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Development and validation of a stability-indicating RP-LC method for the estimation of process-related impurities and degradation products of oxcarbazepine in pharmaceutical formulation

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A stability-indicating gradient reverse-phase liquid chromatographic method was developed for the quantitative determination of process-related impurities and forced degradation products of oxcarbazepine in pharmaceutical formulation. The method was developed by using Inertsil cyano (250 × 4.6 mm) 5 μm column with mobile phase containing a gradient mixture of solvent A (0.01 M sodium dihydrogen phosphate, pH adjusted to 2.7 with orthophosphoric acid and acetonitrile in the ratio of 80:20 v/v) and B (50:40:10 v/v/v mixture of acetonitrile, water, and methanol). The flow rate of mobile phase was 1.0 mL min−1. Column temperature was maintained at 25°C and detection wavelength at 220 nm. Developed reverse-phase high-performance liquid chromatography (RP-HPLC) method can adequately separate and quantitate five impurities of oxcarbazepine, namely imp-A, imp-B, imp-C, imp-D, and imp-E. Oxcarbazepine was subjected to the stress conditions of oxidative, acid, base, hydrolytic, thermal, and photolytic degradation. Oxcarbazepine was found to degrade significantly in acid, base, and oxidative stress conditions. The degradation products were well resolved from oxcarbazepine and its impurities. The developed method was validated as per International Conference on Harmonization (ICH) guidelines with respect to specificity, linearity, limit of detection and quantification, accuracy, precision, and robustness.
Rocznik
Strony
267--282
Opis fizyczny
Bibliogr. 15 poz., rys., tab.
Twórcy
autor
  • IPDO Dr. Reddy’s Laboratories Ltd. Bachupally, Hyderabad 500072 A.P India
autor
  • S. K. University Department of Chemistry Anantapur 515055 A.P. India
autor
  • IPDO Dr. Reddy’s Laboratories Ltd. Bachupally, Hyderabad 500072 A.P India
Bibliografia
  • [1] http://www.rxlist.com/trileptal-drug.htm
  • [2] S.M. Grant and D. Fauld, Drug, 43, 873 (1992)
  • [3] M.L. Qi, P. Wang, L.J. Wang, and R.N. Fu, J. Pharm. Biomed. Anal., 31, 57 (2003)
  • [4] K.S. Rao, N. Belorkar, and M.E.B. Rao, J. Young Pharm., 1, 270 (2009)
  • [5] A. Kumps, J. Liq. Chromatogr., 7, 1235 (1984)
  • [6] M. Klys, S. Rojek, and F. Bolechala, J. Chromatogr. B, 825, 38 (2005)
  • [7] G. Paglia, O. D’Apolito, D. Garofalo, C. Scarano, and G. Corso, J. Chromatogr. B, 860, 153 (2007)
  • [8] M.D.L.LS. Cavazos, V.T.D.L. Cruz, and N.W.D. Torres, J. Liquid Chromatogr. Rel. Tech., 28, 693 (2005)
  • [9] M. Bhatt, S. Shah, and Shivprakash, Biomed. Chromatogr., 25, 751 (2011)
  • [10] H.H. Maurer, C. Kratzsch, A.A. Weber, F.T. Peters, and T. Kraemer, J. Mass Spectro., 37, 687 (2002)
  • [11] G. Srinubabu, B.V. Ratnam, A.A. Rao, and M.N. Rao, Chem. Pharm. Bull., 56, 28 (2008)
  • [12] D.B. Pathare, A.S. Jadhav, and M.S. Shingare, J. Pharm. Biomed. Anal., 43, 1825 (2007)
  • [13] ICH Q1B, Photostability Testing on New Drug Substances and Products, 1996
  • [14] ICH Q1A (R2), Stability Testing of New Drug Substances and Products, 2003
  • [15] ICH Q2 (R1), Validation of Analytical Procedures: Text and Methodology, 2005
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-ef6b8dec-c098-4968-b8af-df8a5ab862a4
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