Christian Østergaard Mariager1, Steffen Ringgaard1, Jan Henrik Ardenkjær-Larsen2,3, and Christoffer Laustsen1
1Department of Clinical Medicine, The MR Research Centre, Aarhus University Hospital, Aarhus N, Denmark, 2Department of Electrical Engineering, Center for Hyperpolarization in Magnetic Resonance, Technical University of Denmark, Kgs. Lyngby, Denmark, 3GE Healthcare, Denmark
Synopsis
Hyperpolarized (HP) 129Xe have been
demonstrated as a useful probe for magnetic resonance (MR) lung imaging and
show promise for in vivo perfusion
imaging and brown adipose tissue characterization. Reports of large polarization enhancements
for 129Xe using dynamic nuclear polarization (DNP) have raised
expectations that DNP can be an alternative to the standard spin exchange
optical pumping (SEOP) method. We show that it is possible to produce HP 129Xe
gas using the clinical GE SpinLab polarizer, thus extending the practical use
of the system beyond the primary purpose of hyperpolarizing liquid biomolecules.
Purpose
Hyperpolarized
(HP) 129Xe for magnetic resonance (MR) has wide use in material
sciences, structural chemistry and medicine. In the medical field 129Xe
has been demonstrated as a useful probe for MR lung imaging and proposed as a
blood tracer for in vivo perfusion imaging1. The xenon probe is
therefore promising for clinical assessment of brain function2, and
may aid in the diagnosis and prognosis of brain diseases. Additionally, HP 129Xe
imaging has been demonstrated as a tracer for the presence and thermogenic
activity of brown adipose tissue (BAT), in relation to the study of weight
regulation3. Standard production of HP 129Xe is via spin
exchange optical pumping (SEOP). However, reports of large polarization
enhancements for 129Xe via dynamic nuclear polarization (DNP)1,4
have raised expectations that DNP can be an alternative method for producing HP
129Xe for patients. We therefore investigated the possibility for
production of HP 129Xe using the clinical GE SpinLab polarizer,
extending the practical use of this system.Materials and methods
Solid
state samples of 0.80 ± 0.01 mL 1-propanol / 12 mM AH111501 radical, infused
with natural abundance (n.a.) or enriched (70% 129Xe) xenon gas at
5.0 ± 0.2 bar partial pressure for 60 ± 1 minutes at room temperature were
prepared, using a custom built gas handling system, see Figure 1. Subsequently, the samples were inserted into
the 5 T SpinLab polarizer at Aarhus University Hospital, depicted in Figure 2.
Microwaves at 140.01 GHz were used to irradiate the samples for 150 ± 2 minutes
at 0.90 ± 0.04 K followed by dissolution, transport and MR measurement. HP / thermal
MR experiments were performed with 9° ± 1° / 90° ± 1° flip angles and TR = 1 s
/ 300 s on a 9.4 T small bore rodent MR scanner (Agilent, UK) using a volume radio
frequency (RF) coil (Doty scientific, US) with 1 / 200 averages. A recorded signal decay curve of the
resulting HP 129Xe gas is shown in Figure 3. Transport times for the n.a. / enriched gas
experiments (n = 2 / 5) were 32 ± 1 s / 26 ± 1 s at earth field. Finally, an
example of the solid state DNP build-up curve is presented in Figure 4. The
solid state data was recorded using the 6.7 T SpinLab polarizer available at
the Technical University of Denmark, using microwaves at 187.96 GHz. Data analysis was performed in
Matlab (MathWorks, Natick, MA, USA).Results
The
experiments resulted in enhancements / polarizations of 214 ± 22 / 0.18 ± 0.02
% and 446 ± 28 / 0.38 ± 0.02 % (n = 2 / 4) with T1 = 29 ± 2 s and 27
± 2 s (n = 2 / 5) for n.a. and enriched gas, respectively. Additionally, solid
state build-up times in the five to six-hour range was determined from the
solid state build-up experiments (n = 2), using the described approach.Discussion and conclusion
The
experiments have shown that it is possible to hyperpolarize 129Xe
using the SpinLab system. However, substantial work is required to shorten
build-up times and to achieve similar enhancements to SEOP. Strides should also
be taken to prolong the T1 lifetime of the resulting HP gas. These
issues can be addressed on multiple fronts, including optimization of the
radical and xenon concentrations, optimization of the polarization build-up
time, using different solvents, improving the phantom and optimizing the
transport conditions. Future uses for this application include the in vivo detection of BAT activity in
animal models as well as lung and perfusion imaging. This will be accomplished
in combination with the implementation of a fast multi-echo balanced
steady state free precession (BSSFP) imaging
scheme, capable of producing high resolution spectroscopic maps of the gaseous
and dissolved xenon phases, using the iterative Dixon type reconstruction
technique (IDEAL)5.Acknowledgements
No acknowledgement found.References
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