Simultaneous determination of anti-diabetic drugs

Detalhes bibliográficos
Autor(a) principal: Sher, Nawab
Data de Publicação: 2019
Outros Autores: Fatima, Nasreen, Perveen, Shahnaz, Siddiqui, Farhan Ahmed
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/180916
Resumo: A novel reverse phase, isocratic HPLC method is described to separate five anti-diabetic drugs i.e., glimepiride, metformin, sitagliptin, rosiglitazone and pioglitazone. Nucleosil C18 analytical column was used as stationary phase, while mobile phase consisted of acetonitrile:phosphate buffer: methanol (40/40/20, v/v) pH 2.0. Effluent was monitored at a flow rate 1 mL/min and detected at wavelength of 240 nm. This research produced excellent chromatography over a wide concentration range of 25‑10000 ng/mL. Sepprated and well resolved quantifiable peaks were obtained and test results were linear in this range. Correlation coefficient of more than 0.9990 was witnessed as well as Low %RSD values i.e., maximum 2.0% documented excellent precision of the method. Good recoveries from pharmaecutical (99-101%), urine and plasma samples (>96%) in a range of concentrtion granted very good linearity, accuracy and precision. The projected method has satisfactory applications in quality control of these molecules as well as quantification of these molecules in urine and plasma samples.
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spelling Simultaneous determination of anti-diabetic drugsMetformin/pharmacokineticsHigh Pressure Liquid ChromatographyUrine/Plasma methodsDetermination/preventionDiabetes Mellitus/drug therapyDrug Liberation/drug effectsA novel reverse phase, isocratic HPLC method is described to separate five anti-diabetic drugs i.e., glimepiride, metformin, sitagliptin, rosiglitazone and pioglitazone. Nucleosil C18 analytical column was used as stationary phase, while mobile phase consisted of acetonitrile:phosphate buffer: methanol (40/40/20, v/v) pH 2.0. Effluent was monitored at a flow rate 1 mL/min and detected at wavelength of 240 nm. This research produced excellent chromatography over a wide concentration range of 25‑10000 ng/mL. Sepprated and well resolved quantifiable peaks were obtained and test results were linear in this range. Correlation coefficient of more than 0.9990 was witnessed as well as Low %RSD values i.e., maximum 2.0% documented excellent precision of the method. Good recoveries from pharmaecutical (99-101%), urine and plasma samples (>96%) in a range of concentrtion granted very good linearity, accuracy and precision. The projected method has satisfactory applications in quality control of these molecules as well as quantification of these molecules in urine and plasma samples.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2019-12-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/18091610.1590/s2175-97902019000217394 Brazilian Journal of Pharmaceutical Sciences; Vol. 55 (2019); e17394Brazilian Journal of Pharmaceutical Sciences; v. 55 (2019); e17394Brazilian Journal of Pharmaceutical Sciences; Vol. 55 (2019); e173942175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/180916/167965Copyright (c) 2019 Brazilian Journal of Pharmaceutical Scienceshttp://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSher, Nawab Fatima, Nasreen Perveen, Shahnaz Siddiqui, Farhan Ahmed 2021-01-19T16:47:29Zoai:revistas.usp.br:article/180916Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2021-01-19T16:47:29Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Simultaneous determination of anti-diabetic drugs
title Simultaneous determination of anti-diabetic drugs
spellingShingle Simultaneous determination of anti-diabetic drugs
Sher, Nawab
Metformin/pharmacokinetics
High Pressure Liquid Chromatography
Urine/Plasma methods
Determination/prevention
Diabetes Mellitus/drug therapy
Drug Liberation/drug effects
title_short Simultaneous determination of anti-diabetic drugs
title_full Simultaneous determination of anti-diabetic drugs
title_fullStr Simultaneous determination of anti-diabetic drugs
title_full_unstemmed Simultaneous determination of anti-diabetic drugs
title_sort Simultaneous determination of anti-diabetic drugs
author Sher, Nawab
author_facet Sher, Nawab
Fatima, Nasreen
Perveen, Shahnaz
Siddiqui, Farhan Ahmed
author_role author
author2 Fatima, Nasreen
Perveen, Shahnaz
Siddiqui, Farhan Ahmed
author2_role author
author
author
dc.contributor.author.fl_str_mv Sher, Nawab
Fatima, Nasreen
Perveen, Shahnaz
Siddiqui, Farhan Ahmed
dc.subject.por.fl_str_mv Metformin/pharmacokinetics
High Pressure Liquid Chromatography
Urine/Plasma methods
Determination/prevention
Diabetes Mellitus/drug therapy
Drug Liberation/drug effects
topic Metformin/pharmacokinetics
High Pressure Liquid Chromatography
Urine/Plasma methods
Determination/prevention
Diabetes Mellitus/drug therapy
Drug Liberation/drug effects
description A novel reverse phase, isocratic HPLC method is described to separate five anti-diabetic drugs i.e., glimepiride, metformin, sitagliptin, rosiglitazone and pioglitazone. Nucleosil C18 analytical column was used as stationary phase, while mobile phase consisted of acetonitrile:phosphate buffer: methanol (40/40/20, v/v) pH 2.0. Effluent was monitored at a flow rate 1 mL/min and detected at wavelength of 240 nm. This research produced excellent chromatography over a wide concentration range of 25‑10000 ng/mL. Sepprated and well resolved quantifiable peaks were obtained and test results were linear in this range. Correlation coefficient of more than 0.9990 was witnessed as well as Low %RSD values i.e., maximum 2.0% documented excellent precision of the method. Good recoveries from pharmaecutical (99-101%), urine and plasma samples (>96%) in a range of concentrtion granted very good linearity, accuracy and precision. The projected method has satisfactory applications in quality control of these molecules as well as quantification of these molecules in urine and plasma samples.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-09
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/180916
10.1590/s2175-97902019000217394
url https://www.revistas.usp.br/bjps/article/view/180916
identifier_str_mv 10.1590/s2175-97902019000217394
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/180916/167965
dc.rights.driver.fl_str_mv Copyright (c) 2019 Brazilian Journal of Pharmaceutical Sciences
http://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2019 Brazilian Journal of Pharmaceutical Sciences
http://creativecommons.org/licenses/by/4.0
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. 55 (2019); e17394
Brazilian Journal of Pharmaceutical Sciences; v. 55 (2019); e17394
Brazilian Journal of Pharmaceutical Sciences; Vol. 55 (2019); e17394
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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