Cape Town - 2026 ISMRM-ISMRT Annual Meeting and Exhibition • 09-14 May 2026
|
666-01-001.
Demonstration of the novel hyperpolarizer technique to monitor in vivo metabolism using cross and direct polarization
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.
|
||
|
666-01-002.
Comparing an iterative least squares frequency decomposition method for non-invasive 3D pH imaging against 13C MRSI in vivo
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.
|
||
|
666-01-003.
Electron irradiation-induced radicals as stable endogenous agents for sodium [1-13C]pyruvate Dynamic Nuclear Polarisation
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.
|
||
|
666-01-004.
Enhancing in vivo SNR of hyperpolarized pH imaging through T1 prolongation by deuteration of 13C-labelled (Z)-OMPD
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.
|
||
|
666-01-005.
A dedicated 13C phantom and protocol for cross-site harmonization in clinical hyperpolarized 13C MRI
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.
|
||
|
666-01-006.
Extending the T1 lifetime of [1-13C]pyruvate to over 4 min
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.
|
||
|
666-01-007.
Multicenter evaluation of the POLARIS PHIP polarizer across models and imaging conditions
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.
|
||
|
666-01-008.
Multi Nuclei Small Animal Insert for in-vivo Hyperpolarized C13 Imaging on a Clinical MRI System
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.
|
||
|
|
666-01-009.
Optimization of [2-13C]Pyruvate Hyperpolarization Via the Addition of Gadolinium
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.
|
||
|
666-01-010.
Optimization of bSSFP passband periodicity for 13C metabolic MRSI at clinical field strengths
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.
|
||
|
666-01-011.
A Dual Multiband RF Pulse Strategy for 3D Volumetric Assessment of Saturable Hyperpolarized 13C Pyruvate Kinetics
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. |
||
|
666-01-012.
Coil Combination of Hyperpolarized C-13 Imaging by Estimating L2-Optimized Sensitivity Maps
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.
|
||
|
666-01-013.
Dynamic Pyruvate-Lactate Exchange Simulation using Arbitrary Phase Encoding Schemes and Sliding-Window Reconstruction
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.
|
||
|
666-01-014.
Spectrally selective Seiffert Spirals for preclinical 13C metabolic MRSI at 11.7 T
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.
|
||
|
666-01-015.
Kinetic-Anchored IDEAL CSI for HP 13C Pyruvate: Center-k Estimation and Voxel-wise Metabolite Imaging
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.
|
© 2026 International Society for Magnetic Resonance in Medicine