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Determination of metformin hydrochloride in human plasma by UPLC/MS/MS: Application in bioequivalence study
Samah Abd Elsabour Mohammed (1,*)
, Mohammed El-Dardiri (2) , Mona Ahmed Elhabak (3) , Khaled Ibrahim Abu Zaid (4) (1) National Organization of Drug Control and Research, Giza, 11843, Egypt
(2) Bioequivalence Center, Modern Science and Arts University, 6th October, 11787, Egypt
(3) Bioequivalence Center, Modern Science and Arts University, 6th October, 11787, Egypt
(4) Bioequivalence Center, Modern Science and Arts University, 6th October, 11787, Egypt
(*) Corresponding Author
Received: 24 Dec 2014, Accepted: 14 Feb 2015, Published: 30 Jun 2015
Abstract
Metformin hydrochloride was quantified in human plasma by Ultra Performance Liquid Chromatography with Tandem Mass spectrometric determination (UPLC-MS/MS). The mobile phase used was (Water + 0.1% Formic acid) and (Acetonitrile + 0.1% Formic acid) in the ratio of 80:20 (v:v). An Acquity UPLC HSS T3 1.8 um 2.1×50 mm column was used. The detection was performed on a mass spectrometer (ESI+) using chlorpheniramine as an internal standard. The method was fully validated and it was applied to bioequivalence study of metformin hydrochloride in two brands of the drug with relative bioequivalence of 94.7%.
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DOI: 10.5155/eurjchem.6.2.178-182.1234
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References
[1]. O'Neil, M. J.; Heckelman P. E.; Koch C. B.; Roman K. J. The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 4th Edition, Merck & Co., Inc., Whitehouse Station, NJ, 2012.
[2]. Goodarzi, M. O.; Bryer-Ash, M. Diabetes Obes. Metab. 2005, 7(6), 654-665.
http://dx.doi.org/10.1111/j.1463-1326.2004.00448.x
[3]. Holt, R. I. G.; Cockram, C.; Flyvbjerg, A.; Goldstein, B. J. Text book for diabetes, 4th edition, John Wiley & Sons, 2009.
[4]. Liu, A.; Coleman, S. P. J. Chromatogr. B 2009, 877(29), 3695-3700.
http://dx.doi.org/10.1016/j.jchromb.2009.09.020
[5]. Chen, L.; Zhou, Z.; Shen, M.; Ma, A. J. Chromatogr. Sci. 2011, 49, 94-100.
http://dx.doi.org/10.1093/chrsci/49.2.94
[6]. Chen, X.; Gu, Q.; Qiu, F.; Dafa, Z. D. J. Chromatogr. B 2004, 802(2), 377-381.
http://dx.doi.org/10.1016/j.jchromb.2003.12.017
[7]. Marlice, A.; Marques, S.; Soares, A.; Pinto, O. W.; Werneck, B. P. T. J. Chromatogr. B 2007, 852, 308-316.
http://dx.doi.org/10.1016/j.jchromb.2007.01.030
[8]. Ding, C. G.; Zhou, Z.; Ge, Q.; Zhi, X.; Ma, L. L. Biomed. Chromatogr. 2007, 21(2), 132-138.
http://dx.doi.org/10.1002/bmc.723
[9]. Ranetti, M. C.; Ionescu, M.; Hinescu, L.; Ionica, E.; Anuta, V.; Ranetti, A. E.; Stecoza, C. E.; Mircioiu, C. Farmacia 2009, 57(6), 728-735.
[10]. Bonde, S. L.; Bhadane, R. P.; Gaikwad, A.; Katale, D.; Gavali, S.; Narendiran, A. S. A. Int. J. Pharm. Sci. 2013, 3, 463-470.
[11]. Amini, H; Ahmadiani, A.; Gazerani, P. J. Chromatogr. B 2005, 824(1-2), 319-322.
http://dx.doi.org/10.1016/j.jchromb.2005.07.009
[12]. Jian, W.; Ying, W. G.; Jing-kai, G. U.; Yan, W. Chem. Res. Chinese. 2005, 21(2), 246-250.
[13]. Zhang, W.; Han, F.; Zhao, H.; Lin, Z. J.; Huang, Q. M.; Weng, N. Biomed. Chromatogr. 2011, 26(10), 1163-1169.
http://dx.doi.org/10.1002/bmc.2673
[14]. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry-Bioanalytical Method validation, MD, 2001.
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DOI Link: https://doi.org/10.5155/eurjchem.6.2.178-182.1234
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