Enhancement of secondary metabolites in Bacopa monnieri (L.) Pennell plants treated with copper‐based nanoparticles in vivo

The study aims to document the effect of starch‐stabilised copper‐based nanoparticles (CuNPs) on the biosynthesis of pharmaceutically valuable secondary metabolites, especially saponins, of the reputed nootropic herb Bacopa monnieri (L.) Pennell. CuNPs were synthesised chemically by the reduction of cupric sulphate pentahydrate with ascorbic acid using starch as the capping agent. They were characterised by UV–visible spectrophotometry, Fourier‐transform infra‐red spectroscopy, X‐ray diffraction, high‐resolution transmission electron microscopy and zeta potential. The nanoparticles consisted of cuprous oxide and metallic copper, were approximately spherical, polydispersed with diameter <20 nm. Hydroponically grown B. monnieri plants were treated in vivo with the CuNPs between the concentrations of 0–100 mg l⁻¹. Spectrophotometric estimation of the total contents of saponins, alkaloids, phenolics, flavonoids and DPPH radical scavenging capacity from the methanolic extracts of the whole plants showed a hormetic increase in the content of secondary metabolites in a concentration‐dependent manner from 5 mg l⁻¹ until it declined at toxic metabolic concentration. This was accompanied by an increase in ROS markers hydrogen peroxide and malondialdehyde as well as a hormetic effect on activities of phenylalanine ammonia lyase and antioxidant enzymes catalase, ascorbate peroxidase and superoxide dismutase. CuNPs at sub‐toxic concentrations were found to enhance secondary metabolism and antioxidant capacity in Bacopa monnieri through ROS‐mediated defence response.Inspec keywords: organic compounds, pharmaceuticals, copper compounds, visible spectra, nanofabrication, hydrogen compounds, transmission electron microscopy, reduction (chemical), ultraviolet spectra, electrokinetic effects, X‐ray diffraction, nanoparticles, toxicology, copper, enzymes, Fourier transform infrared spectra, health and safety, agricultural productsOther keywords: starch‐stabilised copper‐based nanoparticles, secondary metabolites, cupric sulphate pentahydrate, capping agent, UV–visible spectrophotometry, X‐ray diffraction, high‐resolution transmission electron microscopy, DPPH radical scavenging capacity, toxic metabolic concentration, antioxidant capacity, saponin content, chemical reduction, ascorbic acid, Fourier transform infrared spectroscopy, zeta potential, hydroponical growth, methanolic extracts, alkaloid content, flavonoid content, malondialdehyde, phenylalanine ammonia lyase, antioxidant enzymes catalase, ascorbate peroxidase, superoxide dismutase, sub‐toxic concentration, spectrophotometric estimation, phenolic content, Pennell plants, Bacopa monnieri L, in vivo treatment, ROS‐mediated defence response, Cu, Cu₂ O, H₂ O₂ , CuSO₄ H₂ O     

Investigation of ZnO nanoparticles on proline,anthocyanin contents and photosynthetic pigments and lipid peroxidation in the soybean

The interaction between nanoparticles and plants is inevitable. In this study, the effect of different concentrations of ZnO nanoparticles synthesised using olive extract on the soybean was studied. The soybean seeds were cultured in a Hoagland medium containing agar which was treated different concentrations (0, 200 and 400 ppm) of ZnO nanoparticles. After 21 days, the plants were harvested and the parameters of proline, anthocyanin, malondialdehyde (MDA), hydrogen peroxide (H₂ O₂), chlorophyll and carotenoid contents and phenylalanine ammonia‐lyase (PAL) and catalase (CAT) activity in soybeans (Glycine max) were measured. The results showed that the levels of chlorophyll a and b and carotenoid at concentrations of 200 and 400 ppm in comparison with control decreased, while carotenoid content at 200 ppm concentration at a concentration of 400 ppm was not significant. The level of anthocyanin and PAL activity increased with increasing concentration of nanoparticles, while proline content decreased. By increasing the concentration of ZnO nanoparticles, the content of MDA and hydrogen peroxide increased compared to control but CAT activity did not change significantly. This research suggests that ZnO nanoparticles synthesised using olive extract in soybean plants may be toxic by reactive oxygen species production.Inspec keywords: crops, pigments, enzymes, nanoparticles, zinc compounds, toxicology, agricultural safety, nanobiotechnology, hydrogen compoundsOther keywords: carotenoid content, proline content, ZnO nanoparticles, soybean plants, H₂ O₂ , ZnO, time 21.0 d, reactive oxygen species production, toxicity, catalase activity, phenylalanine ammonia‐lyase activity, chlorophyll content, Hoagland medium, olive extract, lipid peroxidation, photosynthetic pigments, hydrogen peroxide, anthocyanin contents     

Gold functionalised attapulgite for discrimination of hydrogen peroxide and oxidising ions

Aiming to monitor hydrogen peroxide and oxidizing ions in aqueous circumstance, functionalized attapulgite [i.e. gold‐modified attapulgite nanocomposites (Au/ATP NCs)] as peroxidase mimics were prepared by loading β‐cysteamine‐capped gold nanoparticles onto attapulgite with the use of electrostatic interactions. As‐prepared Au/ATP NCs were used for the detection of H₂ O₂. The linear range and detection limit for H₂ O₂ were determined by quantitative experiments emerging excellent stability and recyclability. The peroxidase‐like activity of Au/ATP NCs could be expanded for the detection of some oxidative ions (Fe³⁺ and Ag⁺) was also been discovered. Based on the absorption spectrum and steady‐state kinetics, the mechanism for peroxidase mimic reaction is investigated. This work represents the first example of multitarget detection for molecule and cations (H₂ O₂, Fe³⁺ and Ag⁺) using Au/ATP NCs as peroxidase enzyme mimics and holds a promise for future biomedical and analytical applications.Inspec keywords: hydrogen compounds, chemical sensors, nanocomposites, nanosensors, electrostatics, goldOther keywords: Au, H₂ O₂ , biomedical application, enzyme, cation detection, molecule detection, steady‐state kinetics, absorption spectrum, recyclability, stability, electrostatic interaction, β‐cysteamine‐capped gold nanoparticle, peroxidase, Au‐ATP NC, goldmodified attapulgite nanocomposite, oxidising ion, hydrogen peroxide, gold functionalised attapulgite     

Synthesis of nickel oxides nanoparticles on glassy carbon as an electron transfer facilitator for horseradish peroxidase: Direct electron transfer and H2O2 determination

In this study, horseradish peroxidase/nickel oxides nanoparticles/glassy carbon (HRP/NiO NPs/GC) electrode was prepared by first applying nickel oxides nanoparticles on glassy carbon surface and then horseradish peroxidase immobilized on the NiO NPs. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) have been used as a diagnostic tools to identify the synthesized NiO NPs. Immobilized HRP showed an electrochemical redox behavior pertained to HRP(Fe(III)–Fe(II)) by direct electron transfer between protein and nanoparticles with a formal potential (E^0′) of ? 55.5 mV (vs. Ag/AgCl and 141.5 mV vs. NHE) in 50 mM phosphate buffer solution (PBS). The anodic charge transfer coefficient (α) and heterogeneous electron transfer rate constant (k_s) were 0.42 and 0.75 s^? 1, respectively. Biocatalytic activity of HRP/NiO NPs/GC electrode for reduction of hydrogen peroxide and application to hydrogen peroxide determination was exemplified.     

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     

Catalytic hydrolysis of cellobiose using different acid‐functionalised Fe3 O4 magnetic nanoparticles

The present study demonstrated the preparation of three different acid‐functionalised magnetic nanoparticles (MNPs) and evaluation for their catalytic efficacy in hydrolysis of cellobiose. Initially, iron oxide (Fe₃ O₄)MNPs were synthesised, which further modified by applying silica coating (Fe₃ O₄ ‐MNPs@Si) and functionalised with alkylsulfonic acid (Fe₃ O₄ ‐MNPs@Si@AS), butylcarboxylic acid (Fe₃ O₄ ‐MNPs@Si@BCOOH) and sulphonic acid (Fe₃ O₄ ‐MNPs@Si@SO₃ H) groups. The Fourier transform infrared analysis confirmed the presence of above‐mentioned acid functional groups on MNPs. Similarly, X‐ray diffraction pattern and energy dispersive X‐ray spectroscopy analysis confirmed the crystalline nature and elemental composition of MNPs, respectively. TEM micrographs showed the synthesis of spherical and polydispersed nanoparticles having diameter size in the range of 20–80 nm. Cellobiose hydrolysis was used as a model reaction to evaluate the catalytic efficacy of acid‐functionalised nanoparticles. A maximum 74.8% cellobiose conversion was reported in case of Fe₃ O₄ ‐MNPs@Si@SO₃ H in first cycle of hydrolysis. Moreover, thus used acid‐functionalised MNPs were magnetically separated and reused. In second cycle of hydrolysis, Fe₃ O₄ ‐MNPs@Si@SO₃ H showed 49.8% cellobiose conversion followed by Fe₃ O₄ ‐MNPs@Si@AS (45%) and Fe₃ O₄ ‐MNPs@Si@BCOOH (18.3%). However, similar pattern was reported in case of third cycle of hydrolysis. The proposed approach is considered as rapid and convenient. Moreover, reuse of acid‐functionalised MNPs makes the process economically viable.Inspec keywords: scanning electron microscopy, catalysis, magnetic separation, magnetic particles, silicon compounds, iron compounds, nanomagnetics, coatings, X‐ray chemical analysis, nanoparticles, X‐ray diffraction, nanofabrication, Fourier transform infrared spectra, organic compounds, nanocompositesOther keywords: catalytic efficacy, alkylsulfonic acid, butylcarboxylic acid, energy dispersive X‐ray spectroscopy analysis, spherical polydispersed nanoparticles, cellobiose hydrolysis, acid‐functionalised MNPs, acid functional groups, cellobiose conversion, acid‐functionalised magnetic nanoparticle, silica coating, sulphonic acid, Fourier transform infrared analysis, SEM micrograph, X‐ray diffraction pattern, size 20.0 nm to 80.0 nm, Fe₃ O₄ , Si, SiO₂      

Effect of Ag‐NPs synthesised by Chamaemelum nobile extract on the inflammation and oxidative stress induced by carrageenan in mice paw

An environmentally friendly and rapid procedure was developed to synthesise silver nanoparticles (Ag‐NPs) by Chamaemelum nobile extract and to evaluate its in vivo anti‐inflammatory and antioxidant activities. The ultraviolet–visible absorption spectrum of the synthesised Ag‐NPs showed an absorbance peak at 422. The average size of spherical nanoparticles was 24 nm as revealed by transmission electron microscopy. Fourier transform infra‐red spectroscopy analysis supported the presence of biological active compounds involved in the reduction of Ag ion and X‐ray diffraction confirmed the crystalline structure of the metallic Ag. The anti‐inflammatory and antioxidant activity of the Ag‐NPs was investigated against carrageenan‐induced paw oedema in mice. The levels of malondialdehyde (MDA) and antioxidant enzymes superoxide dismutase, catalase, glutathione peroxidase and inflammatory cytokines tumour necrosis factor (TNF‐α), interferon gamma and interleukin (IL)‐6, IL‐1β were assessed in this respect. The results demonstrated that anti‐inflammatory activity of the Ag‐NPs might be due to the ability of the nanoparticles to reduce IL‐1β, IL‐6 and TNF‐α. Moreover, reduction of antioxidant enzymes along with an increase in MDA level shows that the anti‐inflammatory activity of the synthesised Ag‐NPs by C. nobile is attributed to its ameliorating effect on the oxidative damage.Inspec keywords: silver, nanoparticles, nanofabrication, ultraviolet spectra, visible spectra, particle size, transmission electron microscopy, Fourier transform infrared spectra, X‐ray diffraction, crystal structure, enzymes, molecular biophysics, tumours, biomedical materials, nanomedicineOther keywords: Chamaemelum nobile extract, oxidative stress, mice paw, silver nanoparticles, antiinflammatory activity, antioxidant activity, ultraviolet‐visible absorption spectrum, spherical nanoparticle size, transmission electron microscopy, Fourier transform infrared spectroscopy, biological active compounds, X‐ray diffraction, crystalline structure, carrageenan‐induced paw oedema, malondialdehyde, antioxidant enzymes, superoxide dismutase, catalase, glutathione peroxidase, inflammatory cytokines, tumour necrosis factor, interferon gamma, interleukin, IL‐1β, IL‐6, TNF‐α, MDA level, Ag     

In vitro germination and biochemical profiling of citrus reticulata in response to green synthesised zinc and copper nanoparticles

Green synthesis of nanoparticles by using plants is an emerging class of nanobiotechnology. It revolutionizes all the fields of nanobiotechnology by synthesizing chemical‐free nanoparticles for various purposes. In the present study, zinc and copper nanoparticles were synthesized by using the white leaves of Allium cepa and further characterized through Zeta analyzer and Scanning electron microscopy. Zeta analyzer elucidated that zinc nanoparticles ranged from 8‐32 nm while copper nanoparticles ranged from 15‐30 nm. Scanning electron microscopy clarified that zinc nanoparticles were irregular while copper nanoparticles were spherical in shape. The effects of green synthesized nanoparticles were evaluated on the germination frequency and biochemical parameters of plant tissues. The nucellus tissues were inoculated on Murashige and Skoog (MS) medium augmented with 30 µg/ml suspension of zinc and copper nanoparticles. Green synthesized nanoparticles enhanced the in vitro germination parameters because of their low toxicity and high efficacy. Significant results were obtained for germination parameters in response to the applications of zinc nanoparticles as compared to copper nanoparticles. These nanoparticles could also induce stress in plantlets by manipulating the endogenous mechanism as a result various defence compounds are produced which have potential in treating various human ailments. Copper nanoparticles showed higher toxicity as compared to zinc nanoparticles and triggered the production of antioxidative enzymes and non‐ enzymatic compounds.Inspec keywords: botany, zinc, copper, nanoparticles, nanofabrication, biochemistry, scanning electron microscopy, electrokinetic effects, biological tissues, toxicology, nanobiotechnology, biological techniquesOther keywords: in vitro germination, biochemical profiling, citrus reticulata, green synthesised zinc nanoparticles, green synthesised copper nanoparticles, green chemistry, secondary metabolites, nanoparticles synthesis, white leaves, Allium cepa, zeta analyser, scanning electron microscopy, onion extract, nucellus tissues, Murashige‐Skoog medium, biologically synthesised nanoparticles, toxicity, root length, shoot length, seedling vigour index, plantlets, endogenous mechanism, human ailments, antioxidative enzymes, nonenzymatic compounds, size 8 nm to 32 nm, Zn, Cu     

Assessment of AgNPs exposure on physiological and biochemical changes and antioxidative defence system in wheat (Triticum aestivum L) under heat stress

The present study was designed to check the role of silver nanoparticles (AgNPs) on physiological, biochemical parameters and antioxidants of wheat (Triticum aestivum L.) under heat stress. Plant extract of Moringa oleifera was used for AgNPs synthesis followed by characterization through UV–Vis spectroscopy, SEM, XRD and Zeta analyser. Heat stress was applied in range of 35–40°C for 3 hrs/ day for 3 days to wheat plants at trifoliate stage. Heat stress decreased the RWC (13.2%), MSI (16.3%), chl a (5.2%), chl b (4.1%) and TCCs (9.9%). Wheat plants treated with AgNPs showed significant increase in RWC (12.2%), MSI (26.5%), chl a (10%), chl b (16.4%), TCCs (19%), TPC (2.4%), TFC (2.5%), TASC (2.5%), SOD (1.3%), POX (1.5%), CAT (1.8%), APX (1.2%) and GPX (1.4%), under heat stress. Lower concentration of AgNPs (50 mg/l) decreased the sugar (5.8%) and proline contents (4%), while increase was observed in higher AgNPs concentrations. Overall, AgNPs treatment enhanced thermo‐tolerance in wheat plants, but the mechanism of AgNPs action needs further investigation at genome and proteome level in wheat plants under heat stress.Inspec keywords: crops, ultraviolet spectra, X‐ray diffraction, visible spectra, botany, microorganisms, scanning electron microscopy, solubility, agricultural products, nanoparticles, antibacterial activity, sugar, silver, food products, biochemistryOther keywords: heat stress, heat‐stress tolerance, wheat plants, AgNPs exposure, wheat antioxidative defence system, Triticum aestivum L, Moringa oleifera, biochemical parameters, silver nanoparticles, ultraviolet–visible spectroscopy, scanning electron microscopy, X‐ray diffraction, zeta analyser, total chlorophyll contents, TCCs, membrane stability index, MSI, malondialdehyde, sugar level, proline concentration, hydrogen peroxide, RWC, relative water content, total flavonoid content, phenolic content, ascorbate POX, guaiacol POX     

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     

Stimulation of secondary metabolites by copper and gold nanoparticles in submerge adventitious root cultures of Stevia rebaudiana (Bert.)

Nanotechnology is one of the advance technologies that almost found implications in every field of science. The importance is due to the unique properties of nanoparticles. In this study, bimetallic alloys of copper (Cu) and gold (Au) were tested in submerge root cultures of Stevia rebaudiana for production of biomass and secondary metabolites. A known amount of inoculum roots were submerged in liquid Murashige and Skoog medium containing combination of naphthalene acetic acid (NAA; 0.5 mg l⁻¹) and different ratios of nanoparticles (NPs). NAA augmented medium was used as control. The addition of nanoparticles (30 µg l⁻¹) stimulated biomass accumulation (1.447 g/flask) on 27th day of log phases. The maximum total phenolics content (TPC; 16.17 mg/g‐DW) and total flavonoids content (TFC; 4.20 mg/g‐DW) were displayed using AuCu‐NPs (1:3) and NAA. The same combinations enhanced total phenolic production (TPP; 116 mg/L) and total flavonoid production (TFP; 29.5 mg/L) in submerged cultures. A strong correlation was observed between phenolics, flavonoids and dry biomass. Moreover, maximum 1, 1‐diphenyl‐2‐picrylhydrazyl (DPPH) activity of 79% was displayed by addition of AuCu (1:3) nanoparticles. In conclusion, nanoparticles application has shown a positive effect in enhancing biomass and secondary metabolites production in adventitious root cultures of Stevia rebaudiana.Inspec keywords: bimetals, copper, gold, nanoparticles, renewable materials, bioenergy conversion, toxicology, nanofabrication, nanobiotechnology, biochemistry, molecular biophysicsOther keywords: Au‐Ag, time 27 d, maximum DPPH activity, dry biomass, flavonoids, phenolics, NAA enhanced total phenolic production, total flavonoid content, maximum total phenolic content, log phases, bimetallic NPs stimulated biomass accumulation, NAA augmented medium, naphthalene acetic acid, Skoog medium, liquid Murashige, inoculum roots, culture development, seed‐derived roots, bimetallic alloys, nanotechnology, Stevia rebaudiana (Bert.), submerge adventitious root cultures, gold nanoparticles, copper nanoparticles, secondary metabolites     

Synthesis of biopolymeric particles loaded with phosphorus and potassium: characterisation and release tests

The authors synthesised nanoparticles (NPs) loaded with P and K from KH₂ PO₄ using gelatin type‐A and type‐B, and sodium alginate as carriers. Using type‐A and type‐B gelatin, quasi‐spherical particles were obtained, with average sizes of 682 and 856 nm, respectively; with sodium alginate, the resulting NPs exhibited spherical shapes and 600 nm particle average size. The authors found an interaction between KH₂ PO₄ and alginate via the hydrogen bonds existent among the carboxylic groups of the carbohydrate and the OH‐groups of the H₂ PO₄ ‐; interactions among gelatin types with the OH‐groups and the H₂ PO₄ ‐ion were also observed. Adding trypsin to the distilled water solutions of the NPs coated with type‐A gelatin increased the concentration of P in the solution by threefold, while increasing that of K increased by 2.6‐fold. Conversely, adding α ‐amylase to the water solutions with sodium alginate increased the P and K concentrations in the solution by nearly 1.3‐ and 1.1‐fold, respectively. Thus, sodium alginate resulted in NPs with smaller sizes and better spherical formations, though with a high polydispersity index and lower release rate of P and K. This low release rate represents an advantage since plants demand nutrients for long periods, and conventional fertilisers display low use efficiency.Inspec keywords: nanofabrication, nanoparticles, hydrogen bonds, gelatin, biomedical materials, particle size, enzymes, molecular biophysics, biochemistry, nanobiotechnology, polymer films, potassium compoundsOther keywords: sodium alginate, biopolymeric particles, release tests, type‐B gelatin, spherical shapes, carboxylic groups, OH‐groups, distilled water solutions, type‐A gelatin, quasi‐spherical particles, particle average size, hydrogen bonds, trypsin, spherical formations, high polydispersity index, plants, α‐amylase, size 682.0 nm, size 856.0 nm, size 600.0 nm, H₂ PO₄ , KH₂ PO₄      

Photocatalytic degradation of synthetic dyes using iron (III) oxide nanoparticles (Fe2 O3 ‐Nps) synthesised using Rhizophora mucronata Lam

Biosynthesis of nanoparticles through plant extracts is gaining attention due to the toxic free synthesis process. The environmental engineering applications of many metal oxide nanoparticles have been reported. In this study, iron oxide nanoparticles (Fe₂ O₃ ‐Nps) were synthesised using a simple biosynthetic method using a leaf extract of a mangrove plant Rhizophora mucronata through reduction of 0.01 M ferric chloride. Fe₂ O₃ ‐Np synthesis was revealed by a greenish colour formation with a surface plasmon band observed close to 368 nm. The stable Fe₂ O₃ ‐Np possessed excitation and emission wavelength of 368.0 and 370.5 nm, respectively. The Fourier‐transform infrared spectral analysis revealed the changes in functional groups during formation of Fe₂ O₃ ‐Np. Agglomerations of nanoparticles were observed during scanning electron microscopic analysis and energy‐dispersive X‐ray spectroscopic analysis confirmed the ferric oxide nature. The average particle size of Fe₂ O₃ ‐Np based on dynamic light scattering was 65 nm. Based on transmission electron microscopic analysis, particles were spherical in shape and the crystalline size was confirmed by selected area electron diffraction pattern analysis. The synthesised Fe₂ O₃ ‐Np exhibited a good photodegradation efficiency with a reduction of 83 and 95% of phenol red and crystal violet under irradiation of sunlight and florescent light, respectively. This report is a facile synthesis method for Fe₂ O₃ ‐Np with high photodegradation efficiency.Inspec keywords: photochemistry, dyes, nanofabrication, transmission electron microscopy, scanning electron microscopy, nanoparticles, iron compounds, X‐ray diffraction, catalysts, catalysis, particle size, X‐ray chemical analysis, electron diffraction, Fourier transform infrared spectra, surface plasmonsOther keywords: energy‐dispersive X‐ray spectroscopic analysis, ferric oxide nature, transmission electron microscopic analysis, selected area electron diffraction pattern analysis, iron oxide nanoparticles, plant extracts, toxic free synthesis process, metal oxide nanoparticles, metal nanoparticles, nanofiltration, nanobiocides, Rhizophora mucronata Lam, crystalline size, phenol red, crystal violet, sunlight irradiation, florescent light, scanning electron microscopic analysis, Fourier‐transform infrared spectral analysis, surface plasmon, ferric chloride, leaf extract, nanocatalysts, nanoadsorbents, photocatalytic degradation, synthetic dyes, mangrove plant, water remediation, wastewater pollutant, wavelength 370.5 nm, wavelength 368.0 nm, Fe₂ O₃      

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     

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     

Antibacterial,anti‐inflammatory and antioxidant effects of acetyl‐11‐α‐keto‐β‐boswellic acid mediated silver nanoparticles in experimental murine mastitis

Mastitis is an important economic disease causing production losses in dairy industry. Antibiotics are becoming ineffective in controlling mastitis due to the emergence of resistant strains requiring the development of novel therapeutic agents. In this study, the authors present the phytochemical synthesis of silver nanoparticles (AgNPs) with acetyl‐11‐α‐keto‐β‐boswellic acid and evaluation of their activity in Staphylococcus aureus induced murine mastitis. Boswellic acid mediated AgNP (BANS) were oval, polydispersed (99.8 nm) with an minimum inhibitory concentration of 0.033 µg ml⁻¹ against S. aureus, inhibitory concentration (IC₅₀) of 30.04 µg ml⁻¹ on mouse splenocytes and safe at an in vivo acute oral dose of 3.5 mg kg⁻¹ in mice. Mastitis was induced in lactating mice by inoculating S. aureus (log₁₀ 5.60 cfu) and treated 6 h post‐inoculation with BANS (0.12 mg kg⁻¹, intramammary and intraperitoneal), and cefepime (1 mg kg⁻¹, intraperitoneal). S. aureus inoculated mice showed increased bacterial load, neutrophil infiltration in mammary glands and elevated C‐reactive protein (CRP) in serum. Oxidative stress was also observed with elevated malondialdehyde level, superoxide dismutase (SOD) and catalase (CAT) activities. BANS treatment significantly (P  < 0.05) reduced bacterial load, CRP, SOD, CAT activities and neutrophil infiltration in affected mammary glands. BANS could be a potential therapeutic agent for managing bovine mastitis.Inspec keywords: nanomedicine, nanoparticles, silver, antibacterial activity, drugs, diseases, enzymesOther keywords: antibacterial effects, antiinflammatory effects, antioxidant effects, acetyl‐11‐α‐keto‐β‐boswellic acid, mediated silver nanoparticles, experimental murine mastitis, economic disease, dairy industry, resistant strains, phytochemical synthesis, Staphylococcus aureus, minimum inhibitory concentration, inoculating S. aureus, neutrophil infiltration, mammary glands, elevated C‐reactive protein, superoxide dismutase, catalase, bovine mastitis, Ag     

Synthesis of ZnO/Fe3 O4 /rGO nanocomposites and evaluation of antibacterial activities towards E. coli and S. aureus

Antibacterial activity of nanoparticles (NPs) and nanocomposites (NCs) has received wide spread attention in biomedical applications. In this direction, the authors prepared zinc oxide (ZnO), iron oxide (Fe₃ O₄), and their composite including reduced graphene oxide (rGO) by hydrothermal method. The structural and microstructural properties of the synthesised NPs and NCs were investigated by XRD, FT‐IR, UV‐Vis, TGA, and TEM analysis. PEG‐coated ZnO and Fe₃ O₄ form in hexagonal wurtzite and inverse spinel structures, respectively. ZnO forms in rod‐shaped (aspect ratio of ∼3) morphology, whereas well‐dispersed spherical‐shaped morphology of ∼10 nm is observed in Fe₃ O₄ NPs. The ZnO/Fe₃ O₄ composite possesses a homogeneous distribution of above two phases and shows a very good colloidal stability in aqueous solvent. These synthesised particles exhibited varying antibacterial activity against gram‐positive strain Staphylococcus aureus (S. aureus) and gram‐negative strain Escherichia coli (E. coli). The nanocomposite exhibits a better cidal effect on E. coli when compared to S. aureus when treated with 1 mg/ml concentration. Further, the addition of rGO has intensified the anti‐bacterial effect to a much higher extent due to synergistic influence of individual components.Inspec keywords: colloids, visible spectra, II‐VI semiconductors, thermal analysis, nanofabrication, X‐ray diffraction, nanoparticles, biomedical materials, wide band gap semiconductors, transmission electron microscopy, ultraviolet spectra, antibacterial activity, nanocomposites, zinc compounds, nanobiotechnology, Fourier transform infrared spectra, graphene compounds, iron compounds, crystal growth from solution, crystal morphologyOther keywords: antibacterial activity, E. coli, biomedical applications, iron oxide, hydrothermal method, structural properties, microstructural properties, PEG‐coated ZnO, hexagonal wurtzite, inverse spinel structures, gram‐positive strain Staphylococcus aureus, S. aureus, gram‐negative strain Escherichia coli, nanocomposites, nanoparticles, XRD, FTIR spectra, UV‐vis spectra, TGA, TEM, rod‐shaped morphology, spherical‐shaped morphology, colloidal stability, cidal effect, ZnO‐Fe₃ O₄ ‐CO     

Paederia foetida Linn. promoted synthesis of CoFe2 O4 and NiFe2 O4 nanostructures and their photocatalytic efficiency

A facile method of synthesis of cobalt ferrite (CoFe₂ O₄) and nickel ferrite (NiFe₂ O₄) nanoparticles (NPs) was developed using urea as a hydroxylating agent and Paederia foetida Linn. (family: Rubiaceae) leaf extract as a bio‐template. The synthesised ferrite NPs were characterised in a detailed manner by powder X‐ray diffraction (XRD), transmission electron microscopy, Fourier transform‐infrared spectroscopy and vibrating sample magnetometer analysis. The XRD patterns revealed the formation of cubic face‐centred phase for both CoFe₂ O₄ and NiFe₂ O₄ NPs. These quasi‐spherical particles of CoFe₂ O₄ and NiFe₂ O₄ were shown to have sizes in the range of 10–80 and 5–50 nm, respectively. The photocatalytic activity of metal ferrites was evaluated in H₂ O₂ assisted oxidative degradation of methylene blue (MB) and rhodamine B (RhB) under irradiation of solar light. Both metal ferrite photocatalysts exhibited pronounced activity in degradation of MB and RhB, respectively, but relatively higher activity was observed for NiFe₂ O₄. After completion, the catalysts were recovered using an external magnet. Recycling of these recovered catalysts up to five times showed no noticeable change in the efficiency.Inspec keywords: nanoparticles, nanofabrication, photochemistry, catalysts, cobalt compounds, nickel compounds, ferrites, X‐ray diffraction, transmission electron microscopy, Fourier transform infrared spectra, crystal structure, dyesOther keywords: Paederia foetida Linn, nanostructures, photocatalytic efficiency, cobalt ferrite nanoparticles, nickel ferrite nanoparticles, hydroxylating agent, leaf extract, bio‐template, powder X‐ray diffraction, transmission electron microscopy, Fourier transform‐infrared spectroscopy, vibrating sample magnetometer analysis, cubic face‐centred phase, quasi‐spherical particles, photocatalytic activity, methylene blue, rhodamine B, size 5 nm to 80 nm, CoFe₂ O₄ , NiFe₂ O₄      

Gold nanoparticles decorated reduced graphene oxide nanolabel for voltammetric immunosensing

This study describes the development and testing of a simple and novel enzyme‐free nanolabel for the detection and signal amplification in a sandwich immunoassay. Gold nanoparticles decorated reduced graphene oxide (rGOAu) was used as the nanolabel for the quantitative detection of human immunoglobulin G (HIgG). The rGOAu nanolabel was synthesised by one pot chemical reduction of graphene oxide and chloroauric acid using sodium borohydride. The pseudo‐peroxidase behaviour of rGOAu makes the nanolabel unique from other existing labels. The immunosensing platform was fabricated using self‐assembled monolayers of 11‐mercaptoundecanoic acid (11‐MUDA) on a gold disc electrode. The covalent immobilisation of antibody was achieved through the bonding of the carboxyl group of 11‐MUDA and the amino group of the antibody using chemical linkers [1‐ethyl‐3‐(3‐dimethylaminopropyl)carbodiimide] and N ‐hydroxysuccinimide. The fabricated immunosensor exhibited a linear range that included HIgG concentrations of 62.5–500 ng ml⁻¹. The sensor was also used for the testing of HIgG in the blood sample.Inspec keywords: proteins, nanomedicine, reduction (chemical), chemical sensors, nanofabrication, electrochemical sensors, voltammetry (chemical analysis), gold, oxidation, self‐assembly, monolayers, molecular biophysics, biochemistry, biosensors, nanoparticles, nanosensors, blood, grapheneOther keywords: gold nanoparticles, voltammetric immunosensing, enzyme‐free nanolabel, signal amplification, sandwich immunoassay, human immunoglobulin G, rGOAu nanolabel, chloroauric acid, sodium borohydride, 11‐mercaptoundecanoic acid, 11‐MUDA, gold disc electrode, chemical linkers, 1‐ethyl‐3‐(3‐dimethylaminopropyl)carbodiimide], HIgG concentrations, reduced graphene oxide nanolabel, quantitative HIgG detection, one pot chemical reduction, covalent antibody immobilisation, carboxyl group bonding, pseudo‐peroxidase behaviour, self‐assembled monolayers, N‐hydroxysuccinimide, immunosensor, blood sample, Au‐CO