PCL/Gelatin/Graphene Oxide Electrospun Nanofibers: Effect of Surface Functionalization on In Vitro and Antibacterial Response.
Nazirah HamdanWan Khartini Wan Abdul KhodirShafida Abd HamidMohd Hamzah Mohd NasirAhmad Sazali HamzahIriczalli Cruz-MayaVincenzo GuarinoPublished in: Nanomaterials (Basel, Switzerland) (2023)
The emergence of resistance to pathogenic bacteria has resulted from the misuse of antibiotics used in wound treatment. Therefore, nanomaterial-based agents can be used to overcome these limitations. In this study, polycaprolactone (PCL)/gelatin/graphene oxide electrospun nanofibers (PGO) are functionalized via plasma treatment with the monomeric groups diallylamine (PGO-M1), acrylic acid (PGO-M2), and tert -butyl acrylate (PGO-M3) to enhance the action against bacteria cells. The surface functionalization influences the morphology, surface wettability, mechanical properties, and thermal stability of PGO nanofibers. PGO-M1 and PGO-M2 exhibit good antibacterial activity against Staphylococcus aureus and Escherichia coli , whereas PGO-M3 tends to reduce their antibacterial properties compared to PGO nanofibers. The highest proportion of dead bacteria cells is found on the surface of hydrophilic PGO-M1, whereas live cells are colonized on the surface of hydrophobic PGO-M3. Likewise, PGO-M1 shows a good interaction with L929, which is confirmed by the high levels of adhesion and proliferation with respect to the control. All the results confirm that surface functionalization can be strategically used as a tool to engineer PGO nanofibers with controlled antibacterial properties for the fabrication of highly versatile devices suitable for different applications (e.g., health, environmental pollution).
Keyphrases
- induced apoptosis
- escherichia coli
- cell cycle arrest
- staphylococcus aureus
- tissue engineering
- signaling pathway
- healthcare
- risk assessment
- wound healing
- public health
- cell death
- biofilm formation
- oxidative stress
- heavy metals
- multidrug resistant
- human health
- pseudomonas aeruginosa
- social media
- particulate matter
- ionic liquid
- cell proliferation
- combination therapy
- mass spectrometry
- cell migration
- air pollution