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Enhanced spatial resolution in magnetic resonance imaging by dynamic nuclear polarization at 5 K
Spatial resolution in MRI is ultimately limited by the signal detection sensitivity of NMR, since resolution equal to ρ(iso) in all three dimensions requires the detection of NMR signals from a volume ρ(iso)(3). With inductively detected NMR at room temperature, it has therefore proven difficult to...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295792/ https://www.ncbi.nlm.nih.gov/pubmed/35605126 http://dx.doi.org/10.1073/pnas.2201644119 |
Sumario: | Spatial resolution in MRI is ultimately limited by the signal detection sensitivity of NMR, since resolution equal to ρ(iso) in all three dimensions requires the detection of NMR signals from a volume ρ(iso)(3). With inductively detected NMR at room temperature, it has therefore proven difficult to achieve isotropic resolution better than ρ(iso) = 3.0 μm, 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 ρ(iso) = 2.6 μm and ρ(iso) = 1.7 μm, 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 ρ(iso) < 1.0 μm is likely to become feasible, potentially enabling informative studies of structures within typical eukaryotic cells, cell clusters, and tissue samples. |
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