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首页> 外文期刊>Angewandte Chemie >Engineering the Protein Corona Structure on Gold Nanoclusters Enables Red-Shifted Emissions in the Second Near-infrared Window for Gastrointestinal Imaging
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Engineering the Protein Corona Structure on Gold Nanoclusters Enables Red-Shifted Emissions in the Second Near-infrared Window for Gastrointestinal Imaging

机译:在金纳米团簇上设计蛋白质电晕结构,使胃肠道成像的第二个近红外窗口的红移发射成为可能

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The application of NIR-II emitters for gastrointestinal (GI) tract imaging remains challenging due to fluorescence quenching in the digestive microenvironment. Herein, we report that red-shifting of the fluorescence emission of Au nanoclusters (AuNCs) into NIR-II region with improved quantum yields (QY) could be achieved by engineering a protein corona structure consisting of a ribonuclease-A (RNase-A) on the particle surfaces. RNase-A-encapsulated AuNCs (RNase-A@AuNCs) displayed emissions at 1050 nm with a 1.9 QY. Compared to rare earth and silver-based NIR-II emitters, RNase-A@AuNCs had excellent biocompatibility, showing >50-fold higher sensitivity in GI tract, and migrated homogenously during gastrointestinal peristalsis to allow visualization of the detailed structures of the GI tract. RNase-A@AuNCs could successfully examine intestinal tumor mice from healthy mice, indicating a potential utility for early diagnosis of intestinal tumors.
机译:由于消化微环境中的荧光猝灭,NIR-II 发射器在胃肠道 (GI) 成像中的应用仍然具有挑战性。在此,我们报告说,通过在颗粒表面设计由核糖核酸酶-A(RNase-A)组成的蛋白质电晕结构,可以实现Au纳米团簇(AuNCs)向NIR-II区域的荧光发射的红移,并具有更高的量子产率(QY)。RNase-A包封的AuNCs(RNase-A@AuNCs)在1050 nm处的发射为1.9 % QY。 与稀土和银基NIR-II发射器相比,RNase-A@AuNCs具有优异的生物相容性,在胃肠道中的灵敏度高出>50倍,并且在胃肠道蠕动过程中均匀迁移,从而可以可视化胃肠道的详细结构。RNase-A@AuNCs可以成功地从健康小鼠身上检查肠道肿瘤小鼠,表明其对肠道肿瘤的早期诊断具有潜在的效用。

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