Imaging Sequences for Hyperpolarized Solids.
flip angle
hyperpolarization
magnetic resonance imaging
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
30 Dec 2020
30 Dec 2020
Historique:
received:
11
11
2020
revised:
16
12
2020
accepted:
16
12
2020
entrez:
5
1
2021
pubmed:
6
1
2021
medline:
21
9
2021
Statut:
epublish
Résumé
Hyperpolarization is one of the approaches to enhance Nuclear Magnetic Resonance (NMR) and Magnetic Resonance Imaging (MRI) signal by increasing the population difference between the nuclear spin states. Imaging hyperpolarized solids opens up extensive possibilities, yet is challenging to perform. The highly populated state is normally not replenishable to the initial polarization level by spin-lattice relaxation, which regular MRI sequences rely on. This makes it necessary to carefully "budget" the polarization to optimize the image quality. In this paper, we present a theoretical framework to address such challenge under the assumption of either variable flip angles or a constant flip angle. In addition, we analyze the gradient arrangement to perform fast imaging to overcome intrinsic short decoherence in solids. Hyperpolarized diamonds imaging is demonstrated as a prototypical platform to test the theory.
Identifiants
pubmed: 33396762
pii: molecules26010133
doi: 10.3390/molecules26010133
pmc: PMC7795150
pii:
doi:
Substances chimiques
Carbon Isotopes
0
Diamond
7782-40-3
Carbon-13
FDJ0A8596D
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : National Science Foundation
ID : 1903803
Organisme : NIH HHS
ID : 1S10RR013871-01A1
Pays : United States
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