Antioxidant efficacy of chitosan/graphene functionalized superparamagnetic iron oxide nanoparticles

The antioxidant potential of superparamagnetic iron oxide nanoparticles functionalized with chitosan and graphene were examined in the present work. Coprecipitation technique was followed for the synthesis of iron oxide nanoparticles. Graphene-iron oxide nanocomposites were synthesized by mechanical mixing followed by the heat treatment at moderate temperature. The chitosan coated iron oxide nanoparticles were prepared by dispersing nanoparticles in chitosan solution. The nanoparticles/nanocomposites were characterized using XRD, SEM, TEM and HAADF-STEM for phase structure, morphology and elemental analysis. The superparamagnetic behavior of nanoparticles/nanocomposites were confirmed by magnetic measurements using vibrating sample magnetometry. Antioxidant efficacy of these nanoparticles/nanocomposites were investigated in terms of free radical scavenging and reducing potential using an array of in vitro assay system. Ferric reducing antioxidant power (FRAP) and 2,2′-diphenyl-1-picrylhydrazyl (DPPH) were used for the antioxidant capacity. The investigation suggests that the graphene improves the antiradical response of iron oxide nanoparticles at higher concentration which is almost comparable to the ascorbic acid used as standard.     

Ibrutinib conjugated surface-functionalized multiwalled carbon nanotubes and its biopolymer composites for targeting prostate carcinoma

In this report, nanocomposites are composed of surface-functionalized multi-walled carbon nanotubes (f-MWCNTs) and polymers (polyethylene glycol, chitosan) or silver nanoparticles (AgNPs) were successfully synthesized and used as nanocarriers for drug delivery. The drug (Ibrutinib, Ibr) encapsulated with different nanocomposites was used for effective prostate cancer treatment. The as-prepared bioconjugates were confirmed by Fourier transform infrared spectroscopy, X-ray diffraction, and Raman spectroscopy. The drug loading efficiency of 95.5% was achieved for f-MWCNTs/AgNPs composite. The drug release profile showed that the f-MWCNTs/AgNPs composite released 79% in 84 h at pH 5.5 indicating the sustainable drug release. Further, these Ibr-loaded nanocomposites were conjugated with T₃₀ oligonucleotides (T₃₀ ODN) for targeting over-expressed prostate-specific membrane antigen in the prostate gland. The prostate anti-cancer activity was evaluated using PC-3 and MDA-MB-231 cancer cells and the results indicated that the Ibr- loaded nanocomposites conjugated with T₃₀ ODN exhibited higher cell killing efficiency compared to the free Ibr. Therefore, these conjugated nanocomposites are effective drug delivery systems for prostate cancer disease targeted therapy.

     

Lyophilized insulin nanoparticles prepared from quaternized N-aryl derivatives of chitosan as a new strategy for oral delivery of insulin: in vitro,ex vivo and in vivo characterizations

Objective: The purpose of this research was the development, in vitro, ex vivo and in vivo characterization of lyophilized insulin nanoparticles prepared from quaternized N-aryl derivatives of chitosan.

Methods: Insulin nanoparticles were prepared from methylated N-(4-N,N-dimethylaminobenzyl), methylated N-(4 pyridinyl) and methylated N-(benzyl). Insulin nanoparticles containing non-modified chitosan and also trimethyl chiotsan (TMC) were also prepared as control. The effects of the freeze-drying process on physico-chemical properties of nanoparticles were investigated. The release of insulin from the nanoparticles was studied in vitro. The mechanism of the release of insulin from different types of nanoparticles was determined using curve fitting. The secondary structure of the insulin released from the nanoparticles was analyzed using circular dichroism and the cell cytotoxicity of nanoparticles on a Caco-2 cell line was determined. Ex vivo studies were performed on excised rat jejunum using Frantz diffusion cells. In vivo studies were performed on diabetic male Wistar rats and blood glucose level and insulin serum concentration were determined.

Results: Optimized nanoparticles with proper physico-chemical properties were obtained. The lyophilization process was found to cause a decrease in zeta potential and an increase in PdI as well as and a decrease in entrapment efficiency (EE%) and loading efficiency (LE%) but conservation in size of nanoparticles. Atomic force microscopy (AFM) images showed non-aggregated, stable and spherical to sub-spherical nanoparticles. The in vitro release study revealed higher release rates for lyophilized compared to non-lyophilized nanoparticles. Cytotoxicity studies on Caco-2 cells revealed no significant cytotoxicity for prepared nanoparticles after 3-h post-incubation but did show the concentration-dependent cytotoxicity after 24?h. The percentage of cumulative insulin determined from ex vivo studies was significantly higher in nanoparticles prepared from quaternized aromatic derivatives of chitosan. In vivo data showed significantly higher insulin intestinal absorption in nanoparticles prepared from methylated N-(4-N, N-dimethylaminobenzyl) chitosan nanoparticles compared to trimethyl chitosan.

Conclusion: These data obtained demonstrated that as the result of optimized physico-chemical properties, drug release rate, cytotoxicity profile, ex vivo permeation enhancement and increased in vivo absorption, nanoparticles prepared from N-aryl derivatives of chitosan can be considered as valuable method for the oral delivery of insulin.     

Silver nanoparticle-loaded chitosan–starch based films: Fabrication and evaluation of tensile,barrier and antimicrobial properties

The fabrication of silver nanoparticles was accomplished by γ-ray irradiation reduction of silver nitrate in a chitosan solution. The obtained nanoparticles were stable in the solution for more than six months, and showed the characteristic surface plasmon band at 411 nm as well as a positively charged surface with 40.4 ± 2.0 mV. The silver nanoparticles presented a spherical shape with an average size of 20–25 nm, as observed by TEM. Minimum inhibitory concentration (MIC) against E. coli, S. aureus and B. cereus of the silver nanoparticles dispersed in the γ-ray irradiated chitosan solution was 5.64 µg/mL. The silver nanoparticle-loaded chitosan–starch based films were prepared by a solution casting method. The incorporation of silver nanoparticles led to a slight improvement of the tensile and oxygen gas barrier properties of the polysaccharide-based films, with diminished water vapor/moisture barrier properties. In addition, silver nanoparticle-loaded films exhibited enhanced antimicrobial activity against E. coli, S. aureus and B. cereus. The results suggest that silver nanoparticle-loaded chitosan–starch based films can be feasibly used as antimicrobial materials for food packaging and/or biomedical applications.     

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     

Structural analysis of graphene oxide/silver nanocomposites: optical properties,electrochemical sensing and photocatalytic activity

In the present study, graphene oxide/silver (GO/Ag) nanocomposites were synthesized via a facile simple one pot chemical reduction method using ethylene glycol/sodium borohydrate (EG/NaBH₄) as solvent and reducing agent. GO was selected as a substrate and stabilizer to prepare GO/Ag nanocomposites. The synthesized GO/Ag nanocomposites were characterized by a series of techniques. Highly monodispersed stable crystalline silver nanoparticles having a face-centered cubic (fcc) phase were confirmed by X-ray powder diffraction (XRD) on GO signature. Scanning electron microscopy images showed that Ag nanoparticles are deposited on the GO sheet with a narrow size distribution. Transmission electron microscopy observations revealed that large numbers of Ag nanoparticles were uniformly distributed on GO sheet and well separated with an average size of 18 nm. Ultraviolet–visible (UV–Vis) spectroscopic results showed the peak of GO and surface plasmon resonance (SPR) of Ag nanoparticles. The SPR property of GO/Ag nanocomposites showed that there was an interaction between Ag nanoparticles and GO sheet. The intensities of the Raman signal of GO/Ag nanocomposites are gradually increased with attachment of Ag nanoparticles i.e. there is surface-enhanced Raman scattering activity. Electrochemical investigations indicated that the nanocomposites possessed an excellent performance for detecting towards 4-nitrophenol. An application of the obtained GO/Ag nanocomposites as a catalyst in the reduction of 4-nitrophenol to 4-aminophenol by NaBH₄ was demonstrated. The GO/Ag nanocomposites exhibited high activity and stability for the catalytic reduction of 4-nitrophenol. The prepared GO/Ag nanocomposites act as photo-catalysts.     

Solar photocatalytically active,engineered silver nanoparticle synthesis using aqueous extract of mesocarp of Cocos nucifera (Red Spicata Dwarf)

ABSTRACT

Silver nanoparticles synthesised using aqueous extract of Cocos nucifera (CN) mesocarp were evaluated for their photocatalytic activity under solar irradiation. The silver nanoparticles were synthesised by a green method of harnessing bioactive phytocomponents from the mesocarp of Cocos nucifera. Large-scale application of this process necessitates the manoeuvering of the process parameters for increasing the conversion of silver ions to nanoparticles. Process parameters influencing the morphological characteristics of silver nanoparticles such as precursor salt concentration and pH of the synthesis mixture were studied. The crystalline nanoparticles were characterised using UV-vis spectroscopy, XRD, FTIR, SEM and EDX analysis. CN extract and 5 mM silver nitrate solution at a ratio of 1:4 (v/v) in the synthesis mixture was found to be the optimum. Alkaline initial pH of the synthesis mixture was found to favour the synthesis of smaller sized monodispersed silver nanoparticles. Solar energy was harnessed for the photocatalytic degradation of Malachite green dye using silver nanoparticles obtained through the green synthesis method. Overall process aims at utilisation of naturally available resource for the synthesis of silver nanoparticles as well as the degradation of dyes using these nanoparticles, making it useful in the treatment of wastewater.     

Facile synthesis and application of Ag-chemically converted graphene nanocomposite

An in situ chemical synthesis approach has been employed to prepare an Ag-chemically converted graphene (CCG) nanocomposite. The reduction of graphene oxide sheets was accompanied by generation of Ag nanoparticles. The structure and composition of the nanocomposites were confirmed by means of transmission electron microscopy (TEM), atomic force microscopy (AFM) and X-ray diffraction. TEM and AFM results suggest a homogeneous distribution of Ag nanoparticles (5–10 nm in size) on CCG sheets. The intensities of the Raman signals of CCG in such nanocomposites are greatly increased by the attached silver nanoparticles, i.e., there is surface-enhanced Raman scattering activity. In addition, it was found that the antibacterial activity of free Ag nanoparticles is retained in the nanocomposites, which suggests they can be used as graphene-based biomaterials.      

In-situ preparation of epoxy/silver nanocomposites by thermal decomposition of silver–imidazole complex

A novel method for the preparation of epoxy/silver nanocomposites was developed by in-situ formation of silver nanoparticles within the epoxy matrix. The silver–imidazole complex was synthesized by silver acetate and 2-ethyl-4-methylimidazole (2E4MZ). During the cure of epoxy resin, silver nanoparticles were in-situ generated through thermal decomposition of the silver–imidazole complex which was capable of reducing Ag⁺ to Ag⁰ by itself. The simultaneously released imidazole could cure the epoxy. In addition, the in-situ generated silver nanoparticles could be stabilized by the formed epoxy network. Therefore, by using the thermal decomposition method, uniformly dispersed silver nanoparticles of size of around 11.6 nm were in-situ generated in epoxy matrix.     

Synthesis of Starch-Stabilized Silver Nanoparticles and Their Antimicrobial Activity

In this study, silver nanoparticles were prepared using silver nitrate as the metal precursor, starch as protecting agent, and sodium borohydride (NaBH₄) as a reducing agent by the chemical reduction method. The formation of the silver nanoparticles was monitored using ultraviolet-visible absorption spectroscopy, cyclic voltammetry, and particle size analyzer and characterized by transmission electron microscopy (TEM) and x-ray diffraction (XRD). Synthesis of nanoparticles were carried out by varying different parameters, such as reaction temperature, concentration of reducing agent, concentration of silver ion in feed solution, type and concentration of the stabilizing agent, and stirrer speed expressed in terms of particle size and size distribution. Dispersion destabilization of colloidal nanoparticles was detected by Turbiscan. It was observed that size of the starch stabilized silver nanoparticles were lower than 10 nm. The microbial activity of synthesized silver nanoparticles was examined by modified Kirby-Bauer disk diffusion method. Silver nanoparticles were tested for their antibacterial activity against Gram negative bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Gram positive bacteria such as Staphylococcus aureus and Staphylococcus epidermidis. High bacterial activity was observed at very low concentrations of silver (below 1.39 μg/ml). The antifungal activity of silver nanoparticles has been assayed against Candida albicans.     

Properties of polypropylene nanocomposites containing silver nanoparticles

Silver/polypropylene (PP) nanocomposites containing silver nanoparticles smaller than 10 nm were prepared using a new synthetic method. AgNO3 crystals were dissolved into hydrophilic domain of polyoxyethylene maleate-based surfactant (PEOM), which gives self-assembly nano-structures. The AgNO3 in the nano-domains of PEOM was reduced by NaBH4 to form nanoparticles. The colloidal solutions with silver nanoparticles were diluted with ethanol and were mixed with PP pellets. Silver nanocomposites were prepared by extrusion compounding process after drying the pellets. Contents of silver nanoparticles dispersed within PP resin were changed from 100 to 1000 ppm. Formation of silver nanoparticles within PP was confirmed by UV-Vis spectroscopy and TEM. Size and distribution of dispersed silver nanoparticles were also measured by TEM. Silver/PP nanocomposites films showed not only improved thermal stability but also increased mechanical properties compared to neat PP film. Tensile properties of PP nanocomposites were largely improved compared with neat PP resin, and elongation increased also by 175% for the nanocomposites containing 1000 ppm silver nanoparticles.     

Green synthesis of silver nanoparticles from purple acid phosphatase apoenzyme isolated from a new source Limonia acidissima

Green synthesis of nanoparticles is regarded as a safe and non-toxic process whereas conventional synthesis using chemical methods produces toxic substance. This study provides a novel insight for enzymatic synthesis method of silver nanoparticles using purple acid phosphatase, isolated from Limonia acidissima (wood apple) as a new source and used in the synthesis of silver nanoparticles. Stable silver nanoparticles were produced by sonochemical method using apoenzyme as a stabilising and capping agent and were characterised by various physicochemical techniques like UV–Visible spectroscopy, Fourier-transform infrared, X-ray diffraction and transmission electron microscopy. X-ray study shows that nanoparticles are composed of silver and silver oxide. The synthesised nanoparticles exhibited excellent antimicrobial activity against Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus.     

Design,characterization and ex vivo evaluation of chitosan film integrating of insulin nanoparticles composed of thiolated chitosan derivative for buccal delivery of insulin

The purpose of this study is to optimize and characterize of chitosan buccal film for delivery of insulin nanoparticles that were prepared from thiolated dimethyl ethyl chitosan (DMEC-Cys). Insulin nanoparticles composed of chitosan and dimethyl ethyl chitosan (DMEC) were also prepared as control groups. The release of insulin from nanoparticles was studied in vitro in phosphate buffer solution (PBS) pH 7.4. Optimization of chitosan buccal films has been carried out by central composite design (CCD) response surface methodology. Independent variables were different amounts of chitosan and glycerol as mucoadhesive polymer and plasticizer, respectively. Tensile strength and bioadhesion force were considered as dependent variables. Ex vivo study was performed on excised rabbit buccal mucosa. Optimized insulin nanoparticles were obtained with acceptable physicochemical properties. In vitro release profile of insulin nanoparticles revealed that the highest solubility of nanoparticles in aqueous media is related to DMEC-Cys nanoparticles. CCD showed that optimized buccal film containing 4% chitosan and 10% glycerol has 5.81?kg/mm² tensile strength and 2.47?N bioadhesion forces. Results of ex vivo study demonstrated that permeation of insulin nanoparticles through rabbit buccal mucosa is 17.1, 67.89 and 97.18% for chitosan, DMEC and DMEC-Cys nanoparticles, respectively. Thus, this study suggests that DMEC-Cys can act as a potential enhancer for buccal delivery of insulin.     

Sulfobutylether-β-cyclodextrin/chitosan nanoparticles enhance the oral permeability and bioavailability of docetaxel

The aim of this research is to develop novel chitosan nanoparticles including cyclodextrins complexes for docetaxel (DTX), evaluate the performance of nanoparticles which could enhance the oral permeability and bioavailability of DTX in vitro and in vivo. DTX/sulfobutylether-β-cyclodextrin inclusion complexes were made and it was the main ingredient to prepare the DTX/sulfobutylether-β-cyclodextrin/chitosan nanoparticles due to their promising physicochemical properties. DTX/sulfobutylether-β-cyclodextrin/chitosan nanoparticles were prepared by the ionic gelation of chitosan with tripolyphosphate in the presence of cyclodextrins. Results indicated that DTX/sulfobutylether-β-cyclodextrin inclusion complexes and docetaxel/sulfobutylether-β-cyclodextrin/chitosan nanoparticles both had good performances in the studies of release and the rat small intestinal absorption in vitro. DTX/sulfobutylether-β-cyclodextrin/chitosan nanoparticles showed preferable capability in improving the small intestinal absorption and inhibiting the efflux of DTX. In pharmacokinetics study, the DTX/sulfobutylether-β-cyclodextrin/chitosan nanoparticles increased the AUC_0→t and decreased the clearance significantly, and the oral relative bioavailability of the DTX/sulfobutylether-β-cyclodextrin/chitosan nanoparticles was as high as 1447.53% compared to the pure DTX formulation. The DTX/sulfobutylether-β-cyclodextrin/chitosan nanoparticles prepared in this study have a good prospect for oral administration as an alternative of current DTX formulations.     

Modeling of Silver Nanoparticle Synthesis in Ternary Reverse Microemulsion of Cyclohexane/Water/SDS

In the present study, a simple mathematical model has been developed for synthesis of silver nanoparticles. The silver nanoparticles have been synthesized in ternary reverse microemulsion of cyclohexane/water/sodium dodecyl sulfate (SDS). The silver nanoparticles were produced by reaction between silver nitrate in the water droplet core of one microemulsion and hydrazine as reducing agent in the water droplet core of another microemulsion. The dynamic behavior of process was modeled on mass balance equations which were solved using the finite difference method. The kinetic parameters of the critical number size (N _crit ), rate order of nucleation, and growth constants were estimated by minimizing the difference between the average particle size predicted by model and those obtained by experiments. The UV-Vis absorption spectra, transmission electron microscopy (TEM), x-ray diffraction (XRD), x-ray photoelectron spectroscopy (XPS), and dynamic light scattering (DLS) were used to analyze the structure and particle size distribution of silver nanoparticles.     

Antibacterial properties of padded PP/PE nonwovens incorporating nano-sized silver colloids

This paper deals with the effects that nano-sized silver colloids have on the antibacterial properties of PE/PP nonwovens against three kinds of bacteria: Staphylococcus aureus, Klebsiella pneumoniae, and Escherichia coli. These silver colloids comprise silver nanoparticles that are a non-toxic and non-tolerant disinfectant. PE/PP nonwovens are used as back sheets or coverstocks of baby diapers, adult diapers, sanitary napkins, and wipes. These materials are readily contaminated by bacteria present in moisture and dirt and can cause disease. We finished the nonwovens using a normal dipping–pad–dry method. From SEM images, we determined that the silver nanoparticles were generally dispersed well on the surface of the nonwoven fibers. We used the AATCC-100 test method to study the antibacterial properties of the treated fabrics. Bacteria were disinfected completely to below a count of 10 cells after 10 min when using the samples treated with 10 ppm of silver colloids. The ethanol-based silver/sulfur composite colloid (SNSE) has the best antibacterial efficacy when compared with the other nano-sized silver colloids. The silver particles having the smallest sizes gave the higher dispersibilities and the strongest antibacterial efficacies.     

The influence of triangular silver nanoplates on antimicrobial activity and color of cotton fabrics pretreated with chitosan

The effect of cotton fabric pretreatment with biopolymer chitosan (CHT) on deposition of colloidal triangular silver nanoplates was studied. Also, the influence of deposited silver nanoparticles on color and antimicrobial activity of cotton fabrics was evaluated. Characterization of colloidal silver nanoparticles as well as silver nanoparticles deposited on cotton fabrics was performed using electron microscopy (TEM and FESEM), XRD analysis, atomic absorption spectroscopy, UV–Vis absorption, and reflectance spectroscopy. The cotton fabric turned from white to blue color upon deposition of triangular silver nanoplates. Antimicrobial activity of CHT pretreated cotton fabric impregnated with silver nanoparticles was tested against Gram-negative bacteria Escherichia coli, Gram-positive bacteria Staphylococcus aureus, and fungi Candida albicans. Deposited silver nanoparticles imparted excellent antimicrobial properties to cotton fabric. The standard sterilization procedure of cotton fabric for antimicrobial activity testing resulted in color change of the fabric from blue to yellow. This color change is most likely consequence of transformation of triangular silver nanoplates into nanodiscs and/or their agglomeration into spheroids.     

Factors affecting the antibacterial activity of chitosan‐silver nanocomposite

This study provides the optimum preparation parameters of chitosan‐silver nanoparticles composite (CSNC) with promising antibacterial activity against the most common bacterial infections found on burn wounds. CSNC was synthesised by simple green chemical reduction method with different preparation factors. Chitosan was used to reduce silver nitrate and stabilise silver nanoparticles in the medium. For this reason, spectroscopic and microscopic techniques as, ultraviolet‐visible Fourier transform infrared spectroscopy and transmission electron microscopy were used in the study of the molecular and morphological properties of the resultant composites. Furthermore, the composite was assessed in terms of Ag‐ions release by AAS and its efficacy as antibacterial material. As a result, CSNC showed stronger antibacterial effect than its individual components (chitosan and silver nitrate solutions) towards Gram‐positive (Staphylococcus aureus) and Gram‐negative (Pseudomonas aeruginosa and Escherichia coli) bacteria. CSNC prepared in this study showed highest inhibition percentage of bacterial growth up to 96% at concentration of 220 μg/ml.Inspec keywords: silver, nanocomposites, nanoparticles, filled polymers, biomedical materials, nanomedicine, antibacterial activity, wounds, reduction (chemical), ultraviolet spectra, visible spectra, Fourier transform spectra, infrared spectra, transmission electron microscopy, microorganisms, nanofabricationOther keywords: antibacterial activity, chitosan‐silver nanocomposite, optimum preparation parameters, chitosan‐silver nanoparticles composite, CSNC, bacterial infections, burn wounds, green chemical reduction method, ultraviolet‐visible Fourier transform infrared spectroscopy, transmission electron microscopy, molecular properties, morphological properties, Gram‐positive bacteria, Gram‐negative bacteria, Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, bacterial growth, Ag     

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.     

Nickel oxide/polypyrrole/silver nanocomposites with core/shell/shell structure: Synthesis,characterization and their electrochemical behaviour with antimicrobial activities

Magnetic and conducting Nickel oxide–polypyrrole (NiO/PPy) nanoparticles with core–shell structure were prepared in the presence of Nickel oxide (NiO) in aqueous solution containing sodium dodecyl benzenesulfonate (SDBS) as a surfactant as well as dopant. A stable dispersion of silver (Ag) nanoparticles was synthesized by chemical (citrate reduction) method. NiO/PPy nanocomposites were added to the Ag colloid under stirring. Ag nanoparticles could be electrostatically attracted on the surface of NiO/PPy nanocomposites, leading to formation of NiO/PPy/Ag nanocomposites with core/shell/shell structure. The morphology, structure, particle size and composition of the products were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, cyclic voltammetry (CV) and current–voltage (I–V) analysis. The resultant nanocomposites have the good conductivity and excellent electrochemical and catalytic properties of PPy and Ag nanoparticles. Furthermore, the nanocomposites showed excellent antibacterial behaviour due to the presence of Ag nanoparticles in the composite. The thermal stability of NiO–PPy as well as NiO/PPy/Ag nanocomposites was higher than that of pristine PPy. Studies of IR spectra suggest that the increased thermal stability may be due to interactions between NiO and Ag nanoparticles with the PPy backbone.