Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Highly Sensitive Luminescence Assessment of Bile Acid Using a Balofloxacin-Europium(III) Probe in Micellar Medium

  • Cai, Huan (School of Chemistry and Chemical Engineering, Shihezi University, Xinjiang Bintuan Key lab of Chemical Engineering for Green Process) ;
  • Zhao, Fang (School of Chemistry and Chemical Engineering, Shihezi University, Xinjiang Bintuan Key lab of Chemical Engineering for Green Process) ;
  • Si, Hailin (School of Chemistry and Chemical Engineering, Shihezi University, Xinjiang Bintuan Key lab of Chemical Engineering for Green Process) ;
  • Zhang, Shuaishuai (School of Chemistry and Chemical Engineering, Shihezi University, Xinjiang Bintuan Key lab of Chemical Engineering for Green Process) ;
  • Wang, Chunchun (School of Chemistry and Chemical Engineering, Shihezi University, Xinjiang Bintuan Key lab of Chemical Engineering for Green Process) ;
  • Qi, Peirong (School of Chemistry and Chemical Engineering, Shihezi University, Xinjiang Bintuan Key lab of Chemical Engineering for Green Process)
  • Received : 2012.08.05
  • Accepted : 2012.09.28
  • Published : 2012.12.20
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Abstract

A novel and simple method of luminescence enhancement effect for the determination of trace amounts of bile acid was proposed. The procedure was based on the luminescence intensity of the balofloxacin-europium(III) complex that could be strongly enhanced by bile acid in the presence of sodium dodecyl benzene sulfonate (SDBS). Under the optimum conditions, the enhanced luminescence intensity of the system exhibited a good linear relationship with the bile acid concentration in the range $5.0{\times}10^{-9}-7.0{\times}10^{-7}\;mol\;L^{-1}$ with a detection limit of $1.3{\times}10^{-9}\;mol\;L^{-1}$ ($3{\sigma}$). The relative standard deviation (RSD) was 1.7% (n = 11) for $5.0{\times}10^{-8}\;mol\;L^{-1}$ bile acid. The applicability of the method to the determination of bile acid was demonstrated by investigating the effect of potential interferences and by analyzing human serum and urine samples. The possible enhancement mechanism of luminescence intensity in balofloxacin-europium(III)-bile acid-SDBS system was also discussed briefly.

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References

  1. Russell, D. W. Annu. Rev. Biochem. 2003, 72, 137. https://doi.org/10.1146/annurev.biochem.72.121801.161712
  2. Heubi, J. E.; Setchell, K. D. R.; Bove, K. E. Semin. Liver Dis. 2007, 27, 282. https://doi.org/10.1055/s-2007-985073
  3. Vlahcevic, Z. R.; PandaK, W. M.; Stravitz, R. T. Gastroenterol. Clin. North Am. 1999, 28, 1.
  4. Perwaiz,S; Tuchweber, B.; Mignault, D.; Gilat, T.; Yousef, I. M. J. Lipid Res. 2001, 42, 114.
  5. Yousef, I. M.; Tuchweber, B. Can. J. Gastroenterol. 1997, 11, 541.
  6. Ochsenkühn, T.; Bayerdörffer, E.; Meining, A.; Schinkel, M.; Thiede, C.; Nüssler, V.; Sackmann, M.; Hatz, R.; Neubauer, A.; Paumgartner, G. Cancer 1999, 85, 1664. https://doi.org/10.1002/(SICI)1097-0142(19990415)85:8<1664::AID-CNCR4>3.0.CO;2-O
  7. De Kok, T. M. C. M.; Van Faassen, A.; Glinghammar, B.; Pachen, D. M. F. A.; Rafter, J. J.; Baeten, C. G. M. I.; Engels, L. G. J. B.; Kleinjans, J. C. S. Dig. Dis. Sci. 1999, 44, 2218. https://doi.org/10.1023/A:1026644418142
  8. Lee, B. L.; New, A. L.; Ong, C. N. J. Chromatogr. B 1997, 704, 35. https://doi.org/10.1016/S0378-4347(97)00443-X
  9. Roda, A.; Piazza, F.; Baraldini, M. J. Chromatogr. B Biomed. Sci. Appl. 1998, 717, 263. https://doi.org/10.1016/S0378-4347(98)00174-1
  10. Nobilis, M.; Pour, M.; Kunes, J.; Kopecky, J.; Kvetina, J.; Svoboda, Z.; Sladkova, K.; Vortel, J. J. Pharm. Biomed. Anal. 2001, 24, 937. https://doi.org/10.1016/S0731-7085(00)00563-X
  11. You, J. M.; Shi, Y. W.; Ming, Y. F.; Yu, Z. Y.; Yi, Y. J.; Liu, J. Y. Chromatographia 2004, 60, 527. https://doi.org/10.1365/s10337-004-0413-7
  12. Kong, W. J.; Jin, C.; Liu, W.; Xiao, X. H.; Zhao, Y. L.; Li, Z. L.; Zhang, P.; Li, X. F. Food Chemistry 2010, 120, 1193. https://doi.org/10.1016/j.foodchem.2009.11.064
  13. Kakiyama, G.; Hosoda, A.; Iida, T.; Fujimoto, Y.; Goto, T.; Mano, N.; Goto, J.; Nambara, T. J. Chromatogr. A 2006, 1125, 112. https://doi.org/10.1016/j.chroma.2006.05.037
  14. Bentayeb, K.; Batlle, R.; Sanchez, C.; Nerín, C.; Domeno, C. J. Chromatogr. B 2008, 869, 1. https://doi.org/10.1016/j.jchromb.2008.04.045
  15. Xiang, X. Q.; Han, Y.; Neuvonen, M.; Laitila, J.; Neuvonen, P. J.; Niemi, M. J. Chromatogr. B 2010, 878, 51. https://doi.org/10.1016/j.jchromb.2009.11.019
  16. Sergi, M.; Montesano, C.; Napoletano, S.; Pizzoni, D.; Manetti, C.; Colistro. F.; Curini, R.; Compagnone, D. Chromatographia 2012, 75, 479. https://doi.org/10.1007/s10337-012-2218-4
  17. Batta, A. K.; Salen, G.; Batta, P.; Tint, G. S.; Alberts, D. S.; Earnest, D. L. J.Chromatogr. B 2002, 775, 153. https://doi.org/10.1016/S1570-0232(02)00289-1
  18. Fausa, O.; Shalhegg, B. A. Scand J. Gastroenterol 1974, 9, 249.
  19. Gowda, G. A. N.; Ijare, O. B.; Somashekar, B. S.; Sharma, A.; Kapoor, V. K.; Khetrapal, C. L. Lipids 2006, 41, 591. https://doi.org/10.1007/s11745-006-5008-7
  20. Li, Y. S.; Liu, W. P.; Gao, X. F.; Chen, D. D.; Li, W. G. Biosens. Bioelectron. 2008, 24, 538. https://doi.org/10.1016/j.bios.2008.05.001
  21. Bartling, B.; Li, L.; Liu, C. C. Analyst 2009, 134, 973. https://doi.org/10.1039/b900266a
  22. Gultekin, A.; Ersoz, A.; Denizli, A.; Say, R. Sensor. Actuat. BChem. 2012, 162, 153. https://doi.org/10.1016/j.snb.2011.12.053
  23. Psarellis, I. M.; Deftereos, N. T.; Sarantonis, E. G.; Calokerinos, A. C. Anal. Chim. Acta 1994, 294, 27. https://doi.org/10.1016/0003-2670(94)85042-9
  24. Wang, T.; Wang, X. L.; Jiang, C. Q. J. Clin. Lab. Anal. 2007, 21, 207. https://doi.org/10.1002/jcla.20137
  25. Collins, B. J.; Watt, P. C. H.; O'Reilly, T.; McFarland, R. J.; Love, A. H. J. Clin. Pathol. 1984, 37, 313. https://doi.org/10.1136/jcp.37.3.313
  26. Schoelmerich, J.; Roda, A.; Deluca, M. Method. Enzymol. 1986, 133, 215. https://doi.org/10.1016/0076-6879(86)33068-4
  27. Yuan, J. L.; Wang, G. L.; Majima, K.; Matsumoto, K. Anal. Chem. 2001, 73, 1869. https://doi.org/10.1021/ac0013305
  28. Zhao, F.; Qi, Y.; Xiong, W. Bull. Korean Chem. Soc. 2012, 33, 204. https://doi.org/10.5012/bkcs.2012.33.1.204
  29. Bunzli, C.; Piguet, C. Chem. Soc. Rev. 2005, 34, 1048. https://doi.org/10.1039/b406082m
  30. Kamruzzaman, M.; Alam, Al-M.; Lee, S. H.; Kim, Y. H.; Kim, S. H.; Kim, G. M. Bull. Korean Chem. Soc. 2012, 33, 105. https://doi.org/10.5012/bkcs.2012.33.1.105
  31. Wang, L.; Guo, C. C.; Chu, Z. J.; Jiang, W. J. Lumin. 2009, 129, 90. https://doi.org/10.1016/j.jlumin.2008.08.006

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