Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T2 Weighted Magnetic Resonance Imaging

被引:21
|
作者
Mathieu, Paul [1 ,2 ]
Coppel, Yannick [1 ,2 ]
Respaud, Marc [3 ]
Nguyen, Quyen T. [1 ,2 ]
Boutry, Sebastien [4 ,5 ]
Laurent, Sophie [4 ,5 ]
Stanicki, Dimitri [4 ]
Henoumont, Celine [4 ]
Novio, Fernando [6 ]
Lorenzo, Julia [7 ]
Montpeyo, David [7 ]
Amiens, Catherine [1 ,2 ]
机构
[1] CNRS, LCC, 205 Route Narbonne,BP 44099, F-31077 Toulouse 4, France
[2] Univ Toulouse, UPS, INPT, F-31077 Toulouse 4, France
[3] INSA, LPCNO, 135 Ave Rangueil, F-31077 Toulouse 4, France
[4] Univ Mons, Dept Gen Organ & Biomed Chem, NMR & Mol Imaging Lab, 19 Ave Maistriau, B-7000 Mons, Belgium
[5] Univ Mons, UMONS, CMMI, B-6041 Charleroi, Belgium
[6] Univ Autonoma Barcelona, Dept Quim, Campus UAB, E-08193 Barcelona, Spain
[7] Univ Autonoma Barcelona, Inst Biotecnol & Biomed, Dept Bioquim & Biol Mol, Bellaterra 08193, Spain
来源
MOLECULES | 2019年 / 24卷 / 24期
关键词
nanomaterials; nanochemistry; surface functionalization; MRI; toxicity; CORE-SHELL NANOPARTICLES; MRI CONTRAST ENHANCEMENT; IRON NANOPARTICLES; CORE/SHELL NANOPARTICLES; STABILITY; TOXICITY; AGENTS; PHASE;
D O I
10.3390/molecules24244629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The growing concern over the toxicity of Gd-based contrast agents used in magnetic resonance imaging (MRI) motivates the search for less toxic and more effective alternatives. Among these alternatives, iron-iron oxide (Fe@FeOx) core-shell architectures have been long recognized as promising MRI contrast agents while limited information on their engineering is available. Here we report the synthesis of 10 nm large Fe@FeOx nanoparticles, their coating with a 11 nm thick layer of dense silica and functionalization by 5 kDa PEG chains to improve their biocompatibility. The nanomaterials obtained have been characterized by a set of complementary techniques such as infra-red and nuclear magnetic resonance spectroscopies, transmission electron microscopy, dynamic light scattering and zetametry, and magnetometry. They display hydrodynamic diameters in the 100 nm range, zetapotential values around -30 mV, and magnetization values higher than the reference contrast agent RESOVIST (R). They display no cytotoxicity against 1BR3G and HCT116 cell lines and no hemolytic activity against human red blood cells. Their nuclear magnetic relaxation dispersion (NMRD) profiles are typical for nanomaterials of this size and magnetization. They display high r(2) relaxivity values and low r(1) leading to enhanced r(2)/r(1) ratios in comparison with RESOVIST (R). All these data make them promising contrast agents to detect early stage tumors.
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页数:20
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