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Towards hyperpolarized 13C-succinate imaging of brain cancer
We describe a novel 13C enriched precursor molecule, sodium 1- 13C acetylenedicarboxylate, which after hydrogenation by PASADENA (Parahydrogen and Synthesis Allows Dramatically Enhanced Nuclear Alignment) under controlled experimental conditions, becomes hyperpolarized 13C sodium succinate. Fast in...
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Published in: | Journal of magnetic resonance (1997) 2007-05, Vol.186 (1), p.150-155 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We describe a novel
13C enriched precursor molecule, sodium 1-
13C acetylenedicarboxylate, which after hydrogenation by PASADENA (Parahydrogen and Synthesis Allows Dramatically Enhanced Nuclear Alignment) under controlled experimental conditions, becomes hyperpolarized
13C sodium succinate. Fast
in vivo 3D FIESTA MR imaging demonstrated that, following carotid arterial injection, the hyperpolarized
13C-succinate appeared in the head and cerebral circulation of normal and tumor-bearing rats. At this time, no
in vivo hyperpolarized signal has been localized to normal brain or brain tumor. On the other hand,
ex vivo samples of brain harvested from rats bearing a 9L brain tumor, 1
h or more following
in vivo carotid injection of hyperpolarized
13C sodium succinate, contained significant concentrations of the injected substrate,
13C sodium succinate, together with
13C maleate and succinate metabolites 1-
13C-glutamate, 5-
13C-glutamate, 1-
13C-glutamine and 5-
13C-glutamine. The
13C substrates and products were below the limits of NMR detection in
ex vivo samples of normal brain consistent with an intact blood–brain barrier. These
ex vivo results indicate that hyperpolarized
13C sodium succinate may become a useful tool for rapid
in vivo identification of brain tumors, providing novel biomarkers in
13C MR spectral-spatial images. |
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ISSN: | 1090-7807 1096-0856 |
DOI: | 10.1016/j.jmr.2007.01.017 |