Akbar Alipour1, Gaurav Verma1, Michael Bush2, Judy Alper1, and Priti Balchandani1
1Biomedical Engineering and Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States, 2Siemens Medical Solutions USA, Inc, New York, NY, United States
Synopsis
Image quality in the brain periphery at ultra high field MRI is
severely limited by low sensitivity. In this work we illustrate an efficient method for enhancing imaging sensitivity at 7T in a cadaver brain. The method
is based on the application of a wireless coupled-split-ring-resonator array
that amplifies the MR signal during acquisition, which can alleviate the low
sensitivity problem in the brain periphery when low flip angle and low SAR
sequences are needed. Initial ex-vivo 7T MR brain imaging results showed that 2-fold
to 6-fold SNR gain was obtained using this array.
Purpose
To improve the signal sensitivity in the brain on 7T MRI systems by wireless signal amplification during the reception.Introduction
In MR imaging, SNR plays a critical role
in spatial resolution, image quality, and acquisition time. Experimental
results demonstrate approximately linear SNR increase with a static magnetic
field strength up to 4T.1 However, SNR becomes complex when stronger magnetic fields (> 4T) are considered. A comparison of 3T and
7T data obtained under the same imaging
parameters shows an SNR increase by factor of 2 at the center of the head, but
significantly lower gain at the periphery at 7T.1,2
This non-uniform SNR enhancement results from
the inhomogeneous B1 field (due to the wavelength effect) in a volume
head coil, which is more conspicuous at 7T. To improve the receive sensitivity
at the periphery, we developed a wireless, passive, and flexible RF array. The
proposed array can be placed near the area of interest without need for wired
connection to the scanner. The array amplifies the signal at its covered area
during reception, based on the concept of Faraday’s law of induction (Fig.1a).
To prevent B1 field distortion and alleviate potential safety
concerns, the array was decoupled from RF transmission. This array is intended
to be utilized with very low flip angle and low SAR sequences at 7T to improve SNR gain (2 to 6 times in ex-vivo).Method
The proposed array
consists of three coupled-split-ring resonators3 (CSRR)
tuned to the Larmor frequency (297 MHz) of a 7T MR scanner (MAGNETOM 7T,
Siemens Healthcare, Erlangen, Germany). The total dimension of the array is
5.5×2.8 cm2 with each CSRR dimension of 2.5×2.8 cm2 (Fig.1b). Electromagnetic simulation (CST, Germany) was
used to evaluate and optimize the effect of the design parameters. The CSSR is a
multi-layer structure; the first layer is an SRR etched copper on a 25 μm thick flexible substrate (Kapton), then after the CSRR was completed by etching the
second 180°-rotated SRR layer on the other side of the substrate (Fig.1c). When tuning a resonator, it is desirable to
control the capacitance to reach the Larmor frequencies.4 In this design the
overlap area between two SRRs can control the capacitance.
The equivalent electric circuit model of
a single CSRR is shown in figure 1d. All CSRRs electrical characteristics were
measured in the phantom
via an Agilent E5061B network analyzer.
The decoupling among the elements was addressed with critical overlap (Fig.2a).
The RF and imaging safety was provided by decoupling the resonators from RF
excitation using antiparallel PIN diodes (Macom). CSRRs are only coupled during
reception to amplify the receive signal. B1 map was calculated on the phantom (CuSo4 solution) to determine the B1 field distribution in the vicinity of the array
using double angle method.5 Electromagnetic simulation was performed to evaluate
SAR distribution in a gel phantom to identify SAR hotspots. Temperature
measurement was measured in the vicinity of the array in the gel phantom
(dielectric constant = 70; heat capacity = 4454 J/(kg·K); conductivity = 0.65
S/m) under 15-min high SAR MR sequences (GRE: TR/TE=2.6/1.5 ms, flip angle=5°,
slice thickness=10 mm, slice number=2 mm, FOV=220×220 mm2, average=32) to analyze the RF safety. The phantom and ex-vivo MR
experiments were performed to evaluate the array imaging performance by
characterizing image SNR. The flexible and thin structure of the array allow it
to be placed on the curved surfaces (Fig.2b). All images were obtained on a 7T
MR scanner (MAGNETOM 7T, Siemens Healthcare, Erlangen, Germany) using a single-channel
transmitter and 32-channel receiver head coil. GRE (TR/TE =250/10 ms, flip
angle=1°, Matrix size=256×256, slice thickness=3
mm, FOV=180×180 mm2) and inversion recovery (TR/TE/IR
=2000/3.3/300 ms, flip angle=8°, Matrix size=256×256, slice thickness 3
mm, FOV=180×180 mm2) sequences were used to acquire images with/without
the array for comparison.Results
The GRE phantom image shows the enhanced
SNR area (dashed ellipse) (Fig.2c); the corresponding 1D SNR profile along the
dashed line indicates 8-fold SNR gain in the array vicinity (Fig.2d), while moving
away from the array the enhancement is decreased. The B1 map analysis displays a negligible B1 field magnitude distortion in the vicinity of the
array (Fig.3). This distortion can be explained by the fringing effect of the
induced current on the array during the RF transmission. Temperature
measurement recorded by the fiber optic temperature probes (Fig.4a) reported
maximum temperature rise (ΔT) of 0.9 °C with respect to the reference point
(Fig.4b). Ex-vivo MR images acquired with/without the array show that the
highest SNR enhancement of 6-fold and 2-fold were calculated in GRE and
inversion recovery ex-vivo images, respectively.Conclusion
A method of enhancing SNR is proposed and
experimentally demonstrated on a 7T MR system. By positioning an array of
resonators near an imaging sample, SNR of the MR signal can be amplified significantly in the area covered by the array. This method can provide a
solution for the low SNR problem at the brain periphery at high fields. The ex-vivo
experimental results showed an SNR gain up to 6-fold obtained using the
proposed device. Future work can be focused on increasing the area of interest
by increasing the number of elements for the purpose of human imaging.Acknowledgements
Authors would like to thank Derek Smith for his scientific discussion.References
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