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Purpose: Oscillating gradient spin‐echo (OGSE) sequences have demonstrated an ability to probe time‐dependent microstructural features, although they often suffer from low SNR due to increased TEs. In this work we introduce frequency‐tuned bipolar (FTB) gradients as a variation of oscillating gradients with reduced TE and demonstrate their utility by mapping the frequency dispersion of kurtosis in human subjects. Methods: An FTB oscillating gradient waveform is presented that provides encoding of 1.5 net oscillation periods, thereby reducing the TE of the acquisition. Simulations were performed to determine an optimal protocol based on the SNR of kurtosis frequency dispersion—defined as the difference in kurtosis between pulsed and oscillating gradient acquisitions. Healthy human subjects were scanned at 7T using pulsed gradient and an optimized 23 Hz FTB protocol, which featured a maximum b‐value of 2500 s/mm2. In addition, to directly compare existing methods, measurements using traditional cosine OGSE were also acquired. Results: FTB oscillating gradients demonstrated equivalent frequency‐dependent diffusion measurements compared with cosine‐modulated OGSE while enabling a significant reduction in TE. Optimization and in vivo results suggest that FTB gradients provide increased SNR of kurtosis dispersion maps compared with traditional cosine OGSE. The optimized FTB gradient protocol demonstrated consistent reductions in apparent kurtosis values and increased diffusivity in generated frequency dispersion maps. Conclusions: This work presents an alternative to traditional cosine OGSE sequences, enabling more time‐efficient acquisitions of frequency‐dependent diffusion quantities as demonstrated through in vivo kurtosis frequency dispersion maps. [ABSTRACT FROM AUTHOR]

Purpose In order to benefit from the increased spectral bandwidth at ultrahigh field (UHF), the use of parallel transmission (pTx) to mitigate flip-angle inhomogeneity in chemical exchange saturation transfer (CEST) imaging is investigated. Theory and Methods A pTx basis pulse is homogenised by magnitude least-squares (MLS) optimization and expanded to form a frequency-selective saturation pulse for CEST. The pTx saturation pulse was simulated with a three-pool Bloch-McConnell equation to evaluate the impact of pTx on CEST contrast. In vivo CEST imaging performance (7 T) of the pTx saturation pulse and the standard Gaussian saturation in circularly polarized mode were compared. Two-spokes pTx homogeneous excitation was used in all in vivo experiments to ensure fair comparison of the two saturation pulses. Magnetization transfer ratio and inverse Z-spectrum analyses were used as metrics in evaluating the data from 3 healthy volunteers. Results Bloch-McConnell simulations showed that side bands of the pTx saturation pulse at ±20 ppm did not affect any CEST contrast. Improved homogeneity in contrasts and relaxation-compensated CEST metrics were observed in our in vivo data when the pTx saturation pulse was used. Conclusion A pTx-based pulsed CEST presaturation scheme is proposed and validated by simulations and 7T in vivo imaging. Magn Reson Med 78:2216-2225, 2017. © 2017 International Society for Magnetic Resonance in Medicine. [ABSTRACT FROM AUTHOR]