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      Enhancing photocatalytic tetracycline degradation through the fabrication of high surface area CeO 2 from a cerium–organic framework†

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          Abstract

          Water pollution is a global environmental issue, and the presence of pharmaceutical compounds, such as tetracyclines (TCs), in aquatic ecosystems has raised growing concerns due to the potential risks to both the environment and human health. A high surface area CeO 2 was prepared via atmospheric thermal treatment of a metal–organic framework of cerium and benzene-1,3,5-tricarboxylate. The effects of calcination temperature on the morphology, structure, light absorption properties and tetracycline removal efficiency were studied. The best activity of the photocatalysts could be achieved when the heat treatment temperature is 300 °C, which enhances the photocatalytic degradation performance towards tetracycline under visible light. The resulting CeO 2 particles have high capacity for adsorbing TCs from aqueous solution: 90 mg g −1 for 60 mg L −1 TCs. As a result, 98% of the initial TC can be removed under simulated sunlight irradiation. The cooperation of moderate defect concentration and disordered structure showed tetracycline removal activity about 10 times higher than the initial Ce-MOF. An embryotoxicity assessment on zebrafish revealed that treatment with CeO 2 particles significantly decreased the toxicity of TC solutions.

          Abstract

          Water pollution is a global environmental issue, and the presence of pharmaceutical compounds, such as tetracyclines (TCs), in aquatic ecosystems has raised growing concerns due to the potential risks to both the environment and human health.

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          Most cited references51

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          Tetracycline antibiotics: mode of action, applications, molecular biology, and epidemiology of bacterial resistance.

          Tetracyclines were discovered in the 1940s and exhibited activity against a wide range of microorganisms including gram-positive and gram-negative bacteria, chlamydiae, mycoplasmas, rickettsiae, and protozoan parasites. They are inexpensive antibiotics, which have been used extensively in the prophlylaxis and therapy of human and animal infections and also at subtherapeutic levels in animal feed as growth promoters. The first tetracycline-resistant bacterium, Shigella dysenteriae, was isolated in 1953. Tetracycline resistance now occurs in an increasing number of pathogenic, opportunistic, and commensal bacteria. The presence of tetracycline-resistant pathogens limits the use of these agents in treatment of disease. Tetracycline resistance is often due to the acquisition of new genes, which code for energy-dependent efflux of tetracyclines or for a protein that protects bacterial ribosomes from the action of tetracyclines. Many of these genes are associated with mobile plasmids or transposons and can be distinguished from each other using molecular methods including DNA-DNA hybridization with oligonucleotide probes and DNA sequencing. A limited number of bacteria acquire resistance by mutations, which alter the permeability of the outer membrane porins and/or lipopolysaccharides in the outer membrane, change the regulation of innate efflux systems, or alter the 16S rRNA. New tetracycline derivatives are being examined, although their role in treatment is not clear. Changing the use of tetracyclines in human and animal health as well as in food production is needed if we are to continue to use this class of broad-spectrum antimicrobials through the present century.
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            Adsorption and removal of tetracycline antibiotics from aqueous solution by graphene oxide.

            Significant concerns have been raised over pollution of antibiotics including tetracyclines in aquatic environments in recent years. Graphene oxide (GO) is a potential effective absorbent for tetracycline antibiotics and can be used to remove them from aqueous solution. Tetracycline strongly deposited on the GO surface via π-π interaction and cation-π bonding. The adsorption isotherm fits Langmuir and Temkin models well, and the theoretical maximum of adsorption capacity calculated by Langmuir model is 313 mg g(-1), which is approximately in a close agreement with the measured data. The kinetics of adsorption fits pseudo-second-order model perfectly, and it has a better rate constant of sorption (k), 0.065 g mg(-1) h(-1), than other adsorbents. The adsorption capacities of tetracycline on GO decreased with the increase in pH or Na(+) concentration. The adsorption isotherms of oxytetracycline and doxycycline on GO were discussed and compared. Crown Copyright © 2011. Published by Elsevier Inc. All rights reserved.
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              Occurrence, fate, and risk assessment of typical tetracycline antibiotics in the aquatic environment: A review

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                Author and article information

                Journal
                RSC Adv
                RSC Adv
                RA
                RSCACL
                RSC Advances
                The Royal Society of Chemistry
                2046-2069
                30 May 2024
                28 May 2024
                30 May 2024
                : 14
                : 25
                : 17507-17518
                Affiliations
                [a ] Department of Chemistry and Chemical Engineering, University Federal of São Carlos São Carlos Brazil
                [b ] Departament of Chemistry, FFCLRP, University of São Paulo Ribeirão Preto Brazil osaserra@ 123456usp.br
                [c ] Institute of Chemistry, Rural Federal University of Rio de Janeiro-UFRRJ Seropédica Brazil
                [d ] Department of Genetics and Morphology, Institute of Biological Sciences, University Brasilia-UnB Brasilia Brazil
                [e ] Department of Chemistry, University of Warwick Coventry CV4 7AL UK
                Author information
                https://orcid.org/0000-0003-0085-5773
                https://orcid.org/0000-0003-3858-3363
                https://orcid.org/0000-0001-9706-2774
                https://orcid.org/0000-0003-1851-2218
                Article
                d4ra02640c
                10.1039/d4ra02640c
                11138135
                38818361
                12397b4e-bacd-4f2f-8bba-2fe16984d0ba
                This journal is © The Royal Society of Chemistry
                History
                : 8 April 2024
                : 16 May 2024
                Page count
                Pages: 12
                Funding
                Funded by: Conselho Nacional de Desenvolvimento Científico e Tecnológico, doi 10.13039/501100003593;
                Award ID: 311790/2020-8
                Award ID: 426467/2018-3
                Award ID: 432498/2018-4
                Award ID: 150059/2022-1
                Funded by: Fundação de Amparo à Pesquisa do Estado de São Paulo, doi 10.13039/501100001807;
                Award ID: 2021/14904-5
                Award ID: 2018/07514-3
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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