Nanostructured Ag(4)O(4) films with enhanced antibacterial activity

Ag(4)O(4) (i.e.?silver(I)-silver(III) oxide) thin films with tailored structure and morphology at the nanoscale have been grown by reactive pulsed laser deposition (PLD) in an oxygen-containing atmosphere and they are shown to exhibit a very strong antibacterial activity towards Gram-negative bacteria (E. coli) and to completely inhibit the growth of Gram-positive bacteria (S. aureus). The formation of this particular high-valence silver oxide is explained in terms of the reactions occurring during the expansion of the ablated species in the reactive atmosphere, leading to the formation of low-stability Ag-O dimers and atomic oxygen, providing reactive species at the substrate where the film grows. PLD is shown to allow control of the structure (i.e.?crystallinity and grain size) and of the morphology of the films, from compact and columnar to foam-like, thus allowing the deposition of nanocrystalline films with increased porosity and surface area. The antibacterial action towards E. coli is demonstrated and is shown to be superior to that of nanostructured Ag-based medical products. This can be related to the release of Ag ions with high oxidation number, which are known to be very reactive towards bacteria, and to the peculiar morphology at the nanoscale resulting in a large effective surface area.     

Autoclave‐assisted synthesis of AgNPs in Z. officinale extract and assessment of their cytotoxicity,antibacterial and antioxidant activities

In this study, the authors synthesised silver nanoparticles (AgNPs) using autoclave as a simple, unique and eco‐friendly approach. The effect of Zingiber officinale extract was evaluated as a reducing and stabiliser agent. According to transmission electron microscopy results, the AgNPs were in the spherical shape with a particle size of ∼17 nm. The biomedical properties of AgNPs as antibacterial agents and free radical scavenging activity were estimated. Synthesised AgNPs showed significant 1,1‐diphenyl‐2‐picryl‐hydrazyl free radical scavenging. Strong bactericidal activity was shown by the AgNPs on Gram‐positive and Gram‐negative bacteria. A maximum inhibition zone of ∼14 mm was obtained for epidermidis at a concentration of 60 μg/ml for sample fabricated at 24 h. The AgNPs also showed a significant cytotoxic effect against MCF‐7 breast cancer cell lines with an half maximal inhibitory concentration value of 62 μg/ml in 24 h by the MTT assay. It could be concluded that Z. officinale extract can be used effectively in the production of potential antioxidant and antimicrobial AgNPs for commercial application.Inspec keywords: nanoparticles, cancer, organic compounds, antibacterial activity, particle size, microorganisms, silver, visible spectra, ultraviolet spectra, biomedical materials, biochemistry, nanofabrication, free radicals, nanomedicine, toxicology, cellular biophysics, transmission electron microscopyOther keywords: unique approach, eco‐friendly approach, zingiber officinale, reducing agent, stabiliser agent, transmission electron microscopy results, antibacterial agents, free radical scavenging activity, synthesised AgNPs, 1‐diphenyl‐2‐picryl‐hydrazyl free radical scavenging, strong bactericidal activity, antimicrobial AgNPs, autoclave‐assisted synthesis, antioxidant activities, cytotoxic effect, silver nanoparticles, autoclave, time 24.0 hour     

Immobilization of ZnO on Chitosan-Neem seed composite for enhanced thermal and antibacterial activity

Natural and inorganic materials of Chitosan-Zinc oxide-Neem seed (CS-ZnO-NS) hybrid composite were synthesized by chemical precipitation method. The obtained CS-ZnO-NS hybrid composites were characterized for functional group confirmation by Fourier transform infrared spectroscopy and UV–Visible spectroscopy. The ZnO particles connected to biopolymers exhibited small grains and rod, bullet like structure confirmed by scanning electron microscopy and transmission electron microscopy analysis. The size of the prepared CS-ZnO-NS hybrid composite was found to be 20–80?nm. The crystalline behaviors were determined by X-ray diffraction analysis. The surface area of the prepared hybrid composite was determined using BET analysis. The elemental composition was analyzed by energy dispersive X-ray spectroscopy and thermal behaviors by thermo gravimetric analysis. The obtained result shows that zinc oxide was well able to incorporate into chitosan-neem seed composite which enhances the thermal stability. Further, the antibacterial activity evaluated by agar well diffusion method against Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli bacteria exhibits higher inhibition effect because of ZnO particles presence in the chitosan-neem seed. Hence the CS-ZnO-NS is a promising material for biomedical applications.     

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 N-halamine-functionalized silica-polymer core-shell nanoparticles and their enhanced antibacterial activity

N-halamine-functionalized silica-polymer core-shell nanoparticles with enhanced antibacterial activity were synthesized through the encapsulation of silica nanoparticles as support with polymeric N-halamine. The as-synthesized nanoparticles were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive x-ray spectrometry (EDX), dynamic light scattering (DLS), thermogravimetric analysis (TGA), and Fourier transform infrared (FTIR). These N-halamine-functionalized silica-polymer core-shell nanoparticles displayed powerful antibacterial performance against both Gram-positive bacteria and Gram-negative bacteria, and their antibacterial activities have been greatly improved compared with their bulk counterparts. Therefore, these N-halamine-functionalized silica-polymer core-shell nanoparticles have the potential for various significant applications such as in medical devices, healthcare products, water purification systems, hospitals, dental office equipment, food packaging, food storage, household sanitation, etc.     

Role of Ribes khorassanicum in the biosynthesis of AgNPs and their antibacterial properties

Silver nanoparticles (AgNPs) have been biosynthesised through the extracts of Ribes khorassanicum fruits, which served as the reducing agents and capping agents. Biosynthesised AgNPs have been found to be ultraviolet–visible (UV–vis) absorption spectra since they have displayed one surface plasmon resonance peak at 438 nm, attesting the formation of spherical NPs. These particles have been characterised by UV–vis, field‐emission scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, and transmission electron microscopy analysis. The formation of AgNPs at 1.0 mM concentration of AgNO₃ has resulted in NPs that contained mean diameters in a range of 20–40 nm. The green‐synthesised AgNPs have demonstrated high antibacterial effect against pathogenic bacteria (i.e. Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa). Biosynthesising metal NPs through plant extracts can serve as the facile and eco‐friendly alternative for chemical and/or physical methods that are utilised for large‐scale nanometal fabrication in various medical and industrial applications.Inspec keywords: X‐ray diffraction, X‐ray chemical analysis, nanofabrication, surface plasmon resonance, nanoparticles, antibacterial activity, microorganisms, scanning electron microscopy, silver, nanomedicine, visible spectra, ultraviolet spectra, transmission electron microscopy, Fourier transform infrared spectra, field emission scanning electron microscopy, biomedical materialsOther keywords: antibacterial properties, silver nanoparticles, reducing agents, capping agents, surface plasmon resonance peak, spherical NPs, field‐emission scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, X‐ray diffraction, transmission electron microscopy analysis, plant extracts, ultraviolet‐visible absorption spectra, Fourier transform infrared spectroscopy, antibacterial effect, Ribes khorassanicum fruits, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, surface plasmon resonance, AgNO₃ , Ag     

Preparation of an optimized ciprofloxacin-loaded chitosan nanomicelle with enhanced antibacterial activity

Objective: The objective of this study was to evaluate the effect of lipid structure on physicochemical properties of chitosan-fatty acid nanomicelles and prepare an optimum ciprofloxacin-loaded formulation from these conjugates which could enhance the antibacterial effects of drug against some important pathogens like P. aeruginosa.

Significance: Nowadays, resistance in infectious diseases is a growing worldwide concern. Nanocarriers can increase the therapeutic index and consequently reduce the antibiotic resistance. By site-specific delivery of drug, the adverse effects of broad-spectrum antibiotics such as ciprofloxacin would be reduced.

Methods: Fatty acid grafted chitosan conjugates were synthetized in the presence of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide. The effects of fatty acid type (stearic acid, palmitic acid, and linoleic acid) on physicochemical properties of conjugates were investigated. Ciprofloxacin was encapsulated in nanomicelles by thin film hydration method. Also, the preparation process was optimized with a central composite design. The antibacterial effect of optimum formulation against P. aeruginosa, K. pneumoniae, and S. pneumoniae species was determined.

Results: All conjugates were synthetized with high yield values and the substitution degrees ranged between 2.13 and 35.46%. Ciprofloxacin was successfully encapsulated in nanomicelles. The optimum formulation showed high drug loading (≈?19%), with particle size of about 260?nm and a sustained release profile of ciprofloxacin. The minimum inhibitory concentrations of ciprofloxacin in optimum formulation against P. aeruginosa and K. pneumoniae species were 4 and 2 times lower in comparison with the free drug, respectively.

Conclusions: The antibacterial effect of ciprofloxacin was improved by encapsulation of drug in chitosan nanomicelles.     

Embedding ultrasmall Ag nanoclusters in Luria-Bertani extract via light irradiation for enhanced antibacterial activity

Nano Research - Ultrasmall silver nanoclusters (Ag NCs) with rich surface chemistry and good biocompatibility are promising in antibacterial application, however, further development of Ag NCs for...     

Antibiotic-decorated titanium with enhanced antibacterial activity through adhesive polydopamine for dental/bone implant

Implant-associated infections, which are normally induced by microbial adhesion and subsequent biofilm formation, are a major cause of morbidity and mortality. Therefore, practical approaches to prevent implant-associated infections are in great demand. Inspired by adhesive proteins in mussels, here we have developed a novel antibiotic-decorated titanium (Ti) material with enhanced antibacterial activity. In this study, Ti substrate was coated by one-step pH-induced polymerization of dopamine followed by immobilization of the antibiotic cefotaxime sodium (CS) onto the polydopamine-coated Ti through catechol chemistry. Contact angle measurement and X-ray photoelectron spectroscopy confirmed the presence of CS grafted on the Ti surface. Our results demonstrated that the antibiotic-grafted Ti substrate showed good biocompatibility and well-behaved haemocompatibility. In addition, the antibiotic-grafted Ti could effectively prevent adhesion and proliferation of Escherichia coli (Gram-negative) and Streptococcus mutans (Gram-positive). Moreover, the inhibition of biofilm formation on the antibiotic-decorated Ti indicated that the grafted CS could maintain its long-term antibacterial activity. This modified Ti substrate with enhanced antibacterial activity holds great potential as implant material for applications in dental and bone graft substitutes.     

One-step synthesis and characterization of anisotropic silver nanoparticles: application for enhanced antibacterial activity of natural fabric

A simple one-step chemical reduction method was employed for the synthesis of truncated triangular silver nanoparticles (Ag-NPs). The reduction of Ag ions by sodium borohydride was performed in the presence of poly(vinyl pyrrolidone) as a stabilizing agent. The synthesized Ag-NPs were characterized by UV–Vis spectroscopy, transmission electron microscopy, dynamic light scattering, FT-Raman spectrometer and X-ray diffraction in order to study optical, morphological, compositional, and structural properties. The UV–Vis spectrum showed three plasmon peaks located at 340, 412, and 700 nm, confirmed the anisotropic Ag-NPs. The average edge length of 22 ± 5 nm was observed from TEM images for truncated triangular Ag-NPs. From XRD pattern it was confirmed that the Ag-NPs were polycrystalline in nature, with preferential orientation along (111) lattice plane. The antibacterial susceptibility of Ag-NPs-treated fabrics were tested by Kirby–Bauer disk-diffusion test and American Association of Textile Chemists and Colorists (AATCC) test method 100-2004 against Gram-positive and Gram-negative bacteria. The Ag-NPs treated fabrics showed more pronounced antibacterial activity against Gram-negative bacteria than that of Gram-positive bacteria.     

Study of mechanism of enhanced antibacterial activity by green synthesis of silver nanoparticles

The extensive use of silver nanoparticles needs a synthesis process that is greener without compromising their properties. The present study describes a novel green synthesis of silver nanoparticles using Guava (Psidium guajava) leaf extract. In order to compare with the conventionally synthesized ones, we also prepared Ag-NPs by chemical reduction. Their optical and morphological characteristics were thoroughly investigated and tested for their antibacterial properties on Escherichia coli. The green synthesized silver nanoparticles showed better antibacterial properties than their chemical counterparts even though there was not much difference between their morphologies. Fourier transform infrared (FTIR) spectroscopic analysis of the used extract and as-synthesized silver nanoparticles suggests the possible reduction of Ag(+) by the water-soluble ingredients of the guava leaf like tannins, eugenol and flavonoids. The possible reaction mechanism for the reduction of Ag(+) has been proposed and discussed. The time-dependent electron micrographs and the simulation studies indicated that a physical interaction between the silver nanoparticles and the bacterial cell membrane may be responsible for this effect. Based on the findings, it seems very reasonable to believe that this greener way of synthesizing silver nanoparticles is not just an environmentally viable technique but it also opens up scope to improve their antibacterial properties.     

Anticancer activity of green synthesised AgNPs from Cymbopogon citratus (LG) against lung carcinoma cell line A549

The present study is designed to analyse the antibacterial and anticancer effects of silver nanoparticles (AgNPs) synthesised from the Cymbopogon citratus, (lemongrass) (LG‐AgNPs), which is widely used in ayurvedic drugs for treating various diseases. The LG‐AgNPs were synthesised and characterised using ultraviolet (UV) spectroscopy, Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD) and transmission electron microscopy (TEM) analysis. The characterised LG‐AgNPs was subjected to antimicrobial analysis by disc diffusion method against pathogenic bacteria and fungi. Furthermore, the cytotoxicity and anticancer activity of the LG‐AgNPs were assessed with lung alveolar carcinoma cell line A549. Results depict that UV–visible spectra of LG‐AgNPs showed strong absorption peak at 435 nm. The XRD study exposed LG‐AgNPs crystals, which confirmed with TEM analysis exhibiting particle size ranging between 17 and 25.8 nm. The FTIR spectra recorded peaks at 3347, 2126, 1639, 659, 598 and 553 cm⁻¹. The zone of inhibition study proves the LG‐AgNPs possessed both antibacterial and antifungal activities. 3‐(4, 5‐dimethyl thiazoyl‐2‐yl)‐(2,5‐diphenyltetrazolium bromide) results show the cytotoxicity effect of LG‐AgNPs in lung cancer cells. It also inhibited the cell migration and invasion at the dose of 25 µg ml⁻¹ by increasing the apoptotic gene expression. The results reveal LG‐AgNPs possess anticancer activities, proposing that it may be an alternative drug for allopathic drugs with lots of side effects used in lung cancer treatment.Inspec keywords: particle size, Fourier transform spectra, nanomedicine, cellular biophysics, infrared spectra, X‐ray diffraction, antibacterial activity, microorganisms, diseases, nanoparticles, transmission electron microscopy, lung, cancer, toxicology, drugsOther keywords: anticancer activity, green synthesised AgNPs, LG‐AgNPs crystals, lung carcinoma cell line A549, Cymbopogon citratus     

Thermal conductivity of reclaimed asphalt pavement (RAP) and its constituents

Up to the present, most work on the use of reclaimed asphalt pavement (RAP) has been empirical in nature. Very recent advances have demonstrated that finite-element techniques can be effectively used for modelling asphalt mixing drums in order to optimise the relative proportions of new and recycled materials and to determine the amount of time required to achieve full melting inside of the drum. A necessary prerequisite for the modelling is a definitive knowledge of the thermal conductivities of RAP and its components. This need motivated the present experimental work which encompassed RAP particles, RAP particles with the asphalt binder removed, and pure asphalt binder of different degrees of ageing. Also evaluated were taconite tailings, residual rock from the processing of iron-containing ore, and sand. The tailings have been mentioned as a candidate aggregate. The conductivity results for the solid media were related to three metrics: (a) the size ranges of the solids, (b) the density of the sample as a whole and (c) the porosity of the sample. All of the conductivity results for the investigated solid media fell in the range from 17 to 30 W/m °C. The measured conductivities of the binder ranged from 0.17 to 0.19 W/m °C.     

Efficacy of mycosynthesised AgNPs from Earliella scabrosa as an in vitro antibacterial and wound healing agent

The silver nanoparticles (AgNPs) with their unique chemical and physical properties are proving as a new therapeutical agent. In the present study, the AgNPs synthesised from an aqueous extract of a macrofungus, Earliella scabrosa, were characterised by field emission scanning electron microscopy (FESEM), energy dispersive X‐ray analysis (EDX), high‐resolution transmission electron microscopy, X‐ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and further evaluate for its in vitro antibacterial and wound healing efficacy. The mycosynthesised AgNPs exhibited the surface plasmon resonance peak at 410 nm with good stability over a period of a month. The FESEM and EDX analyses revealed the spherical‐shaped AgNPs of an average size of 20 nm and the presence of elemental Ag, respectively. The XRD pattern showed the crystalline nature of AgNPs. The FTIR spectra confirmed the conversion of Ag⁺ ions to AgNPs due to reduction by biomolecules of macrofungus extract. The mycosynthesised AgNPs showed effective antibacterial activity against two Gram‐positive bacteria, namely Bacillus subtilis and Staphylococcus aureus, and two Gram‐negative bacteria Escherichia coli and Pseudomonas aeruginosa. The pathogens were highly sensitive to AgNPs, whereas less sensitive to AgNO₃. The mycosynthesised AgNPs showed significant wound healing potential with 68.58% of wound closure.Inspec keywords: surface plasmon resonance, wounds, X‐ray diffraction, nanoparticles, molecular biophysics, nanomedicine, antibacterial activity, biomedical materials, reduction (chemical), silver, microorganisms, X‐ray chemical analysis, nanofabrication, transmission electron microscopy, particle size, field emission scanning electron microscopy, Fourier transform infrared spectraOther keywords: high‐resolution transmission electron microscopy, healing efficacy, mycosynthesised AgNPs, spherical‐shaped AgNPs, wound healing agent, in vitro antibacterial efficacy, Earliella scabrosa, silver nanoparticles, physical properties, chemical properties, therapeutical agent, aqueous extract, macrofungus, field emission scanning electron microscopy, FESEM, energy dispersive X‐ray analysis, EDX, X‐ray diffraction, XRD, Fourier transform infrared spectroscopy, FTIR spectroscopy, surface plasmon resonance peak, crystalline nature, biomolecules, Gram‐positive bacteria, Bacillus subtilis, Staphylococcus aureus, Gram‐negative bacteria, Escherichia coli, Pseudomonas aeruginosa, pathogens, wound closure, Ag     

Analysis of the size reduction of AgNPs loaded hydrogel and its effect on the anti‐bacterial activity

This article analyses the effect of the size reduced Silver (Ag) loaded hydrogel by (a) lyophilisation (S1) (b) ball milling (S2) techniques and its effect on anti‐bacterial activity. The g loaded hydrogel, S1 and S2 shows an increase in swelling with an increase in pH. The swelling is more for Ag loaded hydrogel in low pH. For pH above 7, the swelling ratio of Ag loaded hydrogel and S1 are almost the same while S2 shows very less swelling. The anti‐bacterial studies reveal that S1 and Ag loaded hydrogel reacted well in S. aureus (Staphylococcus aureus) but no zone formation was seen in S2 .whereas no zone was formed in S1 and S2 for E‐coli (Escherichia coli). As the next step, the anti‐bacterial activity of Ag loaded hydrogel with the addition of curcumin (CS1―size reduced by lyophilisation, CS2―size reduced by ball milling) and turmeric (TS1―size reduced by lyophilisation, TS2―size reduced by ball milling) were investigated. In case of E.coli, a zonal formation of 1.2 cm for TS1 and 1.1 cm for TS2 and 1 cm for CS1 and 0.2 cm for CS2 was observed. For S.aureus, 1.1  and 1 cm were seen for TS1 and CS1. TS2 and CS2 did not show any zone formation. These studies clearly show that size reduction by lyophilisation (S1, TS1 and CS1) is more efficient in all the cases when compared to the ball milling technique (S2, TS2 and CS2). Comparing TS1 with S1 and CS1, TS1 has highly efficient/effective anti‐bacterial properties than S1 and CS1. Therefore, lyophilised hydrogel incorporating turmeric and silver (TS1) is an excellent choice compared to using curcumin for wound dressing applications.     

Preparation of mesoporous tantalum oxide and its enhanced photocatalytic activity

Mesoporous Ta₂O₅ was synthesized by a surfactant-assisted sol-gel method under mild condition. Based on XRD pattern, the products, obtained by calcination at 600 and 700 °C, were found to be in the amorphous and the orthorhombic phases, respectively. The morphology and pore structure of the products were characterized by SEM, TEM and nitrogen adsorption-desorption measurements. The photocatalytic activity was evaluated by measuring the degradation of methylene blue under UV irradiation. Mesoporous orthorhombic Ta₂O₅ showed higher photocatalytic activity than that of the mesoporous sample in the amorphous state, although orthorhombic Ta₂O₅ had a lower surface area. The reason of this enhanced photocatalytic property is discussed.     

Hybrid nanostructured Ag/ZnO decorated powder cellulose fillers for medical plastics with enhanced surface antibacterial activity

Hybrid inorganic–organic fillers based on nanostructured silver/zinc oxide decorations on micro-cellulose carrier particles were prepared by stepwise microwave assisted hydrothermal synthesis using soluble salts as precursors of silver and zinc oxide. Hexamethylenetetramine was used as precipitating agent for zinc oxide and reducing agent for silver. The inorganics covered all available surfaces of the cellulose particles with a morphology resembling a coral reef. Prepared particulate fillers were compounded to medical grade poly(vinyl chloride) matrix. Scanning electron microscopy and powder X-ray diffractometry were used to investigate the morphology and crystalline phase structure of fillers. The scanning electron microscopy was used for morphological study of composites. With respect to prospective application, the composites were tested on electrical and antibacterial properties. A small effect of water absorption in polymer composites on their dielectric properties was observed but no adverse effect of water exposure on prepared materials was manifested. Electrical conductivity of fillers and composites was measured and no influence of water soaking of composites was found at all. The surface antibacterial activity of prepared composites was evaluated according to the standard ISO 22196. Excellent performance against Escherichia coli and very high against Staphylococcus aureus was achieved.     

Preparation and characterization of novel gelatin/cerium (III) fiber with antibacterial activity

Gelatin/Cerium (III) fibers with high tensile strength and good antibacterial activity were prepared by wet spinning method. The fiber structure and properties were investigated. The optical microscope (OPM) results showed that the fiber had a smooth surface and the fiber diameter was in the range of 60-90 µm. The mechanical properties tests showed that the tensile strength of gelatin/cerium (III) fibers increased greatly compared with the pure gelatin fibers. Furthermore, it was found that the gelatin/Ce (III) fibers have the antibacterial activity for Escherichia coli and Staphylococcus aureus.