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A simple, rapid reversed-phase high-performance liquid chromatographic method has been developed and validated for simultaneous estimation of drotaverine and omeprazole in a tablet dosage form. A C 18 column was used with a 60:40 ( v/v ) mixture of methanol and ammonium acetate (0.1 M , pH 5, adjusted with orthophosphoric acid) as mobile phase at a flow rate of 1.5 mL min -1 . UV detection was performed at 319 nm. The method was validated for accuracy, precision, linearity, specificity and sensitivity in accordance with International Conference on Harmonisation guidelines. The method was successfully used for quantitative analysis of Ranipas-DV tablets. Total run time was 10 min, drotaverine and omeprazole were eluted with retention times of 7.969 and 6.538 min respectively. Validation revealed that the method is specific, accurate, precise, reliable and reproducible. Calibration plots were linear over the concentration ranges 5-40 µg mL -1 for drotaverine and 5-50 µg mL -1 for omeprazole, respectively. Limits of detection were 16.2 and 4.8 ng mL -1 and limits of quantification were 49.0 and 14.5 ng mL -1 for drotaverine and omeprazole, respectively. Recovery was in the range 100.66-100.94% and 102.42-102.89% for drotaverine and omeprazole, respectively, and the coefficient of variance was <2.0% for both. The high percentage recovery and low co-efficient of variation confirm the suitability of the method for simultaneous analysis of drotaverine and omeprazole in tablets.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
439--450
Opis fizyczny
Bibliogr. 21 poz., rys., tab.
Twórcy
autor
autor
- Devi Ahilya Vishwavidyalaya School of Pharmacy Takshshila Campus, Khandwa Road Indore M.P. India 452 017, rbsm73@yahoo.co.in
Bibliografia
- [1] K.C. Singh, P. Jain, N. Goel, and A. Saxena, Int. J. Gynecol Obstet., 84 , 17 (2004)
- [2] M.J. Oneil, A. Smith, and P.E. Heckelman, The Merck Index, 13th edn, Merck, Whitehouse Station, New Jersey, 2001, pp. 3489
- [3] V.K. Mahajan, P.P. Dahivelkar, R.A. Fursule, A.A. Shirkhedkar, and S.J. Surana, Indian Drugs, 43 , 656 (2006)
- [4] J.K. Lalla, M.U. Shah, M.B. Jain, and A.H. Sharma, J. Pharm. Biomed. Anal., 11 , 385 (1993)
- [5] O.O. Bolaji and C.O. Onyeji, J. Chromatogr., 622 , 93 (1993)
- [6] P.P. Dahivelkar, V.K. Mahajan, S.B. Bari, A.A. Shirkhedkar, and S.J. Suran, Indian Drugs, 43 , 896 (2006)
- [7] F. Zahran, A.A. Gouda, A.S. Amin, and R. El-Sheikh, Spectrochim. Acta A, 67 , 1088 (2007)
- [8] S. Lakshmi, V. Anilkumar, M. Venkatesan, and T.K. Raja, Indian Drugs, 40 , 589 (2003)
- [9] K.H. Yuen, W.P. Choy, H.Y. Tan, J.W. Wong, and S.P. Yap, J. Pharm. Biomed. Anal, 24 , 715 (2001)
- [10] L. Sivasubramanian and V. Anilkumar, Indian J. Pharm. Sci., 69 , 674 (2007)
- [11] C.S.P. Sastry, P.Y. Naidu, and S.S.N. Murthy, Indian J. Pharm. Sci., 59 , 124 (1997)
- [12] M.E. Bosch, A.J. Sanchez, F.S. Rojas, and C.B. Ojeda, J. Pharm. Biomed. Anal., 44 , 831 (2007)
- [13] R.M. Orlando and P.S. Bonato, J. Chromatogr. B, 795 , 227 (2003)
- [14] Q.B. Cass, V.V. Lima, R.V. Oliveria, N.M. Cassiano, A.L.G. Degani, and J. Pedrazzoli, J. Chromatogr. B, 798 , 275 (2003)
- [15] J.M. Lobenhoffer, I. Reiche, and U. Troger, J. Chromatogr. B, 857 , 301 (2007)
- [16] J. Macek, J. Klima, and P. Ptacek, J. Chromatogr. B, 852 , 282 (2007)
- [17] International Conference on Harmonization (ICH), Q2A: Text on Validation of Analytical Procedures: Definitions and Terminology, Vol. 60, US FDA Federal Register, 1995
- [18] International Conference on Harmonization (ICH), Q2B: Validation of Analytical Procedures: Methodology, Vol. 62, US FDA Federal Register, 1997
- [19] M. Ribani, C.H. Collins, and C.B.G. Bottoli, J. Chromatogr. A, 1156 , 201 (2007)
- [20] The Indian Pharmacopoeia, Vol. I, 1996, p. 532
- [21] R. Sistla, V.S.S.K. Tata, Y.V. Kashyap, D. Candrasekar, and P.V. Diwan, J. Pharm. Biomed. Anal., 39 , 517 (2005).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BATE-0001-0034