4.4 Review

Metabolic and Molecular Imaging with Hyperpolarised Tracers

Journal

MOLECULAR IMAGING AND BIOLOGY
Volume 20, Issue 6, Pages 902-918

Publisher

SPRINGER
DOI: 10.1007/s11307-018-1265-0

Keywords

Imaging; Magnetic resonance imaging MRI; Magnetic resonance spectroscopy MRS; Hyperpolarisation; Metabolic imaging; Molecular imaging; DNP; Parahydrogen; Xenon

Funding

  1. Marie Sklodowska-Curie grant [642773]
  2. CNR-Fondazione Toscana Gabriele Monasterio
  3. Italian Multi-sited Multi-Modal Molecular Imaging site of Eurobioimaging in Pisa
  4. Heinrich-Boll-Stiftung [P131623]
  5. DFG [BE 1824/12-1, GRK 2154]
  6. Cancer Research UK
  7. National Institute of Health Research Biomedical Research Centre
  8. DFG Emmy Noether Programme [HO-4604/2-1, HO-4604/2-2, EXC 306]
  9. Marie Curie Actions (MSCA) [642773] Funding Source: Marie Curie Actions (MSCA)

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Since reaching the clinic, magnetic resonance imaging (MRI) has become an irreplaceable radiological tool because of the macroscopic information it provides across almost all organs and soft tissues within the human body, all without the need for ionising radiation. The sensitivity of MR, however, is too low to take full advantage of the rich chemical information contained in the MR signal. Hyperpolarisation techniques have recently emerged as methods to overcome the sensitivity limitations by enhancing the MR signal by many orders of magnitude compared to the thermal equilibrium, enabling a new class of metabolic and molecular X-nuclei based MR tracers capable of reporting on metabolic processes at the cellular level. These hyperpolarised (HP) tracers have the potential to elucidate the complex metabolic processes of many organs and pathologies, with studies so far focusing on the fields of oncology and cardiology. This review presents an overview of hyperpolarisation techniques that appear most promising for clinical use today, such as dissolution dynamic nuclear polarisation (d-DNP), parahydrogen-induced hyperpolarisation (PHIP), Brute force hyperpolarisation and spin-exchange optical pumping (SEOP), before discussing methods for tracer detection, emerging metabolic tracers and applications and progress in preclinical and clinical application.

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