4.6 Article

Silica-coated super-paramagnetic iron oxide nanoparticles (SPIONPs): a new type contrast agent of T-1 magnetic resonance imaging (MRI)

Journal

JOURNAL OF MATERIALS CHEMISTRY B
Volume 3, Issue 26, Pages 5172-5181

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5tb00300h

Keywords

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Funding

  1. Zhejiang Provincial Natural Science Foundation of China [BSH1401038]
  2. China Postdoctoral Research program [2014M561799]
  3. National Natural Science Foundation of China [U1432114]
  4. Hundred Talents Program of the Chinese Academy of Sciences [2010-735]
  5. Key Breakthrough Program of the Chinese Academy of Sciences [KGZD-EW-T06]
  6. Chinese Academy of Sciences
  7. World Academy of Science [2014FFGB0004]

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Magnetic resonance imaging (MRI), a sophisticated promising three-dimensional tomographic noninvasive diagnostic technique, has an intrinsic advantage in safety compared with radiotracer and optical imaging modalities; however, MRI contrast agents are less sensitive than complexes used in other imaging techniques. Usually the clinically used Gd-based complexes MRI-T-1 contrast agents are toxic; therefore, the demand for nontoxic novel T-1-weighted MRI candidates with ultrasensitive imaging and advanced functionality is very high. In this research, silica-coated ultra-small monodispersed super-paramagnetic iron oxide nanoparticles were synthesized via a thermal decomposition method, which demonstrated themselves as a high performance T-1-weighted MRI contrast agent for heart, liver, kidney and bladder based on in vivo imaging analyses. Transmission electron microscopy (TEM) results illustrated that the diameter of the SPIONPs was in the range of 4 nm and the average size of Fe3O4@SiO2 was about 30-40 nm. X-ray diffraction (XRD) and Raman spectroscopy analyses revealed the phase purity of the prepared SPIONPs. These magnetite nanoparticles exhibited a weak magnetic moment at room temperature because of the spin-canting effect, which promoted a high positive signal enhancement ability. MTT assays and histological analysis demonstrated good biocompatibility of the SPIONPs in vitro and in vivo. In addition, the silica-coated ultrasmall (4 nm sized) magnetite nanoparticles exhibited a good r(1) relaxivity of 1.2 mM(-1) s(-1) and a low r(2)/r(1) ratio of 6.5 mM(-1) s(-1). In vivo T-1-weighted MR imaging of heart, liver, kidney and bladder in mice after intravenous injection of nanoparticles further verified the high sensitivity and biocompatibility of the as-synthesized magnetite nanoparticles. These results reveal silica-coated SPIONPs as a promising candidate for a T-1 contrast agent with extraordinary capability to enhance MR images.

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