Sorption of Cu(II) ions by nano‐scale zero valent iron supported on rubber seed shell

This study focused on synthesising nano‐scale zero valent iron (NZVI) impregnated on a low‐cost agro‐waste material, rubber seed shell (RSS), by borohydride reduction method. The characterisation studies of NZVI‐RSS were performed by Fourier transform infrared spectroscopy, scanning electron microscopy and X‐ray diffraction. The adsorption execution of NZVI‐RSS for Cu(II) ions evacuation from synthetic wastewater was explored by batch studies. The optimum condition for the present adsorption system is as follows: Cu(II) ion concentration = 25 mg/l; solution pH = 6.0; contact time = 30 min; NZVI‐RSS dose = 3 g/l; temperature = 30°C. The sorption data were best portrayed by pseudo‐first‐order and Freundlich models. The outcomes demonstrated the multilayer sorption of Cu(II) ions by NZVI‐RSS. The Langmuir capacity was observed as 48.18 mg/g. Thermodynamic parameters, ΔG °, ΔH ° and ΔS ° were ascertained, and it was watched that the adsorption system was unconstrained and exothermic. The sticking probability for Cu(II) ions by NZVI‐RSS was found to be high at lower temperature. At long last, the research inquire about reasoned that NZVI‐RSS has demonstrated unrivalled adsorption capacity. Also NZVI‐RSS is thought to be really green and financially amicable support for wastewater treatment.Inspec keywords: adsorption, copper, X‐ray diffraction, scanning electron microscopy, wastewater treatment, Fourier transform infrared spectroscopyOther keywords: nano‐scale zero valent iron, rubber seed shell, copper ions, borohydride reduction method, NZVI‐RSS, Fourier transform infrared spectroscopy, scanning electron microscopy, X‐ray diffraction, adsorption execution, synthetic wastewater, Langmuir capacity, Freundlich models, adsorption system, wastewater treatment, adsorption capacity, Cu     

Production of a new platform based on fumed and mesoporous silica nanoparticles for enhanced solubility and oral bioavailability of raloxifene HCl

The purpose of the present study was to compare mesoporous and fumed silica nanoparticles (NPs) to enhance the aqueous solubility and oral bioavailability of raloxifene hydrochloride (RH). Mesoporous silica NPs (MSNs) and fumed silica NPs were used by freeze‐drying or spray‐drying methods. MSNs were obtained with different ratios of cetyltrimethylammonium bromide. Saturation solubility of the NPs was compared with the pure drug. The optimised formulation was characterised by scanning electron microscopy (SEM), X‐ray diffraction (XRD) and differential scanning calorimetry. The pharmacokinetic studies were done by oral administration of a single dose of 15 mg/kg of pure drug or fumed silica NPs of RH in Wistar rats. MSNs enhanced the solubility of RH from 19.88 ± 0.12 to 76.5 μg/ml. Freeze‐dried fumed silica increased the solubility of the drug more than MSNs (140.17 ± 0.45 μg/ml). However, the spray‐dried fumed silica caused about 26‐fold enhancement in its solubility (525.7 ± 93.5 μg/ml). Increasing the ratio of silica NPs enhanced the drug solubility. The results of XRD and SEM analyses displayed RH were in the amorphous state in the NPs. Oral bioavailability of NPs showed 3.5‐fold increase compared to the pure drug. The RH loaded fumed silica NPs prepared by spray‐drying technique could more enhance the solubility and oral bioavailability of RH.Inspec keywords: differential scanning calorimetry, mesoporous materials, freezing, nanofabrication, drug delivery systems, silicon compounds, drying, drugs, solubility, spraying, X‐ray diffraction, biomedical materials, scanning electron microscopy, nanoparticles, biochemistry, amorphous state, nanomedicineOther keywords: freeze‐dried fumed silica, spray‐dried, drug solubility, spray‐drying technique, fumed silica nanoparticles, mesoporous silica nanoparticles, aqueous solubility, mesoporous silica NPs, freeze‐drying, saturation solubility, differential scanning calorimetry, oral administration, fumed silica NPs     

Biogenic copper nanoparticles promote the growth of pigeon pea (Cajanus cajan L.)

Environmental pollution and toxicity have been increasing due to the overuse of chemical fertilisers, which has encouraged nanotechnologists to develop eco‐friendly nano‐biofertilisers. The authors demonstrated the effect of biogenic copper nanoparticles (CuNPs) on the growth of pigeon pea (Cajanus cajan L.). The UV–visible analysis showed absorbance at 615 nm. Nanoparticle tracking and analysis revealed particle concentration of 2.18 × 10⁸ particles/ml, with an average size of 33 nm. Zeta potential was found to be −16.7 mV, which showed stability. X‐ray diffraction pattern depicted the face centred cubic structure of CuNPs; Fourier transform infrared spectroscopy demonstrated the capping due to acidic groups, and transmission electron micrograph showed nanoparticles with size 20–30 nm. The effect of CuNPs (20 ppm) on plant growth was studied, for the absorption of CuNPs by plants on photosynthesis, which was evaluated by measuring chlorophyll a fluorescence using Handy‐Plant Efficiency Analyser. CuNPs treatment showed a remarkable increase in height, root length, fresh and dry weights and performance index of seedlings. The overall growth of plants treated with CuNPs after 4 weeks was recorded. The results revealed that inoculation of CuNPs contribute growth and development of pigeon pea due to growth promoting activity of CuNPs.Inspec keywords: pollution, toxicology, nanotechnology, cropsOther keywords: biogenic copper nanoparticles, pigeon pea, Cajanus cajan L, environmental pollution, toxicity, chemical fertilisers, nanotechnologists, eco‐friendly nano‐biofertilisers, cash crop, UV‐visible analysis, nanoparticle tracking, zeta potential, X‐ray diffraction pattern, Fourier transform infrared spectroscopy, acidic groups, transmission electron micrograph, photosynthesis, chlorophyll, fluorescence, Handy‐Plant Efficiency Analyser, performance index     

Biosynthesis and characterisation of nano‐silica as potential system for carrying streptomycin at nano‐scale drug delivery

A growing trend within nanomedicine has been the fabrication of self‐delivering supramolecular nanomedicines containing a high and fixed drug content ensuring eco‐friendly conditions. This study reports on green synthesis of silica nanoparticles (Si‐NPs) using Azadirachta indica leaves extract as an effective chelating agent. X‐ray diffraction analysis and Fourier transform‐infra‐red spectroscopic examination were studied. Scanning electron microscopy analysis revealed that the average size of particles formed via plant extract as reducing agent without any surfactant is in the range of 100–170 nm while addition of cetyltrimethyl ammonium bromide were more uniform with 200 nm in size. Streptomycin as model drug was successfully loaded to green synthesised Si‐NPs, sustain release of the drug from this conjugate unit were examined. Prolong release pattern of the adsorbed drug ensure that Si‐NPs have great potential in nano‐drug delivery keeping the environment preferably biocompatible, future cytotoxic studies in this connection is helpful in achieving safe mode for nano‐drug delivery.Inspec keywords: silicon compounds, nanofabrication, nanomedicine, drug delivery systems, nanoparticles, X‐ray diffraction, Fourier transform infrared spectra, scanning electron microscopyOther keywords: nanosilica, streptomycin, nanoscale drug delivery, nanomedicine, silica nanoparticles, Azadirachta indica leaves extract, X‐ray diffraction analysis, Fourier transform‐infrared spectroscopy, scanning electron microscopy, cetyltrimethyl ammonium bromide, SiO₂      

Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa

Pseudomonas aeruginosa lectin is purified and nanoparticle‐conjugated in an attempt to inhibit biofilm formation. Thirteen (23.6%) P. aeruginosa isolates are obtained from chicken meat samples, of which 30.8% are biofilm producers and 69.2% are lectin producers. Lectin is purified 36.8‐fold to final specific activity of 506.9 U/mg. Four nanoparticle types are prepared via laser ablation: platinum (Pt), gold (Au), silica oxide (SiO₂), and tin oxide (SnO₂). The four types are characterised, and pulse feeding is used to conjugate the lectin and nanoparticles. Pt, Au, SiO_2, and SnO₂ nanoparticles inhibit biofilm formation, especially SiO₂ nanoparticles, which have higher effectiveness when conjugated with purified lectin. SiO₂‐conjugated lectin significantly (p < 0.05) inhibits biofilm formation more effectively than control and other nanoparticle‐conjugated lectins. Au‐, Pt nanoparticle‐, and SnO₂‐conjugated lectins inhibit biofilm significantly compared with control (p < 0.05), and rhlR gene expression is decreased in the presence of SiO₂‐conjugated lectin. Furthermore, lectin and Pt, Au, SiO₂ and SnO₂ nanoparticles separately, and their conjugated lectins, are effective biofilm inhibitors. Of these, SiO₂‐conjugated lectin was most significant as an anti‐biofilm. Moreover, virulence factors regulon and RhlR were reduced by SiO₂‐conjugated lectin, indicating that this conjugation may also decrease the virulence of P. aeruginosa.     

High‐performance immunosensor for urine albumin using hybrid architectures of ZnO nanowire/carbon nanotube

In this work, the authors reported the hybrid architecture of carbon nanotube (CNT)–zinc oxide (ZnO) nanowire as a multi‐functional probe in amperometric immunosensor for the detection of urine albumin. Low‐cost substrate such as glass is possible because of novel low‐temperature growth process of CNT/ZnO nanowires as a multi‐function electrode in this sensor. Based on Schottky like behaviour this structure exhibit excellent high current density to achieve higher performance. Measurement of urine albumin is a new way for early detection of diabetic and also low concentration of it in culture media is also considered in order to verify the conversion of stem cells to liver cells. Human albumin serum antibody is used as a selective and sensitive part. The amperometric performance of immunosensor is studied and showed excellent performance for detection of albumin in urine samples. Very high linear range (from 3.3 ng/µl to 3.3 mg/µl) with a correlation coefficient of 0.825 and low detection limit (3.3 ng/µl or 4.96 × 10⁻⁸ mol l⁻¹) are the main characteristics of this sensor. Due to the high dynamic range and sensitivity, this sensor was also used in medical diagnosis and biomedical applications.Inspec keywords: biosensors, zinc compounds, wide band gap semiconductors, nanosensors, nanowires, carbon nanotubes, amperometric sensors, II‐VI semiconductors, electrochemical electrodes, Schottky effect, current density, chemical variables measurementOther keywords: amperometric immunosensor, low‐temperature growth process, current density, multifunction electrode probe, nanowire‐carbon nanotube architectures, CNT, human albumin serum antibody detection, Schottky like behaviou, urine albumin measurement, diabetic detection, stem cell conversion, liver cell conversion, medical diagnosis, biomedical applications, ZnO‐C     

Fabrication and characterization of biodegradable PHBV/SiO2 nanocomposite for thermo‐mechanical and antibacterial applications in food packaging

In the present study, biogenic silica nanoparticles (bSNPs) were synthesized from groundnut shells, and thoroughly characterized to understand its phase, and microstructure properties. The biopolymer was synthesized from yeast Wickerhamomyces anomalus and identified as Poly (3‐hydroxybutyrate‐co ‐3‐hydroxyvalerate) (PHBV) by GC‐MS and NMR analysis. The bSNPs were reinforced to fabricate PHBV/SiO₂ nanocomposites via solution casting technique. The fabricated PHBV/SiO₂ nanocomposites revealed intercalated hybrid interaction between the bSNPs and PHBV matrix through XRD analysis. PHBV/SiO₂ nanocomposites showed significant improvement in physical, chemical, thermo‐mechanical and biodegradation properties as compared to the bare PHBV. The cell viability study revealed excellent biocompatibility against L929 mouse fibroblast cells. The antibacterial activity of PHBV/SiO₂ nanocomposites was found to be progressively improved upon increasing bSNPs concentration against E. coli and S. aureus.Inspec keywords: X‐ray diffraction, microorganisms, antibacterial activity, nanoparticles, cellular biophysics, nanofabrication, silicon compounds, nanocomposites, filled polymers, nanomedicine, biomedical materials, casting, biodegradable materials, food packaging, food safety, biological NMROther keywords: antibacterial applications, poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate), PHBV matrix, biodegradable PHBV‐SiO₂ nanocomposite, thermomechanical biodegradation properties, biogenic silica nanoparticles, groundnut shells, microstructure properties, biopolymer, yeast Wickerhamomyces anomalus, GC‐MS, NMR analysis, food packaging, intercalated hybrid interaction, XRD analysis, cell viability study, solution casting, SiO₂      

Targeting microbial biofilms: by Arctium lappa l. synthesised biocompatible CeO2 ‐NPs encapsulated in nano‐chitosan

This study is planned to synthesise new biocompatible, nano antimicrobial formulation against biofilm producing strains. Aqueous root extract of Arctium lappa l. was used to synthesise ceria nanoparticles (CeO₂ ‐NPs). The synthesised nanoparticles were encapsulated with nano‐chitosan by sol–gel method and characterised using standard techniques. Gas chromatography‐mass spectrometer of Arctium lappa l. revealed the presence of ethanol, acetone, 1‐ propanol, 2‐methylethane, 1,1‐di‐ethoxy, 1‐Butanol, and oleic acid acted as reducing and surface stabilising agents for tailoring morphology of CeO₂ ‐NPs. Erythrocyte integrity after treatment with synthesised nanomaterials was evaluated by spectrophotometer measurement of haemoglobin release having biocompatibility. Scanning electron microscopy revealed the formation of mono dispersed beads shaped particles with mean particle size of 26.2 nm. X‐ray diffractometry revealed cubic crystalline structure having size of 28.0 nm. After encapsulation by nano‐chitosan, the size of CeO₂ ‐NPs enhances to 48.8 nm making average coverage of about 22.6 nm. The synthesised nanomaterials were found effective to disrupt biofilm of S. aureus and P. aeruginosa. Interestingly, encapsulated CeO₂ ‐NPs revealed powerful antibacterial and biofilm disruption activity examined by fluorescent live/dead staining using confocal laser scanning microscopy. The superior antibacterial activities exposed by encapsulated CeO₂ ‐NPs lead to the conclusion that they could be useful for controlling biofilm producing multidrug resistance pathogens.Inspec keywords: particle size, microorganisms, organic compounds, nanomedicine, sol‐gel processing, cellular biophysics, scanning electron microscopy, optical microscopy, nanoparticles, antibacterial activity, fluorescence, biomedical materials, nanofabrication, X‐ray diffraction, chromatography, filled polymers, cerium compoundsOther keywords: microbial biofilms, aqueous root extract, sol–gel method, gas chromatography‐mass spectrometer, 1‐di‐ethoxy, 1‐Butanol, nanomaterial synthesis, mean particle size, antibacterial activities, ethanol, acetone, 1‐ propanol, biocompatible ceria‐nanoparticle encapsulation, nano‐chitosan, Arctium lappa l., oleic acid, erythrocyte integrity, spectrophotometer measurement, haemoglobin release, mono dispersed beads shaped particle formation, X‐ray diffractometry, cubic crystalline structure, fluorescent live/dead staining, confocal laser scanning microscopy, multidrug resistance pathogens, size 26.2 nm, size 28.0 nm, size 48.8 nm, size 22.6 nm, CeO₂      

Facile microwave‐assisted synthesis of NiO nanoparticles and its effect on soybean (Glycine max)

NiO nanoparticles in high purity, 15 ± 0.5 nm in size, were prepared via solid‐state microwave irradiation. The [Ni(NH₃)₆](NO₃)₂ complex as a novel source was decomposed in the presence of microwave irradiation for a short time (10 min). The present method is facile, safe, and low‐cost. This method exhibits other advantages; there is no need of a solvent, fuel, surfactant, expensive material, or complex instrument. Synthesised NiO nanoparticles were determined by various analyses. Also, for the first time, NiO nanoparticle effects on biochemical factors in soybean were investigated. Seeds of soybean were grown in the Murashige and Skoog agar medium containing different concentrations of NiO nanoparticles (0, 200, and 400 mg/L) for 21 days under growth chamber conditions. Estimates of malondialdehyde, hydrogen peroxide contents, and antioxidant enzymes (catalase and ascorbate peroxidase) under treatment of NiO nanoparticles were assayed. The result showed that by significantly increasing the concentration of NiO nanoparticles, the activity of catalase and ascorbate peroxidase enzymes was enhanced. Malondialdehyde and hydrogen peroxide contents significantly increased in the presence of NiO nanoparticles. In this study, the increasing activity of catalase and ascorbate peroxidase was not enough for radical oxygen species detoxification.Inspec keywords: nickel compounds, molecular biophysics, biotechnology, microorganisms, nanoparticles, biochemistry, microwave materials processing, hydrogen compounds, enzymes, cellular biophysicsOther keywords: solid‐state microwave irradiation, synthesised NiO nanoparticles, soybean, facile microwave‐assisted synthesis, biochemical factors, Murashige, Skoog agar medium, malondialdehyde, hydrogen peroxide contents, antioxidant enzymes, ascorbate peroxidase enzymes, radical oxygen species detoxification, NiO, [Ni(NH₃)₆](NO₃)₂      

Preparation of alginate oligosaccharide nanoliposomes and an analysis of their inhibitory effects on Caco‐2 cells

The conditions were optimised for preparing Alginate oligosaccharide (AOS) nanoliposomes, and Caco‐2 cell experiments were carried out to examine their antitumour effects. The optimal formulation of AOS nanoliposomes was as follows: a phosphatidylcholine‐to‐cholesterol ratio of 5.12, AOS concentration of 8.44 mg/mL, Tween 80 concentration of 1.11%, and organic phase to aqueous phase ratio of 5.25. Under the above conditions, the experimental encapsulation efficiency was 65.84%, and the AOS nanoliposomes exhibited a small particle size of 323 nm. After Caco‐2 cells were treated with AOS liposomes and AOS for 24 h, AOS nanoliposomes inhibited the growth of Caco‐2 cells to a greater extent than AOS at concentrations of 0.0625, 0.125, 0.25, 0.5 and 1 mg/mL (P  <  0.01). LDH leakage exhibited a concentration‐dependent increase following treatment with 0.5‐1 mg/mL AOS nanoliposomes, and the inhibitory effect of AOS nanoliposomes exhibited a more significant difference than AOS (P  <  0.01). Cells treated with 0.5 mg/mL and 1 mg/mL AOS nanoliposomes displayed a substantial and significant increase in activity compared with AOS (P  < 0.01). Based on these results, AOS nanoliposomes exerted a more significant effect on inhibiting Caco‐2 cell proliferation than AOS.Inspec keywords: evaporation, cellular biophysics, biomedical materials, biomembranes, nanomedicine, enzymes, biochemistry, drug delivery systems, particle size, response surface methodology, molecular biophysics, encapsulation, drugs, lipid bilayers, nanofabrication, materials preparation, polymers, nanostructured materialsOther keywords: reverse‐phase evaporation method, response surface methodology, alginate oligosaccharide nanoliposomes, mitochondrial function, AOS concentration, AOS liposomes, Caco‐2 cell proliferation, AOS nanoliposomes, methyl thiazolyl tetrazolium assay, cell counting kit‐8, lactate dehydrogenase, LDH assay, phosphatidylcholine‐to‐cholesterol ratio, size 323.0 nm, time 24.0 hour     

Fabrication of cellulose nanoparticles through electrospraying

This study reports the fabrication of cellulose nanoparticles through electrospraying the solution of cellulose in N,N ‐dimethylacetamide/lithium chloride solvent as well as investigating the effect of electrospraying conditions and molecular weight on the average size of electrosprayed nanoparticles. Electrospraying of cellulose was carried out with the following range for each factor, namely concentration = 1–3 wt%, voltage = 15–23 kV, nozzle–collector distance = 10–25 cm, and feed rate = 0.03–0.0875 ml/h. The smallest nanoparticles had an average size of around 40 nm. Results showed that lowering the solution concentration and feed rate, as well as increasing the nozzle–collector distance and applied voltage led to a decrease in the average size of the electrosprayed cellulose nanoparticles. Fourier transform infrared analysis proved that no chemical change had occurred in the cellulose structure after the electrospraying process. According to X‐ray diffraction (XRD) results, cellulose nanoparticles showed a lower degree of crystallinity in comparison with the raw cellulose powder. XRD results also proved the absence of LiCl salt in the electrosprayed nanoparticles.Inspec keywords: polymers, nanoparticles, nanofabrication, spraying, molecular weight, particle size, Fourier transform infrared spectra, X‐ray diffraction, polymer structureOther keywords: cellulose nanoparticles, electrospraying, N,N‐dimethylacetamide‐lithium chloride solvent, molecular weight, solution concentration, feed rate, nozzle‐collector distance, Fourier transform infrared analysis, X‐ray diffraction, XRD, crystallinity, cellulose powder, voltage 15 kV to 23 kV     

Protein adsorption on spark plasma sintered 2d‐, 3d‐ and lamellar type mesoporous silicate compacts

The preparation of lamellar type mesoporous silica (MPS) compact through the spark plasma sintering (SPS) and the adsorption/desorption of protein onto MPS compact are reported to be compared with those onto 2d‐hexagonal and 3d‐cubic type MPS compacts. A lamellar‐type MPS powder (MPS‐la) was prepared using triblock copolymer, PEO₅ PPO₆₈ PEO₅, and was compacted in a carbon die and heated at 500°C for 5 min under uniaxial pressure. The products are referred to as MPS‐la‐500. The MPS compacts keep the lamellar type mesoporous configuration. The adsorbed amount of protein onto MPS‐la‐500 was 100 mg/g, while that on MPS‐la was 130 mg/g, and the former decreased by 23%. However, its decreasing ratio of the protein adsorption on MPS‐la‐500 was less than those of 2d‐hexagonal and 3d‐cubic type MPS compacts, which were 73 and 34%, respectively. The released amount of protein into PBS solution from MPS‐la‐500, which was soaked in the protein solution for 48 h, increased with the soaking time, while those from 2d‐ and 3d‐type MPS compacts reached to plateau for 4 h of soaking. The lamellar type MPS compact was found to be easier to absorb and release proteins, which may be due to the large aperture of the mesoporous configuration.Inspec keywords: silicon compounds, polymer blends, mesoporous materials, adsorption, plasma materials processing, proteins, sintering, powders, desorption, compaction, molecular biophysicsOther keywords: lamellar‐type MPS powder, PEO5PPO68PEO5, MPS‐la‐500, protein adsorption, lamellar type MPS compact, 3d‐cubic type MPS compact, spark plasma sintering, 2d‐hexagonal type MPS compacts, lamellar type mesoporous silicate compacts, lamellar type mesoporous silica compact, desorption, triblock copolymer, uniaxial pressure, PBS solution, protein solution, soaking time, temperature 500.0 degC, time 5.0 min, time 48.0 hour, time 4.0 hour, SiO₂      

Rapid synthesis of Bi 2 O 3 nano‐needles via ‘green route’ and evaluation of its anti‐fungal activity

Here, the authors report a rapid, simple, and eco‐friendly process for synthesis of Bi₂ O₃ nano‐needles. Dioscorea alata tuber extract was used as both reducing and capping agent for the first time. These nanoparticles were characterised by X‐ray diffraction, field emission scanning electron microscope, and Fourier transform infrared (FTIR) spectrometry, the nano‐structured Bi₂ O₃ needles have an average diameter of 158 nm with the lengths in the range of 1–3 μm. CLSI M27‐A2 standard was followed for evaluation of anti‐fungal activity. Bi₂ O₃ nano‐needles show remarkable activity against Candida albicans. It exhibits four time greater activity than bulk Bi₂ O₃ powder and two time greater activity than itraconazole, which makes it a potent anti‐fungal drug.Inspec keywords: bismuth compounds, nanoparticles, X‐ray diffraction, field emission scanning electron microscopy, Fourier transform infrared spectra, drugs, nanomedicine, biomedical materials, nanofabricationOther keywords: nanoneedles, antifungal activity, nanoparticles, X‐ray diffraction, field emission scanning electron microscope, Fourier transform infrared spectrometry, CLSI M27‐A2 standard, Candida albicans, itraconazole, antifungal drug, Bi₂ O₃      

Novel nanoplex‐mediated plant transformation approach

Here, a rapid and easy transformation by electroporation technique for gene transfer in plants using cell penetrating amino nanocomplex (nanoplex) has been demonstrated in Nicotiana. Nanoplex was prepared using cell penetrating amino acids (CPAs) such as poly‐L‐lysine (PLL) and Argenine (Arg), in combination with the gold nanoparticles (AuNPs). PLLs‐modified nanoplex with zeta potential of 34.2 ± 1.22 mV charge showed 63.3% efficiency for gene transformation in plant cells as compared to 60% when modified with Arg and the zeta potential was found to be 30.0 ± 0.83 mV; whereas, the transformation efficiency without nanoplex was found to be 6.6%. The findings indicate that the zeta potential of positively charged nanocomplex (AuNPs/CPAs/DNA/CPAs) increases the transformation efficiency because of their ability to protect the DNA from electroporation wave and endogenous enzyme damage. Transformation was confirmed by GUS assay and amplification of npt gene. This technique may open up new possibilities of gene transfer in plants, which will enable to produce large number of transgenic plants.Inspec keywords: biochemistry, electrokinetic effects, DNA, biomedical materials, nanomedicine, nanoparticles, gold, cellular biophysics, enzymes, genetics, molecular biophysics, genomicsOther keywords: nanoplex‐mediated plant transformation approach, electroporation technique, gene transfer, cell penetrating amino nanocomplex, cell penetrating amino acids, poly‐L‐lysine, Arg, gold nanoparticles, PLLs‐modified nanoplex, zeta potential, gene transformation, plant cells, transformation efficiency, positively charged nanocomplex, electroporation wave, npt gene, transgenic plants, AuNPs‐CPAs‐DNA‐CPAs, voltage 32.980000000000004 mV to 35.42 mV, voltage 29.169999999999998 mV to 30.830000000000002 mV, Au     

Superparamagnetic hematite nanoparticle: Cytogenetic impact on onion roots and seed germination response of major crop plants

Augmented escape of nanostructures to the ecosystem has necessitated the comprehensive study of their impact, especially on plants. In the current study, hematite nanoparticles were prepared by employing garlic extract and checked for their cytogenetic effect on onion roots and germination characteristics of five agricultural crops (Vigna radiata, Triticum aestivum, Trigonella foenum‐graecum, Cicer arietinum and Vicia faba) in the concentration range of 20–100 mg/L. Onion roots exhibited an increased mitotic index till 60 mg/L dosage, beyond which trend decreased marginally. Percentage of aberrant chromosomes reported for 100 mg/L exposure was very low (3.358 ± 0.13%) and included common defects such as clumped/sticky metaphase, ring chromosomes, laggards, spindle abnormality, chromosome bridges etc. Moreover, comet assay, DNA laddering experiment and electron micrograph study confirmed negligible damage to onion roots. Seed germination study indicated a positive response in different agronomic traits (germination index, root length, fold change in weight and vigour index) up to 60 mg/L, beyond which either negative or neutral effect was observed. However, none of the samples showed 50% inhibition in germination index; highest being 33.33% inhibition for V. faba, compared to the control. In brief, biogenic hematite nanoparticles caused insignificant phytotoxicity and were likely assimilated as iron source at lower dosage.Inspec keywords: cellular biophysics, agriculture, iron, cellular effects of radiation, crops, biological effects of gamma‐rays, soil pollution, agricultural engineering, DNA, superparamagnetism, nanoparticles, toxicology, food products, biotechnologyOther keywords: mitotic index, aberrant chromosomes, ring chromosomes, chromosome bridges, electron micrograph study, seed germination study, germination index, root length, biogenic hematite nanoparticles, superparamagnetic hematite nanoparticle, Cytogenetic impact, seed germination response, crop plants, cytogenetic effect, germination characteristics, agricultural crops, trigonella foenum‐graecum     

Design a protein gripper to capture a hydrophobic cargo

In recent years, the employment of nano‐robots in intelligent transferring of nano‐cargos and medical treatments has been in the spotlight of researchers. The first step is to present appropriate environmental nano‐parts with the potential ability to transform into nano‐robots. prefoldin, which is a molecular chaperone, is introduced as a new protein nano‐actuator being capable of capturing nano‐cargos with different charges and various sizes, which can also be used in medical applications. By the aid of mutation, in this work authors have designed a new prefoldin nano‐actuator in order to capture hydrophobic nano‐cargo, meaning that the hydrophobic amino acids in the nano‐actuator have substituted hydrophilic amino acids. Then, the interaction between the mutated nano‐actuator and the desired cargo was investigated through the all‐atom molecular dynamics simulations in an explicit solvent environment and at 310 K temperature. The designed nano‐actuator managed to attach to the cargo with four tentacles out of six possible tentacles by leveraging the available attraction between hydrophobic amino acids. Given the results obtained from this research, it can be percieved that the designed prefoldin nano‐actuator can serve as a potential factor in transferring the hydrophobic cargos and inhibiting the pathogenic factors.Inspec keywords: molecular biophysics, molecular dynamics method, hydrophilicity, nanomedicine, biochemistry, proteins, hydrophobicity, grippersOther keywords: protein gripper, hydrophobic cargo, nanorobots, medical treatments, appropriate environmental nanoparts, protein nanoactuator, hydrophobic nanocargo, acids, mutated nanoactuator, desired cargo, designed nanoactuator, designed prefoldin nanoactuator, temperature 310.0 K     

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     

A comparative study on chitosan nanoparticle synthesis methodologies for application in aquaculture through toxicity studies

Chitosan nanoparticles (CSNPs) have been recently used for various applications in aquaculture, especially as drug carriers. The aim of this study was to synthesise and investigate a superlative method of CSNP synthesis for application in aquaculture through aquaculture‐based toxicology screening methods. Two different methods were analysed: the first a direct ionic gelation method (A) and the other involving a low‐molecular‐weight chitosan microparticle intermediate method (B). Dynamic light scattering characterisation revealed that the CSNP particle sizes were 192.7 ± 11.8 and 22.9 nm from methods A and B, respectively. The LC₅₀ values for brine shrimp toxicity were found to be 1.51 and 0.02 ppt in 24 h for methods A and B, respectively. Acute toxicity studies in Litopenaeus vannamei rendered LC₅₀ values of 3235.94 and 2884.03 ppt in 24 h for methods A and B, respectively. Zebrafish toxicity studies revealed mortality rates of 21.67% and 55% at 20 mg/L concentration for methods A and B, respectively, with an increased expression of intracellular reactive oxygen species in method B. From these findings, it can be concluded that a comparatively reduced toxicity of CSNPs derived from ionic gelation method makes it more appropriate for application in aquaculture.     

Fabrication,calibration, and preliminary testing of microcantilever‐based piezoresistive sensor for BioMEMS applications

In this study, the authors demonstrate the fabrication, calibration, and testing of a piezoresistive microcantilever‐based sensor for biomedical microelectromechanical system (BioMEMS) application. To use any sensor in BioMEMS application requires surface modification to capture the targeted biomolecules. The surface alteration comprises self‐assembled monolayer (SAM) formation on gold (Au)/chromium (Cr) thin films. So, the Au/Cr coating is essential for most of the BioMEMS applications. The fabricated sensor uses the piezoresistive technique to capture the targeted biomolecules with the SAM/Au/Cr layer on top of the silicon dioxide layer. The stiffness (k) of the cantilever‐based biosensor is a crucial design parameter for the low‐pressure range and also influence the sensitivity of the microelectromechanical system‐based sensor. Based on the calibration data, the average stiffness of the fabricated microcantilever with and without Au/Cr thin film is 141.39 and 70.53 mN/m, respectively, which is well below the maximum preferred range of stiffness for BioMEMS applications. The fabricated sensor is ultra‐sensitive and selective towards Hg²⁺ ions in the presence of other heavy metal ions (HMIs) and good enough to achieve a lower limit of detection 0.75 ng/ml (3.73 pM/ml).Inspec keywords: molecular biophysics, bioMEMS, chemical sensors, microfabrication, cantilevers, microsensors, self‐assembly, monolayers, gold, piezoresistive devices, calibration, chromium, thin film sensors, mercury (metal), silicon compoundsOther keywords: microcantilever‐based piezoresistive sensor, BioMEMS application, biomedical microelectromechanical system application, targeted biomolecules, piezoresistive technique, cantilever‐based biosensor, microelectromechanical system‐based sensor, microcantilever fabrication, calibration, surface modification, surface alteration, self‐assembled monolayer, SAM, coating, thin films, HMI, heavy metal ion, Au‐Cr‐SiO₂ , Hg     

Graphene oxide‐ellagic acid nanocomposite as effective anticancer and antimicrobial agent

In this study, ellagic acid (ELA), a skin anticancer drug, is capped on the surface(s) of functionalised graphene oxide (GO) nano‐sheets through electrostatic and π–π staking interactions. The prepared ELA‐GO nanocomposite have been thoroughly characterised by using eight techniques: Fourier‐transform infrared spectroscopy (FTIR), zeta potential, X‐ray diffraction (XRD), thermogravimetric analysis (TGA), Raman spectroscopy, atomic force microscopy (AFM) topographic imaging, transmission electron microscopy (TEM), and surface morphology via scanning electron microscopy (SEM). Furthermore, ELA drug loading and release behaviours from ELA‐GO nanocomposite were studied. The ELA‐GO nanocomposite has a uniform size distribution averaging 88 nm and high drug loading capacity of 30 wt.%. The in vitro drug release behaviour of ELA from the nanocomposite was investigated by UV–Vis spectrometry at a wavelength of λ _max 257 nm. The data confirmed prolonged ELA release over 5000 min at physiological pH (7.4). Finally, the IC ₅₀ of this ELA‐GO nanocomposite was found to be 6.16 µg/ml against B16 cell line; ELA and GO did not show any cytotoxic effects up to 50 µg/ml on the same cell lines.