Self-Assembly of Magnetite Nanocrystals with Amphiphilic Polyethylenimine: Structures and Applications in Magnetic Resonance Imaging

被引:51
作者
Wang, Zhiyong [1 ]
Liu, Gang [1 ]
Sun, Jiayu [2 ]
Wu, Bing [2 ]
Gong, Qiyong [2 ]
Song, Bin [2 ]
Ai, Hua [1 ,2 ]
Gu, Zhongwei [1 ]
机构
[1] Sichuan Univ, Natl Engn Res Ctr Biomat, Chengdu 610064, Peoples R China
[2] Sichuan Univ, W China Hosp, Dept Radiol, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Amphiphilic; Polyethylenimine; Iron Oxide; Self-Assembly; MRI; CONTRAST AGENTS; POLYMERIC MICELLES; FE3O4; NANOPARTICLES; COPOLYMERS; DESIGN; PEG; MN; FE; CO;
D O I
10.1166/jnn.2009.J033
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Controlled self-assembly of magnetic nanocrystals has important applications in biomedical fields. In this study, hydrophobic superparamagnetic iron oxide (SPIO) nanocrystals are self-assembled into small clusters (mean diameter <100 nm) in water phase with the help of partially alkylated hyper-branched polycation, polyethylenimine (PEI). The amphiphilic PEI can wrap one or multiple SPIO nanocrystals inside micelle cores depending on different polycation/SPIO mass ratios. These SPIO nanocrystal containing micelles are superparamagnetic at room temperature. At the magnetic field of 1.5 T, single SPIO nanocrystal containing micelles have a T-2 relaxivity of 118 Fe mM(-1)s(-1), while multiple SPIO nanocrystals micelles have relatively higher T-2 relaxivities up to 323 Fe mM(-1)s(-1). Next, these potential magnetic resonance imaging (MRI) probes are tested for labeling rabbit mesenchymal stem cells. The formulation with a low polymer/SPIO ratio (0.2) is biocompatible and effective in labeling. Under a clinical MRI scanner, 3 x 10(6) labeled cells in gelatin phantom present much darker images than controlled ones. The T-2 relaxation rate of the labeled cells is -74.2 s(-1), significantly higher than the control cells of -3.4 s(-1). This new amphiphilic polycation/SPIO nanocomposite may provide opportunities in cell labeling and tracking their behaviors in vivo.
引用
收藏
页码:378 / 385
页数:8
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