荧光
荧光寿命成像显微镜
谷胱甘肽
体内
生物物理学
材料科学
生物相容性
整合素
共焦显微镜
菁
共焦
癌症研究
分子生物学
生物化学
生物
化学
细胞生物学
光学
细胞
冶金
酶
生物技术
物理
作者
Zhenwei Yuan,Lijuan Gui,Jinrong Zheng,Yisha Chen,Sisi Qu,Yuanzhi Shen,Fei Wang,Murat Er,Yueqing Gu,Haiyan Chen
标识
DOI:10.1021/acsami.8b09841
摘要
The development of tumor-associated, stimuli-driven, turn-on near-infrared (NIR) fluorophores requires urgent attention because of their potential in selective and precise tumor diagnosis. Herein, we describe a NIR fluorescent probe (CyA-cRGD) comprised of a fluorescence reporting unit (a cyanine dye) linked with a GSH-responsive unit (nitroazo aryl ether group) and a tumor-targeting unit (cRGD). The NIR fluorescence of CyA-cRGD with sensitive and selective response to GSH can act as a direct off-on signal reporter for GSH monitoring. Notably, CyA-cRGD possesses improved biocompatibility compared with CyA, which is highly desirable for in vivo fluorescence tracking of cancer. Confocal fluorescence imaging confirmed the tumor-targeting capability and GSH detection ability of CyA-cRGD in tumor cells, normal cells, and coincubated tumor /normal cells and in the three-dimensional multicellular tumor spheroid. Furthermore, it was validated that CyA-cRGD could detect tumor precisely in GSH and integrin αvβ 3 high-expressed tumor-bearing mouse models. Importantly, it was confirmed that CyA-cRGD possessed high efficiency for early-stage tumor imaging in mouse models with tumor cells implanted within 72 h. This method provided significant advances toward more in-depth understanding and exploration of tumor imaging, which may potentially be applied for clinical early tumor diagnosis.
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