An innovative, simple, fast, and less toxic high-performance liquid chromatographic method for determination of prednisone in capsules
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , |
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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Brazilian Journal of Pharmaceutical Sciences |
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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 |
_version_ |
1800222913265139712 |