Synthesis of surfactant-modified ZIF-8 with controllable microstructures and their drug loading and sustained release behaviour

被引:22
作者
Xu, Xinyu [1 ]
Liu, Ye [2 ]
Guo, Zhaoming [2 ]
Song, Xue-Zhi [1 ]
Qi, Xiuyu [1 ]
Dai, Zideng [1 ]
Tan, Zhenquan [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Panjin, Liaoning, Peoples R China
[2] Dalian Univ Technol, Sch Life Sci & Med, Panjin, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
nanomedicine; lung; nanofabrication; drug delivery systems; cellular biophysics; nanoparticles; cancer; toxicology; biomedical materials; drugs; organometallic compounds; surfactants; porosity; biodegradable materials; controlled drug sustained release; nanodrugs; controllable microstructures; drug loading; metal-organic frameworks; traditional drug carriers; drug delivery; surfactant-modified ZIF-8 nanoparticles; specific surface area; micropore volumes; doxorubicin; degradation performance; metabolism; cytotoxicity; cellular uptake; intracellular location; A549 human nonsmall-cell lung cancer cell line; cancer chemotherapy; METAL-ORGANIC FRAMEWORKS; NANOPARTICLES; NANOCARRIERS; CHEMOTHERAPY; DELIVERY; THERAPY;
D O I
10.1049/iet-nbt.2020.0076
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metal-organic frameworks (MOFs) as drug carriers have many advantages than traditional drug carriers and have received extensive attention from researchers. However, how to regulate the microstructure of MOFs to improve the efficiency of drug delivery and sustained release behaviour is still a big problem for the clinical application. Herein, the authors synthesise surfactant-modified ZIF-8 nanoparticles with different microstructures by using different types of surfactants to modify ZIF-8. The surfactant-modified ZIF-8 nanoparticles have the larger specific surface area and total micropore volumes than the original ZIF-8, which enables doxorubicin (DOX) to be more effectively loaded on the drug carriers and achieve controlled drug sustained release. Excellent degradation performance of ZIF-8 nanoparticles facilitates the metabolism of drug carriers. The formulation was evaluated for cytotoxicity, cellular uptake and intracellular location in the A549 human non-small-cell lung cancer cell line. ZIF-8/DOX nano drugs exhibit higher cytotoxicity towards cells in comparison with free DOX, suggesting the potential application in nano drugs to cancer chemotherapy.
引用
收藏
页码:595 / 601
页数:7
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