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From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges
Zinc and copper are essential cations involved in numerous biological processes, and variations in their concentrations can cause diseases such as neurodegenerative diseases, diabetes and cancers. Hence, detection and quantification of these cations are of utmost importance for the early diagnosis o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760112/ https://www.ncbi.nlm.nih.gov/pubmed/33266014 http://dx.doi.org/10.3390/ph13120436 |
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author | Malikidogo, Kyangwi P. Martin, Harlei Bonnet, Célia S. |
author_facet | Malikidogo, Kyangwi P. Martin, Harlei Bonnet, Célia S. |
author_sort | Malikidogo, Kyangwi P. |
collection | PubMed |
description | Zinc and copper are essential cations involved in numerous biological processes, and variations in their concentrations can cause diseases such as neurodegenerative diseases, diabetes and cancers. Hence, detection and quantification of these cations are of utmost importance for the early diagnosis of disease. Magnetic resonance imaging (MRI) responsive contrast agents (mainly Lanthanide(+III) complexes), relying on a change in the state of the MRI active part upon interaction with the cation of interest, e.g., switch ON/OFF or vice versa, have been successfully utilized to detect Zn(2+) and are now being developed to detect Cu(2+). These paramagnetic probes mainly exploit the relaxation-based properties (T(1)-based contrast agents), but also the paramagnetic induced hyperfine shift properties (paraCEST and parashift probes) of the contrast agents. The challenges encountered going from Zn(2+) to Cu(2+) detection will be stressed and discussed herein, mainly involving the selectivity of the probes for the cation to detect and their responsivity at physiologically relevant concentrations. Depending on the response mechanism, the use of fast-field cycling MRI seems promising to increase the detection field while keeping a good response. In vivo applications of cation responsive MRI probes are only in their infancy and the recent developments will be described, along with the associated quantification problems. In the case of relaxation agents, the presence of another method of local quantification, e.g., synchrotron X-Ray fluorescence, single-photon emission computed tomography (SPECT) or positron emission tomography (PET) techniques, or (19)F MRI is required, each of which has its own advantages and disadvantages. |
format | Online Article Text |
id | pubmed-7760112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77601122020-12-26 From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges Malikidogo, Kyangwi P. Martin, Harlei Bonnet, Célia S. Pharmaceuticals (Basel) Review Zinc and copper are essential cations involved in numerous biological processes, and variations in their concentrations can cause diseases such as neurodegenerative diseases, diabetes and cancers. Hence, detection and quantification of these cations are of utmost importance for the early diagnosis of disease. Magnetic resonance imaging (MRI) responsive contrast agents (mainly Lanthanide(+III) complexes), relying on a change in the state of the MRI active part upon interaction with the cation of interest, e.g., switch ON/OFF or vice versa, have been successfully utilized to detect Zn(2+) and are now being developed to detect Cu(2+). These paramagnetic probes mainly exploit the relaxation-based properties (T(1)-based contrast agents), but also the paramagnetic induced hyperfine shift properties (paraCEST and parashift probes) of the contrast agents. The challenges encountered going from Zn(2+) to Cu(2+) detection will be stressed and discussed herein, mainly involving the selectivity of the probes for the cation to detect and their responsivity at physiologically relevant concentrations. Depending on the response mechanism, the use of fast-field cycling MRI seems promising to increase the detection field while keeping a good response. In vivo applications of cation responsive MRI probes are only in their infancy and the recent developments will be described, along with the associated quantification problems. In the case of relaxation agents, the presence of another method of local quantification, e.g., synchrotron X-Ray fluorescence, single-photon emission computed tomography (SPECT) or positron emission tomography (PET) techniques, or (19)F MRI is required, each of which has its own advantages and disadvantages. MDPI 2020-11-30 /pmc/articles/PMC7760112/ /pubmed/33266014 http://dx.doi.org/10.3390/ph13120436 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Malikidogo, Kyangwi P. Martin, Harlei Bonnet, Célia S. From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges |
title | From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges |
title_full | From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges |
title_fullStr | From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges |
title_full_unstemmed | From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges |
title_short | From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges |
title_sort | from zn(ii) to cu(ii) detection by mri using metal-based probes: current progress and challenges |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760112/ https://www.ncbi.nlm.nih.gov/pubmed/33266014 http://dx.doi.org/10.3390/ph13120436 |
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