菁
化学
病变
荧光寿命成像显微镜
分子探针
吲哚青绿
分子成像
锁孔
病理
生物物理学
体内
医学
光学
生物化学
荧光
DNA
材料科学
冶金
生物技术
物理
生物
焊接
作者
Lin Qiao,Changsheng Li,Yuhua Wang,Yanqing Zhu,Yueqing Gu
标识
DOI:10.1021/acs.jmedchem.4c00010
摘要
Near-infrared (NIR) fluorescence imaging has attracted much attention in image-guided interventions with unique advantages. However, the clinical translation rate of fluorescence probes is extremely low, primarily due to weak lesion signal contrast and poor specificity. To address this dilemma, a series of small-molecule near-infrared fluorescence probes have been designed for tumor imaging. Among them, YQ-04-03 showed notable optical stability and remarkable sensitivity toward tumor targeting. Moreover, within a specific concentration and time range against oxidizing reducing agents and laser, it demonstrated better stability than ICG. The retention time of YQ-04-03 in tumors was significantly longer compared to other nonspecific uptake sites in the subjects, and its tumor-to-normal tissue ratio (TNR) outperformed ICG. Successful resection of in situ hepatocarcinoma and peritoneal carcinoma was achieved using probe imaging guidance, with the smallest visual lesion resected measuring approximately 1 mm3. Ultimately, this probe holds great potential for advancing tumor tracer.
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