Dion Thomas1, Petrik Galvosas1, Paul D Teal2, Freya G Harrison3,4, Max Berry3,5, Yu-Chieh Tzeng3, and Sergei Obruchkov6
1School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, New Zealand, 2School of Engineering and Computer Science, Victoria University of Wellington, Wellington, New Zealand, 3Centre for Translational Physiology, University of Otago, Wellington, New Zealand, 4Department of Surgery and Anaesthesia, University of Otago, Wellington, New Zealand, 5Department of Paediatrics and Child Health, University of Otago, Wellington, New Zealand, 6Robinson Research Institute, Victoria University of Wellington, Wellington, New Zealand
Synopsis
We have developed a new permanent magnet based single sided magnetic resonance system, which is suitable for relaxometry and diffusion measurement. Our design generates an external region of homogeneous B0 field, a sweet spot, from which signal can be detected. The magnet has been optimised to have a larger penetration depth and higher B field strength than currently existing systems. We have found the system provides good homogeneity and field strength, making it useful for relaxometry. Additionally, we demonstrate it can be used for diffusion-T2 measurements, which will allow further biomedical applications.
Introduction
Single sided NMR systems offer a way of leveraging
Magnetic Resonance techniques away from an expensive MR imaging suite1. Systems are typically based
on arrangements of inexpensive permanent magnets which generate a B0 field with a sweet spot
region which is external to the magnet itself.
In the biomedical field, these systems have been used for measurements of tissue
hydration2,3, breast cancer4, and bone volume fraction5,6. While existing systems can
provide homogeneous B0
fields7–9, the field strength can be
low and the sweet spot region is generally close to the surface ~1cm, which
limits the range of applications.
Our new magnet system generates a homogeneous sweet spot
of 0.21 Tesla with a large penetration depth. The system weighs 30 kg and measures 30x20x20 cm
WxHxL. We show it can be used for relaxometry, and Diffusion-T2 correlation
measurements10,11, using a calibration method
to correct for gradient inhomogeneity12.Method
Our design (Figure 1) is based on an array of Neodymium
block magnets mounted on a metal yoke. The field is augmented with another set
of Neodymium magnets arranged as wings above the base. This is similar to U-shaped magnets, which produce a B0 field parallel to the
surface of the system. The design leaves room for the sample to be placed between
the upper magnets, with room for the RF coil and other hardware underneath the
sample.
To optimise the size and position of the magnet blocks, we simulated
designs in COMSOL Multiphysics. Dimensions were optimised to produce the best
balance between field strength, homogeneity and sweet spot position.
Additionally, an aluminium frame was built to hold the magnet blocks, while
still allowing ample amount of space to accommodate a sample/patient.
The RF coil is a 3 turn solenoid which is stretched in the
y-direction, to match the sensitive volume of the magnet. Adjusting the coil height
effectively moves the sweet spot deeper into the sample. MR experiments were
run using a Magritek Kea 2 console with the internal RF amplifier.
The Diffusion-edited CPMG sequence uses a variable TE for
the 1st echo to allow diffusion through the inhomogeneous field of the magnet to
attenuate the signal12. The data is processed using a 2D Inverse Laplace
Transform13 with a modified kernel to account
for the range of gradients in the sampling volume. The custom inversion kernel
is obtained by performing a calibration measurement on a sample of doped water,
with a known diffusion coefficient12.Results
An in-house built field mapper was used to measure the field
distribution, showing an x-shaped sweet spot which is homogeneous to 1mT (~40 kHz) at a
height of 85 mm above the base plate. The region
is 10 mm wide by 10 mm wide and extends 40 mm in the y-direction of the magnet.
The field strength in this region is 0.21 T (~9.05 MHz) (Figure 2).
To measure the sensitive region, doped water was added
stepwise to a measuring cylinder, with the water height increasing in 1 mm
steps. A series of CPMG experiments were run for each water height, at a range
of frequencies, allowing the change in signal intensity from each step to be
measured (Figure 3). This shows that most signal is detected from the area 84-85
mm above the yoke. It also suggests that changing the excitation frequency can be
used to select different areas along the depth axis.
To test the feasibility of diffusion measurements with this
system, a series of isotropic diffusion phantoms were prepared using 5
different concentrations of K30 polyvinylpyrrolidone (PVP) (Sigma-Aldrich) in
doped water. All experiments took place at room temperature. Diffusion coefficients
for the phantoms were also measured with a Bruker Avance 400 NMR system. The measured DT2 correlation maps from the 9 MHz system show a single peak (Figure 4 Left). Across the different samples, the diffusion
coefficients of the peaks agree with the measurements from the Avance system and with values from the literature14 (Figure 4 Right).Discussion and Conclusion
Our magnet design produces a large homogeneous region of
field deeper in the sample than previous magnet systems. The homogeneity of the
magnet also reduces the effect of diffusive attenuation when measuring using
longer CPMG echo times.
We have found that DT2 measurements within our
new single sided system are in good agreement with the high field measurements for
samples in the physiologically relevant range. This technique can also be used
to identify multiple components in the sample, which may be useful for
characterising tissue.
This magnet design and DT2 experiment will improve
the range of biomedical applications of single sided MR devices.Acknowledgements
This project is funded by the New Zealand Ministry of Business Innovation and EmploymentReferences
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