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Kinetic Spectrophotometric Methods for the Determination of Isatin
Corresponding Author(s) : Masoom Raza Siddiqui
Asian Journal of Chemistry,
Vol. 25 No. 8 (2013): Vol 25 Issue 8
Abstract
Simple, rapid and sensitive kinetic spectrophotometric methods are described for the analysis of isatin in pure form and in mixture. The procedures were based on the kinetic investigations and studies were done upon the oxidation of isatin with potassium permanganate in basic medium. Various parameters affecting the colour developments were investigated and parameters were optimized. The reliability and the analytical performance of the proposed methods were validated for its linearity, range, accuracy and precision. The calibration curves were linear over the range of 5-50 μg mL-1. The limit of detection and limit of quantitation of the two methods ranges from 3.4 × 10-4-0.878 and 1.05 × 10-3-2.663, respectively. The possible mechanism of the reaction is also proposed.
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- P. Zou and H.L. Koh, Rapid Commun. Mass Spectrom., 21, 1239 (2007).
- Silva J.F.M. Da, S.J. Garden and A.C. Pinto, J. Braz. Chem. Soc., 12, 273 (2001).
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- V. Glover, S.K. Bhattacharya, A. Chakrabarti and M. Sandler, Stress Med., 14, 225 (1998).
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- S.K. Battacharya, A. Clow, A. Prareski, J. Halket,V. Glover and M. Sandler, Neurosci. Lett., 132, 44 (1991).
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- V.C. Diculescu, S. Kumbhat and A.M. Oliveira-Brett, Anal. Chim. Acta, 575, 190 (2006).
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References
P. Zou and H.L. Koh, Rapid Commun. Mass Spectrom., 21, 1239 (2007).
Silva J.F.M. Da, S.J. Garden and A.C. Pinto, J. Braz. Chem. Soc., 12, 273 (2001).
N. Hamaue, N. Yamazaki, M. Minami, M. Endo, M. Hirahuji, Y. Monma and H. Togashi, Gen. Pharmacol., 30, 387 (1998).
B. Bhrigu, D. Pathak, N. Siddiqui, M.S. Alam and W. Ahsan, Int. J. Pharm. Sci. Drug Res., 2, 229 (2010).
V. Glover, S.K. Bhattacharya, A. Chakrabarti and M. Sandler, Stress Med., 14, 225 (1998).
V. Glover, M. Reveley and M. Sandler, Biochem. Pharmacol., 29, 467 (1980).
A.E. Medvedev, A. Clow, M. Sandler and V. Glover, Biochem. Pharmacol., 52, 385 (1996).
A. Medvedev, O. Bussygyna, N. Pyatakova, V. Glover and I. Severina, Biochem. Pharmacol., 63, 763 (2002).
S.K. Battacharya, A. Clow, A. Prareski, J. Halket,V. Glover and M. Sandler, Neurosci. Lett., 132, 44 (1991).
H. Xu, D. Wang, W. Zhang, W. Zhu, K. Yamamoto and L. Jin, Anal. Chim. Acta, 577, 207 (2006).
V.C. Diculescu, S. Kumbhat and A.M. Oliveira-Brett, Anal. Chim. Acta, 575, 190 (2006).
V. Manabe,Q. Gao, J. Yuan, T. Takahashi and A. Ueki, J. Chromatogr. B: Biomed. Sci. Appl., 691, 197 (1997).
M. Unger, W. Jacobsen, U. Holzgrabe and L.Z. Benet, J. Chromatogr. B, 767, 245 (2002).
J.M. Halket, P.J. Watkins, A. Przyborowska, B.L. Goodwin, A. Clow, V. Glover and M. Sandler, J. Chromatogr. B: Biomed. Appl., 562, 279 (1991).
K.-I. Mawatari, M. Segawa, R. Masatsuka, Y. Hanawa, F. Iinuma and M. Watanabe, Analyst, 126, 33 (2001).
Z. Xiang-Hui, X. Wei and L. Jun, J. Shanxi Normal Univ., [DOI]:CNKI:SUN:SFDX.0.2008-02-018.http://en.cnki.com.cn/Article_en/CJFDTOTAL-SFDX200802018.htm.
Vogel's Textbook of Quantitative Chemical Analysis, Pearson Education, Singapore, edn. 6, p. 420 (2002).
S. Riahi, F. Hadiloo, S.M.R. Milani, N. Davarkhah, M.R. Ganjali, P. Norouzi and P. Seyfi, Drug Testing Anal., 3, 319 (2011).
N. Rahman, M.R. Siddiqui and S.N.H. Azmi, J. Chin. Chem. Soc., 53, 735 (2006).
C. Hartmann, J. Smeyers-Verbeke, W. Penninck, Y.V. Hayden, P. Venkeerberghen and D.L. Masart, Anal. Chem., 67, 4491 (1995).
Canada Health Protection Branch, Drug Directorate Guidelines, Acceptable Methods, Ministry of National Health and Welfare Draft (1992).
A.M. Ismail and A.A. Zaghloul, Int. J. Chem. Kinet., 30, 463 (1998)