Precise tumor resection under the navigation of Tumor-Microenvironment pH-activated NIR-II fluorescence imaging via calcium Carbonate/Polydopamine Co-packed Nd-doped downshifting nanoprobes

材料科学 荧光 光漂白 兴奋剂 肿瘤微环境 荧光寿命成像显微镜 生物物理学 纳米技术 生物医学工程 光电子学 肿瘤细胞 癌症研究 光学 生物 物理 医学
作者
Jiaqi Li,Kangliang Lou,Yongying Dang,Haina Tian,Qiang Luo,Cailin Huang,Rongliang Liu,Xin Gong,Shifeng Wang,Hui Liu,Peiyuan Wang,Xiaolong Liu
出处
期刊:Materials & Design [Elsevier BV]
卷期号:227: 111703-111703 被引量:4
标识
DOI:10.1016/j.matdes.2023.111703
摘要

Photobleaching resistance, high quantum yield and deep tissue imaging of Nd-doped nanocrystals with fluorescence in the second near infrared region (NIR-II, 1000–1700 nm) occupied an indispensable position for precisely navigating tumor resection. However, these NIR-II nanoprobes often encounter high passive accumulation in reticuloendothelial system (RES) organs that attenuates signal to background ratio (SBR), resulting in the impediment of their application for accurate tumor outline delineation. Herein, a hollow-structured CaCO3 and polydopamine co-packed shell has been co-cladded on the Nd-doped down-shifting nanocrystals ([email protected]). After conjugating folic acid molecules on the hollowed surface ([email protected]), this fascinating NIR-II contrast nanoagent can further specifically enhance tumor targeting capacity and gratifyingly restrain the NIR-II fluorescence in the "OFF" state. It sensitively responds to the weak acid tumor microenvironment, consequently, the hybrid nanoshell is degraded and the NIR-II fluorescence is efficiently turn "ON". Robust fluorescent imaging with the augmented SBR has been demonstrated to accurately identify tumor borderlines from normal tissue. Tumors were thoroughly removed under the navigation of this novel pH stimuli-responsive NIR-II fluorescence imaging with ignorable in situ recurrence or metastases after 28 days post-surgery. This strategy indicates the preclinical potential of tumor microenvironment activated nanoprobes for assisting the accurate delineation of tumor margins.
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