Lance DelaBarre1, Russell L. Lagore1, Yigitcan Eryaman1, Gregor Adriany1, and J. Thomas Vaughan1
1Center for Magnetic Resonance Research - University of Minnesota, Minneapolis, MN, United States
Synopsis
Recently, our 10.5T whole-body MRI magnet achieved field
strength and its installation was completed.
While waiting for IRB and IDE approval, a human-sized porcine model
serves as a surrogate for later human studies, thus allowing development of techniques
in vivo. Using an 8-channel head coil on
a porcine head, the first in vivo images from the 10.5T whole-body MRI were
acquired.Objective
To develop in vivo imaging with pigs as a precursor to human
studies in a whole-body 10.5 T MR system.
Introduction
Recently, our 10.5T MRI magnet achieved field strength and
its installation was completed. This
represents the highest whole-body operational system for human MR imaging. Before imaging humans, however, we must
obtain both IRB and Investigational Device Exemption approval. Until then, we are using anesthetized
human-sized pigs to gather preliminary data for those approvals and taking the
opportunity to refine hardware systems and procedures for in vivo imaging.
Methods
A human-sized pig was anesthetized according to our approved
IACUC protocol and imaged as a surrogate for later human studies. The 10.5T / 88 cm whole body magnet by Agilent
(Santa Clara, CA) is currently the world’s highest strength whole-body MR
magnet. To achieve this field strength,
the passively shielded magnet shown in Figure 1 is 4.1 m long and 3.2 m wide, and contains 433 km
of NbTi wire cooled to below 3 K. The 88 cm
warm-bore accommodates commercial whole-body gradients, which in this case is an
SC72 body gradient (Siemens Healthcare, Erlangen, DE) with 70 mT/m maximum
amplitude and 200 T/m/s maximum slew rate.
Anticipating increased susceptibility inhomogeneities, the system was
outfitted with five 2nd order shims and four 3rd order
shims each driven by a 20 A power supply.
The width of the bore liner tube (patient space) is the standard whole-body
60 cm. The Siemens MAGNETOM console has
32 receive channels and 16 parallel transmit waveform generators driving 16
2-kW RF amplifiers (Stolberg HF-Technik AG, Stolberg, DE). A 16-channel Transmit/Receive interface with
integrated pre-amplifiers (Virtumed LLC, Minneapolis, MN) was connected to an
8-channel end-loaded dipole head coil.
The elements are 16 cm long (two 8 cm segments) and arranged on a
cylinder with an inner diameter of 25 cm.
The end-loaded dipole has a perpendicular plate on the end-walls of the
cylinder to fore-shorten the elements and has been previously modeled.
1 The head of an anesthetized and ventilated 35 kg pig, outfitted with
patient monitoring equipment, was loaded into the coil in supine position. The 8-channel coil was B
1 shimmed
over the brain and the flip angle in the brain was calibrated.
2-4 Gradient echo images were collected with the
following parameters: α = 6°, TR/TE=50/3.39 ms, 256x256, 0.77 x 0.77 x 3 (mm)
3, NEX=2. Turbo spin-echoes with the same resolution,
one acquisition, TR/TE = 5000/60 ms, 130° refocusing pulses, and an echo train
length of 7 were also acquired.
Results
The B
1 shim over the brain resulted in an
excitation pattern in the brain that was higher near the throat but rapidly dropped
off outside the brain in the central area of the throat and intubation tube. Transverse and coronal slices from a GRE sequence
are shown in Figures 2 and 3,
respectively. Figure 4 is a TSE image with
the same slice as Figure 3.
Discussion
The images presented demonstrate that most of the procedures
for in vivo imaging are operational.
There is no evidence of noise leaking into the images. B
1 shimming is working, at least
for this relatively small target. Most
of the animal/patient monitoring equipment either works or needs only minor
adjustments, such as longer cabling to reach into the long bore or to keep
equipment further from the magnet fringe field.
Conclusion
The first in vivo images were collected from the 10.5T
whole-body MRI.
Acknowledgements
NIH-R01-EB006835, NIH-R01 EB007327, NIH-P41-EB015894References
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