The Education Ministry Key Lab of Resource Chemistry, Joint International Research Laboratory of Resource Chemistry, Ministry of Education, Shanghai Key Laboratory of Rare Earth Functional Materials, Shanghai Municipal Education Committee Key Laboratory of Molecular Imaging Probes and Sensors, and Shanghai Frontiers Science Center of Biomimetic Catalysis, College of Chemistry and Materials Science, Shanghai Normal University, Shanghai 200234, China.
Nanoscale. 2023 Jun 8;15(22):9652-9662. doi: 10.1039/d3nr00107e.
The ingenious combination of nano-enzymes with multi-enzyme activities and therapeutic drugs that can promote reactive oxygen species (ROS) production in cancer cells will enhance the therapeutic efficacy of nanomedicines on malignant tumors by amplifying oxidative stress. Herein, PEGylated Ce-doped hollow mesoporous silica nanoparticles (Ce-HMSN-PEG) loaded with saikosaponin A (SSA) are elaborately constructed as a smart nanoplatform for improving the efficiency of tumor therapy. The carrier Ce-HMSN-PEG showed multi-enzyme activities due to the presence of mixed Ce/Ce ions. In the tumor microenvironment, peroxidase-like Ce ions convert endogenous HO into highly toxic ˙OH for chemodynamic therapy, while Ce ions not only show catalase-like activity to reduce tumor hypoxia but also exhibit glutathione (GSH) peroxidase-mimicking properties to effectively deplete GSH in tumor cells. Moreover, the loaded SSA can cause the enrichment of superoxide anions (˙O) and HO within tumor cells by disrupting mitochondrial functions. By integrating the respective advantages of Ce-HMSN-PEG and SSA, the as-prepared SSA@Ce-HMSN-PEG nanoplatform can efficiently trigger cancer cell death and inhibit tumor growth significantly enhanced ROS production. Therefore, this positive combination therapy strategy has a good application prospect for enhancing antitumor efficacy.
纳米酶与具有多种酶活性的治疗药物的巧妙结合可以促进癌细胞中活性氧(ROS)的产生,从而通过放大氧化应激增强纳米药物对恶性肿瘤的治疗效果。在此,通过精心构建负载柴胡皂苷 A(SSA)的聚乙二醇化 Ce 掺杂中空介孔硅纳米粒子(Ce-HMSN-PEG)作为一种智能纳米平台来提高肿瘤治疗的效率。载体 Ce-HMSN-PEG 由于存在混合的 Ce/Ce 离子而具有多种酶活性。在肿瘤微环境中,过氧化物酶样 Ce 离子将内源性 HO 转化为用于化学动力学治疗的高毒性˙OH,而 Ce 离子不仅表现出类似过氧化氢酶的活性来降低肿瘤缺氧,而且还表现出谷胱甘肽(GSH)过氧化物酶模拟特性,以有效地耗尽肿瘤细胞中的 GSH。此外,负载的 SSA 通过破坏线粒体功能导致肿瘤细胞内超氧阴离子(˙O 和 HO 的积累。通过整合 Ce-HMSN-PEG 和 SSA 的各自优势,所制备的 SSA@Ce-HMSN-PEG 纳米平台可以有效地引发癌细胞死亡并抑制肿瘤生长,显著增强 ROS 的产生。因此,这种正组合治疗策略对于增强抗肿瘤疗效具有很好的应用前景。