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      Dye degradation performance, bactericidal behavior and molecular docking analysis of Cu-doped TiO 2 nanoparticles

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      RSC Advances
      The Royal Society of Chemistry

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          Abstract

          Copper-doped TiO 2 was prepared with a sol–gel chemical method. Various concentrations (3, 6, and 9 wt%) of Cu dopant were employed. Several techniques were implemented to assess the structural, optical, morphological and chemical properties of the synthesized samples. Evaluation of elemental composition using SEM-EDS and XRF techniques showed the presence of dopant element in the prepared samples. XRD analysis confirmed the presence of anatase (TiO 2) phase with interstitial doping. Incorporation of dopant was observed to enhance the crystallinity and increase the crystallite size of the synthesized products. SAED profiles revealed a high degree of crystallinity in the prepared specimens, which was also evident in the XRD spectra. Optical properties studied using UV-vis spectroscopy depicted a shift of the maximum absorption to the visible region (redshift) that signified a reduction in the band gap energy of Cu-doped TiO 2 samples. Examination of morphological features with scanning and high-resolution transmission electron microscopes revealed the formation of spherical nanoparticles with a tendency to agglomerate with increasing dopant concentration. Molecular vibrations and the formation of Ti–O–Ti bonds were revealed through FTIR spectra. PL spectroscopy recorded the trapping efficiency and migration of charge carriers, which exhibited electron–hole recombination behavior. Doped nanostructures showed enhanced bactericidal performance and synergism against S. aureus and E. coli. In summary, Cu-doped TiO 2 nanostructures were observed to impede bacteria effectively, which is deemed beneficial in overcoming ailments caused by pathogens such as microbial etiologies. Furthermore, molecular docking analysis was conducted to study the interaction of Cu-doped TiO 2 nanoparticles with multiple proteins namely β-lactamase (binding score: −4.91 kcal mol −1), ddlB (binding score: −5.67 kcal mol −1) and FabI (binding score: −6.13 kcal mol −1) as possible targets with active site residues. Dye degradation/reduction of control and Cu-doped samples were studied through absorption spectroscopy. The obtained outcomes of the performed experiment indicated that the photocatalytic activity of Cu-TiO 2 enhanced with increasing dopant concentration, which is thought to be due to a decreased rate of electron–hole pair recombination. Consequently, it is suggested that Cu-TiO 2 can be exploited as an effective candidate for antibacterial and dye degradation applications.

          Abstract

          Copper-doped TiO 2 was prepared with a sol–gel chemical method.

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          Most cited references79

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          Fundamentals of TiO 2 Photocatalysis: Concepts, Mechanisms, and Challenges

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            Principles and mechanisms of photocatalytic dye degradation on TiO2 based photocatalysts: a comparative overview

            Pictorial representation of all possible dye degradation reaction in UV light initiated indirect dye degradation mechanism. This mechanism is practically more important over visible light initiated direct mechanism. The total annual production of synthetic dye is more than 7 × 10 5 tons. Annually, through only textile waste effluents, around one thousand tons of non-biodegradable textile dyes are discharged into natural streams and water bodies. Therefore, with growing environmental concerns and environmental awareness there is a need for the removal of dyes from local and industrial water effluents with a cost effective technology. In general, these dyes have been found to be resistant to biological as well as physical treatment technologies. In this regard, heterogeneous advanced oxidation processes (AOPs), involving photo-catalyzed degradation of dyes using semiconductor nanoparticles is considered as an efficient cure for dye pollution. In the last two decades TiO 2 has received considerable interest because of its high potential as a photocatalyst to degrade a wide range of organic material including dyes. This review starts with (i) a brief overview on dye pollution, dye classification and dye decolourization/degradation strategies; (ii) focuses on the mechanisms involved in comparatively well understood TiO 2 photocatalysts and (iii) discusses recent advancements to enhance TiO 2 photocatalytic efficiency by (a) doping with metals, non-metals, transition metals, noble metals and lanthanide ions, (b) structural modifications of TiO 2 and (c) immobilization of TiO 2 by using various supports to make it a flexible and cost-effective commercial dye treatment technology.
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              Three decades of beta-lactamase inhibitors.

              Since the introduction of penicillin, beta-lactam antibiotics have been the antimicrobial agents of choice. Unfortunately, the efficacy of these life-saving antibiotics is significantly threatened by bacterial beta-lactamases. beta-Lactamases are now responsible for resistance to penicillins, extended-spectrum cephalosporins, monobactams, and carbapenems. In order to overcome beta-lactamase-mediated resistance, beta-lactamase inhibitors (clavulanate, sulbactam, and tazobactam) were introduced into clinical practice. These inhibitors greatly enhance the efficacy of their partner beta-lactams (amoxicillin, ampicillin, piperacillin, and ticarcillin) in the treatment of serious Enterobacteriaceae and penicillin-resistant staphylococcal infections. However, selective pressure from excess antibiotic use accelerated the emergence of resistance to beta-lactam-beta-lactamase inhibitor combinations. Furthermore, the prevalence of clinically relevant beta-lactamases from other classes that are resistant to inhibition is rapidly increasing. There is an urgent need for effective inhibitors that can restore the activity of beta-lactams. Here, we review the catalytic mechanisms of each beta-lactamase class. We then discuss approaches for circumventing beta-lactamase-mediated resistance, including properties and characteristics of mechanism-based inactivators. We next highlight the mechanisms of action and salient clinical and microbiological features of beta-lactamase inhibitors. We also emphasize their therapeutic applications. We close by focusing on novel compounds and the chemical features of these agents that may contribute to a "second generation" of inhibitors. The goal for the next 3 decades will be to design inhibitors that will be effective for more than a single class of beta-lactamases.
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                Author and article information

                Journal
                RSC Adv
                RSC Adv
                RA
                RSCACL
                RSC Advances
                The Royal Society of Chemistry
                2046-2069
                25 June 2020
                24 June 2020
                25 June 2020
                : 10
                : 41
                : 24215-24233
                Affiliations
                [a] Solar Cell Applications Research Lab, Department of Physics, Government College University Lahore Punjab 54000 Pakistan dr.muhammadikram@ 123456gcu.edu.pk +923005406667
                [b] Department of Clinical Medicine and Surgery, University of Veterinary and Animal Sciences Lahore 54000 Punjab Pakistan
                [c] Department of Physics, Riphah Institute of Computing and Applied Sciences (RICAS), Riphah International University 14 Ali Road Lahore Pakistan
                [d] Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences Tianjin 300308 China
                [e] College of Pharmacy, University of the Punjab Lahore 54000 Pakistan
                [f] Center for Engineering Research, Research Institute, King Fahd University of Petroleum & Minerals Dhahran 31261 Saudi Arabia
                Author notes
                [†]

                M. Ikram and E. Umar are equal contributors.

                Author information
                https://orcid.org/0000-0001-7741-789X
                https://orcid.org/0000-0002-0259-301X
                Article
                d0ra04851h
                10.1039/d0ra04851h
                9055104
                35516171
                8036dbe2-1fb0-4b6a-89fa-fdad0c9ef50d
                This journal is © The Royal Society of Chemistry
                History
                : 1 June 2020
                : 18 June 2020
                Page count
                Pages: 19
                Funding
                Funded by: Higher Education Commission, Pakistan, doi 10.13039/501100004681;
                Award ID: 21-1669
                Funded by: King Fahd University of Petroleum and Minerals, doi 10.13039/501100004055;
                Award ID: Unassigned
                Funded by: Chinese Academy of Sciences, doi 10.13039/501100002367;
                Award ID: Unassigned
                Funded by: The World Academy of Sciences, doi 10.13039/100004457;
                Award ID: Unassigned
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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