4.8 Article

Enhanced spatial resolution in magnetic resonance imaging by dynamic nuclear polarization at 5 K

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.2201644119

关键词

magnetic resonance imaging; magnetic resonance microscopy; hyperpolarization; dynamic nuclear polarization

资金

  1. Intramural Research Program of the National Institute of Diabetes and Digestive and Kidney Diseases, NIH

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The spatial resolution of MRI is limited by signal detection sensitivity, but can be improved by performing measurements at low temperature and using dynamic nuclear polarization (DNP) technique. This allows for higher resolution and shorter data acquisition times, offering a promising direction for high-resolution MRI studies.
Spatial resolution in MRI is ultimately limited by the signal detection sensitivity of NMR, since resolution equal to rho(iso) in all three dimensions requires the detection of NMR signals from a volume rho(3)(iso). With inductively detected NMR at room temperature, it has therefore proven difficult to achieve isotropic resolution better than rho(iso) = 3.0 mu m, even with radio-frequency microcoils, optimized samples, high magnetic fields, optimized pulse sequence methods, and data acquisition times around 60 h. Here we show that spatial resolution can be improved and data acquisition times can be reduced substantially by performing MRI measurements at 5 K and using dynamic nuclear polarization (DNP) to enhance sensitivity. We describe the experimental apparatus and methods, and we report images of test samples with rho(iso) = 2.6 mu m and rho(iso) = 1.7 mu m, with signal-to-noise ratios greater than 15, acquired in 31.5 and 81.6 h, respectively. Image resolutions are verified by quantitative comparisons with simulations. These results establish a promising direction for high-resolution MRI of small samples. With further improvements in the experimental apparatus and in paramagnetic dopants for DNP, DNP-enhanced low-temperature MRI with rho(iso) < 1.0 mu m is likely to become feasible, potentially enabling informative studies of structures within typical eukaryotic cells, cell clusters, and tissue samples.

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