Antifungal effect of green synthesised silver nanoparticles against Setosphaeria turcica

Green synthesis of silver nanoparticles (AgNPs) is an interesting issue of the nanoscience and nanotechnology due to their unique properties. In the present study, Ginkgo biloba L. leaf extract was used to synthesise AgNPs. The effects of quantity of leaves, concentration of Ag nitrate (AgNO₃), reaction temperature, and pH were studied to discover the optimal synthesis system. In addition, antifungal effect of AgNPs against Setosphaeria turcica was measured through inhibition zone method. The optimal biosynthesis system contained 15 g of leaf, 8 mM AgNO₃, and 80°C at pH 9.0. Under mentioned conditions, the resulting synthesised NPs were nearly spherical, with an average size of 14 nm. In tests, AgNPs synthesised at different pH resulted in different inhibition zones, diameters increased gradually at pH from 3.0 to 11.0, while antifungal effect reached maximum at 9.0. Results of this study offer a new approach for biological control plant pathogenic fungi, and it has potential application for screening novel fungistats with high efficiency and low toxicity.Inspec keywords: antibacterial activity, silver, nanoparticles, nanobiotechnology, pHOther keywords: antifungal effect, green synthesised silver nanoparticles, Setosphaeria turcica, nanoscience, nanotechnology, Ginkgo biloba L. leaf extract, reaction temperature, pH, inhibition zone method, inhibition zones, mass 15 g, temperature 80 degC, size 14 nm, Ag     

Effects of surface sterilisation with green synthesised silver nanoparticles on Lamiaceae seeds

Nanoparticles have been used in many areas of biotechnology. In this study, an alternative surface sterilisation method was established for plant tissue cultures. Silver nanoparticles synthesised via green synthesis were used for the surface sterilisation of Lamiaceae seeds (Salvia farinecae, Ocimum basilicum – Large Leaf Italian, Thymus vulgaris, Ocimum basilicum var. purpurascens). Water extracts of dried Alkanna tinctorum rhizomes and Syzygium aromaticum flowers were utilised in the bioreduction of silver ions. The seeds were exposed to 0, 1, 7, 14 and 28 day‐old colloidal solutions of silver nanoparticles and their effects on germination and surface sterilisation were determined. Fresh (0 and 1 day‐old) colloidal solutions of silver nanoparticles were found very effective on surface sterilisation (100%). Moreover, they showed no negative effect on both germination and morphology of plantlets. It was shown that silver nanoparticles can be used as a surface sterilisation agent and they have no adverse effects on seed germination and in vitro plantlet growth.Inspec keywords: nanoparticles, microorganisms, sterilisation (microbiological), silver, nanofabrication, antibacterial activity, colloids, nanobiotechnology, agricultureOther keywords: green synthesised silver nanoparticles, Lamiaceae seeds, silver ions, surface sterilisation agent, seed germination, colloidal solutions, surface sterilisation method, Ag     

Characterisation and antifungal activity of silver nanoparticles biologically synthesised by Amaranthus retroflexus leaf extract

ABSTRACT

Following the emergence of resistant fungal pathogens, silver nanoparticles (AgNPs) biosynthesized by plants have been recognized as promising tools to combat parasitic fungi. This study evaluated the potency of Amaranthus retroflexus in producing AgNPs, followed by testing their antifungal effects. The AgNPs exhibited a maximum absorption at 430 nm through ultraviolet-visible spectroscopy, while the X-ray diffraction indicated that they were crystal in nature. Fourier transform infrared spectroscopy confirmed the conversion of Ag⁺ ions to AgNPs due to the reduction by capping material of plant extract. The transmission electron microscope analysis further revealed that the AgNPs were spherical ranging from 10 nm to 32 nm in size. The AgNPs at the concentrations of 50, 100, 200, and 400 μg/mL were applied to the growth of plant, mushroom, and human pathogenic fungi. The 50% minimum inhibitory concentrations (MIC₅₀) against Macrophomina phaseolina, Alternaria alternata and Fusarium oxysporum were observed to be 159.80 ± 14.49, 337.09 ± 19.72, and 328.05 ± 13.29 μg/mL, respectively. However, no considerable inhibition was observed regarding Trichoderma harzianum or Geotrichum candidum. These findings may suggest A. retroflexus as a green solution for biosynthesizing AgNPs with potent antifungal activities against plant pathogenic fungi.     

Layer-by-layer deposition of green synthesised silver nanoparticles on polyester air filters and its antimicrobial activity

Silver nanoparticles stabilised with anionic polymeric polyelectrolytes were successfully synthesised by high-energy UV reduction. Three types of polyelectrolytes were used including poly(methacrylic acid) (PMA), poly(acrylic acid) (PAA) and poly(4-styrenesulphonic acid-co-maleic acid) (CoPSS). The formation of the prepared solutions exhibited surface plasmon resonance at the wavelength of 475, 730 and 408 nm by using PMA, PAA and CoPSS as the stabilising agents. UV–visible spectrophotometer, transmission electron microscope (TEM) and zeta potential analyser were employed to characterise the formation of the prepared solutions. The silver nanoparticles stabilised with anionic polyelectrolytes were immobilised on polyester air filters using a layer-by-layer technique. This is the sequential dipping of polyester air filters in a dilute solution of cationic poly(diallyldimethylammonium chloride) and anionic polymeric polyelectrolytes capped silver. The surface topography of the polyester air filters were measured by field emission scanning electron microscope. Results showed that silver nanoparticles had the highest surface coverage on the polyester air filters probably because it is a good bonding candidate and insures strong film growth. The multilayers polyester air filters coated silver nanoparticles were tested against the gram positive pathogen Staphylococcus aureus. The deposition of silver nanoparticles onto the polyester air filters resulted in 92.18%, 84.32% and 71.19% of bacteria removal using PMA, PAA and CoPSS as the stabilising agent.     

Seed germination and biochemical profile of Citrus reticulata (Kinnow) exposed to green synthesised silver nanoparticles

The biosynthesis of silver nanoparticles (AgNPs) is substantial for its applications in different fields. The Moringa oleifera leaves were used as reducing and stabilising agent for the biosynthesis of AgNPs. The synthesised AgNPs were characterised through UV–visible spectroscopy, zeta analyser, scanning electron microscopy (SEM) and energy dispersive Xray (EDX). In this study, effects of the synthesised AgNPs were also evaluated on nucellus tissues germination frequency and biochemical parameters of plant tissues. Nucellus tissues of Citrus reticulata were inoculated on MS medium supplemented with 10, 20, 30 and 40 µg/ml suspension of the synthesised AgNPs. Green synthesised AgNPs enhanced the in vitro germination because of low toxicity and nonfriendly issues. Significant results were obtained for germination parameters i.e. root and shoot length and seedling vigour index in response to 30 µg/ml suspension of green synthesised AgNPs. The 30 µ/ml suspension of AgNPs also enhanced antioxidant activity (41%) and SOD activity (0.36 nM/min/mg FW) while total phenolic content (4.7 µg/mg FW) and total flavonoid content (1.1 µg/mg FW) was significantly high when MS medium was fortified with 40 µg/ml suspension of the synthesised AgNPs. The content of total protein was significant (558 µg/BSA Eq/mg FW) in control plantlets as compared to the other treatments.Inspec keywords: antibacterial activity, ultraviolet spectra, X‐ray chemical analysis, proteins, microorganisms, biochemistry, nanofabrication, silver, nanotechnology, visible spectra, surface plasmon resonance, nanoparticles, suspensions, nanomedicine, scanning electron microscopy, electrokinetic effectsOther keywords: green synthesised silver nanoparticles, superoxide dismutase activity, biochemical profile, UV–visible spectroscopy, Citrus reticulata, green synthesised suspension, EDX detector, zeta potential, scanning electron microscopy, SEM, energy dispersive X‐ray, EDX, total phenolic content, total flavonoid content, size 423.0 nm to 425.0 nm, size 8.0 nm to 28.0 nm     

In vitro mutagenic and anti‐mutagenic properties of green synthesised silver nanoparticles

This study is aimed at determining the mutagenic and anti‐mutagenic properties of silver nanoparticles (AgNPs) biosynthesised from Streptomyces griseorubens AU2. To the authors’ knowledge, this is the first study about the investigation of these properties for biogenic AgNPs bacterially synthesised. The mutagenic and anti‐mutagenic potencies were determined by the Ames Salmonella /microsome mutagenicity test using Salmonella typhimurium TA98 and TA100 strains. After determining the cytotoxic dose of green synthesised AgNPs against S. typhimurium TA98 and TA100 strains, subcytotoxic doses (250, 100 and 50 µg/plate) were used in the assays. Biogenic AgNPs at the tested concentrations exhibited no mutagenic effects in the mutagenicity test conducted with the test strains. Moderate anti‐mutagenic effects were observed at high test concentrations. The concentration of 250 µg/plate showed the strongest anti‐mutagenic activity on S. typhimurium TA98. The results did not indicate any mutagenic effect against either of the strains used for screening the mutagenicity of the biogenic AgNPs as they were found to be genotoxically safe. It can be concluded that biogenic AgNPs showed great anti‐mutagenic attributes, standing as a significant factor with respect to medical, pharmaceutical and cosmetic industries.Inspec keywords: biomedical materials, microorganisms, nanomedicine, nanoparticles, silver, toxicologyOther keywords: in vitro mutagenic properties, in vitro antimutagenic properties, green synthesised silver nanoparticles, Streptomyces griseorubens AU2, biogenic silver nanoparticle biosynthesis, microsome mutagenicity test, Salmonella typhimurium TA98 strains, Salmonella typhimurium TA100 strains, subcytotoxic doses, medical industries, pharmaceutical industries, cosmetic industries, Ag     

Removal of toxic contaminants from water by sustainable green synthesised non‐toxic silver nanoparticles

The study describes the synthesis of silver nanoparticles using 21 different plant extracts having medicinal properties. Molecular ultraviolet‐visible spectroscopy shows that the λ _max of nanoparticles synthesised by different plant extracts varied and ranged between 400 and 468 nm. The ultraviolet results revealed that although synthesis of nanoparticles occurred by all plant extracts successfully, their size varies, this was further confirmed by differential light scattering. The synthesised nanoparticles were investigated for their antimicrobial properties. The most promising silver nanoparticles Ocimum sanctum and Artemisia annua assisted were further characterised using transmission electron microscopy and energy dispersive X‐ray spectroscopy (EDX). EDX data confirms that synthesised nanoparticles are highly pure. Further these two plant assisted nanoparticles were studied for chemocatalytic and adsorptive properties. The silver nanoparticles from Ocimum sanctum can catalyse the reduction of 4‐nitrophenol (63%) within 20 min in the presence of NaBH₄, whereas Artemisia annua assisted silver nanoparticles did not show significant chemocatalytic activity. Both the promising nanoparticles can efficiently adsorb textile dyes from aqueous solutions. These synthesised nanoparticles were also exploited to remove microbial and other contaminants from Yamuna River water. The nanoparticles show excellent antimicrobial properties and can be reused repeatedly.Inspec keywords: antibacterial activity, nanofabrication, silver, dyes, light scattering, visible spectra, microorganisms, X‐ray diffraction, transmission electron microscopy, X‐ray chemical analysis, catalysis, nanoparticles, ultraviolet spectra, adsorption, reduction (chemical)Other keywords: sustainable green synthesised nontoxic silver nanoparticles, silver nitrate, molecular ultraviolet–visible spectroscopy, plant assisted nanoparticles, plant extracts, Ocimum sanctum, Artemisia annua, E. coli, C. albicans, plasmon absorbance, differential light scattering, energy dispersive X‐ray spectroscopy, 4‐nitrophenol, chemocatalytic activity, Yamuna River water, antimicrobial properties, time 20.0 min, time 5.0 min to 240.0 hour, size 1.0 nm to 5.0 nm, size 5.0 nm to 20.0 nm, wavelength 400.0 nm to 468.0 nm, NaBH₄ , Ag     

Biofilm reduction,cell proliferation,anthelmintic and cytotoxicity effect of green synthesised silver nanoparticle using Artemisia vulgaris extract

Infectious diseases are caused by etiological agents. Nanotechnology has been used to minimise the effect of clinical pathogens which have resistance to antibiotics. In current research synthesis, characterisation and biological activities of green synthesised nanoparticles using Artemisia vulgaris extract have been done. The characterisation of AgNPs was carried out using Fourier transform infrared spectroscopy, UV‐Vis spectrophotometry, and scanning electron microscopy. Anti‐biofilm, cell viability, antibacterial, brine shrimp lethality, and deoxyribonucleic acid protection effects have been screened. UV‐Vis spectra showed the absorption peak of synthesised nanoparticles at 400 nm. FT‐IR indicated the involvement of the functional group in the preparation of AgNPs. SEM showed the spherical shape of AgNPs with 30 nm diameter. Biological screening results revealed the antibacterial effect against clinical bacterial pathogens. Biofilm reduction and cell viability assay also supported the antibacterial effect. Cytotoxicity effect was recorded as 100% at 200 μg/ml through brine shrimp lethality assay. Protein kinase inhibition zones recorded for AgNPs (16 mm bald) compared with A. vulgaris extract (11 mm bald). It has been concluded that green synthesised AgNPs are more effective against infectious pathogens and could be used as a potential source for therapeutic drugs.Inspec keywords: cellular biophysics, toxicology, silver, nanoparticles, nanomedicine, diseases, microorganisms, ultraviolet spectra, visible spectra, Fourier transform infrared spectra, enzymes, molecular biophysicsOther keywords: biofilm reduction, cell proliferation, anthelmintic effect, cytotoxicity effect, green synthesised silver nanoparticle, Artemisia vulgaris extract, infectious diseases, aetiological agents, Fourier transform infrared spectroscopy, UV‐Vis spectrophotometry, scanning electron microscopy, SEM, antibiofilm, cell viability, brine shrimp lethality, deoxyribonucleic acid protection effects, AgNP, cytotoxicity, protein kinase inhibition zones, therapeutic drugs     

Comparative antibacterial activity of silver nanoparticles synthesised by biological and chemical routes with pluronic F68 as a stabilising agent

The authors report the comparative antibacterial activity of silver nanoparticles synthesised by biological (using Fusarium oxysporum) and chemical routes in the presence and absence of pluronic F68 as a stabilising agent. The production of silver nanoparticles was evidenced by UV–visible spectra, with absorbance at about 420 nm in the case of both biological and chemical synthesis. X‐ray diffraction pattern confirmed the presence of face‐centred cubic structure (FCC plane). The nanoparticles characterised by transmission and scanning electron microscopy showed spherical silver nanoparticles with size range of 5–40 and 10–70 nm in the case of biologically and chemically synthesised nanoparticles, respectively. Addition of pluronic F68 showed the stabilisation of silver nanoparticles. Antibacterial efficacy of silver nanoparticles demonstrated different inhibitory activity against Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus. Overall, biologically synthesised silver nanoparticles showed higher activity as compared with chemically synthesised nanoparticles. Silver nanoparticles synthesised in the presence of pluronic F68 by the chemical route exhibited synergism in antibacterial activity as compared with those synthesised without pluronic F68. On the contrary, biogenic silver nanoparticles without pluronic F68 showed higher antibacterial potential.Inspec keywords: antibacterial activity, nanofabrication, silver, X‐ray diffraction, biomedical materials, nanomedicine, transmission electron microscopy, scanning electron microscopy, ultraviolet spectra, visible spectra, materials preparation, nanoparticlesOther keywords: pluronic F68, stabilising agent, comparative antibacterial activity, Fusarium oxysporum, UV‐visible spectra, biological synthesis, chemical synthesis, X‐ray diffraction pattern, face‐centred cubic structure, FCC plane, transmission electron microscopy, scanning electron microscopy, spherical silver nanoparticles, antibacterial efficacy, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, synergism, biogenic silver nanoparticles, wavelength 420 nm, size 10 nm to 70 nm, size 5 nm to 40 nm, Ag     

Effect of green synthesised silver nanoparticles on morphogenic and biochemical variations in callus cultures of kinnow mandarin (Citrus reticulata L.)

Citrus reticulata is economically important tree fruit crop in Pakistan, fortified with various nutrients and minerals including Vitamin C and secondary metabolites. Nanotechnology is a twenty‐first century science and deals with production of minute particles termed as nanoparticles. In present study, silver nanoparticles (AgNPs) were synthesised through green method by utilising leaves of Olea europea as main reducing and capping agent. The synthesised AgNPs were characterised through UV visible spectroscopy, SEM, and energy dispersive X‐ray. Furthermore, different concentrations of AgNPs (10, 20, 30 ppm) in combination with Thidiazuron (0.5, 1.0 mg/l) were added onto MS medium to study development and secondary metabolites production in callus culture of C. reticulata. Callus induction percentage (96%) was more in 20 ppm AgNPs and 1 mg/l TDZ concentration. Moreover, high total phenolic, flavonoid contents, and antioxidant activity was observed in 20 ppm AgNPs combined with 0.5 and 1 mg/l TDZ. Enzymatic components (SOD, POD and CAT) were increased in MS medium augmented with 30 ppm AgNPs and TDZ. The total protein content (TPC) was significant in callus cultures treated with TDZ only. This study provides the first evidence of green synthesised AgNPs on callus culture developments and further quantification of biochemical profiling in C. reticula. Inspec keywords: nanoparticles, silver, ultraviolet spectra, scanning electron microscopy, antibacterial activity, agricultural products, nanotechnology, biotechnology, agricultural engineering, nanofabrication, genetic engineering, cropsOther keywords: green synthesised silver nanoparticles, morphogenic variations, biochemical variations, kinnow mandarin, citrus reticulata L, nutrients, minerals, green method, UV visible spectroscopy, energy dispersive X‐ray, MS medium, secondary metabolites production, callus induction percentage, TDZ, flavonoid contents, callus culture developments, capping agent, phenolic contents, tree fruit crop     

Broad‐spectrum inhibitory effect of green synthesised silver nanoparticles from Withania somnifera (L.) on microbial growth,biofilm and respiration: a putative mechanistic approach

Multi‐drug resistance in pathogenic bacteria has created immense clinical problem globally. To address these, there is need to develop new therapeutic strategies to combat bacterial infections. Silver nanoparticles (AgNPs) might prove to be next generation nano‐antibiotics. However, improved efficacy and broad‐spectrum activity is still needed to be evaluated and understood. The authors have synthesised AgNPs from Withania somnifera (WS) by green process and characterised. The effect of WS‐AgNPs on growth kinetics, biofilm inhibition as well as eradication of preformed biofilms on both gram‐positive and gram‐negative pathogenic bacteria was evaluated. The authors have demonstrated the inhibitory effect on bacterial respiration and disruption of membrane permeability and integrity. It was found that WS‐AgNPs inhibited growth of pathogenic bacteria even at 16 µg/ml. At sub‐minimum inhibitory concentration concentration, there was approximately 50% inhibition in biofilm formation which was further validated by light and electron microscopy. WS‐AgNPs also eradicated the performed biofilms by varying levels at elevated concentration. The bacterial respiration was also significantly inhibited. Interaction of WS‐AgNPs with test pathogen caused the disruption of cell membrane leading to leakage of cellular content. The production of intracellular reactive oxygen species reveals that WS‐AgNPs exerted oxidative stress inside bacterial cell causing microbial growth inhibition and disrupting cellular functions.Inspec keywords: silver, nanoparticles, nanofabrication, nanomedicine, antibacterial activity, biomedical materials, cellular biophysics, microorganisms, biomembranes, electron microscopy, oxidation, biochemistry, permeabilityOther keywords: broad‐spectrum inhibitory effect, green synthesised silver nanoparticles, Withania somnifera (L.), microbial growth, putative mechanistic approach, multidrug resistance, therapeutic strategies, bacterial infections, next generation nanoantibiotics, broad‐spectrum activity, WS‐AgNPs, growth kinetics, biofilm inhibition, gram‐positive pathogenic bacteria, gram‐negative pathogenic bacteria, bacterial respiration, membrane permeability, membrane integrity, subminimum inhibitory concentration concentration, biofilm formation, light pathogenic bacteria, electron microscopy, cell membrane, cellular content leakage, intracellular reactive oxygen species, oxidative stress, microbial growth inhibition, Ag     

Evaluating the effect of green synthesised copper oxide nanoparticles on oxidative stress and mitochondrial function using murine model

Green synthesis of metal nanoparticles (NPs) has now received the attention of researchers due to ease of preparation and its potential to overcome hazards of these chemicals for an eco‐friendly milieu. In this study, copper oxide (CuO) NPs were synthesised via Desmodium gangeticum aqueous root extract and standard chemical method, further characterised by UV–visible spectroscopy, Fourier transform infrared spectroscopy, X‐ray diffraction, Thermogravimetric analysis and scanning electron microscopy. The nephrotoxicity of the NP obtained from two routes were compared and evaluated at subcellular level in Wistar rat, renal proximal epithelial cells (LLC PK1 cell lines) and isolated renal mitochondria. CuO NP synthesised by chemical route showed prominent nephrotoxicity measured via adverse cytotoxicity to LLC PK1 cells, elevated renal oxidative stress and damage to renal tissue (determined by impaired alanine transaminase, aspartate transaminase, urea, uric acid and creatinine in the blood). However, at the level of cell organelle, CuO NP from both routes are non‐toxic to mitochondrial functional activity. The authors’ finding suggests that CuO NP synthesised by chemical route may induce nephrotoxicity, but may be overcome by co‐administration of antioxidants, as it is not mito‐toxic.Inspec keywords: cellular biophysics, scanning electron microscopy, toxicology, nanomedicine, oxidation, nanoparticles, enzymes, blood, visible spectra, X‐ray diffraction, biochemistry, nanofabrication, antibacterial activity, ultraviolet spectra, copper compounds, Fourier transform infrared spectra, molecular biophysics, thermal analysis, biological tissuesOther keywords: green synthesised copper oxide nanoparticles, murine model, metal nanoparticles, chemicals, eco‐friendly milieu, copper oxide NPs, standard chemical method, X‐ray diffraction, scanning electron microscopy, subcellular level, renal proximal epithelial cells, LLC PK1 cell lines, renal mitochondria, renal tissue, cell organelle, mitochondrial functional activity, UV‐visible spectroscopy, Fourier transform infrared spectroscopy, nephrotoxicity, renal oxidative stress, Desmodium gangeticum aqueous root extract, thermogravimetric analysis, Wistar rat, cytotoxicity, impaired alanine transaminase, aspartate transaminase, urea, uric acid, creatinine, blood, CuO     

Optical and morphological studies of L-histidine functionalised silver nanoparticles synthesised by two different methods

Silver nanoparticles (NPs) functionalised with L-histidine is synthesised by a chemical reduction approach using two different methods of stirring – using a magnetic stirrer and an ultrasonicator. The former method exhibits a strong narrow absorption peak at 396 nm and the latter a blue-shifted weak broad plasmon band for the bare silver NPs. When the capping agent is incorporated, a single broad peak at low intensity evolves for the first method of stirring whereas two distinct peaks are noticed for the second. The Transmission Electron Microscope (TEM) results confirm the spherical shape of the silver NPs in the first case. In the second case, both spherical and elliptical particles are obtained. Zeta potential measurements further confirm the stability of the histidine-capped silver NPs in comparison with the pure silver NPs. A study of the variation of the plasmon peak with pH indicates that a basic medium favours the growth of the histidine-capped silver NPs. A surface-enhanced Raman scattering investigation confirms the adsorption of the capping molecule through the nitrogen of the imidazole ring with the carboxylate group pointing outwards. L-histidine-capped silver NPs can find application in biosensors and biomedicine, particularly when prepared by the magnetic stirrer method due to its greater stability.     

A facile and green route to silver nanoparticles in water

Stable water-dispersible silver nanoparticles with a narrow size distribution are obtained by light-assisted spontaneous reduction of silver nitrate with gelatin, which acts as both the reducing and the stabilizing agents, in water. The formation mechanism of the silver nanoparticles involves an in-situ conversion of Ag(+)-gelatin aggregates to gelatin-stabilized silver nanoparticles via a Ag(+)-mediated oxidation of primary amine groups of the gelatin to carboxylic acid groups. The resultant silver nanoparticles are well within the quantum size domain (10 nm). In addition, the nanoparticles are stable in aqueous solutions and can be separated easily by simple pH adjustment.     

Photocatalytic degradation of dye pollutants under solar,visible and UV lights using green synthesised CuS nanoparticles

A green method for the solvothermal synthesis of copper sulphide nanoparticles (CuS NPs) using xanthan gum as a capping agent was developed. The CuS NPs were characterised by scanning electron microscopy, transmission electron microscopy (TEM), X-ray diffraction, Brunauer–Emment–Teller, zeta analysis, thermal gravimetric– differential thermal analysis, Fourier transform infrared and UV–visible absorption spectra. These characterisations together determine the composition, structural, thermal and optical properties. The UV–visible spectrum had a broad absorption in the visible range. The particle size of the products was observed by TEM in the range of 8–20 nm. The photocatalytic performance of the CuS NPs was evaluated for the degradation of organic dyes (methylene blue, rhodamine B, eosin Y and congo red) under irradiation of solar, visible and UV lights. The CuS NPs showed good photocatalytic activity. Kinetic analyses indicate that the photodegradation rates of dyes usually follow pseudo-first-order kinetics for degradation mechanisms.     

Applications of L-arginine functionalised green synthesised nickel nanoparticles as gene transfer vector and catalyst

Green synthesised nickel nanoparticles (NiGs) using Ocimum sanctum leaf extract have been stabilised with L-arginine (Arg–NiGs) and used as gene transfer vector for bacterial transformation and as catalyst for hydrolytic dehydrogenation. Effective binding of L-arginine with NiGs was confirmed by characterisation of Arg–NiGs. L-arginine coating on NiGs prevented the agglomeration of NiGs and reduced the size of the nanoparticles. Synthesised Arg–NiGs was conjugated with green fluorescent protein (GFP) inserted pUC 18 (pDNA–Arg–NiGs) and employed for transforming non-competent Escherichia coli DH5 α. Transformation efficiency of pDNA–Arg–NiGs was found to be higher (3.8 × 10⁶ µg^–1 DNA) than the CaCl₂-mediated method (2.9 × 10⁵ µg^–1 DNA). Fluorescence micrograph of transformants showed enhanced uptake and transformation of pDNA–Arg–NiGs by bacterial cells. Electrophoretic analysis of expressed GFP confirmed that pDNA could retain its functional activity even after binding with Arg–NiGs. This biocompatible, efficient and economical method could be exploited for transforming non-competent bacterial cells. Arg–NiGs catalysed hydrolytic dehydrogenation of ammonia borane (AB) generated 198 mL of hydrogen in 8 min with 128 mg AB and 10 mL of catalyst at 35 °C. The hydrogen generation rate of Arg–NiGs catalysed AB dehydrogenation was determined to be 24.8 mol H₂ min^–1 with activation energy (E_a) of 34.05 kJ mol^–1 and turnover frequency (TOF) of 12.30 mol H₂ (mol Ni) ^–1 min^–1. Arg–NiGs retained 89% of its initial catalytic activity even after 10 recycles, indicating its high durability in catalytic reactions. Kinetic studies of AB dehydrogenation by Arg–NiGs show the first-order kinetics with respect to catalyst concentration and zero-order kinetics with respect to AB concentration. This efficient and durable catalyst could be applied in hydrolytic dehydrogenation of AB for effective hydrogen storage.     

Role of pH in the green synthesis of silver nanoparticles

The role of pH in the green synthesis of silver nanoparticles (AgNPs) is investigated. For the reduction synthesis of AgNPs we use silver nitrate, glucose, sodium hydroxide and starch respectively to serve as precursor, reducing agent, accelerator and stabilizer. The effect of NaOH addition on the nature of AgNPs is systematically studied. Two reaction pathways are proposed to explain the formation of AgNPs, keeping in view the pH changes that occur on addition of different amounts of NaOH. The aqueous sol of AgNPs prepared at different pH values display different surface plasmon resonance (SPR) behavior. This is explained in terms of size and size distribution of AgNPs.     

Antimicrobial potential and in vitro cytotoxicity study of polyvinyl pyrollidone‐stabilised silver nanoparticles synthesised from Lysinibacillus boronitolerans

The main emphasis herein is on the eco‐friendly synthesis and assessment of the antimicrobial potential of silver nanoparticles (AgNPs) and a cytotoxicity study. Silver nanoparticles were synthesised by an extracellular method using bacterial supernatant. Biosynthesised silver nanoparticles were characterised by UV‐vis spectroscopy, transmission electron microscopy (TEM), Fourier transform infrared spectroscopy, dynamic light scattering, and zeta potential analysis. The synthesised silver nanoparticles exhibited a characteristic peak at 420 nm. TEM analysis depicted the spherical shape and approximately 20 nm size of nanoparticles. Silver nanoparticles carry a charge of −33.75 mV, which confirms their stability. Biogenic polyvinyl pyrrolidone‐coated AgNPs exhibited significant antimicrobial effects against all opportunistic pathogens (Gram‐positive and Gram‐negative bacteria, and fungi). Silver nanoparticles equally affect the growth of both Gram‐positive and Gram‐negative bacteria, with a maximum inhibition zone observed at 22 mm and a minimum at 13 mm against Pseudomonas aeruginosa and Fusarium graminearum, respectively. The minimum inhibitory concentration (MIC) of AgNPs against P. aeruginosa and Staphylococcus aureus was recorded at between 15 and 20 μg/ml. Synthesised nanoparticles exhibited a significant synergistic effect in combination with conventional antibiotics. Cytotoxicity estimates using C2C12 skeletal muscle cell line via 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) test and lactate dehydrogenase assay were directly related to the concentration of AgNPs and length of exposure. On the basis of the MTT test, the IC50 of AgNPs for the C2C12 cell line was approximately 5.45 μg/ml concentration after 4 h exposure.     

Effect of biologically synthesised silver nanoparticles on Staphylococcus aureus biofilm quenching and prevention of biofilm formation

The development of green experimental processes for the synthesis of nanoparticles is a need in the field of nanotechnology. In the present study, the authors reported rapid synthesis of silver nanoparticles using fresh leaves extract of Cymbopogan citratus (lemongrass) with increased stability. The synthesised silver nanoparticles were found to be stable for several months. UV-visible spectrophotometric analysis was carried out to assess the synthesis of silver nanoparticles. The synthesised silver nanoparticles were further characterised by using nanoparticle tracking analyser (NTA), transmission electron microscope (TEM) and energy-dispersive x-ray spectra (EDX). The NTA results showed that the mean size was found to be 32?nm. Silver nanoparticles with controlled size and shape were observed under TEM micrograph. The EDX of the nanoparticles confirmed the presence of elemental silver. These silver nanoparticles showed enhanced quorum quenching activity against Staphylococcus aureus biofilm and prevention of biofilm formation which can be seen under inverted microscope (40X). In the near future, silver nanoparticles synthesised using green methods may be used in the treatment of infections caused by a highly antibiotic resistant biofilm.     

A complete green protocol: wrapping of multiwall carbon nanotubes with silver nanoparticles

Silver nanoparticles have been wrapped on multiwall carbon nanotubes though a green synthesis approach that has advantages over other conventional methods that involve chemical agents associated with environmental toxicity and damage of carbon nanotubes. Acacia was used as a green stabilizer for multiwall carbon nanotubes as well as a stabilizer and reducing agent for silver nanoparticles. Generation of silver-decorated multiwall carbon nanotubes was confirmed by UV-Vis spectrophotometry and X-ray diffraction. Generation of silver nanoparticles (5-10 nm) wrapped on MWCNTs was confirmed by field emission scanning electron microscopy and transmission electron microscopy.