阿霉素
骨肉瘤
细胞凋亡
体内
药理学
癌症研究
化学
药物输送
细胞毒性
活性氧
化疗
抗药性
医学
体外
生物
生物化学
外科
生物技术
有机化学
微生物学
作者
Tao Zhao,Tian‐Jiao Zhou,Chen Zhang,Yingxuan Liu,Wenjia Wang,Chengjun Liu,Xing Liu,Hu‐Lin Jiang
标识
DOI:10.1021/acs.molpharmaceut.3c00068
摘要
Chemotherapy is the main treatment method for osteosarcoma in the clinic. However, drug resistance and its poor antimetastatic effects greatly limit its clinical application. In this work, dual-drug nanoparticles (NPs) containing albendazole (ABZ) and doxorubicin (DOX), named AD@PLGA–PEG NPs, were prepared to solve the problems of chemotherapeutic drug resistance and poor antimetastasis effects. Compared with free DOX, ABZ combined with DOX can increase intracellular reactive oxygen species (ROS) and induce more tumor cell apoptosis; therefore, AD@PLGA–PEG NPs produced more mitochondria-mediated oxidative stress and better apoptosis efficiency. Importantly, ABZ can also effectively inhibit the expression of hypoxia inducible factor-1α (HIF-1α) and then reduce the expression of its downstream vascular endothelial growth factor (VEGF); thus, the AD@PLGA–PEG NPs effectively inhibited tumor metastasis in vivo. Collectively, the dual-drug AD@PLGA–PEG NPs delivery system provided prominent antitumor and antimetastatic efficacy and might be a promising treatment for osteosarcoma.
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