Citation: Hou Jiting, Li Kun, Qin Caiqin, Yu Xiaoqi. Review of the Small Molecular Fluorescent Sensors for Intracellular Reactive Oxygen Species[J]. Chinese Journal of Organic Chemistry, ;2018, 38(3): 612-628. doi: 10.6023/cjoc201709020 shu

Review of the Small Molecular Fluorescent Sensors for Intracellular Reactive Oxygen Species

  • Corresponding author: Qin Caiqin, qincq@hbeu.edu.cn Yu Xiaoqi, 
  • Received Date: 13 September 2017
    Revised Date: 17 October 2017
    Available Online: 31 March 2017

    Fund Project: the National Natrual Science Foundation of China 31371750Project supported by the National Natrual Science Foundation of China (No. 31371750)

Figures(17)

  • Among the numerous bio-active species which are involved in the various chemical reactions in our body, reactive oxygen species (ROS) are a class of important biological species, which are oxidative. ROS can maintain the intracellular redox balance and are tightly related with the cell growth and death. Hence, the fluorescence detection of intracellular ROS has attracted wide attention. However, owining to the inherent features of ROS, such as the short lifetime and high reactivity, fluorescence analysis of ROS is always faced with some problems, like low selectivity and side reactions. Herein, the development of small molecular fluorescent probes for intracellular ROS over the past decade is summarized, and the design mechanisms and bio-applications of these probes are emphasized.
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    1. [1]

      Suh, Y. A.; Arnold, R. S.; Lassegue, B.; Shi, J.; Xu, X.; Sorescu, D.; Chung, A. B.; Griendling, K. K.; Lambeth, J. D. Nature 1999, 401, 79.  doi: 10.1038/43459

    2. [2]

      Koh, C. H.; Whiteman, M.; Li, Q. X.; Halliwell, B.; Jenner, A. M.; Wong, B. S.; Laughton, K. M.; Wenk, M.; Masters, C. L.; Beart, P. M.; Bernard, O.; Cheung, N. S. J. Neurochem. 2006, 98, 1278.  doi: 10.1111/jnc.2006.98.issue-4

    3. [3]

      Rhee, S. G. Science 2006, 312, 1882.  doi: 10.1126/science.1130481

    4. [4]

      Dickinson, B. C.; Srikun, D.; Chang, C. J. Curr. Opin. Chem. Biol. 2010, 14, 50.  doi: 10.1016/j.cbpa.2009.10.014

    5. [5]

      Peteu, S. F.; Boukherroub, R.; Szunerits S. Biosens. Bioelectron. 2014, 58, 359.  doi: 10.1016/j.bios.2014.02.025

    6. [6]

      Yamato, M.; Egashira, T.; Utsumi, H. Free Radical Biol. Med. 2003, 35, 1619.  doi: 10.1016/j.freeradbiomed.2003.09.013

    7. [7]

      de Silva, A. P.; Gunaratne, H. Q. N.; Gunnlaugsson, T.; Huxley, A. J. M.; McCoy, C. P.; Rademacher, J. T.; Rice, T. E. Chem. Rev. 1997, 97, 1515.  doi: 10.1021/cr960386p

    8. [8]

      Berezin, M. Y.; Achilefu, S. Chem. Rev. 2010, 110, 2641.  doi: 10.1021/cr900343z

    9. [9]

      Que, E. L.; Domaille, D. W.; Chang, C. J. Chem. Rev. 2008, 108, 1517.  doi: 10.1021/cr078203u

    10. [10]

      Pradhan, T.; Jung, H. S.; Jang, J. H.; Kim, T. W.; Kang, C.; Kim, J. S. Chem. Soc. Rev. 2014, 43, 4684.  doi: 10.1039/C3CS60477B

    11. [11]

      Chen, X.; Tian, X.; Shin, I.; Yoon, J. Chem. Soc. Rev. 2011, 40, 4783.  doi: 10.1039/c1cs15037e

    12. [12]

      Chen, X.; Wang, F.; Hyun, J. Y.; Wei, T.; Qiang, J.; Ren, X.; Shin, I.; Yoon, J. Chem. Soc. Rev. 2016, 45, 2976.  doi: 10.1039/C6CS00192K

    13. [13]

      Nagano, T. J. Clin. Biochem. Nutr. 2009, 45, 111.  doi: 10.3164/jcbn.R09-66

    14. [14]

      Aratani, Y.; Koyama, H.; Nyui, S.-I.; Suzuki, K.; Kura, F.; Maeda, N. Infect. Immun. 1999, 67, 1828.
       

    15. [15]

      Kenmoku, S.; Urano, Y.; Kojima, H.; Nagano, T. J. Am. Chem. Soc. 2007, 129, 7313.  doi: 10.1021/ja068740g

    16. [16]

      Sun, Z.-N.; Liu, F.-Q.; Chen, Y.; Tam, P. K. H.; Yang, D. Org. Lett. 2008, 10, 2171.  doi: 10.1021/ol800507m

    17. [17]

      Hu, J. J.; Wong N.-K.; Gu, Q.; Bai, X.; Ye, S.; Yang, D. Org. Lett. 2014, 16, 3544.  doi: 10.1021/ol501496n

    18. [18]

      Chen, X.; Wang, X.; Wang, S.; Shi, W.; Wang, K.; Ma, H. Chem. Eur. J. 2008, 14, 4719.  doi: 10.1002/(ISSN)1521-3765

    19. [19]

      Lin, W.; Long, L.; Chen, B.; Tan, W. Chem.-Eur. J. 2009, 15, 2305.  doi: 10.1002/chem.v15:10

    20. [20]

      Yuan, L.; Lin, W.; Song, J.; Yang, Y. Chem. Commun. 2011, 47, 12691.  doi: 10.1039/c1cc15762k

    21. [21]

      Wang, B.; Li, P.; Yu, F.; Song, P.; Sun, X.; Yang, S.; Lou, Z.; Han, K. Chem. Commun. 2013, 49, 1014.  doi: 10.1039/C2CC37803E

    22. [22]

      Zhu, H.; Fan, J.; Wang, J.; Mu, H.; Peng, X. J. Am. Chem. Soc. 2014, 136, 12820.  doi: 10.1021/ja505988g

    23. [23]

      Hou, J.-T.; Wu, M.-Y.; Li, K.; Yang, J.; Yu, K.-K.; Xie, Y.-M.; Yu, X.-Q. Chem. Commun. 2014, 50, 8640.  doi: 10.1039/C4CC02673J

    24. [24]

      Hou, J.-T.; Li, K.; Yang, J.; Yu, K.-K.; Liao, Y.-X.; Ran, Y.-Z.; Liu, Y.-H.; Zhou, X.-D.; Yu, X.-Q. Chem. Commun. 2015, 51, 6781.  doi: 10.1039/C5CC01217A

    25. [25]

      Li, K.; Hou, J.-T.; Yang, J.; Yu, X.-Q. Chem. Commun. 2017, 53, 5539.  doi: 10.1039/C7CC01679D

    26. [26]

      Hu, J. J.; Wong, N.-K.; Lu, M.-Y.; Chen, X.; Ye, S.; Zhao, A. Q.; Gao, P.; Kao, R. Y.-T.; Shen, J.; Yang, D. Chem. Sci. 2016, 7, 2094.  doi: 10.1039/C5SC03855C

    27. [27]

      Yang, D.; Wang, H.-L.; Sun, Z.-N.; Chung, N.-W.; She, J.-G. J. Am. Chem. Soc. 2006, 128, 6004.  doi: 10.1021/ja0603756

    28. [28]

      Sun, Z.-N.; Wang, H.-L.; Liu, F.-Q.; Chen, Y.; Tam, P. K. H.; Yang, D. Org. Lett. 2009, 11, 1887.  doi: 10.1021/ol900279z

    29. [29]

      Peng, T.; Yang, D. Org. Lett. 2010, 12, 4932.  doi: 10.1021/ol102182j

    30. [30]

      Peng, T.; Wong, N.-K.; Chen, X.; Chan, Y.-K.; Ho, D. H.-H.; Sun, Z.; Hu, J. J.; Shen, J.; El-Nezami, H.; Yang, D. J. Am. Chem. Soc. 2014, 136, 11728.  doi: 10.1021/ja504624q

    31. [31]

      Ueno, T.; Urano, Y.; Kojima, H.; Nagano, T. J. Am. Chem. Soc. 2006, 128, 10640.  doi: 10.1021/ja061972v

    32. [32]

      Yu, F.; Li, P.; Li, G.; Zhao, G.; Chu, T.; Han, K. J. Am. Chem. Soc. 2011, 133, 11030.  doi: 10.1021/ja202582x

    33. [33]

      Xu, K.; Chen, H.; Tian, J.; Ding, B.; Xie, Y.; Qiang, M.; Tang, B. Chem. Commun. 2011, 47, 9468.  doi: 10.1039/c1cc12994e

    34. [34]

      Yu, F.; Li, P.; Wang, B.; Han, K. J. Am. Chem. Soc. 2013, 135, 7674.  doi: 10.1021/ja401360a

    35. [35]

      Oushiki, D.; Kojima, H.; Terai, T.; Arita, M.; Hanaoka, K.; Urano, Y.; Nagano, T. J. Am. Chem. Soc. 2010, 132, 2795.  doi: 10.1021/ja910090v

    36. [36]

      Hou, J.-T.; Yang, J.; Li, K.; Liao, Y.-X.; Yu, K.-K.; Xie, Y.-M.; Yu, X.-Q. Chem. Commun. 2014, 50, 9947.  doi: 10.1039/C4CC04192E

    37. [37]

      Cheng, D.; Pan, Y.; Wang, L.; Zeng, Z.; Yuan, L.; Zhang, X.; Chang, Y. T. J. Am. Chem. Soc. 2017, 139, 285.  doi: 10.1021/jacs.6b10508

    38. [38]

      Li, Y.; Xie, X.; Yang, X.; Li, M.; Jiao, X.; Sun, Y.; Wang, X.; Tang, B. Chem. Sci. 2017, 8, 4006.  doi: 10.1039/C7SC00303J

    39. [39]

      Chang, M. C. Y.; Pralle, A.; Isacoff, E. Y.; Chang, C. J. J. Am. Chem. Soc. 2004, 126, 15392.  doi: 10.1021/ja0441716

    40. [40]

      Albers, A. E.; Okreglak, V. S.; Chang, C. J. J. Am. Chem. Soc. 2006, 128, 9640.  doi: 10.1021/ja063308k

    41. [41]

      Miller, E. W.; Tulyathan, O.; Isacoff, E. Y.; Chang, C. J. Nat. Chem. Biol. 2007, 3, 263.  doi: 10.1038/nchembio871

    42. [42]

      Srikun, D.; Miller, E. W.; Domaille, D. W.; Chang, C. J. J. Am. Chem. Soc. 2008, 130, 4596.  doi: 10.1021/ja711480f

    43. [43]

      Dickinson, B. C.; Chang, C. J. J. Am. Chem. Soc. 2008, 130, 9638.  doi: 10.1021/ja802355u

    44. [44]

      Albers, A. E.; Dickinson, B. C.; Miller, E. W.; Chang, C. J. Bioorg. Med. Chem. Lett. 2008, 18, 5948.  doi: 10.1016/j.bmcl.2008.08.035

    45. [45]

      Chung, C.; Srikun, D.; Lim, C. S.; Chang, C. J.; Cho, B. R. Chem. Commun. 2011, 47, 9618.  doi: 10.1039/c1cc13583j

    46. [46]

      Masanta, G.; Heo, C. H.; Lim, C. S.; Bae, S. K.; Cho, B. R.; Kim, H. M. Chem. Commun. 2012, 48, 3518.  doi: 10.1039/c2cc00034b

    47. [47]

      Karton-Lifshin, N.; Segal, E.; Omer, L.; Portnoy, M.; Satchi-Fainaro, R.; Shabat, D. J. Am. Chem. Soc. 2011, 133, 10960.  doi: 10.1021/ja203145v

    48. [48]

      Xu, M.; Han, J.-M.; Zhang, Y.; Yang, X.; Zang, L. Chem. Commun. 2013, 49, 11779.  doi: 10.1039/c3cc47631f

    49. [49]

      Xu, M.; Han, J.-M.; Wang, C.; Yang, X.; Pei, J.; Zang, L. ACS Appl. Mater. Interfaces 2014, 6, 8708.  doi: 10.1021/am501502v

    50. [50]

      Li, G.; Zhu, D.; Liu, Q.; Xue, L.; Jiang, H. Org. Lett. 2013, 15, 924.  doi: 10.1021/ol4000845

    51. [51]

      Hu, F.; Huang, Y.; Zhang, G.; Zhao, R.; Zhang, D. Tetrahedron Lett. 2014, 55, 1471.  doi: 10.1016/j.tetlet.2014.01.056

    52. [52]

      Xu, J.; Li, Q.; Yue, Y.; Guo, Y.; Shao, S. Biosens. Bioelectron. 2014, 56, 58.  doi: 10.1016/j.bios.2013.12.065

    53. [53]

      Sawaki, Y.; Foote, C. S. J. Am. Chem. Soc. 1979, 101, 6292.  doi: 10.1021/ja00515a023

    54. [54]

      Abo, M.; Urano, Y.; Hanaoka, K.; Terai, T.; Komatsu, T.; Nagano, T. J. Am. Chem. Soc. 2011, 133, 10629.  doi: 10.1021/ja203521e

    55. [55]

      Zhang, K.-M.; Dou, W.; Li, P.-X.; Shen, R.; Ru, J.-X.; Liu, W.; Cui, Y.-M.; Chen, C.-Y.; Liu, W.-S.; Bai, D.-C. Biosens. Bioelectron. 2015, 64, 542.  doi: 10.1016/j.bios.2014.09.073

    56. [56]

      Yu, F.; Li, P.; Song, P.; Wang, B.; Zhao, J.; Han, K. Chem. Commun. 2012, 48, 4980.  doi: 10.1039/c2cc30985h

    57. [57]

      Liao, Y.-X.; Li, K.; Wu, M.-Y.; Wu, T.; Yu, X.-Q. Org. Biomol. Chem. 2014, 12, 3004.  doi: 10.1039/c4ob00206g

    58. [58]

      Dong, B.; Song, X.; Kong, X.; Wang, C.; Tang, Y.; Liu, Y.; Lin, W. Adv. Mater. 2016, 28, 8755.  doi: 10.1002/adma.201602939

    59. [59]

      Zhou, X.; Lesiak, L.; Lai, R.; Beck, J. R.; Zhao, J.; Elowsky, C. G.; Li, H.; Stains, C. I. Angew. Chem., Int. Ed. 2017, 56, 4197.  doi: 10.1002/anie.201612628

    60. [60]

      Tang, B.; Zhang, L.; Zhang, L. L. Anal. Biochem. 2004, 326, 176.  doi: 10.1016/j.ab.2003.11.023

    61. [61]

      Gao, J. J.; Xu, K. H.; Tang, B.; Yin, L. L.; Yang, G. W.; An, L. G. FEBS J. 2007, 274, 1725.  doi: 10.1111/j.1742-4658.2007.05720.x

    62. [62]

      Li, P.; Zhang, W.; Li, K.; Liu, X.; Xiao, H.; Zhang, W.; Tang, B. Anal. Chem. 2013, 85, 9877.  doi: 10.1021/ac402409m

    63. [63]

      Maeda, H.; Yamamoto, K.; Nomura, Y.; Kohno, I.; Hafsi, L.; Ueda, N.; Yoshida, S.; Fukuda, M.; Fukuyasu, Y.; Yamauchi, Y.; Itoh, N. J. Am. Chem. Soc. 2005, 127, 68.  doi: 10.1021/ja047018k

    64. [64]

      Maeda, H.; Yamamoto, K.; Kohno, I.; Hafsi, L.; Itoh, N.; Nakagawa, S.; Kanagawa, N.; Suzuki, K.; Uno, T. Chem.-Eur. J. 2007, 13, 1946.  doi: 10.1002/(ISSN)1521-3765

    65. [65]

      Zhang, W.; Li, P.; Yang, F.; Hu, X.; Sun, C.; Zhang, W.; Chen, D.; Tang, B. J. Am. Chem. Soc. 2013, 135, 14956.  doi: 10.1021/ja408524j

    66. [66]

      Zhang, J. J.; Li, C. W.; Zhang, R.; Zhang, F. Y.; Liu, W.; Liu, X. Y.; Lee, S. M. Y.; Zhang, H. X. Chem. Commun. 2016, 52, 2679.  doi: 10.1039/C5CC09976E

    67. [67]

      Xiao, H. B.; Liu, X.; Wu, C. C.; Wu, Y. H.; Li, P.; Guo, X. M.; Tang, B. Biosens. Bioelectron. 2017, 91, 449.  doi: 10.1016/j.bios.2016.12.068

    68. [68]

      Li, R. Q.; Mao, Z. Q.; Rong, L.; Wu, N.; Lei, Q.; Zhu, J. Y.; Zhuang, L.; Zhang, X. Z.; Liu, Z. H. Biosens. Bioelectron. 2017, 87, 73.  doi: 10.1016/j.bios.2016.08.008

    69. [69]

      Pou, S.; Huang, Y. I.; Bhan, A.; Bhadti, V. S.; Hosmane, R. S.; Wu, S. Y.; Cao, G. L.; Rosen, G. M. Anal. Biochem. 1993, 212, 85.  doi: 10.1006/abio.1993.1295

    70. [70]

      Yang, X.-F.; Guo, X.-Q. Anal. Chim. Acta 2001, 434, 169.  doi: 10.1016/S0003-2670(01)00821-2

    71. [71]

      Yang, X. F.; Guo, X. Q. Analyst 2001, 126, 1800.  doi: 10.1039/b103208a

    72. [72]

      Li, P.; Xie, T.; Duan, X.; Yu, F.; Wang, X.; Tang, B. Chem.-Eur. J. 2010, 16, 1834.  doi: 10.1002/chem.v16:6

    73. [73]

      Yuan, L.; Lin, W.; Song, J. Chem. Commun. 2010, 46, 7930.  doi: 10.1039/c0cc02390f

    74. [74]

      Wang, J. Y.; Liu, Z. R.; Ren, M. G.; Kong, X. Q.; Liu, K. Y.; Deng, B. B.; Lin, W. Y. Sens. Actuators, B 2016, 236, 60.  doi: 10.1016/j.snb.2016.04.163

    75. [75]

      Kim, M.; Ko, S.-K.; Kim, H.; Shin, I.; Tae, J. Chem. Commun. 2013, 49, 7959.  doi: 10.1039/c3cc44627a

    76. [76]

      Meng, L.; Wu, Y.; Yi, T. Chem. Commun. 2014, 50, 4843.  doi: 10.1039/C4CC00975D

    77. [77]

      Liu, F.; Du, J.; Song, D.; Xu, M. Y.; Sun, G. P. Chem. Commun. 2016, 52, 4636.  doi: 10.1039/C5CC10658C

    78. [78]

      Steinbeck, M. J.; Khan, A. U.; Karnovsky, M. J. J. Biol. Chem. 1992, 267, 13425.

    79. [79]

      Umezawa, N.; Tanaka, K.; Urano, Y.; Kikuchi, K.; Higuchi, T.; Nagano, T. Angew. Chem., Int. Ed. 1999, 38, 2899.  doi: 10.1002/(ISSN)1521-3773

    80. [80]

      Tanaka, K.; Miura, T.; Umezawa, N.; Urano, Y.; Kikuchi, K.; Higuchi, T.; Nagano, T. J. Am. Chem. Soc. 2001, 123, 2530.  doi: 10.1021/ja0035708

    81. [81]

      Kim, S.; Tachikawa, T.; Fujitsuka, M.; Majima, T. J. Am. Chem. Soc. 2014, 136, 11707.  doi: 10.1021/ja504279r

    82. [82]

      Xu, K.; Wang, L.; Qiang, M.; Wang, L.; Li, P.; Tang, B. Chem. Commun. 2011, 47, 7386.  doi: 10.1039/c1cc12473k

    83. [83]

      Aubry, J.-M.; Pierlot, C.; Rigaudy, J.; Schmidt, R. Acc. Chem. Res. 2003, 36, 668.  doi: 10.1021/ar010086g

    84. [84]

      Song, D.; Cho, S.; Han, Y.; You, Y.; Nam, W. Org. Lett. 2013, 15, 3582.  doi: 10.1021/ol401421r

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