An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules

Detalhes bibliográficos
Autor(a) principal: Silva, Pedro Henrique Reis da
Data de Publicação: 2017
Outros Autores: Enéas, Paula Cristina Rezende, Fernandes, Christian, Pianetti, Gerson Antônio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/134169
Resumo: Prednisone is an anti-inflammatory steroid drug widely used in clinical practice. However, no high-performance liquid chromatographic (HPLC) method has been described in the literature for the determination of prednisone in capsules until now. Thus, an HPLC method was developed using a C18 (250x4.0, 5 µm) column, with methanol:water (70:30) as mobile phase at a flow rate of 1 mL/min and detection at 240 nm. The developed method was validated following current Brazilian legislation. Additionally, linearity was assessed by evaluating the assumptions of normality, homoscedasticity, and independency of residuals, and the fit to the linear model. The method showed linearity (r2>;0.99) over the range of 14.0-26.0 µg/mL, selectivity, precision (RSD
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spelling An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsulesPrednisoneCapsulesHigh performance liquid chromatography/validationLinearity assessment. Prednisone is an anti-inflammatory steroid drug widely used in clinical practice. However, no high-performance liquid chromatographic (HPLC) method has been described in the literature for the determination of prednisone in capsules until now. Thus, an HPLC method was developed using a C18 (250x4.0, 5 µm) column, with methanol:water (70:30) as mobile phase at a flow rate of 1 mL/min and detection at 240 nm. The developed method was validated following current Brazilian legislation. Additionally, linearity was assessed by evaluating the assumptions of normality, homoscedasticity, and independency of residuals, and the fit to the linear model. The method showed linearity (r2>;0.99) over the range of 14.0-26.0 µg/mL, selectivity, precision (RSDUniversidade de São Paulo. Faculdade de Ciências Farmacêuticas2017-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/13416910.1590/s2175-97902017000216064Brazilian Journal of Pharmaceutical Sciences; Vol. 53 Núm. 2 (2017); e16064-Brazilian Journal of Pharmaceutical Sciences; v. 53 n. 2 (2017); e16064-Brazilian Journal of Pharmaceutical Sciences; Vol. 53 No. 2 (2017); e16064-2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/134169/129987Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)info:eu-repo/semantics/openAccessSilva, Pedro Henrique Reis daEnéas, Paula Cristina RezendeFernandes, ChristianPianetti, Gerson Antônio2017-06-29T17:40:27Zoai:revistas.usp.br:article/134169Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2017-06-29T17:40:27Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
title An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
spellingShingle An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
Silva, Pedro Henrique Reis da
Prednisone
Capsules
High performance liquid chromatography/validation
Linearity assessment.
title_short An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
title_full An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
title_fullStr An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
title_full_unstemmed An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
title_sort An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
author Silva, Pedro Henrique Reis da
author_facet Silva, Pedro Henrique Reis da
Enéas, Paula Cristina Rezende
Fernandes, Christian
Pianetti, Gerson Antônio
author_role author
author2 Enéas, Paula Cristina Rezende
Fernandes, Christian
Pianetti, Gerson Antônio
author2_role author
author
author
dc.contributor.author.fl_str_mv Silva, Pedro Henrique Reis da
Enéas, Paula Cristina Rezende
Fernandes, Christian
Pianetti, Gerson Antônio
dc.subject.por.fl_str_mv Prednisone
Capsules
High performance liquid chromatography/validation
Linearity assessment.
topic Prednisone
Capsules
High performance liquid chromatography/validation
Linearity assessment.
description Prednisone is an anti-inflammatory steroid drug widely used in clinical practice. However, no high-performance liquid chromatographic (HPLC) method has been described in the literature for the determination of prednisone in capsules until now. Thus, an HPLC method was developed using a C18 (250x4.0, 5 µm) column, with methanol:water (70:30) as mobile phase at a flow rate of 1 mL/min and detection at 240 nm. The developed method was validated following current Brazilian legislation. Additionally, linearity was assessed by evaluating the assumptions of normality, homoscedasticity, and independency of residuals, and the fit to the linear model. The method showed linearity (r2>;0.99) over the range of 14.0-26.0 µg/mL, selectivity, precision (RSD
publishDate 2017
dc.date.none.fl_str_mv 2017-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/bjps/article/view/134169
10.1590/s2175-97902017000216064
url https://www.revistas.usp.br/bjps/article/view/134169
identifier_str_mv 10.1590/s2175-97902017000216064
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/134169/129987
dc.rights.driver.fl_str_mv Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 53 Núm. 2 (2017); e16064-
Brazilian Journal of Pharmaceutical Sciences; v. 53 n. 2 (2017); e16064-
Brazilian Journal of Pharmaceutical Sciences; Vol. 53 No. 2 (2017); e16064-
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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