Wound infection is arguably the most common, and potentially the most devastating, complication of the wound healing process. The ideal treatment strategy has to eliminate bacteria, alleviate inflammation, and promote wound healing and skin formation. Herein, a multifunctional heterostructure is designed consisting of ultrasmall platinum–ruthenium nanoalloys and porous graphitic carbon nitride C3N5 nanosheets (denoted as PtRu/C3N5), which concurrently possesses piezoelectric enhanced oxidase ‐mimic nanozyme activity and photocatalytic hydrogen gas production capacity. Moreover, these hybrid nanotherapeutics are integrated in natural hyaluronic acid microneedles, which exhibit almost 100% broad‐spectrum antibacterial efficacy against multiple bacterial strains in vitro and in vivo within 10 min ultrasound treatment, and effectively inhibit inflammation reactions after 1 h visible light irradiation, promising for accelerating the cutaneous wound healing in the bacterial infected mice. This study highlights a competitive strategy for development of all‐in‐one antibacterial and anti‐inflammatory therapies.
Nanozymes are promising new-generation antibacterial agents owing to their low cost, high stability, broadspectrum activity, and minimal antimicrobial resistance. However, the inherent low catalytic activity of nanozymes tends to limit their antibacterial efficacy. Herein, a heterostructure of zinc oxide nanorod@graphdiyne nanosheets (ZnO@GDY NR) with unparallel piezocatalytic enzyme mimic activity is reported, which concurrently possesses intrinsic peroxidase-like activity and strong piezoelectric responses and effectively promotes the decomposition of hydrogen peroxide (H 2 O 2 ) and generation of reactive oxygen species under ultrasound irradiation. Moreover, this piezocatalytic nanozyme exhibits almost 100% antibacterial efficacy against multidrug-resistant pathogens involving methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa in vitro and in vivo. In addition, a piezoelectric activatable nanozyme-based skin patch is developed for rapid skin wound disinfections with satisfactory hemocompatibility and cytocompatibility. This work not only sheds light on the development of an innovative piezoelectric activatable nanozyme-based skin patch for rapid wound disinfection but also provides new insights on the engineering of piezocatalytic nanozymes for nanozyme antibacterial therapy.
Treatment of diabetic foot ulcers (DFU) needs to reduce inflammation, relieve hypoxia, lower blood glucose, promote angiogenesis, and eliminate pathogenic bacteria, but the therapeutic efficacy is greatly limited by the diversity and synergy of drug functions as well as the DFU microenvironment itself. Herein, an ultrasoundaugmented multienzyme-like nanozyme hydrogel spray was developed using hyaluronic acid encapsulated L-arginine and ultrasmall gold nanoparticles and Cu 1.6 O nanoparticles coloaded phosphorus doped graphitic carbon nitride nanosheets (ACPCAH). This nanozyme hydrogel spray possesses five types of enzyme-like activities, including superoxide dismutase (SOD)-, catalase (CAT)-, glucose oxidase (GOx)-, peroxidase (POD)-, and nitric oxide synthase (NOS)-like activities. The kinetics and reaction mechanism of the sonodynamic/sonothermal synergistic enhancement of the SOD-CAT-GOx-POD/NOS cascade reaction of ACPCAH are fully investigated. Both in vitro and in vivo tests demonstrate that this nanozyme hydrogel spray can be activated by the DFU microenvironment to reduce inflammation, relieve hypoxia, lower blood glucose, promote angiogenesis, and eliminate pathogenic bacteria, thus accelerating diabetic wound healing effectively. This study highlights a competitive approach based on multienzyme-like nanozymes for the development of all-in-one DFU therapies.
Improving the catalytic activity and broadening the scope of nanozymes are prerequisites to supplement or even supersede natural enzymes. However, the discovery of nanozymes is mostly relied on serendipity with limited fine-tunings of chemical composition, which is often incomprehensive and fragmented. Machine learning (ML) is a promising solution to predict the nanozyme performance and thus accelerate the nanozyme development. Herein, a thorough investigation of the peroxidase (POD) mimic reaction catalyzed by nonmetal atom doped graphdiyne (GDY) is presented and two doped GDYs (B-GDY and N-GDY) with best performance were screened out. Specifically, the extreme gradient boosting (XGB) algorithm can mine the connection between the model parameters and maximum energy barrier (R 2 > 78%) or maximum energy consuming step (accuracy > 65%) from the data set constructed by all the nonmetal atom doped GDYs, which provides a method to effectively reduce 20% calculations. In addition, six nonmetal atom doped GDYs with different expected properties were synthesized, and their activity trends in three related experiments were consistent with the predicted results. This study demonstrates that ML can be a useful tool to assist density functional theory (DFT) computational screening and can serve as a guide for optimizing nanozyme performance, depending on doping strategy.
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