声动力疗法
化学
癌症治疗
肿瘤微环境
肿瘤缺氧
癌症研究
癌症
谷胱甘肽
咪唑酯
生物物理学
沸石咪唑盐骨架
缺氧(环境)
纳米颗粒
纳米医学
细胞
活性氧
联合疗法
纳米技术
癌细胞
转移
细胞凋亡
魔法子弹
细胞生物学
细胞质
共轭体系
膜
肿瘤细胞
磁共振成像
分子成像
癌症治疗
生物化学
磁性纳米粒子
组合化学
作者
Qi Xu,Qiqi Qi,Zhimin Mo,Han Hu,Yanru Shao,Qianyuan He,Zushun Xu
标识
DOI:10.1021/acsanm.5c03736
摘要
Multimodal sonodynamic therapy (SDT) is one of the main approaches for future tumor therapy; however, the application of SDT is still hindered by hypoxia and glutathione (GSH) overexpression in the tumor microenvironment (TME). Based on this, we designed manganese-doped zeolitic imidazolate framework-67 (ZIF-67) nanocrystals and encapsulated them with cell membranes to obtain Mn-ZIF-67@CMs (MF@CMs). The ZIF-67 nanocrystals have natural M-N active sites and show potential for application in SDT. Since the TME contains a large amount of H2O2, which reacts with Mn2+ to release O2. Meanwhile, Co3+ and Mn3+ can consume GSH in the TME, which in turn boosts the effectiveness of SDT. Additionally, the reaction that produces Co2+ and Mn2+ exhibits a Fenton-like mechanism, which further contributes to the therapeutic effects of chemodynamic therapy (CDT). Furthermore, due to the magnetic resonance imaging (MRI) T1 imaging properties of Mn2+, these nanoparticles (MF@CMs) also hold potential for integrated diagnosis and treatment. The MF@CMs designed in this study have good biocompatibility, oxygen-producing capacity, and GSH-consuming capacity, indicating the potential for clinical application.
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