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Journal of Food Quality
Volume 2018, Article ID 6302345, 9 pages
https://doi.org/10.1155/2018/6302345
Research Article

Label-Free Fluorescent Determination of Sunset Yellow in Soft Drinks Based on an Indicator-Displacement Assay

School of Chemical Science and Technology, Yunnan University, Kunming 650091, China

Correspondence should be addressed to Can-Peng Li; moc.anis@4791pppcl

Received 16 June 2017; Revised 12 September 2017; Accepted 22 October 2017; Published 8 February 2018

Academic Editor: Yuxia Fan

Copyright © 2018 Shilian Wu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. L. Ji, Q. Cheng, K. Wu, and X. Yang, “Cu-BTC frameworks-based electrochemical sensing platform for rapid and simple determination of Sunset yellow and Tartrazine,” Sensors and Actuators B: Chemical, vol. 231, pp. 12–17, 2016. View at Publisher · View at Google Scholar · View at Scopus
  2. L. Zhao, F. Zhao, and B. Zeng, “Preparation and application of sunset yellow imprinted ionic liquid polymer - Ionic liquid functionalized graphene composite film coated glassy carbon electrodes,” Electrochimica Acta, vol. 115, pp. 247–254, 2014. View at Publisher · View at Google Scholar · View at Scopus
  3. K. S. Minioti, C. F. Sakellariou, and N. S. Thomaidis, “Determination of 13 synthetic food colorants in water-soluble foods by reversed-phase high-performance liquid chromatography coupled with diode-array detector,” Analytica Chimica Acta, vol. 583, no. 1, pp. 103–110, 2007. View at Publisher · View at Google Scholar · View at Scopus
  4. M. Ma, X. Luo, B. Chen, S. Su, and S. Yao, “Simultaneous determination of water-soluble and fat-soluble synthetic colorants in foodstuff by high-performance liquid chromatography-diode array detection-electrospray mass spectrometry,” Journal of Chromatography A, vol. 1103, no. 1, pp. 170–176, 2006. View at Publisher · View at Google Scholar · View at Scopus
  5. M. Ryvolová, P. Táborský, P. Vrábel, P. Krásenský, and J. Preisler, “Sensitive determination of erythrosine and other red food colorants using capillary electrophoresis with laser-induced fluorescence detection,” Journal of Chromatography A, vol. 1141, no. 2, pp. 206–211, 2007. View at Publisher · View at Google Scholar · View at Scopus
  6. R. Sahraei, A. Farmany, and S. S. Mortazavi, “A nanosilver-based spectrophotometry method for sensitive determination of tartrazine in food samples,” Food Chemistry, vol. 138, no. 2-3, pp. 1239–1242, 2013. View at Publisher · View at Google Scholar · View at Scopus
  7. L. You, D. Zha, and E. V. Anslyn, “Recent Advances in Supramolecular Analytical Chemistry Using Optical Sensing,” Chemical Reviews, vol. 115, no. 15, pp. 7840–7892, 2015. View at Publisher · View at Google Scholar · View at Scopus
  8. F. Biedermann, V. D. Uzunova, O. A. Scherman, W. M. Nau, and A. De Simone, “Release of high-energy water as an essential driving force for the high-affinity binding of cucurbit[n]urils,” Journal of the American Chemical Society, vol. 134, no. 37, pp. 15318–15323, 2012. View at Publisher · View at Google Scholar · View at Scopus
  9. F. Biedermann, M. Vendruscolo, O. A. Scherman, A. De Simone, and W. M. Nau, “Cucurbit[8]uril and blue-box: High-energy water release overwhelms electrostatic interactions,” Journal of the American Chemical Society, vol. 135, no. 39, pp. 14879–14888, 2013. View at Publisher · View at Google Scholar · View at Scopus
  10. G. Ghale and W. M. Nau, “Dynamically analyte-responsive macrocyclic host-fluorophore systems,” Accounts of Chemical Research, vol. 47, no. 7, pp. 2150–2159, 2014. View at Publisher · View at Google Scholar · View at Scopus
  11. X.-L. Ni, X. Xiao, H. Cong et al., “Cucurbit[n]uril-based coordination chemistry: From simple coordination complexes to novel poly-dimensional coordination polymers,” Chemical Society Reviews, vol. 42, no. 24, pp. 9480–9508, 2013. View at Publisher · View at Google Scholar · View at Scopus
  12. K. I. Assaf and W. M. Nau, “Cucurbiturils: from synthesis to high-affinity binding and catalysis,” Chemical Society Reviews, vol. 44, no. 2, pp. 394–418, 2015. View at Publisher · View at Google Scholar
  13. G. Yu, K. Jie, and F. Huang, “Supramolecular Amphiphiles Based on Host-Guest Molecular Recognition Motifs,” Chemical Reviews, vol. 115, no. 15, pp. 7240–7303, 2015. View at Publisher · View at Google Scholar · View at Scopus
  14. D. Shetty, J. K. Khedkar, K. M. Park, and K. Kim, “Can we beat the biotin-avidin pair?: Cucurbit[7]uril-based ultrahigh affinity host-guest complexes and their applications,” Chemical Society Reviews, vol. 44, no. 23, pp. 8747–8761, 2015. View at Publisher · View at Google Scholar · View at Scopus
  15. X.-L. Ni, S. Chen, Y. Yang, and Z. Tao, “Facile Cucurbit[8]uril-Based Supramolecular Approach to Fabricate Tunable Luminescent Materials in Aqueous Solution,” Journal of the American Chemical Society, vol. 138, no. 19, pp. 6177–6183, 2016. View at Publisher · View at Google Scholar · View at Scopus
  16. S. J. Barrow, S. Kasera, M. J. Rowland, J. Del Barrio, and O. A. Scherman, “Cucurbituril-Based Molecular Recognition,” Chemical Reviews, vol. 115, no. 22, pp. 12320–12406, 2015. View at Publisher · View at Google Scholar · View at Scopus
  17. B. Gong, B.-K. Choi, J.-Y. Kim et al., “High Affinity Host-Guest FRET Pair for Single-Vesicle Content-Mixing Assay: Observation of Flickering Fusion Events,” Journal of the American Chemical Society, vol. 137, no. 28, pp. 8908–8911, 2015. View at Publisher · View at Google Scholar · View at Scopus
  18. T.-C. Lee, E. Kalenius, A. I. Lazar et al., “Chemistry inside molecular containers in the gas phase,” Nature Chemistry, vol. 5, no. 5, pp. 376–382, 2013. View at Publisher · View at Google Scholar · View at Scopus
  19. Y. Jiao, K. Liu, G. Wang, Y. Wang, and X. Zhang, “Supramolecular free radicals: Near-infrared organic materials with enhanced photothermal conversion,” Chemical Science, vol. 6, no. 7, pp. 3975–3980, 2015. View at Publisher · View at Google Scholar · View at Scopus
  20. L. C. Smith, D. G. Leach, B. E. Blaylock, O. A. Ali, and A. R. Urbach, “Sequence-Specific, Nanomolar Peptide Binding via Cucurbit[8]uril-Induced Folding and Inclusion of Neighboring Side Chains,” Journal of the American Chemical Society, vol. 137, no. 10, pp. 3663–3669, 2015. View at Publisher · View at Google Scholar · View at Scopus
  21. Q. Zhang and H. Tian, “Effective integrative supramolecular polymerization,” Angewandte Chemie International Edition, vol. 53, no. 40, pp. 10582–10584, 2014. View at Publisher · View at Google Scholar · View at Scopus
  22. M. del Pozo, L. Hernández, and C. Quintana, “A selective spectrofluorimetric method for carbendazim determination in oranges involving inclusion-complex formation with cucurbit[7]uril,” Talanta, vol. 81, no. 4-5, pp. 1542–1546, 2010. View at Publisher · View at Google Scholar · View at Scopus
  23. G.-X. Song, Q. Tang, Y. Huang et al., “A host-guest complexation based fluorescent probe for the detection of paraquat and diquat herbicides in aqueous solutions,” RSC Advances, vol. 5, no. 121, pp. 100316–100321, 2015. View at Publisher · View at Google Scholar · View at Scopus
  24. C. Li, J. Feng, and H. Ju, “Supramolecular interaction of labetalol with cucurbit[7]uril for its sensitive fluorescence detection,” Analyst, vol. 140, no. 1, pp. 230–235, 2015. View at Publisher · View at Google Scholar · View at Scopus
  25. N. Dong, L.-N. Cheng, X.-L. Wang, Q. Li, C.-Y. Dai, and Z. Tao, “Significant fluorescence enhancement by supramolecular complex formation between berberine chloride and cucurbit(n = 7)uril and its analytical application,” Talanta, vol. 84, no. 3, pp. 684–689, 2011. View at Publisher · View at Google Scholar · View at Scopus
  26. S. M. Ghoreishi, M. Behpour, and M. Golestaneh, “Simultaneous determination of Sunset yellow and Tartrazine in soft drinks using gold nanoparticles carbon paste electrode,” Food Chemistry, vol. 132, no. 1, pp. 637–641, 2012. View at Publisher · View at Google Scholar · View at Scopus
  27. M. Chao and X. Ma, “Convenient Electrochemical Determination of Sunset Yellow and Tartrazine in Food Samples Using a Poly(L-Phenylalanine)-Modified Glassy Carbon Electrode,” Food Analytical Methods, vol. 8, no. 1, pp. 130–138, 2015. View at Publisher · View at Google Scholar · View at Scopus
  28. R. A. Medeiros, B. C. Lourencao, R. C. Rocha-Filho, and O. Fatibello-Filho, “Flow injection simultaneous determination of synthetic colorants in food using multiple pulse amperometric detection with a boron-doped diamond electrode,” Talanta, vol. 99, pp. 883–889, 2012. View at Publisher · View at Google Scholar · View at Scopus
  29. M. R. Majidi, R. Fadakar Bajeh Baj, and A. Naseri, “Carbon Nanotube-Ionic Liquid (CNT-IL) Nanocamposite Modified Sol-Gel Derived Carbon-Ceramic Electrode for Simultaneous Determination of Sunset Yellow and Tartrazine in Food Samples,” Food Analytical Methods, vol. 6, no. 5, pp. 1388–1397, 2013. View at Publisher · View at Google Scholar · View at Scopus
  30. L. Yu, M. Shi, X. Yue, and L. Qu, “A novel and sensitive hexadecyltrimethyl ammonium bromide functionalized graphene supported platinum nanoparticles composite modified glassy carbon electrode for determination of sunset yellow in soft drinks,” Sensors and Actuators B: Chemical, vol. 209, pp. 1–8, 2015. View at Publisher · View at Google Scholar · View at Scopus
  31. Y. Zhao, J. Gu, Y. C. Yang, H. Y. Zhu, R. Huang, and B. Jing, “Molecular selective binding of aliphatic oligopeptides by bridged bis(β-cyclodextrin)s with aromatic diamine linkers,” Journal of Molecular Structure, vol. 930, no. 1-3, pp. 72–77, 2009. View at Publisher · View at Google Scholar · View at Scopus