Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy
Autor(a) principal: | |
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Data de Publicação: | 2006 |
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=S0103-50532006000400007 |
Resumo: | This paper describes a very simple and rapid quantitative reflectance spot test procedure for the determination of methyldopa in pharmaceutical formulations. This method is based on the complexation reaction of methyldopa with molybdate ions yielding a yellow stable complex on filter paper. Reflectance measurements were carried out at 410 nm. Under optimal conditions, the calibration graphs obtained for methyldopa by plotting the optical density of the reflectance signal (A R) vs. the log of the concentration were linear from 6.30 x 10-3 to 1.89 x 10-2 mol L-1, with a correlation coefficient of 0.998. The detection limit was 2.74 x 10-3 mol L-1 (R.S.D. = 1.02%) for methyldopa. The common excipients used as additives in pharmaceuticals do not interfere in the proposed method. The method was applied to determine metyldopa in commercial pharmaceutical formulations. The results obtained by the proposed method compare favorably with those obtained by an official procedure at 95% confidence level. |
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Journal of the Brazilian Chemical Society (Online) |
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Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopymethyldopadiffuse reflectancepharmaceuticals formulationsThis paper describes a very simple and rapid quantitative reflectance spot test procedure for the determination of methyldopa in pharmaceutical formulations. This method is based on the complexation reaction of methyldopa with molybdate ions yielding a yellow stable complex on filter paper. Reflectance measurements were carried out at 410 nm. Under optimal conditions, the calibration graphs obtained for methyldopa by plotting the optical density of the reflectance signal (A R) vs. the log of the concentration were linear from 6.30 x 10-3 to 1.89 x 10-2 mol L-1, with a correlation coefficient of 0.998. The detection limit was 2.74 x 10-3 mol L-1 (R.S.D. = 1.02%) for methyldopa. The common excipients used as additives in pharmaceuticals do not interfere in the proposed method. The method was applied to determine metyldopa in commercial pharmaceutical formulations. The results obtained by the proposed method compare favorably with those obtained by an official procedure at 95% confidence level.Sociedade Brasileira de Química2006-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000400007Journal of the Brazilian Chemical Society v.17 n.4 2006reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532006000400007info:eu-repo/semantics/openAccessRibeiro,Paulo Roberto S.Pezza,LeonardoPezza,Helena R.eng2006-08-25T00:00:00Zoai:scielo:S0103-50532006000400007Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2006-08-25T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy |
title |
Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy |
spellingShingle |
Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy Ribeiro,Paulo Roberto S. methyldopa diffuse reflectance pharmaceuticals formulations |
title_short |
Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy |
title_full |
Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy |
title_fullStr |
Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy |
title_full_unstemmed |
Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy |
title_sort |
Determination of methyldopa in pharmaceutical formulations by combined spot test-diffuse reflectance spectroscopy |
author |
Ribeiro,Paulo Roberto S. |
author_facet |
Ribeiro,Paulo Roberto S. Pezza,Leonardo Pezza,Helena R. |
author_role |
author |
author2 |
Pezza,Leonardo Pezza,Helena R. |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Ribeiro,Paulo Roberto S. Pezza,Leonardo Pezza,Helena R. |
dc.subject.por.fl_str_mv |
methyldopa diffuse reflectance pharmaceuticals formulations |
topic |
methyldopa diffuse reflectance pharmaceuticals formulations |
description |
This paper describes a very simple and rapid quantitative reflectance spot test procedure for the determination of methyldopa in pharmaceutical formulations. This method is based on the complexation reaction of methyldopa with molybdate ions yielding a yellow stable complex on filter paper. Reflectance measurements were carried out at 410 nm. Under optimal conditions, the calibration graphs obtained for methyldopa by plotting the optical density of the reflectance signal (A R) vs. the log of the concentration were linear from 6.30 x 10-3 to 1.89 x 10-2 mol L-1, with a correlation coefficient of 0.998. The detection limit was 2.74 x 10-3 mol L-1 (R.S.D. = 1.02%) for methyldopa. The common excipients used as additives in pharmaceuticals do not interfere in the proposed method. The method was applied to determine metyldopa in commercial pharmaceutical formulations. The results obtained by the proposed method compare favorably with those obtained by an official procedure at 95% confidence level. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006-08-01 |
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=S0103-50532006000400007 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000400007 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532006000400007 |
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.17 n.4 2006 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_ |
1750318167302864896 |