Fe3O4/MnO hybrid nanocrystals as a dual contrast agent for both T1- and T2-weighted liver MRI

被引:119
作者
Im, Geun Ho [1 ,2 ]
Kim, Soo Min [3 ]
Lee, Dong-Gyu [3 ]
Lee, Won Jae [1 ]
Lee, Jung Hee [1 ,2 ]
Lee, In Su [3 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Radiol, Seoul 135710, South Korea
[2] Samsung Biomed Res Inst, Ctr Mol & Cellular Imaging, Seoul 135710, South Korea
[3] Pohang Univ Sci & Technol POSTECH, Dept Chem, Gyeongbuk 790784, South Korea
基金
新加坡国家研究基金会;
关键词
Nanoparticle; MRI (magnetic resonance imaging); Contrast agent; Liver; Dual contrast agent; IRON-OXIDE NANOPARTICLES; MAGNETIC-RESONANCE; MANGAFODIPIR TRISODIUM; HEPATOCELLULAR-CARCINOMA; MNO NANOPARTICLES; QUANTUM DOTS; RELAXIVITY; CANCER; SIZE; CELLS;
D O I
10.1016/j.biomaterials.2012.11.054
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
To investigate whether it is possible to develop a dual magnetic resonance (MR) contrast agent, Fe3O4/MnO hybrid nanocrystals were modified to integrate the T-1 and T-2 contrast-enhancing abilities of each compound, and their characteristics as MR contrast agents were investigated. In vitro and in vivo investigations revealed that the Fe3O4/MnO dumbbell-shaped nanocrystal exerted a negative T-2 contrast effect in its intact form and also gave rise to a positive contrast effect in T-1-weighted MR imaging by releasing Mn2+ ions in a low pH environment. This induced organ-specific contrast enhancement for both T-1- and T-2-weighted in vivo MR imaging. The usefulness of the Fe3O4/MnO hybrid nanocrystals as dual contrast agents was evaluated by in vivo MR imaging of an orthotopic xenograft model of human hepatocellular carcinoma (HCC). After injection of the Fe3O4/MnO hybrid nanocrystals, dual contrast-enhanced MR images that synergistically combined the T-2 and T-1 contrast effects from the Fe3O4 grain and released Mn2+ ions were obtained by a single acquisition of MR imaging. This facilitated the detection of HCC with a high degree of conspicuity that could not be achieved with any single contrast agent. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2069 / 2076
页数:8
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