Synthesis,characterisation and anti‐tumour activity of biopolymer based platinum nanoparticles and 5‐fluorouracil loaded platinum nanoparticles

A facile and green synthesis of platinum nanoparticles [gum kondagogu platinum nanoparticles (GKPtNP)] using biopolymer‐ gum kondagogu was developed. The formation of GKPtNP was confirmed by ultraviolet (UV)–visible spectroscopy, scanning electron microscopy–energy dispersive X‐ray spectroscopy, transmission electron microscopy, X‐ray diffraction, Zeta potential, Fourier transform infrared, inductively coupled plasma mass spectroscopy. The formed GKPtNP are well dispersed, homogeneous with a size of 2–4 ± 0.50 nm, having a negative zeta potential (−46.1 mV) indicating good stability. 5‐Fluorouracil (5FU) was loaded onto the synthesised GKPtNP, which leads to the development of a new combination of nanomedicine (5FU–GKPtNP). The in vitro drug release studies of 5FU–GKPtNP in pH 7.4 showed a sustained release profile over a period of 120 min. Agrobacterium tumefaciens induced in vitro potato tumour bioassay was employed for screening the anti‐tumour potentials of GKPtNP, 5FU, and 5FU–GKPtNP. The experimental results suggested a complete tumour inhibition by 5FU–GKPtNP at a lower concentration than the GKPtNP and 5FU. Furthermore, the mechanism of anti‐tumour activity was assessed by their interactions with DNA using agarose gel electrophoresis and UV‐spectroscopic analysis. The electrophoresis results revealed that the 5FU–GKPtNP totally diminishes DNA and the UV‐spectroscopic analysis showed a hyperchromic effect with red shift indicating intercalation type of binding with DNA. Over all, the present study revealed that the combined exposure of the nanoformulation resulted in the enhanced anti‐tumour effect. Inspec keywords: nanoparticles, transmission electron microscopy, biomedical materials, tumours, ultraviolet spectra, DNA, drugs, electrophoresis, polymers, platinum, pH, drug delivery systems, biochemistry, X‐ray chemical analysis, microorganisms, molecular biophysics, electrokinetic effects, X‐ray diffraction, scanning electron microscopy, cancer, nanofabrication, visible spectra, nanomedicine, Fourier transform infrared spectra, materials preparationOther keywords: 5FU–GKPtNP, 5‐fluorouracil loaded platinum nanoparticles, gum kondagogu platinum nanoparticles, antitumour activity, scanning electron microscopy‐energy dispersive X‐ray spectroscopy, biopolymer‐based platinum nanoparticles, biopolymer‐based platinum nanoparticles, ultraviolet‐visible spectroscopy, UV‐visible spectroscopy, transmission electron microscopy, X‐ray diffraction, zeta potential, Fourier transform infrared spectroscopy, inductively coupled plasma mass spectroscopy, nanomedicine, in vitro drug release studies, sustained release profile, Agrobacterium tumefaciens, in vitro potato tumour bioassay, tumour inhibition, tumour activity, agarose gel electrophoresis, UV‐spectroscopic analysis, DNA, time 120.0 min, Pt     

Induction of extrinsic and intrinsic apoptosis in cervical cancer cells by Momordica dioica mediated gold nanoparticles

Bio‐fabrication of gold nanoparticles (AuNPs) has several advantages like biocompatibility, less toxicity, and eco‐friendly in nature over their chemical and physical methods. Currently, the authors fabricated AuNPs using aqueous root extract of Momordica dioica (M. dioica) and explored their anticancer application with mechanistic approaches. Different biophysical techniques such as UV–visible spectroscopy, Fourier transform infrared, X‐ray diffraction, transmission electron microscopy, selected area electron diffraction, and dynamic light scattering were employed for AuNPs characterisation. The synthesised AuNPs were mono‐dispersed, crystalline in nature, anionic surface (−23.9 mV), and spherical particle of an average diameter of 9.4 nm. In addition, the AuNPs were stable in buffers solutions and also biocompatible towards normal human cells (human vascular endothelial cells and human lung cells). The AuNPs were exhibited anticancer activity against different cancer cell lines such as human breast cancer cells, human cervical cancer cells (HeLa) and human lung cancer cells. Further, the pro‐apoptotic genes such as Bcl₂ were down‐regulated and BAX, Caspase‐3, −8, and −9 were up‐regulated in HeLa cells as compared to untreated cells. Annexin‐V‐FITC assay results showed that the AuNPs were induced apoptosis by accumulation of intracellular reactive oxygen species. To their knowledge, this is the first report on the synthesis of bioactive metal nanoparticles from M. dioica and it may open up new avenues in therapeutic applications.Inspec keywords: nanomedicine, tumours, lung, visible spectra, drug delivery systems, cancer, transmission electron microscopy, biomedical materials, molecular biophysics, light scattering, toxicology, electron diffraction, X‐ray diffraction, ultraviolet spectra, biomembranes, drugs, gold, biochemistry, particle size, cellular biophysics, nanoparticles, nanofabrication, Fourier transform infrared spectraOther keywords: extrinsic apoptosis, intrinsic apoptosis, mediated gold nanoparticles, biofabrication, physical methods, biophysical techniques, UV‐visible spectroscopy, X‐ray diffraction, transmission electron microscopy, selected area electron diffraction, AuNPs characterisation, normal human cells, human vascular endothelial cells, cancer cell lines, human breast cancer cells, human cervical cancer cells, human lung cancer cells, HeLa cells, untreated cells, bioactive metal nanoparticles, Momordica dioica mediated gold nanoparticles, Fourier transform infrared spectra, proapoptotic genes, Bcl₂ , BAX, Caspase‐3, Caspase‐9, Caspase‐8, Annexin‐V‐FITC assay, intracellular reactive oxygen species, therapeutic applications, voltage ‐23.9 mV, size 9.4 nm, Au     

Dual‐energy CT imaging of nasopharyngeal cancer cells using multifunctional gold nanoparticles

The purpose of this study is to measure the concentration of gold nanoparticles (AuNPs) attached to folic acid through cysteamin as the linker (FA‐Cys‐AuNPs) and AuNPs in KB human nasopharyngeal cancer cells using dual‐energy CT (DECT). In this study, nanoparticles with a size of ∼15 nm were synthesized and characterised using UV‐Vis, TEM, FTIR and ICP‐OES analyses. The non‐toxicity of nanoparticles was confirmed by MTT assay under various concentrations (40– 100 µg/ml) and incubation times (6, 12 and 24 h). To develop an algorithm for revealing different concentrations of AuNPs in cells, a corresponding physical phantom filled with 0.5 ml vials containing FA‐Cys‐AuNPs was used. The CT scan was performed at two energy levels (80 and 140 kVp). One feature of DECT is material decomposition, which allows separation and identification of different elements. The values obtained from the DECT algorithm were compared with values quantitatively measured by ICP‐OES. Cells were also incubated with AuNPs and FA‐Cys‐AuNPs at different concentrations and incubation times. Subsequently, by increasing the incubation time in the presence of FA‐Cys‐AuNPs, in comparison with AuNPs, DECT pixels were increased. Thus, FA‐Cys‐AuNPs could be a suitable candidate for targeted contrast agent in DECT molecular imaging of nasopharyngeal cancer cells.Inspec keywords: biomedical materials, phantoms, nanoparticles, computerised tomography, nanomedicine, cancer, toxicology, nanofabrication, gold, cellular biophysics, ultraviolet spectra, visible spectra, transmission electron microscopy, Fourier transform infrared spectraOther keywords: Au, time 24.0 hour, time 12.0 hour, time 6.0 hour, head cancer cells, DECT molecular imaging, DECT algorithm, material decomposition, physical phantom, MTT assay, ICP‐OES analyses, FTIR spectra, TEM, UV‐vis spectrophotometry, cysteamin, folic acid, gold nanoparticle concentration, nasopharyngeal cancer cells, dual‐energy CT imaging, neck cancer cells, KB human nasopharyngeal cancer cells, multifunctional gold nanoparticles     

Cross‐linking gold nanoparticles aggregation method based on localised surface plasmon resonance for quantitative detection of miR‐155

MiR‐155 plays a critical role in the formation of cancers and other diseases. In this study, the authors aimed to design and fabricate a biosensor based on cross‐linking gold nanoparticles (AuNPs) aggregation for the detection and quantification of miR‐155. Also, they intended to compare this method with SYBR Green real‐time polymerase chain reaction (PCR). Primers for real‐time PCR, and two thiolated capture probes for biosensor, complementary with miR‐155, were designed. Citrate capped AuNPs (18.7 ± 3.6 nm) were synthesised and thiolated capture probes immobilised to AuNPs. The various concentrations of synthetic miR‐155 were measured by this biosensor and real‐time PCR method. Colorimetric changes were studied, and the calibration curves were plotted. Results showed the detection limit of 10 nM for the fabricated biosensor and real‐time PCR. Also, eye detection using colour showed the weaker detection limit (1 µM), for this biosensor. MiR‐133b as the non‐complementary target could not cause a change in both colour and UV–visible spectrum. The increase in hydrodynamic diameter and negative zeta potential of AuNPs after the addition of probes verified the biosensor accurately fabricated. This fabricated biosensor could detect miR‐155 simpler and faster than previous methods.Inspec keywords: RNA, molecular biophysics, biochemistry, cancer, nanoparticles, gold, aggregation, surface plasmon resonance, molecular configurations, nanosensors, enzymes, calibration, ultraviolet spectra, visible spectra, eye, hydrodynamics, electrokinetic effects, biosensors, nanofabricationOther keywords: cross‐linking gold nanoparticles aggregation method, localised surface plasmon resonance, quantitative detection, cancers, diseases, biosensor, miR‐155 detection, miR‐155 quantification, SYBR green real‐time polymerase chain reaction, thiolated capture probes, citrate capped AuNPs, synthetic miR‐155, real‐time PCR method, colorimetric changes, calibration curves, eye detection, colour, detection limit, MiR‐133b, noncomplementary target, UV‐visible spectrum, hydrodynamic diameter, negative zeta potential, Au     

Biofabrication of gold nanoparticles using marine endophytic fungus – Penicillium citrinum

Nanotechnology is one of the promising fields of research and generating new avenues and applications in medicine. Recently, marine floras such as, marine endophytes are gaining the attention of many researchers due to the myriad of bioactive molecules that they possess. In addition, they find applications in many pharmaceutical and cosmetic industries. In this study, they have studied the green synthesis of gold nanoparticles (AuNPs) from Penicillium citrinum (P. citrinum) and its antioxidant activity. P. citrinum was isolated from brown algae. The identity of the fungus was established by comparing its 18S rDNA sequence. AuNPs were synthesised using P. citrinum and were characterised by UV–visible spectrophotometer (UV–vis), field emission scanning electron microscope (FESEM), X‐ray diffraction, Fourier transform infrared spectroscopy and dynamic light scattering (DLS). AuNPs were tested for free radical scavenging activity by 1,1‐diphenyl‐2‐picrylhydrazyl method. The particle sizes of AuNps were determined by FESEM and DLS. The reduction of gold metal ion was confirmed from the UV–vis spectrum. AuNPs showed significant antioxidant potential and the activity was comparable to the standard ascorbic acid. Further, in vitro and in vivo studies on these AuNPs will help in developing an alternative, cost‐effective and acceptable drug for various ailments.Inspec keywords: microorganisms, nanoparticles, gold, nanofabrication, particle size, nanobiotechnology, DNA, molecular biophysics, molecular configurations, ultraviolet spectra, visible spectra, field emission electron microscopy, scanning electron microscopy, X‐ray diffraction, Fourier transform infrared spectra, light scattering, free radical reactions, biochemistryOther keywords: biofabrication, gold nanoparticles, marine endophytic fungi, Penicillium citrinum, nanotechnology, medicine applications, marine floras, marine endophytes, bioactive molecules, pharmaceutical industries, cosmetic industries, antioxidant activity, brown algae, 18S rDNA sequence, UV‐visible spectrophotometer, field emission scanning electron microscope, FESEM, X‐ray diffraction, Fourier transform infrared spectroscopy, dynamic light scattering, free radical scavenging activity, 1,1‐diphenyl‐2‐picrylhydrazyl method, particle sizes, gold metal ion reduction, antioxidant potential, standard ascorbic acid, drug, ailments, Au     

Cu‐induced assembly of methanobactin‐modified gold nanoparticles and its peroxidase mimic activity

Methanobactin (Mb) is a small copper‐chelating molecule that functions as an agent for copper acquisition, uptake and copper‐containing methane monooxygenase catalysis in methane‐oxidising bacteria. The UV–visible spectral and fluorescence spectral suggested that Mb/Cu coordination complex as a monomer (Mb‐Cu), dimmer (Mb₂ ‐Cu) and tetramer (Mb₄ ‐Cu) could be obtained at different ratios of Mb to Cu (II). The kinetics of the oxidation of hydroquinone with hydrogen peroxide catalysed by the different Mb/Cu coordination complex were investigated. The results suggested that Mb₂ ‐Cu coordination form has highest catalytic capacity. Further, Mb‐modified gold nanoparticles (AuNPs) were obtained by ligand exchange and assembled into two‐ and three‐D nanocluster structure by metal‐organic coordination as driving force. It has been found that AuNPs increased the catalytic activity of Mb₂ ‐Cu on AuNPs. The more significant catalytic activity was exhibited by the nanocluster assembly with multi‐catalytic centres. This may be attributed to the multivalent collaborative characteristics of the catalytic active centres in the nanocluster network assembly. The assembly of Mb‐modified AuNPs can act as excellent nanoenzyme models for imitating peroxidase.Inspec keywords: nanoparticles, catalysis, oxidation, enzymes, microorganisms, nanobiotechnology, gold, organic compounds, reduction (chemical), visible spectra, molecular biophysics, ultraviolet spectra, biochemistry, copper, nanofabrication, fluorescenceOther keywords: Mb‐modified gold nanoparticles, catalytic active centres, Mb‐modified AuNPs, Cu‐induced assembly, methanobactin‐modified gold nanoparticles, peroxidase mimic activity, copper‐chelating molecule, copper‐containing methane monooxygenase catalysis, methane‐oxidising bacteria, fluorescence, Mb/Cu coordination complex, catalytic activity, UV–visible spectra, nanocluster assembly, Cu, Au     

Biosynthesis of gold nanoparticles using fungus Trichoderma sp. WL‐Go and their catalysis in degradation of aromatic pollutants

An efficient green method of gold nanoparticles (AuNPs) biosynthesis was achieved by cell‐free extracts of fungus Trichoderma sp. WL‐Go. Based on UV–Vis spectra, AuNPs biosynthesised by cell‐free extracts with 90 mg/l protein exhibited a characteristic absorption band at 556 nm and was stable for 7 days. Transmission electron microscopy images revealed that the as‐synthesised AuNPs were spherical and pseudo‐spherical, and the average size was calculated to be 9.8 nm with a size range of 1–24 nm. The AuNPs illustrated their good catalytic activities for reduction of nitro‐aromatics (2‐nitrophenol, 3‐nitrophenol, 4‐nitrophenol, 2‐nitroaniline, 3‐nitroaniline) with catalytic rate constants of 7.4 × 10⁻³ s⁻¹, 10.3 × 10⁻³ s⁻¹, 4.9 × 10⁻³ s⁻¹, 5.8 × 10⁻³ s⁻¹, 15.0 × 10⁻³ s⁻¹, respectively. Meanwhile, the AuNPs also showed excellent catalytic performance in decolourisation of azo dyes with decolourisation efficiency from 82.2 to 97.5%. This study provided a green gentle method for AuNPs synthesis as well as exhibiting efficient catalytic capability for degradation of aromatic pollutants.Inspec keywords: catalysts, dyes, particle size, reduction (chemical), nanobiotechnology, nanofabrication, ultraviolet spectra, gold, transmission electron microscopy, nanoparticles, proteins, catalysis, visible spectra, pollution control, microorganismsOther keywords: nitro‐aromatics, catalytic rate constants, decolourisation efficiency, green gentle method, efficient green method, gold nanoparticles biosynthesis, cell‐free extracts, UV–Vis spectra, characteristic absorption band, transmission electron microscopy images, as‐synthesised AuNPs, catalytic performance, protein, catalytic activities, efficient catalytic capability, fungus Trichoderma sp. WL‐Go, aromatic pollutants degradation, 2‐nitrophenol, 3‐nitrophenol, 4‐nitrophenol, 2‐nitroaniline, 3‐nitroaniline, azo dye decolourisation, Au     

Green synthesis of gold nanoparticles using Citrus maxima peel extract and their catalytic/antibacterial activities

The peel of Citrus maxima (C. maxima) is the primary byproducts during the process of fruit or juice in food industries, and it was always considered as biomass waste for further treatments. In this study, the authors reported a simple and eco‐friendly method to synthesise gold nanoparticles (AuNPs) using C. maxima peel extract as reducing and capping agents. The synthesised AuNPs were characterised by UV–visible spectrum, X‐ray diffraction (XRD), transmission electron microscope (TEM) and Fourier‐transform infrared spectroscopy (FTIR). The UV–visible spectrum of the AuNPs colloid showed a characteristic peak at 540 nm. The peaks of XRD analysis at (2θ) 38.30°, 44.28°, 64.62°, 77.57° and 81.75° were assigned to (111), (200), (220), (311) and (222) planes of the face‐centered cubic (fcc) lattice of gold. The TEM images showed that AuNPs were nearly spherical in shape with the size of 8–25 nm. The FTIR spectrum revealed that some bioactive compounds capped the surface of synthesised AuNPs. The biosynthesised AuNPs performed strong catalytic activity in degradation of 4‐nitrophenol to 4‐aminophenol and good antibacterial activity against both gram negative (Escherichia coli) and gram positive (Staphylococcus aureus) bacterium. The synthesis procedure was proved simple, cost effective and environment friendly.Inspec keywords: gold, nanoparticles, nanofabrication, X‐ray diffraction, ultraviolet spectra, visible spectra, transmission electron microscopy, Fourier transform infrared spectra, crystal structure, catalysis, antibacterial activity, nanobiotechnologyOther keywords: gold nanoparticles, Citrus maxima peel extract, UV–visible spectrum, X‐ray diffraction, transmission electron microscope, Fourier‐transform infrared spectroscopy, XRD analysis, faced centre cubic lattice, TEM images, catalytic activity, 4‐nitrophenol, 4‐aminophenol, antibacterial activity, gram negative bacterium, gram positive bacterium, Au     

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     

Method development for optimised green synthesis of gold nanoparticles from Millettia pinnata and their activity in non‐small cell lung cancer cell lines

Green synthesis of gold nanoparticles (GNPs) has received substantial attention, because nanoparticles are produced in an eco‐friendly way using biomolecules present in plant extracts in a single step reaction. This research article highlights GNPs obtained using shade‐dried leaf extracts of Millettia pinnata (L.) with aqueous auric chloride (HAuCl₄) at ambient temperature. In the present study, GNPs with average particle size 37 nm in size were fabricated. Furthermore, the synthesis method to obtain stable and monodispersed GNPs was advanced by optimising enzyme concentration 100 μg/ml, pH 5.4, substrate concentration 0.45 mM and 12 h time of reaction. The confirmation of GNPs formation and characterisation was followed by UV‐vis‐absorption spectroscopy, dynamic light scattering (DLS), and zeta potential (ZP) for the analysis of shape, size, and stability, respectively. TEM images and powder XRD revealed the GNPs synthesis of spherical‐shaped nanoparticles in the face‐centred cubic arrangement. Cytotoxicity of GNPs was studied against A549 lung cancer cells with IC₅₀ 14.76 μg/ml and found lower as compared to doxorubicin IC₅₀ 11.23 μg/ml but significant enough to be used as a vehicle GNPs produced using green source can be used as significant therapeutic agents and drug delivery carriers.Inspec keywords: nanomedicine, molecular biophysics, cancer, electrokinetic effects, pH, transmission electron microscopy, toxicology, gold, cellular biophysics, X‐ray diffraction, lung, biomedical materials, nanofabrication, nanoparticles, particle size, enzymes, visible spectra, ultraviolet spectra, light scattering, biochemistryOther keywords: method development, optimised green synthesis, gold nanoparticles, millettia pinnata, nonsmall cell lung cancer cell lines, plant extracts, single step reaction, shade‐dried leaf extracts, aqueous auric chloride, synthesis method, stable GNPs, monodispersed GNPs, spherical‐shaped nanoparticles, A549 lung cancer cells, green source, particle size, enzyme concentration, substrate concentration, biomolecules, reaction time, UV‐visible‐absorption spectroscopy, dynamic light scattering, zeta potential, TEM images, powder XRD, face‐centred cubic arrangement, cytotoxicity, pH, therapeutic agents, drug delivery carriers, time 12.0 hour, Au     

Multifaceted activities of plant gum synthesised platinum nanoparticles: catalytic,peroxidase, PCR enhancing and antioxidant activities

A single pot, green method for platinum nanoparticles (Pt NP) production was devised with gum ghatti (Anogeissus latifolia). Analytical tools: ultraviolet–visible (UV‐vis), dynamic light scattering, zeta potential, transmission electron microscope, X‐ray diffraction (XRD), and Fourier transform infrared spectroscopy were employed. Wide continuous UV‐vis absorption and black solution colouration proved Pt NP formation. Face‐centred cubic crystalline structure of NP was evidenced from XRD. NPs formed were nearly spherical with a mean particle size of 3 nm. NP demonstrated a myriad of properties including catalytic, peroxidase, polymerase chain reaction (PCR) enhancing and antioxidant activities. Catalytic action of NP was probed via NaBH₄ reduction of arsenazo‐III dye. NP displayed considerable peroxidase activity via catalysis of 3, 3′, 5, 5′‐tetramethylbenzidine oxidation by H₂ O₂. NP showed exceptional stability towards varying pH (3–11), temperature (25–100°C), salt concentration (0–100 mM) and storage time duration (0–12 months). In comparison with horse radish peroxidase, its applicability as an artificial peroxidase is advantageous. NP caused a two‐fold enhancement in PCR yield at 0.4 nM. Also showed significant 1′, 1′ diphenyl picryl‐hydrazyle scavenging (80.1%) at 15 µg/mL. Author envisages that the biogenic Pt NP can be used in a range of biological and environmental applications.Inspec keywords: nanofabrication, ultraviolet spectra, catalysis, molecular biophysics, enzymes, dyes, platinum, electrokinetic effects, transmission electron microscopy, particle size, X‐ray diffraction, visible spectra, pH, nanomedicine, nanoparticles, biochemistry, light scattering, scanning electron microscopy, Fourier transform infrared spectra, reduction (chemical), oxidationOther keywords: antioxidant activities, catalytic action, salt concentration, artificial peroxidase, two‐fold enhancement, PCR yield, multifaceted activities, plant gum synthesised platinum nanoparticles, gum ghatti, anogeissus latifolia, analytical characterisation tools, dynamic light scattering, zeta potential, X‐ray diffraction, XRD, black solution colouration, Pt NP formation, face‐centred cubic crystalline structure, peroxidase activity, ultraviolet‐visible spectroscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, particle size, catalytic activity, PCR enhancing activity, single pot green method, wide continuous UV‐visible absorption, polymerase chain reaction enhancing activity, arsenazo‐III, azo dye decolourisation, 3, 3′, 5, 5′‐tetramethylbenzidine oxidation, pH, environmental conditions, 1′,1′ diphenyl picryl‐hydrazyle scavenging, time 0.0 month to 12.0 month, temperature 25.0 degC to 100.0 degC, Pt     

Bare plasmonic metal nanoparticles: synthesis,characterisation and in vitro toxicity assessment on a liver carcinoma cell line

Metal nanoparticles have generated great interest due to their excellent optical and chemical properties. The widely used chemical method for synthesising nanoparticles involves capping agents for colloidal stability. However, there are scarce reports on the application of metal nanoparticles synthesised without using capping agents. Hence, there is a need to develop pristine nanoparticles devoid of capping that can be used for translational research. Here, the authors developed a facile and rapid method for synthesising bare metal nanoparticles (platinum/silver/gold) that are chemically reactive and stable for a month upon storage. They synthesised bare metal nanoparticles of sub‐15 nm and characterised using standard techniques (UV–VIS‐NIR/DLS/zeta//TEM/XRD). They assessed the safety of the synthesised nanoparticles on the liver carcinoma cell line (HepG2). Bare gold and platinum nanoparticles were non‐toxic in comparison to bare silver nanoparticles. Bare metal nanoparticles were also checked for metal detection wherein antimony, mercury and chromium were detected using bare gold and silver nanoparticles. The spectroscopic shifts of the nanoparticles when bound to metals resulted in blue and red shifting of the plasmon band, indicating the sensing of metals. These results show that bare metal nanoparticles have the potential to emerge as a promising candidate for biomedical and sensing applications.Inspec keywords: ultraviolet spectra, electrokinetic effects, liver, cellular biophysics, nanoparticles, cancer, toxicology, gold, platinum, X‐ray diffraction, silver, colloids, transmission electron microscopy, plasmonics, visible spectra, nanomedicineOther keywords: bare plasmonic metal nanoparticles, liver carcinoma cell line, capping agents, pristine nanoparticles, bare metal nanoparticles, synthesised nanoparticles, platinum nanoparticles, silver nanoparticles, XRD, TEM     

Nutratherapeutics approach against cancer: tomato‐mediated synthesised gold nanoparticles

In this study, an eco‐friendly biosynthesis of stable gold nanoparticles (T‐GNPs) was carried out using different concentrations of tomato juice (nutraceuticals) as a reducing agent and tetrachloroauric acid as a metal precursor to explore their potential application in cancer therapeutics. The synthesis of T‐GNPs was monitored by UV‐visible absorption spectroscopy, which unveiled their formation by exhibiting the typical surface plasmon absorption maxima at 522 nm. The size of T‐GNPs was found to be 10.86 ± 0.6 nm. T‐GNPs were characterised by dynamic light scattering, zeta potential, transmission electron microscopy analysis and Fourier transform infrared spectroscopy. T‐GNPs were further investigated for their anti‐cancer activity against human lung carcinoma cell line (A ₅₄₉) and human cervical cancer cell line wherein the IC₅₀ values were found to be 0.286 and 0.200 mM, respectively. T‐GNPs inhibited the growth of cancer cells by generating ROS and inducing apoptosis. T‐GNPs were found highly effective by virtue of their size, metallic property and capping molecules. Thus, this study opens up the prospects of using nutraceutical (tomato juice) as nutratherapeutic agent (T‐GNPs) against critical diseases like lung cancer and cervical cancer.Inspec keywords: gold, nanoparticles, particle size, cancer, ultraviolet spectra, visible spectra, electrokinetic effects, transmission electron microscopy, Fourier transform infrared spectra, cellular biophysics, spectrochemical analysis, nanomedicine, nanofabricationOther keywords: tomato‐mediated synthesised gold nanoparticles, tomato juice, reducing agent, tetrachloroauric acid, cancer therapeutics, UV‐visible absorption spectroscopy, surface plasmon absorption, dynamic light scattering, zeta potential, transmission electron microscopy analysis, Fourier transform infrared spectroscopy, human lung carcinoma cell line, anticancer activity, human cervical cancer cell line, nutratherapeutic agent, lung cancer, Au     

Biosynthesis of silver nanoparticles using Azadirachta indica leaves: characterisation and impact on Staphylococcus aureus growth and glutathione‐S‐transferase activity

Silver nanoparticles (AgNPs) are toxic to various microbes, but the mechanism of action is not fully understood. The present report explores Azadirachta indica leaf extract as a reducing agent for the rapid biosynthesis of AgNPs. The effects of AgNPs on the growth, glutathione‐S‐transferase (GST) activity, and total protein concentration in Staphylococcus aureus were investigated, as was its antibacterial activity against seven other bacterial strains. Nanoparticle synthesis was confirmed by the UV‐Vis spectrum and colour change of the solution. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential analysis, and infrared spectroscopy were used to characterise the synthesised nanoparticles. The UV‐Visible spectrograph showed an absorbance peak at 420 nm. DLS analysis showed an average AgNP size of 159 nm and a Polydispersity Index of 0.373. SEM analysis showed spherical particle shapes, while TEM established an average AgNP size of 7.5 nm. The element analysis profile showed small peaks for calcium, potassium, zinc, chlorine, with the presence of oxygen and silver. AgNPs markedly affected the growth curves and GST activity in treated bacteria, and produced moderate antibacterial activity. Thus AgNPs synthesised from A. indica leaves can interrupt the growth curve and total protein concentration in bacterial cells.Inspec keywords: ultraviolet spectra, microorganisms, nanomedicine, visible spectra, nanoparticles, electrokinetic effects, antibacterial activity, scanning electron microscopy, infrared spectra, transmission electron microscopy, light scattering, nanofabrication, particle size, silver, enzymes, biochemistry, molecular biophysics, cellular biophysicsOther keywords: silver nanoparticles, glutathione‐S‐transferase activity, green leaves, rapid biosynthesis, total protein concentration, nanoparticle synthesis, colour change, zeta potential analysis, UV‐Visible spectrograph, DLS analysis, SEM analysis, element analysis profile, growth curve, GST activity, bacterial strains, antibacterial activity, staphylococcus aureus growth, microbes, Azadirachta azadirachta indica leaf, reducing agent, scanning electron microscopy, transmission electron microscopy, dynamic light scattering, infrared spectroscopy, absorbance peak, polydispersity index, spherical particle shapes, TEM, bacterial cells, Ag     

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     

Assessment of in‐vivo biocompatibility evaluation of phytogenic gold nanoparticles on Wistar albino male rats

Nanomedicine is an interdisciplinary approach that involves toxicology and other medicinal applications. Gold nanoparticles (AuNPs) may serve as a promising model to address the size and shape‐dependent biological response because they show good biocompatibility. This study is to prepare phytosynthesis AuNPs from ten different Cassia sp. Among them, the aqueous leaf extract of C. roxburghii produced greater efficient and stable AuNPs. The AuNPs were optimised for different physicochemical conditions. Highly stable AuNPs were synthesised at pH 7.0, 37°C, 1.0 ml of C. roxburghii leaf extract and 1.0 mM concentration of HAuCl₄ with the particle size of ∼50 nm and these AuNPs were stable up to 12 months. To determine the safety profile of AuNPs in‐vivo, the nanoparticles were injected intravenously into male Wistar albino rats in varying dosages. The authors noticed no significant difference in body weights, haematological and biochemical parameters and the histopathological sections of all vital organs. Highest accumulation was seen in spleen and least in brain. The authors’ results show that the AuNPs were biocompatible and did not produce any adverse or abnormalities in‐vivo. The implications of the bioaccumulation of AuNPs need to be further studied to rule out any adverse effects on long‐term exposure.Inspec keywords: blood, nanoparticles, cellular biophysics, pH, nanomedicine, particle size, nanofabrication, gold, biomedical materialsOther keywords: in‐vivo biocompatibility evaluation, phytogenic gold nanoparticles, phytosynthesis AuNPs, physicochemical conditions, Wistar albino male rats, nanomedicine, Cassia sp., aqueous leaf extract, C. roxburghii leaf extract, particle size, bioaccumulation, temperature 37.0 degC, Au     

Cytotoxicity of spherical gold nanoparticles synthesised using aqueous extracts of aerial roots of Rhaphidophora aurea (Linden ex Andre) intertwined over Lawsonia inermis and Areca catechu on MCF‐7 cell line

A facile synthesis of gold nanoparticles (GNPs) using the aqueous extracts of the aerial roots of Rhaphidophora aurea (Linden ex Andre) intertwined over Lawsonia inermis and Areca catechu was carried out under different conditions, namely room temperature, higher temperature, sonication, solar irradiation and pH variation. The surface plasmon resonance (SPR) band at 536 and 575 nm obtained in UV–visible spectrum revealed the formation of AuNP''s. The sharp SPR band of the synthesised nanogold indicates the formation of spherical‐shaped and uniform‐sized nanoparticles. The TEM analysis revealed spherical nanogold particles of size 35 and 10 nm for MM and MP extracts. The secondary metabolites present in the aqueous extract are suggested to be responsible for the reduction of metal ions to metal nanoparticles as evidenced from results of FTIR analysis. Rapid synthesis of GNPs by sunlight is the production of microscopic grains of gold due to the dissociation of gold chloride. This may induce the reaction between secondary metabolites and gold chloride solutions and results in GNPs. The cytotoxic activity of the synthesised nanogold studied against human breast cancer cells (MCF‐7) by 3‐[4,5‐dimethylthiazol‐2‐yl]2,5‐diphenyltetrazolium bromide assay showed significant activity at higher concentration.Inspec keywords: toxicology, gold, nanoparticles, nanomedicine, nanofabrication, cellular biophysics, particle size, surface plasmon resonance, ultraviolet spectra, visible spectra, transmission electron microscopy, dissociation, cancer, biological organs, Fourier transform infrared spectraOther keywords: cytotoxicity, spherical gold nanoparticles, aerial roots, Rhaphidophora aurea, Linden ex Andre, Lawsonia inermis, Areca catechu, MCF‐7 cell line, sonication, solar irradiation, pH variation, surface plasmon resonance, UV–visible spectrum, spherical‐shaped nanoparticles, uniform‐sized nanoparticles, TEM analysis, spherical nanogold particles, secondary metabolites, metal ions, FTIR analysis, microscopic grains, dissociation, gold chloride solutions, cytotoxic activity, human breast cancer cells, 3‐[4,5‐dimethylthiazol‐2‐ yl]2,5‐diphenyltetrazolium bromide assay, wavelength 536 nm, wavelength 575 nm, Au     

Assessment of cytotoxicity and immune compatibility of phytochemicals‐mediated biosynthesised silver nanoparticles using Cynara scolymus

The study was focused on the phytochemicals‐mediated biosynthesis of silver nanoparticles using leaf extracts and infusions from Cynara scolymus. To identify the antioxidant activity and total phenolic content, the 1,1‐diphenyl‐1‐picrylhydrazyl and Folin–Ciocalteau methods were applied, respectively. The formation and stability of the reduced silver ions were monitored by UV–vis spectrophotometer. The particle sizes of the silver nanoparticles were characterised using the dynamic light scattering technique and scanning electron microscope. The phase composition of the obtained silver nanoparticles was characterised by X‐ray diffraction. The silver nanoparticles suspension, artichoke infusion, and silver ions were separately tested towards potential cytotoxicity and pro‐inflammatory effect using mouse fibroblasts and human monocytes cell line, respectively. The total phenolic content and antioxidant activity of ethanol extract and infusion were found significantly higher as compared to aqueous extract and infusion. The UV–visible spectrophotometric analysis revealed the presence of the characteristic absorption band of the Ag nanoparticles. Moreover, it was found that with the increasing volume of plant extract, the average size of particles was increased. Biocompatibility results evidently showed that silver nanoparticles do not induce monocyte activation, however in order to avoid their cytotoxicity suspension at a concentration <2 ppm should be applied.Inspec keywords: pharmaceuticals, health and safety, renewable materials, toxicology, organic compounds, antibacterial activity, X‐ray diffraction, nanomedicine, nanoparticles, nanofabrication, suspensions, ultraviolet spectra, visible spectra, scanning electron microscopy, silver, particle sizeOther keywords: phytochemicals‐mediated biosynthesis, antioxidant activity, total phenolic content, dynamic light scattering technique, silver nanoparticles suspension, scanning electron microscopy, Cynara scolymus, 1,1 diphenyl‐1‐picrylhydrazyl method, cytotoxicity, immune compatibility, leaf extracts, UV‐vis spectrophotometry, particle size, Folin‐Ciocalteau methods, phase composition, X‐ray diffraction, artichoke infusion, pro‐inflammatory effect, mouse fibroblasts, human monocytes cell line, Ag     

Phyto‐mediated synthesis,biological and catalytic activity studies of gold nanoparticles

In the present study, a phyto‐mediated synthesis of gold nanoparticles (AuNPs) using an isoflavone, Dalspinosin (5,7‐dihydroxy‐6,3′,4′‐trimethoxy isoflavone) isolated from the alcoholic extract of roots of Dalbergia coromandeliana is reported. It is observed that Dalspinosin itself acts both as a reducing and a capping agent in the synthesis of the nanoparticles (NPs). An ultraviolet–visible (UV–Vis) spectral study showed a surface plasmon resonance band at 526 nm confirming the formation of AuNPs. The NPs formed were characterised by UV–Vis spectroscopy, Fourier transform‐infrared spectroscopy, X‐ray diffraction (XRD), high‐resolution transmission electron microscopy (HR‐TEM) with energy‐dispersive x‐ray spectroscopy (EDX) and dynamic light scattering. HR‐TEM analysis showed the synthesised AuNPs were spherical in shape with a size of 7.5 nm. The AuNPs were found to be stable for seven months when tested by in vitro methods showed good antioxidant and anti‐inflammatory activities. They also showed moderate anti‐microbial activities when tested against Gram positive (Staphylococcus aureus and Streptococcus sp), Gram negative bacterial strains (Klebsiella pneumonia and Klebsiella terrigena) and fungal strain (Candida glabrata). The biosynthesised AuNPs showed significant catalytic activity in the reduction of methylene blue with NaBH₄ to leucomethylene blue.Inspec keywords: biomedical materials, catalysis, Fourier transform infrared spectra, gold, light scattering, microorganisms, nanomedicine, nanoparticles, spectrochemical analysis, surface plasmon resonance, transmission electron microscopy, ultraviolet spectra, visible spectra, X‐ray chemical analysis, X‐ray diffractionOther keywords: phyto‐mediated synthesis, biological activity studies, catalytic activity studies, dalspinosin (5,7‐dihydroxy‐6,3′,4′‐trimethoxy isoflavone), alcoholic extract, roots, Dalbergia coromandeliana, ultraviolet‐visible spectral study, surface plasmon resonance band, UV‐Vis spectroscopy, Fourier transform‐infrared spectroscopy, X‐ray diffraction, high‐resolution transmission electron microscopy, EDX analysis, dynamic light scattering, HR‐TEM analysis, antioxidant activities, antiinflammatory activities, antimicrobial activities, Gram positive bacterial strains, Staphylococcus aureus, Streptococcus sp, Gram negative bacterial strains, wavelength 526 nm, size 7.5 nm, time 7 month, Au     

Evaluation of ‘green’ synthesis and biological activity of gold nanoparticles using Tragopogon dubius leaf extract as an antibacterial agent

Currently, the use of ‘green’ synthesised nanoparticles with environmentally friendly properties is considered a novel therapeutic approach in medicine. Here, the authors evaluated gold nanoparticles (AuNPs) conjugated with Tragopogon dubius leaf extract and their antibacterial activity in vitro and in vivo. Colour changes from yellow to dark brown and a peak at 560 nm on ultraviolet–visible spectroscopy confirmed the formation of nanoparticles. Additionally, transmission electron microscopy, X‐ray diffraction, and Fourier transform infrared spectroscopy analyses were performed to determine particle sizes and functional groups involved in gold reduction. Moreover, using standard micro‐dilution and disc‐diffusion assays against Klebsiella pneumoniae, Bacillus cereus, Escherichia coli, and Staphylococcus aureus, the antimicrobial properties of synthesised AuNPs were investigated. To confirm antibacterial activity, synthesised AuNPs were applied in a rat model on burn wounds infected with S. aureus, and the nanoparticles were as effective as tetracycline in bacterial reduction and wound healing. In conclusion, the synthesis of AuNPs with aqueous T. dubius extract was rapid, simple, and inexpensive, and the synthesised nanoparticles had significant antibacterial activity in vitro and in vivo.Inspec keywords: transmission electron microscopy, wounds, nanoparticles, ultraviolet spectra, reduction (chemical), particle size, nanofabrication, gold, X‐ray diffraction, antibacterial activity, microorganisms, visible spectra, nanomedicine, biomedical materials, Fourier transform infrared spectraOther keywords: biological activity, gold nanoparticles, antibacterial agent, therapeutic approach, colour changes, ultraviolet–visible spectroscopy, transmission electron microscopy, gold reduction, antimicrobial properties, Fourier transform infrared spectroscopy analyses, disc‐diffusion assay, green synthesis, Tragopogon dubius leaf, in vitro antibacterial activity, in vivo antibacterial activity, X‐ray diffraction, particle sizes, functional groups, standard microdilution assay, burn wounds, S. aureus, tetracycline, bacterial reduction, wound healing, wavelength 560.0 nm