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Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip
Author(s) -
Sylwia J. Barker,
Laurynas Dagys,
William Hale,
Barbara Ripka,
James Eills,
Manvendra Sharma,
Malcolm H. Levitt,
Marcel Utz
Publication year - 2022
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.1c05030
Subject(s) - chemistry , hyperpolarization (physics) , microfluidics , metabolite , membrane , nanotechnology , analytical chemistry (journal) , nuclear magnetic resonance spectroscopy , chromatography , stereochemistry , biochemistry , materials science
Microfluidic systems hold great potential for the study of live microscopic cultures of cells, tissue samples, and small organisms. Integration of hyperpolarization would enable quantitative studies of metabolism in such volume limited systems by high-resolution NMR spectroscopy. We demonstrate, for the first time, the integrated generation and detection of a hyperpolarized metabolite on a microfluidic chip. The metabolite [1- 13 C]fumarate is produced in a nuclear hyperpolarized form by (i) introducing para-enriched hydrogen into the solution by diffusion through a polymer membrane, (ii) reaction with a substrate in the presence of a ruthenium-based catalyst, and (iii) conversion of the singlet-polarized reaction product into a magnetized form by the application of a radiofrequency pulse sequence, all on the same microfluidic chip. The microfluidic device delivers a continuous flow of hyperpolarized material at the 2.5 μL/min scale, with a polarization level of 4%. We demonstrate two methods for mitigating singlet-triplet mixing effects which otherwise reduce the achieved polarization level.

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