Silver-zinc oxide nanocomposite: From synthesis to antimicrobial and anticancer properties

A green method by Verbascum speciosum was used to synthesize zinc oxide nanoparticles (ZnO NPs). ZnO NPs were coated with silver to synthesize Ag–ZnO nanocomposite (NCs). The physicochemical properties of Ag–ZnO NCs were analyzed by Fourier-transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), field emission scanning electron microscope (FESEM), transmission electron microscopy (TEM), dynamic light scattering (DLS), and zeta potential. The FTIR indicated the peak of Zn–O vibration and some hydroxyl and carboxyl groups. PXRD analyses confirmed the synthesis of ZnO NPs and Ag–ZnO NCs. Due to the size of the crystallite obtained from PXRD, solid-phase sizes (from FESEM and TEM images), and dynamic sizes from DLS, agglomeration was observed. The Ag–ZnO NCs showed a negative charge surface (?49.3 mV). Ag–ZnO NCs had a high antibacterial activity towards two most important infectious bacteria (i.e., Escherichia coli and Staphylococcus aureus) and anticancer activity against human liver-carcinoma cells (HepG2). Later, it depended on time and concentration of Ag–ZnO NCs. The cytotoxicity properties of Ag–ZnO NCs were also studied against NIH-3T3 as a normal cell, where the results verified the lower cell toxicities of nanocomposite than the HepG2.     

Synthesis of Fe–Pr co-doped ZnO nanoparticles: Structural,optical and antibacterial properties

In the present work, we studied the role of Fe and Pr addition on the structural, optical and antibacterial properties of spherical ZnO nanoparticles synthesized via sol gel method. The lattice constants values increased, while the average crystallite size decreases as the Pr concentration varies from 0.00 to 0.04. The Fe and Pr cations insertion in the Wurtzite structure were also confirmed by the changes in Zn–O bond length (1.9763 Å to 1.9793 Å for 0.00 ≤ y ≤ 0.04). Raman and FTIR spectroscopies validated the ZnO single-phase formation, and the analysis suggests the existence of oxygen vacancies. The samples showed agglomerated spherical morphology and formation of nanoplate homogeneously organized, while the textural properties were affected by the Fe inclusion. All samples presented band gap values lower than expected for bulk ZnO and the lowest values were obtained for samples containing Fe and Pr. The analysis and deconvolution of photoluminescence spectra confirmed the structural defects formation, caused by the synthesis conditions used and dopants ions inclusion. The antimicrobial activity against Escherichia coli and Staphylococcus aureus using the direct contact method showed superior activity for S. aureus due to the nanoparticles-bacteria interactions. The synergistic effect of dopants may have contributed to the better performance observed against S. aureus, while the Pr concentration directly influenced the inhibitory effect of E. coli. Therefore, the synthesized materials are promising to eliminate pathogenic microorganisms.     

Structural,optical, cytotoxicity,and antimicrobial properties of MgO,ZnO and MgO/ZnO nanocomposite for biomedical applications

In this study, MgO nanoparticles were successfully fabricated and incubated inside ZnO NPs to form MgO/ZnO nanocomposite for biomedical applications. The x-ray diffraction analysis of MgO, ZnO, and MgO/ZnO has shown the single-phase x-ray diffraction patterns through X'pert High score. The crystallite sizes were calculated as 18 nm, 42 nm, and 53 nm, respectively. The average particle size of MgO, ZnO, and MgO/ZnO nanopowders depicted from secondary electron images of field emission electron microscopy were 56 nm, 400 nm, and 450 nm, respectively. The presence of MgO NPs inside ZnO NPs was confirmed by transmission electron microscopy. The elemental dispersive spectroscopy of MgO, given the peaks of oxygen and magnesium, also showed only zinc and oxygen peaks in ZnO, which confirms no other impurities in MgO and ZnO powders. The elemental analysis of MgO/ZnO nanocomposite showed the peaks of Zinc and Oxygen, along with a tiny peak of Mg. The photoluminescence and UV–vis spectroscopy revealed the absorbance fluorescence limit of the nanomaterials. Fourier transform infrared spectroscopy confirmed the several groups present in the nanocomposite. The biocompatibility of MgO, ZnO, and MgO/ZnO was observed with human peripheral blood mononuclear cells. The cytotoxicity studies were also performed against human cancer (liver and breast) cell lines. The MgO, ZnO, and MgO/ZnO exhibited the antimicrobial properties against Escherichia coli and Staphylococcus aureus.     

Dye-sensitized solar cell performance and photocatalytic activity enhancement using binary zinc oxide-copper oxide nanocomposites prepared via co-precipitation route

Zinc oxide nanoparticles (ZnO NPs) and binary ZnO–CuO nanocomposites (ZnO–CuO NCs) were prepared through a simple chemical co-precipitation route. The influence of copper (Cu²⁺) ions concentration (0.03, 0.06, 0.09, and 0.12 M) on optical, morphological, structural, and elemental characteristics of the ZnO–CuO NCs was examined by appropriate characterization techniques. The visible light reactive CuO created absorption shift to red region that minimized band gap of the ZnO–CuO NCs. The concentration of Cu²⁺ ions produced appreciable impact on size of the ZnO–CuO NCs. The dye-sensitized solar cell (DSSC) constructed using ZnO–CuO NC photoanode with Cu²⁺ ions concentration of 0.06 M generated a conclusive solar to electrical energy transformation efficiency of 2.56%, which was a 2.2-times greater over the DSSC encompassed pristine photoanode of ZnO NPs. The electrochemical impedance spectroscopy analysis revealed the longer lifetime of the photogenerated electrons and reduction in the charge recombination rate in the ZnO_(0.44)–Cu_(0.06) NC photoanode based DSSC. Furthermore, the ZnO_(0.44)–Cu_(0.06) NC disclosed substantial photocatalytic activity towards methylene blue dye degradation that could be chiefly credited to its particles size induced visible light absorption property.     

Green Synthesis of Zinc Oxide Nanoparticles (ZnO NPs) for Effective Degradation of Dye,Polyethylene and Antibacterial Performance in Waste Water Treatment

At present, there is a vital need for river water purification by developing new approaches to eliminate bacterial biofilms, textile dyes, and Low-Density Polyethylene (LDPE) plastics that pose severe threats to human and environmental health. The current work put forward the construction of an eco-friendly green strategy to synthesize zinc oxide nanoparticles (ZnO NPs) using areca nut (Areca catechu) extract and their application to tackle the challenges in water purification. Prepared biogenic NPs were characterized by X-ray diffraction analysis (XRD), Fourier Transform Infra-Red (FT-IR), Energy Diffraction Spectroscopy (EDS), Scanning Electronic Microscopy (SEM), Transmission Electron Microscopy (TEM) analysis, confirmed the spherical shape in 20 nm and UV–vis spectroscopy. The characteristic absorption band exhibited at 326 nm confirmed the formation of ZnO NPs using UV–vis spectroscopy. Among all the tested bacterial pathogens, the E. coli at 50 µg/mL concentration showed the highest inhibition of biofilm activity, followed by the highest growth curve, cellular leakage, and potassium ion efflux. The ZnO NPs observed with photo-degradation of Rhodamine-B (Rh-B), Methylene Blue (MB), and Nigrosine dyes under sunlight irradiation at different time intervals. Finally, the photocatalytic activity of LDPE-ZnO NPs nanocomposite film showed the highest degradation under solar light irradiation were confirmed through photo-induced weight loss, SEM, FTIR, and MALDI-TOF analysis. This study demonstrates ZnO NPs exhibit efficacy against biofilm formation, degradation of photocatalytic textile dyes, and low-density LDPE film under solar light irradiation, which can be a step forward in water purification.

     

Green synthesis and biomedical behavior of Mg-doped ZnO nanoparticle using leaf extract of Ficus religiosa

Eco-friendly synthesis of Mg doped ZnO NPs was prepared by Ficus religiosa leaf extract. XRD confirmed the crystalline structure of the prepared Mg-doped ZnO. The functional groups and Zn and O bonding were realized from FTIR and Raman analyses. The surface plasma resonance absorption peak at 363 nm affirmed the formation of Mg–ZnO nanoparticles. The 3.32eV bandgap value of Mg–ZnO NPs was calculated by using Tauc's plot. The photoluminescence spectrum showed the emission behavior and point defect arising from zinc, oxygen vacancies. The hexagonal wurtzite structure of the prepared nanoparticles was observed from FESEM images. From the EDAX study, the elemental compositions have confirmed.The Thermal studies(TG/DTA)study,the Mg doped ZnO Material become thermally stable at 600 °C In XPS spectrum shows good formation of Mg doped ZnO nano materialThe facile synthesized Mg–ZnO NPs using Ficus religiosa leaves showed better antimicrobial properties on gram-positive bacterium, Staphylococcus aureus and fungus, Aspergillus niger. The biomedical behavior of prepared Mg–ZnO NPs was clearly understood from antioxidant(500 μg/mL-87), anti-inflammatory(500 μg/mL-89) and anti-diabetic assays(500μg/mL-82)     

Efficient sunlight and UV photocatalytic degradation of Methyl Orange,Methylene Blue and Rhodamine B,using Citrus×paradisi synthesized SnO2 semiconductor nanoparticles

In this work, tin dioxide (SnO2) Nanoparticles (NPs) were synthesized through green synthesis, using Citrus × paradisi extract as a stabilizing (capping). The extract concentrations used were 1, 2 and 4% in relation to the aqueous solution. The resulting SnO2 NPs were used for the degradation of Methyl Orange (MO), Methylene Blue (MB) and Rhodamine B (RhB), under both solar and UV radiation. The NPs were characterized via Attenuated Total Reflectance Infrared Spectroscopy (ATR-IR), X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM-SAED), the Brunauer-Emmett-Teller (BET) theory, Ultraviolet to Visible spectroscopy (UV–Vis), and Photoluminescence spectroscopy (PL); while the photocatalytic degradation was evaluated using UV-VIS. The results showed that the Citrus × paradisi extract is a good medium for the formation of SnO2 NPs. These NPs presented quasi-spherical morphology, particle sizes of 4–8 nm, with a rutile phase crystalline structure, and with banned gap of 2.69 at 3.28 eV. The NPs had excellent photocatalytic properties under solar radiation, degrading 100% of the OM in 180 min. Furthermore, under UV radiation, 100% degradation of the three dyes was achieved in a short time; 20 min for MO, and 60 min for MB and RhB. Therefore, green synthesis is a feasible medium for the formation of SnO2 NPs with good photocatalytic properties.     

Novel ternary poly(vinyl pyrrolidone)/poly(amide-imide)/ZnO nanocomposite: Synthesis,characterization, thermal and optical performance

The present work describes the synthesis and properties of polymer composites based on poly(vinyl pyrrolidone) (PVP) as polymer shell and poly(amide-imide)(PAI)/ZnO nanocomposite (ZNC) as efficient filler. At first, the alanine amino acid containing dicarboxylic acid was grafted on the surface of ZnO NPs. Then, modified ZnO (12 wt%) was incorporated into the PAI matrix under ultrasonic irradiations. The obtained hybrid ZNC showed high thermal stability and the size of the NPs in the TEM image of ZNC was about 31 nm. Secondly, PVP NCs with different ZNC loadings such as 2, 4 and 6 wt% were prepared via ultrasonication. Transmission electron microscopy (TEM) observations showed that the ZnO NPs were uniformly and highly dispersed in the PVP matrix. The UV–vis results exposed that the high UV-shielding efficiency of the obtained composites. Thermal analysis represented that the onset decomposition temperatures of the obtained PVPNCs had remarkable increasing in compared to the neat PVP due to the presence of both ZnO NPs and PAI.     

Enhanced Activity and Sustained Release of Protocatechuic Acid,a Natural Antibacterial Agent,from Hybrid Nanoformulations with Zinc Oxide Nanoparticles

Hybrid nanostructures can be developed with inorganic nanoparticles (NPs) such as zinc oxide (ZnO) and natural antibacterials. ZnO NPs can also exert antibacterial effects, and we used them here to examine their dual action in combination with a natural antibacterial agent, protocatechuic acid (PCA). To produce hybrid nanoformulations, we functionalized ZnO NPs with four types of silane organic molecules and successfully linked them to PCA. Physicochemical assessment confirmed PCA content up to ~18% in hybrid nanoformulations, with a PCA entrapment efficiency of ~72%, indicating successful connection. We then investigated the in vitro release kinetics and antibacterial effects of the hybrid against Staphylococcus aureus. PCA release from hybrid nanoformulations varied with silane surface modification. Within 98 h, only 8% of the total encapsulated PCA was released, suggesting sustained long-term release. We used nanoformulation solutions collected at days 3, 5, and 7 by disc diffusion or log reduction to evaluate their antibacterial effect against S. aureus. The hybrid nanoformulation showed efficient antibacterial and bactericidal effects that also depended on the surface modification and at a lower minimum inhibition concentration compared with the separate components. A hybrid nanoformulation of the PCA prodrug and ZnO NPs offers effective sustained-release inhibition of S. aureus growth.     

Evaluation of the biocompatibility and growth inhibition of bacterial biofilms by ZnO,Fe3O4 and ZnO@Fe3O4 photocatalytic magnetic materials

Magnetic nanostructured materials have found numerous biomedical applications. However, the influence of a magnetic field on the inhibition of pathogenic microorganisms has been poorly explored. Zinc and Iron nano-structured oxides have been widely used due to their biocompatibility and their excellent optoelectronic and magnetic properties. Nevertheless, little effort has been devoted to demonstrate their antibacterial activity at doses that are not harmful to mammalians. In this work, ZnO, Fe₃O₄ (MNPs) and ZnO@Fe₃O₄ (NCs) were synthesized and fully characterized. The materials exhibit good antibacterial activity to inhibit the growth of Staphylococcus aureus (S. aureus) and Helicobacter pylori (H. pylori) both, as planktonic cells and as biofilms structures at low doses. The photocatalytic activity of the materials (NCs) was demonstrated when radiated suspensions of NCs and microorganisms (MOs) exhibited higher inhibition growth of MOs in comparison to non-radiated assays. The materials show better antibacterial activity for biofilm growth inhibition in comparison to commercially available antibiotics. Magnetic antimicrobial films were fabricated by in situ deposition of MNPs in Arabic gum (AG) solution. The films exert enhanced antibacterial activity against S. aureus growth due to Fe³⁺lixiviation and magnetic disruption. Regarding the biocompatibility of the materials, ZnO modifies significantly biochemical parameters in Wistar rats after acute administration. Our results show that the composite ZnO@Fe₃O₄ at low doses: (a) exerts an optimum inhibition on the biofilm formation of microorganisms due to its synergetic activity of lixiviation of ions and oxidative activity; (b) good biocompatibility of the composite with living cells. These properties suit ZnO@Fe₃O₄ as potential candidates for the development of new anti-biofilm formulation.     

A green approach for the preparation of nanostructured zinc oxide: Characterization and promising antibacterial behaviour

In the present study, nanostructured zinc oxide (ZnO) films have been successfully synthesized using fruit extract of Viburnum opulus L. (VO) on glass slides by successive ionic layer adsorption and reaction (SILAR) procedure. The impact of VO concentrations on the structural, morphological, optical, electrical, and antibacterial attributes of ZnO films has been investigated in detail. The samples' XRD patterns present a hexagonal crystal structure with a preferential orientation along the (002) plane. The crystallite size values of ZnO samples were found to be in the ranges from 14.88 to 9.23 nm. The supplementation of VO to the synthesis solution remarkably affected the surface morphological features of the ZnO films. The optical results demonstrated that band gap energy values of the ZnO films at room temperature were decreased from 3.20 to 3.07 eV as a function of VO content in the bath solution. The films' electrical properties were determined by impedance analysis in the frequency range of 20 Hz ?1 MHz. Impedance-frequency measurements showed VO insertion to ZnO thin films cause an increase in impedance value at the low frequencies. Cole-Cole plots with a single semi-circle confirmed the contribution of grain and grain boundary for the electrical conduction process. The agar disk diffusion method was used to test the antibacterial properties of ZnO/VO inserted ZnO and inhibition zones were measured. VO inserted ZnO showed a stronger inhibitory effect on gram-positive bacteria Staphylococcus aureus (ATCC 25923) and gram-negative bacteria Escherichia coli (ATCC 35218) than ampicillin antibiotic used as a control group. In line with the promising bactericidal results of a new generation, VO inserted ZnO, the nanostructured product with this study, it can also be applied in multidrug-resistant clinical isolates obtained from patients.     

Novel bio-mediated Ag/Co3O4 nanocomposites of different weight ratios using aqueous neem leaf extract: Catalytic and microbial behaviour

An environmentally safe, economically, fast, and green synthetic approach was presented in this work for the fabrication of Ag-NP, Co₃O₄-NP and different weight ratio of Ag/Co₃O₄-NC. The synthesized samples were characterized by Fourier-transform infrared spectroscopy (FT-IR) and UV–visible spectrophotometry, Transmission Electron Microscopy (TEM), Scanning electron microscopy (SEM) along with X-ray energy dispersive spectroscopy (EDAX), and X-ray diffraction (XRD). The catalytic behaviour of the synthesized samples toward the reduction reaction of 4-nitrophenol in the presence of NaBH₄ was studied. It is indicated that the synthesized nanocomposites show a satisfactory catalytic activity. The catalytic reduction of p-NP to p-AP obeys first-order kinetics with rate constant in the following order (Ag-NP> (Ag/Co₃O₄-NC) ?1:1 > 1:3 > 3:1> Co₃O₄). This may be attributed to the high dispersion of Ag-NP compared to cobalt oxide nanoparticles. The microbial activity of the samples was analyzed using seven species of pathogenic microorganisms; 1) two species belongs to Gram negative bacteria; Escherichia coli (E.coli), and Salmonella, 2)four species belongs to Gram positive bacteria Marsa, Listeria, Staphylococcus aureus (S. aureus), bacillus subtilis (B.subtilis), and 3) one pathogenic fungal species Candidia. The data show that all samples exhibited an excellent range of inhibition toward all tested pathogenic microorganisms.     

Vitis labruska skin extract assisted green synthesis of ZnO super structures for multifunctional applications

The formation of unique morphologies of zinc oxide (ZnO) super structured frameworks were reported via a simple and eco-friendly route employing Vitis labruska fruit Black Grape Skin (BGS) extract as a fuel. XRD, FTIR, UV–vis, PL, SEM and TEM studies are performed to analyse the formation and characterization of ZnO. XRD confirmed the crystalline nature of the material with hexagonal Wurtzite structure having average crystallite size of ~50 nm. FTIR spectrum shows a band at 532 cm⁻¹ due to the vibrational mode of Zn-O bending. The band gap of the ZnO was found to be 3.26 eV. SEM images confirm the formation of different morphologies like Mysore pak (a popular Indian dessert), canine teeth, hollow pyramids and gems were obtained by varying the weight of BGS. These superstructures were obtained due to the interaction of Zn²⁺ with BGS extract. TEM images clearly shows lattice spacing of 0.29 nm corresponding to the (002) plane of ZnO. Photoluminescence (PL) spectrum shows strong yellow light emission upon excitation at 320 nm due to the Zn-O defects. Synthesized ZnO nanoparticles (Nps) exhibited good photocatalytic activity for the degradation of Methylene blue (MB) dye. The photocatalytic activity was due to the production of OH˙ radicals during photo irradiation on ZnO Nps. ZnO Nps also exhibited superior antibacterial activity against Staphylococcus aureus and Escherichia coli bacteria. Further, ZnO Nps were also used in the development of novel electrochemical sensing platform towards the electrochemical detection of hydrazine as a model system at very low concentrations having a detection limit of 0.3 µM.     

Preparation of 3D crimped ZnO/PAN hybrid nanofiber mats with photocatalytic activity and antibacterial properties by blow-spinning

Zinc oxide (ZnO) nanostructures have received widespread attention due to their unique structure and broad application possibilities, but high preparation costs and agglomeration limit their usage. In this article, low-cost and environmentally friendly cellulose and ZnCl₂ are used to synthesize ZnO nanoparticles (ZnO NPs). Subsequently, multifunctional ZnO/polyacrylonitrile hybrid nanofiber mats (ZnO/PAN@NFMs) with mechanical stability suitable for large-scale application are prepared via solution blow-spinning. The synthesized ZnO/PAN@NFMs exhibit higher photodegradation of organic dyes than earlier reported semiconductors and good recycling performance with an organic dye degradation above 94%–98% after five cycles, which is ascribed to fixation of the ZnO NPs in the nanofibers. In addition, the inhibition rate for Escherichia coli and Staphylococcus aureus is above 99.9% and the bacteriostatic rate against E. coli remains as high as 99% after 10 cycles. From these properties, the synthesized composite ZnO/PAN@NFMs are promising for wastewater cleaning and antibacterial fabrics.     

Facile Synthesis and Characterization of Palm CNF-ZnO Nanocomposites with Antibacterial and Reinforcing Properties

Cellulose nanofibers (CNF) isolated from plant biomass have attracted considerable interests in polymer engineering. The limitations associated with CNF-based nanocomposites are often linked to the time-consuming preparation methods and lack of desired surface functionalities. Herein, we demonstrate the feasibility of preparing a multifunctional CNF-zinc oxide (CNF-ZnO) nanocomposite with dual antibacterial and reinforcing properties via a facile and efficient ultrasound route. We characterized and examined the antibacterial and mechanical reinforcement performances of our ultrasonically induced nanocomposite. Based on our electron microscopy analyses, the ZnO deposited onto the nanofibrous network had a flake-like morphology with particle sizes ranging between 21 to 34 nm. pH levels between 8–10 led to the formation of ultrafine ZnO particles with a uniform size distribution. The resultant CNF-ZnO composite showed improved thermal stability compared to pure CNF. The composite showed potent inhibitory activities against Gram-positive (methicillin-resistant Staphylococcus aureus (MRSA)) and Gram-negative Salmonella typhi (S. typhi) bacteria. A CNF-ZnO-reinforced natural rubber (NR/CNF-ZnO) composite film, which was produced via latex mixing and casting methods, exhibited up to 42% improvement in tensile strength compared with the neat NR. The findings of this study suggest that ultrasonically-synthesized palm CNF-ZnO nanocomposites could find potential applications in the biomedical field and in the development of high strength rubber composites.     

Insight into the impact of zinc doping on the structural,surface, and biological properties of magnasium oxide nanoparticles stabilized by Vateria indica (L.) fruit extract

The present study is an attempt to delineate the effect of zinc doping on the green synthesized magnesium oxide (MgO) NPs. Pure (MgOVI) and zinc doped (ZnMgOVI) NPs were synthesized employing an aqueous fruit extract of V. indica as capping and reducing agents. The various analytical techniques viz. FTIR, PXRD, FESEM, and EDS spectroscopy together with elemental mapping analyses substantiated the formation of pure and doped NPs with crystallite sizes 23.74 and 25.41 nm. The study of surface properties through BET analysis unfolded the formation of mesoporous NPs with a surface area of 7.4 and 5.3 m²g^-1 for pure and doped NPs respectively. Additionally, the refinement of obtained PXRD data through Rietveld refinement corroborated the changes in cell parameters after zinc doping. The anti-inflammatory activity carried out unveiled the biocompatibility of obtained NPs by exhibiting a % HRBCS of 83.65 ± 0.002 and 85.69 ± 0.003 for MgOVI and ZnMgOVI NPs. The in-vitro antidiabetic activity of MgOVI and ZnMgOVI NPs performed revealed their excellent α-amylase inhibition activity (86.29 ± 0.001and 86.44 ± 0.002%). Furthermore, the NPs also displayed anti-microbial activities against Staphylococcus aureus, Bacillus subtulis, Pseudomonas aeroginosa, Pseudomonas syringae, and Escherichia coli. Thus the studies have evinced the superlative antidiabetic and antimicrobial potentialities of MgOVI and ZnMgOVI NPs with high biocompatibility.     

A comprehensive study on copper incorporated bio-glass matrix for its potential antimicrobial applications

In this study, sol-gel derived Cu substituted 70S bioglass (70SiO2-(20-x) CaO–10P2O5-xCuO; where x = 0, 0.5, 1, 1.5) were synthesized as a new multifunctional bioactive glasses (BGs). The effect of Cu substitution in the bio-glass matrix was evaluated for its impact on pathogen (Escherichia coli and Staphylococcus aurous). Fourier Transform Infrared spectroscopy (FT-IR), Thermogravimetric Analysis (TGA), X-Ray Diffraction (XRD), Inductively Coupled Plasma spectroscopy (ICP) and Scanning Electron Microscopy (SEM) revealed that the obtained powders are amorphous silicate glass. The substituted element is present in the desired molar concentration. In vitro bioactivity test was performed in SBF solution by immersion of bioglass pellets. Antibacterial test was carried out against Escherichia coli and Staphylococcus aureus. The results showed that the prepared BGs have a high acellular bioactivity observed by a fast formation of thick and continuous layer of carbonated hydroxyapatite (CHA). The antibacterial properties of the substituted bio-glass matrix was indicated by the growth inhibition of bacterial colonies. The obtained results showed that copper substituted bio-glass is having potential to avoid post-surgical infections and it also represents the capability of hard tissue regeneration.     

Combustion synthesis of β-SnWO4-rGO: Anode material for Li-ion battery and photocatalytic dye degradation

This article reports the synthesis β-SnWO₄–rGO nanocomposite (NC) by a simple solution combustion method followed by low temperature hydrothermal method. The β-SnWO₄–rGO NC has been characterized using various analytical tools such as X-ray diffraction (XRD), Raman spectroscopy, Scanning Electron Microscopy (SEM), High-Resolution Transmission Electron Microscopy (HR-TEM), Ultraviolet-Differential reflectance spectroscopy (UV-DRS). X-ray diffraction pattern shows the formation of cubic structured β-SnWO₄ nanoparticles (NPs) and Raman spectrum shows the presence of rGO in the composite. Transmission Electron Microscopy image shows that SnWO₄ NPs were embedded on the surface of rGO. β-SnWO₄ NPs and β-SnWO₄-rGO NC has been examined as an electrode material for Li-ion battery (LIB). β-SnWO₄ NPs and β-SnWO₄-rGO NC displays an initial discharge capacity of 1351 mAhg^?1 and 1662 mAhg^?1 which is about 23% increase in capacity. Electrochemical performance of β-SnWO₄-rGO NC at different current densities proves that it is one of the good candidates as an electrode material for LIB. β-SnWO₄-rGO NC shows enhanced photocatalytic activity against rose bengal (RB) and methylene blue (MB) compared to pure β-SnWO₄ NPs.     

In vitro anticancer activity and comparative green synthesis of ZnO/Ag nanoparticles by moringa oleifera,mentha piperita,and citrus lemon

This study proposes a simple, effective, and environmentally friendly approach for the synthesis of zinc oxide/silver nanoparticles (ZnO/Ag NPs) using three different plant extracts. The plants used in this study were moringa oleifera (MO), mentha piperita (MP), and citrus lemon (CL). Characterizations of ZnO/Ag NPs were done using ultraviolet–visible spectroscopy (UV vis), X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) along with energy dispersive spectroscopy (EDX), and fourier transform infrared spectroscopy (FTIR). In accordance with size distribution findings, ZnO/Ag NPs synthesized with MO have a narrow size distribution, with the average particle size being 119 ± 36 nm. Among these three reducing agent MO act as the best reducing agent. Moreover, the anticancer activity of silver nanoparticles (Ag NPs), zinc oxide nanoparticles (ZnO NPs) and ZnO/Ag NPs synthesized with MO were demonstrated in human cervical cancer cells (HeLA). The results revealed that ZnO/Ag NPs demonstrate in vitro cell viability of 72%, 81%, and 84% using 2.5, 5, and 10 μgml^?1of ZnO/Ag NPs for 24 h. While Ag NPs and ZnO NPs prepared with MO showed 50% and 60% cell viability using 2.5 μgml^?1concentration for 24 h. This showed that the ZnO/Ag NPs act as a strong anticancer agent compared to Ag NPs and ZnO NPs. Overall, this research proposes a green synthesis approach for ZnO/Ag NPs with a wide range of potential uses, particularly in biomedicine.     

Effective methodology for the production of novel nanocomposite films based on poly(vinyl chloride) and zinc oxide nanoparticles modified with green poly(vinyl alcohol)

Ultrasonic irradiation and solution dispersion methods were used to organize transparent worthwhile poly(vinyl chloride) (PVC) nanocomposite (NC) films which contain different amounts of modified zinc oxide nanoparticles (NP)s. First, modification of ZnO NPs was accomplished by biocompatible poly(vinyl alcohol) (PVA) to increase NCs compatibility and dispersity in the PVC matrix. The investigation followed by the fabrication and characterization of PVC/ZnO‐PVA NCs which obtained via fast and facile ultrasonication irradiation. The measurements of X‐ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and field emission scanning electron microscopy were used for the characterization of properties, structure and morphology of the obtained NPs and their NCs. Furthermore, thermal and optical properties of the resulting NCs were also carried out by thermogravimetric analysis, ultraviolet‐visible transmission, and absorption spectra. Morphology results demonstrate well‐dispersed characteristics of ZnO‐PVA NPs incorporated in the PVC matrix which resulted from modification. Also, modified ZnO NPs enhanced mechanical properties of prepared NC films. Prepared NCs could be categorized as self‐extinguishing materials on the basis of the limiting oxygen index values. POLYM. COMPOS., 38:1800–1809, 2017. © 2015 Society of Plastics Engineers