Synthesis and evaluation of novel absorptive and antibacterial polyurethane membranes as wound dressing

Preparation and evaluation of new polyurethane membranes for wound dressing application was considered in this work. The membranes were prepared through amine curing reaction of epoxy-terminated polyurethane prepolymers and an antibacterial epoxy-functional quaternary ammonium compound (glycidyltriehtylammonium chloride, GTEACl. To render the prepared membranes to be highly absorptive of wound exudates, poly (ethylene glycol) polyols were introduced into the polyurethane networks. Evaluation of biocompatibity via both MTT assay and direct contact with two different cell lines (fibroblast and epidermal keratinocytes) reveled that membranes with appropriate loading of GTEACl showed proper biocompatibility. Promising antibacterial activity of the prepared membranes against Staphylococcus aureus and Escherichia coli bacteria was confirmed by both agar diffusion and shaking flask methods. The membranes with balanced crosslink density and ionic groups' concentration possessed appropriate hydrophilicity and water vapor transmission rate; therefore, they could prevent the accumulation of exudates and decrease the surface inflammation in the wounded area.     

Synthesis and antibacterial properties of silver nanoparticles

Nanometer sized silver particles were synthesized by inert gas condensation and co-condensation techniques. Both techniques are based on the evaporation of a metal into an inert atmosphere with the subsequent cooling for the nucleation and growth of the nanoparticles. The antibacterial efficiency of the nanoparticles was investigated by introducing the particles into a media containing Escherichia coli. The antibacterial investigations were performed in solution and on petri dishes. The silver nanoparticles were found to exhibit antibacterial effects at low concentrations. The antibacterial properties were related to the total surface area of the nanoparticles. Smaller particles with a larger surface to volume ratio provided a more efficient means for antibacterial activity. The nanoparticles were found to be completely cytotoxic to E. coli for surface concentrations as low as 8 microg of Ag/cm2.     

Preparation and evaluation of biocomposites as wound dressing material

Collagen was isolated from the chrome containing leather waste (CCLW) which is a major solid waste in leather industry. Composite films were made using sago starch (SG), soya protein (SY), and collagen (C) and were cross linked with glutaraldehyde (G).The films prepared were characterized for their physico chemical properties like tensile strength, infrared spectra, thermogravimetric analysis, surface morphology, and water absorption studies. Better mechanical properties and surface morphology were observed for SG–SY–G–C films compared to other films prepared using collagen. The composite films prepared were used as wound dressing material on the experimental wounds of rats and healing pattern was evaluated using planimetric, biochemical, and histopathological studies. These studies have revealed better wound healing capacity of SG–SY–G–C film and utilization of CCLW in the preparation of value added product like wound dressing material.     

Green synthesis of silver nanoparticles using Glaucium corniculatum (L.) Curtis extract and evaluation of its antibacterial activity

The metal nanoparticles, due to interesting features such as electrical, optical, chemical and magnetic properties, have been investigated repeatedly. Also, the mentioned nanoparticles have specific uses in terms of their antibacterial activity. The biosynthesis method is more appropriate than the chemical method for producing the nanoparticles because it does not need any special facilities; it is also economically affordable. In the current study, the silver nanoparticles (AgNPs) were obtained by using a very simple and low‐cost method via Glaucium corniculatum (L.) Curtis plant extract. The characteristics of the AgNPs were investigated using techniques including: X‐ray diffraction, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy. The SEM and TEM images showed that the nanoparticles had a spherical shape, and the mean diameter of them was 53.7 and 45 nm, respectively. The results of the disc diffusion test used for measuring the anti‐bacterial activity of the synthesised nanoparticles indicated that the formed nanoparticles possessed a suitable anti‐bacterial activity.Inspec keywords: silver, nanoparticles, antibacterial activity, nanomedicine, nanofabrication, X‐ray diffraction, transmission electron microscopy, scanning electron microscopy, Fourier transform infrared spectraOther keywords: green synthesis, silver nanoparticles, Glaucium corniculatum Curtis extract, antibacterial activity, metal nanoparticles, biosynthesis method, X‐ray diffraction, transmission electron microscopy, scanning electron microscopy, Fourier transform infrared spectroscopy, SEM, TEM, spherical shape, disc diffusion test, Ag     

Synthesis of mesostructured TiO2-based material and its functionalization with silver nanoparticles

We report the results of a template synthesis of a three-dimensional nanostructured material based on titanium(IV) oxide modified with silver nanoparticles. The chemical composition and structure of the material have been determined by scanning electron microscopy, IR spectroscopy, and X-ray diffraction.     

Synthesis of gold and silver nanoparticles using Mukia maderaspatna plant extract and its anticancer activity

The present investigation reveals the in vitro cytotoxic effect of the biosynthesised metal nanoparticles on the MCF 7 breast cancer cell lines. The gold and silver nanoparticles were synthesised through an environmentally admissible route using the Mukia Maderaspatna plant extract. Initially, the biomolecules present in the plant extract were analysed using phytochemical analysis. Further, these biomolecules reduce the metal ion solution resulting from the formation of metal nanoparticles. The reaction parameters were optimised to control the size of nanoparticles which were confirmed by UV visible spectroscopy. Various instrumental techniques such as Fourier transform‐infrared spectroscopy, high resolution transmission electron microscopy, energy dispersive X‐ray and scanning electron microscopy were employed to characterise the synthesised gold and silver nanoparticles. The synthesised gold and silver nanoparticles were found to be 20–50 nm and were of different shapes including spherical, triangle and hexagonal. MTT and dual staining assays were carried out with different concentrations (1, 10, 25, 50 and 100 µg/ml) of gold and silver nanoparticles. The results show that the nanoparticles exhibited significant cytotoxic effects with IC 50 value of 44.8 µg/g for gold nanoparticles and 51.3 µg/g for silver nanoparticles. The observations in this study show that this can be developed as a promising nanomaterial in pharmaceutical and healthcare sector.Inspec keywords: gold, silver, nanoparticles, nanofabrication, nanomedicine, biomedical materials, cancer, cellular biophysics, ultraviolet spectra, visible spectra, Fourier transform infrared spectra, transmission electron microscopy, X‐ray chemical analysis, scanning electron microscopyOther keywords: gold nanoparticle synthesis, silver nanoparticle synthesis, Mukia maderaspatna plant extract, anticancer activity, MCF 7 breast cancer cell line, biomolecule, phytochemical analysis, size 20 nm to 50 nm, healt hcare sector, pharmaceutical sector, nanomaterial, dual staining assay, MTT assay, scanning electron microscopy, energy dispersive X‐ray spectrocopy, high resolution transmission electron microscopy, Fourier transform‐infrared spectroscopy, instrumental technique, ultraviolet‐visible spectroscopy, metal nanoparticle formation, metal ion solution     

Synthesis and characterization of dextran-capped silver nanoparticles with enhanced antibacterial activity

Dextran-capped silver nanoparticles were synthesized by reducing silver nitrate with NaBH4 in the presence of dextran as capping agent. The characters of silver nanoparticles were investigated using UV-Vis spectrophotometer, nano-grainsize analyzer, X-ray diffraction, and transmission electron microscopy. Results showed that the silver nanoparticles capped with dextran were in uniform shape and narrow size distribution. Moreover, compared with polyvinylpyrrolidone (PVP)-capped silver nanoparticles, the dextran-capped ones possessed better stability. Antibacterial tests of these silver nanoparticles were carried out for Escherichia coli, Staphylococcus aureus, Staphylococcus epidermidis, Pseudomonas aeruginosa, and Klebsiella pneumoniae. Results suggested that the dextran-capped silver nanoparticles had high antibacterial activity against both Gram-positive and Gram-negative bacteria. In addition, the cytotoxicity in vitro of the dextran-capped silver nanoparticles was investigated using mouse fibrosarcoma cells (L929). The toxicity was evaluated by the changes of cell morphology and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide assay. Results indicated that these silver nanoparticles had slight effect on the survival and proliferation of L-929 cells at their minimal inhibitory concentration (MIC). After modified by dextran, the physiochemical properties of the silver nanoparticles had been improved. We anticipated that these dextran-capped silver nanoparticles could be integrated into systems for biological and pharmaceutical applications.     

Synthesis of oleic acid-stabilized silver nanoparticles and analysis of their antibacterial activity

The development of new and simple green chemical methods for synthesizing colloidal solutions of functional nanoparticles is desirable for environment-friendly applications. In the present work, we report a feasible method for synthesizing colloidal solutions of silver nanoparticles (Ag NPs) based on the modified Tollens technique. The Ag NPs were stabilized by using oleic acid as a surfactant and were produced for the first time by the reduction of silver ammonium complex [Ag(NH₃)₂]⁺_(aq) by glucose with UV irradiation treatment. A stable and nearly monodisperse aqueous Ag NPs solution with average-sized particles (~ 9–10 nm) was obtained. The Ag NPs exhibited high antibacterial activity against both Gram-negative Escherichia Coli (E. coli) and Gram-positive Staphylococcus aureus bacteria. Electron microscopic images and analyses provided further insights into the interaction and bactericidal mechanism of the Ag NPs. The proposed method of synthesis is an effective way to produce highly bactericidal colloidal solutions for medical, microbiological, and industrial applications.     

银纳米粒子的制备及其在光催化中的应用

在乙醇/水溶剂中,以AgNO3为银源、聚乙烯吡咯烷酮为稳定剂,采用溶剂热还原法合成纳米银.通过调变乙醇-水的相对比例、AgNO3浓度和反应时间等,获得了尺寸均匀的准球形、立方体、线状等不同形貌的银纳米颗粒,利用XRD、SEM、TEM和紫外-可见吸收光谱进行了表征.初步考察了球形纳米银(粒径分布30～70nm)和立方纳米银(粒径80～140nm)修饰介孔二氧化钛对甲基橙的光催化降解性能,结果表明两种纳米银粒子对TiO2的光催化均具有增效作用,且银粒径越小,对光催化活性的提高越显著.     

Synthesis of polypyrrole nanocomposites decorated with silver nanoparticles with electrocatalysis and antibacterial property

Polypyrrole nanowire/silver nanoparticle composites (PPy/Ag) are obtained in aqueous media through a one-pot method without any external stimulus. PPy nanowires were assembled on the reactive self-degraded template of the complex of AgNO₃ and methyl orange (MO). During the synthesis process in the dark surrounding, Ag nanoparticles could be uniformly decorated onto the surface of PPy nanowires in situ by the redox reaction of pyrrole and AgNO₃. Neither additional reducing agents for the growth of silver nanoparticles nor oxidizing agents for the polymerization of pyrrole are utilized. The formation mechanism, morphologies, structural characteristics, and conductivity of the obtained PPy/Ag nanocomposites are reported. The as-prepared PPy/Ag nanocomposites exhibit well-defined response to the electrochemical reduction of hydrogen peroxide. Moreover, the preliminary antibacterial assays indicate that the PPy/Ag nanocomposites also possess antibacterial abilities against Escherichia coli.     

A facile method to prepare size-tunable silver nanoparticles and its antibacterial mechanism

The antibacterial effect of silver nanoparticles (denoted as Ag NPs) is closely related to size. This could partly explain why size controllable synthesis of Ag NPs for bactericidal application is drawing much attention. Thus, we establish a facile and mild route to prepare size-tunable Ag NPs with highly uniform morphologies and narrow size distributions. The as-prepared Ag NPs with averaged sizes of 2, 12 and 32?nm were characterized by transmission electron microscopy (TEM), ultraviolet–visible absorption spectroscopy (UV–vis), X-ray powder diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The antimicrobial effect of the as-prepared Ag NPs with different particles size was assessed by broth dilution and disk diffusion as well as measurement of optical density (OD₆₀₀). Moreover, their antibacterial mechanism was discussed in relation to morphology observation of microorganism by scanning electron microscopy (SEM) and to concentration detection of Ag⁺ by stripping voltammetry. It was found that the parameters such as reactant molar ratio, reaction time, dropping speed, and most of all, pH of the reactant solutions, have significant influences on size-regulation of Ag NPs. The as-prepared Ag NPs exhibit excellent antibacterial properties, and their antimicrobial activities increase with decreasing particles size. Besides, two kinds of mechanisms, i.e., contact action and release of Ag⁺, are responsible for the antimicrobial effect of Ag NPs.     

Investigative evaluation of Cassia absus for antibacterial capacity and biomimetic synthesis of silver nanoparticles

Cassia absus is used for medicinal purposes for a long time all over the world. In this study, the authors report the antimicrobial potential of C. absus extracts obtained with different solvents. The extract(s) obtained with ethyl acetate yielded the best antibacterial effects because of a rich supply of oxalates and alkaloids in it. The same extract was also exploited for reducing Ag⁺ ions (to metallic Ag⁰) for the synthesis of nanoparticles. Electron microscopy revealed that the silver nanoparticles were ∼18–25 nm in diameter. The Fourier‐transform infrared evaluation pointed towards the fact that flavonoids present in the plant extract were acting as reductants while amino groups were the bound stabilisation agents to the synthesised nanoparticles limiting the diameter to a certain threshold and avoiding aggregation naturally. A comparative antibacterial assay of C. absus versus Ag nanoparticles showed that the nanoparticles as well as organic (ethyl acetate) extract of the plant checked the growth of selected (MDR) superbugs. However, the biosynthesised Ag nanoparticles returned better antibacterial efficacies than ethyl acetate extract.Inspec keywords: biomimetics, nanomedicine, nanoparticles, nanofabrication, reduction (chemical), microorganisms, silver, antibacterial activity, Fourier transform infrared spectra, biomedical materials, electron microscopyOther keywords: antibacterial capacity, biomimetic synthesis, silver nanoparticles, antimicrobial potential, ethyl acetate, oxalates, alkaloids, electron microscopy, Fourier‐transform infrared evaluation, antibacterial efficacies, antibacterial assay, organic extract, Cassia absus, flavonoids, Ag     

Green synthesis of silver nanoparticles using flower extract of Malva sylvestris and investigation of their antibacterial activity

High‐quality colloidal silver nanoparticles (AgNP) were synthesised via a green approach by using hydroalcoholic extracts of Malva sylvestris. Silver nitrate was used as a substrate ion while the plant extract successfully played the role of reducing and stabilising agents. The synthesised nanoparticles were carefully characterised by using transmission electron microscopy, atomic‐force microscopy, energy dispersive X‐ray spectroscopy, Fourier transform infrared spectroscopy and UV–vis spectroscopy. The maximum absorption wavelengths of the colloidal solutions synthesised using 70 and 96% ethanol and 100% methanol, as extraction solvents, were 430, 485 and 504 nm, respectively. Interestingly, the size distribution of nanoparticles depended on the used solvent. The best particle size distribution belonged to the nanoparticles synthesised by 70% ethanol extract, which was 20–40 nm. The antibacterial activity of the synthesised nanoparticles was studied on Escherichia coli, Staphylococcus aureus and Streptococcus pyogenes using disk diffusion, minimum inhibitory concentrations and minimum bactericidal concentrations assays. The best antibacterial activity obtained for the AgNPs produced by using 96% ethanolic extract.Inspec keywords: silver, nanoparticles, nanofabrication, antibacterial activity, colloids, particle size, transmission electron microscopy, atomic force microscopy, X‐ray chemical analysis, Fourier transform spectra, infrared spectra, ultraviolet spectra, visible spectra, microorganisms, nanomedicine, biomedical materialsOther keywords: Green synthesis, flower extract, Malva sylvestris, antibacterial activity, high‐quality colloidal silver nanoparticles, hydroalcoholic extracts, plant extract, reducing agents, stabilising agents, transmission electron microscopy, atomic‐force microscopy, energy dispersive X‐ray spectroscopy, Fourier transform infrared spectroscopy, UV– vis spectroscopy, colloidal solutions, particle size distribution, Escherichia coli, Staphylococcus aureus, Streptococcus pyogenes, disk diffusion, minimum inhibitory concentrations, minimum bactericidal concentrations assays, ethanolic extract, size 430 nm, size 485 nm, size 504 nm, size 20 nm to 40 nm, Ag     

Biomedical evaluation of a novel nitrogen oxides releasing wound dressing

Chronic wounds are a major cause for both suffering and economical losses. Management of chronic non-healing wounds requires multipronged approach. They are polymicrobial and agonizing for the patient due to associated pain. Moist dressing providing antimicrobial action is a highly desirable chronic wound management option. Here we report a hydrogel based dressing that possesses the antimicrobial properties of acidified sodium nitrite and the homeostatic property of a hydrogel. The dressing was developed by combining citric acid cross-linked cotton gauze and sodium nitrite loaded gelatin. The cotton gauze was cross-linked with citric acid by pad-dry-curing in presence of nano-titania catalyst. The cotton gauze-gelatin hydrogel combination was gamma-irradiated and freeze-dried. At the time of application, the freeze-dried dressing is wetted by sodium nitrite solution. The dressing has a fluid uptake ability of 90 % (w/v) and the water vapour evaporation rate was estimated to be 2,809 ± 20 g/m²/day. The dressing showed significant antimicrobial activity against both planktonic and biofilm forms and was effective during consecutive re-uses. Cytotoxicity study showed inhibition of fibroblasts, but to a lesser extent than clinically administered concentrations of antiseptic like povidone iodine. Storage at 37 °C over a 3 month period resulted in no significant loss of its antimicrobial activity.     

壳聚糖修饰银纳米颗粒的制备及抗菌性能研究

采用液相化学还原法,以壳聚糖为修饰剂,硼氢化钠为还原剂,制备了壳聚糖修饰银纳米颗粒(chitosan-Ag NPs)。通过X射线粉末衍射仪、透射电子显微镜、傅立叶变换红外光谱仪等对所制备样品的结构和形貌进行了表征。结果表明,所制备纳米颗粒具有面心立方Ag的晶型结构,壳聚糖通过氨基和羟基中的N、O原子与Ag+的化学键合作用修饰在纳米颗粒表面,起到了限制颗粒粒径长大和防止其团聚的作用。采用肉汤连续稀释法检测了样品对大肠杆菌和金黄色葡萄球菌的抑菌杀菌性能,结果表明chitosan-Ag NPs具有优异的抗菌性,抗菌性能受到粒径大小的影响。     

Biofabrication of broad range antibacterial and antibiofilm silver nanoparticles

Silver nanoparticles (AgNPs) were biosynthesized via a green route using ten different plants extracts (GNP1‐ Caryota urens, GNP2‐Pongamia glabra, GNP3‐ Hamelia patens, GNP4‐Thevetia peruviana, GNP5‐Calendula officinalis, GNP6‐Tectona grandis, GNP7‐Ficus petiolaris, GNP8‐ Ficus busking, GNP9‐ Juniper communis, GNP10‐Bauhinia purpurea). AgNPs were tested against drug resistant microbes and their biofilms. These nanoparticles (NPs) were characterised using UV‐vis spectroscopy, transmission electron microscope, Fourier transform infrared spectroscopy, X‐ray diffraction and Image J software. Most of the AgNPs were distributed over a range of 1 of 60 nm size. The results indicated that AgNPs were antibacterial in nature without differentiating between resistant or susceptible strains. Moreover, the effect was more prominent on Gram negative bacteria then Gram positive bacteria and fungus. AgNPs inhibited various classes of microbes with different concentration. It was also evident from the results that the origin or nature of extract did not affect the activity of the NPs. Protein and carbohydrate leakage assays confirmed that the cells lysis is one of the main mechanisms for the killing of microbes by green AgNPs. This study suggests that the action of AgNPs on microbial cells resulted into cell lysis and DNA damage. Excellent microbial biofilm inhibition was also seen by these green AgNPs. AgNPs have proved their candidature as a potential antibacterial and antibiofilm agent against MDR microbes.Inspec keywords: silver, nanoparticles, antibacterial activity, nanofabrication, microorganisms, ultraviolet spectra, visible spectra, transmission electron microscopy, Fourier transform infrared spectra, X‐ray diffraction, proteins, DNA, nanomedicine, biomedical materials, cellular biophysicsOther keywords: biofabrication, broad range antibacterial nanoparticles, antibiofilm silver nanoparticles, plant extract contribution, drug resistant microbes, UV‐vis spectroscopy, transmission electron microscope, Fourier transform infrared spectroscopy, X‐ray diffraction, Image J software, resistant strains, susceptible strains, Gram positive bacteria, fungus, protein leakage assays, carbohydrate leakage assays, cell lysis, DNA damage, Ag     

Biosynthesis of silver nanoparticles using aqueous extract of silky hairs of corn and investigation of its antibacterial and anticandidal synergistic activity and antioxidant potential

This paper investigated the green synthesis of silver nanoparticles (AgNPs) using aqueous extract of silky hairs of corn (Zea mays L.) which is a waste material of the crop, as both a reducing and stabilising/capping agent. The AgNPs were characterised by UV‐visible spectroscopy, scanning electron microscopy (SEM), energy dispersive X‐ray analysis (EDX), thermogravimetric analysis (TGA), X‐ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT‐IR). The average size of AgNPs was found to be 249.12 nm. The AgNPs displayed strong antibacterial activity against five different foodborne pathogenic bacteria with diameter of inhibition zones ranged between (9.23 − 12.81 mm). It also exhibited potent synergistic antibacterial activity together with standard antibiotics, kanamycin (10.6 − 13.65 mm inhibition zones) and rifampicin (10.02 − 12.86 mm inhibition zones) and anticandidal activity with amphotericin b (10.57 − 13.63 mm inhibition zones). The AgNPs exhibited strong antioxidant activity in terms of nitric oxide scavenging (IC₅₀ 91.56 µg/mL), ABTS (2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulphonic acid) radical scavenging (IC₅₀ 115.75 µg/mL), DPPH (1,1‐diphenyl‐2‐picrylhydrazyl) radical scavenging (IC₅₀ 385.87 µg/mL), and reducing power (IC_0.5 23.14 µg/mL). This study demonstrated the synthesis of spherical AgNPs with strong antibacterial, anticandidal and antioxidant properties that could potentially be utilised in the biomedical, cosmetic, food and pharmaceutical industries.Inspec keywords: silver, nanoparticles, nanomedicine, antibacterial activity, biomedical materials, nanofabrication, botany, ultraviolet spectra, visible spectra, scanning electron microscopy, X‐ray chemical analysis, Fourier transform infrared spectra, crystallitesOther keywords: biomedical industry, cosmetic industry, food industry, pharmaceutical industry, Ag, crystallite size, 1,1‐diphenyl‐2‐picrylhydrazyl radical scavenging, 2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulphonic acid) radical scavenging, nitric oxide scavenging, amphotericin b, anticandidal activity, rifampicin, kanamycin, standard antibiotics, inhibition zones, foodborne pathogenic bacteria, Fourier transform infrared spectroscopy, X‐ray diffraction, thermogravimetric analysis, energy‐dispersive X‐ray analysis, scanning electron microscopy, ultraviolet‐visible spectroscopy, Zea mays L, antioxidant potential, anticandidal synergistic activity, antibacterial synergistic activity, corn, silky hair aqueous extract, silver nanoparticles biosynthesis     

Synthesis and characterization of an antibacterial powder based on the covalent bonding of aminosilane-stabilized silver nanoparticles to a colloidal silica

Stable dispersions of silver nanoparticles (Ag NPs) were synthesized employing glycerol as both a solvent and reducing agent, and 3-aminopropyl trimethoxysilane (APTMS) as a stabilizer. Average sizes varied between 13 and 55 nm, depending on the molar ratio of APTMS/Ag. Terminal alkoxysilanes reacted with OH groups of glycerol leading to the covalent bonding of glycerol moieties to the chain ends of the stabilizer. This produced extremely stable colloidal dispersions from which NPs could not be extracted with solvents immiscible with glycerol (as THF). Ag NPs were covalently bonded to the surface of a colloidal silica by hydrolysis/condensation of terminal Si–O–C bonds of the stabilizer with superficial SiOH bonds of silica. TEM images revealed the presence of individual NPs and small clusters of NPs attached to the silica surface. These clusters were presumably generated by intermolecular reactions among chain ends of the stabilizer producing Si–O–Si bonds. The antibacterial properties of the resulting powder were confirmed by conventional tests employing a culture of Escherichia Coli.     

Green synthesis of silver nanoparticles using bovine skin gelatin and its antibacterial effect on clinical bacterial isolates

Nanoparticles are being increasingly used in day‐to‐day life. Therefore, concerns have been raised regarding their interactions with the surrounding environment. This study focused on a simple green method for synthesizing silver nanoparticles (Ag‐NPs) in an autoclave at 15 psi (103 kPa) and 121°C. An aqueous solution of AgNO₃ as a precursor of Ag‐NPs and gelatin (type B) reducing and/or stabilizing (capping) agent were used. The effect of various AgNO₃ concentrations of certain gelatin concentration and various gelatin concentrations at constant AgNO₃ concentration, and autoclaving time, was studied. UV‐Vis spectra ascribed that the presence of localized surface plasmon resonance (SPR) of the synthesized Ag‐NPs. TEM images and the selected area of electron diffraction confirmed, the formation of Ag‐NPs with a diameter of approximately 5 ±0.35 nm. Furthermore, FT‐IR revealed that a gelatin polymer matrix stabilized the synthesized Ag‐NPs. The Well diffusion assay was used to test the effect of Ag‐NPs on six clinical bacterial isolates, where Gram positive bacteria were more susceptible to Ag‐NPs than Gram negative bacteria. Therefore, Ag‐NPs capped by gelatin have remarkable potential effect as an antibacterial agent, and they not only have various medical applications but can also be used in biological, pharmaceutical and industrial fields.Inspec keywords: silver, nanoparticles, nanomedicine, antibacterial activity, microorganisms, nanofabrication, skin, gelatin, ultraviolet spectra, visible spectra, surface plasmon resonance, transmission electron microscopy, electron diffraction, Fourier transform infrared spectra, polymers, biomedical materialsOther keywords: green synthesis, silver nanoparticles, bovine skin gelatin, antibacterial effect, clinical bacterial isolates, autoclave, reducing agent, stabilising agent, ultraviolet‐visible spectra, localised surface plasmon resonance, transmissions electron microscope images, electron diffraction, Fourier transform infrared spectroscopy, gelatin polymer matrix, well diffusion assay, gram negative bacteria, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, gram positive bacteria, Bacillus megaterium, Streptococcus pyogenes, Staphylococcus aureus, temperature 121 degC, Ag     

Preparation and antibacterial properties of hybrid-zirconia films with silver nanoparticles

The antimicrobial effect of incorporating silver nanoparticles (AgNps) into zirconia matrix–polyether glycol was studied. AgNps of 4–6 nm in size were synthesized using the inverse micelles method, and different doses of metallic nanoparticles were incorporated into zirconia–polyether glycol mixtures during the ageing procedure. Atomic force microscopy (AFM) of the modified hybrid film showed a homogenous distribution of 20–80 nm diameter AgNps, indicating agglomeration of these structures during film modification; such agglomerations were greater when increasing the dosage of the colloidal system. The AgNps-hybrid films showed higher antimicrobial activity against Gram-positive bacteria than for Gram-negative bacteria. Hybrid films prepared with dioctyl sodium sulfosuccinate (AOT) stabilized AgNps presented enhanced antibacterial activity compared to that obtained through the addition of a high AgNO₃ concentration (0.3 wt%).