4.1 Article

Fast synthesis and bioconjugation of 68Ga core-doped extremely small iron oxide nanoparticles for PET/MR imaging

Journal

CONTRAST MEDIA & MOLECULAR IMAGING
Volume 11, Issue 3, Pages 203-210

Publisher

WILEY-BLACKWELL
DOI: 10.1002/cmmi.1681

Keywords

chelator-free Ga-68; Iron Oxide; PET; MRI; nano-radiotracer; T-1-MRI

Funding

  1. Spanish ministry of economy [MAT2013-47303-P, SAF2012-1207]
  2. Fundacio La Marato de TV3 [70/C/2012]
  3. Comunidad de Madrid [S2010/BMD-2326, CAM/API1009]
  4. Comunidad de Madrid (Inmunothercan-CM)
  5. Marie Curie Actions - PEOPLE - COFUND Programme
  6. Ministerio de Economia y Competitividad
  7. Pro-CNIC Foundation

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Combination of complementary imaging techniques, like hybrid PET/MRI, allows protocols to be developed that exploit the best features of both. In order to get the best of these combinations the use of dual probes is highly desirable. On this sense the combination of biocompatible iron oxide nanoparticles and 68Ga isotope is a powerful development for the new generation of hybrid systems and multimodality approaches. Our objective was the synthesis and application of a chelator-free 68Ga-iron oxide nanotracer with improved stability, radiolabeling yield and in vivo performance in dual PET/MRI. We carried out the core doping of iron oxide nanoparticles, without the use of any chelator, by a microwave-driven protocol. The synthesis allowed the production of extremely small (2.5 nm) 68Ga core-doped iron oxide nanoparticles. The microwave approach allowed an extremely fast synthesis with a 90% radiolabeling yield and T1 contrast in MRI. With the same microwave approach the nano-radiotracer was functionalized in a fast and efficient way. We finally evaluated these dual targeting nanoparticles in an angiogenesis murine model by PET/MR imaging. Copyright (c) 2016 John Wiley & Sons, Ltd.

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