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Simultaneous RP-HPLC analysis of atenolol, hydrochlorothiazide, and losartan potassium in a tablet formulation

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Simultaneous analysis of atenolol (Atn), hydrochlorothiazide (Hctz) and losartan potassium (Los) in solid dosage forms has been achieved by reversed-phase high-performance liquid chromatography on a C 18 column with a 0.035 M potassium dihydrogen orthophosphate-acetonitrile gradient as mobile phase and UV detection at 225 nm. The retention times for Atn, Hctz, and Los were 2.91, 4.75, and 7.52 min, respectively, with mean recoveries of 99.67, 99.89, and 100.69%. The method was validated in accordance with ICH guidelines. Because of its simplicity and high precision and accuracy, the method can be used for analysis of atenolol, hydrochlorothiazide and losartan potassium in pharmaceutical preparations.
Słowa kluczowe
Rocznik
Strony
219--226
Opis fizyczny
Bibliogr. 14 poz., rys., tab.
Twórcy
autor
  • Padm Dr D.Y. Patil Institute of Pharmaceutical Sciences and Research Department of Pharmaceutical Chemistry Pimpri, Pune 411018 Maharashtra India
autor
  • Padm Dr D.Y. Patil Institute of Pharmaceutical Sciences and Research Department of Pharmaceutical Chemistry Pimpri, Pune 411018 Maharashtra India
autor
  • Padm Dr D.Y. Patil Institute of Pharmaceutical Sciences and Research Department of Pharmaceutical Chemistry Pimpri, Pune 411018 Maharashtra India
  • Padm Dr D.Y. Patil Institute of Pharmaceutical Sciences and Research Department of Pharmaceutical Chemistry Pimpri, Pune 411018 Maharashtra India
  • Padm Dr D.Y. Patil Institute of Pharmaceutical Sciences and Research Department of Pharmaceutical Chemistry Pimpri, Pune 411018 Maharashtra India
autor
  • Padm Dr D.Y. Patil Institute of Pharmaceutical Sciences and Research Department of Pharmaceutical Chemistry Pimpri, Pune 411018 Maharashtra India
autor
  • Padm Dr D.Y. Patil Institute of Pharmaceutical Sciences and Research Department of Pharmaceutical Chemistry Pimpri, Pune 411018 Maharashtra India
  • Padm Dr D.Y. Patil Institute of Pharmaceutical Sciences and Research Department of Pharmaceutical Chemistry Pimpri, Pune 411018 Maharashtra India
Bibliografia
  • [1] Indian Pharmacopoeia, The Controller of Publication, New Delhi, pp. 1194, 1319, 2007
  • [2] British Pharmacopoeia, Vol. 1, Her Majesty’s Stationary Office, London, pp. 137, 1080, 2008
  • [3] The United States Pharmacopoeia, 18th edn, pp. 1893–1896
  • [4] N. Erk, Pharmazie, 58 , 796–800 (2003)
  • [5] N. Erk, J. Pharm. Biomed. Anal., 24 , 603–611 (2001)
  • [6] J. Charles, J. Brault, S. Boyer, C. Langlois, M.S. Cabrero, and L. Dubost, Anal. Lett., 36 , 2485–2495 (2003)
  • [7] E. Satana, S. Altinay, N.G. Goger, S.A. Ozkan, and Z. Senturk, J. Pharm. Biomed. Anal., 25 , 1009–1013 (2001)
  • [8] N.R. Lande, B.M. Shektar, S.S. Kadam, and S.R. Dhaneshwar, Indian Drugs, 37 , 577–581 (2000)
  • [9] T.M. Huag, Z. He, B. Yang, L.P. Shao, X.W. Zheng, and G.L. Duang, J. Pharm. Biomed. Anal., 41 , 644–648 (2006)
  • [10] E. Dinc and O. Ustundag, J. Liq. Chromatogr. Related Technol., 28 , 2179–2194 (2005)
  • [11] S.T. Ulu and S. Saglik, Turk. J. Pharm. Sci., 1 , 165–175 (2004)
  • [12] E. Dinc and O. Ustundag, Chromatographia, 61 , 237–244 (2005)
  • [13] D.L. Hertzog, J.F. McCafferty, X.G. Fang, R.J. Tyrell, and R.A. Reed, J. Pharm. Biomed. Anal., 30 , 747–760 (2002)
  • [14] ICH Guidelines Q2B, Validation of Analytical Procedures-Methodology, 1996
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-cd12e892-aeab-4d14-b255-0fb770ab81f7
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