Stephen Ogier1, John C Bosshard1, and Steven M Wright1
1Electrical and Computer Engineering, Texas A&M University, College Station, TX, United States
Synopsis
In this abstract we report progress and results towards
developing a fully broadband spectrometer for multi-coil multi-nuclear MRI/MRS. This may be of
interest for hyperpolarized MRI and MRS studies due to the very limited
lifetime of the magnetization, as well as for quantitative MRI. A prototype
spectrometer has been developed and tested by simultaneous 1H/2H
imaging on a 1.0T magnet and simultaneous 1H/23Na/2H
spectroscopy on a 4.7T magnet. The system is capable of acquiring data from
four channel array coils for these and other nuclei.Purpose
There has long been interest in performing simultaneous or interleaved
multinuclear studies [1-5]. The development of hyperpolarized MRI and MRS
has brought remarkable improvement in SNR, and the importance of
magnetization management may motivate true simultaneous rather than interleaved
multinuclear studies. Quantitative MRI and MRS also provides
motivation, though interleaved acquisitions may be sufficient for many
applications. This
work reports initial results at developing a broadband spectrometer, capable of
simultaneous acquisition from multiple nuclei, and supporting
array coil acquisition from each nuclei. Results are shown from simultaneous
1H/
2H
imaging on a 1.0T scanner, as well as simultaneous
1H/
2H/
23Na
spectroscopy on a 4.7T scanner. This should be of particular interest in dynamic
experiments where the limited time may not favor ‘conventional’ interleaved
experiments [1, 6, 7], or simply as an
alternative to the switching required in interleaving.
Methods
A broadband NMR spectrometer (Fig. 1) was assembled for true simultaneous
multinuclear transmit and receive. The pulse sequencer employed a National
Instruments PCI-6363 DAQ card to provide analog outputs and digital control. NI
LabVIEW was used as the programming environment. Each gradient amplifier
used a single Apex PA12A operational amplifier, providing a 10 to 90 rise time
to 15 Amps of approximately 200 microseconds. For the spectroscopy experiments,
simultaneous hard pulse excitation at multiple frequencies was accomplished
using an Analog Devices 9959 DDS, a four channel 500 MSPS DDS with 10 bit
amplitude and phase control. For shaped pulses, two independently modulated RF
pulses can be generated at two frequencies using an AD9915 DDS controlled by a
high speed DIO card (National Instruments PCI-6733). The RF pulses are combined and fed to a
conventional broadband amplifier. A triple nuclei coil was assembled from three
nested, single band T/R coils. The three
frequencies were separated following the RF amplifier using a transmission line
duplexing arrangement. Single tuned
coils were used for excitation, with the signals split after the amplifier. All signals were directly digitized using an
Ultraview 16 bit, 250 MS/s/ch, 4 channel digitizer card (Ultraview Corp,
Berkeley, CA). Postprocessing was done offline in Matlab, allowing spectral
widths for the three nuclei to be independently selected during
reconstruction. For comparison, the same
coil was used with a Varian Inova console to acquire single spectra from each
nuclei separately. The unused coils were
simply open-circuited.
Results
Simultaneously excited and acquired
1H and
2H acquisitions
obtained from the spectrometer are shown in Fig. 2. SNR is low due to the long
TR of distilled water in the
1H image, and actually higher in the
2H
image (in the central region) due to the lower resolution and thicker slice, a
result of the lower Larmor constant for
2H. All parameters were
identical except for the output power at each frequency. The
1H and
2H
signals present in each echo were simultaneously digitized by the broadband
receiver card. The nominal resolution at
1H is 120 mm FOV/128 = 0.94
mm. The
2H image, due to the difference in the Larmor constant has a
resolution of 0.94x6.5 = 6 mm. Following demodulation, the separated k-space
data sets were zero-filled in to a 256x256 matrix prior to reconstruction. Figure 3 compares
1H,
23Na
and
2H spectra obtained separately from the Varian scanner as
reference to simultaneously acquired on our spectrometer. The simultaneously acquired spectra were acquired
two ways, with each coil connected to a
separate digitizer channel and then with each coil connected through a 4-way combiner,
following preamplification, to a single
digitizer channel. The latter approach
was of interest because if enables arrays to be used at each frequency. When
combined, additional preamplification was used on the
2H and
23Na
channels, but not
1H. We
believe this caused the lower SNR on the
1H channel (the noise floor
was below the digitizer noise).
However, it was interesting that
the SNR on
2H and
23Na
was significantly better than on our Varian scanner, indicating a problem in
that scanner.
Discussion and Conclusion
Commonly available
electronics hardware now enables construction of custom broadband spectrometers
that can support simultaneous multinuclear imaging and spectroscopy. It would be preferable to have separate
narrow band power amplifiers rather than one broadband amplifier, but the
approach of using a single amplifier proved sufficient and greatly lowers cost and complexity. There are certainly challenges in pulse
sequence design that are easier to overcome with sequential acquisition, but
this abstract demonstrates the ability to excite and acquire multiple nuclei
simultaneously. Because the system has
four channels, it will support array detection at multiple frequencies.
Acknowledgements
Grant support from Samsung Research America is gratefully acknowledgedReferences
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