Optical detection of CA 15.3 breast cancer antigen using CdS quantum dot

The present study focus on optical sensing of breast cancer antigen 15.3 (CA 15.3) using cadmium sulphide quantum dot (CdS‐QD) in saline and serum samples spiked with antigen. The surface of CdS‐QD was modified by cysteamine capping followed by tagging of CA 15.3 antibody. The samples were characterised using UV‐visible absorption spectroscopy (UV‐VIS Spectroscopy), Fourier transform infrared spectroscopy (FTIR), high‐resolution transmission electron microscopy (HRTEM) attached with energy‐dispersive X‐ray spectroscopy, phase contrast inverted epi‐fluorescence microscopy and photoluminescence (PL) spectrophotometry (EDS). The CdS‐QD showed a mean diameter of 3.02 ± 0.6 nm. The complex formed after antigen‐antibody interaction resulted in distinguishable optical and fluorescence intensity with respect to varying concentration of antigen. The PL study revealed that CA 15.3 antibody labelled CdS QD can detect CA 15.3 tumour marker even at very low concentration of 0.002 KU/L with a constant response time of 15 min. This study clearly indicates that detection of CA 15.3 at low concentration is possible using surface modified CdS QD in serum samples and can find immense applications in biosensor development for detection of breast cancer marker similar to various automated detection kits available in market.Inspec keywords: semiconductor quantum dots, cadmium compounds, II‐VI semiconductors, wide band gap semiconductors, cancer, tumours, optical sensors, biosensors, biomedical equipment, visible spectra, ultraviolet spectra, Fourier transform infrared spectra, transmission electron microscopy, X‐ray chemical analysis, fluorescence, optical microscopy, photoluminescence, proteins, molecular biophysics, nanosensors, nanomedicine, nanoparticlesOther keywords: optical detection, CA 15.3 breast cancer antigen, optical sensing, cadmium sulphide quantum dot, saline samples, serum samples, cysteamine capping, CA 15.3 antibody, UV‐visible absorption spectroscopy, Fourier transform infrared spectroscopy, high‐resolution transmission electron microscopy, energy dispersive X‐ray spectroscopy, phase contrast inverted epifluorescence microscopy, photoluminescence spectrophotometry, antigen‐antibody interaction, fluorescence intensity, optical intensity, CA 15.3 tumour marker, surface modified CdS QD, biosensor development, time 15 min, CdS     

Silver nanoparticles biosynthesised using Centella asiatica leaf extract: apoptosis induction in MCF‐7 breast cancer cell line

The aim of this study was to green synthesised silver nanoparticles (AgNPs) using Centella asiatica leaf extract and investigate the cytotoxic and apoptosis‐inducing effects of these nanoparticles in MCF‐7 breast cancer cell line. The characteristics and morphology of the green synthesised AgNPs were evaluated using transmission electron microscopy, scanning electron microscopy, UV–visible spectroscopy, X‐ray diffraction, and Fourier‐transform infrared spectroscopy. The MTT assay was used to investigate the anti‐proliferative activity of biosynthesised nanoparticles in MCF‐7 cells. Apoptosis test was performed using flow cytometry and expression of caspase 3 and 9 genes. The spherical AgNPs with an average size of 19.17 nm were synthesised. The results showed that biosynthesised AgNPs exhibited cytotoxicity, anti‐cancer, apoptosis induction, and increased expression of genes encoding for caspases 3 and 9 in MCF‐7 cancer cells in a concentration‐ and time‐dependent manner. It seems that green synthesised AgNPs have potential uses for pharmaceutical industries.Inspec keywords: ultraviolet spectra, transmission electron microscopy, cellular biophysics, infrared spectra, visible spectra, nanofabrication, cancer, toxicology, nanomedicine, nanoparticles, biomedical materials, scanning electron microscopy, silver, Fourier transform spectra, X‐ray diffraction, genetics, enzymes, botany, biochemistryOther keywords: spherical AgNPs, biosynthesised AgNPs, anti‐cancer, apoptosis induction, green synthesised AgNPs, MCF‐7 breast cancer cell line, green synthesised silver nanoparticles, Ag, caspase gene expression, flow cytometry, anti‐proliferative activity, MTT assay, pharmaceutical industries, cytotoxicity, UV–visible spectroscopy, nanoparticle morphology, scanning electron microscopy, Centella asiatica leaf extract, biosynthesised nanoparticles, Fourier‐transform infrared spectroscopy, transmission electron microscopy     

Bio‐green synthesis ZnO‐NPs in Brassica napus pollen extract: biosynthesis,antioxidant, cytotoxicity and pro‐apoptotic properties

The bio‐green methods of synthesis nanoparticles (NPs) have advantages over chemo‐physical procedures due to cost‐effective and ecofriendly products. The goal of current investigation is biosynthesis of zinc oxide NPs (ZnO‐NPs) and evaluation of their biological assessment. Water extract of Brassica napus pollen [rapeseed (RP)] prepared and used for the synthesis of ZnO‐NPs and synthesised ZnO‐NP characterised using ultraviolet–visible, X‐ray diffraction, Fourier‐transform infrared spectroscopy, field emission scanning electron microscope and transmission electron microscope. Antioxidant properties of ZnO‐NPs, cytotoxic and pro‐apoptotic potentials of NPs were also evaluated. The results showed that ZnO‐NPs have a hexagonal shape with 26 nm size. ZnO‐NPs synthesised in RP (RP/ZnO‐NPs) exhibited the good antioxidant potential compared with the butylated hydroxyanisole as a positive control. These NPs showed the cytotoxic effects against breast cancer cells (M.D. Anderson‐Metastasis Breast cancer (MDA‐MB)) with IC₅₀ about 1, 6 and 6 μg/ml after 24, 48 and 72 h of exposure, respectively. RP/ZnO‐NPs were found effective in increasing the expression of catalase enzyme, the enzyme involved in antioxidants properties of the cells. Bio‐green synthesised RP/ZnO‐NPs showed antioxidant and cytotoxic properties. The results of the present study support the advantages of using the bio‐green procedure for the synthesis of NPs as an antioxidant and as anti‐cancer agents.Inspec keywords: II‐VI semiconductors, wide band gap semiconductors, ultraviolet spectra, toxicology, X‐ray diffraction, biochemistry, zinc compounds, nanomedicine, enzymes, biomedical materials, particle size, antibacterial activity, transmission electron microscopy, molecular biophysics, visible spectra, nanofabrication, cellular biophysics, nanoparticles, cancer, field emission scanning electron microscopy, Fourier transform infrared spectra, semiconductor growthOther keywords: bio‐green synthesis ZnO‐NPs, zinc oxide NPs, synthesised ZnO‐NP, field emission scanning electron microscope, transmission electron microscope, antioxidant properties, bio‐green synthesised RP‐ZnO‐NPs, Fourier‐transform infrared spectroscopy, X‐ray diffraction, breast cancer cells MDA‐MB, pro‐apoptotic potentials, cytotoxic effects, catalase enzyme, bio‐green procedure, time 48.0 hour, time 72.0 hour, size 26.0 nm, time 24.0 hour, ZnO     

Antibacterial and anticancer activity of biosynthesised CuO nanoparticles

The present investigation aims for the synthesis of copper oxide nanoparticles (CuO NPs) using Nilgirianthus ciliatus plant extract. The obtained CuO NPs were characterised by X‐ray diffraction, Fourier transform infrared spectrum, ultraviolet–visible spectroscopy, photoluminescence, scanning electron microscopy and transmission electron microscopy analysis. Significant bacterial activity was manifested by CuO nanoparticles against both Gram‐positive (Staphylococcus aureus and Staphylococcus mutans) and Gram‐negative (Escherichia coli and Pseudomonas aeruginosa) bacteria. The synthesised CuO NPs have good cytotoxicity against both human breast cancer cell line (MCF‐7) and lung cancer cell line (A549) with minimum cytotoxic effect on normal L929 (fibroblast) cell lines.Inspec keywords: microorganisms, ultraviolet spectra, nanomedicine, transmission electron microscopy, visible spectra, cellular biophysics, antibacterial activity, nanoparticles, X‐ray diffraction, lung, copper compounds, cancer, toxicology, biomedical materials, scanning electron microscopy, photoluminescence, Fourier transform infrared spectraOther keywords: antibacterial activity, anticancer activity, biosynthesised CuO nanoparticles, copper oxide nanoparticles, Nilgirianthus ciliatus plant, X‐ray diffraction, infrared spectrum, ultraviolet–visible spectroscopy, transmission electron microscopy analysis, bacterial activity, Gram‐negative bacteria, synthesised CuO NPs, human breast cancer cell line, Staphylococcus aureus, Staphylococcus mutans, CuO     

Analytical study of biosynthesised silver nanoparticles against multi‐drug resistant biofilm‐forming pathogens

The emergence of the huge number of multi‐drug resistant (MDR) bacteria requires an alternative to the drugs. Silver nanoparticles (AgNPs) are a strong candidate for this due to their bactericidal properties, which can be better concluded by understanding their morphology and chemistry. The study hypothesised that AgNPs synthesised using leaves of Syzygium cumini can be used to treat locally emerging MDRs forming biofilms on indwelling medical devices. Synthesised particles were characterised by methods like UV–visible spectroscopy, X‐ray powder diffraction, scanning electron microscopy, transmission electron microscopy, and Zetasizer. Fourier transform infrared spectroscopy, and high‐performance liquid chromatography were used to predict phytochemicals present in the leaves. The shape of particles is revealed to be relatively spherical, with average size to be around 10–100 nm. Phenolic compounds are attributed to the formation of nanoparticles, stability analysis shows particles to be stable, and zeta potential determined the surface charge to be −20.1 mV. Biosynthesised particles are found to possess efficient antibacterial activity MDR bacteria developing biofilms in medical devices; hence, it is concluded that S. cumini based NPs can be used to develop a layer on implant‐related medical devices. Toxicity evaluation against A594 cancer cells portrays AgNPs to be potential tumour reduction agents in a concentration‐dependent manner.Inspec keywords: silver, visible spectra, X‐ray diffraction, transmission electron microscopy, scanning electron microscopy, chromatography, electrokinetic effects, cancer, biomedical materials, reduction (chemical), cellular biophysics, nanofabrication, nanoparticles, antibacterial activity, particle size, drugs, toxicology, nanomedicine, ultraviolet spectra, microorganisms, tumours, Fourier transform infrared spectraOther keywords: Syzygium cumini, biofilms, indwelling medical devices, UV‐visible spectroscopy, X‐ray powder diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, high‐performance liquid chromatography, biosynthesised particles, implant‐related medical devices, biosynthesised silver nanoparticles, multidrug resistant biofilm‐forming pathogens, multidrug resistant bacteria, MDR, bactericidal properties, morphology, scanning electron microscopy, s. cumini based NP, A594 cancer cells, tumour reduction, Ag     

Effect of capping agents on optical and antibacterial properties of cadmium selenide quantum dots

Cadmium selenide quantum dots (CdSe QDs) were synthesized in aqueous phase by the freezing temperature injection technique using different capping agents (viz. thioglycolic acid, 1-thioglycerol, L-cysteine). Absorption spectra of CdSe QDs exhibited a blue shift as compared to its bulk counterpart, which is an indication of quantum confinement effect. The photoluminescence spectra of CdSe QDs confirmed that the particles are poly-dispersed and possess enhanced luminescent property, depending upon the chemical nature of capping agents. The QDs have been characterized by Fourier-transform infrared spectroscopy, atomic absorption spectroscopy and transmission electron microscopy. Further, antimicrobial activity of as-prepared QDs has also been investigated using the disk diffusion method.     

Structural,optical and morphological studies of undoped and Zn-doped CdSe QDs via aqueous route synthesis

Undoped and Zn-doped CdSe quantum dots (QDs) were successfully synthesized by the chemical precipitation method. The structural, optical and morphological properties of the synthesized undoped and Zn-doped CdSe QDs were studied by X-ray diffraction (XRD), UV–visible absorption spectroscopy, photoluminescence (PL) spectroscopy, fluorescence lifetime spectroscopy, scanning electron microscopy (SEM), field emission transmission electron microscopy (FE-TEM) and FTIR. The synthesized undoped and Zn-doped CdSe QDs were in cubic crystalline phase, which was confirmed by the XRD technique. From the UV–visible absorption spectral analysis, the absorption wavelengths of both undoped and Zn-doped CdSe QDs show blue-shift with respect to their bulk counterpart as a result of quantum confinement effect. The highest luminescence intensity was observed for CdSe QDs doped with 4% Zn by PL studies. TEM analysis shows that the prepared QDs are spherical in shape.     

Biosynthesis of Silver Nanoparticles by Streptomyces griseorubens isolated from Soil and Their Antioxidant Activity

Microbial mediated biological synthesis of metallic nanoparticles was carried out ecofriendly in the present study. Silver nanoparticles (AgNPs) were extracellularly biosynthesised from Streptomyces griseorubens AU2 and extensively characterised by ultraviolet–visible (UV–vis) and Fourier transform infrared spectroscopy, high‐resolution transmission electron microscopy, scanning electron microscopy and X‐ray diffraction analysis. Elemental analysis of nanoparticles was also carried out using energy dispersive X‐ray spectroscopy. The biosynthesised AgNPs showed the characteristic absorption spectra in UV–vis at 422 nm which confirmed the presence of metallic AgNPs. According to the further characterisation analysis, the biosynthesised AgNPs were found to be spherical and crystalline particles with 5–20 nm average size. Antioxidant properties of the biosynthesised AgNPs were determined by 2,2‐diphenyl‐1‐picrylhydrazyl free radical scavenging assay and was found to increase in a dose‐dependent matter. The identification of the strain was determined by molecular characterisation method using 16s rDNA sequencing. The present study is the first report on the microbial biosynthesis of AgNPs using S. griseorubens isolated from soil and provides that the active biological components found in the cell‐free culture supernatant of S. griseorubens AU2 enable the synthesis of AgNPs.Inspec keywords: silver, microorganisms, nanoparticles, nanofabrication, DNA, molecular biophysics, ultraviolet spectra, visible spectra, scanning electron microscopy, Fourier transform infrared spectra, transmission electron microscopy, X‐ray diffraction, X‐ray chemical analysis, absorption coefficients, cellular biophysicsOther keywords: silver nanoparticles, Streptomyces griseorubens AU2, soil, antioxidant activity, microbial mediated biological synthesis, ultraviolet‐visible spectroscopy, Fourier transform infrared spectroscopy, UV‐vis spectroscopy, high‐resolution transmission electron microscopy, scanning electron microscopy, X‐ray diffraction, elemental analysis, energy dispersive X‐ray spectroscopy, absorption spectra, spherical particles, crystalline particles, 2,2‐diphenyl‐1‐picrylhydrazyl free radical scavenging assay, strain identification, molecular characterisation method, rDNA sequencing, active biological components, cell‐free culture supernatant, wavelength 422 nm, size 5 nm to 20 nm, Ag     

Biosynthesis of zinc oxide nanoparticles using anjbar (root of Persicaria bistorta) extract and their cytotoxic effects on human breast cancer cell line (MCF‐7)

Biosynthesis of nanoparticles (NPs) using biomass is now one of the best methods for synthesising NPs due to their nontoxic and biocompatibility. Plants are the best choice among all biomass to synthesise large‐scale NPs. The objectives of this study were to synthesise zinc oxide nanoparticles (ZnO‐NPs) using Anjbar (root of Persicaria bistorta) [An/ZnO‐NPs] and investigate the cytotoxic and anti‐oxidant effects. For this purpose, the An/ZnO‐NPs were synthesised by using Bistort extract and characterised using UV–Visible spectroscopy, transmission electron microscope, field emission scanning electron microscope, x‐ray diffraction and Fourier‐transform infrared spectroscopy. The cytotoxic effects of the An/ZnO‐NPs on MCF‐7 cells were followed by 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide assays at 24, 48, and 72 h. Nuclear morphology changed and apoptosis in cells was investigated using acridine orange/propodium iodide (AO/PI) staining and flow cytometry analysis. The pure biosynthesised ZnO‐NPs were spherical in shape and particles sizes ranged from 1 to 50 nm. Treated MCF‐7 cells with different concentrations of ZnO‐NPs inhibited cell viability in a time‐ and dose‐dependent manner with IC50 about 32 μg/ml after 48 h of incubation. In flow cytometry analysis the sub‐G1 population, which indicated apoptotic cells, increased from 12.6% at 0 μg/ml (control) to 92.8% at 60 μg/ml, 48 h after exposure. AO/PI staining showed that the treated cells displayed morphologic evidence of apoptosis, compared to untreated groups. Inspec keywords: cancer, cellular biophysics, toxicology, particle size, nanofabrication, X‐ray diffraction, nanomedicine, nanoparticles, ultraviolet spectra, scanning electron microscopy, visible spectra, transmission electron microscopy, patient treatment, field emission electron microscopy, Fourier transform infrared spectra, drug delivery systemsOther keywords: anjbar, cytotoxic effects, human breast cancer cell line, biomass, transmission electron microscope, field emission scanning electron microscope, Fourier‐transform infrared spectroscopy, flow cytometry analysis, ZnO‐NPs inhibited cell viability, antioxidant effects, MCF‐7 cells, biosynthesised ZnO‐NP, biosynthesised ZnO‐NP, acridine orange‐propodium iodide staining, An‐ZnO‐NP, Persicaria bistorta, zinc oxide nanoparticle biosynthesis, 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide     

Green synthesis of highly stable carbon nanodots and their photocatalytic performance

The present study reports a novel, facile, biosynthesis route for the synthesis of carbon nanodots (CDs) with an approximate quantum yield of 38.5%, using Musk melon extract as a naturally derived‐precursor material. The synthesis of CDs was established by using ultraviolet–visible (UV–vis) spectroscopy, Dynamic light scattering, photoluminescence spectroscopy, X‐ray diffraction, transmission electron microscopy and Fourier transform infrared (FTIR) spectroscopy. The as‐prepared CDs possess an eminent fluorescence under UV–light (λ _ex  = 365 nm). The size range of CDs was found to be in the range of 5–10 nm. The authors further explored the use of such biosynthesised CDs as a photocatalyst material for removal of industrial dye. Degradation of methylene blue dye was performed in a photocatalytic reactor and monitored using UV–vis spectroscopy. The CDs show excellent dye degradation capability of 37.08% in 60 min and reaction rate of 0.0032 min⁻¹. This study shows that synthesised CDs are highly stable in nature, and possess potential application in wastewater treatment.Inspec keywords: carbon, nanostructured materials, nanofabrication, catalysis, photochemistry, ultraviolet spectra, visible spectra, photoluminescence, X‐ray diffraction, transmission electron microscopy, Fourier transform infrared spectra, fluorescence, dyesOther keywords: green synthesis, highly stable CD, photocatalytic performance, biosynthesis route, carbon nanodots, quantum yield, Musk melon extract, naturally derived‐precursor material, ultraviolet‐visible spectroscopy, dynamic light scattering, photoluminescence spectroscopy, X‐ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, FTIR spectroscopy, fluorescence, biosynthesised CD, photocatalyst material, industrial dye, methylene blue dye degradation, photocatalytic reactor, UV‐vis spectroscopy, wastewater treatment, size 5 nm to 10 nm, time 60 min     

Improvement of efficacy and decrement cytotoxicity of oxaliplatin anticancer drug using bovine serum albumin nanoparticles: synthesis,characterisation and release behaviour

To sustained release of an anticancer drug, oxaliplatin (OX), a non‐toxic and biocompatible nanocarrier based on bovine serum albumin (BSA) were synthesised by desolvation method and characterised using Fourier‐transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM) and dynamic light scattering. The results showed that the BSA nanoparticles (BSANPs) with a mean magnitude of 187.9 ± 1.2 nm have spherical morphology with a smooth surface and a uniform distribution. Furthermore, OX was loaded onto the BSANPs and the loading was confirmed by FTIR, AFM and FESEM techniques. The percentage of encapsulation efficiency and drug loading were determined by absorption spectroscopy (UV–vis). The drug release studies showed that release of OX from BSANPs exhibited slower release rate. However, the release kinetics followed the first‐order kinetic for both of them with the non‐Fickian release behaviour. The electrochemical analysis showed stability of OX loaded onto the BSANPs (OX@BSANPs) and confirmed the diffusion mechanism. Furthermore, the results of MTT assay revealed increasing of normal cell viability and cancer cell death in the OX@BSANPs compared to only OX. It was shown that the BSANPs could be safely used as a biocompatible nanocarrier for the sustained release of OX.Inspec keywords: nanoparticles, drug delivery systems, molecular biophysics, encapsulation, cancer, proteins, drugs, cellular biophysics, light scattering, nanofabrication, atomic force microscopy, biomedical materials, diffusion, toxicology, nanomedicine, field emission scanning electron microscopy, Fourier transform infrared spectra, ultraviolet spectra, visible spectra, surface morphologyOther keywords: cytotoxicity, biocompatible nanocarrier, bovine serum albumin nanoparticles, desolvation method, atomic force microscopy, dynamic light scattering, BSA nanoparticles, FESEM, UV‐visible absorption spectroscopy, drug release rate, nonFickian release behaviour, oxaliplatin anticancer drug, Fourier‐transform infrared spectroscopy, FTIR spectroscopy, spherical morphology, encapsulation efficiency, release kinetics, first‐order kinetics, electrochemical analysis, diffusion mechanism, MTT assay, cell viability, cancer cell death     

Biosynthesis of Selenium Nanoparticles using yeast Nematospora coryli and examination of their anti‐candida and anti‐oxidant activities

Selenium (Se) is a rare and essential element for the human body and other living organisms because of its role in the structure of several proteins and having anti‐oxidant properties to reduce oxidative stress at cells. Some microorganisms can absorb Se oxyanions and convert them into zero‐valent Se (Se0) in the nanoscale dimensions, which can be used for producing Se nanoparticles (SeNPs). In the present study, SeNPs were intracellularly biosynthesised by yeast Nematospora coryli, which is an inexpensive method and does not involve using materials hazardous for human and environment. The produced NPs were refined by a two‐phase system and then characterised and identified by ultraviolet–visible, X‐ray diffraction, X‐ray fluorescence, transmission electron microscope, and Fourier transform infrared spectroscopy analyses. The structural analysis of biosynthesised SeNPs showed spherical‐shaped NPs with size ranging from 50 to 250 nm. Also, extracted NPs were applied to explore their anti‐candida and anti‐oxidant activities. The results of this investigation confirm the biological properties of Se.Inspec keywords: X‐ray diffraction, microorganisms, oxidation, transmission electron microscopy, reduction (chemical), nanomedicine, biomedical materials, visible spectra, nanoparticles, proteins, nanofabrication, selenium, ultraviolet spectra, particle size, Fourier transform infrared spectra, antibacterial activityOther keywords: proteins, oxidative stress, Se oxyanions, yeast, biosynthesised SeNPs, anti‐oxidant activities, human body, living organisms, Se nanoparticles, Nematospora coryli, anti‐candida activities, biosynthesis, ultraviolet–visible analysis, X‐ray diffraction, X‐ray fluorescence, transmission electron microscope, Fourier transform infrared spectroscopy, structural analysis, size 50.0 nm to 250.0 nm, Se     

Biocompatibility enhancement of graphene oxide‐silver nanocomposite by functionalisation with polyvinylpyrrolidone

Several materials such as silver are used to enhance graphene oxide (GO) sheets antimicrobial activity. However, these toxic materials decrease its biocompatibility and hinder its usage in many biological applications. Therefore, there is an urgent need to develop nanocomposites that can preserve both the antimicrobial activity and biocompatibility simultaneously. This work highlights the importance of functionalisation of GO sheets using Polyvinylpyrrolidone (PVP) and decorating them with silver nanoparticles (AgNPs) in order to enhance their antimicrobial activity and biocompatibility at the same time. The structural and morphological characterisations were performed by UV‐Visible, Fourier transform infrared (FTIR), and Raman spectroscopic techniques, X‐ray diffraction (XRD), and high‐resolution transmission electron microscopy (HR‐TEM). The antimicrobial activities of the prepared samples against Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans were studied. The cytotoxicity of prepared materials was tested against BJ1 normal skin fibroblasts. The results indicated that the decoration with AgNPs showed a significant increase in the antimicrobial activity of GO and FGO sheets, and functionalisation of GO sheets and GO‐Ag nanocomposite with PVP improved the cell viability about 40 and 35%, respectively.Inspec keywords: biomedical materials, nanocomposites, visible spectra, ultraviolet spectra, X‐ray diffraction, cellular biophysics, nanoparticles, Raman spectra, filled polymers, transmission electron microscopy, silver, microorganisms, antibacterial activity, nanomedicine, nanofabrication, graphene compounds, toxicology, Fourier transform infrared spectraOther keywords: graphene oxide‐silver nanocomposite, polyvinylpyrrolidone, toxic materials, biocompatibility, antimicrobial activity, morphological characterisations, structural characterisations, UV‐visible spectra, Fourier transform infrared spectra, Raman spectra, X‐ray diffraction, high‐resolution transmission electron microscopy, Staphylococcus aureus, Pseudomonas aeruginosa, Candida albicans, cytotoxicity, BJ1 normal skin fibroblasts, cell viability, CO‐Ag     

Green wet chemical route to synthesize capped CdSe quantum dots

In the present work, we report green synthesis of tartaric acid (TA) and triethanolamine (TEA) capped cadmium selenide quantum dots (CdSe QDs) employing chemical bath deposition (CBD) method. The mechanism of capping using non-toxic binary capping agents is also discussed. Stable QDs of various sizes were obtained by varying pH of the bath. The structural, morphological and spectroscopic characterization of the as-prepared samples by XRD, SEM, optical absorption and photoluminescence (PL) is also reported.     

Simple,green approach for the synthesis of solid support‐embedded PdNPs for ligand exchange

Green approaches have the potential to significantly reduce the costs and environmental impact of chemical syntheses. Here, the authors used green tea (GT) leaf extract to synthesise and anchor palladium nanoparticles (PdNPs) to silica. The synthesised PdNPs in GT extract were characterised by ultraviolet–visible spectroscopy, Fourier‐transform infrared spectroscopy, X‐ray diffraction, and transmission electron microscopy. PdNPs primarily formed as capped NPs dispersed in GT extract before reduction completed after 24 h. This capped phytochemical solution was employed as a green precursor solution to synthesise PdNP‐embedded solid supports. The morphology of PdNPs anchored to silica differed to that of PdNPs in solution. Silica‐embedded PdNPs was employed as a new ligand exchanger to isolate trace polycyclic aromatic sulphur heterocycles from a hydrocarbon matrix. The isolation efficiency of the new, greener ligand exchanger was the same as an efficient chemical ligand exchanger and may, therefore, hold promise for future applications.Inspec keywords: nanofabrication, palladium, visible spectra, transmission electron microscopy, nanoparticles, reduction (chemical), ultraviolet spectra, X‐ray diffraction, Fourier transform infrared spectra, surface morphologyOther keywords: ultraviolet–visible spectroscopy, Fourier‐transform infrared spectroscopy, transmission electron microscopy, phytochemical solution, green precursor solution, PdNP‐embedded solid supports, solid support‐embedded PdNPs, green tea leaf extract, chemical ligand exchanger, anchor palladium nanoparticles, X‐ray diffraction, isolate trace polycyclic aromatic sulphur heterocycles, hydrocarbon matrix, green synthesis, time 24.0 hour, Pd     

Synthesis and size dependent optical studies in CdSe quantum dots via inverse micelle technique

Cadmium selenide quantum dots (CdSe QDs) were successfully synthesized without using trioctylphosphine (TOP). The XRD pattern showed zinc-blend phase of the CdSe QDs. The absorption and PL spectra exhibit a strong blue shift as the QDs size decreases due to the quantum confinement effect. In addition, the quantum efficiency of CdSe QDs with TOP capping is higher than CdSe QDs with oleic acid capping. TEM image shows a spherical shape, compact and dense structure of CdSe QDs. A good agreement between the Tauc's model and experimentally measured absorption spectra of CdSe QDs is achieved. The FTIR peak at ～1712 cm^?1 spectra confirms the influence of oleic acid as a capping agent.     

Plasmonic photothermal therapy of colon cancer cells utilising gold nanoshells: an in vitro study

In this study, gold nanoshell (GNS) were synthesised utilising the Halas method. The obtained nanoparticles (NPs) were characterised by Fourier‐transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–Vis spectroscopy and dynamic light scattering. FTIR spectra demonstrated the successful functionalisation of silica NP with 3‐aminopropyl trimethoxysilane. SEM and TEM images showed the morphology and diameter of the synthesised silica NPs (137 ± 26 nm) and GNS. UV–Vis spectrum illustrated the maximum absorbance of the resultant GNS and their average hydrodynamic diameter was 159 nm. For in vitro study, HCT‐116 cells were exposed to gold nanoshells and intense pulsed light in different experiment groups. The results showed that exposing the cells to nanoshells and 30 s irradiation would efficiently decrease the viability percentage of the cells to about 30% compared with the control. A continued exposure of 4 min decreased the viability of the cancer cells to 20%. The results demonstrated that photothermal therapy would be promising in treatment of colon cancer cells utilising gold nanoshells.Inspec keywords: gold, silicon compounds, nanomedicine, plasmonics, radiation therapy, bio‐optics, cancer, cellular biophysics, nanoparticles, Fourier transform spectra, infrared spectra, scanning electron microscopy, transmission electron microscopy, ultraviolet spectra, visible spectraOther keywords: plasmonic photothermal therapy, colon cancer cells, gold‐silica nanoshells, GNS, Halas method, Fourier transform infrared spectroscopy, FTIR, scanning electron microscopy, SEM, transmission electron microscopy, TEM, UV‐vis spectroscopy, dynamic light scattering, FTIR spectra, 3‐aminopropyl trimethoxysilane, morphology, in vitro study, HCT‐116 cells, cell viability, nanoparticles, time 30 s, time 4 min, Au     

Sunlight induced biosynthesis of silver nanoparticle from the bark extract of Amentotaxus assamica D.K. Ferguson and its antibacterial activity against Escherichia coli and Staphylococcus aureus

Green synthesis of nanoparticles has gained importance due to its eco‐friendly, low toxicity and cost effective nature. This study deals with the biosynthesis of silver nanoparticles (AgNPs) from the bark extract of Amentotaxus assamica. The AgNPs have been synthesised by reducing the silver ions into stable AgNPs using the bark extract of Amentotaxus assamica under the influence of sunlight irradiation. The characterisation of the biosynthesised AgNPs was carried out by UV–vis spectroscopy, X‐ray diffraction analysis (XRD), Fourier transform infrared spectroscopy, scanning electron microscopy (SEM) and energy dispersive X‐ray analysis. The UV–vis spectrum showed a broad peak at 472 nm. Also, the XRD confirmed the crystalline structure of the AgNPs. Moreover, the SEM analysis revealed that the biosynthesised AgNPs were spherical in shape. Also, dynamic light scattering techniques were used to evaluate the size distribution profile of the biosynthesised AgNPs. Furthermore, the biosynthesised AgNPs showed a prominent inhibitory effect against both Escherichia coli (MTCC 111) and Staphylococcus aureus (MTCC 97). Thus the biosynthesis of AgNPs from the bark extract of Amentotaxus assamica is found to eco‐friendly way of producing AgNPs compared to chemical method.Inspec keywords: X‐ray chemical analysis, microorganisms, transmission electron microscopy, nanoparticles, toxicology, scanning electron microscopy, ultraviolet spectra, particle size, Fourier transform spectra, X‐ray diffraction, antibacterial activity, visible spectra, infrared spectra, nanomedicine, silverOther keywords: stable AgNP, biosynthesised AgNP, SEM analysis, sunlight irradiation, silver ions, silver nanoparticle, amentotaxus assamica, biosynthesis, escherichia coli     

Structural and physicochemical properties of Rheum emodi mediated Mg(OH)2 nanoparticles and their antibacterial and cytotoxic potential

In the present investigation, Rheum emodi roots extract mediated magnesium hydroxide nanoparticles [Mg(OH)₂ NPs] through the bio‐inspired experimental technique were synthesised. Mg(OH)₂ NPs were characterised by using various characterisation techniques such as field emission scanning electron microscopy, transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), and ultraviolet–visible spectroscopy. The formation of Mg(OH)₂ NPs was confirmed by X‐ray diffraction. The structural analysis confirmed the hexagonal crystal symmetry of Mg(OH)₂ NPs with space group P‐3m1 and space group no. 164 using the Rietveld refinement technique. TEM micrographs illustrated the nano‐size formation of Mg(OH)₂ NPs of spherical shape and size ∼14.86 nm. With the aid of FTIR data, plant metabolites such as anthraquinones have been identified as a stabilising and reducing agent for the synthesis of biogenic Mg(OH)₂ NPs. The synthesised Mg(OH)₂ NPs showed antimicrobial and cytotoxic potential against Gram‐negative and Gram‐positive bacteria such as Escherichia coli (ATCC 25922) and Staphylococcus aureus (ATCC 25923) and MDA‐MB‐231 human breast cancer cell lines.Inspec keywords: antibacterial activity, microorganisms, visible spectra, cancer, X‐ray diffraction, cellular biophysics, nanomedicine, ultraviolet spectra, nanoparticles, transmission electron microscopy, nanofabrication, field emission scanning electron microscopy, Fourier transform infrared spectra, particle size, magnesium compounds, space groups, toxicologyOther keywords: physicochemical properties, structural properties, Rheum emodi root extract mediated magnesium hydroxide nanoparticles, bio‐inspired experimental technique, field emission scanning electron microscopy, transmission electron microscopy, TEM, Fourier transform infrared spectroscopy, FTIR spectroscopy, ultraviolet‐visible spectroscopy, X‐ray diffraction, hexagonal crystal symmetry, space group P‐3m1, space group no. 164, Rietveld refinement technique, nanosize formation, plant metabolites, spherical shape, antibacterial potential, cytotoxic potential, reducing agent, anthraquinones, stabilising agent, Gram‐positive bacteria, Gram‐negative bacteria, Escherichia coli, Staphylococcus aureus, MDA‐MB‐231 human breast cancer cell lines, Mg(OH)₂      

Postprandial anti‐hyperglycemic activity of marine Streptomyces coelicoflavus SRBVIT13 mediated gold nanoparticles in streptozotocin induced diabetic male albino Wister rats

The present study focuses on the biosynthesis of gold nanoparticles (AuNPs) using Streptomyces coelicoflavus (S. coelicoflavus) SRBVIT13 isolated from marine salt pan soils collected from Ongole, Andhra Pradesh, India. The biosynthesised AuNPs are characterised by UV–visible spectroscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, high‐resolution transmission electron microscopy and energy‐dispersive X‐ray analysis. Transmission electron microscopy study suggests that the biosynthesised AuNPs are spherical in shape within a size range of 12–20 nm (mean diameter as 14 nm). The anti‐type II diabetes activity of AuNPs is carried out by testing it in vitro α ‐glucosidase and α ‐amylase enzyme inhibition activity and in vivo postprandial anti‐hyperglycemic activity in sucrose and glucose‐loaded streptozotocin induced diabetic albino Wister rats. AuNPs has shown a significant inhibitory activity of 84.70 and 87.82% with IC₅₀ values of 67.65 and 65.59 μg/mL to α ‐glucosidase and α ‐amylase enzymes, while the diabetic rats have shown significant reduction in the post postprandial blood glucose level by 57.80 and 88.09%, respectively compared with control group after AuNPs treatment at the concentration of 300 and 600 mg/kg body weight. Hence, this biosynthesised AuNPs might be useful in combating type II diabetes mellitus for the betterment of human life.Inspec keywords: gold, nanoparticles, ultraviolet spectra, visible spectra, X‐ray diffraction, Fourier transform infrared spectra, transmission electron microscopy, X‐ray chemical analysis, diseases, enzymes, nanomedicine, biochemistry, spectrochemical analysisOther keywords: gold nanoparticles, Streptomyces coelicoflavus SRBVIT13, biosynthesis, UV–visible spectroscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, high‐resolution transmission electron microscopy, energy‐dispersive X‐ray analysis, antitype II diabetes activity, in vitro enzyme inhibition activity, in vivo postprandial antihyperglycemic activity, streptozotocin induced diabetic albino Wister rats, type II diabetes mellitus, Au