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      Oxygen-Rich Graphene/ZnO2-Ag nanoframeworks with pH-Switchable Catalase/Peroxidase activity as O2 Nanobubble-Self generator for bacterial inactivation

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      Journal of Colloid and Interface Science
      Elsevier BV

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          Abstract

          The oxygen-rich organic/inorganic (reduced graphene oxide (rGO)/ZnO2-Ag) nanoframeworks as suppliers of O2 nanobubbles (NBs) with dual pH-and-temperature-sensitive behavior were developed to suppress bacterial growth. It was demonstrated that not only the rate but also the final product of oxygen-rich ZnO2 decomposition (to an intermediate product of H2O2) rate was dramatically controlled by pH adjustment. Furthermore, in the presence of Ag nanoparticles, ̇OH radical generation switched to O2 NBs evolution by shifting the pH from acidic to basic/neutral conditions, demonstrating an adjustable nanozyme function-ability between catalase and peroxidase-like activity, respectively. Antibacterial properties of the in-situ generated O2 NBs substantially enhanced against bacterial models including methicillin-resistant Staphylococcus aureus in the presence of rGO. In fact, deflecting the electrons from their main respiratory chain to an oxygen-rich bypath through rGO significantly stimulated reactive oxygen species (ROS) generation, combating bacteria more efficiently. Moreover, NIR laser irradiation-induced temperature rise (due to the inherent photothermal properties of rGO) facilitated ZnO2 decomposition and accelerated growth and collapse of NBs. The simultaneous microscale thermal and mechanical destructions induced stronger antibacterial behavior. These results hold great promises for designing simple organic/inorganic nanoframeworks as solid sources of NBs with tunable enzyme-like ability in response to environmental conditions suitable for forthcoming graphene-based bio-applications.

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          Biofilms: an emergent form of bacterial life.

          Bacterial biofilms are formed by communities that are embedded in a self-produced matrix of extracellular polymeric substances (EPS). Importantly, bacteria in biofilms exhibit a set of 'emergent properties' that differ substantially from free-living bacterial cells. In this Review, we consider the fundamental role of the biofilm matrix in establishing the emergent properties of biofilms, describing how the characteristic features of biofilms - such as social cooperation, resource capture and enhanced survival of exposure to antimicrobials - all rely on the structural and functional properties of the matrix. Finally, we highlight the value of an ecological perspective in the study of the emergent properties of biofilms, which enables an appreciation of the ecological success of biofilms as habitat formers and, more generally, as a bacterial lifestyle.
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            Antibacterial activity of graphite, graphite oxide, graphene oxide, and reduced graphene oxide: membrane and oxidative stress.

            Health and environmental impacts of graphene-based materials need to be thoroughly evaluated before their potential applications. Graphene has strong cytotoxicity toward bacteria. To better understand its antimicrobial mechanism, we compared the antibacterial activity of four types of graphene-based materials (graphite (Gt), graphite oxide (GtO), graphene oxide (GO), and reduced graphene oxide (rGO)) toward a bacterial model-Escherichia coli. Under similar concentration and incubation conditions, GO dispersion shows the highest antibacterial activity, sequentially followed by rGO, Gt, and GtO. Scanning electron microscope (SEM) and dynamic light scattering analyses show that GO aggregates have the smallest average size among the four types of materials. SEM images display that the direct contacts with graphene nanosheets disrupt cell membrane. No superoxide anion (O(2)(•-)) induced reactive oxygen species (ROS) production is detected. However, the four types of materials can oxidize glutathione, which serves as redox state mediator in bacteria. Conductive rGO and Gt have higher oxidation capacities than insulating GO and GtO. Results suggest that antimicrobial actions are contributed by both membrane and oxidation stress. We propose that a three-step antimicrobial mechanism, previously used for carbon nanotubes, is applicable to graphene-based materials. It includes initial cell deposition on graphene-based materials, membrane stress caused by direct contact with sharp nanosheets, and the ensuing superoxide anion-independent oxidation. We envision that physicochemical properties of graphene-based materials, such as density of functional groups, size, and conductivity, can be precisely tailored to either reducing their health and environmental risks or increasing their application potentials. © 2011 American Chemical Society
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              Toxicity of graphene and graphene oxide nanowalls against bacteria.

              Bacterial toxicity of graphene nanosheets in the form of graphene nanowalls deposited on stainless steel substrates was investigated for both gram-positive and gram-negative models of bacteria. The graphene oxide nanowalls were obtained by electrophoretic deposition of Mg(2+)-graphene oxide nanosheets synthesized by a chemical exfoliation method. On the basis of measuring the efflux of cytoplasmic materials of the bacteria, it was found that the cell membrane damage of the bacteria caused by direct contact of the bacteria with the extremely sharp edges of the nanowalls was the effective mechanism in the bacterial inactivation. In this regard, the gram-negative Escherichia coli bacteria with an outer membrane were more resistant to the cell membrane damage caused by the nanowalls than the gram-positive Staphylococcus aureus lacking the outer membrane. Moreover, the graphene oxide nanowalls reduced by hydrazine were more toxic to the bacteria than the unreduced graphene oxide nanowalls. The better antibacterial activity of the reduced nanowalls was assigned to the better charge transfer between the bacteria and the more sharpened edges of the reduced nanowalls, during the contact interaction.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Journal of Colloid and Interface Science
                Journal of Colloid and Interface Science
                Elsevier BV
                00219797
                May 2023
                May 2023
                : 637
                : 237-250
                Article
                10.1016/j.jcis.2023.01.079
                36701869
                91e0ebe8-5b5d-4178-8b84-c873532f9f34
                © 2023

                https://www.elsevier.com/tdm/userlicense/1.0/

                https://doi.org/10.15223/policy-017

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-012

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-004

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