Metal cation responsive anionic microgels: behaviour towards biologically relevant divalent and trivalent ions.
Vittoria Chimisso1, Simona Conti1, Phally Kong1
1Department of Chemistry, University of Basel, Mattenstrasse 24/a, 4002, Basel, Switzerland. wolfgang.meier@unibas.ch.
Soft Matter
|November 21, 2020
Summary
Anionic microgels can bind and release divalent cations, including Mg2+, Sr2+, Cu2+, and Fe3+. These biocompatible chelating agents show potential for treating iron overaccumulation in the digestive tract.
Area of Science:
- Polymer Chemistry
- Materials Science
- Biotechnology
Background:
- Anionic microgels offer tunable properties for ion binding.
- Metal ion interactions with charged polymer networks are crucial for responsive materials.
Purpose of the Study:
- To synthesize and characterize anionic poly(vinylcaprolactam-co-itaconicacid-co-dimethylitaconate) microgels.
- To investigate the microgels' responsiveness to various cations (Mg2+, Sr2+, Cu2+, Fe3+).
- To evaluate the potential of these microgels as biocompatible chelating agents, particularly for iron overload.
Main Methods:
- Dispersion polymerization for microgel synthesis.
- Dynamic Light Scattering (DLS) to measure microgel size changes in response to ions.
- Ion chromatography to quantify bound and released metal ions.
- Protonation studies to demonstrate ion release mechanisms.
Main Results:
- Synthesized anionic microgels demonstrated cation-induced crosslinking and size reduction.
- Microgels showed reversible binding and release of divalent cations over multiple cycles.
- Selective entrapment of Fe3+ over divalent cations was observed.
- Ion chromatography confirmed quantitative binding and release of Mg2+, Sr2+, Cu2+, and Fe3+.
Conclusions:
- The synthesized microgels exhibit reversible cation-binding capabilities, functioning effectively over multiple cycles.
- The selective Fe3+ entrapment highlights their potential application in managing iron overload conditions.
- These biocompatible microgels show promise as chelating agents for therapeutic applications in the digestive tract.
Related Concept Videos
Extraction: Advanced Methods
864
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
864
Metal-Ligand Bonds
23.1K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
23.1K
Formation of Complex Ions
25.0K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
25.0K
Complexation Equilibria: Factors Influencing Stability of Complexes
655
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
655
Complexation Equilibria: The Chelate Effect
921
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
921
Qualitative Analysis
23.3K
For solutions containing mixtures of different cations, the identity of each cation can be determined by qualitative analysis. This technique involves a series of selective precipitations with different chemical reagents, each reaction producing a characteristic precipitate for a specific group of cations. Metal ions within a group are further separated by varying the pH, heating the mixture to redissolve a precipitate, or adding other reagents to form complex ions.
For instance, group IV...
For instance, group IV...
23.3K


