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pH Dependence of MRI Contrast in Magnetic Nanoparticle Suspensions Demonstrates Inner-Sphere Relaxivity Contributions and Reveals the Mechanism of Dissolution
[Image: see text] Superparamagnetic iron oxide nanoparticles, MNPs, are under investigation as stimulus-responsive nanocarriers that can be tracked by magnetic resonance imaging. However, fundamental questions remain, including the effect of differing surface chemistries on MR image contrast efficac...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933532/ https://www.ncbi.nlm.nih.gov/pubmed/36734523 http://dx.doi.org/10.1021/acs.langmuir.2c02621 |
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author | MacMahon, Eoghan Brougham, Dermot F. |
author_facet | MacMahon, Eoghan Brougham, Dermot F. |
author_sort | MacMahon, Eoghan |
collection | PubMed |
description | [Image: see text] Superparamagnetic iron oxide nanoparticles, MNPs, are under investigation as stimulus-responsive nanocarriers that can be tracked by magnetic resonance imaging. However, fundamental questions remain, including the effect of differing surface chemistries on MR image contrast efficacy (relaxivity), both initially and over time in the biological environment. The effects of pH and ligand type on the relaxivity of electrostatically and sterically stabilized spherical 8.8 nm superparamagnetic MNP suspensions are described. It is shown for the first time that across the pH ranges, within which the particles are fully dispersed, increasing acidity progressively reduces relaxivity for all ligand types. This effect is stronger for electrostatically (citrate or APTES) than for sterically stabilized (PEG5000) MNPs. NMR relaxation profiles (relaxivity as a function of (1)H Larmor frequency) identified an inner-sphere effect, arising from the protonation of bare oxide or low-molecular-weight-bound species, as the cause. The suppression is not accounted for by the accepted model (SPM theory) and is contrary to previous reports of increased relaxivity at lower pH for paramagnetic iron oxide nanoparticles. We propose that the suppression arises from the orientation of water molecules, with the oxygen atom facing the surface increasingly preferred with increasing surface protonation. For APTES-stabilized MNPs, pendant amines and the silane layer confer exceptional chemical and colloidal stability at low pH. Dissolution of these particles at pH 1.8 was monitored over several months by combining in situ measurements of relaxation profiles with dynamic light scattering. It was shown that particles are magnetically intact for extended periods until they rapidly dissolve, once the silane layer is breached, in a process that is apparently second order in particle concentration. The findings are of interest for tracking MNP fate, for quantitation, and for retention of magnetic responsiveness in biological settings. |
format | Online Article Text |
id | pubmed-9933532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99335322023-02-17 pH Dependence of MRI Contrast in Magnetic Nanoparticle Suspensions Demonstrates Inner-Sphere Relaxivity Contributions and Reveals the Mechanism of Dissolution MacMahon, Eoghan Brougham, Dermot F. Langmuir [Image: see text] Superparamagnetic iron oxide nanoparticles, MNPs, are under investigation as stimulus-responsive nanocarriers that can be tracked by magnetic resonance imaging. However, fundamental questions remain, including the effect of differing surface chemistries on MR image contrast efficacy (relaxivity), both initially and over time in the biological environment. The effects of pH and ligand type on the relaxivity of electrostatically and sterically stabilized spherical 8.8 nm superparamagnetic MNP suspensions are described. It is shown for the first time that across the pH ranges, within which the particles are fully dispersed, increasing acidity progressively reduces relaxivity for all ligand types. This effect is stronger for electrostatically (citrate or APTES) than for sterically stabilized (PEG5000) MNPs. NMR relaxation profiles (relaxivity as a function of (1)H Larmor frequency) identified an inner-sphere effect, arising from the protonation of bare oxide or low-molecular-weight-bound species, as the cause. The suppression is not accounted for by the accepted model (SPM theory) and is contrary to previous reports of increased relaxivity at lower pH for paramagnetic iron oxide nanoparticles. We propose that the suppression arises from the orientation of water molecules, with the oxygen atom facing the surface increasingly preferred with increasing surface protonation. For APTES-stabilized MNPs, pendant amines and the silane layer confer exceptional chemical and colloidal stability at low pH. Dissolution of these particles at pH 1.8 was monitored over several months by combining in situ measurements of relaxation profiles with dynamic light scattering. It was shown that particles are magnetically intact for extended periods until they rapidly dissolve, once the silane layer is breached, in a process that is apparently second order in particle concentration. The findings are of interest for tracking MNP fate, for quantitation, and for retention of magnetic responsiveness in biological settings. American Chemical Society 2023-02-03 /pmc/articles/PMC9933532/ /pubmed/36734523 http://dx.doi.org/10.1021/acs.langmuir.2c02621 Text en © 2023 The Authors. Published by 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 | MacMahon, Eoghan Brougham, Dermot F. pH Dependence of MRI Contrast in Magnetic Nanoparticle Suspensions Demonstrates Inner-Sphere Relaxivity Contributions and Reveals the Mechanism of Dissolution |
title | pH Dependence
of MRI Contrast in Magnetic Nanoparticle
Suspensions Demonstrates Inner-Sphere Relaxivity Contributions and
Reveals the Mechanism of Dissolution |
title_full | pH Dependence
of MRI Contrast in Magnetic Nanoparticle
Suspensions Demonstrates Inner-Sphere Relaxivity Contributions and
Reveals the Mechanism of Dissolution |
title_fullStr | pH Dependence
of MRI Contrast in Magnetic Nanoparticle
Suspensions Demonstrates Inner-Sphere Relaxivity Contributions and
Reveals the Mechanism of Dissolution |
title_full_unstemmed | pH Dependence
of MRI Contrast in Magnetic Nanoparticle
Suspensions Demonstrates Inner-Sphere Relaxivity Contributions and
Reveals the Mechanism of Dissolution |
title_short | pH Dependence
of MRI Contrast in Magnetic Nanoparticle
Suspensions Demonstrates Inner-Sphere Relaxivity Contributions and
Reveals the Mechanism of Dissolution |
title_sort | ph dependence
of mri contrast in magnetic nanoparticle
suspensions demonstrates inner-sphere relaxivity contributions and
reveals the mechanism of dissolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933532/ https://www.ncbi.nlm.nih.gov/pubmed/36734523 http://dx.doi.org/10.1021/acs.langmuir.2c02621 |
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