Smart gold nanocages for mild heat-triggered drug release and breaking chemoresistance

阿霉素 纳米笼 光热治疗 抗药性 化学 化疗 药理学 癌细胞 药品 副作用(计算机科学) 脂质体 癌症研究 纳米技术 癌症 医学 材料科学 外科 生物 生物化学 内科学 催化作用 程序设计语言 微生物学 计算机科学
作者
Huamei He,Lanlan Liu,Shengping Zhang,Mingbin Zheng,Ai-Qing Ma,Ze Chen,Hong Pan,Haimei Zhou,Ruijing Liang,Lintao Cai
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:323: 387-397 被引量:44
标识
DOI:10.1016/j.jconrel.2020.04.029
摘要

Chemotherapy is an important modality available for cancer treatment. However, the present chemotherapy is still far from being satisfactory mainly owing to the severe side effects of the chemotherapeutic agents and drug resistance of cancer cells. Thus, reversing drug resistance by constructing an ideal chemotherapeutic strategy with the least side effects and the best efficacy is greatly needed. Here, we designed a smart nanosystem of thermo-sensitive liposome coated gold nanocages with doxorubicin (DOX) loading (LAD) for near-infrared (NIR)-triggered drug release and chemo-photothermal combination therapy. The biocompatible liposomes coating facilitated the cellular uptake of LAD and meanwhile avoided drug leakage during the circulation. More importantly, LAD exhibited controllable photothermal conversion property and produced mild heat under NIR irradiation, which not only triggered DOX release and transferred DOX from lysosome to nucleus, but also elicited the mild heat cell killing effect to improve the curative efficiency. Further mechanism study revealed that mild heat could reverse drug resistance by down-regulation of the chemoresistance-related markers (e.g., HSF-1, p53, P-gp), and inhibited DOX export and increased drug sensitiveness, thereby prominently increased the anticancer efficiency. This versatile nanoplatform with enhanced curative efficacy and lower side effect is promising to apply in the field of drug controlled release and combination tumor therapy.
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