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...

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Main Authors: Kyangwi P. Malikidogo, Harlei Martin, Célia S. Bonnet
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/13/12/436
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author Kyangwi P. Malikidogo
Harlei Martin
Célia S. Bonnet
author_facet Kyangwi P. Malikidogo
Harlei Martin
Célia S. Bonnet
author_sort Kyangwi P. Malikidogo
collection DOAJ
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<sup>2+</sup> and are now being developed to detect Cu<sup>2+</sup>. These paramagnetic probes mainly exploit the relaxation-based properties (T<sub>1</sub>-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<sup>2+</sup> to Cu<sup>2+</sup> 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 <sup>19</sup>F MRI is required, each of which has its own advantages and disadvantages.
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spelling doaj.art-2bbb568f545f4b189987db4be5246ba22023-11-20T22:56:41ZengMDPI AGPharmaceuticals1424-82472020-11-01131243610.3390/ph13120436From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and ChallengesKyangwi P. Malikidogo0Harlei Martin1Célia S. Bonnet2Centre de Biophysique Moléculaire, Université d’Orléans, Rue Charles Sadron, F-45071 Orléans 2, FranceCentre de Biophysique Moléculaire, Université d’Orléans, Rue Charles Sadron, F-45071 Orléans 2, FranceCentre de Biophysique Moléculaire, Université d’Orléans, Rue Charles Sadron, F-45071 Orléans 2, FranceZinc 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<sup>2+</sup> and are now being developed to detect Cu<sup>2+</sup>. These paramagnetic probes mainly exploit the relaxation-based properties (T<sub>1</sub>-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<sup>2+</sup> to Cu<sup>2+</sup> 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 <sup>19</sup>F MRI is required, each of which has its own advantages and disadvantages.https://www.mdpi.com/1424-8247/13/12/436zinc detectioncopper detectionMRIresponsive contrast agentslanthanidesmolecular imaging
spellingShingle Kyangwi P. Malikidogo
Harlei Martin
Célia S. Bonnet
From Zn(II) to Cu(II) Detection by MRI Using Metal-Based Probes: Current Progress and Challenges
Pharmaceuticals
zinc detection
copper detection
MRI
responsive contrast agents
lanthanides
molecular imaging
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 zinc detection
copper detection
MRI
responsive contrast agents
lanthanides
molecular imaging
url https://www.mdpi.com/1424-8247/13/12/436
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