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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.
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页数:6
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