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Validated reversed-phase high-performance liquid chromatographic and high-performance thin-layer chromatographic methods for simultaneous analysis of tamsulosin hydrochloride and dutasteride in pharmaceutical dosage forms

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
In this research paper we describe validated high-performance liquid chromatographic (HPLC) and high-performance thin-layer chromatographic (HPTLC) methods for simultaneous analysis of tamsulosin hydrochloride and dutasteride in tablet formulations. HPLC was performed on a C 18 column with 85:15 ( υ/υ ) methanol-0.02 M ammonium acetate buffer (pH 9.5, adjusted with triethylamine) as mobile phase. HPTLC was performed on aluminium foil-backed silica gel G60F 254 layers with toluene-methanol-triethylamine 9:1.5:1 ( υ/υ/υ ) as mobile phase. In HPLC, quantification was achieved by photo diode-array (PDA) detection at 274 nm over the concentration range 1–20 μg mL -1 for both; mean recovery was 98.18 ± 0.698 and 99.94 ± 0.611% for TAM and DUTA, respectively. In HPTLC, quantification was achieved by UV detection at 280 nm over the concentration range 200–2000 ng per band for both; mean recovery was 99.66 ± 0.892 and 100.05 ± 1.012% for TAM and DUTA, respectively. These methods are simple, precise, and sensitive, and are suitable for simultaneous analysis of TAM and DUTA in tablet formulations.
Rocznik
Strony
419--431
Opis fizyczny
Bibliogr. 23 poz., rys., tab.
Twórcy
autor
  • Ganpat University Department of Pharmaceutical Chemistry, S.K. Patel College of Pharmaceutical Education and Research Kherva, Mehsana 382711 Gujarat India
autor
  • Ganpat University Department of Pharmaceutical Chemistry, S.K. Patel College of Pharmaceutical Education and Research Kherva, Mehsana 382711 Gujarat India
Bibliografia
  • [1] J.G. Hardman, L.E. Limbard and A.G. Gilman (eds), Goodman & Gilman’s: The Pharmacological Basis of Therapeutics, 9th ed., McGraw-Hill, New York, 2001, pp. 232–235
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  • [4] C. Page, M. Walker, and M. Curtis (eds), Integrated Pharmacology, Mosby, New York, 2002, pp. 489–492
  • [5] The Merck Index, An Encyclopedia of Chemicals, Drugs and Biologicals 14th ed., Merck Research Laboratories, Division of Merck & Co., Inc., Whitehouse Station, NJ, 2006, pp. 1728–1730
  • [6] C.J. Dunn, A. Matheson, and D.M. Faulds, Drugs Aging, 19 , 135–161 (2002)
  • [7] M. Marberger, Nat. Clin. Pract. Urol., 3 , 495–497 (2006)
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  • [9] M. Qi, P. Wang and L. Liu, J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci., 805 , 7–11 (2004)
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  • [12] L. Din, L. Li, P. Tao, J. Yang, and Z. Zhang, J. Chromatogr. B, 767 , 75–81 (2002)
  • [13] J. Macek, J. Klima, and P. Ptacek, J. Chromatogr. B, 809 , 307–311 (2004)
  • [14] N.V. Ramakrishna, K.N. Vishwottam, S. Manoj, M. Koteshwara, S. Wishu, and D.P. Varma, Biomed. Chromatogr., 19 , 709–719 (2005)
  • [15] S.A. Ozkan, B. Uslu, and H.Y. Enein, Talanta, 61 , 147–156 (2003)
  • [16] V. Maier, J. Horakova, J. Petr, E. Tesarova, P. Coufal, and J. Sevcik, J. Pharm. Biomed. Anal., 39 , 691–696 (2005)
  • [17] S.K. Sudhir, B.C. Vishal, T.V. Vinayak, and S.P. Swarup, J. Chromatogr. 67 , 911–918 (2008)
  • [18] D.V. Subba Rao and P. Radhakrishnanand, J. Chromatogr., 67 , 841–845 (2008)
  • [19] N.V. Ramakrishna, K.N. Vishwottam, S. Puran, M. Koteshwara, S. Manoj, and M. Santosh, J. Chromatogr. B, 809 , 117–124 (2004)
  • [20] S.K. Sudhir, B.C. Vishal, T.V. Vinayak and S.P. Swarup, Asian J. Chem., 20 , 5514–5518 (2008)
  • [21] A. Sangita, K. Veeran, S. Amlan, G. Debotri, B. Uttam, C. Tapas, and P. Tapan, J. Chromatogr., 67 , 893–903 (2008)
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  • [23] International Conference on Harmonisation, Q2B, Validation of Analytical Methods: Methodology. The Third International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), Guideline on Validation of Analytical Procedure-Methodology , Geneva, Switzerland, 1996
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-c1a09eb3-b9a7-4af0-9462-b8a200051d40
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