光热治疗
吡非尼酮
转移
肿瘤微环境
纳米颗粒
癌症研究
肿瘤进展
材料科学
癌症
阿霉素
纳米技术
药物输送
化疗
医学
特发性肺纤维化
肿瘤细胞
肺
内科学
作者
Huizi Deng,Yifan Yang,Tiantian Zuo,Tianxu Fang,Yingxin Xu,Jie Yang,Jun Zhang,Qi Shen
标识
DOI:10.1016/j.nano.2021.102399
摘要
The poor drug delivery and unsatisfying therapeutic effects remain to be the primary challenges for cancer therapy. Nanosystem that combines multiple functions into a single platform is an ideal strategy. Here, a smart drug delivery nanoplatform (Z@C-D/P) based on ZnO@CuS nanoparticles, loaded with doxorubicin (DOX) and pirfenidone (PFD) was constructed. Importantly, the β-CD-DMA and PEG-DMA could be activated in the mild acidic tumor microenvironment, then the nanosystem underwent charge reversal and PFD release. PFD could inhibit cancer-associated fibroblasts (CAFs) activation and enhance tumor penetration. And the residual nanostructure ZnO@CuS could trigger cascade amplified ROS generation to induce tumor cell death. The photothermal effect further strengthened the anti-tumor efficacy. Finally, the nanosystem showed remarkable inhibition of tumor growth (89.7%) and lung metastasis. The innovatively designed nanosystem integrating chemotherapy and photothermal effect would provide a promising strategy in breast cancer therapy.
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