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基于谷胱甘肽的高亲和性αβ 整合素激活近红外光致点亮荧光探针用于精确早期肿瘤识别。

GSH-Activated Light-Up Near-Infrared Fluorescent Probe with High Affinity to αβ Integrin for Precise Early Tumor Identification.

机构信息

Department of Biomedical Engineering, School of Engineering , China Pharmaceutical University , 24 Tongjia Lane , Gulou District, Nanjing 210009 , China.

出版信息

ACS Appl Mater Interfaces. 2018 Sep 19;10(37):30994-31007. doi: 10.1021/acsami.8b09841. Epub 2018 Sep 6.

Abstract

The development of tumor-associated, stimuli-driven, turn-on near-infrared (NIR) fluorophores requires urgent attention because of their potential in selective and precise tumor diagnosis. Herein, we describe a NIR fluorescent probe (CyA-cRGD) comprised of a fluorescence reporting unit (a cyanine dye) linked with a GSH-responsive unit (nitroazo aryl ether group) and a tumor-targeting unit (cRGD). The NIR fluorescence of CyA-cRGD with sensitive and selective response to GSH can act as a direct off-on signal reporter for GSH monitoring. Notably, CyA-cRGD possesses improved biocompatibility compared with CyA, which is highly desirable for in vivo fluorescence tracking of cancer. Confocal fluorescence imaging confirmed the tumor-targeting capability and GSH detection ability of CyA-cRGD in tumor cells, normal cells, and coincubated tumor /normal cells and in the three-dimensional multicellular tumor spheroid. Furthermore, it was validated that CyA-cRGD could detect tumor precisely in GSH and integrin αβ high-expressed tumor-bearing mouse models. Importantly, it was confirmed that CyA-cRGD possessed high efficiency for early-stage tumor imaging in mouse models with tumor cells implanted within 72 h. This method provided significant advances toward more in-depth understanding and exploration of tumor imaging, which may potentially be applied for clinical early tumor diagnosis.

摘要

由于其在选择性和精确性肿瘤诊断中的潜在应用,开发与肿瘤相关的、刺激驱动的、开启型近红外(NIR)荧光团受到了迫切关注。在此,我们描述了一种由荧光报告单元(菁染料)与谷胱甘肽响应单元(硝基偶氮芳基醚基团)和肿瘤靶向单元(cRGD)连接而成的 NIR 荧光探针(CyA-cRGD)。CyA-cRGD 对 GSH 具有敏感和选择性的 NIR 荧光响应,可以作为 GSH 监测的直接关开信号报告器。值得注意的是,CyA-cRGD 与 CyA 相比具有更好的生物相容性,这对于癌症的体内荧光跟踪非常理想。共聚焦荧光成像证实了 CyA-cRGD 在肿瘤细胞、正常细胞以及共孵育的肿瘤/正常细胞和三维多细胞肿瘤球体中的肿瘤靶向能力和 GSH 检测能力。此外,还验证了 CyA-cRGD 可以在 GSH 和整合素 αβ 高表达的荷瘤小鼠模型中精确检测肿瘤。重要的是,证实了 CyA-cRGD 可以在植入肿瘤细胞 72 小时内的小鼠模型中进行早期肿瘤成像,具有高效性。该方法为更深入地了解和探索肿瘤成像提供了重要进展,可能有望应用于临床早期肿瘤诊断。

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