CAD/CAM scaffolds for bone tissue engineering: investigation of biocompatibility of selective laser melted lightweight titanium

The objective of the current in‐vitro study was to evaluate the biocompatibility of a new type of CAD/CAM scaffold for bone tissue engineering by using human cells. Porous lightweight titanium scaffolds and Bio‐Oss® scaffolds as well as their eluates were used for incubation with human osteoblasts, fibroblasts and osteosarcoma cells. The cell viability was assessed by using fluorescein diazo‐acetate propidium iodide staining. Cell proliferation and metabolism was examined by using MTT‐, WST‐Test and BrdU‐ELISA tests. Scanning electron microscope was used for investigation of the cell adhesion behaviour. The number of devitalised cells in all treatment groups did not significantly deviate from the control group. According to MTT and WST results, the number of metabolically active cells was decreased by the eluates of both test groups with a more pronounced impact of the eluate from Bio‐Oss®. The proliferation of the cells was inhibited by the addition of the eluates. Both scaffolds showed a partial surface coverage after 1 week and an extensive to complete coverage after 3 weeks. The CAD/CAM titanium scaffolds showed favourable biocompatibility compared to Bio‐Oss® scaffolds in vitro. The opportunity of a defect‐specific design and rapid prototyping by selective laser melting are relevant advantages in the field of bone tissue engineering and regenerative medicine.Inspec keywords: calcium compounds, scanning electron microscopy, adhesion, titanium, CAD/CAM, tissue engineering, bone, biomedical materials, cellular biophysics, biomechanics, laser materials processing, meltingOther keywords: bone tissue engineering, human cells, porous lightweight titanium scaffolds, human osteoblasts, osteosarcoma cells, cell viability, fluorescein diazo‐acetate propidium iodide staining, cell proliferation, MTT tests, WST‐Test, BrdU‐ELISA tests, cell adhesion, devitalised cells, metabolically active cells, biocompatibility, selective laser melting, CAD‐CAM scaffolds, cell metabolism, scanning electron microscopy, Ti     

Properties of scaffolds based on chitosan and collagen with bioglass 45S5

Scaffolds based on chitosan (CTS), collagen (Coll) and glycosaminoglycans (GAG) mixtures cross‐linked by tannic acid (TA) with bioglass 45S5 addition were obtained with the use of the freeze‐drying method. The prepared scaffolds were characterised for morphology, mechanical strength and degradation rate. Moreover, cell viability on the obtained scaffolds was measured with and without the presence of ascorbic acid and dexamethasone. The main purpose of the research was to compare the effectiveness of bioglass 45S5 influence on the physicochemical and biological properties of scaffolds. The results demonstrated that the scaffolds based on the blends of biopolymers cross‐linked by TA are stable in an aqueous environment. Scanning electron microscope images allowed the observation of a porous scaffold structure with interconnected pores. The addition of bioglass nanoparticles improved the mechanical properties and decreased the degradation rate of composite materials. The biological properties were improved for 20% tannic acid addition compared to 5%. However, the addition of bioglass 45S5 did not change to cells response significantly.Inspec keywords: biomedical materials, drying, porous materials, freezing, tissue engineering, proteins, nanofabrication, bone, scanning electron microscopy, polymers, molecular biophysics, cellular biophysics, nanoparticles, porosityOther keywords: chitosan, collagen, glycosaminoglycans, bioglass 45S5 addition, freeze‐drying method, degradation rate, ascorbic acid, dexamethasone, physicochemical properties, biological properties, porous scaffold structure, bioglass nanoparticles, mechanical properties, tannic acid addition, scanning electron microscopy     

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)     

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

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

Effect of green GO/Au nanocomposite on in‐vitro amplification of human DNA

Recently nanomaterials have attracted interest for increasing efficiency of polymerase chain reaction (PCR) systems. Here, the authors report on the usefulness of green graphene oxide/gold (GO/Au) nanocomposites for enhancement of PCR reactions. In this study, green GO/Au nanocomposite was prepared with Matricaria chamomilla extract as reducing/capping agent for site‐directed nucleation of Au^o atoms on surface of GO sheets. The as‐prepared green GO/Au nanocomposites were then characterised with UV–VIS spectrophotometer and scanning electron microscopy. Later, the effect of these nanocomposites was studied on end‐point and real‐time PCR employed for amplification of human glyceraldehyde‐3‐phosphate dehydrogenase gene. The results indicated that GO/Au nanocomposite can improve both end‐point and real‐time PCR methods at the optimum concentrations, possibly through interaction between GO/Au nanocomposite and the materials in PCR reaction, and through providing increased thermal convection by the GO surface as well as the Au nanostructures. In conclusion, it can be suggested that green GO/Au nanocomposite is a biocompatible and eco‐friendly candidate as enhancer of in‐vitro molecular amplification strategies.Inspec keywords: graphene, molecular biophysics, nucleation, enzymes, gold, nanofabrication, nanocomposites, scanning electron microscopy, nanoparticles, DNA, nanomedicine, ultraviolet spectra, visible spectra, graphene compoundsOther keywords: green GO/Au nanocomposite, polymerase chain reaction systems, green graphene oxide/gold, PCR reaction, as‐prepared green GO/Au nanocomposites, real‐time PCR methods, Au nanostructures, in‐vitro amplification, human DNA, Matricaria chamomilla extract, site‐directed nucleation, Au, CO, CO‐Au     

Iron oxide/gold nanoparticles‐decorated reduced graphene oxide nanohybrid as the thermo‐radiotherapy agent

The main focus of the current study is the fabrication of a multifunctional nanohybrid based on graphene oxide (GO)/iron oxide/gold nanoparticles (NPs) as the combinatorial cancer treatment agent. Gold and iron oxide NPs formed on the GONPs via the in situ synthesis approach. The characterisations showed that gold and iron oxide NPs formed onto the GO. Cell toxicity assessment revealed that the fabricated nanohybrid exhibited negligible toxicity against MCF‐7 cells in low doses (<50 ppm). Temperature measurement showed a time and dose‐dependent heat elevation under the interaction of the nanohybrid with the radio frequency (RF) wave. The highest temperature was recorded using 200 ppm concentration nanohybrid during 40 min exposure. The combinatorial treatments demonstrated that the maximum cell death (average of 53%) was induced with the combination of the nanohybrid with RF waves and radiotherapy (RT). The mechanistic study using the flow cytometry technique illustrated that early apoptosis was the main underlying cell death. Moreover, the dose enhancement factor of 1.63 and 2.63 were obtained from RT and RF, respectively. To sum up, the authors’ findings indicated that the prepared nanohybrid could be considered as multifunctional and combinatorial cancer therapy agents.Inspec keywords: radiation therapy, toxicology, gold, biomedical materials, nanofabrication, nanoparticles, iron compounds, cancer, nanomedicine, cellular biophysics, tumours, graphene compounds, biothermicsOther keywords: graphene oxide nanohybrid, combinatorial cancer treatment agent, cell toxicity assessment, MCF‐7 cells, dose‐dependent heat elevation, multifunctional cancer therapy agents, thermoradiotherapy agent, graphene oxide‐iron oxide‐gold nanoparticles, temperature measurement, radiofrequency wave, flow cytometry, time 40.0 min, CO‐FeO‐Au     

Ferulic acid‐loaded collagen hydrolysate and polycaprolactone nanofibres for tissue engineering applications

There is a great need for the progress of composite biomaterials, which are effective for tissue engineering applications. In this work, the development of composite electrospun nanofibres based on polycaprolactone (PCL) and collagen hydrolysate (CH) loaded with ferulic acid (FA) for the treatment of chronic wounds. Response Surface Methodology (RSM) has been applied to nanofibres factor manufacturing assisted by electrospinning. For wound healing applications, the authors have created the efficacy of CH, and PCL membranes can act as a stable, protective cover for wound, enabling continuous FA release. The findings of the RSM showed a reasonably good fit with a polynomial equation of the second order which was statistically acceptable at P  < 0.05. The optimised parameters include the quantity of hydrolysate collagen, the voltage applied and the distance from tip‐to‐collector. Based on the Box–Behnken design, the RSM was used to create a mathematical model and optimise nanofibres with minimum diameter production conditions. Using FTIR, TGA and SEM, optimised nanofibres were defined. In vitro, cytocompatibility trials showed that there was an important cytocompatibility of the optimised nanofibres, which was proved by cell proliferation and cell morphology. In this research, the mixed nanofibres of PCL and CH with ferulic could be a potential biomaterial for wound healing.Inspec keywords: tissue engineering, polymer fibres, wounds, electrospinning, nanofibres, response surface methodology, cellular biophysics, proteins, molecular biophysics, scanning electron microscopy, biomedical materials, nanomedicine, nanocomposites, nanofabrication, Fourier transform infrared spectraOther keywords: wound healing applications, PCL membranes, stable cover, protective cover, continuous FA release, RSM, optimised parameters, hydrolysate collagen, mathematical model, optimised nanofibres, polycaprolactone nanofibres, tissue engineering applications, composite biomaterials, composite electrospun nanofibres, collagen hydrolysate, ferulic acid, chronic wounds, Response Surface Methodology, nanofibres factor     

Fabrication and characterisation of super‐paramagnetic responsive PLGA–gelatine–magnetite scaffolds with the unidirectional porous structure: a physicochemical,mechanical, and in vitro evaluation

Architecture and composition of Scaffolds are influential factors in the regeneration of defects. Herein, synthesised iron oxide (magnetite) nanoparticles (MNPs) by co‐precipitation technique were evenly distributed in polylactic‐co‐glycolic acid (PLGA)–gelatine Scaffolds. Hybrid structures were fabricated by freeze‐casting method to the creation of a matrix with tunable pores. The synthesised MNPs were characterised by transmission electron microscopy, Fourier transform infrared spectroscopy, X‐ray diffraction spectroscopy, and vibrating sample magnetometer analysis. Scanning electron microscopy micrographs of porous Scaffolds confirmed the formation of unidirectional microstructure, so that pore size measurement indicated the orientation of pores in the direction of solvent solidification. The addition of MNPs to the PLGA–gelatine Scaffolds had no particular effect on the morphology of the pores, but reduced slightly pore size distribution. The MNPs contained constructs demonstrated increased mechanical strength, but a reduced absorption capacity and biodegradation ratio. Stability of the MNPs and lack of iron release was the point of strength in this investigation and were determined by atomic absorption spectroscopy. The evolution of rat bone marrow mesenchymal stem cells performance on the hybrid structure under a static magnetic field indicated the potential of super‐paramagnetic constructs for further pre‐clinical and clinical studies in the field of neural regeneration.Inspec keywords: transmission electron microscopy, biodegradable materials, nanofabrication, freezing, mechanical strength, tissue engineering, X‐ray diffraction, cellular biophysics, precipitation (physical chemistry), biomedical materials, iron compounds, porosity, scanning electron microscopy, atomic absorption spectroscopy, gelatin, nanoparticles, porous materials, bone, nanocomposites, Fourier transform infrared spectraOther keywords: unidirectional microstructure, pore size measurement, mechanical strength, atomic absorption spectroscopy, hybrid structure, super‐paramagnetic responsive PLGA–gelatine–magnetite scaffolds, unidirectional porous structure, tissue engineering Scaffolds, co‐precipitation technique, polylactic‐co‐glycolic acid–gelatine Scaffolds, freeze‐casting method, transmission electron microscopy, Fourier‐transform infrared spectroscopy, X‐ray diffraction spectroscopy, scanning electron microscopy micrographs, pore size distribution, absorption capacity, iron oxide nanoparticles, Fe₃ O₄      

Atorvastatin lipid nanocapsules and gold nanoparticles embedded in injectable thermo‐gelling hydrogel scaffold containing adipose tissue extracellular matrix for myocardial tissue regeneration

This study aimed to prepare, optimise, and characterise the novel hybrid hydrogel scaffold containing atorvastatin lipid nanocapsules (LNCs) and gold nanoparticles (NPs) to improve cardiomyoblasts proliferation and regeneration of myocardium. A thermo‐responsive aminated guaran (AGG) hydrogel was prepared to encompass extracellular matrix (ECM) fetched from human adipose tissue. Emulsion phase‐inversion technique was used to obtain LNCs. Biocompatibility, tensile strength, conductivity, and proliferation of human myocardial cells of the optimised formulation were studied. The LNCs have a spherical shape, and the optimised formulation showed a mean particle size of 18.79 nm, the zeta potential of − 11.4 mV, drug loading of 99.99%, and release efficiency percent over 72 h was 18.73%. The injectable thermo‐sensitive hydrogel prepared using 1 w/v% of AGG, 35 w/w% of ECM, ∼0.5 mg/ml of gold NPs and atorvastatin loaded LNCs showed the best physical characteristics. The hybrid scaffold loaded with atorvastatin and gold NPs improved the proliferation of cardiomyoblasts more than sevenfold with enhanced cell attachment to the scaffold. The tensile strength and the conductivity of the scaffold were 300 kPa and 0.14 S/m, respectively. Injectable hybrid adipose tissue prepared by ECM and AGG hydrogel loaded with atorvastatin and gold NPs showed promising physical characteristics for myocardial tissue engineering.Inspec keywords: biological tissues, nanoparticles, tensile strength, electrokinetic effects, particle size, nanomedicine, emulsions, biomedical materials, cellular biophysics, nanofabrication, drugs, drug delivery systems, molecular biophysics, tissue engineering, hydrogels, goldOther keywords: Au, cardiomyoblast, hybrid hydrogel scaffold, myocardial tissue engineering, AGG hydrogel, injectable hybrid adipose tissue, atorvastatin loaded LNCs, gold NPs, thermo‐sensitive hydrogel, drug loading, human myocardial cells, tensile strength, emulsion phase‐inversion technique, human adipose tissue, ECM, thermo‐responsive aminated guaran hydrogel, cardiomyoblasts proliferation, atorvastatin lipid nanocapsules, myocardial tissue regeneration, adipose tissue extracellular matrix, thermo‐gelling hydrogel scaffold, gold nanoparticles     

Fabrication of conductive human bio‐nanoelectrode from graphene oxide modified with polyvinyl alcohol

It is time for electrodes prepared from graphene oxide (GO) to replace the traditional electrodes. However, GO is an electrically insulating material. However, in this study, a conductive electrode was prepared from GO modification with glycerol (GL) under the esterification reaction at 90°C for 3 h with sulphuric acid as a catalyst under vacuum conditions. Polyvinyl alcohol (PVA) acts as a polymer host. It was mixed with GO and modification was carried out under heating conditions. The mixture of the GO/GL/PVA nanocomposite was rapidly cooled and poured into the electrode mould. Finally, it is placed in a desiccator at room temperature for two days. The characterisation (Fourier transform infrared spectroscopy, X‐ray diffraction, and scanning electron microscopy) proved that the ester bond was formed and a complete distribution of GO/GL into the matrix of PVA was verified. The GO/GL/PVA nanocomposite was tested for electrocardiogram (ECG) electrodes. The biopic instrument was used to compare the behaviour of the GO/GL/PVA plastic electrode and the commercial one. The results indicated that the GO/GL/PVA plastic electrode efficiently detected ECG signals after two months with high conductivity and lower noise than the commercial electrode. The GO/GL/PVA plastic electrode has been reported for the first time in the literature.Inspec keywords: catalysts, scanning electron microscopy, filled polymers, nanofabrication, X‐ray diffraction, moulding, nanocomposites, graphene compounds, Fourier transform infrared spectra, nanomedicine, biomedical electrodes, electrocardiography, electrical conductivity, medical signal detection, bonds (chemical)Other keywords: graphene oxide, polyvinyl alcohol, electrode mould, electrocardiogram electrodes, conductive human bionanoelectrode, electrically insulating material, GO‐GL‐PVA nanocomposite, GO‐GL‐PVA plastic electrode, esterification reaction, sulphuric acid, catalyst, vacuum conditions, polymer host, heating conditions, desiccator, glycerol, Fourier transform infrared spectroscopy, X‐ray diffraction, scanning electron microscopy, ester bond, biopic instrument, ECG signal detection, electrical conductivity, temperature 90.0 degC, time 3.0 hour, temperature 293 K to 298 K, time 2 day, CO     

Preparing a novel magnesium‐doped hyaluronan/polyethyleneimine nanoparticle to improve endothelial functionalisation

Nowadays, tissue engineering vascularisation has become an important means of organ repair and treatment of major traumatic diseases. Vascular endothelial layer regeneration and endothelial functionalisation are prerequisites and important components of tissue engineering vascularisation. The present researches of endothelial functionalisation mainly focus on tissue engineering scaffold preparation and implant surface modification. Few studies have reported the interaction of endothelial functionalisation and scaled materials, especially the nanomaterials. Magnesium (Mg), as an essential cytotropic active element in the human body, should promote the growth of endothelial cells. However, the authors’ previous work found that the Mg in the alloys had a defect of delayed endothelialisation, which may be attributed to the non‐uniform scales of the degradation products from Mg alloys. To validate this hypothesis and fabricate a novel nanomaterial for tissue engineering vascularisation, the authors prepared Mg‐doped hyaluronan (HA)/polyethyleneimine (PEI) nanoparticles for endothelial cells testing. Their data showed that the Mg‐doped HA/PEI nanoparticle with small scales (diameter <150 nm) presented better ability on improving endothelial cells growth, functionalisation and nitric oxide release.Inspec keywords: diseases, tissue engineering, biomedical materials, contact angle, cellular biophysics, nanoparticles, filled polymers, nanocomposites, nanomedicine, magnesium compounds, nanofabricationOther keywords: tissue engineering vascularisation, vascular endothelial layer regeneration, endothelial functionalisation, tissue engineering scaffold preparation, nitric oxide release, magnesium‐doped hyaluronan‐polyethyleneimine nanoparticle, endothelial cell testing, traumatic diseases, implant surface modification, human body, Mg‐doped hyaluronan‐polyethyleneimine nanoparticles, endothelial cell growth     

One‐step method for the preparation of poly(methyl methacrylate) modified titanium‐bioactive glass three‐dimensional scaffolds for bone tissue engineering

A novel three‐dimensional (3D) titanium (Ti)‐doping meso‐macroporous bioactive glasses (BGs)/poly(methyl methacrylate) (PMMA) composite was synthesised using PMMA and EO₂₀ PO₇₀ EO₂₀ (P₁₂₃) as the macroporous and mesoporous templates, respectively. Unlike the usual calcination method, the acid steam technique was used to improve the polycondensation of Ti‐BGs, and then PMMA was partially extracted via chloroform to induce the macroporous structure. Simultaneously, the residual PMMA which remained in the wall enhanced the compressive strength to 2.4 MPa (0.3 MPa for pure BGs). It is a simple and green method to prepare the macro‐mesoporous Ti‐BGs/PMMA. The materials showed the 3D interconnected hierarchical structure (250 and 3.4 nm), making the fast inducing‐hydroxyapatite growth and the controlled drug release. Besides mentioned above, the good antimicrobial property and biocompatible of the scaffold also ensure it is further of clinical use. Herein, the fabricated materials are expected to have potential application on bone tissue regeneration.Inspec keywords: titanium, bone, tissue engineering, glass, materials preparation, biomedical materials, polymers, porous materials, drug delivery systems, nanomedicineOther keywords: poly(methyl methacrylate), PMMA preparation, 3D titanium‐bioactive glass scaffold, bone tissue engineering, titanium‐doping mesomacroporous bioactive glass, bioactive glass‐PMMA composite, macroporous template, mesoporous template, calcination method, acid steam technique, titanium‐bioactive glass polycondensation, macroporous structure, green method, macromesoporous titanium‐bioactive glass‐PMMA, 3D interconnected hierarchical structure, fast inducing‐hydroxyapatite growth, controlled drug release, bone tissue regeneration, Ti     

Directional preparation of superhydrophobic magnetic CNF/PVA/MWCNT carbon aerogel

Carbon aerogels have attracted considerable attention in basic research and for their potential applications in many fields. Here, the fabrication of a magnetic cellulose nanofibre (CNF)/poly(vinyl alcohol) (PVA)/multiwalled carbon nanotubes (MWCNT) carbon aerogel (m‐CPMCA) is reported using a simple freeze‐drying followed by a carbonisation process, and direct immobilisation of Fe₃ O₄ nanoparticle on the surface of aerogels. The obtained target aerogel has the characteristics of low density (0.098 g/cm³), high porosity (>90%) and 3D interpenetrating porous structures. Furthermore, m‐CPMCA has a surprising compressive strength (about 0.35 MPa) which is obviously higher than many other cellulose‐based carbon aerogels. After Carbonization, m‐CPMCA exhibits superhydrophobicity, selective absorption for organic solvents and fire‐resistance. The m‐CPMCA also exhibited a magnetic response and can absorb oil on the water surface and can be actuated by a small magnet. More importantly, the m‐CPMCA could be recycled many times by combustion, which showed economic significance. To sum up, the authors believe that m‐CPMCA will become a very potential adsorbent for dealing with the increasingly serious problem of organic pollution.Inspec keywords: hydrophobicity, compressive strength, nanocomposites, nanofabrication, nanoparticles, porous materials, freezing, porosity, nanofibres, water, drying, aerogels, multi‐wall carbon nanotubes, filled polymersOther keywords: 3D interpenetrating porous structures, m‐CPMCA, cellulose‐based carbon aerogels, magnetic response, directional preparation, superhydrophobic magnetic CNF/PVA/MWCNT carbon aerogel, magnetic cellulose nanofibre/poly(vinyl alcohol)/multiwalled carbon nanotubes carbon aerogel, aerogel, freeze‐drying, carbonisation, direct immobilisation, Fe₃ O₄ nanoparticle, porosity, compressive strength, superhydrophobicity, fire‐resistance, combustion, Fe₃ O₄ , C     

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     

Honokiol–camptothecin loaded graphene oxide nanoparticle towards combinatorial anti‐cancer drug delivery

Honokiol (HK) is a natural product isolated from the bark, cones, seeds and leaves of plants belonging to the genus Magnolia. It possesses anti‐cancer activity which can efficiently impede the growth and bring about apoptosis of a diversity of cancer cells. The major concerns of using HK are its poor solubility and lack of targeted drug delivery. In this study, a combinatorial drug is prepared by combining HK and camptothecin (CPT). Both CPT and HK belong to the Magnolian genus and induce apoptosis by cell cycle arrest at the S‐phase and G1 phase, respectively. The combinatorial drug thus synthesised was loaded onto a chitosan functionalised graphene oxide nanoparticles, predecorated with folic acid for site‐specific drug delivery. The CPT drug‐loaded nanocarrier was characterised by X‐ray diffractometer, scanning electron microscope, transmission electron microscope, UV–vis spectroscopy and fluorescence spectroscopy, atomic force microscopy. The antioxidant properties, haemolytic activity and anti‐inflammatory activities were analysed. The cellular toxicity was analysed by 3‐(4,5‐Dimethylthiazol‐2‐yl)‐2,5‐Diphenyltetrazolium Bromide (MTT assay) and Sulforhodamine B (SRB) assay against breast cancer (MCF‐7) cell lines.Inspec keywords: nanofabrication, cancer, nanoparticles, atomic force microscopy, graphene, scanning electron microscopy, cellular biophysics, toxicology, transmission electron microscopy, drug delivery systems, nanomedicine, tumours, solubilityOther keywords: targeted drug delivery, combinatorial drug, Magnolian genus, apoptosis, cell cycle, chitosan functionalised graphene oxide nanoparticles, site‐specific drug delivery, CPT drug‐loaded nanocarrier, transmission electron microscope, fluorescence spectroscopy, haemolytic activity, antiinflammatory activities, breast cancer cell lines, honokiol–camptothecin loaded graphene oxide nanoparticle, combinatorial anti‐cancer drug delivery, natural product, genus Magnolia, anticancer activity, cancer cells     

In vitro biological evaluation of anti‐diabetic activity of organic–inorganic hybrid gold nanoparticles

Diabetes mellitus has been considered as a heterogeneous metabolic disorder characterised by complete or relative impairment in the production of insulin by pancreatic β‐cells or insulin resistance. In the present study, propanoic acid, an active biocomponent isolated from Cassia auriculata is employed for the synthesis of propanoic acid functionalised gold nanoparticles (Pa@AuNPs) and its anti‐diabetic activity has been demonstrated in vitro. In vitro cytotoxicity of synthesised Pa@AuNPs was performed in L6 myotubes. The mode of action of Pa@AuNPs exhibiting anti‐diabetic potential was validated by glucose uptake assay in the presence of Genistein (insulin receptor tyrosine kinase inhibitor) and Wortmannin (Phosphatidyl inositide kinase inhibitor). Pa@AuNPs exhibited significant glucose uptake in L6 myotubes with maximum uptake at 50 ng/ml. Assays were performed to study the potential of Pa@AuNPs in the inhibition of protein‐tyrosine phosphatase 1B, α‐glucosidases, and α‐amylase activity.Inspec keywords: molecular biophysics, biomedical materials, sugar, enzymes, nanofabrication, gold, patient treatment, organic‐inorganic hybrid materials, biochemistry, diseases, cellular biophysics, nanoparticles, toxicology, nanomedicineOther keywords: glucose uptake assay, α‐amylase activity, organic–inorganic hybrid gold nanoparticles, diabetes mellitus, heterogeneous metabolic disorder, pancreatic β‐cells, insulin resistance, propanoic acid, antidiabetic potential, antidiabetic activity, in vitro cytotoxicity, L6 myotubes, Genistein, IRTK inhibitor, Wortmannin, P13K inhibitor, protein‐tyrosine phosphatase 1B, α‐glucosidases, Cassia auriculata, Au     

Penetration Depth in Nanoparticles Incorporated Radiofrequency Hyperthermia into the Tissue: Comprehensive Study with Histology and Pathology Observations

In present study, the effective penetration of radiofrequency (RF) induced gold decorated iron oxide nanoparticles (GS@IONPs) hyperthermia was investigated. The effective penetration depth of RF also the damage potency of hyperthermia was evaluated during histopathology observations which were done on the chicken breast tissue and hepatocellular carcinoma (HCC) models. The thermal damages are well‐ documented in our previous cellular study which was engaged with potency of RF hyperthermia in Epithelial adenocarcinoma (MCF‐7) and fibroblast (L‐929) cells deaths [1]. In recent work, PEGylated iron oxide nanoparticles (IONPs) were used as base platform for gold magnetic nanoparticles (GS@IONPs) formation. The 144.00015 MHz, 180W RF generator was applied for stimulating the nanoparticles. The chicken breast tissue and the hepatocellular tumor model was considered in the experimental section. In histology studies, the structural changes also the effective penetration depth of RF induced nanoparticles was observed through microscopic monitoring of the tissue slices in histology observations (Gazi medical school). The highest damage level was seen in 8.0 µm tissue slices where lower damages were seen in depth of 1.0 cm and more inside tissue. The histology observations clarified the effective penetration depth of RF waves and irreversible damages in the 2.0 cm inside the tissue.Inspec keywords: nanomedicine, tumours, biomedical materials, cellular biophysics, nanoparticles, gold, cancer, hyperthermia, magnetic particles, iron compounds, radiation therapyOther keywords: Au‐Fe₃ O₄ , depth 1.0 cm, depth 8.0 mum, power 180.0 W, size 2.0 cm, frequency 144.00015 MHz, microscopic monitoring, structural changes, hepatocellular tumour model, standing wave ratio, propylene glycol, thermal damages, hepatocellular carcinoma models, radiofrequency hyperthermia, nanoparticle dispersion, tissue alterations, modified tissues, gold shell magnetic nanoparticles, chicken breast tissue, gold‐coated iron oxide nanoparticles, pathology observations, effective penetration depth, histology observations, tissue slices     

Folate encapsulation in PEG‐diamine grafted mesoporous Fe3 O4 nanoparticles for hyperthermia and in vitro assessment

Effective and targeted delivery of the antitumour drugs towards the specific cancer spot is the major motive of drug delivery. In this direction, suitably functionalised magnetic iron oxide nanoparticles (NPs) have been utilised as a theranostic agent for imaging, hyperthermia and drug delivery applications. Herein, the authors reported the preparation of multifunctional polyethyleneglycol‐diamine functionalised mesoporous superparamagnetic iron oxide NPs (SPION) prepared by a facile solvothermal method for biomedical applications. To endow targeting ability towards tumour site, folic acid (FA) is attached to the amine groups which are present on the NPs surface by 1‐ethyl‐3‐(3‐dimethylaminopropyl) carbodiimide hydrochloride/N‐hydroxysuccinimide chemistry. FA attached SPION shows good colloidal stability and possesses high drug‐loading efficiency of ∼ 96% owing to its mesoporous nature and the electrostatic attachment of daunosamine (NH₃ ⁺) group of doxorubicin (DOX) towards the negative surface charge of carboxyl and hydroxyl group. The NPs possess superior magnetic properties in result endowed with high hyperthermic ability under alternating magnetic field reaching the hyperthermic temperature of 43°C within 223 s at NP''s concentration of 1 mg/ml. The functionalised NPs possess non‐appreciable toxicity in breast cancer cells (MCF‐7) which is triggered under DOX‐loaded SPION.Inspec keywords: nanoparticles, nanocomposites, mesoporous materials, colloids, biochemistry, nanomagnetics, molecular biophysics, tumours, superparamagnetism, drugs, toxicology, biomedical materials, nanofabrication, hyperthermia, cancer, magnetic particles, cellular biophysics, nanomedicine, iron compounds, drug delivery systems, filled polymers, biological organs, liquid phase depositionOther keywords: NP surface, colloidal stability, drug‐loading efficiency, hydroxyl group, magnetic properties, high hyperthermic ability, magnetic field, DOX‐loaded SPION, folate encapsulation, targeted delivery, antitumour drugs, specific cancer spot, magnetic iron oxide nanoparticles, theranostic agent, drug delivery applications, multifunctional polyethyleneglycol‐diamine, facile solvothermal method, biomedical applications, tumour site, amine groups, mesoporous superparamagnetic nanoparticles, PEG‐diamine grafted mesoporous nanoparticles, 1‐ethyl‐3‐(3‐dimethylaminopropyl) carbodiimide hydrochloride‐N‐hydroxysuccinimide chemistry, daunosamine group, carboxyl group, breast cancer cells, temperature 43.0 degC, Fe₃ O₄