scholarly journals Formation of a Bacteriostatic Surface on ZrNb Alloy via Anodization in a Solution Containing Cu Nanoparticles

Materials ◽  
2020 ◽  
Vol 13 (18) ◽  
pp. 3913 ◽  
Author(s):  
Viktoriia Korniienko ◽  
Oleksandr Oleshko ◽  
Yevheniia Husak ◽  
Volodymyr Deineka ◽  
Viktoriia Holubnycha ◽  
...  

High strength, excellent corrosion resistance, high biocompatibility, osseointegration ability, and low bacteria adhesion are critical properties of metal implants. Additionally, the implant surface plays a critical role as the cell and bacteria host, and the development of a simultaneously antibacterial and biocompatible implant is still a crucial challenge. Copper nanoparticles (CuNPs) could be a promising alternative to silver in antibacterial surface engineering due to low cell toxicity. In our study, we assessed the biocompatibility and antibacterial properties of a PEO (plasma electrolytic oxidation) coating incorporated with CuNPs (Cu nanoparticles). The structural and chemical parameters of the CuNP and PEO coating were studied with TEM/SEM (Transmission Electron Microscopy/Scanning Electron Microscopy), EDX (Energy-Dispersive X-ray Dpectroscopy), and XRD (X-ray Diffraction) methods. Cell toxicity and bacteria adhesion tests were used to prove the surface safety and antibacterial properties. We can conclude that PEO on a ZrNb alloy in Ca–P solution with CuNPs formed a stable ceramic layer incorporated with Cu nanoparticles. The new surface provided better osteoblast adhesion in all time-points compared with the nontreated metal and showed medium grade antibacterial activities. PEO at 450 V provided better antibacterial properties that are recommended for further investigation.

Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1138
Author(s):  
Abdulmohsen Ali Alshehri ◽  
Maqsood Ahmad Malik

Biomolecules from plant extracts have gained significant interest in the synthesis of nanoparticles owing to their sustainable properties, cost efficiency, and environmental wellbeing. An eco-friendly and facile method has been developed to prepare Cu-Co-Ni trimetallic nanoparticles with simultaneous bio-reduction of Cu-Co-Ni metal precursors by aqueous extract of oregano (Origanum vulgare) leaves. Dramatic changes in physicochemical properties of trimetallic nanoparticles occur due to synergistic interactions between individual metal precursors, which in turn outclass the properties of corresponding monometallic nanoparticles in various aspects. The as biosynthesized Cu-Co-Ni trimetallic nanoparticles were initially analyzed using ultraviolet (UV)–visible spectroscopy. The morphology, structure, shape, and size of biosynthesized trimetallic nanoparticles were confirmed by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and X-ray diffraction (XRD) spectroscopy. The elemental analysis was carried out by energy-dispersive X-ray (EDX) spectroscopy. Fourier transform infrared (FTIR) microscopy was carried out to explain the critical role of the biomolecules in the Origanum vulgare leaf extract as capping and stabilizing agents in the nanoparticle formation. Additionally, simultaneous thermogravimetric analysis (TGA) and differential thermogravimetry (DTG) analysis was also performed to estimate the mass evaluation and rate of the material weight changes. The photocatalytic activity of as biosynthesized trimetallic nanoparticles was investigated towards methylene blue (MB) dye degradation and was found to be an efficient photocatalyst for dye degradation. Kinetic experiments have shown that photocatalytic degradation of MB dye followed pseudo-first-order kinetics. The mechanism of the photodegradation process of biogenic Cu-Co-Ni trimetallic nanoparticles was also addressed.


2020 ◽  
Vol 35 (4-5) ◽  
pp. 389-398
Author(s):  
Tarık Eren ◽  
Gülay Baysal ◽  
Faik Doğan

There is a growing interest in new type of biocidal compounds with antibacterial properties against bacteria. In this study, new antibacterial synthetic materials bearing curcumin and cationic polymers were synthesized. In the synthesis stage, the methacrylate functional cationic monomer was synthesized via the Michael addition route by using 3-acryloxy-2-hydroxypropyl methacrylate and 3-amino pyridine to obtain Monomer 1. Monomer 1 was further quaternized with hexyl bromide to obtain a cationic methacrylate functional monomer. Free-radical polymerization of Monomer 1 and methyl acrylate was conducted in the presence of azobisisobutyronitrile under dimethylformamide solvent. The composite formulation was conducted by using turmeric extract Curcuma longa (curcumin), hydroxyapatite, montmorillonite, and silver nitrate. The materials were analyzed by using the methods of X-ray diffraction, nuclear magnetic resonance, Fourier transform infrared spectroscopy, and scanning electron microscopy. The biocidal activities against the bacteria Escherichia coli, Listeria monocytogenes, Salmonella, and Staphylococcus aureus were analyzed using agar well diffusion method. From the Fourier transform infrared, X-ray diffraction, and scanning electron microscopy analysis results of the synthesized nanocomposites, it is seen that they form strong connections with the components added to the composites and form an exfoliated structure. According to the antibacterial analysis results, the nanocomposites obtained have showed a strong antibacterial resistance against E.coli, L.monocytogenes, Salmonella, and S. aureus bacteria, and the high inhibition zone areas were obtained.


2020 ◽  
Vol 2020 ◽  
pp. 1-12
Author(s):  
Xuan Nui Pham ◽  
Hoa Thi Nguyen ◽  
Ngan Thi Pham

In recent years, the green synthesis of nanoparticles via biological processes has attracted considerable attention. Herein, we introduce a facile and green approach for the synthesis of poriferous silver nanoparticles (Ag-NPs) decorated hydroxylapatite (HAp@Ag) nanoparticles with excellent antibacterial properties. All the nanocomposites were fully characterized in the solid state via various techniques such as X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectrometer (EDX), in which the synthesized Ag-NPs (24 nm in diameter) and their homogeneous incorporation on HAp have been studied by ultraviolet-visible (UV-vis) technique, transmission electron microscopy (TEM), and dynamic light scattering (DLS) analysis. The obtained results indicate that the structure and morphology of HAp have no significant changes after the incorporation of Ag-NPs on its surface. Moreover, an impressive antibacterial activity of HAp@Ag nanocomposite against Gram-positive bacterium Staphylococcus aureus and Gram-negative bacteria Escherichia coli and Pseudomonas aeruginosa has been recorded by using the agar well diffusion method. As a result, the HAp@Ag nanocomposite promises to be a great biomedical material with high antibacterial properties.


2020 ◽  
Author(s):  
Ross Anderson ◽  
et al.

Supplemental methodological details, antibacterial properties of clays, other minerals with distinct fossil/matrix distributions, summaries of mineralogy by taxon, data tables, statistical summaries, and light/scanning electron microscopy–energy-dispersive X-ray spectroscopy images of fossil specimens showing X-ray diffraction selected areas.<br>


2011 ◽  
Vol 287-290 ◽  
pp. 169-172
Author(s):  
Hong Wang ◽  
Xi Yang He ◽  
Ying Wang

The flower-like α-Fe2O3superstructures were fabricated by a novel hydrothermal route and sequential annealing at 600 °C for 1 h using FeCl3×6H2O as the starting precursor. The structures and morphologies of the synthesized flower-like superstructures have been characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM). It is revealed that the flower-like α-Fe2O3nanostructures consist of nanorods with the average diameter of about 70 nm and an average length of about 200nm growing from the centers. The critical role of urea in the hydrothermal synthesis of the flower-like nanostructures is discussed.


2020 ◽  
Author(s):  
Ross Anderson ◽  
et al.

Supplemental methodological details, antibacterial properties of clays, other minerals with distinct fossil/matrix distributions, summaries of mineralogy by taxon, data tables, statistical summaries, and light/scanning electron microscopy–energy-dispersive X-ray spectroscopy images of fossil specimens showing X-ray diffraction selected areas.<br>


Metals ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 858 ◽  
Author(s):  
Yen-Hao Chang ◽  
Chih-Yeh Chao ◽  
Yuan-Ting Chang ◽  
Je-Kang Du

Titanium alloys are widely employed for the fabrication of biomedical devices. In this study, we designed and developed a Ti-5Al-2.5Cu alloy, which exhibited antibacterial properties. Microstructure and elemental analyses were performed using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and transmission electron microscopy (TEM). We evaluated the alloy’s antibacterial properties using Escherichia coli in the plate-count method. The cytotoxicity was examined using the MG-63 cell response by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays. Microstructural analysis revealed that Ti-5Al-2.5Cu exhibited an equiaxed α’ martensite structure after short-term annealing. The heterogeneous and homogeneous α → α + Ti2Cu phase transitions occurred at ~840 and 920 °C, respectively. The antibacterial property for Ti-5Al-2.5Cu was varied by volume fraction in the Ti2Cu and Cu-rich phase, which was obtained using different heat treatments. The high volume fraction of the Ti2Cu and Cu-rich phase was observed after long-term annealing at 720–840 °C and thus exhibited a higher antibacterial rate. The relationship between phase distribution and the antibacterial property could be satisfied by a positive linear regression equation. Cytotoxicity results showed that heat treatments at different temperatures for Ti-5Al-2.5Cu alloys had no effect on cell viability. The optimal heat treatment for Ti-5Al-2.5Cu alloy was annealing at 760 °C for 24 h. After, the alloy exhibited both promising antibacterial performance and good cytocompatibility.


2012 ◽  
Vol 535-537 ◽  
pp. 436-439 ◽  
Author(s):  
Noppakun Sanpo ◽  
James Wang ◽  
Christopher C. Berndt

Zinc substituted cobalt ferrite nanopowders with the general formula Co(1-x)ZnxFe2O4(with x = 0, 0.3, 0.5, 0.7, and 1) were prepared via the sol-gel route using citric acid as a chelating agent. The influence of zinc concentration on the microstructure, crystal structure and antibacterial property of zinc substituted cobalt ferrite nanopowders has been systematically investigated. The microstructure and elemental composition were characterized using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX), respectively. Phase analysis of cobalt ferrite nanopowders was performed using X-ray diffractometry (XRD). The antibacterial properties of zinc substituted cobalt ferrite nanopowders were investigated. The results indicate that the substitution of zinc influences strongly the microstructure, crystal structure and antibacterial property of the cobalt ferrite nanopowders.


2014 ◽  
Vol 1061-1062 ◽  
pp. 256-261
Author(s):  
Peng Xu ◽  
Shao Wei ◽  
Jing Yang ◽  
Yi Xi Che ◽  
Xiao Yong Cao ◽  
...  

In this paper, a novel anti-bacterial agent of Ag-deposited silica-coated Fe3O4 magnetic nanoparticles was prepared by a template-activated strategy, which possess a silica coated magnetic core and silver nanoparticles on the outer shell. The as-synthesized nanoparticles have been characterized by transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX). The obtained products exhibited dispersibility and high magnetization, which also show a good recycling antibacterial activity, and the antibacterial rates against Escherichia coli was all 100 % for 3 cycles.


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Philipp Sahrmann ◽  
Sophie Winkler ◽  
Andrea Gubler ◽  
Thomas Attin

Abstract Background To assess the changes of implant surfaces of different roughness after instrumentation with ultrasonic-driven scaler tips of different materials. Methods Experiments were performed on two moderately rough surfaces (I—Inicell® and II—SLA®), one surface without pre-treatment (III) and one smooth machined surface (IV). Scaler tips made of steel (A), PEEK (B), titanium (C), carbon (D) and resin (E) were used for instrumentation with a standardized pressure of 100 g for ten seconds and under continuous automatic motion. Each combination of scaler tip and implant surface was performed three times on 8 titanium discs. After instrumentation roughness was assessed by profilometry, morphological changes were assessed by scanning electron microscopy, and element distribution on the utmost surface by energy dispersive X-ray spectroscopy. Results The surface roughness of discs I and II were significantly reduced by instrumentation with all tips except E. For disc III and IV roughness was enhanced by tip A and C and, only for IV, by tip D. Instrumentation with tips B, D and E left extensive residuals on surface I, II and III. The element analysis of these deposits proved consistent with the elemental composition of the respective tip materials. Conclusion All ultrasonic instruments led to microscopic alterations of all types of implants surfaces assessed in the present study. The least change of implant surfaces might result from resin or carbon tips on machined surfaces.


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