Application of a Cascaded Nanozyme in Infected Wound Recovery of Diabetic Mice.
Yanfang ZhangDanxia LiYuanhong XuYusheng NiuPublished in: ACS biomaterials science & engineering (2022)
The emergence of peroxidase (POD)-like nanozyme-derived catalytic therapy has provided a promising choice for reactive oxygen species (ROS)-mediated broad-spectrum antibacterials to replace antibiotics, but it still suffers from limitations of low therapeutic efficiency and unusual addition of unstable H 2 O 2 . Considering that the higher blood glucose in diabetic wounds provides much more numerous nutrients for bacterial growth, a cascade nanoenzymatic active material was developed by coating glucose oxidase (GOx) onto POD-like Fe 2 (MoO 4 ) 3 [Fe 2 (MoO 4 ) 3 @GOx]. GOx could consume the nutrient of glucose to produce gluconic acid (weakly acidic) and H 2 O 2 , which could be subsequently converted into highly oxidative • OH via the catalysis of POD-like Fe 2 (MoO 4 ) 3 . Accordingly, the synergistic effect of starvation and ROS-mediated therapy showed significantly efficient antibacterial effect while avoiding the external addition of H 2 O 2 that affects the stability and efficacy of the therapy system. Compared with the bactericidal rates of 46.2-59.404% of GOx or Fe 2 (MoO 4 ) 3 alone on extended-spectrum β-lactamases producing Escherichia coli and methicillin-resistant Staphylococcus aureus , those of the Fe 2 (MoO 4 ) 3 @GOx group are 98.396 and 98.776%, respectively. Animal experiments showed that the as-synthesized Fe 2 (MoO 4 ) 3 @GOx could much efficiently promote the recovery of infected wounds in type 2 diabetic mice while showing low cytotoxicity in vivo .
Keyphrases
- blood glucose
- reactive oxygen species
- methicillin resistant staphylococcus aureus
- escherichia coli
- metal organic framework
- wound healing
- aqueous solution
- visible light
- dna damage
- cell death
- glycemic control
- heavy metals
- insulin resistance
- drug delivery
- ionic liquid
- oxidative stress
- decision making
- mesenchymal stem cells
- biofilm formation
- replacement therapy