放射增敏剂
生物相容性
辐照
钌
活性氧
化学
纳米结构
纳米技术
辐射
材料科学
放射治疗
催化作用
光学
医学
有机化学
生物化学
物理
核物理学
内科学
作者
Qixuan Dai,Lin Wang,En Ren,Hu Chen,Xing Gao,Hongwei Cheng,Yibo An,Chengchao Chu,Gang Liu
标识
DOI:10.1002/ange.202211674
摘要
Abstract A lack of targeting accuracy and radiosensitivity severely limits clinical radiotherapy. In this study, we developed a radiosensitizer comprised of Ru‐based metal–organic nanostructures (ZrRuMn‐MONs@mem) to optimize irradiation by maximizing reactive oxygen species (ROS) generation and CO release in X‐ray‐induced dynamic therapy (XDT). The well‐designed nanostructures increase the direct absorption of radiation doses (primary radiation) and promote the deposition of photons and electrons (secondary radiation). The secondary electrons were trapped and transferred in the constrained MONs where they induce a cascade of reactions to increase the therapeutic efficiency. Meanwhile, the full‐length antiglypican 3 (GPC3) antibody (hGC33) expressed a cell membrane coating enabling active targeting of tumor sites with optimized biocompatibility. The ZrRuMn‐MONs@mem represents a starting point for advancing an all‐around radiosensitizer that operates efficiently in clinical XDT.
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