声动力疗法
共价键
超顺磁性
佐剂
化学
纳米颗粒
材料科学
纳米技术
光动力疗法
有机化学
医学
肿瘤科
磁化
量子力学
磁场
物理
作者
Dianwei Wang,Tong Li,Lin Lin,Meng Meng,Kai Hao,Zhaopei Guo,Jie Chen,Huayu Tian,Xuesi Chen
出处
期刊:Nano Today
[Elsevier]
日期:2023-12-04
卷期号:54: 102088-102088
被引量:2
标识
DOI:10.1016/j.nantod.2023.102088
摘要
Superior sonosensitizer and targeted delivery of sonosensitizer are critical factors in determining the effectiveness of sonodynamic therapy (SDT). We developed magnetic targeting covalent organic framework (COF) nanoparticles to act as sonosensitizer and nanoadjuvant to multi-amplify the SDT effect at tumor sites. First, core-shell Fe3O4 @COF nanoparticles with uniform size were prepared by “molecule exchange method” based on imine exchange reaction and further cationized, finally loaded with unmethylated cytosine-phosphate-guanine (CpG) adjuvant. The structural confinement of the porphyrin-based COF enhanced the sonodynamic performance, and the Fe3O4 endowed the COF with chemodynamic effect to enhance SDT effect. More importantly, the superparamagnetism of Fe3O4 could enable magnetic COF nanoparticles to actively target tumor sites, which further increased the treatment effect of SDT against simulated deep-seated tumors. Because of the presence of CpG adjuvant, this nanoplatform could be used as an in situ vaccine to achieve effective tumor immunotherapy to further amplify the treatment effect. This innovative method of preparing COF with core-shell structure and the enhanced SDT strategy effectively inhibited tumor growth and prevented tumor recurrence and metastasis, providing a new reference for clinical application.
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