Cape Town - 2026 ISMRM-ISMRT Annual Meeting and Exhibition • 09-14 May 2026

Digital Poster

Hyperpolarization: Novel Methods

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Hyperpolarization: Novel Methods
Digital Poster
Contrast Mechanisms
Thursday, 14 May 2026
Digital Posters Row G
08:30 - 09:25
Session Number: 666-01
No CME/CE Credit
This session focuses on technology development and applications in hyperpolarization particularly for 13C.

  Figure 666-01-001.  Demonstration of the novel hyperpolarizer technique to monitor in vivo metabolism using cross and direct polarization
Donghyun Hong, Dmitry Eshchenko, Meetu Wadhwa, Pinelopi Moutzouri, Paola Porcari, agnes glemot, Alia Hassan, Marco Sacher, Marc Rossire, Marc Schnell, Stefan Zollinger, Denis Lohner, Joerg Hinderer, Valentin Krebs, Benjamin Beyeler, Alec Beaton, Roberto Melzi, Kristin Granlund, Dan Vigneron, James Kempf, Renuka Sriram
University Of California, San Francisco (UCSF), United States of America
Impact: This work establishes cross-polarization hyperpolarization as a rapid, high-SNR method for in vivo 13C metabolic imaging, reducing polarization time from >60 to 10 minutes. It enables efficient, multi-organ metabolic studies and accelerates the translation of hyperpolarized MRI toward clinical applications.
  Figure 666-01-002.  Comparing an iterative least squares frequency decomposition method for non-invasive 3D pH imaging against 13C MRSI in vivo
Jakob Gaubatz, Florian Gaksch, Sandra Sühnel, Oscar Georgiev, Luca Nagel, Martin Grashei, Franz Schilling
TUM School of Medicine and Health, TUM University Hospital, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany
Impact: A new approach for 3D pH imaging using hyperpolarised 13C-labelled Z-OMPD was compared to conventional FID-CSI. With agreement confirmed, the method’s faster readout and greater volume coverage can now enable novel 3D insights into tumour acidification or kidney pH.
  Figure 666-01-003.  Electron irradiation-induced radicals as stable endogenous agents for sodium [1-13C]pyruvate Dynamic Nuclear Polarisation
Zoe Richardson, William Myers, Iain Tullis, Nichlas Vous Christensen, Duy Anh Dang, Esben Hansen, Zhuang Liu, Lotte Bonde Bertelsen, Kristoffer Petersson, Christoffer Laustsen, Damian Tyler, Jack Miller, Catriona Rooney
University College London, London, United Kingdom
Impact: One of the barriers to clinical scaling of hyperpolarised MRI is the need for unstable exogenous radicals. Using endogenous electron irradiation-induced radicals simplifies DNP. It removes the need for filtration and sterilisation and could allow centralised manufacturing of the radicals.
  Figure 666-01-004.  Enhancing in vivo SNR of hyperpolarized pH imaging through T1 prolongation by deuteration of 13C-labelled (Z)-OMPD
Florian Gaksch, Alexander Huber, Jakob Gaubatz, Sandra Sühnel, Kristin Koetz, Nadine Setzer, Silvester Bartsch, Martin Grashei, Franz Schilling
TUM School of Medicine and Health, TUM University Hospital, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany
Impact: T₁-prolongation by deuteration of ZOMPD substantially enhances in vivo SNR of hyperpolarized pH-imaging when avoiding co-polarization with [13C]urea and high injection concentrations. This allows for higher spatial resolution in hyperpolarized in vivo pH-imaging and extended perfusion times to study pH-compartments.


  Figure 666-01-005.  A dedicated 13C phantom and protocol for cross-site harmonization in clinical hyperpolarized 13C MRI
Kristina Jacobsen, Ingeborg Skre, Rie Olin, Mathilde Lerche
Technical University of Denmark, Kgs. Lyngby, Denmark
Impact: A dedicated ¹³C phantom and protocol provide a common framework for identifying and assessing inter-site variability, promoting consistent acquisition in forthcoming multi-center hyperpolarized ¹³C MRI studies.
  Figure 666-01-006.  Extending the T1 lifetime of [1-13C]pyruvate to over 4 min
Josh Philipp Peters, Florin Teleanu, Charbel Assaf, Huijing Zou, Jan-Bernd Hövener, Alexej Jerschow, Andrey Pravdivtsev
Kiel University, Kiel, Germany
Impact: More than 4 minutes T1 enables essentially polarization loss-free transport, quality assurance and administration of hyperpolarized [1-13C]pyruvate for biomedical applications. Understanding and reducing relaxation sources extended the nuclear relaxation lifetimes by >600%, setting a new reference for pyruvate hyperpolarization studies.
  Figure 666-01-007.  Multicenter evaluation of the POLARIS PHIP polarizer across models and imaging conditions
Vencel Somai, Hadrien Dyvorne, Galen Reed, Christoph Müller, Catriona Rooney, Meret Cepero Malo, Andrei Chekushin, Senay Karaali, Zumrud Ahmodova, Martin Grashei, Jonas Handwerker, Felix Josten, Pascal P.R. Ruetten, Luca Nagel, Miriam Kirst, Sandra Sühnel, Martin Grashei, Franz Schilling, Stephen Lai, Qing Wang, Yunyun Chen, José Enriquez, James Bankson, David Gomez-Cabeza, Lluís Mangas, Gergo Matajsz, Alba Herrero Gómez, Vincent Ribas, Irene Marco-Rius, Renuka Sriram, Dan Vigneron, Jeremy Gordon, Meetu Wadhwa, Xiao Gao, Tamara Vasilkovska, Max Bullock, rafat chowdhury, Shonit Punwani, Mario Chang, Saket Patel, Roberta Pigliapocchi, Thasin Peyear, Kayvan Keshari, Ilai Schwartz, Stephan Knecht, Myriam Chaumeil
NVision Imaging Technologies GmbH, Ulm, Germany
Impact: POLARIS delivers fast, reliable, and reproducible [1-¹³C]pyruvate hyperpolarization, enabling standardized metabolic MRI across centers, field strengths, and models. This breakthrough accelerates translational research and multicenter studies, driving clinical adoption of real-time metabolic imaging in oncology, neurology, and cardiovascular disease.
  Figure 666-01-008.  Multi Nuclei Small Animal Insert for in-vivo Hyperpolarized C13 Imaging on a Clinical MRI System
Tobias Haase b. Lobmeyer, Miriam Kirst, Kristin Koetz, Sybille Reder, Martin Grashei, Franz Schilling, Volker Rasche
Ulm University, Medical Center, Ulm, Germany
Impact: The easy-to-use system shows adequate SNR (1H and 13C) for imaging in small animals without modifying scanner hardware. Using the clinical scanners console, sequences, main magnetic field and gradient system, allow for a high degree of transferability to clinical trials.
  Figure 666-01-009.  Optimization of [2-13C]Pyruvate Hyperpolarization Via the Addition of Gadolinium
Zhuang Liu, Damian Tyler, Ladislav Valkovič, James Grist
Oxford Centre for Clinical MR Research (OCMR), University of Oxford, Oxford, United Kingdom
Impact: The liquid-state polarization level of [2-13C]pyruvate in the pre-clinical polarizer is possible to be nearly doubled with our optimized Gd concentration, which can significantly increase the signal-to-noise ratio (SNR) and is promising for metabolic imaging in clinical practice.
  Figure 666-01-010.  Optimization of bSSFP passband periodicity for 13C metabolic MRSI at clinical field strengths
Stefan Menzel, Julian Schüle, Fabian Bschorr, Tobias Speidel, Christoph Müller, Volker Rasche
Ulm University, Medical Center, Ulm, Germany
Impact: Optimization of passband periodicity in the bSSFP transient phase improves SNR and acquisition speed for hyperpolarized ¹³C-MRSI at clinical field strengths, enabling more efficient metabolite-separated imaging, and facilitating translation of optimized bSSFP techniques to preclinical and in-vivo metabolic studies.
  Figure 666-01-011.  A Dual Multiband RF Pulse Strategy for 3D Volumetric Assessment of Saturable Hyperpolarized 13C Pyruvate Kinetics
Abubakr Eldirdiri, Joshua Rogers, Dirk Mayer
University of Maryland School of Medicine, Baltimore, United States of America
Impact: 
Metabolic rates from first-order kinetic modeling in hyperpolarized ¹³C experiments are often dose-dependent, complicating comparisons across experiments. Our 3D acquisition strategy provides a metabolic metric ($V_{max}$) that is independent of substrate concentration, reducing variability in hyperpolarized 13C studies.
  Figure 666-01-012.  Coil Combination of Hyperpolarized C-13 Imaging by Estimating L2-Optimized Sensitivity Maps
Anna Bennett Haller, Minjie Zhu, Peder Larson, Jeremy Gordon, Nicholas Dwork
University Of California, San Francisco (UCSF), United States of America
Impact: Implementation of an L2-optimization-based sensitivity map estimator, using both substrate and product metabolite images as input, has been shown to improve SNR in HP C13 datasets.
  Figure 666-01-013.  Dynamic Pyruvate-Lactate Exchange Simulation using Arbitrary Phase Encoding Schemes and Sliding-Window Reconstruction
Pia Gebhard, Tobias Speidel, Fabian Bschorr, Julian Schüle, Volker Rasche
Ulm University, Medical Center, Ulm, Germany
Impact: A new BART-based simulation framework for dynamic 13-C metabolic imaging enables realistic pyruvate–lactate exchange studies for arbitrary phase encoding schemes. The combination of information-based undersampling and tiny golden angle refinement supports accurate, temporally resolved reconstructions using non-uniform FFT methods.
  Figure 666-01-014.  Spectrally selective Seiffert Spirals for preclinical 13C metabolic MRSI at 11.7 T
Julian Schüle, Fabian Bschorr, Tobias Speidel, Christoph Müller, Volker Rasche
Ulm University, Medical Center, Ulm, Germany
Impact: Spectrally selective Seiffert Spirals enable rapid, metabolite-specific imaging with high SNR and a lower number of readouts compared to other acquisition techniques, possibly enabling single-shot trajectories to be combined with high-field hyperpolarized ¹³C studies.
  Figure 666-01-015.  Kinetic-Anchored IDEAL CSI for HP 13C Pyruvate: Center-k Estimation and Voxel-wise Metabolite Imaging
Ching-Yi Hsieh, Ying-Chieh Lai, Kuan-Ying Lu, Gigin Lin
Chang Gung University, Taoyuan, Taiwan
Impact: This work establishes a kinetics-anchored IDEAL-CSI framework enabling accurate voxel-wise metabolic mapping in hyperpolarized $^{13}$C MRI, improving quantification of pyruvate–lactate dynamics and supporting robust, clinically adaptable assessment of metabolic alterations in irradiated and control cell models.

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