NIR-activated quercetin-based nanogels embedded with CuS nanoclusters for the treatment of drug-resistant biofilms and accelerated chronic wound healing.
Amit NainYu-Ting TsengAkash GuptaYu-Feng LinArumugam SangiliYu-Fen HuangChih-Ching HuangHuan-Tsung ChangPublished in: Nanoscale horizons (2023)
We have developed multifunctional nanogels with antimicrobial, antioxidant, and anti-inflammatory properties, facilitating rapid wound healing. To prepare the multifunctional nanogels, we utilized quercetin (Qu) and a mild carbonization process to form carbonized nanogels (CNGs). These CNGs possess excellent antioxidative and bacterial targeting properties. Subsequently, we utilized the Qu-CNGs as templates to prepare nanogels incorporating copper sulfide (CuS) nanoclusters, further enhancing their functionality. Notably, the CuS/Qu-CNGs nanocomposites demonstrated an exceptional minimum inhibitory concentration against tested bacteria, approximately 125-fold lower than monomeric Qu or Qu-CNGs. This enhanced antimicrobial effect was achieved by leveraging near-infrared II (NIR-II) light irradiation. Additionally, the CuS/Qu-CNGs exhibited efficient penetration into the extracellular biofilm matrix, eradicating methicillin-resistant Staphylococcus aureus -associated biofilms in diabetic mice wounds. Furthermore, the nanocomposites were found to suppress proinflammatory cytokines, such as IL-1β, at the wound sites while regulating the expression of anti-inflammatory factors, including IL-10 and TGF-β1, throughout the recovery process. The presence of CuS/Qu-CNGs promoted angiogenesis, epithelialization, and collagen synthesis, thereby accelerating wound healing. Our developed CuS/Qu-CNGs nanocomposites have great potential in addressing the challenges associated with delayed wound healing caused by microbial pathogenesis.
Keyphrases
- wound healing
- anti inflammatory
- drug resistant
- staphylococcus aureus
- methicillin resistant staphylococcus aureus
- candida albicans
- cancer therapy
- drug delivery
- multidrug resistant
- fluorescent probe
- microbial community
- oxidative stress
- poor prognosis
- reduced graphene oxide
- acinetobacter baumannii
- escherichia coli
- pseudomonas aeruginosa
- radiation therapy
- gold nanoparticles
- epithelial mesenchymal transition
- carbon nanotubes
- biofilm formation
- cystic fibrosis
- risk assessment
- drug release
- radiation induced
- long non coding rna
- loop mediated isothermal amplification