光动力疗法
材料科学
光子上转换
发光
能量转移
免疫疗法
金属有机骨架
异质结
光电子学
癌症研究
纳米技术
癌症
化学
医学
吸附
有机化学
内科学
分子物理学
作者
Qi-Xian Wang,Yuanfan Yang,X. C. Yang,Yue Pan,Ling‐Dong Sun,Wenyuan Zhang,Yulei Shao,Jie Shen,Jian Lin,Lele Li,Chun‐Hua Yan
出处
期刊:Nano Today
[Elsevier]
日期:2022-03-03
卷期号:43: 101439-101439
被引量:60
标识
DOI:10.1016/j.nantod.2022.101439
摘要
Heterostructures of NaLnF4 and porphyrinic metal-organic frameworks (MOF) have been reported as a promising platform for near-infrared (NIR)-driven photodynamic therapy (PDT), while the energy transfer from NaLnF4 to MOF greatly decreased the upconversion emissions. To develop NaLnF4 and MOF heterostructures with significantly improved PDT and imaging simultaneously is important to track their location to implement therapy accurately. Herein, we constructed Er3+-doped NaLnF4@MOF [email protected] nanoparticles to integrate NIR-driven PDT and NIR-II imaging. NaLnF4 nanoparticles are designed with upconversion and NIR emission simultaneously under a single 980 nm excitation, where the upconversion luminescence (UCL) overlaps well with the absorption of Zr-based porphyrin MOF, enabling efficient energy transfer from NaLnF4 to the MOF shell to generate 1O2. And the NIR luminescence, which gave out under a lower excitation power than that of UCL, could be used to track the location and distribution of the heterostructures via NIR-II imaging. Moreover, antiprogrammed death-ligand 1 (α-PD-L1) immunotherapy was introduced synergistically to improve antitumor immunity efficacy. The combination of NaLnF4@MOF and α-PD-L1 not only inhibited primary tumors but also suppressed distant one, leading to an effective tumor inhibition rate of 95%. This work provides an integrated nanoplatform for boosting NIR-II imaging-guided PDT/immunotherapy efficacy toward tumor treatment.
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