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Liquid Selective Electrodes for Warfarin Sodium Based on Poly(vinyl chloride) Matrix Membrane
Corresponding Author(s) : Yehya K. Al-Bayati
Asian Journal of Chemistry,
Vol. 28 No. 9 (2016): Vol 28 Issue 9
Abstract
An accurate, sensitive, selective and reproducible method for quantification of warfarin sodium in pharmaceutical preparation has been developed. This method is based on construction of selective liquid membrane electrodes using phosphotungstic acid as an active material and oleic acid, tri-n-butylphosphate, nitrobenzene, acetophenone and di-octyl phthalate as plasticizers and PVC as matrix. The results showed that the linear concentration is between 1 × 10–1 and 1 × 10–5 M, correlation coefficient of (0.9984 and 0.99949), slope of (20.04 -29.6) mV/decade, detection limit of (6 × 10–6 to 4 × 10–5) M and the life time were (10-40) days. This study also included the measurements of selectivity coefficients of these electrodes in the presence of common cations and some amino acid they found to be less than one. The electrodes were successfully applied for determination of warfarin sodium in pure form and in pharmaceutical tablets.
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References
Martindale, The Complete Drug Reference, Pharmaceutical Press Publication Division of Royal Pharmaceutical Society, Great Britain, edn 33, p. 998 (2002).
K.D. Tripathi, Essentials of Medical Pharmacology, edn 3, p. 555 (1985).
S.G. Kini, S. Choudhary and M. Mubeen, J. Computat. Methods Mol. Des., 2, 51 (2012).
M.P. Teotia, D.K. Rastogi and W.U. Malik, Anal. Chim. Acta, 7, 339 (1973).
D. Singh and H.B. Singh, Indian J. Chem., 14, 781 (1976).
U. Yasar, E. Eliasson, M. Dahl, I. Johansson, M. Ingelman-Sundberg and F. Sjoqvist, Biochem. Biophys. Res. Commun., 254, 628 (1999); doi:10.1006/bbrc.1998.9992.
A.T.M. Serajuddin, Adv. Drug Deliv. Rev., 59, 603 (2007); doi:10.1016/j.addr.2007.05.010.
D. Gao and M.B. Maurin, AAPS PharmSci, 3, 18 (2001); doi:10.1208/ps030103.
A. Vacobi, J.A. Udall and G. Levy, Clin. Pharmacol. Ther., 19, 552 (1976); doi:10.1002/cpt1976195part1552.
F.V. Lucas, A. Duncan, R. Jay, R. Coleman, P. Craft, B. Chan, L. Winfrey, D.R. Mungall and J. Hirsh, Am. J. Clin. Pathol., 88, 442 (1987); doi:10.1093/ajcp/88.4.442.
Y.A. Chua, W.Z. Abdullah and S.H. Gan, Turk. J. Med. Sci., 42, 930 (2012).
I. Locatelli, V. Kmetec, A. Mrhar and I. Grabnar, J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 818, 191 (2005); doi:10.1016/j.jchromb.2004.12.024.
C. Banfield and M. Rowlandx, J. Pharm. Sci., 73, 1392 (1984); doi:10.1002/jps.2600731017.
H. Takahashi, T. Kashima, S. Kimura, N. Muramoto, H. Nakahata, S. Kubo, Y. Shimoyama, M. Kajiwara and H. Echizen, J. Chromatogr. B Biomed. Sci. Appl., 701, 71 (1997); doi:10.1016/S0378-4347(97)00346-0.
A. Duffield, P.H. Duffield, D.J. Birkett, M. Kennedy and D.N. Wade, Biomed. Mass Spectrom., 6, 208 (1979); doi:10.1002/bms.1200060508.
M.R. Nateghi, M.H. Mosslemin, A. Hakimi and S. Kavoosi, Asian J. Chem., 22, 3516 (2010).
M.M. Ghoneim and A. Tawfik, Anal. Chim. Acta, 511, 63 (2004); doi:10.1016/j.aca.2004.01.037.
T.D. Smirnova, N.V. Nevryueva, S.N. Shtykov, V.I. Kochubei and D.A. Zhemerichkin, J. Anal. Chem., 64, 1114 (2009); doi:10.1134/S1061934809110045.
Z. Chang and H.T. Yan, J. Lumin., 132, 811 (2012); doi:10.1016/j.jlumin.2011.11.013.
Q. Zhou, W.P. Yau and E. Chan, Electrophoresis, 24, 2617 (2003); doi:10.1002/elps.200305441.
P. Gareil, J.P. Gramond and F. Guyon, J. Chromatogr. B, 615, 317 (1993); doi:10.1016/0378-4347(93)80347-7.
F. Faridbod, M.R. Ganjali, R. Dinarvand and P. Norouzi, Afr. J. Biotechnol., 6, 2960 (2007).
Y. Umezawa, K. Umezawa and H. Sato, Pure Appl. Chem., 67, 507 (1995); doi:10.1351/pac199567030507.
Ch.C. Rundl, A Beginners Guide to Ion Selective Electrodes Measurement, Nico2000 Ltd., London, UK (2004).