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Deferoxamine-Modified Hybrid Materials for Direct Chelation of Fe(III) Ions from Aqueous Solutions and Indication of the Competitiveness of In Vitro Complexing toward a Biological System
[Image: see text] Deferoxamine (DFO) is one of the most potent iron ion complexing agent belonging to a class of trihydroxamic acids. The extremely high stability constant of the DFO–Fe complex (log β = 30.6) prompts the use of deferoxamine as a targeted receptor for scavenging Fe(III) ions. The fol...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210399/ https://www.ncbi.nlm.nih.gov/pubmed/34151096 http://dx.doi.org/10.1021/acsomega.1c01411 |
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author | Pawlaczyk, Mateusz Schroeder, Grzegorz |
author_facet | Pawlaczyk, Mateusz Schroeder, Grzegorz |
author_sort | Pawlaczyk, Mateusz |
collection | PubMed |
description | [Image: see text] Deferoxamine (DFO) is one of the most potent iron ion complexing agent belonging to a class of trihydroxamic acids. The extremely high stability constant of the DFO–Fe complex (log β = 30.6) prompts the use of deferoxamine as a targeted receptor for scavenging Fe(III) ions. The following study aimed at deferoxamine immobilization on three different supports: poly(methyl vinyl ether-alt-maleic anhydride), silica particles, and magnetite nanoparticles, leading to a class of hybrid materials exhibiting effectiveness in ferric ion adsorption. The formed deferoxamine-loaded hybrid materials were characterized with several analytical techniques. Their adsorptive properties toward Fe(III) ions in aqueous samples, including pH-dependence, isothermal, kinetic, and thermodynamic experiments, were investigated. The materials were described with high values of maximal adsorption capacity q(m), which varied between 87.41 and 140.65 mg g(–1), indicating the high adsorptive potential of the DFO-functionalized materials. The adsorption processes were also described as intense, endothermic, and spontaneous. Moreover, an exemplary magnetically active deferoxamine-modified material has been proven for competitive in vitro binding of ferric ions from the biological complex protoporphyrin IX–Fe(III), which may lead to a further examination of the materials’ biological or medical applicability. |
format | Online Article Text |
id | pubmed-8210399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82103992021-06-17 Deferoxamine-Modified Hybrid Materials for Direct Chelation of Fe(III) Ions from Aqueous Solutions and Indication of the Competitiveness of In Vitro Complexing toward a Biological System Pawlaczyk, Mateusz Schroeder, Grzegorz ACS Omega [Image: see text] Deferoxamine (DFO) is one of the most potent iron ion complexing agent belonging to a class of trihydroxamic acids. The extremely high stability constant of the DFO–Fe complex (log β = 30.6) prompts the use of deferoxamine as a targeted receptor for scavenging Fe(III) ions. The following study aimed at deferoxamine immobilization on three different supports: poly(methyl vinyl ether-alt-maleic anhydride), silica particles, and magnetite nanoparticles, leading to a class of hybrid materials exhibiting effectiveness in ferric ion adsorption. The formed deferoxamine-loaded hybrid materials were characterized with several analytical techniques. Their adsorptive properties toward Fe(III) ions in aqueous samples, including pH-dependence, isothermal, kinetic, and thermodynamic experiments, were investigated. The materials were described with high values of maximal adsorption capacity q(m), which varied between 87.41 and 140.65 mg g(–1), indicating the high adsorptive potential of the DFO-functionalized materials. The adsorption processes were also described as intense, endothermic, and spontaneous. Moreover, an exemplary magnetically active deferoxamine-modified material has been proven for competitive in vitro binding of ferric ions from the biological complex protoporphyrin IX–Fe(III), which may lead to a further examination of the materials’ biological or medical applicability. American Chemical Society 2021-06-03 /pmc/articles/PMC8210399/ /pubmed/34151096 http://dx.doi.org/10.1021/acsomega.1c01411 Text en © 2021 The Authors. Published by American Chemical Society 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 | Pawlaczyk, Mateusz Schroeder, Grzegorz Deferoxamine-Modified Hybrid Materials for Direct Chelation of Fe(III) Ions from Aqueous Solutions and Indication of the Competitiveness of In Vitro Complexing toward a Biological System |
title | Deferoxamine-Modified Hybrid Materials for Direct
Chelation of Fe(III) Ions from Aqueous Solutions and Indication of
the Competitiveness of In Vitro Complexing toward
a Biological System |
title_full | Deferoxamine-Modified Hybrid Materials for Direct
Chelation of Fe(III) Ions from Aqueous Solutions and Indication of
the Competitiveness of In Vitro Complexing toward
a Biological System |
title_fullStr | Deferoxamine-Modified Hybrid Materials for Direct
Chelation of Fe(III) Ions from Aqueous Solutions and Indication of
the Competitiveness of In Vitro Complexing toward
a Biological System |
title_full_unstemmed | Deferoxamine-Modified Hybrid Materials for Direct
Chelation of Fe(III) Ions from Aqueous Solutions and Indication of
the Competitiveness of In Vitro Complexing toward
a Biological System |
title_short | Deferoxamine-Modified Hybrid Materials for Direct
Chelation of Fe(III) Ions from Aqueous Solutions and Indication of
the Competitiveness of In Vitro Complexing toward
a Biological System |
title_sort | deferoxamine-modified hybrid materials for direct
chelation of fe(iii) ions from aqueous solutions and indication of
the competitiveness of in vitro complexing toward
a biological system |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210399/ https://www.ncbi.nlm.nih.gov/pubmed/34151096 http://dx.doi.org/10.1021/acsomega.1c01411 |
work_keys_str_mv | AT pawlaczykmateusz deferoxaminemodifiedhybridmaterialsfordirectchelationoffeiiiionsfromaqueoussolutionsandindicationofthecompetitivenessofinvitrocomplexingtowardabiologicalsystem AT schroedergrzegorz deferoxaminemodifiedhybridmaterialsfordirectchelationoffeiiiionsfromaqueoussolutionsandindicationofthecompetitivenessofinvitrocomplexingtowardabiologicalsystem |