Issue
Korean Journal of Chemical Engineering,
Vol.32, No.10, 2103-2108, 2015
Choline chloride-based deep eutectic solvents as additives for optimizing chromatographic behavior of caffeic acid
A series of deep eutectic solvents (DESs) were prepared using glycerol and choline chloride (ChCl), and Fourier transform infrared spectrometer (FT-IR) was used to analyze the spectra of glycerol, choline chloride and DESs based on glycerol and choline chloride. Then DESs were used as the additives of mobile phase to optimize chromatographic behavior of caffeic acid in high performance liquid chromatography (HPLC). A 17-run Box-Behnken design (BBD) was employed to evaluate effect of DESs as additives by analyzing the maximum theoretical plate number. Three factors, reaction temperature (60 oC, 80 oC, 100 oC), molar ratio of glycerol and choline chloride (2 : 1, 3 : 1, 4 : 1, n/n), and volume percent of additives (0.05%, 0.10%, 0.15%, v/v), were investigated in BBD. The optimum experiment condition was that of reaction temperature (80 oC), molar ratio of glycerol and ChCl (3 : 1, n/n), and volume percent of additive (0.10%, v/v). The mean chromatographic theoretical plate number of the caffeic acid this condition was 1567.5, and DESs as additives shorten the retention time and modify the chromatogram shape, proving DESs as additives for effective theoretical plate number and column efficiency in HPLC.
[References]
  1. Berner M, Krug D, Bihlmaier C, Vente A, Muller R, Bechthold A, J. Bacteriol., 188(7), 2666, 2006
  2. Celik S, Erdogan S, Tuzcu M, J. Pharmacol. Res., 60(4), 270, 2009
  3. Prasad NR, Karthikeyan A, Karthikeyan S, Bandugula VR, Mol. Cell. Biochem., 349, 11, 2011
  4. Maurya DK, Devasagayam TPA, Food Chem. Toxicol., 48(12), 3369, 2010
  5. Joyeux M, Lobstein A, Anton R, Mortier F, Planta. Med., 61(12), 6, 1995
  6. Miles EA, Zoubouli P, Calder PC, Phil D, Nutrition, 21, 389, 2005
  7. Bose JS, Gangan V, Jain SK, Manna SK, Clin. Immunol., 29, 90, 2009
  8. Michaluart P, Masferrer JL, Carothers AM, Subbaramaiah K, Zweifel BS, Koboldt C, Mestre JR, Grunberger D, Sacks PG, Tanabe T, Dannenberg AJ, Cancer. Res., 59, 2347, 1999
  9. Temerdashev ZA, Frolova NA, Kolychev IA, J. Anal. Chem., 66, 407, 2011
  10. Widmer TL, Laurent N, Eur. J. Plant. Path., 115, 377, 2006
  11. Song YH, Wang S, J. Anhui Med. Pharm., 11(16), 2, 2012
  12. Gupta S, Manohar CS, Struct. Saf., 26, 123, 2004
  13. Lobo HR, Singh BS, Shankarling GS, Green. Chem. Lett. Rev., 5, 487, 2012
  14. Maugeri Z, Maria PD, RSC Adv., 2, 421, 2012
  15. Durand E, Lecomte J, Villeneuve P, Eur. J. Lipid. Sci. Tech., 115, 379, 2013
  16. Tang B, Tian M, Row KH, J. Chromatogr. A, 1285, 22, 2013
  17. Weingartner H, Chem. Int. Ed. Eng., 47, 654, 2008
  18. Baldelli S, Acc. Chem. Res., 41, 421, 2008
  19. Bonhote P, Dias AP, Papageorgiou N, Kalyanasundaram K, Gratzel M, Inorg. Chem., 35(5), 1168, 1996
  20. Li JH, Shen YF, Zhang YJ, Liu Y, Chem. Commun., 3, 360, 2005
  21. Thomas DP, Foley JP, J. Chromatogr. A, 1205, 36, 2008
  22. Zhou MH, Xiao GM, Hong M, Res. Chem. Intermed., 38, 9, 2012
  23. Tittel G, Wagner H, Chem. Lab. Prac., 2, 343, 1986
  24. Tang BK, Row KH, Monatsh. Chem., 144, 1427, 2013
  25. Abbott AP, Bell TJ, Handa S, Stoddart B, Green Chem., 7, 705, 2005
  26. Abbott AP, Capper G, Davis DL, Tambyrajahv RKR, Chem. Commun., 1(70), 1, 2003
  27. Jimenez AE, Bermudez MD, Tribol. Lett., 40, 237, 2010
  28. Lobo HR, Singh BS, Shankarling GS, Green. Chem. Lett. Rev., 5, 487, 2012
  29. Shahbaz K, Mjalli FS, Hashim MA, AlNashef IM, Fluid Phase Equilib., 319, 48, 2012
  30. Abbott AP, Capper G, Davies DL, McKenzie KJ, Obi SU, J. Chem. Eng. Data, 51(4), 1280, 2006
  31. Ngo HL, LeCompte K, Hargens L, McEwen AB, Thermochim. Acta, 357, 97, 2000
  32. Box GEP, Wilson KB, J. Roy. Stat. Soc. B., 13, 1, 1951
  33. RenJie L, Carbohydr. Polym., 74, 858, 2008
  34. Varnalis AI, Brennan JG, MacDougall DB, Gilmour SG, J. Food Eng., 61(2), 153, 2004
  35. Zhu T, Row KH, J. Liq. Chromatogr. Relat. Technol., 34(12), 1036, 2011
  36. Xu H, Sun LP, Shi YZ, Wu YH, Zhang B, Zhao DQ, Biochem. Eng. J., 39, 66, 2008
  37. Sun Y, Li T, Yan J, Liu J, Carbohydr. Polym., 80, 242, 2010
  38. Wu Y, Cui SW, Tan JX, Food. Chem., 105, 1599, 2007
  39. Zhong K, Wang Q, Carbohydr. Polym., 80, 19, 2010
  40. Zhu T, Row KH, Sep. Sci. Technol., 48(10), 1510, 2013