| Literature DB >> 25267650 |
David Gajan1, Aurélien Bornet2, Basile Vuichoud2, Jonas Milani2, Roberto Melzi3, Henri A van Kalkeren4, Laurent Veyre4, Chloé Thieuleux4, Matthew P Conley5, Wolfram R Grüning5, Martin Schwarzwälder5, Anne Lesage1, Christophe Copéret5, Geoffrey Bodenhausen6, Lyndon Emsley7, Sami Jannin2.
Abstract
Hyperpolarization of substrates for magnetic resonance spectroscopy (MRS) and imaging (MRI) by dissolution dynamic nuclear polarization (D-DNP) usually involves saturating the ESR transitions of polarizing agents (PAs; e.g., persistent radicals embedded in frozen glassy matrices). This approach has shown enormous potential to achieve greatly enhanced nuclear spin polarization, but the presence of PAs and/or glassing agents in the sample after dissolution can raise concerns for in vivo MRI applications, such as perturbing molecular interactions, and may induce the erosion of hyperpolarization in spectroscopy and MRI. We show that D-DNP can be performed efficiently with hybrid polarizing solids (HYPSOs) with 2,2,6,6-tetramethyl-piperidine-1-oxyl radicals incorporated in a mesostructured silica material and homogeneously distributed along its pore channels. The powder is wetted with a solution containing molecules of interest (for example, metabolites for MRS or MRI) to fill the pore channels (incipient wetness impregnation), and DNP is performed at low temperatures in a very efficient manner. This approach allows high polarization without the need for glass-forming agents and is applicable to a broad range of substrates, including peptides and metabolites. During dissolution, HYPSO is physically retained by simple filtration in the cryostat of the DNP polarizer, and a pure hyperpolarized solution is collected within a few seconds. The resulting solution contains the pure substrate, is free from any paramagnetic or other pollutants, and is ready for in vivo infusion.Entities:
Keywords: D-DNP; NMR signal enhancement; mesostructured hybrid silica; molecular imaging; porous materials
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Year: 2014 PMID: 25267650 PMCID: PMC4205634 DOI: 10.1073/pnas.1407730111
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205