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Semi-adiabatic Shinnar–Le Roux pulses and their application to diffusion tensor imaging of humans at 7T
Authors:Priti Balchandani  Deqiang Qiu
Institution:1. Department of Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA;2. Department of Radiology, Stanford University, Stanford, CA, USA;3. Department of Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, GA, USA
Abstract:The adiabatic Shinnar–Le Roux (SLR) algorithm for radiofrequency (RF) pulse design enables systematic control of pulse parameters such as bandwidth, RF energy distribution and duration. Some applications, such as diffusion-weighted imaging (DWI) at high magnetic fields, would benefit from RF pulses that can provide greater B1 insensitivity while adhering to echo time and specific absorption rate (SAR) limits. In this study, the adiabatic SLR algorithm was employed to generate 6-ms and 4-ms 180° semi-adiabatic RF pulses which were used to replace the refocusing pulses in a twice-refocused spin echo (TRSE) diffusion-weighted echo planar imaging (DW-EPI) sequence to create two versions of a twice-refocused adiabatic spin echo (TRASE) sequence. The two versions were designed for different trade-offs between adiabaticity and echo time. Since a pair of identical refocusing pulses is applied, the quadratic phase imposed by the first is unwound by the second, preserving the linear phase created by the excitation pulse. In vivo images of the human brain obtained at 7 Testa (7 T) demonstrate that both versions of the TRASE sequence developed in this study achieve more homogeneous signal in the diffusion-weighted images than the conventional TRSE sequence. Semi-adiabatic SLR pulses offer a more B1-insensitive solution for diffusion preparation at 7 T, while operating within SAR constraints. This method may be coupled with any EPI readout trajectory and parallel imaging scheme to provide more uniform coverage for diffusion tensor imaging at 7 T and 3 T.
Keywords:Adiabatic  Shinnar&ndash  Le Roux  RF excitation  Diffusion-weighted imaging    T  B1-insensitive
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