Peroxidase-like Nanozymes for Point-of-Care SERS Sensing and Wound Healing

The emergence of nanozymes provides a potential method for combating multidrug-resistant bacteria resulted from the abuse of antibiotics. However, in nanozyme-catalyzed systems, few studies have addressed the actual hydrogen peroxide (H2O2) level involved in sterilization. Herein, we designed a high-efficiency peroxidase-mimicking nanozyme with surface-enhanced Raman scattering (SERS) property by assembling gold nanoparticles on single-layer Cu2+-C3N4 (AuNP-Cu2+-C3N4). The nanozyme effectively converts the low-active Raman reporter 3,3 ',5,5 '- tetramethylbenzidine (TMB) into its oxidized form with H2O2, resulting in SERS signal changes, thereby achieving highly sensitive quantification of H2O2 with limit of detection as low as 0.60 mu M. More importantly, the nanozyme can specifically catalyze H2O2 into antibacterial hydroxyl radicals. In vitro and in vivo evaluations demonstrate the remarkable antibacterial efficacy of the nanozyme/H2O2 combination against Staphylococcus aureus (up to 99.9%), which could promote wound healing in mice and allow point-of-care monitoring the amount of H2O2 participated in effective sterilization. This study not only displays great potential in combining multiple functionalities of nanomaterials for versatile bioassays but also provides a promising approach to design nanozymes for biomedical and catalytic applications.

Automated summary

The emergence of nanozymes provides a potential method for combating multidrug-resistant bacteria resulted from the abuse of antibiotics. In this study, a high-efficiency peroxidase-mimicking nanozyme with surface-enhanced Raman scattering (SERS) property was designed. The nanozyme effectively converts the low-active Raman reporter 3,3 ',5,5 '- tetramethylbenzidine (TMB) into its oxidized form with H2O2, resulting in SERS signal changes, thereby achieving highly sensitive quantification of H2O2. Moreover, the nanozyme can specifically catalyze H2O2 into antibacterial hydroxyl radicals, demonstrating remarkable antibacterial efficacy against Staphylococcus aureus.