Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design

Detalhes bibliográficos
Autor(a) principal: Polonini,Hudson C
Data de Publicação: 2011
Outros Autores: Oliveira,Marcone A. L. de, Ferreira,Anderson O, Raposo,Nádia R. B, Grossi,Lívia N, Brandão,Marcos A. F
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=S0103-50532011000700011
Resumo: In this work, a dissolution test for oxcarbazepine capsules was developed and validated. For the screening study, a mixed-level factorial design containing factors at three and two levels (3² × 2) was used in order to select the stirring speed, the dissolution medium and the dissolution apparatus. This strategy is needful for reducing the time of method development and to provide less ambiguous data. The best in vitro percentage dissolution was obtained using apparatus paddle at 80 rpm and sodium lauryl sulfate 1% m/v aqueous solution as the dissolution medium. The quantification of the mass dissolved was obtained by UV-Vis spectrophotometric analysis at 304 nm. The validation results demonstrate that the method was precise and linear over the range of 83-249 µg mL-1 of oxcarbazepine. Thus, the method is useful and adequate for oxcarbazepine capsules dissolution test, once there is no official monograph regarding it.
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spelling Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial designoxcarbazepinedissolution testmixed-level factorial designIn this work, a dissolution test for oxcarbazepine capsules was developed and validated. For the screening study, a mixed-level factorial design containing factors at three and two levels (3² × 2) was used in order to select the stirring speed, the dissolution medium and the dissolution apparatus. This strategy is needful for reducing the time of method development and to provide less ambiguous data. The best in vitro percentage dissolution was obtained using apparatus paddle at 80 rpm and sodium lauryl sulfate 1% m/v aqueous solution as the dissolution medium. The quantification of the mass dissolved was obtained by UV-Vis spectrophotometric analysis at 304 nm. The validation results demonstrate that the method was precise and linear over the range of 83-249 µg mL-1 of oxcarbazepine. Thus, the method is useful and adequate for oxcarbazepine capsules dissolution test, once there is no official monograph regarding it.Sociedade Brasileira de Química2011-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700011Journal of the Brazilian Chemical Society v.22 n.7 2011reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532011000700011info:eu-repo/semantics/openAccessPolonini,Hudson COliveira,Marcone A. L. deFerreira,Anderson ORaposo,Nádia R. BGrossi,Lívia NBrandão,Marcos A. Feng2011-07-22T00:00:00Zoai:scielo:S0103-50532011000700011Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-07-22T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
title Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
spellingShingle Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
Polonini,Hudson C
oxcarbazepine
dissolution test
mixed-level factorial design
title_short Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
title_full Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
title_fullStr Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
title_full_unstemmed Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
title_sort Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
author Polonini,Hudson C
author_facet Polonini,Hudson C
Oliveira,Marcone A. L. de
Ferreira,Anderson O
Raposo,Nádia R. B
Grossi,Lívia N
Brandão,Marcos A. F
author_role author
author2 Oliveira,Marcone A. L. de
Ferreira,Anderson O
Raposo,Nádia R. B
Grossi,Lívia N
Brandão,Marcos A. F
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Polonini,Hudson C
Oliveira,Marcone A. L. de
Ferreira,Anderson O
Raposo,Nádia R. B
Grossi,Lívia N
Brandão,Marcos A. F
dc.subject.por.fl_str_mv oxcarbazepine
dissolution test
mixed-level factorial design
topic oxcarbazepine
dissolution test
mixed-level factorial design
description In this work, a dissolution test for oxcarbazepine capsules was developed and validated. For the screening study, a mixed-level factorial design containing factors at three and two levels (3² × 2) was used in order to select the stirring speed, the dissolution medium and the dissolution apparatus. This strategy is needful for reducing the time of method development and to provide less ambiguous data. The best in vitro percentage dissolution was obtained using apparatus paddle at 80 rpm and sodium lauryl sulfate 1% m/v aqueous solution as the dissolution medium. The quantification of the mass dissolved was obtained by UV-Vis spectrophotometric analysis at 304 nm. The validation results demonstrate that the method was precise and linear over the range of 83-249 µg mL-1 of oxcarbazepine. Thus, the method is useful and adequate for oxcarbazepine capsules dissolution test, once there is no official monograph regarding it.
publishDate 2011
dc.date.none.fl_str_mv 2011-07-01
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=S0103-50532011000700011
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532011000700011
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.7 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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