胶质母细胞瘤
胶质瘤
放射治疗
血脑屏障
医学
放射科
病理
生物医学工程
化学
癌症研究
内科学
中枢神经系统
作者
Lichao Su,Kang Zhu,Xiaoguang Ge,Ying Wu,Jieping Zhang,Guoyu Wang,Liu Daojia,Ling Chen,Qingqing Li,Junqiang Chen,Jibin Song
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-03-18
卷期号:24 (12): 3727-3736
被引量:4
标识
DOI:10.1021/acs.nanolett.4c00223
摘要
The permeability of the highly selective blood–brain barrier (BBB) to anticancer drugs and the difficulties in defining deep tumor boundaries often reduce the effectiveness of glioma treatment. Thus, exploring the combination of multiple treatment modalities under the guidance of second-generation near-infrared (NIR-II) window fluorescence (FL) imaging is considered a strategic approach in glioma theranostics. Herein, a hybrid X-ray-activated nanoprodrug was developed to precisely visualize the structural features of glioma microvasculature and delineate the boundary of glioma for synergistic chemo-radiotherapy. The nanoprodrug comprised down-converted nanoparticle (DCNP) coated with X-ray sensitive poly(Se-Se/DOX-co-acrylic acid) and targeted Angiopep-2 peptide (DCNP@P(Se-DOX)@ANG). Because of its ultrasmall size and the presence of DOX, the nanoprodrug could easily cross BBB to precisely monitor and localize glioblastoma via intracranial NIR-II FL imaging and synergistically administer antiglioblastoma chemo-radiotherapy through specific X-ray-induced DOX release and radiosensitization. This study provides a novel and effective strategy for glioblastoma imaging and chemo-radiotherapy.
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