The Institute for Advanced Studies, and College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, P. R. China.
State Key Laboratory of Medicinal Chemical Biology, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Research Center for Analytical Sciences, College of Chemistry, Frontiers Science Center for New Organic Matter, State Key Laboratory of Elemento-Organic Chemistry, Department of Chemical Biology, Frontiers Science Center for Cell Responses, and Haihe Laboratory of Sustainable Chemical Transformations, Nankai University, Tianjin 300071, P. R. China.
Anal Chem. 2023 Oct 24;95(42):15540-15548. doi: 10.1021/acs.analchem.3c01967. Epub 2023 Oct 13.
With the development of near-infrared II (NIR-II) fluorescence imaging, AgSe quantum dots (QDs) have become promising label candidates due to their negligible toxicity and narrow band gap. Despite their potential for gastrointestinal (GI) imaging, the application of AgSe QDs still presents significant challenges due to issues such as fluorescence extinction or poor stability in the complex digestive microenvironment. Herein, we have proposed a novel approach to the continuous production of Se precursors using glutathione (GSH) as the reductant under acidic conditions, realizing the continuous growth of water-dispersible AgSe QDs. The AgSe QDs emitting at 600-1100 nm have been successfully synthesized. Meanwhile, the silver-rich surface of the synthesized NIR-II AgSe QDs has been passivated well with the dense GSH, resulting in exceptional colloidal stability and photostability and endowing them with acid resistance. As a result, the obtained NIR-II AgSe QDs have exhibited remarkable stability in gastric acid, thus enabling their utilization for long-term real-time monitoring of GI peristalsis via NIR-II fluorescence imaging. Moreover, in contrast to conventional barium meal-based X-ray imaging, NIR-II fluorescence imaging with as-prepared NIR-II AgSe QDs can offer clearer visualization of fine intestinal structures, with a width as small as 1.07 mm. The developed strategy has offered a new opportunity for the synthesis of acid-resistant nanocrystals, and the acid-resistant, low-toxicity, and biocompatible NIR-II AgSe QDs synthesized in this work show a great promise for GI imaging and diagnosis of GI diseases in vivo.
随着近红外二区(NIR-II)荧光成像的发展,由于 AgSe 量子点(QDs)的毒性可以忽略不计且带隙较窄,因此它们成为有前途的标记候选物。尽管它们具有胃肠道(GI)成像的潜力,但由于在复杂的消化微环境中荧光猝灭或稳定性差等问题,AgSe QDs 的应用仍然存在重大挑战。在此,我们提出了一种新方法,即在酸性条件下使用谷胱甘肽(GSH)作为还原剂连续制备 Se 前体,从而实现水散性 AgSe QDs 的连续生长。成功合成了发射波长在 600-1100nm 的 AgSe QDs。同时,合成的 NIR-II AgSe QDs 中富含银的表面被密集的 GSH 很好地钝化,从而具有出色的胶体稳定性和光稳定性,并赋予其耐酸性。结果,所获得的 NIR-II AgSe QDs 在胃酸中表现出优异的稳定性,从而可以通过 NIR-II 荧光成像对 GI 蠕动进行长期实时监测。此外,与传统的基于钡餐的 X 射线成像相比,用所制备的 NIR-II AgSe QDs 进行的 NIR-II 荧光成像可以更清晰地可视化细小的肠道结构,其宽度小至 1.07mm。所开发的策略为合成耐酸纳米晶体提供了新的机会,并且本工作中合成的耐酸、低毒性和生物相容性的 NIR-II AgSe QDs 为 GI 成像和体内 GI 疾病的诊断提供了很好的应用前景。