TY - JOUR
T1 - Surface metal cation doping of maghemite nanoparticles
T2 - Modulation of MRI relaxivity features and chelator-free 68Garadiolabelling for dual MRI-PET imaging
AU - Israel, Liron L.
AU - Karimi, Farhad
AU - Bianchessi, Silvia
AU - Scanziani, Eugenio
AU - Passoni, Lorena
AU - Matteoli, Michela
AU - Langström, Bengt
AU - Lellouche, Jean Paul
N1 - Publisher Copyright:
© 2015 IOP Publishing Ltd.
PY - 2015/9
Y1 - 2015/9
N2 - Magnetically responsive maghemite (γ-Fe2O3) nanoparticles (NPs) are the subject of current interest due to their potential use as contrast agents for in vivo magnetic resonance imaging (MRI). In addition, PET (positron emission tomography) is another non-invasive molecular imaging modality based on nuclear medicine and short-lived positron radionuclides incorporated in various bioprobes. In previous work (Haviv et al 2010 J. Am. Chem. Soc. 132 12519-12521), Massart magnetite (Fe3O4) oxidation using ceric ammonium nitrate (CAN) was explored. The resulting hydrophilic maghemite (γ-Fe2O3) NPs formed a stable aqueous colloid/ferrofluid that disclosed a low level ofNP surface doping by Ce3/4+ atoms/cations. In this work, magnetically responsive gallium(III) or various other lanthanide(III) cation-doped maghemite NPs were prepared in different ways which influenced their r2∗ MRI relaxivities, which were usually strengthened vs those of known FDA approved ferrofluids. In addition, this resulting NPsurface chemistry enabled their direct labeling with PET-enabled 68Ga(III) cations (scheme 1) without using any attached chelating organic species/polymer, providing PETenabled radioactive magnetic NPs towards a novel dual PET/MRI imaging nanoscale agent.
AB - Magnetically responsive maghemite (γ-Fe2O3) nanoparticles (NPs) are the subject of current interest due to their potential use as contrast agents for in vivo magnetic resonance imaging (MRI). In addition, PET (positron emission tomography) is another non-invasive molecular imaging modality based on nuclear medicine and short-lived positron radionuclides incorporated in various bioprobes. In previous work (Haviv et al 2010 J. Am. Chem. Soc. 132 12519-12521), Massart magnetite (Fe3O4) oxidation using ceric ammonium nitrate (CAN) was explored. The resulting hydrophilic maghemite (γ-Fe2O3) NPs formed a stable aqueous colloid/ferrofluid that disclosed a low level ofNP surface doping by Ce3/4+ atoms/cations. In this work, magnetically responsive gallium(III) or various other lanthanide(III) cation-doped maghemite NPs were prepared in different ways which influenced their r2∗ MRI relaxivities, which were usually strengthened vs those of known FDA approved ferrofluids. In addition, this resulting NPsurface chemistry enabled their direct labeling with PET-enabled 68Ga(III) cations (scheme 1) without using any attached chelating organic species/polymer, providing PETenabled radioactive magnetic NPs towards a novel dual PET/MRI imaging nanoscale agent.
KW - Chelator free labeling of NPs
KW - Functional maghemite NPs
KW - Ga-labelling of NPs
KW - MRI/PET dual nanoparticulate imaging agents
KW - Metal cation doping process for NPsurface engineering
UR - http://www.scopus.com/inward/record.url?scp=84953255749&partnerID=8YFLogxK
U2 - 10.1088/2053-1591/2/9/095009
DO - 10.1088/2053-1591/2/9/095009
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SN - 2053-1591
VL - 2
JO - Materials Research Express
JF - Materials Research Express
IS - 9
M1 - 095009
ER -