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Determination of nalidixic acid using dispersive liquid-liquid microextraction followed by HPLC-UV

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A fast, simple, and sensitive sample preparation procedure based on dispersive liquid-liquid microextraction (DLLME) followed by high-performance liquid chromatography and ultraviolet (HPLC-UV) detection was developed for the determination of nalidixic acid in a human urine sample. A mixture of extraction solvent (35 μL carbon tetrachloride) and disperser solvent (1.0 mL acetonitrile) were rapidly injected into an aqueous sample (5.0 mL) for the formation of cloudy solution; the analyte in the sample was extracted into the fine droplets of carbon tetrachloride. After extraction, phase separation was performed by centrifugation and the enriched analyte in the sedimented phase was determined by HPLC-UV. The influence of several important parameters on extraction efficiency of nalidixic acid was evaluated. Under optimized experimental conditions, the calibration graph was linear in the concentration range of 1–800 μg L-1 with the coefficient of determination being 0.9994. The limits of detection and quantification were 0.2 and 0.7 μg L-1, respectively. The relative standard deviations (RSDs) and accuracies were in the range of 1.1–8.7% and 92.7–104.9%, respectively. This procedure was successfully applied to the determination of nalidixic acid in spiked urine samples with satisfactory results. The relative recoveries of urine samples ranged from 103.1% to 105.1%, with RSDs varying from 0.8% to 2.4%.
Rocznik
Strony
567--577
Opis fizyczny
Bibliogr. 30 poz., rys., tab.
Twórcy
autor
  • Ilam University Department of Chemistry, Faculty of Science Ilam 69315-516 Iran
autor
  • Ilam University Department of Chemistry, Faculty of Science Ilam 69315-516 Iran
autor
  • Ilam University Department of Chemistry, Faculty of Science Ilam 69315-516 Iran
Bibliografia
  • [1] U. Schröder and A. Machetzki, Eur. Food Res. Technol., 225, 627 (2007)
  • [2] J.E. Renew and C.H. Huang, J. Chromatogr. A, 1042, 113 (2004)
  • [3] M. Diaz-Alvarez, A. Turiel, and A. Martin-Esteban, Anal. Bioanal. Chem., 393, 899 (2009)
  • [4] A. Guiberteau, T.G. Diaz, M.I.R. Caceres, J.M.O. Burguillos, I.D. Meras, and F.S. Lopez, Talanta, 62, 357 (2004)
  • [5] M.A. Garcia, C. Solans, A. Calvo, M. Royo, E. Hernandez, R. Rey, and M.A. Bregante, Chromatographia, 54, 577 (2001)
  • [6] B. Toussaint, G. Bordin, A. Janosi, and A.R. Rodriguez, J. Chromatogr. A, 976, 195 (2002)
  • [7] G. Johnson, S. Westwood, and R. Houghton, Chromatographia, 55, S–127 (2002)
  • [8] E. Turiel, A. Martin-Esteban, and J.L. Tadeo, Anal. Chim. Acta, 562, 30 (2006)
  • [9] I.D. Meras, T.G. Diaz, F.S. Lopez, and M.I.R. Caceres, Chromatographia, 51, 163 (2000)
  • [10] Y.F. Mestre, L.L. Zamora, and J.M. Calatayud, Anal. Chim. Acta, 438, 93 (2001)
  • [11] H. Zhang, Y. Ren, and X. Bao, J. Pharm. Biomed. Anal., 49, 367 (2009)
  • [12] Y. Xiao, H. Chang, A. Jia, and J. Hu, J. Chromatogr. A, 1214, 100 (2008)
  • [13] V. Samanidou, E. Evaggelopoulou, M. Trotzmuller, X. Guo, and E. Lankmayr, J. Chromatogr. A, 1203, 115 (2008)
  • [14] F. Tamtam, F. Mercier, J. Eurin, M. Chevreuil, and B.L. Bot, Anal. Bioanal. Chem., 393, 1709 (2009)
  • [15] Y. Shi, J.H. Zhang, D. Shi, M. Jiang, Y.X. Zhu, S.R. Mei, Y.K. Zhou, K. Dai, and B. Lu, J. Pharm. Biomed. Anal., 42, 549 (2006)
  • [16] S. Almeda, L. Nozal, L. Arce, and M. Valcarcel, Anal. Chim. Acta, 587, 97 (2007)
  • [17] N. Fattahi, Y. Assadi, M.R.M. Hosseini, and E.Z. Jahromi, J. Chromatogr. A, 1157, 23 (2007)
  • [18] R.R. Kozani, Y. Assadi, F. Shemirani, M.R.M. Hosseini, and M.R. Jamali, Talanta, 72, 387 (2007)
  • [19] L. Farina, E. Boido, F. Carrau, and E. Dellacassa, J. Chromatogr. A, 1157, 46 (2007)
  • [20] M.G. Lopez, I. Rodriguez, and R. Cela, J. Chromatogr. A, 1166, 9 (2007)
  • [21] M.B. Melwanki, W.S. Chen, H.Y. Bai, T.Y. Lin, and M.R. Fuh, Talanta, 78, 618 (2009)
  • [22] H. Chen, H. Chen, J. Ying, J. Huang, and L. Liao, Anal. Chim. Acta, 632, 80 (2009)
  • [23] X. Zang, J. Wang, O. Wang, M. Wang, J. Ma, G. Xi, and Z. Wang, Anal. Bioanal. Chem., 392, 749 (2008)
  • [24] R.S. Zhao, C.P. Diao, X. Wang, T. Jiang, and J.P. Yuan, Anal. Bioanal. Chem., 391, 2915 (2008)
  • [25] M. Rezaee, Y. Assadi, M.R.M. Hosseini, E. Aghaee, F. Ahmadi, and S. Berijani, J. Chromatogr. A, 1116, 1 (2006)
  • [26] D. Nagaraju and S.D. Huang, J. Chromatogr. A, 1161, 89 (2007)
  • [27] J.S. Chiang and S.D. Huang, Talanta, 75, 70 (2008)
  • [28] P. Liang, J. Xu, and Q. Li, Anal. Chim. Acta, 609, 53 (2008)
  • [29] H. Yan, B. Liu, J. Du, G. Yang, and K.H. Row, J. Chromatogr. A, 1217, 5152 (2010)
  • [30] U.S. Food and Drug Administration, Guidance for Industry, Bioanalytical Method Validation, Centre for Drug Evaluation and Research, 2001
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-1bf748d4-8e8f-46f0-a7c5-4c83f85a15dd
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