Folic Acid Functionalized Zirconium-Based Metal-Organic Frameworks as Drug Carriers for Active Tumor-Targeted Drug Delivery

被引:106
作者
Dong, Hong [1 ]
Yang, Gui-Xin [1 ]
Zhang, Xin [1 ]
Meng, Xiang-Bin [1 ]
Sheng, Jing-Li [1 ]
Sun, Xiao-Jun [1 ]
Feng, Yu-Jie [2 ]
Zhang, Feng-Ming [1 ]
机构
[1] Harbin Univ Sci & Technol, Coll Chem & Environm Engn, Sch Mat Sci & Engn, Harbin 150040, Heilongjiang, Peoples R China
[2] Harbin Inst Technol, Sch Municipal & Environm Engn, Harbin 150090, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
active tumor-targeted; drug delivery; folic acid; metal-organic frameworks; zirconium; CANCER-THERAPY; PROTON CONDUCTION; MOF MATERIALS; NANOPARTICLES; CELLS; IONS; SIZE;
D O I
10.1002/chem.201804153
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoscale metal-organic frameworks (NMOFs) have proven to be a class of promising drug carriers as a result of their high porosity, crystalline nature with definite structure information, and potential for further functionality. However, MOF-based drug carriers with active tumor-targeting function have not been extensively researched until now. Here we show a strategy for constructing active tumor-targeted NMOF drug carriers by anchoring functional folic acid (FA) molecules onto the metal clusters of NMOFs. Two zirconium-based MOFs, MOF-808 and NH2-UiO-66, were chosen as models to reduce to the nanoscale for application as drug carriers, and then the terminal carboxylates of FA molecules were coordinated to Zr-6 clusters on the surfaces of the nanoparticles by substitution of the original formate or terminal -OH ligands. The successful modification with FA was confirmed by solid-state C-13 MAS NMR and UV/Vis spectroscopy and other characterization methods. Drug loading and controlled release behavior at different pH were determined by utilizing the anticancer drug 5-fluorouracil (5-FU) as the model drug. Confocal laser scanning microscopy measurements further demonstrated that 5-FU-loaded FA-NMOFs have excellent targeting ability through the efficient cellular uptake of FA-NMOFs. This work opens up a new avenue to the construction of active tumor-targeted NMOF-based drug carriers with potential for cancer therapies.
引用
收藏
页码:17148 / 17154
页数:7
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