Dataset Information

Chitosan Encapsulation of FerrateVI for Controlled Release to Water:Mechanistic Insights and Degradation of Organic Contaminant.

ABSTRACT: Tetraoxy-anion of iron in +6 oxidation state (FeVIO42-, FeVI), commonly called ferrate, has shown tremendous potential as a green oxidative agent for decontaminating water and air. Encapsulation of solid potassium salt of ferrate (K2FeO4) circumvents the inherent drawbacks of the instability of ferrate under humid conditions. In the encapsulated strategy, controlled release without exposing the solid ferrate to the humid environment avoids self-decomposition of the oxidant by water in the air, and the ferrate is mostly used to decontaminate water efficiently. This study demonstrated the formulation of oxidative microcapsules with natural materials present in chitosan, whose release rate of the core material can be controlled by the type of intermediate hydrocarbon layer and the pH-dependent swelling of chitosan shell. The pH played a pivotal role in swelling chitosan shell and releasing the core oxidant. In a strong acidic solution, chitosan tended to swell quickly and release FeVI at a faster rate than under neutral conditions. Additionally, among the several long-chain hydrocarbon compounds, oleic acid exhibited the strongest "locking" effect when applied as the intermediate layer, giving rise to the slow release of FeVI. Coconut oil and mineral oil, in comparison, allowed FeVI to penetrate the layer within shorter lengths of time and showed comparable degrees of degradation of target contaminant, methylene orange, under ambient temperature and near-neutral conditions. These findings have practical ramifications for remediating environmental and industrial processes.

SUBMITTER: Chen BY

PROVIDER: S-EPMC6892851 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature

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Chitosan Encapsulation of FerrateVI for Controlled Release to Water:Mechanistic Insights and Degradation of Organic Contaminant.

Chen Bo-Yen BY Kuo Hsuen-Wen HW Sharma Virender K VK Den Walter W

Scientific reports 20191204 1

Tetraoxy-anion of iron in +6 oxidation state (FeVIO42-, FeVI), commonly called ferrate, has shown tremendous potential as a green oxidative agent for decontaminating water and air. Encapsulation of solid potassium salt of ferrate (K2FeO4) circumvents the inherent drawbacks of the instability of ferrate under humid conditions. In the encapsulated strategy, controlled release without exposing the solid ferrate to the humid environme ...[more]

PMID: 31797977

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Project description:Glycol chitosan (GC) is a hydrophilic chitosan derivative, known for its aqueous solubility. Previously, we have demonstrated the feasibility of preparing injectable, enzymatically crosslinked hydrogels from HPP [3-(4-Hydroxyphenyl)-propionic acid (98%)]-modified GC. However, HPP-GC gels showed very slow degradation, which presents challenges as an in vivo protein delivery vehicle. This study reports the potential of acetylated HPP-GC hydrogels as a biodegradable hydrogel platform for sustained protein delivery. Enzymatic crosslinking was used to prepare injectable, biodegradable hydrogels from HPP-GC with various degrees of acetylation (DA). The acetylated polymers were characterized using Fourier transform infrared and nuclear magnetic resonance spectroscopy. Rheological methods were used to characterize the mechanical behavior of the hydrogels. In vitro degradation and protein release were performed in the presence and absence of lysozyme. In vivo degradation was studied using a mouse subcutaneous implantation model. Finally, two hydrogel formulations with distinct in vitro/in vivo degradation and in vitro protein release were evaluated in 477-SKH1-Elite mice using live animal imaging to understand in vivo protein release profiles. The lysozyme-mediated degradation of the gels was demonstrated in vitro and the degradation rate was found to be dependent on the DA of the polymers. In vivo degradation study further confirmed that gels formed from polymers with higher DA degraded faster. In vitro protein release demonstrated the feasibility to achieve lysozyme-mediated protein release from the gels and that the rate of protein release can be modulated by varying the DA. In vivo protein release study further confirmed the feasibility to achieve differential protein release by varying the DA. The feasibility to develop degradable enzymatically crosslinked GC hydrogels is demonstrated. Gels with a wide spectrum of degradation time ranging from less than a week and more than 6 weeks can be developed using this approach. The study also showed the feasibility to fine tune in vivo protein release by modulating HPP-GC acetylation. The hydrogel platform therefore holds significant promise as a protein delivery vehicle for various biomedical and regenerative engineering applications. Impact statement The study describes the feasibility to develop a novel enzyme sensitive biodegradable and injectable hydrogel, where in the in vivo degradation rate and protein release profile can be modulated over a wide range. The described hydrogel platform has the potential to develop into a clinically relevant injectable and tunable protein delivery vehicle for a wide range of biomedical applications.

Dataset Information

Chitosan Encapsulation of FerrateVI for Controlled Release to Water:Mechanistic Insights and Degradation of Organic Contaminant.

Publications

Chitosan Encapsulation of Ferrate<sup>VI</sup> for Controlled Release to Water:Mechanistic Insights and Degradation of Organic Contaminant.

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