化学
药品
细胞毒性
癌细胞
哈卡特
药物输送
细胞凋亡
生物物理学
纳米颗粒
癌症研究
药理学
纳米技术
癌症
材料科学
生物化学
体外
有机化学
医学
生物
内科学
作者
Can Tao,Fang Zhao,Ziwei Tang,Luxi Zhang,Qiang Niu,Gao Cao,Limin Zhao,Wenhuan Huang,Ping Zhao
标识
DOI:10.1016/j.jssc.2021.122489
摘要
Magnetic mesoporous ZrO2 (Fe3O4@ZrO2, MMZr) nanoparticles blocked by bismuth oxide (Bi2O3) are presented and efficiently deliver chemotherapeutic agent daunomycin (DNM) to the targeted tumor cells. Bi2O3 not only rapidly dissolves in the acidic condition of cancer cells to release the loaded chemotherapeutic drug but also enhances the anti-cancer effect through synergistic effects of the chemotherapy and Bi3+ ions. By monitoring the treatment process, compared with the free drug DNM, the drug loaded DDS exhibit more significant suppression against cancerous cells growth such as A549 and MCF-7 cancer cells and lower cytotoxicity against normal Hacat cells. Mechanism research indicates that the drug loaded DDS can arrest the cell cycle at G0/G1 phase, change the mitochondrial membrane potential and finally induced the apoptosis of the cancerous cells. These results indicate that the Bi2O3-gated ZrO2 platform is a promising approach to serve as a pH-sensitive DDS in the treatment of various cancers by chemo/ionic synergistic effects.
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