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The study aims to compare different approaches and efficacies during the biological production of nanoparticles (NPs). Gold nanoparticles (AuNPs) are produced by Fusarium oxysporum at two different temperatures. One flask is incubated at 37 °C ("Common") and the other is directly heated for 5 min at 80 °C ("Heat‐treated"). Obtained AuNPs are analyzed and compared by spectrophotometry, transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X‐ray spectroscopy (EDS), dynamic light scattering (DLS), and Fourier transform infrared spectroscopy (FTIR). Graphite furnace atomic absorption spectroscopy (GF‐AAS) is used to determine the particle concentration after the AuNPs production. The AuNPs prepared by both (the Common and the Heat‐treated) methods exhibit maximum absorption peaks at 541 and 528 nm, respectively, and have round shapes and sizes of less than 50 nm. Their zeta potential is about −28 mV. GF‐AAS shows that the efficiency of AuNP production in Common‐ and Heat‐treated samples is equal, between 65% and 68%. Since the Heat‐treated sample shows a better size distribution, the use of higher temperature and shorter time period is preferable for the bioproduction of AuNPs. It seems that shortening the time for the production of AuNPs prevents the formation of larger NPs. [ABSTRACT FROM AUTHOR]

The biological method for synthesis of silver nanoparticles (AgNPs) using Bacopa monneri leaves and its anti‐proliferation against human lung adenocarcinoma cell line (A549) was studied. The AgNPs synthesis was determined by an ultraviolet–visible spectrum and was confirmed primarily by the colour change and surface plasmon resonance was observed at 450 nm and its reduction of functional groups stretched in AgNPs was identified by Fourier transform infrared and the crystalline nature of AgNPs was confirmed by X‐ray diffraction. The structural morphology of the AgNPs was found to be spherical and polygonal shape and size (> 35 nm) were determined by field emission scanning electron microscopy analysis and its purity was identified by energy dispersive analysis of X‐rays (EDAX). A further, antibacterial activity of biosynthesised AgNPs against Gram negative and Gram positive bacteria was assessed. The cytotoxic effect of synthesised AgNPs was analysed against human lung adenocarcinoma cells by 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide assay. The GI50 was found to be 20 µg/ml at 24 h incubation. The apoptosis cells containing condensate and marginalised chromatin stages were analysed by propidium iodide staining and DNA damage was observed in A549 treated cells. The present study strongly emphasised that the bioactive molecule‐coated AgNPs could have potential for biomedical applications and significant anticancer effects against human lung adenocarcinoma cells. [ABSTRACT FROM AUTHOR]

A biological method for synthesising silver nanoparticles (AgNPs) was developed using the callus extracts from Artemisia annua L. under sunlight at 25,000 lx. The AgNPs were characterised using transmission electron microscopy, atomic force microscope, X‐ray diffraction and Fourier transform infrared spectroscopy. The AgNPs were mostly spherical with the size of 2.1 to 45.2 nm (average 10.9 nm). Pulse treatments of AgNPs at 125, 250 and 500 mg/l for 1 h extended vase life of cut carnation (Dianthus caryophyllus cv. Green Land) flowers. Four dominant bacteria strains Arthrobacter arilaitensis, Kocuria sp., Staphylococcus equorum and Microbacterium oxydans were isolated from the stem‐ends of cut D. caryophyllus flowers. AgNP pulse inhibited significantly bacterial growth in vase solution and cut stem ends during all of the vase period. The bacteria related blockage in the stem‐ends was significantly alleviated by AgNP pulse because of its higher antibacterial efficacy against the dominant bacteria. In addition, ethylene release of cut carnation flowers was inhibited in response to AgNP pulse. This is the first time that the biologically synthesised AgNPs could be applied as a promising preservative agent for cut carnation flowers. [ABSTRACT FROM AUTHOR]

A novel combination of titanium oxide (TiO2)/gold (Au)/multiwalled carbon nanotubes (MWCNTs) nanocomposite (NC) was synthesised by sol– gel method. MWCNT functionalisation by modified Hummers method. TiO2 /Au nanoparticles (NPs) were synthesised by biological method using Terminalia chebula bark extract. MWCNT/TiO2 /Au NC samples were characterised by X‐ray diffraction, ultraviolet–visible–diffuse reflectance spectra, microRaman, scanning electron microscopy and high‐resolution‐transmission electron microscopy analyses. The photocatalytic performance of the obtained for NC toward the decomposition of congo‐red and the antimicrobial activity for inhibition of Gram positive (Bacillus subtilis, Streptococcus pneumonia and Staphylococcus aureus), Gram negative (Shigella dysenderiae, Proteus vulgaris and Klebsiella pneumonia) and fungal strains have been evaluated and the results are compared with positive control ampicillin. The metal and metal–oxide NPs have a lower sorption capacity. The herbicidal bond to the tested CNTs by the combination of electron donor–acceptor interactions and hydrogen bonds. In particular, the dispersion of NC and control of sodium borohydride, it has more efficient effect on the photodegradation and antibacterial activity of positive control of ampicillin. The NC material has exhibited maximum photodegradation and antibacterial activity results of zone of inhibition when compared with control samples. [ABSTRACT FROM AUTHOR]