Preparation and Evaluation of Chitosan/PVA Based Hydrogel Films Loaded with Honey for Wound Healing Application

In the present study, chitosan/polyvinyl alcohol (PVA)-based honey hydrogel films were developed for potential wound healing application. The hydrogel films were developed by a solvent-casting method and were evaluated in terms of thickness, weight variation, folding endurance, moisture content and moisture uptake. The water vapor transmission rate was found to range between 1650.50 +/- 35.86 and 2698.65 +/- 76.29 g/m(2)/day. The tensile strength and elongation at break were found to range between 4.74 +/- 0.83 and 38.36 +/- 5.39 N, and 30.58 +/- 3.64 and 33.51 +/- 2.47 mm, respectively, indicating significant mechanical properties of the films. SEM images indicated smooth surface morphology of the films. FTIR, DSC and in silico analysis were performed, which highlighted the docking energies of the protein-ligand complex and binding interactions such as hydrogen bonding, Pi-Pi bonding, and Pi-H bonding between the selected compounds and target proteins; hence, we concluded, with the three best molecules (lumichrome, galagin and chitosan), that there was wound healing potential. In vitro studies pointed toward a sustained release of honey from the films. The antimicrobial performance of the films was investigated against Staphylococcus aureus. Overall, the results signaled the potential application of chitosan/PVA based hydrogel films as wound dressings. Furthermore, in vivo experiments may be required to evaluate the clinical efficacy of honey-loaded chitosan/PVA hydrogel films in wound healing.

Automated summary

In this study, chitosan/polyvinyl alcohol (PVA)-based hydrogel films loaded with honey were developed for potential wound healing applications. The films were evaluated for their physical and mechanical properties, as well as their antimicrobial performance against Staphylococcus aureus. The results demonstrated the potential of these films as wound dressings and suggested the need for further in vivo experiments to evaluate their clinical efficacy.