Mitochondria-targeting zeolitic imidazole frameworks to overcome platinum-resistant ovarian cancer

被引:18
|
作者
Xing, Yan [1 ]
Jiang, Zhenqi [2 ,3 ]
Akakuru, Ozioma Udochukwu [2 ,3 ]
He, Yan [4 ]
Li, Aiguo [4 ]
Li, Juan [2 ]
Wu, Aiguo [2 ]
机构
[1] Ningbo First Hosp, Dept Gynecol, Ningbo 315010, Peoples R China
[2] Chinese Acad Sci, Key Lab Addit Mfg Mat Zhejiang Prov, Ningbo Inst Mat Technol & Engn, CAS Key Lab Magnet Mat & Devices,Cixi Inst Biomed, Ningbo 315201, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
基金
国家重点研发计划;
关键词
ZIF-90; Ovarian cancer; A2780; cells; Proliferation; Drug resistance; METAL-ORGANIC FRAMEWORKS; ONE-POT SYNTHESIS; ZIF-90; MEMBRANE; FAVORABLE BIOCOMPATIBILITY; DRUG-RESISTANCE; DELIVERY; NANOPARTICLES; SELECTIVITY; DOXORUBICIN; ATP;
D O I
10.1016/j.colsurfb.2020.110837
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Epithelial ovarian cancer is still the leading cause of death in gynecology due to its resistance to platinum-based first-line chemotherapeutic drugs. The utilization of mitochondria-targeted drugs has become an important direction in anti-tumor drug research and development. In this work, cisplatin (DDP)-loaded ZIF-90 with mitochondrial-targeting was synthesized at room temperature with a high drug loading (11.7 %, calculated based on Pt content). The ZIF-90@DDP showed high cellular uptake and less toxicity in both non- and DDP-resistant ovarian cancer cells with effective pH- and ATP-responsive drug release. Both mitochondria-targeting and responsive drug release could increase the drug concentration in mitochondria of drug-resistant cancer cells to reverse such resistance. Conclusively, the mitochondria-targeting ZIF-90@DDP with high drug loading could trigger responsive drug release in mitochondria of epithelial ovarian cancer cells, inhibit DPP-resistant epithelial ovarian cancer cells, and reverse drug resistance.
引用
收藏
页数:6
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