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A dual-tuned concentric multimodal RF coil for 7 T 1H/31P MRSI: concurrently enhancing B1 efficiency over
Yunkun Zhao1, Xiaoliang Zhang2
1Department of Biomedical Engineering, State University of New York at Buffalo, Buffalo, NY, United States.
Abstract:
This study presents the design, simulation, and experimental validation of a dual-tuned concentric multimodal surface coil for 7 T 1H/31P magnetic resonance spectroscopic imaging (MRSI), developed to significantly enhance 31P B1 efficiency while improving 1H performance. The coil architecture utilizes two interleaved sets of three concentric loop resonators. Intra-nucleus electromagnetic coupling within each three-loop set generates a spectrum of eigenmodes; the operational modes for 1H and 31P were specifically selected because their co-directed current distributions reinforce the magnetic field at the center, yielding B1 patterns that resemble those of conventional single-loop surface coils but with superior efficiency. Full-wave electromagnetic simulations and bench measurements on a fabricated prototype were conducted to characterize the multimodal resonance behavior, scattering parameters, B1 distribution, and 10-g local SAR, using size-matched conventional single-tuned loops as references. The results confirmed that the design reproducibly generated the predicted eigenmode ordering with sufficient spectral separation to prevent interference from parasitic or undesired modes. Notably, the multimodal design achieved an 83% boost in 31P B1 efficiency and a 21% boost in 1H B1 efficiency at the coil center compared to same-sized single-tuned references. Sufficient inter-nuclear decoupling was achieved to prevent signal leakage between channels, and simulations with a human head model confirmed that the peak 10-g local SAR remained comparable to conventional designs. These findings demonstrate that this multimodal concentric design offers a robust and highly efficient solution for multinuclear MRSI at ultrahigh fields, effectively mitigating the sensitivity limitations of X-nuclei without compromising proton-based imaging capabilities.
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