PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

A validated stability-indicating RP-LC method for the estimation of process-related impurities and degradation products of quetiapine fumarate in solid oral dosage form

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A simple, selective, and stability-indicating reverse phase liquid chromatographic method has been developed and validated for the simultaneous determination of impurities and forced degradation products of quetiapine fumarate. The chromatographic separation was achieved on Inertsil-3 C8, 150 mm × 4.6 mm, 5 μm column at 35°C with UV detection at 217 nm using gradient mobile phase at a flow rate of 1.0 mL/min. Mobile phase A contains a mixture of 0.01 M di-potassium hydrogen orthophosphate (pH 6.8) and acetonitrile in the ratio of 80:20 (v/v), respectively, and mobile phase B contains a mixture of 0.01 M di-potassium hydrogen orthophosphate (pH 6.8) and acetonitrile in the ratio of 20:80 (v/v), respectively. The drug product was subjected to the stress conditions of oxidative, hydrolysis (acid and base), hydrolytic, thermal, and photolytic degradation. Quetiapine fumarate was found to degrade significantly in acid, base, and oxidative stress conditions. The degradation products were well resolved from main peak and its impurities. The mass balance was found to be in the range of 96.6–102.2% in all the stressed conditions, thus proved the stability-indicating power of the method. The developed method was validated as per ICH guidelines with respect to specificity, linearity, limit of detection and quantification, accuracy, precision, and robustness.
Rocznik
Strony
393--409
Opis fizyczny
Bibliogr. 25 poz., rys., tab.
Twórcy
autor
  • IPDO Dr. Reddy’s Laboratories Ltd. Bachupally, Hyderabad 500072 A.P India
  • .I.T. University Department of Chemistry, S.A.S. Vellore 632014 Tamilnadu India
autor
  • .I.T. University Department of Chemistry, S.A.S. Vellore 632014 Tamilnadu India
autor
  • IPDO Dr. Reddy’s Laboratories Ltd. Bachupally, Hyderabad 500072 A.P India
autor
  • IPDO Dr. Reddy’s Laboratories Ltd. Bachupally, Hyderabad 500072 A.P India
Bibliografia
  • [1] J.G. Small, S.R. Hirsch, L.A. Arvanitis, B.G. Miller, and C.G. Link, Arch. Gen. Psychiatry, 54, 549 (1997)
  • [2] http://www.rxlist.com/seroquel-drug.htm
  • [3] N. Rajendraprasad, K. Basavaiah, and K. B. Vinay, J. Pre-Clin. Clin. Res., 4, 24 (2010)
  • [4] K. Basavaiah, N. Rajendraprasad, P.J. Ramesh, and K.B. Vinay, Thai J. Pharm. Sci., 34, 146 (2010)
  • [5] S.R. Dhaneshwar, N.G. Patre, and M.V. Mahadik, Acta Chromatogr., 21, 83 (2009)
  • [6] B. Dhandapani, A. Somasundaram, S.H. Raseed, M. Raja, and K. Dhanabal, Int. J. PharmTech Res., 1, 139 (2009)
  • [7] S.A. Jadhav, S.B. Landge, S.S. Shelke, N.C. Niphade, R.K. Panchangam, V.T. Mathad, S. R. Bembalkar, Chromatographia, 71, 1055 (2010)
  • [8] D. Suneetha and A.L. Rao, E-J. Chem., 7, 261 (2010)
  • [9] S. Hillaert, L. Snoeck and W. Van den Bossche, J. Chromatogr. A, 1033, 357 (2004)
  • [10] N. El-Enany, A. El-Brashy, F. Belal, and N. El-Bahay, Port. Electrochim. Acta, 27, 113, (2009)
  • [11] L. Mercolini, M. Grillo, C. Bartoletti, G. Boncompagni, and M.A. Raggi, Anal. Bioanal. Chem., 388, 235 (2007)
  • [12] F. Belal, A. Elbrashy, M. Eid, and J.J. Nasr, J. Liq. Chromatogr. Relat. Technol., 31, 1283 (2008)
  • [13] P.C. Davis, O. Bravo, M. Gehrke, and C.T. Azumaya, J. Pharm. Biomed. Anal., 51, 1113 (2010)
  • [14] R. Mandrioli, S. Fanali, A. Ferranti, and M.A. Raggi, J. Pharm. Biomed. Anal., 30, 969 (2002)
  • [15] Z. Zhou, X. Li, K. Li, Z. Xie, Z. Cheng, W. Peng, F. Wang, R. Zhu, and H. Li, J. Chromatogr. B, 802, 257 (2004)
  • [16] E.U. Stolarczyk, L. Kaczmarek, K. Eksanow, M. Kubiszewski, M. Glice, and A. Kutner, Pharm. Dev. Technol., 14, 27 (2009)
  • [17] H. Xu, D. Wang, C. Sun, Y. Pan, and M. Zhou, J. Pharm. Biomed. Anal., 44, 414 (2007)
  • [18] Ch. Bharathi, K.J. Prabahar, Ch.S. Prasad, M.S. Rao, G.N. Trinadhachary, V.K. Handa, R. Dandala, and A. Naidu, Pharmazie, 63, 14 (2008)
  • [19] V. Mittapelli, L. Vadali, D.A. Sivalakshmi, and M.V. Suryanarayana, Rasayan J. Chem., 3, 677 (2010)
  • [20] R.K. Trivedi and M.C. Patel, Sci. Pharm., 79, 97 (2011)
  • [21] S.R. Krishna, B.M. Rao and N.S. Rao, Rasayan J. Chem., 1, 466 (2008)
  • [22] M. Bakshi and S. Singh, J. Pharm. Biomed. Anal., 28, 1011 (2002)
  • [23] ICH Q1A (R2), Stability Testing of New Drug Substances and Products, 2000
  • [24] ICH Q1B, Photostability testing on new drug substances and products, 1996
  • [25] ICH Q2 (R1), Validation of Analytical Procedures: Text and Methodology, 2005
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-a0849ddc-d9b4-40d6-ab9a-9646198137fb
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.