CP421, Polarized Gas Targets and
Polarized Beams: Seventh International Workshop
edited by Roy J. Holt and Michael A. Miller
©1998 The American Institute of Physics 1/56396-700-6/98/$15.00
Polarized Noble Gas MRI
James R. Brookeman1,2, John P. Mugler III1,2,
Paul Bogorad5, Thomas M. Daniel3, Eduard E. de Lange1,
Bastiaan Driehuys5, Jack Knight-Scott1, Therese Maier1,
Jonathon D.
Truwit4, Gordon Cates5, and William Happer5
Departments of Radiology1, Biomedical Engineering2,
Surgery3
and Internal Medicine4, University of Virginia Health Sciences Center,
Charlottesville, Virginia 22908, and Department of Physics5, Princeton
University, Princeton, New Jersey 08544
Abstract. The development of convenient methods to polarize liter
quantities of the noble gases helium-3 and xenon-129 has provided the opportunity for a
new MRI method to visualize the internal air spaces of the human lung. These spaces are
usuall y poorly seen with hydrogen-based MRI, because of the limited water content of the
lung and the low thermal polarization of the water protons achieved in conventional
magnets. In addition, xenon, which has a relatively high solubility and a sufficiently p
ersistent polarization level in blood and biological tissue, offers the prospect of
providing perfusion images of the lung, brain and other organs.
Techniques employed for creating laser-polarized spin targets for
high-energy physics have been adapted (1) to polarizing liter quantities of the noble
gases 3He and 129Xe, that when inhaled make possible magnetic
resonance (MR) imag es of the human lung spaces. Although the noble gas density achieved
in the lung is considerably less than the water density in most human tissues, the gain in
magnetization achieved by the laser polarization process is so great (>105)
that ex cellent quality lung space images can be obtained with 129Xe and 3He
MRI.
MR STUDIES WITH 129XE
Early MRI studies of rats and mice with 129Xe
(2) showed the potential for polarized noble gas MRI and provided the incentive to develop
laser gas polarizers suitable for human studies. In April 1996 a prototype laser
diode-array polarizer for 129Xe was assembled by the Princeton physics group at
the University of Virginia. Enriched xenon gas (71% 129Xe), polarized via spin
exchange with an optically pumped rubidium vapor, was accumulated as a solid in a cold
finger from a gas stream of 1% Xe, 1% N2, and 98% 4He. The frozen
xenon was then sublimed and collected in a 500 cm3 plastic bag for delivery to
the subject positioned in a 1.5 Tesla whole-body MR
scanner (Magnetom Vision, Siemens Medical Systems, Iselin,
NJ). With polarization levels of approximately 2% cross-sectional images of the lung
gas-spaces were acquired during a 12 second breathhold (see Figure 1). In separate MR
spectroscopy experiments , three dissolved-phase peaks were detected from the chest (see
Figure 2), and a single prominent peak, shifted 196 ppm from the gas peak, was observed in
the human brain (3).
MR STUDIES WITH 3HE
In April 1997 lung images with 3He were obtained
at the University of Virginia (see Figure 3), employing an investigational noble gas
polarizer (Magnetic Imaging Technologies Inc., Durham, NC). This system, which is similar
in operation to th e 129Xe polarizer, is capable of producing 2-3 liters of
15-25% polarized 3He gas in a
3-4 hour accumulation. In a typical 3He MR lung
study, the volunteer inhales a liter of 3He from a small plastic bag, and 10 to
15 contiguous 1-cm sections of the lung field are obtained during a 15-22 second
breathhold. The first human lung studies with optically polarized 3He reported
in 1 996 (4,5,6) showed healthy volunteers with a near homogeneous MR signal observed
throughout the lung field, except for areas where the gas was displaced by normal
structures, such as vessels. In patient studies (5), lesions were apparent as MR signal de
fects, and obstructive lung disease was depicted with severely inhomogeneous signal
intensity. Our study of a patient with chronic obstructive pulmonary disease (COPD) has
similar findings (see Figure 4) with significant signal voids that correspond to
ventilation defects seen in a nuclear medicine study of the same patient.
SUMMARY
The precise role that this type of imaging procedure might play in a
patient's evaluation and the relative merits of 3He versus 129Xe are
yet to be determined; but the initial results are sufficiently encouraging to warrant
further s tudy. The possibility of imaging the dissolved phases of 3Xe in the
lung and brain to provide images of tissue perfusion is particularly attractive. This
would require higher polarization levels (> 20%) and probably some form of echo-train
pu lse sequence to take advantage of the long T2 values of these dissolved
phases.
Continued improvements in the technology of laser polarized noble gas
MRI can be expected to enhance the potential diagnostic value of this new method of
imaging, which is readily transferable to many of the MRI centers located worldwide with
simple addit ions to the basic MR platform. It is also possible that very low field MR
systems could be developed to reduce the cost of the procedure, since the MR signal
strength for this technology does not depend primarily on the value of the applied
magnetic fiel d. Furthermore, for some applications, it may be advantageous to introduce
polarized dissolved-phase xenon directly into blood or tissue using a compatible solvent
carrier as proposed by Bifone et al. (7). This could considerably reduce the burden of xe
non in the lung, and also significantly increase the MR signal for regional perfusion
studies.
ACKNOWLEDGMENTS
The authors thank Joe Camaratta, Wilhelm Dürr, Andreas Potthast, and
Phillip Belcher of Siemens Medical Systems for important contributions in bringing the
broadband imaging/spectroscopy option and the helium and xenon RF coils into operation,
and Stuart Berr, John Christopher, Denise Hinton, and Shella Keilholz, for valuable
assistance with the MR studies. This research was supported by the University of Virginia
Pratt Fund, the Dean of the Medical School, Dr. Robert M. Carey, and Siemens Medical
System s.
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