Hyperpolarized fumarate is a promising biosensor for carbon-13 magnetic resonance metabolic imaging. Such molecular imaging applications require nuclear hyperpolarization to attain sufficient signal strength. Dissolution dynamic nuclear polarization is the current state-of-the-art methodology for hyperpolarizing fumarate, but this is expensive and relatively slow. Alternatively, this important biomolecule can be hyperpolarized in a cheap and convenient manner using parahydrogen-induced polarization. However, this process requires a chemical reaction, and the resulting solutions are contaminated with the catalyst, unreacted reagents, and reaction side-product molecules, and are hence unsuitable for use in vivo. In this work we show that the hyperpolarized fumarate can be purified from these contaminants by acid precipitation as a pure solid, and later redissolved to a desired concentration in a clean aqueous solvent. Significant advances in the reaction conditions and reactor equipment allow for formation of hyperpolarized fumarate at C polarization levels of 30-45%.
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http://dx.doi.org/10.1073/pnas.2025383118 | DOI Listing |
Anal Chem
October 2024
Section Biomedical Imaging, Molecular Imaging North Competence Center (MOIN CC), Department of Radiology and Neuroradiology, University Medical Center Kiel, Kiel University, Am Botanischen Garten 18, Kiel 24118, Germany.
Metabolic changes in an organism often occur much earlier than macroscopic manifestations of disease, such as invasive tumors. Therefore, noninvasive tools to monitor metabolism are fundamental as they provide insights into in vivo biochemistry. NMR represents one of the gold standards for such insights by observing metabolites.
View Article and Find Full Text PDFMol Cancer Ther
October 2024
National Cancer Institute, Bethesda, MD, United States.
Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) is an inherited cancer syndrome caused by germline pathogenic variants in the fumarate hydratase (FH) gene. Affected individuals are at risk for developing cutaneous and uterine leiomyomas and aggressive FH-deficient renal cell carcinoma (RCC) with a papillary histology. Due to a disrupted TCA cycle, FH-deficient kidney cancers rely on aerobic glycolysis for energy production, potentially creating compensatory metabolic vulnerabilities.
View Article and Find Full Text PDFACS Appl Mater Interfaces
July 2024
Advanced Imaging Research Center, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
Hyperpolarized C-labeled fumarate probes tissue necrosis via the production of C-malate. Despite its promises in detecting tumor necrosis and kidney injuries, its clinical translation has been limited, primarily due to the low solubility in conventional glassing solvents. In this study, we introduce a new formulation of fumarate for dissolution dynamic nuclear polarization (DNP) by using meglumine as a counterion, a nonmetabolizable derivative of sorbitol.
View Article and Find Full Text PDFJ Am Chem Soc
July 2024
School of Chemistry, University of Southampton, Southampton SO17 1BJ, United Kingdom.
We show the direct production and detection of C-hyperpolarized fumarate by parahydrogen-induced polarization (PHIP) in a microfluidic lab-on-a-chip (LoC) device and achieve 8.5% C polarization. This is the first demonstration of C-hyperpolarization of a metabolite by PHIP in a microfluidic device.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2024
NVision Imaging Technologies GmbH, 89081, Ulm, Germany.
Parahydrogen-induced polarization (PHIP) is an inexpensive way to produce hyperpolarized molecules with polarization levels of >10 % in the solution-state, but is strongly limited in generality since it requires chemical reactions/ interactions with H. Here we report a new method to widen the scope of PHIP hyperpolarization: a source molecule is produced via PHIP with high C polarization, and precipitated out of solution together with a target species. Spin diffusion within the solid carries the polarization onto C spins of the target, which can then be dissolved for solution-state applications.
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