A novel colorimetric and ratiometric NIR fluorescent sensor for glutathione based on dicyanomethylene-4H-pyran in living cells
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  • 作者:Xumeng Wu ; Andong Shao ; Shiqin Zhu ; Zhiqian Guo ; Weihong Zhu
  • 关键词:near ; infrared ; GSH ; ratiometric ; colorimetric ; fluorescent sensor
  • 刊名:SCIENCE CHINA Chemistry
  • 出版年:2016
  • 出版时间:January 2016
  • 年:2016
  • 卷:59
  • 期:1
  • 页码:62-69
  • 全文大小:1,267 KB
  • 参考文献:1.Chen XQ, Zhou Y, Peng XJ, Yoon J. Chem Soc Rev, 2010, 39: 2120–2135CrossRef
    2.Hou YC, Guo ZM, Li J, Wang PG. Biochem Biophys Res Commun, 1996, 228: 88–93CrossRef
    3.Wu XM, Sum XR, Guo ZQ, Tang JB, Shen YQ, James TD, Tian H, Zhu WH. J Am Chem Soc, 2014, 136: 3579–3588CrossRef
    4.Wood ZA, Schröder E, Harris JR, Poole LB. Trends Biochem Sci, 2003, 28: 32–40CrossRef
    5.Finkel T, Holbrook NJ. Nature, 2000, 408: 239–247CrossRef
    6.Hou SG, Liang L, Deng SSH, Chen JF, Huang Q, Cheng Y, Fan CH. Sci China Chem, 2014, 57: 100–106CrossRef
    7.Kizek R, Vacek J, Trnková L, Jelen F. Bioelectrochemistry, 2004, 63: 19–24CrossRef
    8.Feng LH, Liu LB, Lv FT, Bazan GC, Wang S. Adv Mater, 2014, 26: 3926–3930CrossRef
    9.Vacek J, Klejdus B, Petrlová J, Lojková L, Kubán V. Analyst, 2006, 131: 1167–1174CrossRef
    10.Ling YY, Yin XF, Fang ZL. Electrophoresis, 2005, 26: 4759–4766CrossRef
    11.Satoh I, Arakawa S, Okamoto A. Sens Actuators B, 1991, 5: 245–247CrossRef
    12.Pastore A, Federici G, Bertini E, Piemonte F. Clin Clim Acta, 2003, 333: 19–39CrossRef
    13.Li K, Yu X, Tong AJ, Tang BZ. Sci China Chem, 2014, 57: 248–251CrossRef
    14.Miao QQ, Li Q, Yuan QP, Li LL, Hai ZJ, Liu S, Liang GL. Anal Chem, 2015, 87: 3460–3466CrossRef
    15.Zheng MM, Huang HX, Zhou M, Wang YQ, Zhang Y, Ye DJ, Chen HY. Chem Eur J, 2015, 21: 10506–10512CrossRef
    16.Yin J, Kwon Y, Kim D, Lee D, Kim G, Hu Y, Ryu JH, Yoon J. J Am Chem Soc, 2014, 136: 5351–5358CrossRef
    17.Lee MH, Han JH, Kwon P, Bhuniya S, Kim JY, Sessler JL, Kang C, Kim JS. J Am Chem Soc, 2012, 134: 1316–1322CrossRef
    18.Lou ZR, Li P, Sun XF, Yang SQ, Wang BS, Han KL. Chem Commun, 2013, 49: 391–393CrossRef
    19.Long LL, Lin WY, Chen BB, Gao WS, Yuan L. Chem Commun, 2011, 47: 893–895CrossRef
    20.Niu LY, Guan YS, Chen YZ, Wu LZ, Tung CH, Yang QZ. J Am Chem Soc, 2012, 134: 18928–18931CrossRef
    21.Wang FY, Zhou L, Zhao CC, Wang R, Fei Q, Luo SH, Guo ZQ, Tian H, Zhu WH. Chem Sci, 2015, 6: 2584–2589CrossRef
    22.Jung HS, Ko KC, Kim GH, Lee AR, Na YC, Kang C, Lee JY, Kim JS. Org Lett, 2011, 13: 1498–1501CrossRef
    23.Sreejith S, Divya KP, Ajayaghosh A. Angew Chem Int Ed, 2008, 47: 7883–7887CrossRef
    24.Ding J, Li HY, Wang C, Yang J, Xie YJ, Peng Q, Li QQ, Li Z. ACS Appl Mater Interf, 2015, 7: 11369–11376CrossRef
    25.Frangioni JV. Curr Opin Chem Biol, 2003, 7: 626–634CrossRef
    26.Majumdar P, Yuan XL, Li SF, Guennic BL, Ma J, Zhang CS, Jacqueminde D, Zhao JZ. J Mater Chem B, 2014, 2: 2838–2854CrossRef
    27.Li YH, Sun Y, Li JC, Su QQ, Yuan W, Dai Y, Han CM, Wang QH, Feng W, Li FY. J Am Chem Soc, 2015, 137: 6407–6416CrossRef
    28.Sun W, Fan JL, Hu C, Cao JF, Zhang H, Xiong XQ, Wang JY, Cui S, Sun SG, Peng XJ. Chem Commun, 2013, 49: 3890–3892CrossRef
    29.Wu XM, Chang S, Sun XR, Guo ZQ, Li YS, Tang JB, Shen YQ, Shi JL, Tian H, Zhu WH. Chem Sci, 2013, 4: 1221–1228CrossRef
    30.Samanta A, Vendrell M, Das R, Chang YT. Chem Commun, 2010, 46: 7406–7408CrossRef
    31.Shank NI, Pham HH, Waggoner AS, Armitage BA. J Am Chem Soc, 2013, 135: 242–251CrossRef
    32.Altman RB, Zheng QS, Zhou Z, Terry DS, Warren JD, Blanchard SC. Nat Method, 2012, 9: 428–429CrossRef
    33.Barbon A, Bott ED, Brustolon M, Fabris M, Kahr B, Kaminsky W, Reid PJ, Wong SM, Wustholz KL, Zanré R. J Am Chem Soc, 2009, 131: 11548–11557CrossRef
    34.Guo ZQ, Zhu WH, Shen LJ, Tian H. Angew Chem Int Ed, 2007, 46: 5549–5553CrossRef
    35.Guo ZQ, Zhu WH, Xiong YY, Tian H. Macromolecules, 2009, 42: 1448–1453CrossRef
    36.Liu B, Li XY, Liu MY, Ning ZJ, Zhang Q, Li C, Müllen K, Zhu WH. Dyes Pigm, 2012, 94: 23–27CrossRef
    37.Guo ZQ, Zhu WH, Tian H. Chem Commun, 2012, 48: 6073–6084CrossRef
    38.Zhu WH, Huang XM, Guo ZQ, Wu XM, Yu HH, Tian H. Chem Commun, 2012, 48: 1784–1786CrossRef
    39.Lee MH, Yang ZG, Lim CW, Lee YH, Dongbang S, Kang C, Kim JS. Chem Rev, 2013, 113: 5071–5109CrossRef
    40.Li M, Wu XM, Wang Y, Li YS, Zhu WH, James TD. Chem Commun, 2014, 50: 1751–1753CrossRef
    41.Yang ZG, Lee JH, Jeon HM, Han JH, Park N, He YX, Lee H, Hong KS, Kang C, Kim JS. J Am Chem Soc, 2013, 135: 11657–11662CrossRef
    42.Mahato R, Tai W, Cheng K. Adv Drug Delivery Rev, 2011, 63: 659–670CrossRef
    43.Belsky I, Dodiuk H, Shvo Y. J Org Chem, 1974, 39: 989–995CrossRef
    44.Hammond PR. Opt Commun, 1979, 29: 331–333CrossRef
    45.Chung C, Srikun D, Lim CS, Chang CJ, Cho BR. Chem Commun, 2011, 47: 9618–9620CrossRef
    46.Lim CS, Masanta G, Kim HJ, Han JH, Kim HM, Cho BR. J Am Chem Soc, 2011, 133: 11132–11135CrossRef
    47.He XX, Wang YS, Wang KM, Chen M, Chen SY. Anal Chem, 2012, 84: 9056–9064
    48.Wang G, Chang XM, Peng JX, Liu KQ, Zhao K, Yu CM, Fang Y. Phys Chem Chem Phys, 2015, 17: 5441–5449CrossRef
    49.Guo T, Cui L, Shen JN, Wang R, Zhu WP, Xu YF, Qian XH. Chem Commun, 2013, 49: 1862–1864CrossRef
    50.Altman RB, Terry DS, Zhou Z, Zheng QS, Geggier P, Kolster RA, Zhao YF, Javitch JA, Warren JD, Blanchard SC. Nat Method, 2012, 9: 68–71CrossRef
  • 作者单位:Xumeng Wu (1) (2) (3)
    Andong Shao (1) (2) (3)
    Shiqin Zhu (1) (2) (3)
    Zhiqian Guo (1) (2) (3)
    Weihong Zhu (1) (2) (3)

    1. Shanghai Key Laboratory of Functional Materials Chemistry, Shanghai, 200237, China
    2. Key Laboratory for Advanced Materials and Institute of Fine Chemicals, Shanghai, 200237, China
    3. East China University of Science and Technology, Shanghai, 200237, China
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Chinese Library of Science
    Chemistry
  • 出版者:Science China Press, co-published with Springer
  • ISSN:1869-1870
文摘
Glutathione (GSH) plays a critical role in maintaining oxidation-reduction homeostasis in biological systems. Considering the detection of GSH by fluorescence sensors is limited by either the short wavelength emission or the poor photostability, a highly stable colorimetric and ratiometric NIR fluorescent sensor (DCM-S) for GSH detection has been constructed on the basis of dicyanomethylene-4H-pyran (DCM) chromophore. The specific disulfide bond is incorporated via a carbamate linker as the GSH responsive group, which simultaneously blue-shifts and quenches the fluorescence. Upon addition of GSH, DCM-S exhibits outstanding colorimetric (from yellow to red) and ratiometric fluorescent response with the 6-fold enhancement of NIR fluorescence at 665 nm in quantum yield. More importantly, the GSH-treated DCM-S (DCM-NH2 actually) possesses 20-fold longer fluorescence half-life period as well as much better photostability than the FDA-approved ICG. Finally, the ratiometric detection of GSH is also successfully operated in the living cell imaging, exhibiting NIR fluorescence and large Stokes shift (215 nm) with nearly no background fluorescence interference. As a consequence, DCM-S can be utilized as colorimetric and ratiometric NIR fluorescent sensor for GSH, with a great potential in the development of GSH-induced drug delivery system.

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