Qualitative and quantitative hard-tissue MRI with portable Halbach scanners
Jose Borreguero, Luiz G. C. Santos, Lorena Vega Cid, Elisa Castañón, Marina Fernández-García, Pablo Benlloch, Rubén Bosch, Jesús Conejero, Pablo García-Cristóbal, Alba González-Cebrián, Teresa Guallart-Naval, Eduardo Pallás, Laia Porcar, Lucas Swistunow, Jose Miguel Algarín, Fernando Galve, Joseba Alonso
TL;DR
This study tackles the challenge of imaging hard tissues with portable, low-field MRI by implementing a ZTE-like PETRA framework on a Halbach-based system. It couples pre-emphasis RF pulse control, an extended SPDS protocol for simultaneous $B_0$ and $B_1$ mapping, and model-based reconstruction to mitigate strong field inhomogeneities, enabling in vivo imaging of ligaments, tendons, cartilage, and cortical bone in under 15 minutes. The authors introduce VFA-PETRA to achieve quantitative $T_1$ mapping across soft and hard tissues at $B_0\approx 0.09$ T, validated in phantoms and knees, with in vivo knee/ankle demonstrations. They show that with field-PK aided reconstruction, hard-tissue visualization and $T_1$ quantification become feasible on portable Halbach systems, marking a step toward affordable, non-ionizing musculoskeletal imaging in point-of-care and remote settings. The work highlights practical limitations (SNR, resolution, partial-volume effects) and lays out a clear pathway for hardware and algorithm improvements to broaden clinical impact.
Abstract
Purpose: To demonstrate the feasibility of performing in vivo imaging and quantitative relaxation mapping of soft and hard tissues using a low-cost, portable MRI scanner, and to establish the methodological foundations for zero echo time (ZTE) imaging in systems affected by strong field inhomogeneities. Methods: A complete framework for artifact-free ZTE imaging at low field was developed, including: (i) RF pulse pre/counteremphasis calibration to minimize ring-down and electronics switching time; (ii) an extension of a recent single-point double-shot (SPDS) protocol for simultaneous B0 and B1 mapping; and (iii) a model-based reconstruction incorporating these field maps into the encoding matrix. ZTE imaging and variable flip angle (VFA) T1 mapping were performed on phantoms and in vivo human knees and ankles, and benchmarked against standard RARE and STIR acquisitions. Results: The optimized PETRA sequence produced 3D images of knees and ankles within clinically compatible times (< 15 min), revealing hard tissues such as ligaments, tendons, cartilage, and bone that are invisible in spin-echo sequences. The extended SPDS method enabled accurate field mapping, while the VFA approach provided the first in vivo T1 measurements of hard tissues at B0 < 0.1 T. Conclusions: The proposed framework broadens the range of pulse sequences feasible in portable low-field MRI and demonstrates the potential of ZTE for quantitative and structural imaging of musculoskeletal tissues in affordable Halbach-based systems.
