Facile synthesis of polypyrrole@metal-organic framework core-shell nanocomposites for dual-mode imaging and synergistic chemo-photothermal therapy of cancer cells

被引:108
|
作者
Chen, Xiangjun [1 ]
Zhang, Manjie [1 ]
Li, Shengnan [1 ]
Li, Lu [1 ]
Zhang, Lingyu [1 ]
Wang, Tingting [2 ]
Yu, Min [1 ]
Mou, Zhongcheng [1 ]
Wang, Chungang [1 ]
机构
[1] Northeast Normal Univ, Dept Chem, Natl & Local United Engn Lab Power Battery, Changchun 130024, Peoples R China
[2] Changchun Univ Sci & Technol, Sch Chem & Environm Engn, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
NEAR-INFRARED LIGHT; IN-VIVO; DRUG-DELIVERY; NANOPARTICLES; CHEMOTHERAPY; CARRIER; AGENT;
D O I
10.1039/c6tb03218d
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In our work, we report a facile approach to fabricate well-dispersed polypyrrole@metal-organic framework (PPy@MOF) core-shell nanocomposites (NCs) with a polypyrrole (PPy) core and an MIL-100(Fe) shell. The adsorbed Fe(III) ions on the as-fabricated PPy surface were utilized as reactive sites for further growth of the MIL-100(Fe) in the presence of trimesic acid (H(3)btc). The resulting NCs exhibited strong absorption in the near infrared (NIR) region and possessed an excellent photothermal efficiency of B40% resulting from the PPy core. The MOF structure based on Fe(III) carboxylate materials held great ability for storage/delivery of the hydrophilic anti-cancer drug, doxorubicin (DOX). The released DOX continuously increased due to the damage of the shell at low pH values. When the DOX-loaded PPy@MIL-100(Fe) NCs were exposed to NIR irradiation, owing to the heat produced by the NCs, the local temperature increased, resulting in a faster release of DOX from the MIL-100(Fe) shell. Furthermore, PPy@MIL-100(Fe) NCs were successfully employed for dual-mode magnetic resonance imaging (MRI)/photoacoustic imaging (PAI) and synergistic chemo-photothermal therapy of cancer cells. Therefore, our work could encourage further study in the construction of a multifunctional platform using different MOF nanomaterials for cancer theranostics.
引用
收藏
页码:1772 / 1778
页数:7
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