Tomohisa Okada1, Shinya Handa2, Bill Ding2, Shin-ichi Urayama1, Koji Fujimoto1, Atsushi Shima3, Takashi Ayaki4, Nobukatsu Sawamoto3, Ryosuke Takahashi4, Hirotaka Onoe1, Tadashi Isa1, and Labros Petropoulos2
1Human Brain Research Center, Kyoto University, Kyoto, Japan, 2Quality Electrodynamics, Mayfield Village, OH, United States, 3Department of Human Health Sciences, Kyoto University, Kyoto, Japan, 4Department of Neurology, Kyoto University, Kyoto, Japan
Synopsis
MR imaging is frequently correlated to histopathology of specimen, and
their high-resolution imaging is required. However, it is not usually feasible using
the whole-body human MR scanner. We implemented inductively coupled small
diameter coils insertable to the knee coil at 7T without modification of the
coil interface. Up to isotropic 50 μm imaging was successfully conducted, and
fine details of the specimen could be visualized using the same sequence for in
vivo scans. The proposed coils are easy to use and will facilitate
investigation of image-histopathology correlation.
Introduction
The human 7T MR scanner is gradually becoming widely available and enables high-resolution
imaging using latest pulse sequences. Validation of image finding on specimen
or animal model is occasionally required, and some animal systems are used to
scan small samples. However, some pulse sequences are provided solely to a
human scanner. If we could visualize them using the same human MR scanner, it
is highly convenient. At 7T, 3 times higher SNR than at 3T can be attained, but
it requires an appropriate coil.1 In addition, latest human MR systems have a multi-channel capability. Building
multi-array coils2-6 are possible options, but construction of such a multi-element
coil is not always feasible. However, the latest system is usually furnished
with large-sized multi-element coils. If a small-size coil with high local
sensitivity can be inserted and used in the human coils without wiring, it
would be highly advantageous.
A small-size volume coil has been
used to scan small objects with a very high SNR. If designed appropriately, a small-size
volume coil can be used inductively coupled with a larger-size coil without
wiring. Here, we fabricated an unplugged insert-type volume coils and examined
their capability to visualize small objects using a human 7T MR system.Methods
An investigational whole-body human 7T scanner
(MAGNETOM 7T, Siemens Healthineers, Erlangen, Germany) and a Tx and 28-ch Rx knee coil (Quality Electrodynamics, Mayfield
Village, OH, USA) was selected as the baseline system. The inner diameter of
the knee coil is 150mm. Unplugged insert-type volume coils were designed to fit
into the knee coil with diameter of 26 and 64 mm (D26 and D64 coils). The D26
coil was consisted with a 3-turn solenoid coil (total length: 500 mm, three
passive only decoupling circuits). The D64 coil was consisted with a quadrature
saddle coil and capacitive decoupling network (total length: 8 cm, four passive
decoupling circuits). See Figure 1. Placement
of these coils inside of the knee coil is presented in Figure 2. No wiring was
required. During the knee coil transmit,
the insertable volume coils were detuned by the built-in passive decoupling
circuits and no B1 field enhancement or distortion induced by the insertable
volume coils. When the knee coil was in receive state, the insertable coils
were inductively coupled to the 28ch knee receive array coil and generate a
high sensitivity and undistorted B1 field distribution within the localized
resonator.
Ex vivo brain specimen were measured soaked in proton-free
susceptibility-matching fluid (Fluorinert FC-43, 3M Corp., MN, USA) using a 3D
gradient-echo sequence for T2*-weighted images. An excised brain part of an Alzheimer’s
disease (AD) patient and a macaque whole brain were scanned using the D26 and
D64 coils in isotropic 50 μm resolution (FOV 20 mm, TR/TE 200/23 ms,
BW 40 Hz/pixel) and 150 μm resolution (FOV 57 mm, TR/TE 100/20 ms, BW 40
Hz/pixel), respectively. Scan time was
approximately 4 hours for each scan. Results
Representative images of the specimen are shown in Figures 3 (D26) and 4
(D64). In Figure 3, many small dark holes are observed located at the cerebral
cortex of the AD patient. These are considered to be amyloid plaques (50 – 100
μm) with iron deposition. The small plaques could be visualized on T2*-weighted images because of blooming
effect caused by their high susceptibility in addition to high spatial
resolution. In Figure 3, fine laminar structures of the hippocampus and
lateral geniculate nucleus can be observed. Structural details of the
cerebellar folia, brain stem, basal ganglia and thalamus are also depicted. Discussion
High-resolution imaging on a human 7T-MRI system was feasible, when the unplugged
insertable volume coils were used. They can be used with the knee coil without
modification of the coil interface, and their setup is very easy. Scan
parameters need to be optimized dependent on the sample size and target
contrast. The recommended scan is T2*-weighted imaging because narrower BW is
required to retain signal from very small voxels. The long axis of the coils
needs to be placed orthogonal to the B0 direction, which is the direction of
the knee coil diameter of approximately 15 cm. Even though the current
configuration of insert-type volume coils has a limited flexibility of sample
size and orientation, that could be improved with different configuration of
inductively coupled resonators such as birdcage coils or dielectric resonators7 which could accommodate horizontal bore access for in-vivo animal scans under
anesthesia. The inductively coupled
small-diameter volume coils may perform well even at 3T and 1.5T, although it
is left to be validated. Conclusion
Inductively coupled small diameter coils that can
be inserted to the knee coil could successfully visualize fine structures of
the specimen. They are easy to handle and enable MR microscopy using the same
whole-body 7T-MRI system that is used for in vivo scans. Acknowledgements
This research was supported by the Agency for
Medical Research and Development, Japan (Grant Number: JP20dm030700). References
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