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Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip

[Image: see text] 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. W...

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Autores principales: Barker, Sylwia J., Dagys, Laurynas, Hale, William, Ripka, Barbara, Eills, James, Sharma, Manvendra, Levitt, Malcolm H., Utz, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096798/
https://www.ncbi.nlm.nih.gov/pubmed/35147413
http://dx.doi.org/10.1021/acs.analchem.1c05030
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author Barker, Sylwia J.
Dagys, Laurynas
Hale, William
Ripka, Barbara
Eills, James
Sharma, Manvendra
Levitt, Malcolm H.
Utz, Marcel
author_facet Barker, Sylwia J.
Dagys, Laurynas
Hale, William
Ripka, Barbara
Eills, James
Sharma, Manvendra
Levitt, Malcolm H.
Utz, Marcel
author_sort Barker, Sylwia J.
collection PubMed
description [Image: see text] 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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spelling pubmed-90967982022-05-13 Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip Barker, Sylwia J. Dagys, Laurynas Hale, William Ripka, Barbara Eills, James Sharma, Manvendra Levitt, Malcolm H. Utz, Marcel Anal Chem [Image: see text] 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. American Chemical Society 2022-02-11 2022-02-22 /pmc/articles/PMC9096798/ /pubmed/35147413 http://dx.doi.org/10.1021/acs.analchem.1c05030 Text en © 2022 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Barker, Sylwia J.
Dagys, Laurynas
Hale, William
Ripka, Barbara
Eills, James
Sharma, Manvendra
Levitt, Malcolm H.
Utz, Marcel
Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip
title Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip
title_full Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip
title_fullStr Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip
title_full_unstemmed Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip
title_short Direct Production of a Hyperpolarized Metabolite on a Microfluidic Chip
title_sort direct production of a hyperpolarized metabolite on a microfluidic chip
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096798/
https://www.ncbi.nlm.nih.gov/pubmed/35147413
http://dx.doi.org/10.1021/acs.analchem.1c05030
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