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RP-HPLC-PDA method development and validation for the estimation of oxcarbazepine in bulk and formulations

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A simple, precise, rapid, and accurate liquid chromatography-mass spectrometry (LC-MS) compatible reversed phase high-performance liquid chromatography-photodiode array detection (RP-HPLC-PDA) method has been developed and validated for the estimation of oxcarbazepine (OXC) in bulk and tablet formulations. The chromatographic separation was achieved on Phenomenex C18 column (150 mm • 4.6 mm, 5.0 μm particle size) using the mobile phase comprising methanol-formic acid (0.02% v/v in water) in the ratio of 50:50 (v/v) at a flow rate of 1 mL min -1, and OXC was eluted at 6.4 min. Quantification and linearity were achieved at 229 nm over the concentration range of 10–50 μg mL -1, and the mean percentage of assay was found to be 100.03. The method was validated for specificity, linearity, accuracy, precision, limit of detection (LOD), limit of quantification (LOQ), stability, and robustness as per the International Conference on Harmonisation (ICH) guidelines and it is suitable to be employed in quality control.
Rocznik
Strony
519--529
Opis fizyczny
Bibliogr. 20 poz., rys., tab.
Twórcy
autor
  • K.V.S.R Siddhartha College of Pharmaceutical Sciences Vijayawada 520010 AP India
autor
  • K.V.S.R Siddhartha College of Pharmaceutical Sciences Vijayawada 520010 AP India
  • K.V.S.R Siddhartha College of Pharmaceutical Sciences Vijayawada 520010 AP India
  • K.V.S.R Siddhartha College of Pharmaceutical Sciences Vijayawada 520010 AP India
Bibliografia
  • [1] E.S. Tecoma, Epilepsis, 40, S37 (1999)
  • [2] M.J. Mclean, M. Schmutz, and A.W. Wamil, Epilepsis, 35, S5–S9 (1994)
  • [3] L.U. Zhi-cheng and Y.U. Qing-sheng, Chin. J. Clin. Pharmacol., 19, 134–137 (2003)
  • [4] M. Mazza, G. Della Marca, M. Di Nicola, G. Martinotti, G. Pozzi, L. Janiri, P. Bria, and S. Mazza, Epilepsy Behav., 10, 397–401 (2007)
  • [5] A.R. Rosa, N. Cruz, M. Comes, and E. Vieta, Euro. Neuropsychopharmacol., 19, S75–S76 (2009)
  • [6] K. Lanckmans, R. Clinckers, A. Van Eeckhaut, S. Sarre, I. Smolders, and Y.J. Michotte, J. Chromatogr. B, 831, 205–212 (2006)
  • [7] H. Levert, P. Odou, and H. Robert, Biomed. Chromatogr., 16, 19–24 (2002)
  • [8] H. Levert, P. Odou, and H Robert, J. Pharm. Biomed. Anal., 28, 517–525 (2002)
  • [9] R. Mandrioli, N. Ghedini, F. Albani, E. Kenndler, and M.A. Raggi, J. Chromatogr. B, 783, 253–263 (2003)
  • [10] H. Breton, M. Cociglio, F. Bressolle, H. Peyriere, J.P. Blayac, and D. Hillaire-Buys, J. Chromatogr. B, 828, 8090 (2005)
  • [11] M.C. Rouan, M. Decherf, V. Le Clanche, J.B. Lecaillon, and J. Godbillon, J. Chromatogr. B, 658, 167–172 (1994)
  • [12] G. Menge and J.P. Dubois, J. Chromatogr. B, 275, 189–194 (1983)
  • [13] G. Paglia, O. D’Apolito, D. Garofalo, C. Scarano, and G. Corso, J. Chromatogr. B, 860, 153–159 (2007)
  • [14] B.S. Maria, F.N. Demetrius, L.M. Ismael, N.C. Adriano, E.G. Francisco, and A.F. Fernando, J. Pharm. Biomed. Anal., 45, 304–311(2007).
  • [15] M.L. Qi, P. Wang, L.J. Wang, and R.N. Fu, J. Pharm. Biomed. Anal., 31, 57–62 (2003)
  • [16] A. Appa Rao, Afr. J. Pure Appl. Chem., 2, 1–5 (2008)
  • [17] K.S. Rao, N. Belorkar, and M.E.B. Rao, J. Young Pharmacists, 1, 270–277 (2009)
  • [18] D.B. Pathare, A.S. Jadhav, and M.S. Shingare, J. Pharm. Biomed. Anal., 43, 1825–1830 (2007)
  • [19] H. Levert, P. Odou, and H. Robert, J. Pharm. Biomed. Anal., 28, 517–525 (2002)
  • [20] Guidance for Industry — Q2B Validation of Analytical Procedures: Methodology; http://www.fda.gov/cder/guidance/index.htm
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-73abfd08-84e5-40d0-9152-07eed88f11ac
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