Adsorption of gum Arabic on bioceramic nanoparticles

Surface modification agents can be used to tailor the surface chemistry and biological activity of bioceramic nanoparticles in very intriguing ways. However, the specific modes of interactions between macromolecules and nanoparticles can be difficult to characterize. The aim of this study was to investigate the adsorption of gum Arabic on hydroxyapatite (HAp) and magnetic nanoparticles (MNP) using the bicinchoninic acid (BCA) test. Gum Arabic (GA) is a natural gum that has been widely used as an emulsifying agent and shows promise for dispersing nanoparticles in aqueous solutions. The adsorption of GA onto HAp nanoparticles followed a Langmuir isotherm with an adsorption plateau occurring at 0.2 g GA/g HAp. The adsorption of GA onto MNP attained a maximum value of 0.6 g GA/g MNP, after which it decreased to approximately 0.2 g GA/g MNP. The maximum adsorption density of GA on both MNP and HAp is equivalent when normalized to the specific surface area (4 × 10^− 3 g GA/m²). Adsorbed GA molecules were displaced from the surface of HAp and MNP in the presence of phosphate ions.     

Magnetite nanoparticles with high heating efficiencies for application in the hyperthermia of cancer

Magnetic hyperthermia is a safe method for cancer therapy. A gap-type alternating current magnetic field (100 kHz, 100–300 Oe) is expected to be clinically applicable for magnetic hyperthermia. In this study, magnetite nanoparticles (MNPs) varying in size from 8 to 413 nm were synthesized using a chemical coprecipitation and an oxidation precipitation method to find the optimum particle size that shows a high heating efficiency in an applied magnetic field. The particles' in vitro heating efficiency in an agar phantom at an MNP concentration of 58 mg Fe/ml was measured in an applied magnetic field. In a magnetic field of 120 Oe, the temperature increase (ΔT) of the agar phantom within 30 s was 9.3 °C for MNPs with a size of 8 nm, but was less for the other samples, while in a magnetic field of 300 Oe, ΔT = 55 °C for MNPs with a size of 24 nm, and ΔT = 25 °C for MNPs with a size of 8 nm. The excellent heating efficiency of MNPs with a size of 24 nm in a magnetic field of 300 Oe may be due to a combination of the effects of both relaxation and hysteresis losses of the magnetic particles. It is believed that MNPs with a size of 8–24 nm will be useful for the in situ hyperthermia treatment of cancer.     

Hydrothermal synthesis of ZnO nanorod arrays with the addition of polyethyleneimine

ZnO nanorod arrays were synthesized on glass substrates coated by a ZnO seeding layer via a hydrothermal technique by adding polyethyleneimine (PEI) to the growth solution. The XRD and SEM results show that the ZnO nanorods have the single crystal wurtzite structure with the (0 0 2) direction normal to the substrates. In 50 ml growth solution of 0.05 M zinc salts, the average diameter of the nanorods was reduced drastically from 300 nm to 40 nm with the PEI amount increasing from 0 ml to 6 ml. The diameter distribution and the polycrystalline layer at the bottom of the nanorods were improved. Longer nanorods were obtained by prolonging the growth time. Based on the results, possible mechanisms that PEI adsorbs on the non-polar facets of ZnO nanorods and its coordination to zinc ions were proposed to elucidate the effect of PEI on reducing the diameters and improving the morphologies of nanorods.     

Recyclable and stable silver deposited magnetic nanoparticles with poly (vinyl pyrrolidone)-catechol coated iron oxide for antimicrobial activity

This paper introduces a facile method to make highly stable and recyclable antimicrobial magnetic nanoparticles (NPs). Initially, magnetic iron oxide nanoparticles (IONPs) were coated with poly (vinyl pyrrolidone) conjugated catechol (PVP-CCDP). Afterward, silver nanoparticles (Ag⁰) were deposited onto PVP-CCDP coated IONPs using remain catechol. The prepared nanoparticles showed long term (~ 4 weeks) colloidal stability and redispersibility, respectively, against external magnetic field and over a broad range of pH (4–12). The NPs were characterized by UV–vis, SEM, XPS, and XRD measurements. TEM and DLS analyses showed that the mean particle size of PVP-CCDP coated IONPs/Ag⁰ were about 72 nm. The recyclable magnetic NPs possessed a high antibacterial effect against the model microbes Staphylococcus aureus and Escherichia coli and could be separated easily using magnet following antibacterial test for repeated uses and maintained 100% antibacterial efficiency during three cycles. In MTT assay, the magnetic nanoparticles possessed no measureable cytotoxicity to live cells.     

Electrospun nanofibers composed of poly(ε-caprolactone) and polyethylenimine for tissue engineering applications

Poly(ε-caprolactone) (PCL) electrospun nanofibers have been reported as a scaffold for tissue engineering application. However, high hydrophobicity of PCL limits use of functional scaffold. In this study, PCL/polyethylenimine (PEI) blend electrospun nanofibers were prepared to overcome the limitation of PCL ones because the PEI as a cationic polymer can increase cell adhesion and can improve the electrospinnability of PCL. The structure, mechanical properties and biological activity of the PCL/PEI electrospun nanofibers were studied. The diameters of the PCL/PEI nanofibers ranged from 150.4 ± 33 to 220.4 ± 32 nm. The PCL/PEI nanofibers showed suitable mechanical properties with adequate porosity and increased hydrophilic behavior. The cell adhesion and cell proliferation of PCL nanofibers were increased by blending with PEI due to the hydrophilic properties of PEI.     

Influence of the coating material on the loosing of dental implant abutment screw joints

Dental implant abutment screw joints tend to loosen and prosthesis rotation has been observed under clinical conditions. Some dental implant manufacturers suggest coated abutment screw to prevent the displacement of dental prosthesis. In the present work, the opening torque (N cm) was measured as a function of tightening torque (N cm) for dental implant abutment screws coated with four different materials (TiC, TiCN, Teflon and Parylene) to clarify the influence of the coating material on abutment screw stability and to analyze the relationship between preload and opening torque. On a first series of tests, closing and opening torque (N cm) of abutment screws without coating and with coating tightened to 20, 30, 32, 35 and 40 N cm was recorded. In a second series of tests, changes in opening torque values were analyzed after successive closures that were tightened at constant values of 30, 32 and 35 N cm. On a third series of tests, abutment screws without coating and with Teflon coating were tightened to 32 N cm and submitted to cyclic loading. The results showed that for all abutment screws the opening torque was less than the tightening torque. For a given applied tightening torque (35 N cm), the screws without a coating had the highest opening torque (31.6 ± 0.9 N cm [mean ± S.D.]). The screw coated with TiN had the smallest average opening torque (12.2 ± 0.6 N cm) after tightening at 20 N cm. A progressive decrease in opening torque values was measured in all screw groups after repeated closures. After six retightenings (35 N cm) a statistically significant difference (P < .05) was observed in opening torque among uncoated Ti screw group (31.5 ± 0.6 N cm) and coated screw tested groups (Parylene = 29.6 ± 0.4, Teflon = 29.1 ± 0.7). Under cyclic loading Ti screws without coating are more stable than Teflon coated screws. The present work suggests that one must be aware of the magnitude of the opening torque when specifying a certain coating/preload combination. The present methodology shows how to calculate the relevant quantities.     

Biosensor based on laccase immobilized on plasma polymerized allylamine/carbon electrode

In this work, a simple and rapid method was used to functionalize carbon electrode in order to efficiently immobilize laccase for biosensor application. A stable allylamine coating was deposited using a low pressure inductively excited RF tubular plasma reactor under mild plasma conditions (low plasma power (10 W), few minutes) to generate high density amine groups (N/C ratio up to 0.18) on rough carbon surface electrodes. The longer was the allylamine plasma deposition time; the better was the surface coverage. Laccase from Trametes versicolor was physisorbed and covalently bound to these allylamine modified carbon surfaces. The laccase activities and current outputs measured in the presence of 2,2′-azinobis-(3-ethylbenzothiazole-6-sulfonic acid) (ABTS) showed that the best efficiency was obtained for electrode plasma coated during 30 min. They showed also that for all the tested electrodes, the activities and current outputs of the covalently immobilized laccases were twice higher than the physically adsorbed ones. The sensitivity of these biocompatible bioelectrodes was evaluated by measuring their catalytic efficiency for oxygen reduction in the presence of ABTS as non-phenolic redox substrate and 2,6-dimethoxyphenol (DMP) as phenolic one. Sensitivities of around 4.8 μA mg^? 1 L and 2.7 μA mg^? 1 L were attained for ABTS and DMP respectively. An excellent stability of this laccase biosensor was observed for over 6 months.     

Synthesis and characterization of the iron oxide magnetic particles coated with chitosan biopolymer

Magnetic particles are extremely interesting for several biomedical applications; amongst these are therapeutic applications, such as: hyperthermia and release of drugs. The use of magnetic particles to induce hyperthermia in biological tissues is an important factor in cancer therapy. The aim of this study was to prepare and characterize iron oxide magnetic particles coated with biopolymer chitosan, and also to produce ferrofluids from the magnetic particles. The iron oxide magnetic particles (IOMP) were coated with chitosan (CS) by spray-drying method using two IOMP/coating ratios (IOMP/CS = 1.6 and IOMP/CS = 4.5). The magnetic particles were characterized by way of scanning electronic microscopy and energy-dispersive X-ray. The analysis by energy-dispersive X-ray was carried out to determine the chemical composition of particles in samples. The size distribution the iron oxide magnetic particles uncoated and coated were evaluated by the laser diffraction analysis and image analysis, respectively. Amongst the prepared ferrofluids, the sample IOMP/CS = 1.6 proved to be the one that has brought about the best results in therapeutics applications, such as in hyperthermia treatment. This sample was placed within an alternating magnetic field during 40 min, it was observed that 1 °C heated in 3 min and underwent a temperature variation of 7 °C, since it varied from 25 °C to 32 °C. Considering that the experiment would be carried out at body temperature 37 °C, probably, the temperature variation would be very close to the one reported at 25 °C. In such a way, the cancerous cells would reach 44–45 °C and at such temperatures the cancer cells generally perish.     

Electric isolation of porous silicon by electro generated polyethyleneimine film,comparison to thermal oxide

Electrochemical oxidation of diethylenetriamine (DETA) charged with 0.1 M LiSO₃CF₃, leads to a polymeric coating (polyethyleneimine film: PEI) on the porous silicon (PS) surface. The obtained passivated electrode is characterized through IRTF spectrometry and through C(V) curves on PS/PEI structures showing good insulating properties of the PEI film. The passivated electrode presents a linear pH sensitivity close to 62 mV per pH unit. Such sensitivity is higher compared to flat PEI passivated silicon electrode. The results were fitted with the generalized site-binding theory and the following parameters were found: the surface site density N_s was found to be equal to 3.6 × 10¹⁶ cm^− 2 and pK_H (K_H acido-basic constant of the amino group) is − 5.54.     

Kinetics of elimination and distribution in blood and liver of biocompatible ferrofluids based on Fe3O4 nanoparticles: An EPR and XRF study

In this study, we evaluated the biodistribution and the elimination kinetics of a biocompatible magnetic fluid, Endorem™, based on dextran-coated Fe₃O₄ nanoparticles endovenously injected into Winstar rats. The iron content in blood and liver samples was recorded using electron paramagnetic resonance (EPR) and X-ray fluorescence (XRF) techniques. The EPR line intensity at g = 2.1 was found to be proportional to the concentration of magnetic nanoparticles and the best temperature for spectra acquisition was 298 K. Both EPR and XRF analysis indicated that the maximum concentration of iron in the liver occurred 95 min after the ferrofluid administration. The half-life of the magnetic nanoparticles (MNP) in the blood was (11.6 ± 0.6) min measured by EPR and (12.6 ± 0.6) min determined by XRF. These results indicate that both EPR and XRF are very useful and appropriate techniques for the study of kinetics of ferrofluid elimination and biodistribution after its administration into the organism.     

Preparation of N,O-carboxymethyl chitosan coated alginate microcapsules and their application to Bifidobacterium longum BIOMA 5920

In order to greatly improve vitality of probiotic bacteria within the application, a novel biocompatible vehicle, N,O-carboxymethyl chitosan (NOCs) with appropriate degrees of substitution coat alginate (ALg) microparticles, was prepared by electrostatic droplet generation. The amount of chitosan (Cs) and N,O-carboxymethyl chitosan (NOCs) coated on the ALg microparticles was determined by differential scanning calorimetry. The surface morphology of ALg microparticles, Cs coated ALg microparticles and NOCs coated ALg microparticles was determined using scanning electron microscopy. The coating thickness of Cs coated ALg microparticles and that of NOCs coated ALg microparticles was directly observed with confocal laser scanning microscopy. In order to assess pH sensitivity of microparticles, the bovine serum albumin release from the microspheres was tested in acid solution (pH 2.0) for 2 h and subsequently in alkaline solution (pH 7.0) for 2 h. The survival of Bifidobacterium longum BIOMA 5920 loaded in NOCs coated with ALg microparticle was improved in simulated gastric juice (pH 2.0, for 2 h) compared to that of B. longum BIOMA 5920 loaded in ALg microparticles and Cs coated ALg microparticles. After incubation in simulated intestinal juices (pH 7.0, 2 h), the release of microencapsulated B. longum BIOMA 5920 was investigated.     

Improving the electromechanical performance of dielectric elastomers using silicone rubber and dopamine coated barium titanate

In this work, a new soft dielectric elastomer (DE) was fabricated from dopamine coated barium titanate particles and silicone rubber (SR). The results showed that the barium titanate (BaTiO₃, BT) was coated by dopamine and the coated particles were highly compatible with SR. In order to achieve a maximum voltage-induced deformation, the minimum secant moduli of DEs were obtained in experimentation at a stretch ratio of approximately 1.6 by applying equi-biaxial tensile strain using the bubble inflation method. Additionally, it was found that the addition of DP-BT into SR led to an increased dielectric constant and decreased dielectric loss tangent for the matrix by comparison with SR/BT composites. Furthermore, the electromechanical properties of the SR/DP-BT composites were greatly improved in terms of voltage-induced deformation (s_a), electromechanical energy density (e) and coupling efficiency (K²). A maximum actuated area strain of approximately 78%, which was 30% larger than that of the SR/BT composites, was achieved for the sample having a DP-BT content of 20 wt.%. This strain corresponded to a low dielectric strength of around 53 V/μm, the composite exhibited a maximum energy density of 0.07 MJ/m³ and coupling efficiency of 0.68.     

Magnetic nanoparticle-based solder composites for electronic packaging applications

Sn–Ag–Cu (SAC) alloys are regarded as the most promising alternative for traditional Pb–Sn solders used in electronic packaging applications. However, the higher reflow temperature requirement, possible intermetallic formation, and reliability issues of SAC alloys generate several key challenges for successful adoption of Pb-free solder for next generation electronic packaging needs. Localized heating in interconnects can alleviate thermal stresses by preventing subjection of entire package to the higher reflow temperatures associated with the SAC solders. It had been demonstrated that SAC solder–FeCo magnetic nanoparticles (MNPs) composite paste can be reflowed locally with AC magnetic fields, enabling interconnect formation in area array packages while minimizing eddy current heating in the printed circuit board.Solder/magnetic nanocomposite pastes with varying MNP concentration were reflowed using AC magnetic fields. Differential scanning calorimetry results show a reduced undercooling of the composite pastes with the addition of MNPs. TEM results show that the FeCo MNPs are distributed in Sn matrix of the reflowed solder composites. Optical and SEM micrographs show a decrease in Sn dendrite regions as well as smaller and more homogeneous dispersed Ag₃Sn with the addition of MNPs. The MNPs promote Sn solidification by providing more heterogeneous nucleation sites at relatively low undercoolings. The mechanical properties were measured by nanoindentation. The modulus, hardness, and creep resistance, increase with the MNP concentration. The enhanced mechanical properties are attributed to grain boundary and dispersion strengthening.The reflow of solder composites have been modeled based on eddy current power loss in the substrate and magnetic power losses in the solder bumps. Induction reflow of pure solder bumps (<300 μm) in an area array package using 500 Oe magnetic field at 300 kHz requires excessive eddy current power loss in the substrate, resulting in extreme temperatures that lead to blistering and delamination of the substrate. Solder–MNP composites with modest MNP loading showed temperature increases sufficient to achieve solder reflow when subjected to the same AC magnetic fields. Thermomechanical behavior of a solder joint was also modeled under cyclic temperature variations. The stress and strain are highly localized at the interface between solder and substrate. Plastic work accumulated per cycle can be used for lifetime prediction.In this article we review lead-containing and lead-free solder systems, and the electronic packaging technologies pertinent to soldering process. Recent research on the effects of MNPs on localized heating, microstructure evolution, mechanical properties, and thermomechanical reliability are summarized.     

Enteric coating process of diclofenac sodium pellets in a fluid bed coater with a wurster insert: Influence of process variables on coating performance and release profile

The objective of this work was to study the coating process of diclofenac sodium pellets, with the commercial aqueous coating suspension for enteric release – Acryl-Eze® MP, in a fluid bed coater with a Wurster insert. Coating experiments were performed following a 2² factorial design to determine the influence of process variables on coating performance, measured by the two response variables: efficiency (η_%) and agglomeration index (m_agg%). Both response variables were found to be affected by inlet temperature and suspension flow rate with a 95% confidence level. This work also studied the release of diclofenac sodium coated and uncoated pellets in HCl 0.1 N and pH 6.8 phosphate buffer media. Results showed that the release of diclofenac sodium during the buffer stage was affected by the prior exposure to the HCl 0.1 N medium and a polymer weight gain above 9.7% (2.7 mg/cm²), was needed to modify the release in such a way that it remained below 10% for the first 120 min in HCl 0.1 N and above 75% in pH 6.8 for the next 45 min. Neither the drug content nor the release profiles were significantly affected by storage at 40 °C and 75% relative humidity.     

Synthesis and characterization of magnetite nanoparticles via the chemical co-precipitation method

Magnetite nanoparticles were synthesized via the chemical co-precipitation method using ammonium hydroxide as the precipitating agent. The size of the magnetite nanoparticles was carefully controlled by varying the reaction temperature and through the surface modification. Herein, the hexanoic acid and oleic acid were introduced as the coating agents during the initial crystallization phase of the magnetite. Their structure and morphology were characterized by the Fourier transform infrared spectroscopy (FTIR), the X-ray diffraction (XRD) and the field-emission scanning electron microscopy (FE-SEM). Moreover, the electrical and magnetic properties were studied by using a conductivity meter and a vibrating sample magnetometer (VSM), respectively. Both of the bare magnetite and the coated magnetite were of the cubic spinel structure and the spherical-shaped morphology. The reaction temperature and the surface modification critically affected the particle size, the electrical conductivity, and the magnetic properties of these particles. The particle size of the magnetite was increased through the surface modification and reaction temperature. In this study, the particle size of the magnetite nanoparticles was successfully controlled to be in the range of 10–40 nm, suitable for various biomedical applications. The electrical conductivity of the smallest particle size was 1.3 × 10^?3 S/cm, within the semi-conductive materials range, which was higher than that of the largest particle by about 5 times. All of the magnetite nanoparticles showed the superparamagnetic behavior with high saturation magnetization. Furthermore, the highest magnetization was 58.72 emu/g obtained from the hexanoic acid coated magnetite nanoparticles.     

Magnetic refrigerator for hydrogen liquefaction

This paper reviews the status of magnetic refrigeration system for hydrogen liquefaction. There is no doubt that hydrogen is one of most important energy sources in the near future. In particular, liquid hydrogen can be utilized for infrastructure construction consisting of storage and transportation. When we compare the consuming energy of hydrogen liquefaction with high pressurized hydrogen gas, FOM must be larger than 0.57 for hydrogen liquefaction. Thus, we need to develop a highly efficient liquefaction method. Magnetic refrigeration using the magneto-caloric effect has potential to realize not only the higher liquefaction efficiency >50%, but also to be environmentally friendly and cost effective. Our hydrogen magnetic refrigeration system consists of Carnot cycle for liquefaction stage and AMR (active magnetic regenerator) cycle for precooling stages. For the Carnot cycle, we develop the high efficient system with >80% liquefaction efficiency by using the heat pipe. For the AMR cycle, we studied two kinds of displacer systems, which transferred the working fluid. We confirmed the AMR effect with the cooling temperature span of 12 K for 1.8 T of the magnetic field and 6 s of the cycle. By using the simulation, we estimate the efficiency of the hydrogen liquefaction plant for 10 kg/day. A FOM of 0.47 is obtained for operation temperature between 20 K and 77 K including LN₂ work input.     

O-Carboxymethyl-chitosan/organosilica hybrid nanoparticles as non-viral vectors for gene delivery

Polymeric non-viral vectors, such as chitosan nanoparticles show good biocompatibility, but low transfection efficiency. The objective of this study was to improve the transfection efficiency of chitosan based non-viral vectors by using o-carboxymethyl-chitosan which is a kind of water-soluble chitosan derivative and also has good biocompatibility. O-Carboxymethyl-chitosan-organosilica hybrid nanoparticles (CMG NPs) were synthesized through a rapid one-step aqueous synthetic approach for gene delivery. The size of nanoparticles was 276 ± 25 nm and zeta potential was 31.6 ± 0.4 mV in deionized water. Zeta potential increased with the decrease of pH, and it had been discovered that pH = 5.5 is the best point for CMG NPs to bond with plasmid DNA. DNA inclusion and integrity was evaluated by gel electrophoresis, and it is indicated that CMG NPs could protect DNA against DNase I and serum degradation. The results of MTT for cell viability and in vitro transfection also support the idea that CMG NPs could be used as efficient and safe vectors for gene delivery.     

PHEMA cryogel for in-vitro removal of anti-dsDNA antibodies from SLE plasma

Supermacroporous poly(2-hydroxyethyl methacrylate) (PHEMA) cryogel carrying DNA was used in the removal of anti-dsDNA antibodies from systemic lupus erythematosus (SLE) patient plasma. The PHEMA cryogel was prepared by bulk polymerization which proceeds in an aqueous solution of monomer frozen inside a plastic syringe. After thawing, the PHEMA cryogel contains a continuous matrix having interconnected macropores of 10–200 μm size. Pore volume in the PHEMA cryogel was 67.5%. Ester groups in the PHEMA structure were converted to imine groups by reacting with poly(ethyleneimine) (PEI) in the presence of NaHCO₃. Amino (? NH₂) content of PEI-modified PHEMA cryogel was determined as 82 mg PEI/g. Then, DNA was attached onto the PHEMA cryogel via amino groups (53.4 mg DNA/g cryogel). Anti-dsDNA-antibody concentration declined significantly from 780 IU/ml to 80 IU/ml with the time. The maximum anti-dsDNA-antibody adsorption amount was 70 × 10³ IU/g. Anti-dsDNA-antibodies could be repeatedly adsorbed and eluted without noticeable loss in the anti-dsDNA-antibody adsorption amount.     

Magnetic properties of nanocrystalline ɛ-Fe3N and Co4N phases synthesized by newer precursor route

Nanocrystalline ɛ-Fe₃N and Co₄N nitride phases are synthesized first time by using tris(1,2-diaminoethane)iron(II) chloride and tris(1,2-diaminoethane)cobalt(III) chloride precursors, respectively. To prepare ɛ-Fe₃N and Co₄N nitride phases, the synthesized precursors were mixed with urea in 1:12 ratio and heat treated at various temperatures in the range of 450–900 °C under the ultrapure nitrogen gas atmosphere. The precursors are confirmed by FT-IR study. The ɛ-Fe₃N phase crystallizes in hexagonal structure with unit cell parameters, a = 4.76 Å and c = 4.41 Å. The Co₄N phase crystallizes in face centred cubic (fcc) structure with unit cell parameters, a = 3.55 Å. The estimated crystallite size for ɛ-Fe₃N and Co₄N phases are 29 nm and 22 nm, respectively. The scanning electron microscopy (SEM) studies confirm the nanocrystalline nature of the materials. The values of saturation magnetization for ɛ-Fe₃N and Co₄N phases are found to be 28.1 emu/g and 123.6 emu/g, respectively. The reduction of magnetic moments in ultrafine materials compared to bulk materials have been explained by spin pairing effect, lattice expansion, superparamagnetic behaviour and canted spin structures at the surface of the particles.     

Preparation of high performance soft magnetic alloy Fe-4Si-0.8P by metal injection molding

Fe-4Si-0.8P soft magnetic alloy was prepared by metal injection molding (MIM). Ferrophosphorus liquid phase sintering promoted densification and enhanced magnetic properties. The sample with nearly full density, the saturation induction of 1.59 T, maximum permeability of 2467, coercive force of 130 A/m and resistivity of 81.2 μΩ·cm was obtained at 1300 °C for 4 h. Competitive properties contributed toward achieving low magnetic losses. Therefore, MIM Fe-4Si-0.8P can be widely used in the field of magnetic materials.