Anti-quenching NIR-II molecular fluorophores for in vivo high-contrast imaging and pH sensing

被引:345
作者
Wang, Shangfeng [1 ,2 ]
Fan, Yong [1 ,2 ]
Li, Dandan [1 ,2 ]
Sun, Caixia [1 ,2 ]
Lei, Zuhai [1 ,2 ]
Lu, Lingfei [1 ,2 ]
Wang, Ting [1 ,2 ]
Zhang, Fan [1 ,2 ]
机构
[1] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, State Key Lab Mol Engn Polymers, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, iChem, Shanghai 200433, Peoples R China
关键词
FLUORESCENT-PROBES; DYES; GLUTATHIONE; BRIGHT;
D O I
10.1038/s41467-019-09043-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The contrast and sensitivity of in vivo fluorescence imaging has been revolutionized by molecular fluorophores operating in the second near-infrared window (NIR-II; 1000-1700 nm), but an ongoing challenge is the solvatochromism-caused quenching in aqueous solution for the long-wavelength absorbing fluorophores. Herein, we develop a series of antiquenching pentamethine cyanine fluorophores that significantly overcome the severe solvatochromism, thus affording stable absorption/ emission beyond 1000 nm with up to similar to 44-fold enhanced brightness and superior photostability in aqueous solution. These advantages allow for deep optical penetration (8 mm) as well as high-contrast and highly-stable lymphatic imaging superior to clinical-approved indocyanine green. Additionally, these fluorophores exhibit pH-responsive fluorescence, allowing for noninvasive ratiometric fluorescence imaging and quantification of gastric pH in vivo. The results demonstrate reliable accuracy in tissue as deep as 4 mm, comparable to standard pH electrode method. This work unlocks the potential of anti-quenching pentamethine cyanines for NIR-II biological applications.
引用
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页数:11
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