Glycerol-Enhanced Gum Karaya Hydrogel Films with a Sandwich-like Structure Enriched with Octenidine for Antibacterial Action against Multidrug-Resistant Bacteria

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Date
2025-07-02
Authors
Černá, Eva
Neděla, Vilém
Tihlaříková, Eva
Brtníková, Jana
Fohlerová, Zdenka
Lipový, Břetislav
Vacek, Lukáš
Růžička, Filip
Matulová, Jana
Vojtová, Lucy
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Referee
Mark
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Abstract
This study explores the innovative approach in the development of freeze-dried hydrogel films, leveraging the unique properties of gum Karaya (GK), poly(vinyl alcohol) (PVA), poly(ethylene glycol) (PEG), and glycerol with a coating of octenidine dihydrochloride (OCT). These innovative hydrogel films exhibit at a certain glycerol concentration a sandwich-like structure, achieved through a tailored freeze-drying process, which enhances transparency and mechanical stability. OCT provides superior antibacterial performance, effectively combating multidrug-resistant bacteria with a controlled and gradual release mechanism, surpassing conventional OCT solutions that require frequent reapplication for infected wound treatment without the creation of bacterial resistance. Advanced environmental scanning electron microscopy (A-ESEM) reveals the complex microstructure of the hydrogel, highlighting the dense surface layer and interconnected porous bulk. Variations in glycerol concentrations proved to significantly impact hydrogels' properties. Increasing the glycerol concentration decreases the pore size (around 4.5 mu m) while enhancing the polymer network density and flexibility. However, low concentration increases the pore size (7.8-15.6 mu m), impacting enhanced swelling behavior and hydrolytic stability. OCT's rapid antibacterial action, releasing over 30% within the first hour and maintaining prolonged activity for up to 2 weeks, emphasizes the material's potential for diverse applications. Hydrogels' remarkable transparency, porosity, structural stability, and antibacterial efficacy against both Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli strains suggest promising uses as transparent dressings, biomedical devices, and infection-resistant surfaces.
This study explores the innovative approach in the development of freeze-dried hydrogel films, leveraging the unique properties of gum Karaya (GK), poly(vinyl alcohol) (PVA), poly(ethylene glycol) (PEG), and glycerol with a coating of octenidine dihydrochloride (OCT). These innovative hydrogel films exhibit at a certain glycerol concentration a sandwich-like structure, achieved through a tailored freeze-drying process, which enhances transparency and mechanical stability. OCT provides superior antibacterial performance, effectively combating multidrug-resistant bacteria with a controlled and gradual release mechanism, surpassing conventional OCT solutions that require frequent reapplication for infected wound treatment without the creation of bacterial resistance. Advanced environmental scanning electron microscopy (A-ESEM) reveals the complex microstructure of the hydrogel, highlighting the dense surface layer and interconnected porous bulk. Variations in glycerol concentrations proved to significantly impact hydrogels' properties. Increasing the glycerol concentration decreases the pore size (around 4.5 mu m) while enhancing the polymer network density and flexibility. However, low concentration increases the pore size (7.8-15.6 mu m), impacting enhanced swelling behavior and hydrolytic stability. OCT's rapid antibacterial action, releasing over 30% within the first hour and maintaining prolonged activity for up to 2 weeks, emphasizes the material's potential for diverse applications. Hydrogels' remarkable transparency, porosity, structural stability, and antibacterial efficacy against both Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli strains suggest promising uses as transparent dressings, biomedical devices, and infection-resistant surfaces.
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ACS Omega. 2025, vol. 10, issue 27, p. 29530-29546.
https://pubs.acs.org/doi/10.1021/acsomega.5c02915
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Peer-reviewed
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en
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Creative Commons Attribution 4.0 International
http://creativecommons.org/licenses/by/4.0/
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