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Novel benzo-bis(125-thiadiazole) fluorophores for in vivo NIR-II imaging of cancer

机译:用于癌症的体内NIR-II成像的新型苯并双(125-噻二唑)荧光团

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摘要

Optical imaging of diseases represents a highly dynamic and multidisciplinary research area, and second near-infrared window (NIR-II, 1000–1700 nm) imaging is at the forefront of the research on optical imaging techniques. Small-molecule based NIR-II (1000–1700 nm) dyes are highly promising candidates for in vivo molecular imaging because of their high biocompatibility, fast excretion, and high clinical translation ability. However, research reports on small-molecule based NIR-II dyes and probes are rare. Herein, we designed a series of fluorescent compounds (>Q1, >Q2, >Q3, and >Q4) and investigated the relationships between their structures and absorption/fluorescence properties. >Q4 (maximum emission at 1100 nm) stood out as the dye with the best physical properties and thus was selected as a scaffold for the facile construction of two types of water-soluble and biocompatible NIR-II probes (>Q4NPs and >SCH1100). Highly specific gastrin-releasing peptide receptor (GRPR) targeted NIR-II imaging of prostate cancer in living mice was achieved using the small-molecule probe >SCH1100, which represents the first small peptide based NIR-II probe for targeted cancer imaging. The attractive imaging properties of >Q4-based NIR-II probes open up many opportunities for molecular imaging and clinical translation in the unique NIR-II window.
机译:疾病的光学成像是一个高度动态和跨学科的研究领域,而第二次近红外窗口(NIR-II,1000-1700 nm)成像则是光学成像技术研究的前沿。基于小分子的NIR-II(1000-1700 nm)染料具有高度的生物相容性,快速的排泄能力和较高的临床翻译能力,因此非常适合用于体内分子成像。然而,关于基于小分子的NIR-II染料和探针的研究报告很少。在此,我们设计了一系列荧光化合物(> Q1 ,> Q2 ,> Q3 和> Q4 ),并研究了它们的结构与吸收/荧光性质之间的关系。 > Q4 (在1100 nm处的最大发射)脱颖而出,是具有最佳物理性能的染料,因此被选作方便构建两种水溶性和生物相容性NIR-II探针的支架( > Q4NP 和> SCH1100 )。使用小分子探针> SCH1100 实现了针对活体小鼠前列腺癌的高特异性胃泌素释放肽受体(GRPR)的NIR-II成像,这是首款基于小肽的NIR-II探针靶向癌症成像。基于> Q4 的NIR-II探针具有吸引人的成像特性,在独特的NIR-II窗口中为分子成像和临床翻译打开了许多机会。

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