Facile synthesis of hyaluronic acid-modified Fe3O4/Au composite nanoparticles for targeted dual mode MR/CT imaging of tumors

被引:47
作者
Hu, Yong [1 ]
Yang, Jia [2 ]
Wei, Ping [1 ]
Li, Jingchao [1 ]
Ding, Ling [1 ]
Zhang, Guixiang [2 ]
Shi, Xiangyang [1 ]
Shen, Mingwu [1 ]
机构
[1] Donghua Univ, Coll Chem Chem Engn & Biotechnol, Shanghai 201620, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Shanghai Gen Hosp, Dept Radiol, Shanghai 200080, Peoples R China
基金
中国国家自然科学基金;
关键词
IRON-OXIDE NANOPARTICLES; ENTRAPPED GOLD NANOPARTICLES; MAGNETIC-RESONANCE; IN-VIVO; PHOTOTHERMAL THERAPY; COMPUTED-TOMOGRAPHY; CONTRAST; CANCER; MR; NANOCOMPOSITES;
D O I
10.1039/c5tb02040a
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
A facile co-precipitation approach for synthesizing hyaluronic acid (HA)-modified Fe3O4/Au composite nanoparticles (CNPs) for targeted dual mode tumor magnetic resonance (MR) and computed tomography (CT) imaging is reported. In this work, polyethyleneimine (PEI) was employed as a stabilizer to form gold NPs (PEI-Au NPs). In the presence of the PEI-Au NPs, controlled co-precipitation of Fe(II) and Fe(III) salts was performed, leading to the formation of the Fe3O4/Au-PEI CNPs, which were further modified with hyaluronic acid (HA). We show that the formed Fe3O4/Au-PEI-HA CNPs are colloidally stable, hemocompatible and cytocompatible in a given concentration range, and have a high affinity to target CD44 receptor-overexpressing cancer cells. Due to the presence of Fe3O4 and Au components, the formed Fe3O4/Au-PEI-HA CNPs display a high r(2) relaxivity (264.16 mM(-1) s(-1)) and good X-ray attenuation property, rendering them with an ability to be used as a nanoprobe for targeted dual mode MR/CT imaging of CD44 receptor-overexpressing cancer cells in vitro and a xenografted tumor model in vivo. The Fe3O4/Au-PEI-HA CNPs developed via this facile approach may hold great promise to be used as a unique platform for precision imaging of CD44 receptor-overexpressing tumors.
引用
收藏
页码:9098 / 9108
页数:11
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