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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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. |
format | Online Article Text |
id | pubmed-9096798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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