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Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities

This article reviews the recent developments in the synthesis, antibacterial activity, and visible-light photocatalytic bacterial inactivation of nano-zinc oxide. Polycrystalline wurtzite ZnO nanostructures with a hexagonal lattice having different shapes can be synthesized by means of vapor-, liqui...

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Autores principales: Li, Yuchao, Liao, Chengzhu, Tjong, Sie Chin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700383/
https://www.ncbi.nlm.nih.gov/pubmed/33266476
http://dx.doi.org/10.3390/ijms21228836
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author Li, Yuchao
Liao, Chengzhu
Tjong, Sie Chin
author_facet Li, Yuchao
Liao, Chengzhu
Tjong, Sie Chin
author_sort Li, Yuchao
collection PubMed
description This article reviews the recent developments in the synthesis, antibacterial activity, and visible-light photocatalytic bacterial inactivation of nano-zinc oxide. Polycrystalline wurtzite ZnO nanostructures with a hexagonal lattice having different shapes can be synthesized by means of vapor-, liquid-, and solid-phase processing techniques. Among these, ZnO hierarchical nanostructures prepared from the liquid phase route are commonly used for antimicrobial activity. In particular, plant extract-mediated biosynthesis is a single step process for preparing nano-ZnO without using surfactants and toxic chemicals. The phytochemical molecules of natural plant extracts are attractive agents for reducing and stabilizing zinc ions of zinc salt precursors to form green ZnO nanostructures. The peel extracts of certain citrus fruits like grapefruits, lemons and oranges, acting as excellent chelating agents for zinc ions. Furthermore, phytochemicals of the plant extracts capped on ZnO nanomaterials are very effective for killing various bacterial strains, leading to low minimum inhibitory concentration (MIC) values. Bioactive phytocompounds from green ZnO also inhibit hemolysis of Staphylococcus aureus infected red blood cells and inflammatory activity of mammalian immune system. In general, three mechanisms have been adopted to explain bactericidal activity of ZnO nanomaterials, including direct contact killing, reactive oxygen species (ROS) production, and released zinc ion inactivation. These toxic effects lead to the destruction of bacterial membrane, denaturation of enzyme, inhibition of cellular respiration and deoxyribonucleic acid replication, causing leakage of the cytoplasmic content and eventual cell death. Meanwhile, antimicrobial activity of doped and modified ZnO nanomaterials under visible light can be attributed to photogeneration of ROS on their surfaces. Thus particular attention is paid to the design and synthesis of visible light-activated ZnO photocatalysts with antibacterial properties
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spelling pubmed-77003832020-11-30 Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities Li, Yuchao Liao, Chengzhu Tjong, Sie Chin Int J Mol Sci Review This article reviews the recent developments in the synthesis, antibacterial activity, and visible-light photocatalytic bacterial inactivation of nano-zinc oxide. Polycrystalline wurtzite ZnO nanostructures with a hexagonal lattice having different shapes can be synthesized by means of vapor-, liquid-, and solid-phase processing techniques. Among these, ZnO hierarchical nanostructures prepared from the liquid phase route are commonly used for antimicrobial activity. In particular, plant extract-mediated biosynthesis is a single step process for preparing nano-ZnO without using surfactants and toxic chemicals. The phytochemical molecules of natural plant extracts are attractive agents for reducing and stabilizing zinc ions of zinc salt precursors to form green ZnO nanostructures. The peel extracts of certain citrus fruits like grapefruits, lemons and oranges, acting as excellent chelating agents for zinc ions. Furthermore, phytochemicals of the plant extracts capped on ZnO nanomaterials are very effective for killing various bacterial strains, leading to low minimum inhibitory concentration (MIC) values. Bioactive phytocompounds from green ZnO also inhibit hemolysis of Staphylococcus aureus infected red blood cells and inflammatory activity of mammalian immune system. In general, three mechanisms have been adopted to explain bactericidal activity of ZnO nanomaterials, including direct contact killing, reactive oxygen species (ROS) production, and released zinc ion inactivation. These toxic effects lead to the destruction of bacterial membrane, denaturation of enzyme, inhibition of cellular respiration and deoxyribonucleic acid replication, causing leakage of the cytoplasmic content and eventual cell death. Meanwhile, antimicrobial activity of doped and modified ZnO nanomaterials under visible light can be attributed to photogeneration of ROS on their surfaces. Thus particular attention is paid to the design and synthesis of visible light-activated ZnO photocatalysts with antibacterial properties MDPI 2020-11-22 /pmc/articles/PMC7700383/ /pubmed/33266476 http://dx.doi.org/10.3390/ijms21228836 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Li, Yuchao
Liao, Chengzhu
Tjong, Sie Chin
Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities
title Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities
title_full Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities
title_fullStr Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities
title_full_unstemmed Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities
title_short Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities
title_sort recent advances in zinc oxide nanostructures with antimicrobial activities
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700383/
https://www.ncbi.nlm.nih.gov/pubmed/33266476
http://dx.doi.org/10.3390/ijms21228836
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