Flow-injection iodimetric determination of captopril in pharmaceutical preparations

Detalhes bibliográficos
Autor(a) principal: Schmidt Jr.,Erlando
Data de Publicação: 2009
Outros Autores: Melchert,Wanessa R., Rocha,Fábio R. P.
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=S0103-50532009000200007
Resumo: A simple, fast and low cost procedure for spectrophotometric determination of captopril in pharmaceutical preparations is described. The procedure is based on a flow-injection system exploiting the on-line formation of the triiodide reagent, which is consumed in the presence of the analyte generating a transient signal. Linear response was observed up to 200 µmol L-1 with a detection limit of 1.0 µmol L-1 (99.7% confidence level). The coefficient of variation (n = 20) and the sampling rate were estimated as 1.2% and 72 determinations per hour, respectively. The main excipients found in pharmaceutical preparations did not affect the captopril determination. The zone sampling approach was exploited to implement on-line dilutions, aiming direct analysis of sample extracts. Results of the analysis of commercial samples agreed with the obtained by the titrimetric reference procedure described in the US-Pharmacopeia at the 95% confidence level. The reagent consumption was estimated as 18 µg of KMnO4 and 10 mg of KI per determination, with a cost of US$ 2.50 per 1000 determinations.
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spelling Flow-injection iodimetric determination of captopril in pharmaceutical preparationsflow injectionspectrophotometryiodimetrycaptoprilanti-hypertensiveA simple, fast and low cost procedure for spectrophotometric determination of captopril in pharmaceutical preparations is described. The procedure is based on a flow-injection system exploiting the on-line formation of the triiodide reagent, which is consumed in the presence of the analyte generating a transient signal. Linear response was observed up to 200 µmol L-1 with a detection limit of 1.0 µmol L-1 (99.7% confidence level). The coefficient of variation (n = 20) and the sampling rate were estimated as 1.2% and 72 determinations per hour, respectively. The main excipients found in pharmaceutical preparations did not affect the captopril determination. The zone sampling approach was exploited to implement on-line dilutions, aiming direct analysis of sample extracts. Results of the analysis of commercial samples agreed with the obtained by the titrimetric reference procedure described in the US-Pharmacopeia at the 95% confidence level. The reagent consumption was estimated as 18 µg of KMnO4 and 10 mg of KI per determination, with a cost of US$ 2.50 per 1000 determinations.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000200007Journal of the Brazilian Chemical Society v.20 n.2 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009000200007info:eu-repo/semantics/openAccessSchmidt Jr.,ErlandoMelchert,Wanessa R.Rocha,Fábio R. P.eng2009-02-27T00:00:00Zoai:scielo:S0103-50532009000200007Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2009-02-27T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Flow-injection iodimetric determination of captopril in pharmaceutical preparations
title Flow-injection iodimetric determination of captopril in pharmaceutical preparations
spellingShingle Flow-injection iodimetric determination of captopril in pharmaceutical preparations
Schmidt Jr.,Erlando
flow injection
spectrophotometry
iodimetry
captopril
anti-hypertensive
title_short Flow-injection iodimetric determination of captopril in pharmaceutical preparations
title_full Flow-injection iodimetric determination of captopril in pharmaceutical preparations
title_fullStr Flow-injection iodimetric determination of captopril in pharmaceutical preparations
title_full_unstemmed Flow-injection iodimetric determination of captopril in pharmaceutical preparations
title_sort Flow-injection iodimetric determination of captopril in pharmaceutical preparations
author Schmidt Jr.,Erlando
author_facet Schmidt Jr.,Erlando
Melchert,Wanessa R.
Rocha,Fábio R. P.
author_role author
author2 Melchert,Wanessa R.
Rocha,Fábio R. P.
author2_role author
author
dc.contributor.author.fl_str_mv Schmidt Jr.,Erlando
Melchert,Wanessa R.
Rocha,Fábio R. P.
dc.subject.por.fl_str_mv flow injection
spectrophotometry
iodimetry
captopril
anti-hypertensive
topic flow injection
spectrophotometry
iodimetry
captopril
anti-hypertensive
description A simple, fast and low cost procedure for spectrophotometric determination of captopril in pharmaceutical preparations is described. The procedure is based on a flow-injection system exploiting the on-line formation of the triiodide reagent, which is consumed in the presence of the analyte generating a transient signal. Linear response was observed up to 200 µmol L-1 with a detection limit of 1.0 µmol L-1 (99.7% confidence level). The coefficient of variation (n = 20) and the sampling rate were estimated as 1.2% and 72 determinations per hour, respectively. The main excipients found in pharmaceutical preparations did not affect the captopril determination. The zone sampling approach was exploited to implement on-line dilutions, aiming direct analysis of sample extracts. Results of the analysis of commercial samples agreed with the obtained by the titrimetric reference procedure described in the US-Pharmacopeia at the 95% confidence level. The reagent consumption was estimated as 18 µg of KMnO4 and 10 mg of KI per determination, with a cost of US$ 2.50 per 1000 determinations.
publishDate 2009
dc.date.none.fl_str_mv 2009-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000200007
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000200007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532009000200007
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.20 n.2 2009
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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