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Adv Mater ; 33(8): e2005477, 2021 Feb.
Article in English | MEDLINE | ID: covidwho-1039151

ABSTRACT

Besides the pandemic caused by the coronavirus outbreak, many other pathogenic microbes also pose a devastating threat to human health, for instance, pathogenic bacteria. Due to the lack of broad-spectrum antibiotics, it is urgent to develop nonantibiotic strategies to fight bacteria. Herein, inspired by the localized "capture and killing" action of bacteriophages, a virus-like peroxidase-mimic (V-POD-M) is synthesized for efficient bacterial capture (mesoporous spiky structures) and synergistic catalytic sterilization (metal-organic-framework-derived catalytic core). Experimental and theoretical calculations show that the active compound, MoO3 , can serve as a peroxo-complex-intermediate to reduce the free energy for catalyzing H2 O2 , which mainly benefits the generation of •OH radicals. The unique virus-like spikes endow the V-POD-M with fast bacterial capture and killing abilities (nearly 100% at 16 µg mL-1 ). Furthermore, the in vivo experiments show that V-POD-M possesses similar disinfection treatment and wound skin recovery efficiencies to vancomycin. It is suggested that this inexpensive, durable, and highly reactive oxygen species (ROS) catalytic active V-POD-M provides a promising broad-spectrum therapy for nonantibiotic disinfection.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Biomimetic Materials/chemical synthesis , Oxides/chemical synthesis , Peroxidase/chemistry , Anti-Bacterial Agents/pharmacology , Biocompatible Materials/chemistry , Biomimetic Materials/pharmacology , Catalysis , Humans , Hydrogen Peroxide/metabolism , Metal-Organic Frameworks/chemistry , Metal-Organic Frameworks/pharmacology , Molecular Dynamics Simulation , Molybdenum/pharmacology , Oxides/pharmacology , Peroxidase/metabolism , Sterilization , Vancomycin/pharmacology
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