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Simultaneous determination of celiprolol HCl and chlorthalidone in tablets and biological fluids using high-performance liquid chromatography

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A simple, accurate, and sensitive reversed-phase HPLC method was developed for the simultaneous determination of celiprolol HCl (CE) and chlorthalidone (CT). Good chromatographic separation was achieved using a 250 mm × 4.6 mm i.d., 5 μm particle size Hypurity C8 column. Mobile phase containing a mixture of methanol and 0.04 M phosphate buffer (35:65, υ/υ) at pH 7.0 was pumped at a flow rate of 1.2 mL min-1 with UV detection at 225 nm. Lisinopril dihydrate (LIS) was used as internal standard. The method showed good linearity in the ranges 0.2–20 and 0.2–10 μg mL-1 with limits of detection 0.06 and 0.04 μg mL-1 and limits of quantification 0.20 and 0.14μg mL-1 for CE and CT, respectively. The suggested method was successfully applied to the simultaneous analysis of the studied drugs in their synthetic mixture and coformulated tablet. The method was further extended to the determination of CE in biological fluids. The proposed method was also applied to the determination of the studied drugs in presence of some coadministered or related drugs such as atenolol, propranolol, acetazolamide, enalapril, nicardipine, triamterene, and hydrochlorothiazide without any interference.
Rocznik
Strony
185--206
Opis fizyczny
Bibliogr. 27 poz., rys., tab.
Twórcy
autor
  • University of Mansoura Department of Analytical Chemistry, Faculty of Pharmacy 35516 Mansoura Egypt
  • University of Mansoura Department of Analytical Chemistry, Faculty of Pharmacy 35516 Mansoura Egypt
autor
  • University of Mansoura Department of Analytical Chemistry, Faculty of Pharmacy 35516 Mansoura Egypt
autor
  • University of Mansoura Department of Analytical Chemistry, Faculty of Pharmacy 35516 Mansoura Egypt
Bibliografia
  • [1] S. Budavari (Ed.), The Merck Index, 12th edn, Merck & Co. Inc., Whitehouse Station, New Jersey, 1996; Electronic version
  • [2] S.C. Sweetman (Ed.), Martindale: The Complete Drug Reference, 35th edn, The Pharmaceutical Press, London, 2009; Electronic version
  • [3] The British Pharmacopoeia 2007, The Stationery Office, London; Electronic version
  • [4] D.J. Mazzo, C.L. Obetz, and J.E. Shuster, In: K. Florey (Ed.) Analytical Profiles of Drug Substances, Academic Press, California, 1991, vol. 20, pp. 237–301
  • [5] M. Delamoye, C. Duverneuil, F. Paraire, P. de-Mazancourt, and J.C. Alvarez, Forensic Sci. Int., 141, 23 (2004)
  • [6] E. Caudron, S. Laurent, E.M. Billaud, and P. Prognon, J. Chromatogr. B., 801, 339 (2004)
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  • [8] L.Y. Li, B.Y. Qian, R.Y. Gao, and Q.S. Wang, Fenxi Ceshi Xuebao, 22, 83 (2003)
  • [9] N. Grobuschek, M.G. Schmid, J. Koidl, and G. Guebitz, J. Sep. Sci., 25, 1297 (2002)
  • [10] A. Detroyer, Y. Vander-Heyden, S. Carda-Broch, M.C. Garcia-Alvarez-Coque, and D.L. Massart, J. Chromatogr. A, 912, 211 (2001)
  • [11] Rapado-Martinez, M.C. Garcia-Alvarez-Coque, and R.M. Villanueva-Camanas, J. Chromatogr. A, 765, 221 (1997)
  • [12] H.H. Maurer, O. Tenberken, C. Kratzsch, A.A. Weber, and F.T. Peters, J. Chromatogr. A, 1058, 169 (2004)
  • [13] K. Deventer, P. Van-Eenoo, and F.T. Delbeke, Rapid Commun. Mass Spectrom., 19, 90 (2005)
  • [14] C.A. Mueller, W. Weinmann, S. Dresen, A. Schreiber, and M. Gergov, Rapid Commun. Mass Spectrom., 19, 1332 (2005)
  • [15] The United States Pharmacopoeia 30, the National Formulary 25, US Pharmacopeial Convention, Rockville, MD, 2007; Electronic version
  • [16] A. El-Gindy, S. Emara, and A. Mostafa, Farmaco, 60, 269 (2005)
  • [17] A.A. Elshanawane, S.M. Mostafa, and M.S. Elgawish, J. AOAC Int., 92, 404 (2009)
  • [18] O. Gonzalez, G. Iriarte, N. Ferreirós, M.I. Maguregui, R.M. Alonso, and R.M. Jiménez, J. Pharm. Biomed. Anal., 50, 630 (2009)
  • [19] A. El-Gindy, S. Sallam, and R.A. Abdel-Salam, J. Sep. Sci. 31, 677 (2008)
  • [20] S. Pous-Torres, J.R. Torres-Lapasió, J.J. Baeza-Baeza, and M.C. García-Alvarez-Coque, J. Chromatogr. A, 1163, 49 (2007)
  • [21] M.J. Ruiz-Angel, J.R. Torres-Lapasió, and M.C. García-Alvarez-Coque, J. Chromatogr. A, 1022, 51 (2004)
  • [22] R. Herráez-Hernández and P. Campíns-Falcó, J. Chromatogr. B: Biomed. Sci. Appl., 740, 169 (2000)
  • [23] Y. Lu, J. Chen, B. Chen, and S. Yao, Se Pu, 27, 44 (2009)
  • [24] A. Vonaparti, M. Kazanis, and I. Panderi, J. Mass Spectrom., 41, 593 (2006)
  • [25] J.N. Miller and J.C. Miller, Statistics and Chemometrics for Analytical Chemistry, 5th edn, Pearson Education Limited, Harlow, England, 2005, pp. 39–73, 107–149, 256
  • [26] ICH Harmonized Tripartite Guideline, Validation of Analytical Procedures: Text and Methodology, Q2(R1), Current Step 4 Version, Parent Guidelines on Methodology, dated November 6 1996, incorporated in November 2005: http://www.ich.org/LOB/media/MEDIA417.pdf (accessed February 15, 2008)
  • [27] A.C. Moffat, M.D. Osselton, B. Widdop and L.Y. Galichet (Eds), Clark’s Analysis of Drugs and Poisons in Pharmaceuticals, Body Fluids and Postmortem Material, 3rd edn, The Pharmaceutical Press, London, 2004, vol. 2, pp. 768, 797
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-87618088-4101-4585-a713-76e312ad41f5
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