Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum

Detalhes bibliográficos
Autor(a) principal: Ghoneim,Mohamed M.
Data de Publicação: 2012
Outros Autores: Hassanein,Amera. M., Salahuddin,Nehal A., El-Desoky,Hanaa S., Elfiky,Mona N.
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=S0103-50532012000900003
Resumo: Raloxifene HCl (RLX) was found to strongly adsorb onto surface of the mercury electrode in a monolayer surface coverage of 5.724 × 10-10 mol cm-2. Two precise, rapid and extraction-free linear sweep and square wave adsorptive cathodic stripping voltammetry (LS-AdCSV and SW-AdCSV, respectively) methods are described for trace quantitation of RLX in bulk form, commercial formulation and human serum. Limits of quantification (LOQ) of 2.0 × 10-9 and 5.0 × 10-11 mol L-1 RLX in bulk form and 4.0 × 10-9 and 1.0 × 10-10 mol L-1 RLX in spiked human serum were achieved by the described LS-AdCSV and SW-AdCSV methods, respectively. Insignificant interferences from some common excipients, metal ions and co-administrated drugs were obtained. LOQ achieved by the methods are low as well as they offer good possibilities for determination of drug in low-dosage pharmaceutical preparations. However, the SW-AdCSV method described is sensitive enough to assay the drug also in human serum.
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spelling Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serumraloxifene HCldeterminationstripping voltammetryRaloxifene HCl (RLX) was found to strongly adsorb onto surface of the mercury electrode in a monolayer surface coverage of 5.724 × 10-10 mol cm-2. Two precise, rapid and extraction-free linear sweep and square wave adsorptive cathodic stripping voltammetry (LS-AdCSV and SW-AdCSV, respectively) methods are described for trace quantitation of RLX in bulk form, commercial formulation and human serum. Limits of quantification (LOQ) of 2.0 × 10-9 and 5.0 × 10-11 mol L-1 RLX in bulk form and 4.0 × 10-9 and 1.0 × 10-10 mol L-1 RLX in spiked human serum were achieved by the described LS-AdCSV and SW-AdCSV methods, respectively. Insignificant interferences from some common excipients, metal ions and co-administrated drugs were obtained. LOQ achieved by the methods are low as well as they offer good possibilities for determination of drug in low-dosage pharmaceutical preparations. However, the SW-AdCSV method described is sensitive enough to assay the drug also in human serum.Sociedade Brasileira de Química2012-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000900003Journal of the Brazilian Chemical Society v.23 n.9 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012005000016info:eu-repo/semantics/openAccessGhoneim,Mohamed M.Hassanein,Amera. M.Salahuddin,Nehal A.El-Desoky,Hanaa S.Elfiky,Mona N.eng2012-10-15T00:00:00Zoai:scielo:S0103-50532012000900003Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-10-15T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum
title Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum
spellingShingle Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum
Ghoneim,Mohamed M.
raloxifene HCl
determination
stripping voltammetry
title_short Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum
title_full Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum
title_fullStr Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum
title_full_unstemmed Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum
title_sort Adsorptive stripping voltammetry determination of the hormone therapy Raloxifene HCl in formulation and human serum
author Ghoneim,Mohamed M.
author_facet Ghoneim,Mohamed M.
Hassanein,Amera. M.
Salahuddin,Nehal A.
El-Desoky,Hanaa S.
Elfiky,Mona N.
author_role author
author2 Hassanein,Amera. M.
Salahuddin,Nehal A.
El-Desoky,Hanaa S.
Elfiky,Mona N.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Ghoneim,Mohamed M.
Hassanein,Amera. M.
Salahuddin,Nehal A.
El-Desoky,Hanaa S.
Elfiky,Mona N.
dc.subject.por.fl_str_mv raloxifene HCl
determination
stripping voltammetry
topic raloxifene HCl
determination
stripping voltammetry
description Raloxifene HCl (RLX) was found to strongly adsorb onto surface of the mercury electrode in a monolayer surface coverage of 5.724 × 10-10 mol cm-2. Two precise, rapid and extraction-free linear sweep and square wave adsorptive cathodic stripping voltammetry (LS-AdCSV and SW-AdCSV, respectively) methods are described for trace quantitation of RLX in bulk form, commercial formulation and human serum. Limits of quantification (LOQ) of 2.0 × 10-9 and 5.0 × 10-11 mol L-1 RLX in bulk form and 4.0 × 10-9 and 1.0 × 10-10 mol L-1 RLX in spiked human serum were achieved by the described LS-AdCSV and SW-AdCSV methods, respectively. Insignificant interferences from some common excipients, metal ions and co-administrated drugs were obtained. LOQ achieved by the methods are low as well as they offer good possibilities for determination of drug in low-dosage pharmaceutical preparations. However, the SW-AdCSV method described is sensitive enough to assay the drug also in human serum.
publishDate 2012
dc.date.none.fl_str_mv 2012-09-01
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=S0103-50532012000900003
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000900003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532012005000016
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.9 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
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