Abstract

A growth of bacterial infections and over-and inefficient release of antibiotics forces one to search new antibacterial agents and/or strategies. In this study, a novel strategy towards biocompatible and antibacterial bilayer wound dressing was proposed by a two-step spin coating method combined with in-situ crosslinking polymerization. First, through in-situ crosslinking polymerization, [2-(methacryloyloxy) ethyl] trimethylammonium chloride ([MTA][Cl]) was polymerized and crosslinked in polycaprolactone (PCL) solution and PCL/PMTA solution was obtained. Then, the PCL/PMTA solution was spinning-coated as the antibacterial top layer and the mixture of PCL and gelatin (Gel) (PCL/Gel) as the biocompatible bottom layer. The obvious bi-layered structure and boundary between the two layers was distinctly showed in scanning electron microscope (SEM) pictures. X-ray diffraction (XRD), attenuated total reflection flourier transformed infrared spectroscopy (ATR-FTIR), differential scanning calorimeter (DSC), thermo-gravimetric analysis (TGA) and water contact angle (WCA) analysis were used to investigate the physical and chemical properties and obtained results demonstrated the successful preparation of the bi-layered membranes. The prepared bi-layered wound dressing displayed both strong antibacterial activity and good biocompatibility in vitro. The bilayered membranes with biocompatible and antibacterial properties would be next generation of wound dressing.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.