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Rational design of a super-contrast NIR-II fluorophore affords high-performance NIR-II molecular imaging guided microsurgery

机译:合理设计的超对比度NIR-II荧光团可提供高性能的NIR-II分子成像引导显微外科手术

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摘要

In vivo molecular imaging in the “transparent” near-infrared II (NIR-II) window has demonstrated impressive benefits in reaching millimeter penetration depths with high specificity and imaging quality. Previous NIR-II molecular imaging generally relied on high hepatic uptake fluorophores with an unclear mechanism and antibody-derived conjugates, suffering from inevitable nonspecific retention in the main organs/skin with a relatively low signal-to-background ratio. It is still challenging to synthesize a NIR-II fluorophore with both high quantum yield and minimal liver-retention feature. Herein, we identified the structural design and excretion mechanism of novel NIR-II fluorophores for NIR-II molecular imaging with an extremely clean background. With the optimized renally excreted fluorophore–peptide conjugates, superior NIR-II targeting imaging was accompanied by the improved signal-to-background ratio during tumor detection with reducing off-target tissue exposure. An unprecedented NIR-II imaging-guided microsurgery was achieved using such an imaging platform, which provides us with a great preclinical example to accelerate the potential clinical translation of NIR-II imaging.
机译:在“透明”近红外II(NIR-II)窗口中进行的体内分子成像已显示出以高特异性和成像质量达到毫米穿透深度的显着优势。以前的NIR-II分子成像通常依赖于机制不清楚的高肝摄取荧光团和抗体衍生的缀合物,它们在主要器官/皮肤中不可避免地具有非特异性保留,且信噪比相对较低。合成具有高量子产率和最小肝滞留特征的NIR-II荧光团仍然具有挑战性。在本文中,我们确定了具有非常干净背景的用于NIR-II分子成像的新型NIR-II荧光团的结构设计和排泄机制。通过优化的肾脏排泄的荧光团-肽共轭物,卓越的NIR-II靶向成像伴随着改善的肿瘤检测过程中的信噪比,同时减少了脱靶组织的暴露。使用这种成像平台实现了前所未有的NIR-II成像引导显微外科手术,这为我们提供了一个很好的临床前实例,可加快NIR-II成像的潜在临床翻译速度。

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