Glypican-3 antibody functionalized Prussian blue nanoparticles for targeted MR imaging and photothermal therapy of hepatocellular carcinoma

被引:67
|
作者
Li, Zhenglin [1 ,2 ]
Zeng, Yongyi [1 ,2 ,3 ]
Zhang, Da [1 ,2 ]
Wu, Ming [1 ,2 ]
Wu, Lingjie [1 ,2 ]
Huang, Aimin [2 ,4 ]
Yang, Huanghao [5 ]
Liu, Xiaolong [1 ,2 ]
Liu, Jingfeng [1 ,2 ,3 ]
机构
[1] Fujian Med Univ, Mengchao Hepatobiliary Hosp, Fuzhou 350025, Peoples R China
[2] Fujian Med Univ, Liver Ctr Fujian Prov, Fuzhou 350025, Peoples R China
[3] Fujian Med Univ, Liver Dis Ctr, Affiliated Hosp 1, Fuzhou 350005, Peoples R China
[4] Fujian Med Univ, Sch Basic Med Sci, Dept Pathol, Fuzhou 350004, Peoples R China
[5] Fuzhou Univ, Coll Chem, Key Lab Anal & Detect Technol Food Safety MOE, Fuzhou 350002, Peoples R China
基金
中国国家自然科学基金;
关键词
IRON-OXIDE NANOPARTICLES; IN-VIVO; THERMAL THERAPY; CANCER; ABLATION; AGENT; CELLS; LASER; TUMORS; PROBE;
D O I
10.1039/c4tb00516c
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
MRI-guided photothermal therapy is becoming a more widely accepted minimally invasive technique. In this study, glypican-3 monoclonal antibody functionalized Prussian blue nanoparticles (antiGPC3-PBNPs) were developed as a novel theranostic agent for the targeted MR imaging and photothermal therapy of hepatocellular carcinoma. The physical properties of the antiGPC3-PBNPs were characterized by SEM, TEM and Vis-NIR absorption spectra, which showed that the developed nanoprobe formed well defined nanocubes with an average diameter of 21 nm. The significantly increased targeting cellular uptake efficiency in HepG2 cells via receptor-mediated endocytosis was confirmed by confocal fluorescence microscopy and ICP-MS. Furthermore, the high photothermal cytotoxicity, excellent MR imaging contrast enhancement ability and biocompatibility of the developed nanoprobe were also confirmed. Hence, the developed antiGPC3-PBNPs could be used as a promising nanoprobe for targeted MRI diagnosis and efficient photothermal therapy for hepatocellular carcinoma.
引用
收藏
页码:3686 / 3696
页数:11
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