Surface and Interfacial Engineering of Iron Oxide Nanoplates for Highly Efficient Magnetic Resonance Angiography

被引:128
作者
Zhou, Zijian [1 ,2 ]
Wu, Changqiang [3 ,4 ]
Liu, Hanyu [1 ,2 ]
Zhu, Xianglong [1 ,2 ]
Zhao, Zhenghuan [1 ,2 ]
Wang, Lirong [1 ,2 ]
Xu, Ye [3 ,4 ]
Ai, Hua [3 ,4 ]
Gao, Jinhao [1 ,2 ]
机构
[1] Xiamen Univ, Key Lab Chem Biol Fujian Prov, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Dept Biol Chem, Xiamen 361005, Peoples R China
[3] Sichuan Univ, West China Hosp, Natl Engn Res Ctr Biomat, Chengdu 610064, Peoples R China
[4] Sichuan Univ, West China Hosp, Dept Radiol, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
blood pool contrast agents; surface structure; interface; MRA; high-performance; CONTRAST AGENTS; MR-ANGIOGRAPHY; NANOPARTICLES; RELAXATION; NANOCUBES; TOXICITY; PROGRESS; CORONA; STATE; SIZE;
D O I
10.1021/nn507193f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Magnetic resonance angiography using gadolinium-based molecular contrast agents suffers from short diagnostic window; relatively low resolution and risk of toxicity. Taking into account the chemical exchange between metal Centers and surrounding protons; magnetic nanoparticles with suitable surface and interfacial features may serve as alternative T-1 contrast agents. Herein, we report the engineering on surface structure of iron oxide nanoplates to boost T-1 contrast ability through synergistic effects between exposed metal-rich Fe3O4(100) facets and embedded Gd2O3 clusters. The nanoplates show prominent T-1 contrast in a wide range of magnetic fields with an ultrahigh r(1) value up to 61.5 MM-1 s(-1). Moreover, engineering on nanobio interface through zwitterionic molecules adjusts the in vivo behaviors of nanoplates for highly efficient magnetic resonance angiography with steady-state acquisition Window, Superhigh resolution in vascular details, and low toxicity. This study provides a powerful tool for sophisticated design of MRI contrast agents for diverse use in bioimaging applications.
引用
收藏
页码:3012 / 3022
页数:11
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