Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure
Autor(a) principal: | |
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Data de Publicação: | 2011 |
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=S0103-50532011000500008 |
Resumo: | An alternative method for ethambutol (ETB) determination by UV spectrophotometry in pharmaceutical formulations using ETB complexation with Cu(II) was optimized employing a 3² full experimental design having Cu(II) and aqueous acetic acid/sodium acetate buffer at pH 4.6 as variables. The predominant complex stoichiometry in aqueous buffer solution at this pH and formation constant were obtained by using Job's method and Scatchard diagram, respectively. The complex crystalline structure of monocrystal was obtained by X-ray diffraction. The developed method was applied to the pharmaceutical formulation analysis being found: 408.0 ± 11.9 mg of ETB·2HCl, recovery range of 100.9-104.0% and detection and quantification limits of 0.8 and 2.8 mg L-1, respectively. The spectrophotometric method was compared to zone capillary electrophoresis and no significant difference was found within the 95% confidence interval |
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Journal of the Brazilian Chemical Society (Online) |
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Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structureethambutolcomplexationspectrophotometrycrystal structureAn alternative method for ethambutol (ETB) determination by UV spectrophotometry in pharmaceutical formulations using ETB complexation with Cu(II) was optimized employing a 3² full experimental design having Cu(II) and aqueous acetic acid/sodium acetate buffer at pH 4.6 as variables. The predominant complex stoichiometry in aqueous buffer solution at this pH and formation constant were obtained by using Job's method and Scatchard diagram, respectively. The complex crystalline structure of monocrystal was obtained by X-ray diffraction. The developed method was applied to the pharmaceutical formulation analysis being found: 408.0 ± 11.9 mg of ETB·2HCl, recovery range of 100.9-104.0% and detection and quantification limits of 0.8 and 2.8 mg L-1, respectively. The spectrophotometric method was compared to zone capillary electrophoresis and no significant difference was found within the 95% confidence intervalSociedade Brasileira de Química2011-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000500008Journal of the Brazilian Chemical Society v.22 n.5 2011reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532011000500008info:eu-repo/semantics/openAccessFaria,Adriana FMarcellos,Luiza FVasconcelos,Juliana PSouza,Marcus V. N. deS. Júnior,Antônio LCarmo,Weberton R. doDiniz,RenataOliveira,Marcone A. L. deeng2011-05-16T00:00:00Zoai:scielo:S0103-50532011000500008Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-05-16T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure |
title |
Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure |
spellingShingle |
Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure Faria,Adriana F ethambutol complexation spectrophotometry crystal structure |
title_short |
Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure |
title_full |
Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure |
title_fullStr |
Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure |
title_full_unstemmed |
Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure |
title_sort |
Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure |
author |
Faria,Adriana F |
author_facet |
Faria,Adriana F Marcellos,Luiza F Vasconcelos,Juliana P Souza,Marcus V. N. de S. Júnior,Antônio L Carmo,Weberton R. do Diniz,Renata Oliveira,Marcone A. L. de |
author_role |
author |
author2 |
Marcellos,Luiza F Vasconcelos,Juliana P Souza,Marcus V. N. de S. Júnior,Antônio L Carmo,Weberton R. do Diniz,Renata Oliveira,Marcone A. L. de |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Faria,Adriana F Marcellos,Luiza F Vasconcelos,Juliana P Souza,Marcus V. N. de S. Júnior,Antônio L Carmo,Weberton R. do Diniz,Renata Oliveira,Marcone A. L. de |
dc.subject.por.fl_str_mv |
ethambutol complexation spectrophotometry crystal structure |
topic |
ethambutol complexation spectrophotometry crystal structure |
description |
An alternative method for ethambutol (ETB) determination by UV spectrophotometry in pharmaceutical formulations using ETB complexation with Cu(II) was optimized employing a 3² full experimental design having Cu(II) and aqueous acetic acid/sodium acetate buffer at pH 4.6 as variables. The predominant complex stoichiometry in aqueous buffer solution at this pH and formation constant were obtained by using Job's method and Scatchard diagram, respectively. The complex crystalline structure of monocrystal was obtained by X-ray diffraction. The developed method was applied to the pharmaceutical formulation analysis being found: 408.0 ± 11.9 mg of ETB·2HCl, recovery range of 100.9-104.0% and detection and quantification limits of 0.8 and 2.8 mg L-1, respectively. The spectrophotometric method was compared to zone capillary electrophoresis and no significant difference was found within the 95% confidence interval |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-05-01 |
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=S0103-50532011000500008 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000500008 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532011000500008 |
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.22 n.5 2011 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_ |
1750318172252143616 |