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Progress in Chemistry 2022, Vol. 34 Issue (5): 1136-1152 DOI: 10.7536/PC210537 Previous Articles   Next Articles

• Review •

The Fluorescent Probe for Detecting Glutathione

Fanyong Yan(), Yueyan Zang, Yuyang Zhang, Xiang Li, Ruijie Wang, Zhentong Lu   

  1. State Key Laboratory of Separation Membrane and Membrane Processes/National International Joint Research Center for Separation Membrane Science and Technology, School of Chemical Engineering and Technology, Tiangong University,Tianjin 300387, China
  • Received: Revised: Online: Published:
  • Contact: Fanyong Yan
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As the most abundant non-protein sulfhydryl compound in cells, glutathione plays an important role in maintaining normal physiological activities of the human body. Therefore, it is of great significance to be able to detect glutathione efficiently and sensitively. Fluorescent probe method has become the main method for the determination of glutathione in biological samples due to its advantages of convenient operation, excellent specificity and high sensitivity. The successful application of fluorescent probe method is also attributed to the special structural features of GSH, such as the nucleophilicity of sulfhydryl groups, reduction, high affinity for metal ions and the synergistic reaction ability of amino groups. Based on the classification of the probe structure, the fluorescent probes that can specifically detect glutathione in the past five years are divided into two categories: organic fluorescent probes and inorganic fluorescent probes. According to the structural characteristics of coumarin, BODIPY, rhodamine, cyanine, benzothiazole, naphthalimide, metal-organic framework, semiconductor quantum dots, carbon dots, metal nano, manganese dioxide nanosheet, graphene quantum dots, etc., organic fluorescent probes/inorganic fluorescent probes, the sensing mechanisms of Michael addition reaction, nucleophilic substitution, reduction reaction, and thiol-induced breakage reaction and complexation reaction of 2,4-dinitrobenzenesulfonyl are reviewed. Meanwhile, the design strategy, response model for glutathione and practical application of the probes are described and analyzed. We really look forward to providing a new idea for the construction of a new glutathione fluorescent probe.

Contents

1 Introduction

2 Organic small molecule fluorescent probes for GSH

2.1 Coumarin-based fluorescent probes for GSH

2.2 BODIPY-based fluorescent probes for GSH

2.3 Rhodamine-based fluorescent probes for GSH

2.4 Cyanine-based fluorescent probes for GSH

2.5 Benzothiazole-based fluorescent probes for GSH

2.6 Naphthalimide-based fluorescent probes for GSH

2.7 Metal-organic framework-based fluorescent probes for GSH

2.8 Other organic fluorescent probes for GSH

3 Inorganic nano-fluorescent probes for GSH

3.1 Semiconductor quantum dots for GSH

3.2 Carbon dots for GSH

3.3 Metal nano-fluorescent probes for GSH

3.4 Manganese dioxide nanosheet-based fluorescent probes for GSH

4 Conclusion and outlook

Key words: glutathione, fluorescent probe, detect, organic, inorganic
Fig. 1 The detection mechanism of Coumarin-based fluorescent probe based on Michael addition for GSH
Fig. 2 The detection mechanism of probe G-1 for GSH[20]
Fig. 3 The detection mechanism of probe G-2 and G-3for GSH[21,22]
Fig. 4 The detection mechanism of nucleophilic substituted glutathione-coumarin-based fluorescent probe
Fig. 5 The detection mechanism of probe G-4 and G-5 for GSH[23,24]
Fig. 6 The detection mechanism of probe G-6 for GSH[25]
Fig. 7 The detection mechanism of probe G-7 for GSH[26]
Fig. 8 The detection mechanism of Coumarin-based fluorescent probe based on demetallization reaction for GSH
Fig. 9 The detection mechanism of probe G-8 and G-9 for GSH[27,28]
Fig. 10 The detection mechanism of BODIPY-based fluorescent probe based on aromatic ring substitution for GSH
Fig. 11 The detection mechanism of probe G-10 for GSH[29]
Fig. 12 The detection mechanism of probe G-11 for GSH[30]
Fig. 13 The detection mechanism of probe G-12 for GSH[31]
Fig. 14 The detection mechanism of BODIPY-based fluorescent probe with sulfhydryl cutting as design strategy for GSH
Fig. 15 The detection mechanism of probe G-13 for GSH[32]
Fig. 16 The detection mechanism of probe G-14 for GSH[33]
Fig. 17 The detection mechanism of Rhodamine-based fluorescent probes for GSH
Fig. 18 The detection mechanism of probe G-15 for GSH[34]
Fig. 19 The detection mechanism of probe G-16 for GSH[35]
Fig. 20 The detection mechanism of probe G-17 and G-18 for GSH[36,37]
Fig. 21 The detection mechanism of Cyanine-based fluorescent probe with thioether bond and ether bond as recognition site for GSH
Fig. 22 The detection mechanism of probe G-19 and G-20 for GSH[38]
Fig. 23 The detection mechanism of probe G-21 for GSH[39]
Fig. 24 The detection mechanism of Benzothiazole-based fluorescent probes for GSH
Fig. 25 The detection mechanism of probe G-22 and G-23 for GSH[40,41]
Fig. 26 The detection mechanism of probe G-24 for GSH[42]
Fig. 27 The detection mechanism of Naphthalimide-based fluorescent probes for GSH
Fig. 28 The detection mechanism of probe G-25 and G-26 for GSH[43]
Fig. 29 The detection mechanism of probe G-27 for GSH[44]
Fig. 30 The detection mechanism of probe G-28 for GSH[45]
Fig. 31 The detection mechanism of probe G-29 for GSH[46]
Fig. 32 The detection mechanism of probe G-30 for GSH[47]
Fig. 33 The detection mechanism of probe G-31 for GSH[48]
Fig. 34 The detection mechanism of probe G-32 for GSH[49]
Fig. 35 The detection mechanism of probe G-33 for GSH[50]
Fig. 36 The detection mechanism of probe based on disulfide bond-mercaptan exchange reactions for GSH
Fig. 37 The detection mechanism of probe G-35 for GSH[52]
Fig. 38 The detection mechanism of probe G-36 for GSH[53]
Fig. 39 The detection mechanism of probe G-37 for GSH[54]
Fig. 40 The detection mechanism of probe G-38 for GSH[55]
Fig. 41 The detection mechanism of probe G-40 for GSH[57]
Fig. 42 The detection mechanism of probe G-41 for GSH[58]
Fig. 43 The detection mechanism of probe G-45 for GSH[63]
Fig. 44 The detection mechanism of probe G-46 for GSH[64]
Fig. 45 The detection mechanism of probe G-49 for GSH[66,67]
Fig. 46 The detection mechanism of probe G-51 for GSH[69]
Fig. 47 The detection mechanism of probe G-52 for GSH[70]
Fig. 48 The detection mechanism of probe G-53 for GSH[71]
Fig. 49 The detection mechanism of probe G-55 for GSH[73]
Table 1 Comparison of GSH Probe Sensing Performance and Applications
Probe Fluorophore Detection limit (μmol·L-1) Detection range (μmol·L-1) Application ref
G-6 Coumarin 90 0~15 000 tumor margin recognition 25
G-9 Coumarin 0.12 / endogenous GSH 28
G-12 BODIPY 0.056 0~100 RAW 264.7 cells 31
G-14 BODIPY 1.07 / cervical cancer cell 33
G-16 Rhodamine 0.17 5~50 cell redox state 35
G-18 Rhodamine 0.07 1~3 human serum samples 37
G-20 Cyanine 0.33 0~100 identification and
sequence detection		 38
G-23 Benzothiazole 0.33 0~1000 living cells and zebrafish 41
G-27 Naphthalimide 0.10 2~150 tracer lysosomes 44
G-29 Metal-organic framework 97.5 500~10 000 clinical medicine 46
G-30 Metal-organic framework 0.57 1~70 human serum samples 47
G-38 Semiconductor quantum dots 0.92 1.95~104 indirect fluorometry 55
G-47 Carbon dots 0.076 5~32 H1299 cells 64
G-49 Carbon dots 1.53 10~2000 tumor targeted 67
G-50 Metal nano-fluorescent probes / 0~200 HeLa cells 68
G-55 Manganese dioxide nanosheet 0.22 0.5~20 pH and GSH dual sensing 73
[1]
Bjørklund G, Tinkov A A, Hosnedlová B, Kizek R, Ajsuvakova O P, Chirumbolo S, Skalnaya M G, Peana M, Dadar M, El-Ansary A, Qasem H, Adams J B, Aaseth J, Skalny A V. Free Radical. Bio. Med., 2020, 160: 149.

doi: S0891-5849(20)31153-9 pmid: 32745763
[2]
Lv H, Zhen C X, Liu J Y, Yang P F, Hu L J, Shang P. Oxidative Med. Cell. Longev., 2019, 2019: 1.
[3]
Tsugawa S, Noda Y, Tarumi R, Mimura Y, Yoshida K, Iwata Y, Elsalhy M, Kuromiya M, Kurose S, Masuda F, Morita S, Ogyu K, Plitman E, Wada M, Miyazaki T, Graff-Guerrero A, Mimura M, Nakajima S. J. Psychopharmacol., 2019, 33(10): 1199.

doi: 10.1177/0269881119845820 pmid: 31039654
[4]
Wang L X, Ahn Y J, Asmis R. Redox Biol., 2020, 31: 101410.

doi: 10.1016/j.redox.2019.101410
[5]
Li J, Kwon Y, Chung K S, Lim C S, Lee D, Yue Y K, Yoon J, Kim G, Nam S J, Chung Y W, Kim H M, Yin C X, Ryu J H, Yoon J,. Theranostics, 2018, 8(5): 1411.

doi: 10.7150/thno.22252
[6]
Hanko M, Švorc L’, Planková A, Mikuš P. Anal. Chimica Acta, 2019, 1062: 1.

doi: 10.1016/j.aca.2019.02.052
[7]
Nesakumar N, Berchmans S, Alwarappan S. Sens. Actuat. B: Chem., 2018, 264: 448.

doi: 10.1016/j.snb.2018.01.224
[8]
Liu T, Yue Y, Zhai Y, Guo Z, Zhao W, Yang X, Chen D, Yin C. Chem.Commun., 2021, 57(100), 13764.
[9]
Tian M, Liu Y, Jiang F L. Anal. Chem., 2020, 92(21): 14285.

doi: 10.1021/acs.analchem.0c03418
[10]
Xu Z Y, Qin T Y, Zhou X F, Wang L, Liu B. Trac Trends Anal. Chem., 2019, 121: 115672.

doi: 10.1016/j.trac.2019.115672
[11]
Shen B X, Zhu W, Zhi X, Qian Y. Talanta, 2020, 208: 120461.

doi: 10.1016/j.talanta.2019.120461
[12]
Wang T T. Master Dissertation of Lanzhou University, 2019.
(王婷婷. 兰州大学硕士论文, 2019.).
[13]
Chen D, Feng Y. Crit. Rev. Anal. Chem., 2022, 52(3): 649.

doi: 10.1080/10408347.2020.1819193
[14]
Chen L, Li J B, Chen D G. Chinese Journal of Organic Chemistry, 2021, 41(2): 611.

doi: 10.6023/cjoc202006046
(陈莉, 黎俊波, 陈杜刚. 有机化学, 2020, 41(2): 611.)
[15]
Lee S, Li J, Zhou X, Yin J, Yoon J. Coord. Chem. Rev., 2018, 366: 29.

doi: 10.1016/j.ccr.2018.03.021
[16]
Yang J J. Master Dissertation of Nanjing Normal University, 2017.
(杨敬敬. 南京师范大学硕士论文, 2017.).
[17]
Dai J N, Ma C G, Zhang P, Fu Y Q, Shen B X. Dyes Pigments, 2020, 177: 108321.

doi: 10.1016/j.dyepig.2020.108321
[18]
Zamir G,. Khan P O P. Microchem. J., 2020, 157: 105011.

doi: 10.1016/j.microc.2020.105011
[19]
Tian M, Feng Y L, Jiang L. Anal. Chem., 2020, 92: 14285.

doi: 10.1021/acs.analchem.0c03418
[20]
Chen Z Y, Sun Q, Yao Y H, Fan X X, Zhang W B, Qian J H. Biosens. Bioelectron., 2017, 91: 553.

doi: 10.1016/j.bios.2017.01.013
[21]
Khatun S, Yang S, Zhao T Q, Lu Y X. Anal. Chem., 2020, 92: 10989.

doi: 10.1021/acs.analchem.9b05175
[22]
Tian M, Yang M, Liu Y, Jiang F L. ACS Appl. Bio Mater., 2019, 2(10): 4503.

doi: 10.1021/acsabm.9b00642
[23]
Li Y, Liu W M, Zhang P P, Zhang H Y, Wu J S, Ge J C, Wang P F. Biosens. Bioelectron., 2017, 90: 117.

doi: 10.1016/j.bios.2016.11.021
[24]
Yin G X, Niu T T, Gan Y B, Yu T, Yin P, Chen H M, Zhang Y Y, Li H T, Yao S Z. Angew. Chem. Int. Ed., 2018, 57(18): 4991.

doi: 10.1002/anie.201800485
[25]
Zou Y X, Li M S, Xing Y L, Duan T T, Zhou X J, Yu F B. ACS Sens., 2020, 5(1): 242.

doi: 10.1021/acssensors.9b02118
[26]
Yang Y, Wang Y Z, Feng Y, Cao C, Song X R, Zhang G L, Liu W S. J. Mater. Chem. B, 2019, 7(48): 7723.

doi: 10.1039/c9tb01645g pmid: 31746929
[27]
He G J, Li J, Wang Z Q, Liu C X, Liu X L, Ji L G, Xie C Y, Wang Q Z. Tetrahedron, 2017, 73(3): 272.

doi: 10.1016/j.tet.2016.12.012
[28]
He G J, Hua X B, Yang N, Li L L, Xu J H, Yang L L, Wang Q Z, Ji L G. Bioorg. Chem., 2019, 91: 103176.

doi: 10.1016/j.bioorg.2019.103176
[29]
Liu X L, Niu L Y, Chen Y Z, Zheng M L, Yang Y X, Yang Q Z. Org. Biomol. Chem., 2017, 15(5): 1072.

doi: 10.1039/C6OB02407F
[30]
Xiang H J, Tham H P, Nguyen M D, Fiona Phua S Z, Lim W Q, Liu J G, Zhao Y L. Chem. Commun., 2017, 53(37): 5220.

doi: 10.1039/C7CC01814B
[31]
Chen X X, Niu L Y, Shao N, Yang Q Z. Anal. Chem., 2019, 91(7): 4301.

doi: 10.1021/acs.analchem.9b00169
[32]
Wang F F, Fan X Y, Liu Y J, Gao T, Huang R, Jiang F L, Liu Y. Dyes Pigments, 2017, 145: 451.

doi: 10.1016/j.dyepig.2017.06.033
[33]
Liu X L, Niu L Y, Chen Y Z, Yang Y X, Yang Q Z. Biosens. Bioelectron., 2017, 90: 403.

doi: 10.1016/j.bios.2016.06.076
[34]
Ouyang J, Li C Y, Li Y F, Fei J J, Xu F, Li S J, Nie S X. Sens. Actuat. B: Chem., 2017, 240: 1165.

doi: 10.1016/j.snb.2016.09.074
[35]
Chen L Y, Park J S, Wu D, Kim C H, Yoon J. Sens. Actuat. B: Chem., 2018, 262: 306.

doi: 10.1016/j.snb.2018.02.023
[36]
Tong L L, Qian Y. J. Mater. Chem. B, 2018, 6(12): 1791.

doi: 10.1039/C7TB03199H
[37]
Yang X, Qian Y. J. Mater. Chem. B, 2018, 6(45): 7486.

doi: 10.1039/c8tb02309c pmid: 32254750
[38]
Lee D, Jeong K, Luo X, Kim G, Yang Y J, Chen X Q, Kim S, Yoon J. J. Mater. Chem. B, 2018, 6(17): 2541.

doi: 10.1039/C7TB01560G
[39]
He L W, Yang X L, Xu K X, Kong X Q, Lin W Y. Chem. Sci., 2017, 8(9): 6257.

doi: 10.1039/C7SC00423K
[40]
Chen S, Li H M, Hou P. Tetrahedron, 2017, 73(5): 589.

doi: 10.1016/j.tet.2016.12.049
[41]
Zheng Y L, Zhang H C, Tian D H, Duan D C, Dai F, Zhou B. Spectrochimica Acta A: Mol. Biomol. Spectrosc., 2020, 238: 118429.

doi: 10.1016/j.saa.2020.118429
[42]
Zhang S W, Wu D D, Jiang X, Xie F, Jia X D, Song X L, Yuan Y. Sens. Actuat. B: Chem., 2019, 290: 691.

doi: 10.1016/j.snb.2019.04.028
[43]
Liu G T, Han X, Zhang J, Xu Z Q, Liu S H, Zeng L T, Yin J. Dyes Pigments, 2018, 148: 292.

doi: 10.1016/j.dyepig.2017.09.016
[44]
Xu Z Q, Zhang M X, Li G J, Chen X Q, Liu S H, Chen H Y, Yin J. Dyes Pigments, 2019, 171: 107685.

doi: 10.1016/j.dyepig.2019.107685
[45]
Zong H C, Peng J Y, Li X R, Liu M, Hu Y Z, Li J, Zang Y, Li X, James T D. Chem. Commun., 2020, 56(4): 515.

doi: 10.1039/C9CC07753G
[46]
Zhu J Y, Xia T F, Cui Y J, Yang Y, Qian G D. J. Solid State Chem., 2019, 270: 317.

doi: 10.1016/j.jssc.2018.11.032
[47]
Wang N, Xie M G, Wang M K, Li Z X, Su X G. Talanta, 2020, 220: 121352.

doi: 10.1016/j.talanta.2020.121352
[48]
Jalili R, Khataee A, Rashidi M R, Luque R. Sens. Actuat. B: Chem., 2019, 297: 126775.

doi: 10.1016/j.snb.2019.126775
[49]
Cui M M, Li W T, Wang L Y, Gong L S, Tang H, Cao D R. J. Mater. Chem. C, 2019, 7(13): 3779.

doi: 10.1039/C8TC05360J
[50]
Hou P, Sun J W, Wang H J, Liu L, Zou L W, Chen S. Sens. Actuat. B: Chem., 2020, 304: 127244.

doi: 10.1016/j.snb.2019.127244
[51]
Chen J, Ma Q, Hu X Y, Gao Y J, Yan X Y, Qin D D, Lu X Q. Sens. Actuat. B: Chem., 2018, 254: 475.

doi: 10.1016/j.snb.2017.07.125
[52]
Hu L L, Wei X, Meng J, Wang X Y, Chen X W, Wang J H. Sens. Actuat. B: Chem., 2018, 268: 264.

doi: 10.1016/j.snb.2018.04.114
[53]
Zheng Z M, Huyan Y C, Li H J, Sun S G, Xu Y Q. Sens. Actuat. B: Chem., 2019, 301: 127065.

doi: 10.1016/j.snb.2019.127065
[54]
Sheng Z, Chen L G. Anal. Bioanal. Chem., 2017, 409(26): 6081.

doi: 10.1007/s00216-017-0541-1 pmid: 28799001
[55]
Amouzegar Z, Afkhami A, Madrakian T. Microchimica Acta, 2019, 186(3): 205.

doi: 10.1007/s00604-019-3310-3
[56]
Sun J L, Liu F, Yu W Q, Jiang Q Y, Hu J L, Liu Y H, Wang F A, Liu X Q. Nanoscale, 2019, 11(11): 5014.

doi: 10.1039/C8NR09801H
[57]
Yang R, Guo X F, Jia L H, Zhang Y. Microchimica Acta, 2017, 184(4): 1143.

doi: 10.1007/s00604-017-2076-8
[58]
Pan J H, Zheng Z Y, Yang J Y, Wu Y Y, Lu F S, Chen Y W, Gao W H. Talanta, 2017, 166: 1.

doi: 10.1016/j.talanta.2017.01.033
[59]
Huang T, Song X, Cai M, Zhang D, Duan L. Mater Today Energy, 2021, 21: 100705.
[60]
Yan F Y, Ye Q H, Xu J X, He J J, Chen L, Zhou X G. Sens. Actuat. B: Chem., 2017, 251: 753.

doi: 10.1016/j.snb.2017.05.050
[61]
Wu D, Li G L, Chen X F, Qiu N N, Shi X X, Chen G, Sun Z W, You J M, Wu Y N. Microchimica Acta, 2017, 184(7): 1923.

doi: 10.1007/s00604-017-2187-2
[62]
Jia R N, Jin K F, Zhang J M, Zheng X J, Wang S, Zhang J. Sens. Actuat. B: Chem., 2020, 321: 128506.

doi: 10.1016/j.snb.2020.128506
[63]
Wang J P, Wang X Y, Pan X H, Pan W, Li Y, Liang X Y, Sun X B. Microchimica Acta, 2020, 187(6): 330.

doi: 10.1007/s00604-020-04311-w
[64]
Li L, Shi L, Jia J, Eltayeb O, Lu W, Tang Y, Dong C, Shuang S. ACS Appl. Mater. Inter., 2020, 12 (16): 18250.

doi: 10.1021/acsami.0c00283
[65]
Yan F, Bai Z, Zu F, Zhang Y, Sun X, Ma T, Chen L. Microchim Acta, 2019, 186 (2): 113.

doi: 10.1007/s00604-018-3221-8
[66]
Wang Q, Li L F, Wang X D, Dong C, Shuang S M. Talanta, 2020, 219: 121180.

doi: 10.1016/j.talanta.2020.121180
[67]
Guo Y X, Zhang X D, Wu F G. J. Colloid Interface Sci., 2018, 530: 511.

doi: 10.1016/j.jcis.2018.06.041
[68]
Li Q J, Sun A N, Si Y S, Chen M, Wu L M. Chem. Mater., 2017, 29(16): 6758.

doi: 10.1021/acs.chemmater.7b01649
[69]
Li J F, Huang P C, Wu F Y. Sens. Actuat. B: Chem., 2017, 240: 553.

doi: 10.1016/j.snb.2016.09.018
[70]
Ji D Y, Meng H M, Ge J, Zhang L, Wang H Q, Bai D M, Li J J, Qu L B, Li Z H. Microchimica Acta, 2017, 184(9): 3325.

doi: 10.1007/s00604-017-2343-8
[71]
Yao C P, Wang J, Zheng A X, Wu L J, Zhang X L, Liu X L. Sens. Actuat. B: Chem., 2017, 252: 30.

doi: 10.1016/j.snb.2017.05.136
[72]
Zhang X B, Kong R M, Tan Q Q, Qu F, Qu F L. Talanta, 2017, 169: 1.

doi: 10.1016/j.talanta.2017.03.050
[73]
Fu L, Du Y L, Zhang Z X, Sun H Y, Zheng A X, Liu X L. Microchimica Acta, 2019, 186(8): 491.

doi: 10.1007/s00604-019-3590-7
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