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      

TiO2 /chondroitin‐4‐sulphate nanocomposite coating on Ti–6Al–4V for implants and prostheses applications

Nano‐titania, chondroitin‐4‐sulphate, and titania/chondroitin‐4‐sulphate nanocomposite were separately deposited on Ti–6Al–4V alloys by repetitive spin coating. Surface characterisation techniques were used to find out the crystalline nature, chemical bonding, surface homogeneity, and elemental composition. Biological studies of nanocomposite‐coated alloys revealed the formation of stable hydroxyapatite (Ca/P = 1.678), superior corrosion resistance, and ∼12 mm zone of inhibition against Staphylococcus sp. However, the cell line studies revealed the better response on polymer‐coated alloy than the uncoated and composite‐coated alloy. It has been found that the nanocomposite coating can synergistically increase the thickness of the pre‐existing passive layer and thereby improve the corrosion resistance of Ti–6Al–4V implant in simulated body fluid. The nanocomposite coatings improved the corrosion resistance of the bare Ti–6Al–4V implant specimens by decreasing the i _corr. The formation of hydroxyapatite on nanocomposite‐coated alloy may have ability to inhibit the release of toxic substance to the adjacent tissues. In addition, the in vitro cell line study confers that the nanocomposite‐coated Ti–6Al–4V induces cell attachment and proliferation, and it eventually help to new bone cell formation than the uncoated one. Overall, this nanocomposite coating can be applied in orthopedic applications for effective biomimic bone regeneration.Inspec keywords: titanium compounds, nanocomposites, titanium alloys, aluminium alloys, vanadium alloys, nanomedicine, biomedical materials, prosthetics, X‐ray diffraction, Fourier transform spectra, infrared spectra, scanning electron microscopy, fluorescence, corrosion resistance, polymer films, calcium compounds, cellular biophysics, boneOther keywords: chondroitin‐4‐sulphate nanocomposite coating, implants, prostheses, nano‐titania, repetitive spin coating, surface characterisation, X‐ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, X‐ray fluorescence, TiAlV, TiO₂ , effective biomimic bone regeneration, orthopaedic applications, bone cell formation, osteoblast cells, cell proliferation, cell attachment, simulated body fluid solution, composite‐coated alloy, polymer‐coated alloy, Staphylococcus sp, corrosion resistance, hydroxyapatite, elemental composition, surface homogeneity, chemical bonding, crystalline nature     

In vitro evaluation of biodegradable nHAP‐Chitosan‐Gelatin‐based scaffold for tissue engineering application

The present study focuses on fabrication and characterisation of porous composite scaffold containing hydroxyapatite (HAP), chitosan, and gelatin with an average pore size of 250–1010 nm for improving wound repair and regeneration by Electrospinning method. From the results of X ‐Ray Diffraction (XRD) study, the peaks correspond to crystallographic structure of HAP powder. The presence of functional group bonds of HAP powder, Chitosan and scaffold was studied using Fourier Transform Infrared Spectroscopy (FTIR). The surface morphology of the scaffold was observed using Scanning Electron Microscope (SEM). The Bioactivity of the Nano composite scaffolds was studied using simulated body fluid solution at 37 ± 1°C. The biodegradability test was studied using Tris‐Buffer solution for the prepared nanocomposites [nano Chitosan, nano Chitosan gelatin, Nano based Hydroxyapatite Chitosan gelatin]. The cell migration and potential biocompatibility of nHAP‐chitosan‐gelatin scaffold was assessed via wound scratch assay and were compared to povedeen as control. Cytocompatibility evaluation for Vero Cells using wound scratch assay showed that the fabricated porous nanocomposite scaffold possess higher cell proliferation and growth than that of povedeen. Thus, the study showed that the developed nanocomposite scaffolds are potential candidates for regenerating damaged cell tissue in wound healing process.Inspec keywords: nanofabrication, tissue engineering, electrospinning, wounds, cellular biophysics, scanning electron microscopy, surface morphology, X‐ray diffraction, biomedical materials, nanomedicine, porosity, biodegradable materials, nanoporous materials, calcium compounds, gelatin, nanocomposites, Fourier transform infrared spectra, nanoparticles, precipitation (physical chemistry)Other keywords: average pore size, wound repair, crystallographic structure, HAP powder, functional group bonds, simulated body fluid solution, biodegradability test, Tris‐Buffer solution, cell migration, wound scratch assay, tissue engineering, electrospinning method, X‐ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, biocompatibility, cytocompatibility, porous nanocomposite scaffold, cell tissue, nHAP‐chitosan‐gelatin scaffold composites, wet chemical precipitation method, surface morphology, nanohydroxyapatite‐nanochitosan‐gelatin scaffold composites, cell proliferation, wound healing, (Ca₁₀ (PO₄)₆ (OH)₂)     

Characterisation of sol–gel method synthesised MgZnFe2 O4 nanoparticles and its cytotoxic effects on breast cancer cell line,MDA MB‐231 in vitro

In this study, nanocrystalline magnesium zinc ferrite nanoparticles were successfully prepared by a simple sol–gel method using copper nitrate and ferric nitrate as raw materials. The calcined samples were characterised by differential thermal analysis/thermogravimetric analysis, Fourier transform infrared spectroscopy and X‐ray diffraction. Transmission electron microscopy revealed that the average particle size of the calcined sample was in a range of 17–41 nm with an average of 29 nm and has spherical size. A cytotoxicity test was performed on human breast cancer cells (MDA MB‐231) and (MCF‐7) at various concentrations starting from (0 µg/ml) to (800 µg/ml). The sample possessed a mild toxic effect toward MDA MB‐231 and MCF‐7 after being examined with MTT (3‐[4, 5‐dimethylthiazol‐2‐yl]‐2, 5 diphenyltetrazolium bromide) assay for up to 72 h of incubation. Higher reduction of cells viability was observed as the concentration of sample was increased in MDA MB‐231 cell line than in MCF‐7. Therefore, further cytotoxicity tests were performed on MDA MB‐231 cell line.Inspec keywords: sol‐gel processing, nanoparticles, nanofabrication, magnesium compounds, zinc compounds, toxicology, biological organs, cancer, cellular biophysics, nanomedicine, calcination, differential thermal analysis, Fourier transform infrared spectra, X‐ray diffraction, transmission electron microscopy, particle size, organic compoundsOther keywords: sol‐gel method, cytotoxic effects, breast cancer cell line, MDA MB‐231 in vitro, nanocrystalline magnesium zinc ferrite nanoparticles, copper nitrate, ferric nitrate, raw materials, calcined samples, differential thermal analysis, thermogravimetric analysis, Fourier transform infrared spectroscopy, X‐ray diffraction, transmission electron microscopy, average particle size, cytotoxicity testing, human breast cancer cells, mild toxic effect, 3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5 diphenyltetrazolium bromide) assay, cell viability, MCF‐7, MDA MB‐231 cell line, size 17 nm to 41 nm     

In‐situ fabrication of zirconium–titanium nano‐composite and its coating on Ti‐6Al‐4V for biomedical applications

In this study, nanocomposite powder consisting of zirconia and titania (Zr–Ti) have been synthesised by sol–gel method, with the aim of protecting Ti‐6Al‐4V surface. A simple and low cost electrophoretic deposition (EPD) technique has been employed for coating the nanocomposite material on Ti‐6Al‐4V. The prepared nanocomposite powder was characterised for its functional groups, phase purity, surface topography by Fourier transform infrared spectroscopy, powder X‐ray diffraction and scanning electron microscopy. Further, the biocompatibility nature of the composite powder was studied by [3‐(4, 5‐dimethylthiazol‐2‐yl)‐2, 5‐diphenyltetrazolium bromide] colorimetric assay and fluorescence analysis with MG63 osteoblast cell lines. The electrochemical behaviour of composite coating was investigated by potentiodynamic polarization and electrochemical impedance method. The results obtained from the electrochemical techniques indicate more corrosion resistance behaviour with increase of R _ct value with the corresponding decrease in R _dl values. From the above findings, the composite coating acts as a barrier layer against corrosion by preventing the leaching of metal ions from a dense and defect free coating. A scratch test analyser was used to assess the integrity of the coating; the lower traction force value of composite coating with increase in load has confirmed the presence of thick adherent layer on the substrate.Inspec keywords: zirconium compounds, titanium compounds, titanium alloys, aluminium alloys, vanadium alloys, nanofabrication, nanocomposites, nanoparticles, sol‐gel processing, electrophoretic coating techniques, surface topography, Fourier transform infrared spectra, X‐ray diffraction, scanning electron microscopy, X‐ray chemical analysis, fluorescence, cellular biophysics, biomedical materials, electrochemical impedance spectroscopy, corrosion resistance, corrosion protection, corrosion protective coatings, adhesionOther keywords: in‐situ fabrication, zirconium‐titanium nanocomposite powder, biomedical applications, zirconia, titania, sol‐gel method, electrophoretic deposition, EPD, functional groups, phase purity, surface topography, Fourier transform infrared spectroscopy, powder X‐ray diffraction, scanning electron microscopy, energy dispersive X‐ray analysis, biocompatibility, 3‐(4, 5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide colorimetric assay, acridine range fluorescence analysis, MG63 osteoblast cell lines, electrochemical behaviour, composite coating, potentiodynamic polarization, electrochemical impedance spectroscopy, corrosion resistance, barrier layer, leaching, defect free coating layer, scratch test analysis, adherent layer, TiAlV‐ZrO₂ ‐TiO₂      

Electrophoretic deposition of hydroxyapatite‐shrimp crusts nanocomposite thin films for bone implant studies

Hydroxyapatite‐shrimp crusts nanocomposite thin films were deposited on titanium substrates by electrophoretic technique, under different preparation conditions, for bone implant applications. Fourier transform infrared spectrometer, atomic force microscope, X‐ray diffraction (XRD), optical microscope, and scanning electron microscope were employed to characterise the synthesised films. Vickers’ micro‐hardness measurements revealed a value of 502 HV for the hydroxyapatite films and 314.55 HV for the nanocomposite films. XRD results confirmed the polycrystalline nature of the hydroxyapatite and hydroxyapatite‐shrimp nanocomposite films. The in‐vitro bioactivity test of the synthesised films in simulated body fluid showed very low dissolution rate. Antibacterial activity of synthesised films was investigated against E. coli bacteria.Inspec keywords: electrophoretic coating techniques, thin films, nanocomposites, antibacterial activity, bone, prosthetics, nanomedicine, calcium compounds, bioceramics, nanofabrication, Fourier transform infrared spectra, atomic force microscopy, X‐ray diffraction, optical microscopy, scanning electron microscopy, Vickers hardness, microhardness, microorganisms, dissolvingOther keywords: Ti, Ca₁₀ (PO₄)₆ (OH)₂ , E. coli bacteria, antibacterial activity, dissolution rate, simulated body fluid, in‐vitro bioactivity test, polycrystalline nature, Vickers microhardness measurements, XRD, scanning electron microscopy, optical microscopy, X‐ray diffraction, atomic force microscopy, Fourier transform infrared spectrometer, bone implant applications, titanium substrates, hydroxyapatite‐shrimp crust nanocomposite thin films, electrophoretic deposition     

Development and characterisation of novel Ce‐doped hydroxyapatite–Fe3 O4 nanocomposites and their in vitro biological evaluations for biomedical applications

Hydroxyapatite (HAP: Ca₁₀ (PO₄)₆ (OH)₂) is extensively used in biomedical field because of its biocompatibility, osteoconductivity and non‐toxicity properties. However, HAP exhibits poor mechanical strength and bacterial restriction behavior. To overcome these drawbacks, various metal ions such as Ag⁺, Zn²⁺, Cu²⁺, Ti⁴⁺ and Ce^4+/3+ are incorporated in HAP matrix to increase the mechanical and biological properties. Among these, Cerium (Ce) is selected as antibacterial agent due to its high thermal stability and its applications in dental fillings, bone healing and catheters. Fe₃ O₄ nanoparticles were used in hyperthermia treatment, magnetic fluid recordings and catalysis. In this present study, we have synthesized nanocomposites consisting of 1.25% Ce doped HAP with various concentrations of Fe₃ O₄ NPs as 90:10 (C‐1), 70:30 (C‐2) and 50:50 wt% (C‐3) using ball milling technique. The obtained Ce@HAP‐Fe₃ O₄ nanocomposites were characterized by ATR‐FTIR, XRD, VSM, SEM‐EDAX and TEM analysis. Further, the fabricated Ce@HAP‐Fe₃ O₄ nanocomposites were tested for its antibacterial activity towards Staphylococcus aureus (S. aureus) and Escherichia coli (E.coli), where C‐3 composites exhibit the excellent pathogen inhibition towards E.coli. In addition, the cytotoxicity evaluation on C‐3 nanocomposites by in vitro biocompatibility study using MG‐63 cells shows the prominent viable cell enhancement up to 400µg/mL concentrations.Inspec keywords: nanocomposites, iron compounds, calcium compounds, cerium, mechanical strength, antibacterial activity, biomedical materials, dentistry, bone, nanoparticles, nanofabrication, ball milling, Fourier transform infrared spectra, attenuated total reflection, X‐ray diffraction, magnetometry, scanning electron microscopy, transmission electron microscopy, microorganisms, cellular biophysics, nanomedicineOther keywords: Ce‐doped HAP–Fe3O4 nanocomposite, hydroxyapatite, in vitro biological evaluation, mechanical strength, bacterial restriction behaviour, metal ion, silver ion, zinc ion, copper ion, titanium ion, cerium ion, HAP matrix, antibacterial agent, thermal stability, dental filling, bone healing, catheter, Fe3O4 nanoparticle, hyperthermia treatment, magnetic fluid recording, catalysis, ball milling technique, Fourier transform infrared spectroscopy, attenuated total reflectance spectroscopy, X‐ray diffraction, vibrating sample magnetometry, scanning electron microscopy, SEM‐energy dispersive spectroscopy, transmission electron microscopy, TEM analysis, antibacterial activity, Staphylococcus aureus, Escherichia coli, pathogen inhibition, in vitro biocompatibility, MG‐63 osteoblast cell, cell enhancement, Ca₅ (PO₄)₃ (OH):Ce, Fe₃ O₄      

Screening the UV‐blocking and antimicrobial properties of herbal nanoparticles prepared from Aloe vera leaves for textile applications

Nanomaterials play a vital role in textile industries due to their unique properties and applications. There is an increase in the use of nanoscale phyto products in textiles to control the bacterial infection in fabrics. Here, natural herbal nanoparticles of different sizes were prepared from shade‐dried Aloe vera plant leaves using ball milling technique without any additives. The amorphous herbal A. vera nanoparticles possess an average particle size of 40 ± 2 nm and UV‐absorption maximum at 269 nm. A. vera nanopowders–chitosan nanocomposites were prepared and coated on cotton fabrics using pad‐dry cure method. The evaluation of antibacterial activity against Escherichia coli (22.05 ± 0.06 mm) and Staphylococcus aureus (27.17 ± 0.02 mm), UV‐protection properties (UV‐protection factor = 57.2 ± 0.1), and superhydrophobic nature (155 ± 3°) of the prepared herbal nanoparticles and their composites were analysed by disc diffusion, UV–visible spectral analysis, and contact angle analysis. Understanding the functional properties of herbal nanoparticles, coated particles on fabrics highlights their potential applications in protective clothing with better antimicrobial properties, hydrophobicity, and UV‐protection properties. This study of using A. vera herbal nanoparticles in textiles significantly enhances the fabric performance to develop protective textile fabrics in defence and biomedical fields.Inspec keywords: nanoparticles, particle size, nanofabrication, nanomedicine, antibacterial activity, biomedical materials, hydrophobicity, ultraviolet spectra, visible spectra, radiation protection, textile fibres, cotton fabrics, ball milling, X‐ray diffraction, light scattering, scanning electron microscopy, X‐ray fluorescence analysis, fluorescence, amorphous state, nanocomposites, filled polymers, protective coatings, curing, microorganisms, biodiffusion, contact angle, surface morphology, protective clothingOther keywords: UV‐blocking, antimicrobial properties, disc diffusion, UV‐visible spectral analysis, contact angle analysis, morphological characteristics, protective clothing, protective textile fabrics, biomedical fields, superhydrophobic nature, UV‐protection factor, UV‐protection properties, Staphylococcus aureus, Escherichia coli, pad‐dry cure method, cotton fabrics, A. vera nanopowders‐chitosan nanocomposites, UV‐absorption maximum, average particle size, amorphous herbal A. vera nanoparticles, X‐ray fluorescence spectrometry, scanning electron microscopy, dynamic light scattering, UV‐visible spectrophotometry, X‐ray diffraction, ball milling, shade‐dried Aloe vera plant leaves, natural herbal nanoparticle size, bacterial infection, nanoscale phyto products, textile industries, nanomaterials, textile applications     

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     

Synthesis and comparative assessment of antiradical activity,toxicity, and biodistribution of κ‐carrageenan‐capped selenium nanoparticles of different size: in vivo and in vitro study

In the present study, water‐soluble hybrid selenium‐containing nanocomposites have been synthesised via soft oxidation of selenide‐anions, preliminarily generated from elemental bulk‐selenium in the base‐reduction system ‘N₂ H₄ –NaOH’. The nanocomposites obtained consist of Se⁰ NPs (4.6–24.5 nm) stabilised by κ‐carrageenan biocompatible polysaccharide. The structure of these composite nanomaterials has been proven using complementary physical–chemical methods: X‐ray diffraction analysis, transmission electron microscopy, optical spectroscopy, and dynamic light scattering. Optical ranges of ‘emission/excitation’ of aqueous solutions of nanocomposites with Se⁰ NPs of different sizes are established and the most important parameters of their luminescence are determined. For the obtained nanocomposites, the expressed antiradical activity against free radicals 2,2‐diphenyl‐1‐picrylhydrazyl and 2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulphonic acid has been found, the value of which depends on the size of selenium nanoparticles. It is experimentally revealed that all obtained nanocomposites are low toxic (LD₅₀ >2000 mg/kg). It is also found that small selenium nanoparticles (6.8 nm), in contrast to larger nanoparticles (24.5 nm), are accumulated in organisms to significantly increase the level of selenium in the liver, kidneys, and brain (in lesser amounts) of rats.Inspec keywords: nanobiotechnology, free radical reactions, oxidation, enzymes, selenium, solubility, nanofabrication, transmission electron microscopy, X‐ray diffraction, free radicals, reduction (chemical), biomedical materials, nanoparticles, nanomedicine, light scattering, organic‐inorganic hybrid materials, biochemistry, nanocompositesOther keywords: κ‐carrageenan biocompatible polysaccharide, composite nanomaterials, complementary physical–chemical methods, X‐ray diffraction analysis, transmission electron microscopy, optical spectroscopy, dynamic light scattering, optical ranges, expressed antiradical activity, 2,2‐diphenyl‐1‐picrylhydrazyl, 3‐ethylbenzothiazoline‐6‐sulphonic acid, comparative assessment, toxicity, κ‐carrageenan‐capped selenium nanoparticles, water‐soluble hybrid selenium‐containing nanocomposites, soft oxidation, selenide‐anions, elemental bulk‐selenium, base‐reduction system, free radicals, 2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulphonic acid, selenium nanoparticles, nanocomposites, liver, kidneys, brain, luminescence, size 4.6 nm to 24.5 nm     

Synthesis of biotin‐targeted chitosan/poly (methyl vinyl ether‐alt ‐maleic acid) copolymeric micelles for delivery of doxorubicin

Biotinylated chitosan/poly(methyl vinyl ether‐alt ‐maleic acid) (PMVEMA) copolymer was synthesised by an amide reaction in two steps. Structural characterisation was performed using ¹ HNMR and Fourier transform infra‐red (FTIR) spectra. Critical micelle concentration (CMC) of the copolymer was determined by pyrene as a fluorescent probe. Doxorubicin (DOX) was loaded in the micelles by the direct dissolution method. The effects of different variables including type of copolymer, copolymer concentration, stirring rate and stirring time were studied on the physicochemical properties of the micelles including: particle size, zeta potential, release efficiency and loading efficiency of nanoparticles using an irregular factorial design. The in vitro cytotoxicity of DOX‐loaded biotin‐targeted micelles was studied in HepG2 cells which over express biotin receptors by 3, 5‐[dimethylthiazol‐2‐yl]‐2, 5‐diphenyl tetrazolium bromide assay. The successful synthesis of the biotinylated copolymer of chitosan/PMVEMA was confirmed by FTIR and ¹ HNMR. The optimised micelles showed the CMC of 33 μg/ml, particle size of 247 ± 2 nm, zeta potential of +9.46 mV, polydispersity index of 0.22, drug‐loading efficiency of 71% and release efficiency of 84.5 ± 1.6%. The synthesised copolymer was not cytotoxic. The cytotoxicity of DOX‐loaded in targeted micelles on HepG2 cell line was about 2.2‐fold compared with free drug.Inspec keywords: biomedical materials, cellular biophysics, dissolving, drug delivery systems, drugs, electrokinetic effects, fluorescence, Fourier transform infrared spectra, particle size, polymer blends, spectrochemical analysis, toxicologyOther keywords: ¹ HNMR spectra, biotin‐targeted chitosan‐poly (methyl vinyl ether‐alt‐maleic acid) copolymeric micelles, doxorubicin delivery, amide reaction, structural characterisation, Fourier transform infrared spectra, pyrene, fluorescent probe, direct dissolution method, physicochemical properties, particle size, zeta potential, nanoparticles, irregular factorial design, in vitro cytotoxicity, DOX‐loaded biotin‐targeted micelles, 3, 5‐[dimethylthiazol‐2‐yl]‐2, 5‐diphenyl tetrazolium bromide assay, polydispersity index, drug‐loading efficiency, HepG2 cell line, voltage 9.46 mV     

Biogenic gold nanoparticles for reduction of 4‐nitrophenol to 4‐aminophenol: an eco‐friendly bioremediation

The present study investigated the synthesis of gold nanoparticles (AuNPs) using mangrove plant extract from Avicennia marina as bioreductant for eco‐friendly bioremediation of 4‐nitrophenol (4‐NP). The AuNPs synthesised were confirmed by UV spectrum, transmission electron microscopy (TEM), X‐ray diffraction, Fourier transmission infrared spectroscopy (FTIR), dynamic light scattering (DLS), and zeta potential. The AuNPs were found to be spherical in shape with size ranging from 4 to 13 nm, as evident by TEM and DLS. Further, the AuNPs were encapsulated with sodium alginate in the form of gold nano beads and used as heterogeneous catalyst and degrading agent to reduce 4‐NP. This reduction in 4‐NP into 4‐aminophenol was confirmed by UV and FTIR. The aqueous solution of 4‐NP peaked its absorbance at 320 nm, and shifted to 400 nm, with an intense yellow colour, appeared due to formation of 4‐nitrophenolate ion. After the addition of AuNps, the 4‐NP solution became colourless and peaked at 400 nm and reduced to 290 nm corresponding to the formation of 4‐aminophenol. Hence, the present work suggested the AuNPs as the potent, eco‐friendly bionanocomposite catalyst for bioremediation of 4‐NP.Inspec keywords: gold, nanoparticles, nanobiotechnology, nanofabrication, ultraviolet spectra, transmission electron microscopy, X‐ray diffraction, Fourier transform spectra, infrared spectra, electrokinetic effects, catalysts, nanocomposites, biochemistryOther keywords: biogenic gold nanoparticles, 4‐nitrophenol, 4‐aminophenol, eco‐friendly bioremediation, mangrove plant extract, Avicennia marina, bioreductant, UV spectrum, transmission electron microscopy, TEM, X‐ray diffraction, Fourier transmission infrared spectroscopy, FTIR, dynamic light scattering, DLS, zeta potential, degrading agent, 4‐nitrophenolate, bionanocomposite catalyst, size 4 nm to 13 nm, wavelength 400 nm, wavelength 290 nm, Au     

Facile synthesis of mesoporous alumina using hexadecyltrimethylammonium bromide (HTAB) as template: simplified sol‐gel approach

Herein the authors present the synthesis of surface functionalised mesoporous alumina (MeAl) for textural characterisation by a simplified sol–gel method obtained by using hexadecyltrimethylammonium bromide as a template. Etoricoxib (ETOX) was used as a model drug for the study. Alumina supported mesoporous material containing drug was characterised using instrumental technique namely Brunauer–Emmett–Teller surface area, Fourier transform‐infrared, differential scanning calorimetry, transmission electron microscopy, X‐ray diffraction, and field emission scanning electron microscopy. Diffusion study using a dialysis bag method used to check the release pattern of ETOX‐loaded‐MeAl. Results of characterisation study revealed the successful surface functionalisation of the drug on nanocomposite. The IC₅₀ value obtained from cell viability study demonstrated the non‐toxic behaviour of synthesised drug‐loaded mesoporous alumina up to the tested concentration range. The present work has demonstrated that synthesised MeAl showed excellent stability with an expanded surface area suitable for carrier material for drug delivery system.Inspec keywords: Fourier transform spectra, adsorption, biomedical materials, silicon compounds, drug delivery systems, X‐ray diffraction, alumina, differential scanning calorimetry, nanocomposites, field emission electron microscopy, nanofabrication, nanomedicine, mesoporous materials, transmission electron microscopy, sol‐gel processing, scanning electron microscopyOther keywords: ETOX‐loaded‐MeAl, successful surface functionalisation, synthesised drug‐loaded mesoporous alumina, synthesised MeAl, expanded surface area, drug delivery system, hexadecyltrimethylammonium bromide, sol‐gel approach, surface functionalised mesoporous alumina, simplified sol–gel method, mesoporous material containing drug, Brunauer–Emmett–Teller surface area, Fourier transform‐infrared, differential scanning calorimetry, transmission electron microscopy, X‐ray diffraction, field emission scanning electron microscopy, dialysis bag method     

Solvothermal‐assisted green synthesis of hybrid Chi‐Fe3 O4 nanocomposites: a potential antibacterial and antibiofilm material

In this present study, a hybrid Chi‐Fe₃ O₄ was prepared, characterised and evaluated for its antibacterial and antibiofilm potential against Staphylococcus aureus and Staphylococcus marcescens bacterial pathogens. Intense peak around 260 nm in the ultraviolet–visible spectrum specify the formation of magnetite nanoparticles. Spherical‐shaped particles with less agglomeration and particle size distribution of 3.78–46.40 nm were observed using transmission electron microscopy analysis and strong interaction of chitosan with the surface of magnetite nanoparticles was studied using field emission scanning microscopy (FESEM). X‐ray diffraction analysis exhibited the polycrystalline and spinel structure configuration of the nanocomposite. Presence of Fe and O, C and Cl elements were confirmed using energy dispersive X‐ray microanalysis. Fourier transform infrared spectroscopic analysis showed the reduction and formation of Chi‐Fe₃ O₄ nanocomposite. The antibacterial activity by deformation of the bacterial cell walls on treatment with Chi‐Fe₃ O₄ nanocomposite and its interaction was visualised using FESEM and the antibiofilm activity was determined using antibiofilm assay. In conclusion, this present study shows the green synthesis of Chi‐Fe₃ O₄ nanocomposite and evaluation of its antibacterial and antibiofilm potential, proving its significance in medical and biological applicationsInspec keywords: visible spectra, particle size, magnetic particles, nanocomposites, nanoparticles, X‐ray diffraction, nanofabrication, transmission electron microscopy, X‐ray chemical analysis, nanomagnetics, microorganisms, antibacterial activity, iron compounds, ultraviolet spectra, biomedical materials, field emission scanning electron microscopy, Fourier transform infrared spectra, filled polymers, crystal growth from solution, polymer structureOther keywords: potential antibacterial material, antibiofilm potential, magnetite nanoparticles, solvothermal‐assisted green synthesis, hybrid Chi‐Fe₃ O₄ nanocomposites, staphylococcus aureus, staphylococcus marcescens, bacterial pathogens, ultraviolet–visible spectrum, spherical‐shaped particles, particle size, transmission electron microscopy, FESEM, field emission scanning electron microscopy, X‐ray diffraction, spinel structure, polycrystalline structure, energy dispersive X‐ray microanalysis, Fourier transform infrared spectroscopic analysis, deformation, bacterial cell walls, Fe₃ O₄      

Factors affecting the antibacterial activity of chitosan‐silver nanocomposite

This study provides the optimum preparation parameters of chitosan‐silver nanoparticles composite (CSNC) with promising antibacterial activity against the most common bacterial infections found on burn wounds. CSNC was synthesised by simple green chemical reduction method with different preparation factors. Chitosan was used to reduce silver nitrate and stabilise silver nanoparticles in the medium. For this reason, spectroscopic and microscopic techniques as, ultraviolet‐visible Fourier transform infrared spectroscopy and transmission electron microscopy were used in the study of the molecular and morphological properties of the resultant composites. Furthermore, the composite was assessed in terms of Ag‐ions release by AAS and its efficacy as antibacterial material. As a result, CSNC showed stronger antibacterial effect than its individual components (chitosan and silver nitrate solutions) towards Gram‐positive (Staphylococcus aureus) and Gram‐negative (Pseudomonas aeruginosa and Escherichia coli) bacteria. CSNC prepared in this study showed highest inhibition percentage of bacterial growth up to 96% at concentration of 220 μg/ml.Inspec keywords: silver, nanocomposites, nanoparticles, filled polymers, biomedical materials, nanomedicine, antibacterial activity, wounds, reduction (chemical), ultraviolet spectra, visible spectra, Fourier transform spectra, infrared spectra, transmission electron microscopy, microorganisms, nanofabricationOther keywords: antibacterial activity, chitosan‐silver nanocomposite, optimum preparation parameters, chitosan‐silver nanoparticles composite, CSNC, bacterial infections, burn wounds, green chemical reduction method, ultraviolet‐visible Fourier transform infrared spectroscopy, transmission electron microscopy, molecular properties, morphological properties, Gram‐positive bacteria, Gram‐negative bacteria, Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, bacterial growth, Ag     

The use of slow releasing nanoparticle encapsulated Azadirachtin formulations for the management of Caryedon serratus O. (groundnut bruchid)

Nanobiotechnology is one of the emerging fields and its interventions in agriculture is been attracting the scientific community. Herein, the authors first to report on control of groundnut bruchid (Caryedon serratus O.) using nanoscale zinc oxide (ZnONPs) particles and nanoscale chitosan (CNPs) particles‐based Azadirachtin formulations. ZnONPs and CNPs were prepared using sol–gel and ion tropic gelation techniques, respectively. Neem seed kernel extract (NSKE) 5% and Neem oil (3000 and 1000 ppm) were encapsulated using the prepared nanoscale materials and characterised using the techniques such as dynamic light scattering, high‐resolution transmission electron microscopy. Spherical‐shaped nanoparticles were formed after encapsulation with the required bio‐materials (ZnONPs 33.1 nm; CNPs 78.8 nm; neem oil encapsulated (3000 ppm) ZnONPs 182.9 nm; NSKE encapsulated ZnONPs 84.9 nm) and observed that the particles are stable (52.3 mV for ZnONPs, −36.2 mV for CNPs, −43.0 mV for neem oil encapsulated (3000 ppm) ZnONPs and −39.4 mV for NSKE encapsulated ZnONPs). NSKE encapsulated CNPs were able to contain groundnut bruchid up to 180 days with 54.61% weight loss compared to other formulations tested. Thus biomaterial encapsulated nanoscale material formulations are proved to be effective in controlling stored grain pests to reduce huge economic losses.Inspec keywords: nanobiotechnology, agricultural products, toxicology, agrochemicals, food safety, sol‐gel processing, food preservation, agriculture, II‐VI semiconductors, storage, nanoparticles, transmission electron microscopy, encapsulation, nanofabrication, zinc compounds, wide band gap semiconductors, food processing industry, light scattering, materials preparation, pest control, nanocompositesOther keywords: voltage ‐36.2 mV, voltage ‐43.0 mV, voltage ‐39.4 mV, voltage 52.3 mV, size 84.9 nm, size 182.9 nm, size 78.8 nm, size 33.1 nm, NSKE, neem seed kernel extract, caryedon serratus O., CNPs, bio‐materials, nanoscale materials, nanoparticle, encapsulation, spherical‐shaped nanoparticles, high‐resolution transmission electron microscopy, neem oil, ion tropic gelation techniques, sol–gel, nanoscale chitosan particles, nanoscale zinc oxide particles, scientific community, groundnut bruchid, Azadirachtin formulations, biomaterial encapsulated nanoscale material formulations     

Poly (ɛ‐caprolactone)–chitosan–poly (vinyl alcohol) nanofibrous scaffolds for skin excisional and burn wounds in a canine model

Poly (ɛ‐caprolactone)–chitosan–poly (vinyl alcohol) (PCL: Cs: PVA) nanofibrous blend scaffolds were known as useful materials for skin wound healing and would help the healing process about 50% faster at the final time point. From the previous studies by the authors, PCL: Cs: PVA (in 2: 1: 1.5 mass ratio) nanofibres showed high efficacy in healing on rat models. In this study, the scaffolds were examined in burn and excision wounds healing on dogs as bigger models. The scaffolds were applied on dorsum skin wounds (n  = 5) then macroscopic and microscopic investigations were carried out to measure the wounds areas and to track healing rate, respectively. Macroscopic results showed good aspect healing effect of scaffolds compared with control wounds especially after 21 days post‐operating for both cutting and burn wounds. Pathological studies showed that the healing rates of the wounds covered with PCL: Cs: PVA nanofibrous scaffolds were much rapid compared to untreated wounds in control group. The immunogenicity of the scaffolds in canine model was also investigated. The findings showed that nanofibrous blend scaffolds was not immunogenic in humoural immune responses. All these results indicated that PCL: Cs: PVA nanofibrous web could be considered as promising materials for wounds healings.Inspec keywords: nanofibres, nanomedicine, biomedical materials, polymer fibres, polymer blends, skin, woundsOther keywords: poly(ε‐caprolactone)‐chitosan‐poly (vinyl alcohol) nanofibrous blend scaffolds, skin excisional wounds, burn wounds, canine model, skin wound healing, dorsum skin wounds, macroscopic investigations, microscopic investigations, healing rate, cutting wounds, pathological study, humoural immune responses, nanofibrous web, immunogenicity, time 21 day     

Co–Sn–Cu oxides/graphene nanocomposites as green catalysts for preparing 1,8‐dioxo‐octahydroxanthenes and apoptosis‐inducing agents in MCF‐7 human breast cancer cells

In this work, Co–Sn–Cu oxides/graphene nanocomposite, 30–40 ± 0.5 nm in size, was synthesized by solid‐state microwave irradiation. This method presents several advantages such as operational simplicity, fast, low cost, safe and energy efficient, and suitability for production of high purity of nanoparticles. Other advantages of this method are there is no need for the use of solvent, fuel, and surfactant. Co–Sn–Cu oxides/graphene nanocomposites have been characterized by Fourier transform infrared spectroscopy, X‐ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, vibrating sample magnetometer, energy‐dispersive X–ray spectroscopy, and UV–Vis spectroscopy. The synthesized nanocomposites were used as novel highly efficient catalysts for the synthesis of 1,8‐dioxo‐octahydroxanthenes at room temperature. The catalysts are recoverable and can be reused for six runs without loss of their activity. Also, the obtained nanocomposites exhibited significant anticancer activity against breast cancer cells and they could induce apoptosis in cancer cells.     

Biocompatibility assessment of SiO2 –TiO2 composite powder on MG63 osteoblast cell lines for orthopaedic applications

The objective of this study is to evaluate the biocompatibility of composite powder consisting of silica and titania (SiO₂ –TiO₂) for biomedical applications. The advancement of nanoscience and nanotechnology encourages researchers to actively participate in reinvention of existing materials with improved physical, chemical and biological properties. Hence, a composite/hybrid material has given birth of new materials with intriguing properties. In the present investigation, SiO₂ –TiO₂ composite powder was synthesised by sol‐gel method and the prepared nanocomposite was characterised for its phase purity, functional groups, surface topography by powder X‐ray diffraction (XRD), Fourier transform infrared spectroscopy (FT‐IR) and scanning electron microscopy. Furthermore, to understand the adverse effects of composite, biocompatibility test was analysed by cell culture method using MG63 osteoblast cell lines as a basic screening method. From the results, it was observed that typical Si–O–Ti peaks in FT‐IR confirms the formation of composite and the crystallinity of the composite powder was analysed by XRD analysis. Further in vitro biocompatibility and acridine orange results have indicated better biocompatibility at different concentrations on osteoblast cell lines. On the basis of these observations, we envision that the prepared silica–titania nanocomposite is an intriguing biomaterial for better biomedical applications.Inspec keywords: bioceramics, nanocomposites, silicon compounds, titanium compounds, nanofabrication, sol‐gel processing, surface topography, X‐ray diffraction, Fourier transform infrared spectra, scanning electron microscopy, X‐ray chemical analysis, cellular biophysics, nanomedicineOther keywords: MG63 osteoblast cell lines, orthopaedic applications, biomedical applications, nanoscience, nanotechnology, nanotoxicology, physical properties, chemical properties, biological properties, biological applications, biomaterial synthesis, composite‐hybrid materials, intriguing properties, sol‐gel method, surface properties, ceramic nanocomposite, phase purity, functional groups, surface topography, powder X‐ray diffraction, Fourier transform infrared spectroscopy, FT‐IR spectroscopy, scanning electron microscopy, energy dispersive X‐ray analysis, biocompatibility test, cell culture method, screening method, crystallinity, XRD, in vitro biocompatibility, acridine orange, silica‐titania nanocomposite powder, SiO₂ ‐TiO₂      

In vitro degradation,haemolysis and cytotoxicity study of Mg‐0.4Ce/ZnO2 nanocomposites

Magnesium is an ideal candidate for biodegradable implants, but the major concern is its uncontrollable degradation for application as a biomaterial. The in vitro corrosion and cytotoxicity of Mg‐0.4Ce/ZnO₂ (magnesium nanocomposites) were studied to determine its suitability as a biodegradable material. The polycrystalline nature of Mg‐0.4Ce/ZnO₂ was assessed using an optical microscope. The hydrophobic nature of Mg‐0.4Ce/ZnO₂ was determined by contact angle measurements. The corrosion resistance of magnesium nanocomposites was tested in phosphate buffer solution (PBS) and it was improved by the gradual deposition of a protective layer on its surface after 48 h. The cytotoxicity of Mg‐0.4Ce/ZnO₂ was evaluated by 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) assay and calcium deposition by Alizarin red staining using sarcoma osteogenic (Saos2) cells. The haemocompatibility test of Mg‐0.4Ce/ZnO₂ showed 30% haemolysis, which is higher than the safe value for biomaterials, and cell viability was reduced after 24 h in comparison with control groups. The calcium deposition by sarcoma osteogenic cells showed a brick red colour deposition in both the control group and Mg‐0.4Ce/ZnO₂ after 24 h. The preliminary degradation results of Mg‐0.4Ce/ZnO₂ showed good corrosion resistance; however further improvement is needed in haemolysis and cytotoxicity studies for its use as a biodegradable material for orthopaedic applications.