UV spectrophotometric method for quantitative determination of agomelatine in coated tablets
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/177563 |
Resumo: | UV spectrophotometry is an analytical technique used routinely for qualitative and quantitative assay due the low cost and reliability during analysis. In this work, it was validated a quantitative UV method for determination of agomelatine in coated tablets. The parameters specificity, linearity, precision, accuracy and robustness were evaluated according to official guidelines. Methanol was selected as solvent and the maximum wavelength for drug analysis was 230 nm. The purposed assay showed to be specific and the linearity was proved in a range of 0.5 - 2.5 μg/mL. The RSD values obtained during precision assay (inter-day RSD = 1.75%) indicated the method reproducibility, and the accuracy testing showed good results from recovery test. Robustness assay was complementary and showed that the purposed method is adequate for drug quantitation in commercial samples, being a reliable alternative to chromatographic assay. |
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Barbosa, Fábio de SouzaRodrigues, Vanise CotyVolpato, Nadia MariaSchapoval, Elfrides Eva SchermanSteppe, MartinGarcia, Cassia VirginiaMendez, Andreas Sebastian Loureiro2018-05-05T03:16:11Z20172527-2616http://hdl.handle.net/10183/177563001058385UV spectrophotometry is an analytical technique used routinely for qualitative and quantitative assay due the low cost and reliability during analysis. In this work, it was validated a quantitative UV method for determination of agomelatine in coated tablets. The parameters specificity, linearity, precision, accuracy and robustness were evaluated according to official guidelines. Methanol was selected as solvent and the maximum wavelength for drug analysis was 230 nm. The purposed assay showed to be specific and the linearity was proved in a range of 0.5 - 2.5 μg/mL. The RSD values obtained during precision assay (inter-day RSD = 1.75%) indicated the method reproducibility, and the accuracy testing showed good results from recovery test. Robustness assay was complementary and showed that the purposed method is adequate for drug quantitation in commercial samples, being a reliable alternative to chromatographic assay.application/pdfengDrug Analytical Research. Porto Alegre, RS. Vol. 1, no. 2 (2017), p. 24-29EspectrofotometriaAntidepressivosAgomelatineUV spectrophotometryValidationQuantitationUV spectrophotometric method for quantitative determination of agomelatine in coated tabletsinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001058385.pdf001058385.pdfTexto completo (inglês)application/pdf157647http://www.lume.ufrgs.br/bitstream/10183/177563/1/001058385.pdf5f58deaac359918df9d5a5ab24bfef98MD51TEXT001058385.pdf.txt001058385.pdf.txtExtracted Texttext/plain17919http://www.lume.ufrgs.br/bitstream/10183/177563/2/001058385.pdf.txt564b80bcfcc46ead29c94989f6191443MD5210183/1775632018-05-06 02:26:37.775268oai:www.lume.ufrgs.br:10183/177563Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-05-06T05:26:37Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
UV spectrophotometric method for quantitative determination of agomelatine in coated tablets |
title |
UV spectrophotometric method for quantitative determination of agomelatine in coated tablets |
spellingShingle |
UV spectrophotometric method for quantitative determination of agomelatine in coated tablets Barbosa, Fábio de Souza Espectrofotometria Antidepressivos Agomelatine UV spectrophotometry Validation Quantitation |
title_short |
UV spectrophotometric method for quantitative determination of agomelatine in coated tablets |
title_full |
UV spectrophotometric method for quantitative determination of agomelatine in coated tablets |
title_fullStr |
UV spectrophotometric method for quantitative determination of agomelatine in coated tablets |
title_full_unstemmed |
UV spectrophotometric method for quantitative determination of agomelatine in coated tablets |
title_sort |
UV spectrophotometric method for quantitative determination of agomelatine in coated tablets |
author |
Barbosa, Fábio de Souza |
author_facet |
Barbosa, Fábio de Souza Rodrigues, Vanise Coty Volpato, Nadia Maria Schapoval, Elfrides Eva Scherman Steppe, Martin Garcia, Cassia Virginia Mendez, Andreas Sebastian Loureiro |
author_role |
author |
author2 |
Rodrigues, Vanise Coty Volpato, Nadia Maria Schapoval, Elfrides Eva Scherman Steppe, Martin Garcia, Cassia Virginia Mendez, Andreas Sebastian Loureiro |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Barbosa, Fábio de Souza Rodrigues, Vanise Coty Volpato, Nadia Maria Schapoval, Elfrides Eva Scherman Steppe, Martin Garcia, Cassia Virginia Mendez, Andreas Sebastian Loureiro |
dc.subject.por.fl_str_mv |
Espectrofotometria Antidepressivos |
topic |
Espectrofotometria Antidepressivos Agomelatine UV spectrophotometry Validation Quantitation |
dc.subject.eng.fl_str_mv |
Agomelatine UV spectrophotometry Validation Quantitation |
description |
UV spectrophotometry is an analytical technique used routinely for qualitative and quantitative assay due the low cost and reliability during analysis. In this work, it was validated a quantitative UV method for determination of agomelatine in coated tablets. The parameters specificity, linearity, precision, accuracy and robustness were evaluated according to official guidelines. Methanol was selected as solvent and the maximum wavelength for drug analysis was 230 nm. The purposed assay showed to be specific and the linearity was proved in a range of 0.5 - 2.5 μg/mL. The RSD values obtained during precision assay (inter-day RSD = 1.75%) indicated the method reproducibility, and the accuracy testing showed good results from recovery test. Robustness assay was complementary and showed that the purposed method is adequate for drug quantitation in commercial samples, being a reliable alternative to chromatographic assay. |
publishDate |
2017 |
dc.date.issued.fl_str_mv |
2017 |
dc.date.accessioned.fl_str_mv |
2018-05-05T03:16:11Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/other |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/177563 |
dc.identifier.issn.pt_BR.fl_str_mv |
2527-2616 |
dc.identifier.nrb.pt_BR.fl_str_mv |
001058385 |
identifier_str_mv |
2527-2616 001058385 |
url |
http://hdl.handle.net/10183/177563 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Drug Analytical Research. Porto Alegre, RS. Vol. 1, no. 2 (2017), p. 24-29 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFRGS instname:Universidade Federal do Rio Grande do Sul (UFRGS) instacron:UFRGS |
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UFRGS |
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Repositório Institucional da UFRGS |
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Repositório Institucional da UFRGS |
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