A UPLC/DAD method for simultaneous determination of empagliflozin and three related substances in spiked human plasma

Abstract A simple, rapid and sensitive ultrahigh performance liquid chromatographic method was developed for the determination of the anti-diabetic drug: empagliflozin (EMPA) and three related substances in spiked human plasma, using dapagliflozin (DAPA) as an internal standard and tetrahydrofuran a...

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Main Authors: Mokhtar M. Mabrouk, Suzan M. Soliman, Heba M. El-Agizy, Fotouh R. Mansour
Format: Article
Language:English
Published: BMC 2019-07-01
Series:BMC Chemistry
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13065-019-0604-9
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spelling doaj-4871aaa39bf8483195d087e285cb1ad22020-11-25T03:12:40ZengBMCBMC Chemistry2661-801X2019-07-011311910.1186/s13065-019-0604-9A UPLC/DAD method for simultaneous determination of empagliflozin and three related substances in spiked human plasmaMokhtar M. Mabrouk0Suzan M. Soliman1Heba M. El-Agizy2Fotouh R. Mansour3Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta UniversityNational Organization for Drug Control and Research (NODCAR)National Organization for Drug Control and Research (NODCAR)Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta UniversityAbstract A simple, rapid and sensitive ultrahigh performance liquid chromatographic method was developed for the determination of the anti-diabetic drug: empagliflozin (EMPA) and three related substances in spiked human plasma, using dapagliflozin (DAPA) as an internal standard and tetrahydrofuran as a plasma protein precipitating agent. The chromatographic separation was achieved on an Acquity “UPLC® BEH” C18 column (50 mm × 2.1 mm i.d, 1.7 µm particle size), and a mobile phase consisting of aqueous trifluoroacetic acid (0.1%, pH 2.5): acetonitrile (60:40, v/v) at a flow rate of 0.5 mL/min. Upon using the UPLC system, the run time could be reduced to less than 1.2 min, and the solvents consumption decreased to 0.36 mL of acetonitrile per run. The response was linear over a concentration range of 50–700 ng/mL and 40–200 ng/mL (r2 = 0.9994–0.9999) with lower limits of detection and quantification (LOD/LOQ) of 15/50, 11.5/40, 12/40 and 12.5/40 ng/mL for EMPA and the three related substances, respectively. Good accuracy was obtained with mean percentage recoveries ≥ 96.97% for the studied compounds. The method was validated according to the ICH guidelines and was found suitable for routine analysis of EMPA and its related substances in human plasma.http://link.springer.com/article/10.1186/s13065-019-0604-9EmpagliflozinRelated substancesUPLCSpiked human plasmaTHF protein precipitation
collection DOAJ
language English
format Article
sources DOAJ
author Mokhtar M. Mabrouk
Suzan M. Soliman
Heba M. El-Agizy
Fotouh R. Mansour
spellingShingle Mokhtar M. Mabrouk
Suzan M. Soliman
Heba M. El-Agizy
Fotouh R. Mansour
A UPLC/DAD method for simultaneous determination of empagliflozin and three related substances in spiked human plasma
BMC Chemistry
Empagliflozin
Related substances
UPLC
Spiked human plasma
THF protein precipitation
author_facet Mokhtar M. Mabrouk
Suzan M. Soliman
Heba M. El-Agizy
Fotouh R. Mansour
author_sort Mokhtar M. Mabrouk
title A UPLC/DAD method for simultaneous determination of empagliflozin and three related substances in spiked human plasma
title_short A UPLC/DAD method for simultaneous determination of empagliflozin and three related substances in spiked human plasma
title_full A UPLC/DAD method for simultaneous determination of empagliflozin and three related substances in spiked human plasma
title_fullStr A UPLC/DAD method for simultaneous determination of empagliflozin and three related substances in spiked human plasma
title_full_unstemmed A UPLC/DAD method for simultaneous determination of empagliflozin and three related substances in spiked human plasma
title_sort uplc/dad method for simultaneous determination of empagliflozin and three related substances in spiked human plasma
publisher BMC
series BMC Chemistry
issn 2661-801X
publishDate 2019-07-01
description Abstract A simple, rapid and sensitive ultrahigh performance liquid chromatographic method was developed for the determination of the anti-diabetic drug: empagliflozin (EMPA) and three related substances in spiked human plasma, using dapagliflozin (DAPA) as an internal standard and tetrahydrofuran as a plasma protein precipitating agent. The chromatographic separation was achieved on an Acquity “UPLC® BEH” C18 column (50 mm × 2.1 mm i.d, 1.7 µm particle size), and a mobile phase consisting of aqueous trifluoroacetic acid (0.1%, pH 2.5): acetonitrile (60:40, v/v) at a flow rate of 0.5 mL/min. Upon using the UPLC system, the run time could be reduced to less than 1.2 min, and the solvents consumption decreased to 0.36 mL of acetonitrile per run. The response was linear over a concentration range of 50–700 ng/mL and 40–200 ng/mL (r2 = 0.9994–0.9999) with lower limits of detection and quantification (LOD/LOQ) of 15/50, 11.5/40, 12/40 and 12.5/40 ng/mL for EMPA and the three related substances, respectively. Good accuracy was obtained with mean percentage recoveries ≥ 96.97% for the studied compounds. The method was validated according to the ICH guidelines and was found suitable for routine analysis of EMPA and its related substances in human plasma.
topic Empagliflozin
Related substances
UPLC
Spiked human plasma
THF protein precipitation
url http://link.springer.com/article/10.1186/s13065-019-0604-9
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