Simultaneous determination of anti-diabetic drugs
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Pharmaceutical Sciences |
DOI: | 10.1590/s2175-97902019000217394 |
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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Brazilian Journal of Pharmaceutical Sciences |
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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 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 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 Simultaneous determination of anti-diabetic drugs |
title_full_unstemmed |
Simultaneous determination of anti-diabetic drugs Simultaneous determination of anti-diabetic drugs |
title_sort |
Simultaneous determination of anti-diabetic drugs |
author |
Sher, Nawab |
author_facet |
Sher, Nawab Sher, Nawab Fatima, Nasreen Perveen, Shahnaz Siddiqui, Farhan Ahmed 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 |
_version_ |
1822181823068766208 |
dc.identifier.doi.none.fl_str_mv |
10.1590/s2175-97902019000217394 |