Tissue Adhesive, Biocompatible, Antioxidant, and Antibacterial Hydrogels Based on Tannic Acid and Fungal-Derived Carboxymethyl Chitosan for Wound-Dressing Applications.
Kummara Madhususdana RaoUluvangada Thammaiah UthappaHyeon Jin KimSung Soo HanPublished in: Gels (Basel, Switzerland) (2023)
This study aimed to develop hydrogels for tissue adhesion that are biocompatible, antioxidant, and antibacterial. We achieved this by using tannic acid (TA) and fungal-derived carboxymethyl chitosan (FCMCS) incorporated in a polyacrylamide (PAM) network using free-radical polymerization. The concentration of TA greatly influenced the physicochemical and biological properties of the hydrogels. Scanning electron microscopy showed that the nanoporous structure of the FCMCS hydrogel was retained with the addition of TA, resulting in a nanoporous surface structure. Equilibrium-swelling experiments revealed that increasing the concentration of TA significantly improved water uptake capacity. Antioxidant radical-scavenging assays and porcine skin adhesion tests confirmed the excellent adhesive properties of the hydrogels, with adhesion strengths of up to 39.8 ± 1.2 kPa for 1.0TA-FCMCS due to the presence of abundant phenolic groups on TA. The hydrogels were also found to be biocompatible with skin fibroblast cells. Furthermore, the presence of TA significantly enhanced the antibacterial properties of the hydrogels against both Gram-positive ( Staphylococcus aureus ) and Gram-negative ( Escherichia coli ) bacteria. Therefore, the developed drug-free antibacterial and tissue-adhesive hydrogels can potentially be used as wound dressings for infected wounds.
Keyphrases
- wound healing
- drug delivery
- gram negative
- drug release
- hyaluronic acid
- escherichia coli
- biofilm formation
- electron microscopy
- staphylococcus aureus
- multidrug resistant
- oxidative stress
- anti inflammatory
- induced apoptosis
- extracellular matrix
- cystic fibrosis
- ionic liquid
- signaling pathway
- high throughput
- endoplasmic reticulum stress
- molecular dynamics
- cell proliferation
- cell migration
- molecular dynamics simulations
- klebsiella pneumoniae
- drug induced
- mass spectrometry