Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection
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=S0103-50532012001000010 |
Resumo: | A novel and fast electroanalytical method for naproxen determination in pharmaceutical formulations using batch injection analysis (BIA) with pulsed amperometric detection is described. Bare glassy carbon electrode was used as working electrode and 0.05 mol L-1 phosphate buffer solution as supporting electrolyte. The amperometric method involved the continuous application of two sequential potential pulses to the working electrode in order to detect naproxen by its electrochemical oxidation (+1.5 V for 200 ms) and to clean the electrode surface from adsorption products (+1.0 V for 100 ms), avoiding electrode contamination. The proposed method has several advantages for routine analysis, including: a low relative standard deviation between injections (3.0%, n = 10), high analytical frequency (90 h-1), satisfactory accuracy (based on comparative determinations by spectrofluorimetry) and low limit of detection (0.3 µmol L-1). |
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Journal of the Brazilian Chemical Society (Online) |
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Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detectionbatch injection analysismultiple-pulse amperometrynon-steroidal anti-inflammatory drugA novel and fast electroanalytical method for naproxen determination in pharmaceutical formulations using batch injection analysis (BIA) with pulsed amperometric detection is described. Bare glassy carbon electrode was used as working electrode and 0.05 mol L-1 phosphate buffer solution as supporting electrolyte. The amperometric method involved the continuous application of two sequential potential pulses to the working electrode in order to detect naproxen by its electrochemical oxidation (+1.5 V for 200 ms) and to clean the electrode surface from adsorption products (+1.0 V for 100 ms), avoiding electrode contamination. The proposed method has several advantages for routine analysis, including: a low relative standard deviation between injections (3.0%, n = 10), high analytical frequency (90 h-1), satisfactory accuracy (based on comparative determinations by spectrofluorimetry) and low limit of detection (0.3 µmol L-1).Sociedade Brasileira de Química2012-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012001000010Journal of the Brazilian Chemical Society v.23 n.10 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012005000055info:eu-repo/semantics/openAccessStefano,Jessica S.Lima,Ana Paula deMontes,Rodrigo H. O.Richter,Eduardo M.Muñoz,Rodrigo A. A.eng2012-12-05T00:00:00Zoai:scielo:S0103-50532012001000010Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-12-05T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection |
title |
Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection |
spellingShingle |
Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection Stefano,Jessica S. batch injection analysis multiple-pulse amperometry non-steroidal anti-inflammatory drug |
title_short |
Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection |
title_full |
Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection |
title_fullStr |
Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection |
title_full_unstemmed |
Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection |
title_sort |
Fast determination of naproxen in pharmaceutical formulations by batch injection analysis with pulsed amperometric detection |
author |
Stefano,Jessica S. |
author_facet |
Stefano,Jessica S. Lima,Ana Paula de Montes,Rodrigo H. O. Richter,Eduardo M. Muñoz,Rodrigo A. A. |
author_role |
author |
author2 |
Lima,Ana Paula de Montes,Rodrigo H. O. Richter,Eduardo M. Muñoz,Rodrigo A. A. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Stefano,Jessica S. Lima,Ana Paula de Montes,Rodrigo H. O. Richter,Eduardo M. Muñoz,Rodrigo A. A. |
dc.subject.por.fl_str_mv |
batch injection analysis multiple-pulse amperometry non-steroidal anti-inflammatory drug |
topic |
batch injection analysis multiple-pulse amperometry non-steroidal anti-inflammatory drug |
description |
A novel and fast electroanalytical method for naproxen determination in pharmaceutical formulations using batch injection analysis (BIA) with pulsed amperometric detection is described. Bare glassy carbon electrode was used as working electrode and 0.05 mol L-1 phosphate buffer solution as supporting electrolyte. The amperometric method involved the continuous application of two sequential potential pulses to the working electrode in order to detect naproxen by its electrochemical oxidation (+1.5 V for 200 ms) and to clean the electrode surface from adsorption products (+1.0 V for 100 ms), avoiding electrode contamination. The proposed method has several advantages for routine analysis, including: a low relative standard deviation between injections (3.0%, n = 10), high analytical frequency (90 h-1), satisfactory accuracy (based on comparative determinations by spectrofluorimetry) and low limit of detection (0.3 µmol L-1). |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-10-01 |
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=S0103-50532012001000010 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012001000010 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532012005000055 |
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.10 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_ |
1750318174378655744 |