Abstract

Stable chitosan/PVA-based hydrogels were obtained by combining covalent and physical cross-linking methods. As covalent cross-linkers, epoxy agents with different chain lengths were used, while freeze–thaw cycles were applied for additional physical cross-linking. The chemical structure of the hydrogel was examined by FTIR spectroscopy whereas the morphology was analyzed by SEM, showing well-defined pores with dimensions of around 50 μm in diameter. It was proved that gel fraction and the network morphology were deeply influenced by the synthesis conditions. Chitosan/PVA hydrogel showed a relative high swelling rate, reaching equilibrium in the first hour. The values obtained for the elastic modulus were relatively low (3–30 kPa); as a result, these hydrogels are soft and very flexible, and are ideal candidates for medical applications as wound or oral dressings. In addition, the natural antimicrobial activity of chitosan was enhanced by in situ generation of silver nanoparticles (AgNPs) under UV irradiation. The total amount of Ag from hydrogel was determined by elemental analyses and its crystalline state was confirmed by XRD. The CS/PVA hydrogels entrapped with AgNPs exhibited high inhibitory activity against S. aureus and K. pneumonia. The vitality tests confirmed the lack of cytotoxicity of CS/PVA hydrogels without and with AgNPs.

Highlights

  • IntroductionThe healing time can be influenced by different factors such as genetic vulnerability, nutritional status, age, coexisting illnesses, the time of organism exposure to bacterial agents, excessive drugs intake, and air pollution [1]

  • This paper presents original results regarding a novel method for the synthesis of stable CS/poly(vinyl alcohol) (PVA)-based hydrogels by a double cross-linking procedure: physically by a freeze–thawing method and covalently using an epoxy cross-linking agent

  • The new CS/PVA-based hydrogels were successfully obtained, from diluted solutions of PVA, by combining two cross-linking techniques: (a) in the first stage, the covalent cross-linking of the CS chains was performed at room temperature (RT) with Ethylene glycol diglycidyl ether (EGDGE) or butanediol diglycidyl ether (BDDGE), known to have low toxicity [48,49]; (b) in the second stage, the physical cross-linking of the PVA

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Summary

Introduction

The healing time can be influenced by different factors such as genetic vulnerability, nutritional status, age, coexisting illnesses, the time of organism exposure to bacterial agents, excessive drugs intake, and air pollution [1]. Effective treatment consists of antibiotics administration, but an increasing body resistance or unwanted secondary effects have been observed, and for this reason, new therapeutic devices or drug delivery systems are being developed [2]. For treating infected skin wounds, oral or intestinal mucosal diseases, polysaccharide-based hydrogels with prolonged antimicrobial activity are frequently used [3]. Hydrogels can be impregnated with antibiotics, antimicrobial agents, and silver or gold nanoparticles, acting through non-stereospecific mechanisms that involve bacterial membrane disruption or biofilm generation [3,4]

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