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      Visible light-induced photocatalytic and antibacterial adhesion properties of superhydrophilic TiO 2 nanoparticles

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          Abstract

          Bacterial infections triggered by patient or healthcare worker contact with surfaces are a major cause of medically acquired infections. By controlling the kinetics of tetrabutyl titanate hydrolysis and condensation during the sol–gel process, it is possible to regulate the content of Ti 3+ and oxygen vacancies (OVs) in TiO 2, and adjust the associated visible light-induced photocatalytic performance and anti-bacterial adhesion properties. The results have shown that the Ti 3+ content in TiO 2 was 9.87% at the calcination temperature of the reaction system was 300 °C and pH was 1.0, corresponding to optimal photocatalytic and hydrophilic properties. The formation of a hydrated layer on the superhydrophilic surface provided resistance to bacterial adhesion, preventing cross-contamination on high-touch surfaces. The excellent photocatalytic self-cleaning performance and anti-bacterial adhesion properties can be attributed to synergistic effects associated with the high specific surface area of TiO 2 nanoparticles, the mesoporous structure, and the presence of Ti 3+ and OVs. The formation of superhydrophilic self-cleaning surfaces under visible light can serve as the basis for the development of a new class of anti-bacterial adhesion materials.

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          Mechanisms of SARS-CoV-2 entry into cells

          The unprecedented public health and economic impact of the COVID-19 pandemic caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been met with an equally unprecedented scientific response. Much of this response has focused, appropriately, on the mechanisms of SARS-CoV-2 entry into host cells, and in particular the binding of the spike (S) protein to its receptor, angiotensin-converting enzyme 2 (ACE2), and subsequent membrane fusion. This Review provides the structural and cellular foundations for understanding the multistep SARS-CoV-2 entry process, including S protein synthesis, S protein structure, conformational transitions necessary for association of the S protein with ACE2, engagement of the receptor-binding domain of the S protein with ACE2, proteolytic activation of the S protein, endocytosis and membrane fusion. We define the roles of furin-like proteases, transmembrane protease, serine 2 (TMPRSS2) and cathepsin L in these processes, and delineate the features of ACE2 orthologues in reservoir animal species and S protein adaptations that facilitate efficient human transmission. We also examine the utility of vaccines, antibodies and other potential therapeutics targeting SARS-CoV-2 entry mechanisms. Finally, we present key outstanding questions associated with this critical process. Entry of SARS-CoV-2 into host cells is mediated by the interaction between the viral spike protein and its receptor angiotensin-converting enzyme 2, followed by virus–cell membrane fusion. Worldwide research efforts have provided a detailed understanding of this process at the structural and cellular levels, enabling successful vaccine development for a rapid response to the COVID-19 pandemic.
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            Implant infections: adhesion, biofilm formation and immune evasion

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              Bioinspired Surfaces with Superwettability: New Insight on Theory, Design, and Applications.

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                Author and article information

                Contributors
                chenlili@cqut.edu.cn
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                4 April 2024
                4 April 2024
                2024
                : 14
                : 7940
                Affiliations
                School of Chemistry and Chemical Engineering, Chongqing University of Technology, ( https://ror.org/04vgbd477) Chongqing, 400054 China
                Article
                58660
                10.1038/s41598-024-58660-0
                10995203
                38575777
                87631c3c-903a-472c-a766-4a76bda7ca55
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 4 January 2024
                : 2 April 2024
                Funding
                Funded by: Scientific Research Foundation of Chongqing University of Technology
                Award ID: 0115220003
                Award ID: 0115220003
                Award ID: 0115220003
                Award ID: 0115220003
                Funded by: Science and Technology Research Program of Chongqing Municipal Education Commission of China
                Award ID: KJQN202201118
                Award ID: KJQN202201118
                Award ID: KJQN202201118
                Award ID: KJQN202201118
                Categories
                Article
                Custom metadata
                © Springer Nature Limited 2024

                Uncategorized
                anatase tio2,ti3+/ovs,hydrophilicity,photocatalysis,anti-bacterial adhesion,materials science,biomaterials,materials for energy and catalysis,materials for optics,nanoscale materials

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