Biologically‐synthesised ZnO/CuO/Ag nanocomposite using propolis extract and coated on the gauze for wound healing applications

Wound healing has long been recognised as a major clinical challenge for which stablishing more effective wound therapies is necessary. The generation of metallic nanocomposites using biological compounds is emerging as a new promising strategy for this purpose. In this study, four metallic nanoparticles (NPs) with propolis extract (Ext) and one without propolis including ZnO/Ext, ZnO/Ag/Ext, ZnO/CuO/Ext, ZnO/Ag/CuO/Ext and ZnO/W were prepared by microwave method and assessed for their wound healing activity on excision experimental model of wounds in rats. The developed nanocomposites have been characterised by physico‐chemical methods such as X‐ray diffraction, scanning electron microscopy, diffuse reflectance UV–vis spectroscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis and Brunauer–Emmett–Teller analyses. The wounded animals treated with the NPs/Ext in five groups for 18 days. Every 6 days, for measuring wound closure rate, three samples of each group were examined for histopathological analysis. The prepared tissue sections were investigated by haematoxylin and Eosin stainings for the formation of epidermis, dermis and muscular and Masson''s trichrome staining for the formation of collagen fibres. These findings toughly support the probability of using this new ZnO/Ag/Ext materials dressing for a wound care performance with significant effect compared to other NPs.Inspec keywords: nanomedicine, X‐ray diffraction, II‐VI semiconductors, visible spectra, ultraviolet spectra, nanocomposites, biomedical materials, proteins, wounds, nanoparticles, scanning electron microscopy, nanofabrication, skin, zinc compounds, silver, antibacterial activity, Fourier transform infrared spectra, copper compounds, molecular biophysicsOther keywords: propolis, wound healing applications, effective wound, metallic nanocomposites, biological compounds, metallic nanoparticles, microwave method, wound healing activity, physico‐chemical methods, Fourier transform infrared spectroscopy, diffuse reflectance UV‐vis spectroscopy, Brunauer‐Emmett‐Teller analyses, wounded animals, wound closure rate, wound care performance, histopathological analysis, scanning electron microscopy, X‐ray diffraction, thermogravimetric analysis, haematoxylin, Eosin stainings, Masson trichrome, epidermis, muscular trichrome, collagen fibres, time 18.0 d, time 6.0 d, ZnO‐CuO‐Ag     

Enhanced wound healing activity of Ag–ZnO composite NPs in Wistar Albino rats

In the present study, silver (Ag) and Ag–zinc oxide (ZnO) composite nanoparticles (NPs) were synthesised and studied their wound‐healing efficacy on rat model. Ultraviolet–visible spectroscopy of AgNPs displayed an intense surface plasmon (SP) resonance absorption at 450 nm. After the addition of aqueous Zn acetate solution, SP resonance band has shown at 413.2 nm indicating a distinct blue shift of about 37 nm. X‐ray diffraction analysis Ag–ZnO composite NPs displayed existence of two mixed sets of diffraction peaks, i.e. both Ag and ZnO, whereas AgNPs exhibited face‐centred cubic structures of metallic Ag. Scanning electron microscope (EM) and transmission EM analyses of Ag–ZnO composite NPs revealed the morphology to be monodispersed hexagonal and quasi‐hexagonal NPs with distribution of particle size of 20–40 nm. Furthermore, the authors investigated the wound‐healing properties of Ag–ZnO composite NPs in an animal model and found that rapid healing within 10 days when compared with pure AgNPs and standard drug dermazin.Inspec keywords: wounds, tissue engineering, biomedical materials, nanocomposites, nanofabrication, nanomedicine, silver, zinc compounds, II‐VI semiconductors, wide band gap semiconductors, ultraviolet spectra, visible spectra, nanoparticles, particle size, surface plasmon resonance, spectral line shift, X‐ray diffraction, scanning electron microscopy, transmission electron microscopyOther keywords: enhanced wound healing activity, Ag‐ZnO composite nanoparticles, Wistar Albino rats, wound‐healing efficacy, ultraviolet‐visible spectroscopy, intense surface plasmon resonance absorption, aqueous Zn acetate solution, SP resonance band, blue shift, X‐ray diffraction analysis, diffraction peaks, face‐centred cubic structures, scanning electron microscope, SEM, transmission electron microscope, TEM, monodispersed hexagonal nanoparticles, quasihexagonal nanoparticles, particle size, animal model, time 10 d, size 20 nm to 40 nm, Ag‐ZnO     

Silver coated bioactive glass particles for wound healing applications

Bioactive glass particles (0.42SiO₂–0.15CaO–0.23Na₂O–0.20ZnO) of varying size (<90 μm and 425–850 μm) were synthesized and coated with silver (Ag) to produce Ag coated particles (PAg). These were compared against the uncoated analogous particles (Pcon.). Surface area analysis determined that Ag coating of the glass particles resulted in increased the surface area from 2.90 to 9.12 m²/g (90 μm) and 1.09–7.71 m²/g (425–850 μm). Scanning electron microscopy determined that the Ag coating remained at the surface and there was little diffusion through the bulk. Antibacterial (Escherichia coli—13 mm and Staphylococcus epidermidis—12 mm) and antifungal testing (Candida albicans—7.7 mm) determined that small Ag-coated glass particles exhibited the largest inhibition zones compared to uncoated particles. pH analysis determined an overall higher pH consider in the smaller particles, where after 24 h the large uncoated and Ag coated particles were 8.27 and 8.74 respectively, while the smaller uncoated and Ag coated particles attained pH values of 9.63 and 9.35 respectively.     

Green antimicrobial coating based on quaternised chitosan/organic montmorillonite/Ag NPs nanocomposites

This work is aimed at developing a green antimicrobial coating. First, a green antimicrobial agent, quaternised chitosan (QCS)/organic montmorillonite (OMMT)/silver nanoparticles (Ag NPs) (QOMA) nanocomposite was fabricated through an environmental-friendly one-step approach. Morphological and structural characteristics of QOMA were investigated, and good antimicrobial activity was proved. QOMA was then incorporated into powder coating formulations to form a homogeneous coating on steel plates, which was studied by scanning electron images. Besides, the physical and mechanical properties as well as the antimicrobial performances of the coatings were discussed. The results showed that the addition of QOMA imparted good antimicrobial capacity to the powder coating, but did not affect its physical and mechanical properties. The coatings were able to effectively inactivate Gram-negative bacteria (Escherichia coli), Gram-positive bacteria (Staphylococcus aureus) and fungi (Aspergillus niger, Penicillium funiculosum, Chaetomium globasum, Paecilomyces varioti, Asp. terreus and Aureobasidium pullulans). Our findings demonstrate the possibilities of green antimicrobial coating containing QOMA for practical applications in medical devices, domestic appliances and other solid surfaces concerning bacterial infection and contamination.     

Synthesis of Ag‐NPs impregnated cellulose composite material: its possible role in wound healing and photocatalysis

Cellulose is the natural biopolymer normally used as supporting agent with enhanced applicability and properties. In present study, cellulose isolated from citrus waste is used for silver nanoparticles (Ag‐NPs) impregnation by a simple and reproducible method. The Ag‐NPs fabricated cellulose (Ag‐Cel) was characterised by powder X‐rays diffraction, Fortier transform infrared spectroscopy and scanning electron microscopy. The thermal stability was studied by thermo‐gravimetric analysis. The antibacterial activity performed by disc diffusion assay reveals good zone of inhibition against Staphylococcus aureus and Escherichia coli by Ag‐Cel as compared Ag‐NPs. The discs also displayed more than 90% reduction of S. aureus culture in broth within 150 min. The Ag‐Cel discs also demonstrated minor 2,2‐diphenyl 1‐picryl‐hydrazyl radical scavenging activity and total reducing power ability while moderate total antioxidant potential was observed. Ag‐Cel effectively degrades methylene‐blue dye up to 63.16% under sunlight irradiation in limited exposure time of 60 min. The Ag‐NPs impregnated cellulose can be effectively used in wound dressing to prevent bacterial attack and scavenger of free radicals at wound site, and also as filters for bioremediation and wastewater purification.Inspec keywords: silver, nanoparticles, particle reinforced composites, nanocomposites, filled polymers, wounds, nanomedicine, biomedical materials, photochemistry, catalysis, X‐ray diffraction, Fourier transform infrared spectra, scanning electron microscopy, thermal stability, thermal analysis, antibacterial activity, dyes, wastewater treatment, contaminated site remediation, nanofabricationOther keywords: silver nanoparticles, impregnated cellulose composite, wound healing, photocatalysis, natural biopolymer, citrus waste, powder X‐ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, thermal stability, thermo‐gravimetric analysis, antibacterial activity, disc diffusion assay, Staphylococcus aureus, Escherichia coli, inhibition zone, broth, 2,2‐diphenyl 1‐picryl‐hydrazyl radical scavenging activity, total reducing power ability, total antioxidant potential, methylene‐blue dye, sunlight irradiation, wound dressing, bacterial attack, free radical scavenger, wastewater purification, bioremediation filters, wound site, time 60 min, Ag     

Synthesis and studies of bay‐substituted perylene diimide‐based D–A–D‐type SM acceptors for OSC and antimicrobial applications

In this study, the synthesis of a series of bay‐substituted donor–acceptor–donor (D–A–D) type perylene diimide derivatives (3a–3d) has been reported as an acceptor for the small‐molecule‐based organic solar cells (SM‐OSCs) by the Suzuki coupling method. It has been evaluated for the antimicrobial activity against some of the bacteria and fungi. The synthesised SMs were confirmed by Fourier transform‐infrared spectroscopy, nuclear magnetic resonance (NMR), and high resolution mass spectroscopy (HR‐MS). The SMs showed absorption up to 750 nm, which eventually reduced the optical band gap Egopt to  < 2 eV. SMs showed thermal stability up to 400 °C. In the SM‐OSC, the SMs showed a power conversion efficiency of  < 1% with the P3HT donor in bulk hetero‐junction device structure. Additionally, the new SMs showed antimicrobial activity against Gram‐negative bacteria such as Escherichia coli Gram‐positive bacteria such as Bacillus subtilis and antifungal activity against the Candida albicans, and Aspergillus niger. Cytotoxicity studies were carried out against the breast cancer cell lines MCF‐7 using MTT assay method. The results revealed that the SMs was able to inhibit the cancer cells. LD₅₀ s calculated for the SMs 3a–3d were between 200 and 400 µg/ml.Inspec keywords: antibacterial activity, solar cells, microorganisms, Fourier transform spectra, infrared spectra, nuclear magnetic resonance, photonic band gap, thermal stability, cellular biophysics, toxicology, cancer, nanomedicine, organic semiconductors, mass spectroscopy, biomedical materialsOther keywords: bay‐substituted perylene diimide‐based D‐A‐D‐type SM acceptors, donor‐acceptor‐donor type perylene diimide derivatives, small‐molecule‐based organic solar cells, SM‐OSC, Suzuki coupling method, antimicrobial activity, bacteria, fungi, Fourier transform infrared spectroscopy, NMR, HR‐MS, optical band gap, P3HT donor, bulk hetero‐junction device structure, Gram‐negative bacteria, Escherichia coli Gram‐positive bacteria, Bacillus subtilis, antifungal activity, Candida albicans, Aspergillus niger, cytotoxicity, breast cancer cell lines MCF‐7, MTT assay method, cancer cells, wavelength 750 nm, temperature 400 degC     

Fabrication of electrospun polycaprolactone coated withchitosan-silver nanoparticles membranes for wound dressing applications

In this study, electrospun polycaprolactone membrane coated with chitosan-silver nanoparticles (CsAg), electrospun polycaprolactone/chitosan/Ag nanoparticles, was fabricated by immersing the plasma-treated electrospun polycaprolactone membrane in the CsAg gel. The plasma modification of electrospun polycaprolactone membrane prior to CsAg coating was tested by methylene blue stain and scanning electron microscope. The presence of silver and chitosan on the plasma-treated electrospun polycaprolactone membrane was confirmed by energy-dispersive X-ray spectroscopy and FT-IR spectrum. Scanning electron microscope observation was employed to observe the morphology of the membranes. The release of Ag ions from electrospun polycaprolactone/chitosan/Ag nanoparticles membrane was tested using atomic absorption spectrometry. Electrospun polycaprolactone/chitosan/Ag nanoparticles membrane inherited advantages from both CsAg gel and electrospun polycaprolactone membrane such as: increasing biocompatibility, mechanical strength, and antibacterial activity against both Gram-negative and Gram-positive bacteria. Thus, this investigation introduces a highly potential membrane that can increase the efficacy of the wound dressing process.     

Development of a novel porous cryo-foam for potential wound healing applications

This body of work describes the development of a porous hydrogel for wound healing applications. In the present study poly (vinyl alcohol) (PVA) and poly (acrylic acid) (PAA) based hydrogels were prepared, and their properties were examined. Varying concentrations of the polymers and distilled water were used to prepare the hydrogels. The use of a high shear mixer, for foaming the PVA and PVA/PAA gels, and how this physical change can affect the structure and porosity of the hydrogel in question, represents a key feature of this work. The mechanical and thermal properties were determined by parallel plate rheometry and modulated differential scanning calorimetry (MDSC) respectively. The results indicated that the hydrogels containing low concentration of PVA and high volume of H₂O are significantly weaker than those synthesised with higher concentrations of PVA. The thermal analysis shows distinct endotherms and provides evidence of crystallisation. The chemical structure of the hydrogels was confirmed by means of attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR).     

Putative mechanism for anticancer properties of Ag–PP (NPs) extract

One of the most important challenges in treating cancer is the invasion and the angiogenesis of cancer cells. The synthesis of green nanoparticles (NPs) and their use in therapeutic fields is one of the most effective methods with minimal side effects in cancer treatment. In this study, cytotoxic and anti‐angiogenic effects of silver NPs (AgNPs) coated with palm pollen extract [Ag–PP(NPs)] were evaluated. For this purpose, the cells were treated with NPs and then were subjected to trypan blue testing (48 h). Then, the cancer invasion was evaluated by the scratch procedure and the expressions of the vascular endothelial growth factor (VEGF) and its receptor (VEGF‐R) genes were estimated using real‐time PCR assay. Also, the angiogenesis effect of the NPs was investigated with chick chorioallantoic membrane (CAM) assay. The Ag–PP(NPs) induced cytotoxicity on MCF7 cells. The findings also showed that Ag–PP(NPs) inhibit invasive cancer cells and reduce the expression of VEGF and VEGF‐R and significantly reduced the number and vessels lengths and the lengths and weights of the embryos in CAM assay. Ag–PP(NPs) with the induction of cytotoxic effects, metastatic inhibition and anti‐angiogenesis properties should be considered as an appropriate option for treatment of cancerInspec keywords: nanomedicine, genetics, cellular biophysics, toxicology, patient treatment, silver, cancer, biochemistry, biomedical materials, nanoparticles, nanofabrication, membranesOther keywords: minimal side effects, cancer treatment, silver NPs, cancer invasion, vascular endothelial growth factor, receptor genes, VEGF‐R, real‐time polymerase chain reaction assay, angiogenesis effect, chick chorioallantoic membrane assay, MCF7 cells, invasive cancer cells, cytotoxic effects, putative mechanism, anticancer properties, antiangiogenic effects, antiangiogenesis properties, Ag–PP‐induced cytotoxicity, metastatic inhibition, palm pollen extraction, trypan blue testing, time 48.0 hour, Ag     

Physical, antibacterial and antioxidant properties of chitosan films incorporated with thyme oil for potential wound healing applications

Chitosan films incorporated with thyme oil for potential applications of wound dressing were successfully prepared by solvent casting method. The water vapor permeability, oxygen transmission rate, and mechanical properties of the films were determined. Surface and cross-section morphologies and the film thicknesses were determined by Scanning Electron Microscopy (SEM). Fourier transform infrared (FT-IR) spectroscopy was conducted to determine functional group interactions between the chitosan and thyme oil. Thermal behaviors of the films were analyzed by Thermal Gravimetry (TGA) and Differential Scanning Calorimetry (DSC). In addition, the antimicrobial and the antioxidant activities of the films were investigated. The antimicrobial test was carried by agar diffusion method and the growth inhibition effects of the films including different amount of thyme oil were tested on the gram negative microorganisms of Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and a gram positive microorganism of Staphylococcus aureus. The minimum thyme oil concentration in chitosan films showing the antimicrobial activity on all microorganisms used in the study was found as 1.2 % (v/v). In addition, this concentration showed the highest antioxidant activity due to mainly the carvacrol in thyme oil. Water vapor permeability and oxygen transmission rate of the films slightly increased, however, mechanical properties decreased with thyme oil incorporation. The results revealed that the thyme oil has a good potential to be incorporated into chitosan to make antibacterial and permeable films for wound healing applications.     

Rheological and thermal characteristics of a two phase hydrogel system for potential wound healing applications

Hydrogels fabricated from single polymers have been extensively investigated for wound healing applications. However, in many cases a single polymer cannot meet divergent demands in terms of both properties and performance. In this work, a two phase hydrogel was prepared by physically imbedding a xerogel in the core of a freeze thawed hydrogel. The outer hydrogel was prepared by freeze thawing poly (vinyl alcohol) (PVA) and poly (acrylic acid) (PAA) while the xerogels were prepared by UV polymerisation of 1-vinyl-2-pyrrolidinone (NVP). The rheological results indicated that the two phase hydrogels over a period of 2 weeks formed a strong interface and demonstrated greater physical strength. This suggested that the inner gel containing PVP diffused into the PVA/PAA hydrogel, which in turn increased hydrogen bonding, resulting in the overall increase in the stiffness of the gel. Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) confirmed hydrogen bonding had occurred between the constituents of the two phase hydrogels. Thermal analysis suggested that T _g of each of the samples was above 80 °C, which indicated no impact on the behaviour of the gel at body temperature, but did however, give an indication of the stiffness of the dry polymer.     

Biosynthesis of bimetallic and core–shell nanoparticles: their biomedical applications – a review

Recently, researchers succeeded in designing and manufacturing a new class of nanoparticles (NPs) called hybrid NPs. Among hybrid NPs, bimetallic and core–shell NPs were a revolutionary step in NPs science. A large number of green physiochemical and methods for nanostructures synthesis have been published. Eventually, physiochemical methods are either expensive or require the use of chemical compounds for the synthesis of bimetallic and core–shell nanostructures. The main challenges that scientists are facing are making the process cheaper, facile and eco‐friendly efficient synthesis process. Green synthesis (biosynthesis) refers to the use of bio‐resources (such as bacteria, fungi, plants or their derivatives) for the synthesis of nanostructures. The popularity of the green synthesis of nanostructures is due to their environmental friendliness and no usage of toxic materials, environmental friendliness for the synthesis or stability of nanostructure. Bimetallic and core–shell NPs have many biomedical applications such as removing heavy metals, parasitology, molecular and microbial sensor, gene carrier, single bacterial detection, oligonucleotide detection and so on. The purpose of this study is to discuss briefly the biosynthesised bimetallic and core–shell NPs, their biomedical applications.Inspec keywords: nanofabrication, nanoparticles, biosensors, microorganisms, molecular biophysics, nanobiotechnologyOther keywords: biosynthesised bimetallic –shell, environmental friendliness, green synthesis, eco‐friendly efficient synthesis process, core–shell nanostructures, bimetallic –shell nanostructures, physiochemical methods, nanostructures synthesis, green physiochemical, NPs science, hybrid NPs, biomedical applications, core–shell nanoparticles, bimetallic –shell nanoparticles, biosynthesis     

Biogenic synthesis of Au,Ag and Au–Ag alloy nanoparticles using Cannabis sativa leaf extract

Biogenic synthesis of gold (Au), silver (Ag) and bimetallic alloy Au–Ag nanoparticles (NPs) from aqueous solutions using Cannabis sativa as reducing and stabilising agent has been presented in this report. Formation of NPs was monitored using UV–visible spectroscopy. Morphology of the synthesised metallic and bimetallic NPs was investigated using X‐ray diffraction and scanning electron microscopy. Elemental composition and the surface chemical state of NPs were confirmed by energy dispersive X‐ray spectroscopy analysis. Fourier transform‐infrared spectroscopy was utilised to identify the possible biomolecules responsible for the reduction and stabilisation of the NPs. Biological applicability of biosynthesised NPs was tested against five bacterial strains namely Klebsiella pneumonia, Bacillus subtilis (B. subtilis), Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa (P. aeruginosa) and Leishmania major promastigotes. The results showed considerable antibacterial and anti‐leishmanial activity. The Au–Ag bimetallic NPs showed improved antibacterial activity against B. subtilis and P. aeruginosa as compared to Au and Ag alone, while maximum anti‐leishmanial activity was observed at 250 μg ml⁻¹ NP concentration. These results suggest that biosynthesised NPs can be used as potent antibiotic and anti‐leishmanial agents.Inspec keywords: silver, silver alloys, gold, gold alloys, nanoparticles, nanofabrication, reduction (chemical), ultraviolet spectra, visible spectra, X‐ray diffraction, scanning electron microscopy, X‐ray chemical analysis, Fourier transform infrared spectra, microorganisms, antibacterial activityOther keywords: biogenic synthesis, Cannabis sativa leaf extract, bimetallic alloy Au–Ag nanoparticles, aqueous solutions, reducing agent, stabilising agent, UV–visible spectroscopy, X‐ray diffraction, scanning electron microscopy, elemental composition, surface chemical state, energy dispersive X‐ray spectroscopy analysis, Fourier transform‐infrared spectroscopy, biomolecules, bacterial strains, Klebsiella pneumonia, Bacillus subtilis, Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Leishmania major promastigotes, antibacterial activity, anti‐leishmanial activity, Ag, Au, AuAg     

FSE–Ag complex NS: preparation and evaluation of antibacterial activity

Silver (Ag) complexes of drugs and their nanosystems have great potential as antibacterials. Recently, an Ag complex of furosemide (Ag–FSE) has shown to be a promising antimicrobial. However, poor solubility of Ag–FSE could hamper its introduction into clinics. Therefore, the authors developed a nanosuspension of Ag–FSE (Ag–FSE_NS) for its solubility and antibacterial activity enhancement. The aim of this study was to introduce a novel nanoantibiotic with enhanced antibacterial efficacy. Ag–FSE_NS was prepared by precipitation–ultrasonication technique. Size, polydispersity index (PI) and zeta potential (ZP) of prepared Ag–FSE_NS were measured by dynamic light scattering, whereas surface morphology was determined using scanning electron microscopy (SEM). In vitro antibacterial activity was evaluated against Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa using broth microdilution method. Size, PI and ZP of optimised Ag–FSE_NS1 were 191.2 ± 19.34 nm, 0.465 ± 0.059 and −55.7 ± 8.18 mV, respectively. SEM revealed that Ag–FSE_NS1 particles were rod or needle‐like with smooth surfaces. Saturation solubility of Ag–FSE in NS increased eight‐fold than pure Ag–FSE. Ag–FSE_NS1 exhibited two‐fold and eight‐fold enhancements in activity against E. coli and S. aureus, respectively. The results obtained showed that developed Ag–FSE_NS1 holds a promise as a topical antibacterial.Inspec keywords: nanomedicine, nanofabrication, light scattering, surface morphology, silver, particle size, solubility, suspensions, scanning electron microscopy, electrokinetic effects, drugs, biomedical materials, antibacterial activity, microorganisms, nanoparticles, drug delivery systems, transmission electron microscopyOther keywords: saturation solubility, topical antibacterial, size 171.86 nm to 210.54 nm, voltage ‐47.52 mV to ‐63.88 mV, Ag, broth microdilution method, Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, SEM, scanning electron microscopy, surface morphology, dynamic light scattering, particle size, polydispersity index, precipitation–ultrasonication technique, nanoantibiotic, nanosuspension, furosemide, nanosystems, drugs, Ag–FSE_NS preparation, in vitro antibacterial activity, pure Ag–FSE, Ag–FSE_NS1 particles, optimised Ag–FSE_NS1, zeta potential, enhanced antibacterial efficacy, antibacterials     

Antibacterial activity of hybrid chitosan–cupric oxide nanoparticles on cotton fabric

In this study, cupric oxide (CuO) nanoparticles were prepared using sonochemical method. The prepared nanoparticles were studied using X‐ray diffraction (XRD) pattern, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM) methods. The colloidal chitosan (CS) solution was prepared using ultrasound irradiation method and simultaneously mixed with CuO nanoparticles. The coatings of colloidal solution with and without CuO nanoparticles were studied through TEM images. The cotton fabrics were separately soaked in the prepared nanoparticle‐containing (hybrid) solutions by sonication method followed by pad‐dry‐cure method. The structural, functional, and morphological analyses of the coated and uncoated fabrics were performed using XRD, FTIR‐attenuated total reflectance, and SEM analyses, respectively. The hybrid‐coated cotton fabrics showed better antibacterial activity against Staphylococcus aureus and Escherichia coli. The bioactivity performance of the coated fabrics was in the order of CuO‐coated fabric > CS‐coated fabric.Inspec keywords: cotton fabrics, nanoparticles, antibacterial activity, transmission electron microscopy, Fourier transform spectroscopy, infrared spectroscopy, scanning electron microscopy, copper compoundsOther keywords: antibacterial activity, hybrid chitosan‐cupric oxide nanoparticles, cotton fabric, cupric oxide nanoparticles, sonochemical method, X‐ray diffraction, XRD pattern, Fourier transform infrared spectroscopy, FTIR spectroscopy, scanning electron microscopy, SEM, transmission electron microscopy, TEM methods, colloidal chitosan solution, ultrasound irradiation method, colloidal solution, TEM images, cotton fabrics, nanoparticle‐containing solutions, sonication method, pad‐dry‐cure method, morphological analyses, structural analyses, functional analyses, FTIR‐attenuated total reflectance, SEM analyses, hybrid‐coated cotton fabrics, Staphylococcus aureus, Escherichia coli, bioactivity performance, CuO     

Studies on binding of single‐stranded DNA with reduced graphene oxide–silver nanocomposites

The binding reaction of reduced graphene oxide–silver nanocomposites (rGO–AgNCs) with calf thymus single‐stranded DNA (ssDNA) was studied by ultraviolet–visible absorption, fluorescence spectroscopy and circular dichroism (CD), using berberine hemisulphate (BR) dye as a fluorescence probe. The absorbance of ssDNA increases, but the fluorescence intensity is quenched with the addition of rGO–AgNCs. The binding of rGO–AgNCs with ssDNA was able to increase the quenching effects of BR and ssDNA, and induce the changes in CD spectra. All of the evidence indicated that there was a relatively strong interaction between ssDNA and rGO–AgNCs. The data obtained from fluorescence experiments revealed that the quenching process of ssDNA caused by rGO–AgNCs is primarily due to complex formation, i.e. static quenching. The increasing trend of the binding equilibrium constant (K a) with rising temperature indicated that the binding process was an endothermic reaction. The calculated thermodynamic parameters showed that the binding process was thermodynamically spontaneous, and hydrophobic association played predominant roles in the binding of ssDNA to the surface of rGO–AgNCs.Inspec keywords: DNA, fluorescence spectroscopy, circular dichroism, nanofabrication, nanobiotechnology, silver, hydrophobicity, molecular biophysics, radiation quenching, biochemistry, nanocomposites, visible spectra, ultraviolet spectra, dyes, fluorescence, association, graphene compoundsOther keywords: ssDNA increases, fluorescence intensity, fluorescence experiments, binding equilibrium constant, binding process, reduced graphene oxide‐silver nanocomposites, binding reaction, calf thymus single‐stranded DNA, fluorescence spectroscopy, fluorescence probe, complex formation, static quenching, calculated thermodynamic parameters, rGO‐AgNCs binding, ultraviolet‐visible absorption, berberine hemisulphate dye, circular dichroism, CO‐Ag     

Nitrobacter sp. extract mediated biosynthesis of Ag2 O NPs with excellent antioxidant and antibacterial potential for biomedical application

In this study, extracellular extract of plant growth promoting bacterium, Nitrobacter sp. is used for the bioconversion of AgNO₃ (silver nitrate) into Ag₂ O (silver oxide nanoparticles). It is an easy, ecofriendly and single step method for Ag₂ O NPs synthesis. The bio‐synthesized nanoparticles were characterized using different techniques. UV‐Vis results showed the maximum absorbance around 450 nm. XRD result shows the particles to have faced centered cubic (fcc) crystalline nature. FTIR analysis reveals the functional groups that are involved in bioconversion such as C–N, N–H and C=O. Energy‐dispersive X‐ray spectroscopy (EDAX) spectrum confirms that the prepared nanoparticle is Ag₂ O NPs. Particle size distribution result reveals that the average particle size is around 40 nm. The synthesized Ag₂ O NPs found to be almost spherical in shape. Biosynthesized Ag₂ O NPs possess good antibacterial activity against selected Gram positive and Gram negative bacterial strains namely Salmonella typhimurium, Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae when compared to standard antibiotic. In addition, Ag₂ O NPs exhibits excellent free radical scavenging activity with respect to dosage. Thus, this study is a new approach to use soil bacterial extract for the production of Ag₂ O NPs for biomedical application.Inspec keywords: nanomedicine, nanoparticles, silver compounds, antibacterial activity, ultraviolet spectra, visible spectra, X‐ray diffraction, Fourier transform infrared spectra, X‐ray chemical analysis, particle size, free radicalsOther keywords: free radical scavenging activity, Ag₂ O, AgNO₃ , Klebsiella pneumoniae, Escherichia coli, Staphylococcus aureus, Salmonella typhimurium, Gram negative bacterial strains, Gram positive bacterial strains, particle size distribution, energy‐dispersive X‐ray spectroscopy spectrum, functional groups, Fourier transform infrared analysis, faced centred cubic crystalline nature, XRD, UV‐Vis results, bio‐synthesised nanoparticles, silver oxide nanoparticles, silver nitrate bioconversion, plant growth promoting bacterium, extracellular extract, biomedical application, antibacterial potential, antioxidant potential, Ag₂ O NPs, extract mediated biosynthesis, Nitrobacter sp     

镀Au键合Ag线性能对键合质量的影响研究

利用扫描电镜、能谱仪、拉力-剪切力测试仪等研究了不同镀Au厚度的镀Au键合Ag线Free Air Ball(FAB)特性和不同力学性能的镀Au键合Ag线对键合强度及其可靠性的影响规律，研究结果表明：镀Au键合Ag线镀层厚度过小会造成Electronic-Flame-Off(EFO)过程中的FAB偏球及球焊点形状不稳定，镀层厚度过大会导致FAB变尖；高强度、低伸长率会造成焊点颈部产生裂纹而造成焊点的拉力偏低并在颈部断裂，低强度、高伸长率引起颈部晶粒粗大进而降低颈部连接强度；镀Au键合Ag线颈部应力集中或内部组织结构不均匀，在冷热冲击周期性形变作用下，球焊点颈部产生裂纹并引起电阻增加，进而导致器件失效.     

Fabrication of biopolymer based nanocomposite wound dressing: evaluation of wound healing properties and wound microbial load

The aim of this study is to introduce natural‐based polymers, chitosan and starch, to design a remedial nanocomposite, comprising of cerium oxide nanoparticles and silver nanoparticles, to investigate their effects in accelerating wound healing and in wound microbial load. Cerium oxide nanoparticles synthesized in starch solution added to the colloidal dispersion of synthesized silver nanoparticles in chitosan to make a three‐component nanomaterial. Mice were anaesthetized and two parallel full‐thickness round wounds were excised under aseptic conditions with the help of sterile dermal biopsy punch. Furthermore, effects of silver‐chitosan and silver‐cerium‐chitosan nanocomposite had evaluated on rate of wound closure and collagen density and on microbial load of wound in full‐thickness model. Results showed that both silver chitosan and silver‐cerium‐chitosan had significant impact on acceleration of wound closure and collagen content and on reduction of wound microbial load in comparison with control group, which was, received no treatments. However, the silver‐cerium‐chitosan nanocomposite is more potent than silver‐chitosan group and control group in wound closure. The wound healing effects of silver‐cerium‐chitosan nanocomposite are due to unique features of its three components and this nanocomposite promises impressive remedies for clinical application.Inspec keywords: wounds, nanocomposites, nanomedicine, nanoparticles, proteins, cerium, silver, polymers, colloids, patient treatmentOther keywords: biopolymer‐based nanocomposite wound dressing, wound healing properties, wound microbial load, natural‐based polymers, chitosan, remedial nanocomposite, cerium oxide nanoparticles, nanoceria, silver nanoparticles, starch solution, three‐component nanomaterial, synthesised silver nanoparticles, ketamine intraperitoneal injection, silver‐cerium‐chitosan nanocomposite, wound closure, collagen density, wound healing effects, wound care, aseptic conditions, sterile dermal biopsy punch, Ag‐Ce