光热治疗
生物相容性
索拉非尼
纳米材料
癌症治疗
纳米颗粒
体内
介孔材料
癌症研究
活性氧
医学
纳米技术
肝细胞癌
化学
癌症
材料科学
内科学
生物
生物化学
催化作用
生物技术
有机化学
作者
Qingqing Guan,Ruomi Guo,Shihui Huang,Fan Zhang,Jie Liu,Zhiyong Wang,Xi Yang,Xintao Shuai,Zhong Cao
标识
DOI:10.1016/j.jconrel.2020.01.048
摘要
Iron-based nanomaterials as the main ferroptosis-inducing platforms are more promising because iron itself is a key component in the Fenton reaction to produce ROS. However, the Fe dose needs to be very high in order to induce ferroptosis-based cancer treatment using the SPIO NPs. Therefore, it is still of great challenge to enhance the efficacy of ferroptosis-based cancer therapy by associating the iron-based nanomaterials with other components and therapeutic modalities. In this study, sorafenib (SRF) and ultrasmall SPIO nanoparticles were loaded into the mesopores and onto the surface of MPDA NPs to form [email protected] nanoparticles. SPIO loading endowed the system with iron-supply for ferroptosis and made the system MRI-visible. Meanwhile, SRF was able to induce ferroptosis in cancer cells with lower Fe dose. Furthermore, the heat generated by MPDA NPs upon laser irradiation offered a moderate PTT to boost the ferroptosis effect. The [email protected] exhibited biocompatibility highly desirable for in vivo application and superior anticancer therapy via the combination of ferroptosis and photothermal therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI