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Quantum chemical insight into the effects of the local electron environment on T-2-based MRI
Journal article   Open access   Peer reviewed

Quantum chemical insight into the effects of the local electron environment on T-2-based MRI

M. S. Petronek, J. J. St-Aubin, C. Y. Lee, D. R. Spitz, E. G. Gillan, B. G. Allen and V. A. Magnotta
Scientific reports, Vol.11(1), p.20817
10/21/2021
DOI: 10.1038/s41598-021-00305-7
PMCID: PMC8531323
PMID: 34675308
url
https://doi.org/10.1038/s41598-021-00305-7View
Published (Version of record) Open Access

Abstract

T-2* relaxation is an intrinsic magnetic resonance imaging (MRI) parameter that is sensitive to local magnetic field inhomogeneities created by the deposition of endogenous paramagnetic material (e.g. iron). Recent studies suggest that T-2* mapping is sensitive to iron oxidation state. In this study, we evaluate the spin state-dependence of T-2* relaxation using T-2* mapping. We experimentally tested this physical principle using a series of phantom experiments showing that T-2* relaxation times are directly proportional to the spin magnetic moment of different transition metals along with their associated magnetic susceptibility. We previously showed that T-2* relaxation time can detect the oxidation of Fe2+. In this paper, we demonstrate that T-2* relaxation times are significantly longer for the diamagnetic, d(10) metal Ga3+, compared to the paramagnetic, d(5) metal Fe3+. We also show in a cell culture model that cells supplemented with Ga3+ (S = 0) have a significantly longer relaxation time compared to cells supplemented with Fe3+ (S = 5/2). These data support the hypothesis that dipole-dipole interactions between protons and electrons are driven by the strength of the electron spin magnetic moment in the surrounding environment giving rise to T-2* relaxation.
Multidisciplinary Sciences Science & Technology Science & Technology - Other Topics

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