Optimization of a new dissolution test for oxcarbazepine capsules using mixed-level factorial design
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=S0103-50532011000700011 |
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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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 |
_version_ |
1750318172327641088 |