Rapidly liver-clearable rare-earth core-shell nanoprobe for dual-modal breast cancer imaging in the second near-infrared window.
Rapidly liver-clearable rare-earth core-shell nanoprobe for dual-modal breast cancer imaging in the second near-infrared window.
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可快速肝脏清除的稀土核壳纳米探针,用于第二近红外窗口中的双模式乳腺癌成像
DOI:
10.1186/s12951-021-01112-y
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发表时间:
2021-11-17
影响因子:
10.2
通讯作者:
Gao M
中科院分区:
文献类型:
--
作者:
Wei Z;Duan G;Huang B;Qiu S;Zhou D;Zeng J;Cui J;Hu C;Wang X;Wen L;Gao M
Fluorescence imaging as the beacon for optical navigation has wildly developed in preclinical studies due to its prominent advantages, including noninvasiveness and superior temporal resolution. However, the traditional optical methods based on ultraviolet (UV, 200–400 nm) and visible light (Vis, 400–650 nm) limited by their low penetration, signal-to-noise ratio, and high background auto-fluorescence interference. Therefore, the development of near-infrared-II (NIR-II 1000–1700 nm) nanoprobe attracted significant attentions toward in vivo imaging. Regrettably, most of the NIR-II fluorescence probes, especially for inorganic NPs, were hardly excreted from the reticuloendothelial system (RES), yielding the anonymous long-term circulatory safety issue. Here, we develop a facile strategy for the fabrication of Nd3+-doped rare-earth core–shell nanoparticles (Nd-RENPs), NaGdF4:5%Nd@NaLuF4, with strong emission in the NIR-II window. What’s more, the Nd-RENPs could be quickly eliminated from the hepatobiliary pathway, reducing the potential risk with the long-term retention in the RES. Further, the Nd-RENPs are successfully utilized for NIR-II in vivo imaging and magnetic resonance imaging (MRI) contrast agents, enabling the precise detection of breast cancer. The rationally designed Nd-RENPs nanoprobes manifest rapid-clearance property revealing the potential application toward the noninvasive preoperative imaging of tumor lesions and real-time intra-operative supervision. The online version contains supplementary material available at 10.1186/s12951-021-01112-y.
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影响因子:
10.8
作者:
He, Shuqing;Chen, Si;Cheng, Zhen
通讯作者:
Cheng, Zhen
影响因子:
16.6
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Cheng Z
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16.6
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通讯作者:
Moghe, P. V.
影响因子:
13.3
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通讯作者:
Gao, Mingyuan