菁
荧光
溶剂变色
吲哚青绿
猝灭(荧光)
水溶液
光化学
体内
化学
荧光寿命成像显微镜
深铬移
吸收(声学)
临床前影像学
材料科学
荧光团
近红外光谱
光学
有机化学
生物技术
复合材料
物理
生物
作者
Shangfeng Wang,Yong Fan,Dandan Li,Caixia Sun,Zuhai Lei,Lingfei Lu,Ting Wang,Fan Zhang
标识
DOI:10.1038/s41467-019-09043-x
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 anti-quenching pentamethine cyanine fluorophores that significantly overcome the severe solvatochromism, thus affording stable absorption/emission beyond 1000 nm with up 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.
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