
captopril thioguanine copper(II) adsorptive cathodic stripping voltammetry |
description |
A reliable, highly selective and sensitive procedure is presented for simultaneous determination of captopril and thioguanine based on cathodic adsorptive stripping of Cu(I)-captopril and Cu(I)-thioguanine complexes on a hanging mercury drop electrode. Captopril and thioguanine were preconcentrated onto the surface of hanging mercury drop electrode using Cu(II) as a suitable probe, with accumulation time of 90 s. Then the preconcentrated complexes were analyzed by cathodic stripping differential pulse voltammetry. The effect of various parameters such as pH, concentration of copper, accumulation potential, accumulation time and scan rate on the sensitivity were studied. The optimum conditions for simultaneous determination of captopril and thioguanine include pH=3.5, 45.0 ng mL-1 copper(II) concentration, accumulation potential of -0.10 V and scan rate of 60 mV s-1. Under the optimum conditions and for an accumulation time of 90 s, the measured peak currents at about -0.15 V and -0.40 V (vs. Ag/AgCl) are proportional to the concentrations of thioguanine and captopril over the ranges of 0.15-180 and 0.5-100 nmol L-1, respectively. The limits of detection are 0.08 and 0.3 nmol L-1 for thioguanine and captopril, respectively. The relative standard deviations for five replicate analyses of 20.0 nmol L-1 captopril and thioguanine are 2.5% and 2.1%, respectively. The method was applied to the determination of captopril and thioguanine in synthetic mixed samples, pharmaceutical samples and human serum with satisfactory results. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-01-01 |
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=S0103-50532008000300006 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000300006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532008000300006 |
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.19 n.3 2008 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_ |
1750318168638750720 |