Light-degradable nanocomposite hydrogels for antibacterial wound dressing applications.
Changhao FangQiming ShenYingnan ZhangKaren KanemaruMichael J SerpePublished in: Journal of materials chemistry. B (2024)
Skin injuries infected by bacteria can cause life-threatening human diseases if not treated properly. In this work, we developed a light-degradable nanocomposite hydrogel to achieve both controlled antibiotic delivery and hydrogel degradation using light as the sole stimulus. Specifically, we incorporated triclosan-loaded, poly( N -isopropylacrylamide)-based nanogels (TCS-NGs) that exhibited potent antibacterial efficacy, into a light-degradable poly (ethylene glycol) (PEG)-based hydrogel matrix via simple physical entrapment method. Upon exposure to 365 nm light, the hydrogel matrix could rapidly degrade, which subsequently released the entrapped TCS-NGs into the surrounding environment. Our results demonstrated that TCS-NGs released from light-degradable nanocomposite hydrogels still possessed remarkable antibacterial efficacy by inhibiting the growth of Staphylococcus aureus both in solution (a fivefold reduction in optical density compared to the blank control) and on bacteria-infected porcine skins (a fivefold reduction in colony-forming units compared to the blank control). Finally, using an alamarBlue assay on human dermal fibroblasts, we determined that each component of the nanocomposite hydrogel exhibited excellent biocompatibility (>90% cell viability) and would not cause significant cytotoxicity. Overall, the fabricated light-degradable nanocomposite hydrogels could serve as novel material for antibacterial wound dressing applications.
Keyphrases
- wound healing
- drug delivery
- hyaluronic acid
- tissue engineering
- reduced graphene oxide
- staphylococcus aureus
- endothelial cells
- quantum dots
- drug release
- extracellular matrix
- photodynamic therapy
- induced pluripotent stem cells
- physical activity
- cystic fibrosis
- single cell
- simultaneous determination
- essential oil
- pluripotent stem cells
- tandem mass spectrometry