Zhang Wen, Li Mengmei, Wang Xin, Zhang Wei, Wang Hui, Li Ping, Tang Bo
College of Chemistry, Chemical Engineering and Materials Science, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Shandong Normal University, Jinan 250014, China.
Anal Chem. 2023 Jan 31;95(4):2382-2389. doi: 10.1021/acs.analchem.2c04395. Epub 2023 Jan 18.
Thrombus are blood clots formed by abnormal hemostasis in blood vessels and are closely associated with various diseases such as pulmonary embolism, myocardial infarction and stroke. Early diagnosis and treatment of thrombus is the key to reducing the high risk of thrombotic disease. Given that early thrombus is small in early size, free instability, wide regional distribution and fast formation, it is urgent to develop all-inclusive detection methods that combine high signal-to-noise ratio, in situ dynamic and rapid in-depth tissue imaging. Near-infrared (NIR) fluorescence imaging, with its excellent high spatiotemporal resolution and tissue penetration depth, is a powerful technique for direct visualization of thrombotic events in situ. Considering the fibrin highly expressed in the thrombus is a typical thrombotic target. Moreover, the viscosity of the thrombus is markedly higher than its surroundings. Therefore, we developed a fibrin-targeting and viscosity-activating thrombus NIR fluorescent probe (TIR-V) for high-resolution and high-sensitivity in situ lighten-up thrombus. TIR-V has the advantages of good thrombus targeting, significant "off-on" fluorescence specific response to viscosity, bright NIR fluorescence and good biocompatibility. The thrombus is clearly delineated by a high signal-to-noise ratio NIR fluorescence imaging, enabling imaging detection and precise navigation of thrombotic regions. This work demonstrates the potential of TIR-V as a bifunctional probe for definitive diagnostic imaging and direct navigation of thrombotic lesions in clinical applications.
血栓是血管内异常止血形成的血凝块,与肺栓塞、心肌梗死和中风等多种疾病密切相关。血栓的早期诊断和治疗是降低血栓性疾病高风险的关键。鉴于早期血栓体积小、游离不稳定、区域分布广且形成迅速,迫切需要开发一种包含高信噪比、原位动态和快速深度组织成像的全面检测方法。近红外(NIR)荧光成像具有出色的高时空分辨率和组织穿透深度,是一种直接原位可视化血栓形成事件的强大技术。考虑到血栓中高表达的纤维蛋白是典型的血栓靶点。此外,血栓的粘度明显高于其周围环境。因此,我们开发了一种纤维蛋白靶向和粘度激活的血栓近红外荧光探针(TIR-V),用于高分辨率和高灵敏度的原位点亮血栓。TIR-V具有良好的血栓靶向性、对粘度有显著的“开-关”荧光特异性响应、明亮的近红外荧光和良好的生物相容性。通过高信噪比的近红外荧光成像可以清晰地勾勒出血栓,实现血栓区域的成像检测和精确导航。这项工作证明了TIR-V作为一种双功能探针在临床应用中对血栓性病变进行确定性诊断成像和直接导航的潜力。