A colorimetric and ratiometric fluorescent probe for selective detection and cellular imaging of glutathione

Biosensors and Bioelectronics

Volumn 72, Issue , 2015, Pages 275-281

  Xu, Chang ^a   Li, Hongda ^b   Yin, Bingzhu ^a  

^a YANBIAN UNIVERSITY   (China)

^b National Police University of China   (China)

Author keywords

Cell imaging; Chlorinated coumarinyl aldehyde; Cysteine; Glutathione detection; Homocysteine; Ratiometric fluorescent probe

Indexed keywords

ALDEHYDES; AMINO ACIDS; COLOR; COLORIMETRY; FLUORESCENCE; FLUORESCENCE SPECTROSCOPY; MOBILE SECURITY; PEPTIDES;

CELL IMAGING; CYSTEINE; FLUORESCENT PROBES; GLUTATHIONES; HOMOCYSTEINES;

PROBES;

ALDEHYDE; CHLORINATED COUMARINYL ALDEHYDE; COUMARIN DERIVATIVE; CYSTEINE; GLUTATHIONE; HOMOCYSTEINE; UNCLASSIFIED DRUG; COUMARIN; FLUORESCENT DYE;

ABSORPTION; ARTICLE; CELL MEMBRANE PERMEABILITY; CHEMICAL REACTION; COLORIMETRY; CONTROLLED STUDY; CYTOTOXICITY; FLUORESCENCE ANALYSIS; HUMAN; HUMAN CELL; MOLECULAR IMAGING; MOLECULAR PROBE; SENSITIVITY ANALYSIS; CHEMISTRY; FLUORESCENCE IMAGING; FLUORESCENCE MICROSCOPY; HELA CELL LINE; SPECTROFLUOROMETRY;

COLORIMETRY; COUMARINS; CYSTEINE; FLUORESCENT DYES; GLUTATHIONE; HELA CELLS; HOMOCYSTEINE; HUMANS; MICROSCOPY, FLUORESCENCE; OPTICAL IMAGING; SPECTROMETRY, FLUORESCENCE;

EID: 84929312052     PISSN: 09565663     EISSN: 18734235     Source Type: Journal    
DOI: 10.1016/j.bios.2015.05.030     Document Type: Article

References (46)

1. Chen.H., Zhao Q., Wu Y., Li F., Yang H., Yi T., Huang C. Inorg. Chem. 2007, 46:11075-11081.
2. Chen X., Zhou Y., Peng X., Yoon J. Chem. Soc. Rev. 2010, 39:2120-2135.
3. Dale T.J., Rebek J. J. Am. Chem. Soc. 2006, 128:4500-4501.
4. Feuster E.K., Glass T.E. J. Am. Chem. Soc. 2003, 125:16174-16175.
5. Fu L., Jiang F.-L., Fortin D., Harvey P.D., Liu Y. Chem. Commun. 2011, 47:5503-5505.
6. Guo Y., Wang H., Sun Y., Qu B. Chem. Commun. 2012, 48:3221-3223.
7. Guo Y., Yang X., Hakuna L., Barve A., Escobedo J.O., Lowry M., Strongin R.M. Sensors 2012, 12:5940-5950.
8. Guo Z., Nam S.W., Park S., Yoon J. Chem. Sci. 2012, 3:2760-2765.
9. Guy J., Caron K., Dufresne S., Michnick S.W., Skene W.G., Keillor J.W. J. Am. Chem. Soc. 2007, 129:11969-11977.
10. Hu R., Feng J., Hu D., Wang S., Li S., Li Y., Yang G. Angew. Chem. Int. Ed. 2010, 49:4915-4918.
11. Hwang C., Sinskey A.J., Lodish H.F. Science 1992, 257:1496-1502.
12. Jia M.-Y., Niu L.-Y., Zhang Y., Yang Q.-A., Tung C.-H., Guan Y.-F., Feng L. ACS Appl. Mater. Interfaces 2015, 7:5907-5914.
13. Jung H.S., Han J.H., Pradhan T., Kim S., Lee S.W., Sessler J.L., Kim T.W., Kang C., Kim J.S. Biomaterials 2012, 33:945-953.
14. Jung H.S., Pradhan T., Han J.H., Heo K.J., Lee J.H., Kang C., Kim J.S. Biomaterials 2012, 33:8495-8502.
15. Klockow J.L., Glass T.E. Org. Lett. 2013, 15:235-237.
16. Lee M.H., Han J.H., Kwon P.-S., Bhuniya S., Kim J.Y., Sessler J.L., Kang C., Kim J.S. J. Am. Chem. Soc. 2012, 134:1316-1322.
17. Li H., Jin L.-Y., Kan Y., Yin B. Sens. Actuators B: Chem. 2014, 196:546-554.
18. Lim S.-Y., Hong K.-H., Kim D.I., Kwon H., Kim H.-J. J. Am. Chem. Soc. 2014, 136:7018-7025.
19. Liu J., Sun Y.-Q., Zhang H., Huo Y., Shi Y., Guo W. Chem. Sci. 2014, 5:3183-3188.
20. Liu Y., Lv X., Liu J., Yuan-Qiang Sun Y.-Q., Guo.W. Chem. Eur. J. 2015, 21:4747-4754.
21. Ma L., Qian J., Tian H., Lan M., Zhang W. Analyst 2012, 137:5046-5050.
22. Meister A. J. Biol. Chem. 1988, 263:17205-17208.
23. Miller E.W., Bian S.X., Chang C.J. J. Am. Chem. Soc. 2007, 129:3458-3459.
24. Niu L.-Y., Guan Y.-S., Chen Y.-Z., Wu L.-Z., Tung C.-H., Yang Q.-Z. J. Am. Chem. Soc. 2012, 134:18928-18931.
25. Niu L.-Y., Guan Y.-S., Chen Y.-Z., Wu L.-Z., Tung C.-H., Yang Q.-Z. Chem. Commun. 2013, 49:1294-1296.
26. Pires M.M., Chmielewski J. Org. Lett. 2008, 10:837-840.
27. Rusin O., Luce N.N., Agbaria R.A., Escobedo J.O., jiang S., Warner I.M., Dawan F.B., Lian K., Strongin R.M. J. Am. Chem. Soc. 2004, 126:438-439.
28. Secor K.E., Glass T.E. Org. Lett. 2004, 6:3727-3730.
29. Secor K.E., Plante J., Avetta C., Glass T. J. Mater. Chem. 2005, 15:4073-4077.
30. Shao J., Sun H., Guo H., Ji S., Zhao J., Wu W., Yuan X., Zhang C., James T.D. Chem. Sci. 2012, 3:1049-1061.
31. Shao N., Jin J., Wang H., Zheng J., Yang R., Chan W., Abliz Z. J. Am. Chem. Soc. 2010, 132:725-736.
32. Sun Y., Liu Y., Chen M., Guo W. Talanta 2009, 80:996-1000.
33. Tang B., Xing Y., Li P., Zhang N., Yu F., Yang G. J. Am. Chem. Soc. 2007, 129:11666-11667.
34. Townsend D.M., Tew K.D., Tapiero H. Biomed. Pharmacother. 2003, 57:145-155.
35. Wang F., Li Zhou L., Zhao C., Wang R., Fei Q., Luo S., Guo Z., Tian H., Zhu W.-H. Chem. Sci. 2015, 6:2584-2589.
36. Xu Y., Li B., Han P., Sun S., Pang Y. Analyst 2013, 138:1004-1007.
37. Yang X.-F., Huang Q., Zhong Y., Li Z., Li H., Lowry M., Escobedoc J.O., Strongin R.M. Chem. Sci. 2014, 5:2177-2183.
38. Yang X., Guo Y., Strongin R.M. Angew. Chem. Int. Ed. 2011, 50:10690-10693.
39. Yang X., Guo Y., Strongin R.M. Org. Biomol. Chem. 2012, 10:2739-2741.
40. Yang Z., Zhao N., Sun Y., Miao F., Liu Y., Liu X., Zhang Y., Ai W., Song G., Shen X., Yu X., Sun J., Wong W.-Y. Chem. Commun. 2012, 48:3442-3444.
41. Yin J., Kwon Y., Kim D., Lee D., Kim G., Hu Y., Ryu J.-H., Yoon J. J. Am. Chem. Soc. 2014, 136:5351-5358.
42. Yuan L., Lin W., Yang Y. Chem. Commun. 2011, 47:6275-6277.
43. Zhang J., Shibata A., Ito M., Shuto S., Ito Y., Mannervik B., Abe H., Morgenstern R. J. Am. Chem. Soc. 2011, 133:14109-14119.
44. Zhang M., Yu M., Li F., Zhu M., Li M., Gao Y., Li L., Liu Z., Zhang J., Zhang D., Yi T., Huang C. J. Am. Chem. Soc. 2007, 129:10322-10323.
45. Zhang M., Wu Y., Zhang S., Zhu H., Wu Q., Jiao L., Hao E. Chem. Commun. 2012, 48:8925-8927.
46. Zhou X., Jin X., Sun G., Li D., Wu X. Chem. Commun. 2012, 48:8793-8795.