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Signal amplification by reversible exchange for COVID-19 antiviral drug candidates
Several drug candidates have been proposed and tested as the latest clinical treatment for coronavirus pneumonia (COVID-19). Chloroquine, hydroxychloroquine, ritonavir/lopinavir, and favipiravir are under trials for the treatment of this disease. The hyperpolarization technique has the ability to fu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459298/ https://www.ncbi.nlm.nih.gov/pubmed/32868801 http://dx.doi.org/10.1038/s41598-020-71282-6 |
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author | Jeong, Hye Jin Min, Sein Chae, Heelim Kim, Sarah Lee, Gunwoo Namgoong, Sung Keon Jeong, Keunhong |
author_facet | Jeong, Hye Jin Min, Sein Chae, Heelim Kim, Sarah Lee, Gunwoo Namgoong, Sung Keon Jeong, Keunhong |
author_sort | Jeong, Hye Jin |
collection | PubMed |
description | Several drug candidates have been proposed and tested as the latest clinical treatment for coronavirus pneumonia (COVID-19). Chloroquine, hydroxychloroquine, ritonavir/lopinavir, and favipiravir are under trials for the treatment of this disease. The hyperpolarization technique has the ability to further provide a better understanding of the roles of these drugs at the molecular scale and in different applications in the field of nuclear magnetic resonance/magnetic resonance imaging. This technique may provide new opportunities in diagnosis and research of COVID-19. Signal amplification by reversible exchange-based hyperpolarization studies on large-sized drug candidates were carried out. We observed hyperpolarized proton signals from whole structures, due to the unprecedented long-distance polarization transfer by para-hydrogen. We also found that the optimal magnetic field for the maximum polarization transfer yield was dependent on the molecular structure. We can expect further research on the hyperpolarization of other important large molecules, isotope labeling, as well as polarization transfer on nuclei with a long spin relaxation time. A clinical perspective of these features on drug molecules can broaden the application of hyperpolarization techniques for therapeutic studies. |
format | Online Article Text |
id | pubmed-7459298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74592982020-09-01 Signal amplification by reversible exchange for COVID-19 antiviral drug candidates Jeong, Hye Jin Min, Sein Chae, Heelim Kim, Sarah Lee, Gunwoo Namgoong, Sung Keon Jeong, Keunhong Sci Rep Article Several drug candidates have been proposed and tested as the latest clinical treatment for coronavirus pneumonia (COVID-19). Chloroquine, hydroxychloroquine, ritonavir/lopinavir, and favipiravir are under trials for the treatment of this disease. The hyperpolarization technique has the ability to further provide a better understanding of the roles of these drugs at the molecular scale and in different applications in the field of nuclear magnetic resonance/magnetic resonance imaging. This technique may provide new opportunities in diagnosis and research of COVID-19. Signal amplification by reversible exchange-based hyperpolarization studies on large-sized drug candidates were carried out. We observed hyperpolarized proton signals from whole structures, due to the unprecedented long-distance polarization transfer by para-hydrogen. We also found that the optimal magnetic field for the maximum polarization transfer yield was dependent on the molecular structure. We can expect further research on the hyperpolarization of other important large molecules, isotope labeling, as well as polarization transfer on nuclei with a long spin relaxation time. A clinical perspective of these features on drug molecules can broaden the application of hyperpolarization techniques for therapeutic studies. Nature Publishing Group UK 2020-08-31 /pmc/articles/PMC7459298/ /pubmed/32868801 http://dx.doi.org/10.1038/s41598-020-71282-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jeong, Hye Jin Min, Sein Chae, Heelim Kim, Sarah Lee, Gunwoo Namgoong, Sung Keon Jeong, Keunhong Signal amplification by reversible exchange for COVID-19 antiviral drug candidates |
title | Signal amplification by reversible exchange for COVID-19 antiviral drug candidates |
title_full | Signal amplification by reversible exchange for COVID-19 antiviral drug candidates |
title_fullStr | Signal amplification by reversible exchange for COVID-19 antiviral drug candidates |
title_full_unstemmed | Signal amplification by reversible exchange for COVID-19 antiviral drug candidates |
title_short | Signal amplification by reversible exchange for COVID-19 antiviral drug candidates |
title_sort | signal amplification by reversible exchange for covid-19 antiviral drug candidates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459298/ https://www.ncbi.nlm.nih.gov/pubmed/32868801 http://dx.doi.org/10.1038/s41598-020-71282-6 |
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