Dual antibacterial activities of a chitosan-modified upconversion photodynamic therapy system against drug-resistant bacteria in deep tissue.
Siwen LiSisi CuiDeyan YinQiuyun ZhuYuxiang MaZhiyu QianYueqing GuPublished in: Nanoscale (2018)
Photodynamic therapy (PDT) has recently been proposed as an innovative approach to combat multi-drug resistant (MDR) bacteria. To improve the penetration depth of current PDT, a core-shell upconversion nanoparticle (UCNP) based PDT system, composed of a cationic N-octyl chitosan (OC) coated UCNP loaded with the photosensitizer zinc phthalocyanine (OC-UCNP-ZnPc), was constructed to enhance the antibacterial efficacy against MDR bacteria in deep tissue. The core-shell UCNPs displayed a higher upconversion fluorescence efficiency compared to the inner UCNP core. Dual antibacterial activities induced by chitosan and PDT-induced ROS were demonstrated, independent of the bacterial species. In particular, these nanoconstructs exhibited excellent antibacterial effects on the MDR bacteria including methicillin-resistant Staphylococcus aureus (MRSA) and β-lactamase-producing Escherichia coli. In vivo antibacterial therapy for murine MRSA-infected abscesses in the deep tissue (1 cm) strongly confirmed the outstanding anti-MRSA efficacy of OC-UCNP-ZnPc. Our results indicated that the OC-UCNP-ZnPc based PDT system triggered by deep-penetrating NIR light has a prominent antibacterial effect on MDR bacteria, which could be a promising strategy for deep-tissue infections.
Keyphrases
- photodynamic therapy
- drug resistant
- multidrug resistant
- methicillin resistant staphylococcus aureus
- wound healing
- silver nanoparticles
- acinetobacter baumannii
- staphylococcus aureus
- drug delivery
- fluorescence imaging
- escherichia coli
- klebsiella pneumoniae
- anti inflammatory
- hyaluronic acid
- biofilm formation
- cell death
- single molecule
- cancer therapy
- cystic fibrosis
- drug release
- candida albicans