Abstract

Microporous chitosan nanofibers functionalized with different amounts of an antimicrobial agent via imine linkage were prepared by a three-step procedure including the electrospinning of a chitosan/PEO blend, PEO removal and acid condensation reaction in a heterogeneous system with 2-formylphenylboronic acid. The fibers’ characterization was undertaken keeping in mind their application to wound healing. Thus, by FTIR and 1H-NMR spectroscopy, it was confirmed the successful imination of the fibers and the conversion degree of the amine groups of chitosan into imine units. The fiber morphology in terms of fiber diameter, crystallinity, inter- and intra-fiber porosity and strength of intermolecular forces was investigated using scanning electron microscopy, polarized light microscopy, water vapor sorption and thermogravimetric analysis. The swelling ability was estimated in water and phosphate buffer by calculating the mass equilibrium swelling. The fiber biodegradation was explored in five media of different pH, corresponding to different stages of wound healing and the antimicrobial activity against the opportunistic pathogens inflicting wound infection was investigated according to standard tests. The biocompatibility and bioadhesivity were studied on normal human dermal fibroblast cells by direct contact procedure. The dynamic character of the imine linkage of the functionalized fibers was monitored by UV-vis spectroscopy. The results showed that the functionalization of the chitosan microporous nanofibers with antimicrobial agents via imine linkage is a great route towards bio-absorbable wound dressings with “on demand” antimicrobial properties and biodegradation rate matching the healing stages.

Highlights

  • MaterialsChitosan (126 kDa, DA = 97%) was prepared by basic hydrolysis (Figures S1 and S2)

  • Introduction iationsWound healing is a frequent skin trauma that severely impacts public health

  • 2A series of microporous chitosan nanofibers functionalized via imine linkage formylphenylboronic acid were prepared and characterized with the aim to develop a a

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Summary

Materials

Chitosan (126 kDa, DA = 97%) was prepared by basic hydrolysis (Figures S1 and S2). 2-Formylphenylboronic acid (Aldrich, 97%) was purified by column chromatography (Figures S3 and S4). Polyethylene oxide (1000 kDa), acetic acid (99, 89%), sodium hydroxide (95%) and ethanol (98.89%) were purchased from Aldrich. Ethanol was dried on molecular sieves before use

Fiber Preparation
Equipment
Results and Discussion
Structural Characterization of the Imino-Chitosan Fibers
12 Mat Morphology
Graphical representation the BA release
Swelling Behaviour
Antimicrobial Activity
Biocompatibility
Conclusions
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