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Stability-indicating RP-HPLC method for analysis of eplerenone in the bulk drug and in a pharmaceutical dosage form

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A novel stability-indicating reversed-phase (RP) HPLC method has been developed and validated for quantitative analysis of eplerenone in the bulk drug and in a pharmaceutical dosage form. Use of a 250 mm × 4.6 mm, 5-μm particle, C18 column with 55:45 ( v/v ) 50 mM ammonium acetate buffer (pH 7)-acetonitrile as isocratic mobile phase enabled separation of the drug from its degradation products. UV detection was performed at 240 nm. The method was validated for linearity, accuracy (recovery), precision, specificity, and robustness. The linearity of the method was excellent over the range 10–100 μg mL -1 (correlation coefficient 0.999). The limits of detection and quantification were 0.019 and 0.053 μg mL -1, respectively. Recovery of eplerenone from the pharmaceutical dosage form ranged from 100.97 to 101.25%. Eplerenone was subjected to stress conditions (hydrolysis (acid, base), oxidation, photolysis, and thermal degradation) and the stressed samples were analysed by use of the method. Degradation was observed in acid, base, and 30% H 2 O 2 . The drug was stable under the other stress conditions investigated. The degradation products were well resolved from main peak. The forced degradation studies prove the stability indicating power of the method.
Rocznik
Strony
619--629
Opis fizyczny
Bibliogr. 14 poz., rys., tab.
Twórcy
autor
  • Dr Babasaheb Ambedkar Marathwada University Department of Chemical Technology Aurangabad 431004 (MS) India
  • Wockhardt Research Centre Aurangabad 431210 (MS) India
autor
  • Dr Babasaheb Ambedkar Marathwada University Department of Chemical Technology Aurangabad 431004 (MS) India
  • Wockhardt Research Centre Aurangabad 431210 (MS) India
  • Wockhardt Research Centre Aurangabad 431210 (MS) India
autor
  • Wockhardt Research Centre Aurangabad 431210 (MS) India
autor
  • Dr Babasaheb Ambedkar Marathwada University Department of Chemical Technology Aurangabad 431004 (MS) India
Bibliografia
  • [1] J.A. Spertus, J. Tooley, P. Jones, C. Poston, E. Mahoney, P. Deedwania, S. Hurley, B. Pitt, and W.S. Weintraub, Am. Heart J., 143 , 636 (2002)
  • [2] E.G. McMahon, Curr. Opin. Pharmacol., 1 , 190 (2001)
  • [3] J.A. Delyani, R. Rocha, C.S. Cook, D.S. Tolbert, S. Levin, B. Roniker, D.L. Workman, Y.L. Sing, and B. Whelihan, Cardiovasc. Drug Rev., 19 , 185 (2001)
  • [4] C.T. Stier, P.N. Chander Jr, and R. Rocha, Cardiology Rev., 10 , 97 (2002)
  • [5] J. Staessen, P. Lijnen, R. Fagard, L. Verschuren, and A. Amery, J. Endocrinol., 91 , 457 (1981)
  • [6] R.J. MacFadyen, C.S. Barr, and A.D. Struthers, Cardiovasc. Res, 35 , 30 (1997)
  • [7] International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, Stability testing of New Drug Substances and Products. QIA (R2), August, 2003
  • [8] J.Y. Zhang, D.M. Fast, and A.P. Breau, J. Pharm. Biomed. Anal., 31 , 103–115 (2003)
  • [9] J.Y. Zhang, D.M. Fast, and A.P. Breau, J. Chromatogr. B, 787 , 333–344 (2003)
  • [10] F. Varin, T. Minh, F. Benoit, J.P. Villeneuve, and Y. Theoret, J. Chromatogr., 574 , 57 (1992)
  • [11] A.M. Kaukonen, P. Vuorela, H. Vuorela, and J.P. Mannermaa, J. Chromatogr., 797 , 271 (1998)
  • [12] A. Jankowski, A. Skorek-Jankowaska, and H. Lamparezyk, J. Pharm. Biomed. Anal., 14 , 1359 (1996)
  • [13] Drug Information Branch (HFD-210), Validation of analytical procedure: Methodology. Step 4. In: ICH Harmonized Tripartite Guidelines Q2B. Center for Drug Evaluation and Research, Rockville, MD, November, 6 (1996)
  • [14] M. Bakshi, B. Singh, A. Singh, and S. Singh, J. Pharm. Biomed. Anal., 26 , 1011–1040 (2001)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-21022dde-2362-4ecb-bb43-4aa0aa49da94
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