Jones, NE, Burnett, CA, Salamon, S et al. (9 more authors) (2018) Fluoride doped γ-Fe₂O₃ nanoparticles with increased MRI relaxivity. Journal of Materials Chemistry B, 6 (22). pp. 3665-3673. ISSN 2050-750X
Abstract
Iron oxide nanoparticles (IONs) are being actively researched and experimented with as contrast agents for Magnetic Resonance Imaging (MRI), as well as image-directed delivery of therapeutics. The efficiency of an MRI contrast agent can be described by its longitudinal and transverse relaxivities, r₁ and r₂. γ-Fe₂O₃ nanoparticles – doped with fluoride in a controlled manner and functionalised with citric acid – showed a 3-fold increase in r₁ and a 17-fold increase in r₂ in a magnetic field of 3 T and almost 6-fold increase in r₁ and a 14-fold increase in r₂ at 11 T. Following fluorination, PXRD shows that the crystal structure of γ-Fe₂O₃ is maintained, Mössbauer spectroscopy shows that the oxidation state of the Fe cation is unchanged and HREM shows that the particle size does not vary. However, magnetisation curves show a large increase in the coercive field, pointing towards a large increase in the magnetic anisotropy for the fluorinated nanoparticles compared to the un-doped γ-Fe₂O₃ nanoparticles. Therefore, a chemically induced increase in magnetic anisotropy appears to be the most relevant parameter responsible for the large increase in relaxivity for γ-Fe₂O₃ nanoparticles.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2018, The Royal Society of Chemistry. This is an author produced version of a paper published in Journal of Materials Chemistry B. Uploaded in accordance with the publisher's self-archiving policy. |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Physics and Astronomy (Leeds) > Molecular & Nanoscale Physics |
Depositing User: | Symplectic Publications |
Date Deposited: | 25 Jun 2018 13:55 |
Last Modified: | 04 Apr 2019 00:43 |
Status: | Published |
Publisher: | Royal Society of Chemistry |
Identification Number: | 10.1039/C8TB00360B |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:132477 |