Copyright (c) 2015 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Field-Amplified on-line Sample Stacking for Separation and Determination of Adefovir and Tenofovir Using Capillary Electrophoresis
Corresponding Author(s) : Yixiang Duan
Asian Journal of Chemistry,
Vol. 27 No. 9 (2015): Vol 27 Issue 9
Abstract
An on-line sample stacking method known as field amplified sample stacking, using hydroxypropylmethyl cellulose as electro-osmotic flow suppressant, was developed for separation and identification of adefovir and tenofovir for the first time. A water plug (hydrodynamic injection for 15 s, 2.0 psi) was added to the system prior to the loading of sample (electrokinetic injection at cathode end (14.6 kV, 20 s)) in the capillary (80 cm × 75 μm). The separation was performed using phosphate solution containing 0.3 % hydroxypropylmethyl cellulose and measured at 18 kV and 214 nm. Comparing with the conventional capillary electrophoresis, the signal enhancement factor was found to be 146 for adefovir (LOD = 2.67 ng mL-1) and 137 for tenofovir (LOD = 3.22 ng mL-1) (S/N = 3). The proposed method has potential application in pharmacokinetics and can reach detection limits comparable to mass spectrometry, a more complicated and costly procedures.
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T. Delahunty, L. Bushman and C.V. Fletcher, J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 830, 6 (2006); doi:10.1016/j.jchromb.2005.10.015.
K. Vavrova, K. Lorencova, J. Klimentova, J. Novotný and A. Hrabálek, J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 853, 198 (2007); doi:10.1016/j.jchromb.2007.03.012.
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R.T. Kennedy, I. German, J.E. Thompson and S.R. Witowski, Chem. Rev., 99, 3081 (1999); doi:10.1021/cr980134j.
J.P. Quirino, J.-B. Kim and S. Terabe, J. Chromatogr. A, 965, 357 (2002); doi:10.1016/S0021-9673(01)01499-6.
Y. Zhao, K. McLaughlin and C.E. Lunte, Anal. Chem., 70, 4578 (1998); doi:10.1021/ac980427c.
E. van der Vlis, M. Mazereeuw, U.R. Tjaden, H. Irth and J. van der Greef, J. Chromatogr. A, 687, 333 (1994); doi:10.1016/0021-9673(94)00776-4.
A.K. Korir, V.K. Almeida, D.S. Malkin and C.K. Larive, Anal. Chem., 77, 5998 (2005); doi:10.1021/ac050669u.
A. Riaz, B. Kim and D.S. Chung, Electrophoresis, 24, 2788 (2003); doi:10.1002/elps.200305537.
W.F. Smyth, G.B. Harland, S. McClean, G. McGrath and D. Oxspring, J. Chromatogr. A, 772, 161 (1997); doi:10.1016/S0021-9673(97)00182-9.
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C.-X. Zhang and W. Thormann, Anal. Chem., 68, 2523 (1996); doi:10.1021/ac951250e.
J.C. Sanders, M.C. Breadmore, Y.C. Kwok, K.M. Horsman and J.P. Landers, Anal. Chem., 75, 986 (2003); doi:10.1021/ac020425z.
R.-L. Chien and D.S. Burgi, J. Chromatogr. A, 559, 141 (1991); doi:10.1016/0021-9673(91)80066-P.
J.Z. Song, J. Chen, S.J. Tian and Z.-P. Sun, J. Pharm. Biomed. Anal., 21, 569 (1999); doi:10.1016/S0731-7085(99)00158-2.
A. Zinellu, S. Sotgia, L. Deiana and C. Carru, Electrophoresis, 32, 1893 (2011); doi:10.1002/elps.201100056.
X.L. Hou, D.L. Deng, X. Wu, Y. Lv and J. Zhang, J. Chromatogr. A, 1217, 5622 (2010); doi:10.1016/j.chroma.2010.06.070.
Y.F. Shi, Y. Huang, J.P. Duan, H. Chen and G. Chen, J. Chromatogr. A, 1125, 124 (2006); doi:10.1016/j.chroma.2006.04.061.