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近红外二区金纳米簇组装体的发光性能和生物命运得到改善,可用于 HS 的体内比率成像。

Near-Infrared II Gold Nanocluster Assemblies with Improved Luminescence and Biofate for In Vivo Ratiometric Imaging of HS.

机构信息

MOE Key Laboratory for Analytical Science of Food Safety and Biology, College of Chemistry, Fuzhou University, Fuzhou, Fujian 350116, China.

Qingyuan Innovation Laboratory, 1# Xueyuan Road, Quanzhou, Fujian 362801, China.

出版信息

Anal Chem. 2022 Feb 8;94(5):2641-2647. doi: 10.1021/acs.analchem.1c05154. Epub 2022 Jan 27.

Abstract

Ultrasmall gold nanoclusters (AuNCs) are emerging as promising luminescent nanoprobes for bioimaging due to their fantastic photoluminescence (PL) and renal-clearable ability. However, it remains a great challenge to design them for in vivo sensitive molecular imaging in desired tissues. Herein, we have developed a strategy to tailor the PL and biofate of near-infrared II (NIR-II)-emitting AuNCs via ligand anchoring for improved bioimaging. By optimizing the ligand types in AuNCs and using Er-doped lanthanide (Ln) nanoparticles as models, core-satellite Ln@AuNCs assemblies were rationally constructed, which enabled 2.5-fold PL enhancement of AuNCs at 1100 nm and prolonged blood circulation compared to AuNCs. Significantly, Ln@AuNCs with dual intense NIR-II PL (from AuNCs and Er) can effectively accumulate in the liver for ratiometric NIR-II imaging of HS, facilitated by HS-mediated selective PL quenching of AuNCs. We have then demonstrated the real-time imaging evaluation of liver delivery efficacy and dynamics of two HS prodrugs. This shows a paradigm to visualize liver HS delivery and its prodrug screening in vivo. Note that Ln@AuNCs are body-clearable via the hepatobiliary excretion pathway, thus reducing potential long-term toxicity. Such findings may propel the engineering of AuNC nanoprobes for advancing in vivo bioimaging analysis.

摘要

超小的金纳米团簇(AuNCs)由于其出色的光致发光(PL)和肾脏清除能力,正在成为生物成像中很有前途的发光纳米探针。然而,设计用于在所需组织中进行体内敏感分子成像的 AuNCs 仍然是一个巨大的挑战。在此,我们开发了一种通过配体锚定来定制近红外二区(NIR-II)发射 AuNCs 的 PL 和生物命运的策略,以改善生物成像。通过优化 AuNCs 中的配体类型,并以掺铒的镧系(Ln)纳米颗粒作为模型,合理构建了核-卫星 Ln@AuNCs 组装体,与 AuNCs 相比,AuNCs 在 1100nm 处的 PL 增强了 2.5 倍,血液循环时间延长。值得注意的是,具有双重强烈近红外二区 PL(来自 AuNCs 和 Er)的 Ln@AuNCs 可以有效地在肝脏中积累,用于 HS 的比率型近红外二区成像,这得益于 HS 介导的 AuNCs 的选择性 PL 猝灭。我们随后证明了两种 HS 前药肝递送效果和动力学的实时成像评估。这表明了一种可视化肝 HS 递送及其体内前药筛选的范例。请注意,Ln@AuNCs 可通过肝胆排泄途径清除,从而降低潜在的长期毒性。这些发现可能推动 AuNC 纳米探针的工程设计,以推进体内生物成像分析。

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