13C Hyperpolarization

MR with Hyperpolarized Spin Systems

3D graph depicting the relationship between amplitude, time, and frequency concerning metabolites like pyruvate, lactate, and alanine. Arrows indicate key compounds and reactions in metabolic pathways. On the right, a molecular structure of hyperpolarized 13C1-pyruvate is presented, with a note on its administration.
Dynamic ¹³C MRS after the administration of hyperpolarized Pyruvate (signal at 172 ppm, with its hydrated form at 180 ppm) into living tissue to assess enzymatic activity in vivo. After transport via Monocarboxylate Transporters (MCT) into cells, Lactate Dehydrogenase (LDH) transfers hyperpolarization to Lactate (signal at 184 ppm), and Alanine-Aminotransferase (ALT) to Alanine (signal at 176 ppm). The hyperpolarization decays after a few minutes.

The MR signal in living tissue is fundamentally limited by extremely low thermal polarization. Using hyperpolarization techniques such as dissolution Dynamic Nuclear Polarization (d-DNP), polarization of carbon-13 (13C) can be increased by several orders of magnitude, enabling metabolic MR applications of unprecedented sensitivity. After administration of hyperpolarized 13C-labeled substrates such as [1-13C]pyruvate, cellular metabolism transfers the 13C label to downstream molecules. Because each metabolite exhibits a distinct 13C resonance frequency, dynamic 13C MR allows real-time tracking of metabolic conversion rates, including pathways highly relevant in cancer biology, such as pyruvate-to-lactate flux. 

Our research integrates physics, chemistry, biomedical engineering, and clinical/pharmaceutical sciences, creating a highly interdisciplinary environment for developing and applying hyperpolarized 13C MR. The current focus of our work lies on preclinical applications in oncology and neuroscience, ranging from controlled in vitro systems to small-animal studies, using the SpinAligner (Polarize) system for polarization. Alongside these experimental efforts, we are advancing fast and quantitative 13C MR sequence design and developing new molecular probes to broaden the accessible metabolic landscape.

In parallel, we are working on the clinical translation of hyperpolarized 13C metabolic MRI, using the Spinlab (GE Healthcare) polarizing system. This combined preclinical and translational effort aims to extend the diagnostic and mechanistic power of metabolic MR toward clinically relevant questions in oncology and neuroscience.

Contact

  • Employee image

    Dr. Helen Abeln

    Group leader

  • Employee image

    Dr. Alexandra Lipka

    Group leader

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