纳米医学
生物相容性
中子俘获
材料科学
胶质瘤
纳米颗粒
硼
癌症治疗
纳米技术
放射化学
癌症研究
癌症
化学
医学
有机化学
冶金
内科学
作者
Liqun Dai,Jie Liu,Xiaosheng Zhao,Yuhao Li,Siming Zhou,Liping Yuan,Diyun Shu,Lili Pan,Yuan‐hao Liu,Zhiyong Qian
标识
DOI:10.1002/adfm.202214145
摘要
Abstract Boron neutron capture therapy (BNCT) is a promising therapy for refractory cancer based on the cytotoxic reaction of 10 B (n, α) 7 Li. Although two BNCT agents are clinically available, they are quickly metabolized and show modest enrichment in tumor sites, partially limiting BNCT widespread application. Consequently, novel agents that perform active targeting and show good biocompatibility have to be developed. Herein, boronophenylalanine‐containing polydopamine (B‐PDA) nanoparticles are easily fabricated by encapsulating boronophenylalanine (BPA) in polydopamine via nitrogen‐boronate coordination. In this study, B‐PDA achieves increased tumor accumulation and prolonged retention effects in the tumor site and superior antitumor activity post neutron irradiation in the orthotopic xenograft glioma model. In brief, this study offers a novel strategy for BPA delivery and may broaden the perspective on nanomedicine design for BNCT.
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