Self-Assembly of SiO2/Gd-DTPA-Polyethylenimine Nanocomposites as Magnetic Resonance Imaging Probes

被引:20
|
作者
Luo, Kui [1 ]
Tian, Jing [1 ]
Liu, Gang [1 ]
Sun, Jiayu [2 ]
Xia, Chunchao [2 ]
Tang, Hehan [2 ]
Lin, Ling [2 ]
Miao, Tianxin [1 ]
Zha, Xuna [3 ]
Gao, Fabao [2 ]
Gong, Qiyong [2 ]
Song, Bin [2 ]
Shuai, Xintao [4 ]
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
[3] Philips Healthcare, Beijing 100020, Peoples R China
[4] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Gadolinium; Polyethylenimine; Layer-by-Layer; Self-Assembly; MRI; MRI CONTRAST AGENTS; GENE DELIVERY; IN-VIVO; POLYELECTROLYTE MULTILAYER; GADOPENTETATE DIMEGLUMINE; BIOMEDICAL APPLICATIONS; RELEASE PROPERTIES; SUSTAINED-RELEASE; LIVER METASTASES; SILICONE-RUBBER;
D O I
10.1166/jnn.2010.1742
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Controlled self-assembly of organic/inorganic magnetic hybrid materials have important applications in magnetic resonance imaging (MRI). In this study, a widely used polycation polyethylenimine was conjugated with gadopentetic acid (Gd-DTPA) as a gadolinium bearing polyelectrolyte (Gd-DTPA-PEI). Next, multilayers; of Gd-DTPA-PEI were coated on silica nanoparticles through layer-by-layer (LbL) self-assembly with polyanions as monitored by dynamic light scattering, zeta-potential, and scanning electron microscopy. The thickness of the multilayer film was estimated from quartz crystal microbalance based on counting frequency change of each adsorbed layer. The magnetic relaxation of SiO2/(Gd-DTPA-PEI/polyanion)(n) core-shell nanocomposite was tested at 1.5 T magnetic field in a clinical MRI scanner, and a 3-fold increase in T-1 relaxivity to 15.1 Gd mM(-1)s(-1) was noticed comparing to Gd-DTPA small molecules. Dextran sulfate was coated as the outermost layer on the nanocomposite for better biocompatibility as verified by in vitro cytotoxicity studies. This formulation provides good signal intensity enhancement of mouse liver in vivo with only 1/25 dose of clinical standard at 30 and 60 minutes after intravenous injection. This sensitive imaging probe with unique core-shell structures may find broad applications in cellular and molecular imaging.
引用
收藏
页码:540 / 548
页数:9
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