Lucas Soustelle1, Paulo Loureiro de Sousa1, Sascha Koehler2, Chrystelle Po1, François Rousseau3, and Jean-Paul Armspach1
1Université de Strasbourg, CNRS, ICube, FMTS, Strasbourg, France, 2Bruker BioSpin MRI, Ettlingen, Germany, 3Institut Mines Télécom, Télécome Bretagne, INSERM LaTIM, Brest, France
Synopsis
The Variable-rate
Selective Excitation (VERSE) approach allows to achieve very short echo time in 2D-UTE sequences when applied on a selective half-pulse and its paired slice selection gradient. Unfortunately, the latter may suffer from non-linearities and eddy current effects, all the more important on preclinical scanners equipped with strong gradient systems.
An efficient method was implemented on a 7T preclinical scanner to measure the real slice selection gradient profile. A reshaping of the corresponding pulse was made, improving the slice selectivity.
Purpose
The Variable-rate
Selective Excitation (VERSE) algorithm is a valuable selective RF pulse
reshaping technique1 to assess ultra-short T2 content (T2 < 1 ms) in
2D-UTE sequence2 since it allows very short TE (when used in pair
with a half-pulse), typically capped to the delay for switching the system from
a transmitting to a receiving state. Its design has been improved using a
Time-Optimal approach3, offering a simple way to shape a pair of RF pulse and slice
selection gradient to obtain a Minimum-Time VERSE4 (MT-VERSE) or a Delay-Insensitive
VERSE5 design. Due to relaxation during excitation, the observed ultra-short
T2 components suffer from an increase in width of their slice profiles as
well as an attenuation of their nominal amplitudes if the RF duration is greater
or comparable to the acquired T26. To this end, we use MT-VERSE to shape a
short duration selective RF pulse. However, the slice selection gradient may
suffer from significant non-linearities and eddy current effects, especially on
preclinical systems. Thus, the real gradient shape may present a delay
during its ramp down, leading consecutively to a non-respect of the ordered
weighting function1, and degrading the desired slice profile.
We propose here an efficient method for RF
pulse reshaping, in the sense of MT-VERSE, which takes into account gradient
imperfections while taking advantage of the scanner's limit performances in a
preclinical context.
Material & Methods
Figure 1
shows the pipeline used for correction purpose. An initial pair {B1(t); G(t)}
is MT-VERSEd and implemented on the scanner's system. Using a built-in trajectory
measurement method7, the real gradient profile is calculated, with respect
to the pulse and geometry constraints. This yields an efficient
correction, since the behavior of the ramp down may vary, e.g. with the
maximum amplitude of the requested slice selection gradient. Then, a reshaping of
the original MT-VERSEd pulse is done by taking into account the real slice
selection gradient waveform undergoing distortions and delays from
non-linearities and eddy current effects.
Two phantoms
were used to assess the improvement of slice selection after correction: one
composed of a piece of eraser (T2 ≈ 520 μs at 7T) surrounded by a 1.5% agar gel
(T2 = 100 ms at 7T; Sigma-Aldrich), and one plastic (T2 ≈ 500 μs at 7T; LEGO)
surrounded by doped agar with paramagnetic Ni2+ agent.
Experiments
were conducted on a 7T BioSpec 70/30 USR small animal MRI system (Bruker
BioSpin MRI GmbH, Ettlingen, Germany) equipped with a gradient system providing
a maximum amplitude of 442 mT/m and a peak slew rate of 3440 T/m/s. We used a volume
transmit/receive resonator of 7.2 cm in diameter, providing a maximum B1
amplitude of 150 μT. The 2D-UTE Bruker sequence was modified to
include a VERSE excitation.
A SLR half-pulse was used in the experiments (Time Bandwidth Product = 3, tRF
= 128 μs when MT-VERSEd, Flip Angle = 30°). The followed parameters were used:
matrix = 128x128, FOV = 40x40 mm², Slice Thickness = 1 mm (number of radial projections
= 402), with TR/TE = 500/0.05 ms and receiver Bandwidth = 100 kHz.
Results
Figure 2
shows the difference between requested and measured slice selection gradient
shapes, which emphasizes the need of a correction (delay between respective approximately
null amplitude reach Δt ≈ 50 μs). Figure 3 shows slice profiles before and after correction. Figure 4 shows slices before and after correction,
and presents the decrease of out-of-slice contamination when using the
correction.
Discussion
The
use of MT-VERSE allows to excite a broader bandwidth compared to
classical VERSE (consisting in a reshaping of B
1 to take into account the ramp
down of the slice selection gradient), which represents an advantage when
dealing with ultra-short T
2 components, especially at high fields. Preliminary
results seem promising and demonstrate the feasibility of using a short
selective RF pulse while ensuring good slice selectivity in the presence of a
non-ideal and strong slice selection gradient, and offers perspectives for
ultra-short T
2 excitation, such as lipidic myelin content assessment using a
proper long-T
2 suppression scheme. Nevertheless,
the method imposes an extra step (i.e. measuring G’
v(t) and reshaping B
1v(t)),
and relies strongly on system performances.
Conclusion
In
this work, an efficient pipeline was implemented for MT-VERSE improvement in preclinical scanner use. The use of the measured slice selection gradient,
instead of the theoretical one, highly improves the slice selectivity.
Acknowledgements
The authors thanks Geneviève Guillot and Daniel Gounot for useful discussions.References
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