Ethambutol analysis by copper complexation in pharmaceutical formulations: spectrophotometry and crystal structure

Detalhes bibliográficos
Autor(a) principal: Faria,Adriana F
Data de Publicação: 2011
Outros Autores: 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
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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spelling 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
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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
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