Citation: Zhang Yahui, Liu Gang, Xu Hui. Progress in Electrochemical Methods for Chiral Recognition[J]. Chemistry, ;2017, 80(8): 699-707. shu

Progress in Electrochemical Methods for Chiral Recognition

School of Chemistry and Materials Science, Ludong University, Yantai 264025

Corresponding author: Xu Hui, xuhui235@163.com
Received Date: 9 December 2016
Accepted Date: 18 April 2017

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At present, chromatographic, spectroscopic, microscopic and electrochemical methods have been successfully used in the qualitative and quantitative study of separation and analysis of chiral compounds, and many significant progresses have been made over the past years. Among these approaches, electrochemical methods have attracted a lot of attention owing to the advantages of high sensitivity, simple instrument and fast detection. In this article, the research progress of electrochemical method for chiral recognition was reviewed, and the prospects of this field were also put forward.
- Electrochemical sensor,
- Chiral recognition
1. [1]
2. [2]
3. [3]
4. [4]
  T Q Yan, C Orihuela. J. Chromatogr. A, 2007, 1156(1~2):220~227.
5. [5]
  Y Matsuoka, N Kanda, Y M Lee et al. J. Memb. Sci., 2006, 280(s 1~2):116~123.
6. [6]
  H Tabani, M Mahyari, A Sahragard et al. Electrophoresis, 2015, 36(2):305~311.
7. [7]
  I M Mavridis, K Yannakopoulou. Int. J. Pharm., 2015, 492(1~2):275~290.
8. [8]
  Y Ma, H Zhang, Z U Rahman et al. Electrophoresis, 2014, 35(19):2772~2777.
9. [9]
  I Ali, M M Sanagi, H Y Aboul-Enein. Electrophoresis, 2014, 35(7):926~936.
10. [10]
  M Dabrowska, M Starek. Food. Chem., 2014, 142(3):220~232.
11. [11]
  E A Christodoulou. Curr. Org. Chem., 2010, 14(19):2337~2347.
12. [12]
  L Challier, F Mavré, J Moreau et al. Anal. Chem., 2012, 84(12):5415~5420.
13. [13]
  H Y Xie, Z R Wang, Z F Fu. J. Pharm. Anal., 2014, 4(6):412~416.
14. [14]
  Z Jie, Y Wang, L Yun et al. Anal.Chim.Acta, 2015, 868:73~79.
15. [15]
  P Nowak, M Garnysz, M P Mitoraj et al. J. Chromatogr. A, 2015, 1377:106~113.
16. [16]
  L Libo, L Xia, L Quan et al. Talanta, 2015, 142:28~34.
17. [17]
  G Neumajer, T Sohajda, A Darcsi et al. J. Pharm. Biomed. Anal, 2012, 62(62):42~47.
18. [18]
  Z I Szabó, G Tóth, G V lgyi et al. J. Pharm. Biomed. Anal., 2015, 30(4):359~360.
19. [19]
  I Ali, D R Sahoo, Z A Alothman et al. J. Chromatogr. A, 2015, 1406:201~209.
20. [20]
  T Sheng, B Qin, C Wei et al. J. Chromatogr. A, 2016, 1440:112~122.
21. [21]
  C Lin, J Fan, W N Liu et al. J. Pharm. Biomed. Anal., 2014, 98(10):221~227.
22. [22]
  V Kannappan, S S Mannemala. J. Pharm. Biomed. Anal., 2015, 120(2):270~278.
23. [23]
24. [24]
  M H Xu, J Lin, Q S Hu et al. J. Am. Chem. Soc., 2002, 124(47):14239~14246.
25. [25]
  H L Liu, P Qian, Y D Wu et al. Angew. Chem. Int. Ed., 2010, 49(3):612~616.
26. [26]
  S O Fakayode, I M Swamidoss, M A Busch et al. Talanta, 2005, 65(4):838~845.
27. [27]
  C Guo, R D Shah, R K Dukor et al. Anal. Chem., 2004, 76(76):6956~6966.
28. [28]
  W A Tao, R G Cooks. Anal. Chem., 2003, (1):25A~31A.
29. [29]
  A Kühnle, T R Linderoth, B Hammer et al. Nature, 2002, 415(6874):891~893.
30. [30]
  W S Kim, H Y Lee, T Kawai et al. Sens. Actuat. B, 2008, 129(1):126~133.
31. [31]
32. [32]
33. [33]
  J Huang, Z Wei, J Chen et al. Sens. Actuat. B, 2008, 134(2):573~578.
34. [34]
  E Granot, R Tel Vered, O Lioubashevski et al. Adv. Funct. Mater., 2008, 18(3):478~484.
35. [35]
36. [36]
37. [37]
  J Damen, D C Neckers. Tetrahed. Lett., 1980, 21(20):1913~1916.
38. [38]
  L Andersson, B Sellergren, K Mosbach. Tetrahed. Lett., 1984, 25(45):5211~5214.
39. [39]
  S Fireman-Shoresh, I Turyan, D Mandler et al. Langmuir, 2005, 21(17):7842~7847.
40. [40]
  S Sekine, Y Watanabe, Y Yoshimi et al. Sens. Actuat. B, 2007, 127(2):512~517.
41. [41]
  H Liao, Z Zhang, L Nie et al. J. Biochem. Bioph. Meth., 2004, 59(1):75~87.
42. [42]
  B B Prasad, S Srivastava, K Tiwari et al. Mater. Sci. Eng:C, 2009, 29(6):1781~1789.
43. [43]
  B B Prasad, D Kumar, R Madhuri et al. Biosens. Bioelectron., 2011, 28(1):117~126.
44. [44]
  B B Prasad, I Pandey. Sens. Actuat. B, 2013, 186(18):407~416.
45. [45]
  T Sajini, B Mathew. J. Surf. Sci. Technol., 2014, 30(3~4):201~208.
46. [46]
  B C Iacob, E Bodoki, A Florea et al. Anal. Chem., 2015, 87(5):2755~2763.
47. [47]
48. [48]
  B Deore, Z Chen, T Nagaoka. Anal. Chem., 2000, 72(17):3989~3994.
49. [49]
  V Syritski, J Reut, A Menaker et al. Electrochim. Acta, 2008, 53(6):2729~2736.
50. [50]
  I Basozabal, A Gómez-Caballero, N Unceta et al. Electrochim. Acta, 2011, 58(1):729~735.
51. [51]
  B B Prasad, I Pandey, A Srivastava et al. Sens. Actuat. B, 2013, 176(6):863~874.
52. [52]
  J Gu, H Dai, Y Kong et al. Syn. Met., 2016, 222:137~143.
53. [53]
  A Rubinstein. Drug Dev. Res., 2000, 50(3~4):435~439.
54. [54]
  B C Son, K Park, S H Song et al. Korean J. Chem. Eng., 2004, 21(6):1168~1172.
55. [55]
  S Wang, Y Dai, J Wu et al. J. Chromatogr. A, 2013, 1277:84~92.
56. [56]
  T Jian, Y Lu, Y Wang et al. Talanta, 2014, 128:460~465.
57. [57]
  M Monier, D M Ayad, Y Wei et al. Biochem. Eng. J, 2010, 51(3):140~146.
58. [58]
  J H Kim, J Jegal, J H Kim et al. J. Appl. Polym. Sci, 2003, 89(11):3046~3051.
59. [59]
  Y Wang, S Zhu, Y Liao et al. J. Polym. Res., 2014, 21(12):1~7.
60. [60]
  F Ortega-Caballero, C Rousseau, B Christensen et al. J. Am. Chem. Soc., 2005, 127(10):3238~3239.
61. [61]
62. [62]
63. [63]
  Y Tao, J Dai, Y Kong et al. Anal. Chem., 2014, 86(5):2633~2639.
64. [64]
  W Feng, C Liu, S Lu et al. Microchim. Acta, 2014, 181(5~6):501~509.
65. [65]
  Y Tao, X Gu, L Deng et al. J. Phys. Chem. C, 2015, 119(15):8183~8190.
66. [66]
  Y Chen, Y Huang, D Guo et al. J. Solid. State. Electrochem., 2014, 18(12):3463~3469.
67. [67]
  J Xu, Q Wang, C Xuan et al. Electroanalysis, 2016, 28(4):868~873.
68. [68]
  K J Huang, C X Xu, W Z Xie et al. Colloid. Surf. B, 2009, 74(1):167~171.
69. [69]
  Y Fan, J H Liu, H T Lu et al. Microchim. Acta, 2011, 173(1~2):241~247.
70. [70]
  Y Tao, X Gu, B Yang et al. Anal. Chem., 2017, 89(3):1900~1906.
71. [71]
  X Gu, Y Tao, Y Pan et al. Anal. Chem., 2015, 87(18):9481~9486.
72. [72]
  J Ou, Y Tao, J Xue et al. Electrochem. Commun., 2015, 57:5~9.
73. [73]
  L Y Yu, Q Liu, X W Wu et al. RSC Adv., 2015, 5(119):98020~98025.
74. [74]
75. [75]
  Y Wang, Q Han, Q Zhang et al. J. Solid State Electrochem., 2013, 17(3):627~633.
76. [76]
  Y Fu, Q Chen, J Zhou et al. Anal. Biochem., 2012, 421(1):103~107.
77. [77]
  E Zor, I H Patir, H Bingol et al. Biosens. Bioelectron., 2013, 42:321~325.
78. [78]
  B Kasinathan, R M Zawawi, N L Hong. J. Appl. Electrochem., 2015, 45(10):1085~1099.
79. [79]
  M Trojanowicz. Electrochem. Commun., 2014, 38(1):47~52.
80. [80]
  B Wei, N Liu, J Zhang et al. Anal. Chem., 2015, 87(4):2058~2062.
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