化学
硝基还原酶
体内
荧光寿命成像显微镜
分子成像
肾
荧光
肾脏疾病
急性肾损伤
临床前影像学
体外
生物标志物
分子探针
病理
医学影像学
生物物理学
癌症研究
离体
光学成像
肾功能
荧光显微镜
体外毒理学
作者
Zhangkang Lv,Xinrong Lin,Jingting Huang,Yujie Huang,Fang Shen,Xing‐Can Shen,Hua Chen
标识
DOI:10.1021/acs.analchem.6c04500
摘要
Abstract Precise renal optical imaging is crucial for the early detection of renal cell carcinoma (RCC) and renal ischemia-reperfusion injury (IRI), as well as improving therapeutic outcomes. However, the majority of currently available fluorescent probes are preferentially taken up by the liver or only respond to a single analyte, resulting in limited accuracy in renal imaging and severely impairing their performance in renal function imaging. Herein, based on a novel “two birds with one stone” strategy, we report the renal-clearable and nitroreductase (NTR)/viscosity dual-activated fluorescent probe V-NTR for precise in vivo kidney disease imaging and diagnosis. Notably, the probe displays a remarkable 31.3-fold fluorescence enhancement upon dual stimulation by NTR and elevated viscosity, significantly improving detection specificity. In vivo NIR fluorescence imaging and in vitro urine analysis studies have collectively demonstrated that V-NTR enables precise imaging of RCC and real-time monitoring of injury induced during the early ischemic phase of renal IRI. Thus, this study not only provides a novel and reliable molecular tool for the early diagnosis and real-time monitoring of kidney diseases, but also offers a generalizable chemical design platform for the development of kidney-specific molecular imaging probes.
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