Effect of Gentamicin Sulfate and Polymeric Polyethylene Glycol Coating on the Degradation and Cytotoxicity of Iron-Based Biomaterials.

The work is focused on the degradation, cytotoxicity, and antibacterial properties, of iron-based biomaterials with a bioactive coating layer. The foam and the compact iron samples were coated with a polyethylene glycol (PEG) polymer layer without and with gentamicin sulfate (PEG + Ge). The corrosion properties of coated and uncoated samples were studied using the degradation testing in Hanks' solution at 37 °C. The electrochemical and static immersion corrosion tests revealed that the PEG-coated samples corroded faster than samples with the bioactive PEG + Ge coating and uncoated samples. The foam samples corroded faster compared with the compact samples. To determine the cytotoxicity, cell viability was monitored in the presence of porous foam and compact iron samples. The antibacterial activity of the samples with PEG and PEG + Ge against Escherichia coli CCM 3954 and Staphylococcus aureus CCM 4223 strains was also tested. Tested PEG + Ge samples showed significant antibacterial activity against both bacterial strains. Therefore, the biodegradable iron-based materials with a bioactive coating could be a suitable successor to the metal materials studied thus far as well as the materials used in the field of medicine.

SERS Performance of Ti3C2Tx MXene-Based Substrates Correlates with Surface Morphology.

The surface-enhanced Raman scattering (SERS) properties of low-dimensional semiconducting MXene nanoflakes have been investigated over the last decade. Despite this fact, the relationship between the surface characteristics and SERSing performance of a MXene layer has yet to be comprehensively investigated and elucidated. This work shows the importance of surface morphology on the overall SERS effect by studying few-layer Ti3C2Tx MXene-based SERS substrates fabricated by vacuum-assisted filtration (VAF) and spray coating on filter paper. The VAF deposition results in a dense MXene layer suitable for SERS with high spot-to-spot and substrate-to-substrate reproducibility, with a significant limit of detection (LoD) of 20 nM for Rhodamine B analyte. The spray-coated MXenes film revealed lower uniformity, with a LoD of 50 nM for drop-casted analytes. Moreover, we concluded that the distribution of the analyte deposited onto the MXene layer is affected by the presence of MXene aggregates created during the deposition of the MXene layer. Accumulation of the analyte molecules in the vicinity of MXene aggregates was observed for drop-casted deposition of the analyte, which affects the resulting SERS enhancement. Ti3C2Tx MXene layers deposited on filter paper by VAF offer great potential as a cost-effective, easy-to-manufacture, yet robust, platform for sensing applications.

Anticorrosion and Antimicrobial Tannic Acid-Functionalized Ti-Metallic Glass Ribbons for Dental Abutment.

In this study, a recently reported Ti-based metallic glass (MG), without any toxic element, but with a significant amount of metalloid (Si-Ge-B, 18 atom %) and minor soft element (Sn, 2 atom %), was produced in ribbon form using conventional single-roller melt-spinning. The produced Ti60Zr20Si8Ge7B3Sn2 ribbons were investigated by differential scanning calorimetry and X-ray diffraction to confirm their amorphous structure, and their corrosion properties were further investigated by open-circuit potential and cyclic polarization tests. The ribbon's surface was functionalized by tannic acid, a natural plant-based polyphenol, to enhance its performance in terms of corrosion prevention and antimicrobial efficacy. These properties can potentially be exploited in the premucosal parts of dental implants (abutments). The Folin and Ciocalteu test was used for the quantification of tannic acid (TA) grafted on the ribbon surface and of its redox activity. Fluorescent microscopy and ζ-potential measurements were used to confirm the presence of TA on the surfaces of the ribbons. The cytocompatibility evaluation (indirect and direct) of TA-functionalized Ti60Zr20Si8Ge7B3Sn2 MG ribbons toward primary human gingival fibroblast demonstrated that no significant differences in cell viability were detected between the functionalized and as-produced (control) MG ribbons. Finally, the antibacterial investigation of TA-functionalized samples against Staphylococcus aureus demonstrated the specimens' antimicrobial properties, shown by scanning electron microscopy images after 24 h, presenting a few single colonies remaining on their surfaces. The thickness of bacterial aggregations (biofilm-like) that were formed on the surface of the as-produced samples reduced from 3.5 to 1.5 µm.

Selective Tumor Hypoxia Targeting Using M75 Antibody Conjugated Photothermally Active MoOx Nanoparticles.

Photothermal therapy (PTT) mediated at the nanoscale has a unique advantage over currently used cancer treatments, by being spatially highly specific and minimally invasive. Although PTT combats traditional tumor treatment approaches, its clinical implementation has not yet been successful. The reasons for its disadvantage include an insufficient treatment efficiency or low tumor accumulation. Here, we present a promising new PTT platform combining a recently emerged two-dimensional (2D) inorganic nanomaterial, MoOx, and a tumor hypoxia targeting element, the monoclonal antibody M75. M75 specifically binds to carbonic anhydrase IX (CAIX), a hypoxia marker associated with many solid tumors with a poor prognosis. The as-prepared nanoconjugates showed highly specific binding to cancer cells expressing CAIX while being able to produce significant photothermal yield after irradiation with near-IR wavelengths. Small aminophosphonic acid linkers were recognized to be more effective over the combination of poly(ethylene glycol) chain and biotin-avidin-biotin bridge in constructing a PTT platform with high tumor-binding efficacy. The in vitro cellular uptake of nanoconjugates was visualized by high-resolution fluorescence microscopy and label-free live cell confocal Raman microscopy. The key to effective cancer treatment may be the synergistic employment of active targeting and noninvasive, tumor-selective therapeutic approaches, such as nanoscale-mediated PTT. The use of active targeting can streamline nanoparticle delivery increasing photothermal yield and therapeutic success.

Preparation and properties of novel binary and ternary highly amorphous poly(vinyl alcohol)-based composites with hybrid nanofillers.

Smart protective coatings and devices are currently of great interest. In particular, they can absorb or reflect harmful waves of electromagnetic interference (EMI). In this work, novel binary and ternary composites with highly amorphous poly(vinyl alcohol) (HAVOH) as a matrix and single-walled carbon nanotubes (SWCNTs) and MXenes as nanofillers were prepared. HAVOH is a recently patented kind of poly(vinyl alcohol) (PVOH) that was modified with diol monomers. MXenes are a new type of inorganic two-dimensional (2D) nanoparticle consisting of carbides, nitrides and carbonitrides. Three series of composites, HAVOH/SWCNTs, HAVOH/MXenes and HAVOH/SWCNTs/MXenes, were prepared using the solvent casting method. Samples were tested with various methods to study their structure, electrical properties, thermal behavior and EMI-shielding properties. HAVOH/3.0 wt.% SWCNTs/3.0 wt.% MXene specimens revealed a shielding effectiveness of 55 dB, which is 122 times better than that of the neat matrix. These results are promising for the fabrication of films with protective effects against EMI.

Insight into the Li-Storage Property of Surface-Modified Ti2Nb10O29 Anode Material for High-Rate Application.

Ti-based anode materials are considered to be an alternative to graphite anodes to accomplish high-rate application requirements. Ti2Nb10O29 (TNO15) has attracted much attention due to its high lithium storage capacity through the utilization of multiple redox couples and a suitable operating voltage window of 1.0 to 2.0 V vs Li/Li+. However, poor intrinsic electronic conductivity has limited the futuristic applicability of this material to the battery anode. In this work, we report the modification of TNO15 by introducing oxygen vacancies and using few-layered carbon and copper coatings on the surface to improve its Li+ storage property. With the support of the galvanostatic intermittent titration technique (GITT), we found that the diffusion coefficient of carbon/copper coated TNO15 is 2 orders of magnitude higher than that of the uncoated sample. Here, highly conductive copper metal on the surface of the carbon-coated oxygen-vacancy-incorporated TNO15 increases the overall electronic and ionic conductivity. The prepared TNO15-800-C-Cu-700 half-cell shows a significant rate capability of 92% when there is a 10-fold increase in the current density. In addition, the interconnected TNO15 nanoparticles create a porous microsphere structure, which enables better Li-ion transportation during charge/discharge process, and experiences an enhancement after the carbon and copper coating on the surface of the primary TNO15 nanocrystallites.

Morphological, Mechanical and Gas Penetration Properties of Elastomer Composites with Hybrid Fillers.

Ethylene-propylene-diene monomer (EPDM)-based composites including four different types of graphene nanoplatelets (GnPs) were prepared to evaluate the size effects of GnPs in terms of both specific surface area and lateral size on the morphological, mechanical, and viscoelastic properties, swelling ratio, crosslink density, and oxygen permeability. EPDM-based hybrid composites with GnPs and carbon black (CB) fillers were prepared, with the concentrations of 20 and 50 phr of CB and GnPs up to 7 phr. All samples were prepared using the melt mixing method, followed by compression molding. The specific surface area of GnPs is a more important key factor for mechanical and viscoelastic properties than its lateral size. The presence of GnPs leads to a decrease in the swelling ratio and oxygen permeability of the matrix while an increase in the crosslinking density. For a given specific surface area of GnPs (170 m2/g) and the same thickness (5 nm), the optimum lateral size for mechanical properties, swelling ratio, and crosslinking density is about 30 µm. There is a distinct synergic effect on the mentioned properties when hybrid fillers are used. For hybrid composites, the optimum total and each filler concentration are found to be important for achieving the best performance in terms of mechanical properties, swelling ratio, and crosslink density.

Nanofriction Properties of Mono- and Double-Layer Ti3C2Tx MXenes.

Unique structure and ability to control the surface termination groups of MXenes make these materials extremely promising for solid lubrication applications. Due to the challenging delamination process, the tribological properties of two-dimensional MXenes particles have been mostly investigated as additive components in the solvents working in the macrosystem, while the understanding of the nanotribological properties of mono- and few-layer MXenes is still limited. Here, we investigate the nanotribological properties of mono- and double-layer Ti3C2Tx MXenes deposited by the Langmuir-Schaefer technique on SiO2/Si substrates. The friction of all of the samples demonstrated superior lubrication properties with respect to SiO2 substrate, while the friction force of the monolayers was found to be slightly higher compared to double- and three-layer flakes, which demonstrated similar friction. The coefficient of friction was estimated to be 0.087 ± 0.002 and 0.082 ± 0.003 for mono- and double-layer flakes, respectively. The viscous regime was suggested as the dominant friction mechanism at high scanning velocities, while the meniscus forces affected by contamination of the MXenes surface were proposed to control the friction at low sliding velocities.

Wettability of MXene films.

HYPOTHESIS: One of the highlighted properties of Ti3C2Tx MXene compared to other 2D nanomaterials is its hydrophilicity. However, the broad range of static contact angles of Ti3C2Tx reported in the literature is misleading. To elucidate the experimental values of the static contact angles and get reproducible contact angle data, it is wiser to perform the advancing and receding contact angle measurements on smooth and compact Ti3C2Tx layers and focus on deep understanding of the physical basis behind the wettability, which is provided by contact angle hysteresis. EXPERIMENTS: Measurements of the advancing and receding contact angle on mono-, bi, and trilayer Ti3C2Tx on two different substrates were performed. As substrates, UV-ozone treated silicon wafer and silicon wafer functionalized by (3-aminopropyl)triethoxysilane, were used. FINDINGS: The values of the advancing contact angle on Ti3C2Tx on both substrates were proved to be independent of the number of Ti3C2Tx layers, demonstrating a negligible effect of the background substrate wettability. In addition, a giant contact angle hysteresis (44-52 °) was observed on very smooth surface, most likely as a result of chemical heterogeneity arising from the diversity of surface terminal groups (F, O, and OH). The findings reported in this study provide a comprehensive understanding of the wettability of MXene.

Electrochemical performance of composite electrodes based on rGO, Mn/Cu metal-organic frameworks, and PANI.

Benzendicarboxylic acid (BDC)-based metal-organic frameworks (MOFs) have been widely utilized in various applications, including supercapacitor electrode materials. Manganese and copper have solid diamond frames formed with BDC linkers among transition metals chosen for MOF formation. They have shown the possibility to enlarge capacitance at different combinations of MOFs and polyaniline (PANI). Herein, reduced graphene oxide (rGO) was used as the matrix to fabricate electrochemical double-layer SCs. PANI and Mn/Cu-MOF's effect on the properties of electrode materials was investigated through electrochemical analysis. As a result, the highest specific capacitance of about 276 F/g at a current density of 0.5 A/g was obtained for rGO/Cu-MOF@PANI composite.

Plastic ingestion by the Wels catfish (Silurus glanis L.): detailed chemical analysis and degradation state evaluation.

Plastic ingestion by various organisms within different trophic levels, including humans, is becoming a serious problem worldwide. Plastic waste samples are often found concentrated in an organism's digestive tract and can be degraded and further translocate to the surrounding tissue or circulatory systems and accumulate in food chains. In the present work, we report a detailed chemical analysis and degradation state evaluation of a relatively large piece of plastic waste found in the gastrointestinal tract of a Wels catfish (Silurus glanis L.) caught in the Bodrog River (Danube River basin), eastern Slovakia. Chemical analysis by surface-sensitive X-ray photoelectron spectroscopy (XPS) was performed to identify the surface composition of the digested plastic piece. Micro-Fourier transform infrared (µFTIR) spectroscopy showed that the plastic waste was oxidized low-density polyethylene (LDPE), with some nylon fibers adhered on the surface. Glyceraldehyde adhered onto LDPE was also detected, which might come from the carbohydrate metabolism of that fish. A morphology study by digital optical microscopy indicated solid inorganic particles attached to the surface of LDPE. A degradation study by differential scanning calorimetry (DSC) showed considerable oxidation of LDPE, leading to fragmentation and disintegration of the plastic waste material.

Enhancement of Interfacial Hydrogen Interactions with Nanoporous Gold-Containing Metallic Glass.

Contrary to the electrochemical energy storage in Pd nanofilms challenged by diffusion limitations, extensive metal-hydrogen interactions in Pd-based metallic glasses result from their grain-free structure and presence of free volume. This contribution investigates the kinetics of hydrogen-metal interactions in gold-containing Pd-based metallic glass (MG) and crystalline Pd nanofilms for two different pore architectures and nonporous substrates. Fully amorphous MGs obtained by physical vapor deposition (PVD) co-sputtering are electrochemically hydrogenated by chronoamperometry. High-resolution (scanning) transmission electron microscopy and corresponding energy-dispersive X-ray analysis after hydrogenation corroborate the existence of several nanometer-sized crystals homogeneously dispersed throughout the matrix. These nanocrystals are induced by PdHx formation, which was confirmed by depth-resolved X-ray photoelectron spectroscopy, indicating an oxide-free inner layer of the nanofilm. With a larger pore diameter and spacing in the substrate (Pore40), the MG attains a frequency-independent impedance at low frequencies (∼500 Hz) with very high Bode magnitude stability accounting for enhanced ionic diffusion. On the contrary, on a substrate with a smaller pore diameter and spacing (Pore25), the MG shows a larger low-frequency (0.1 Hz) capacitance, linked to enhanced ionic transfer in the near-DC region. Hence, the nanoporosity of amorphous and crystalline metallic materials can be systematically adjusted depending on AC- and DC-type applications.

Discharge Plasma Treatment as an Efficient Tool for Improved Poly(lactide) Adhesive-Wood Interactions.

Poly(lactide) (PLA) films obtained by thermoforming or solution-casting were modified by diffuse coplanar surface barrier discharge plasma (300 W and 60 s). PLA films were used as hot-melt adhesive in joints in oak wood. It was demonstrated that lap shear strength increased from 3.4 to 8.2 MPa, respectively, for the untreated and plasma-treated series. Pull-off tests performed on particleboard for the untreated and treated PLA films showed 100% cohesive failure. Pull-off strength tests on solid oak demonstrated adhesion enhancement from 3.3 MPa with the adhesion failure mode to 6.6 MPa with the cohesion failure mode for untreated and treated PLA. XPS revealed that carbonyl oxygen content increased by two-to-three-fold, which was confirmed in the Fourier-transform infrared spectroscopy experiments of the treated PLA. The water contact angle decreased from 66.4° for the pristine PLA to 49.8° after treatment. Subsequently, the surface free energy increased from 47.9 to 61.05 mJ/m2. Thus, it was clearly proven that discharge air plasma can be an efficient tool to change surface properties and to strengthen adhesive interactions between PLA and woody substrates.

Targeting of carbonic anhydrase IX-positive cancer cells by glycine-coated superparamagnetic nanoparticles.

Antibody-modified magnetic nanoparticles were prepared to study their cellular uptake in 3D multicellular spheroidal cell cultures. For this purpose, carbonic anhydrase IX specific monoclonal antibody VII/20 was selected to conjugate on the surface of positively charged glycine coated magnetic nanoparticles in a form of a stable magnetic fluid. In this work, glycine-functionalized magnetic nanoparticles were characterized by different methods. X-ray photoelectron analysis confirmed the binding of glycine to the magnetic nanoparticles, and quantification of the glycine coating on the surface of the magnetic nanoparticles was conducted by thermogravimetric analysis. The optimal weight ratio of glycine to magnetic nanoparticles was determined to be 5 showing good colloid stability due to the high surface charge density of protonated glycine coating shown by the great zeta potential (⁓40 mV). The antibody conjugation to the functionalized magnetic nanoparticles was performed at an antibody to magnetic nanoparticles weight ratio equal to 0.5. Applications of antibody-modified magnetic nanoparticles in cancer therapy rely on their ability to specifically target cancer tissues and enter the tumour intracellular space. Here, we show that antibody coupled nanoparticle internalization was triggered by selective binding to tumour cells expressing hypoxic marker carbonic anhydrase IX. Moreover, our results confirmed specific penetration of conjugated nanoparticles into the tumour cell spheroids.

Origin of Electrocatalytic Activity in Amorphous Nickel-Metalloid Electrodeposits.

In transition metal-based alloys, the nonlinearity of the current at large cathodic potentials reduces the credibility of the linear Tafel slopes for the evaluation of electrocatalytic hydrogen activity. High-precision nonlinear fitting at low current densities describing the kinetics of electrochemical reactions due to charge transfer can overcome this challenge. To show its effectiveness, we introduce a glassy alloy with a highly asymmetric energy barrier: amorphous NiP electrocoatings (with different C and O inclusions) via changing the applied DC and pulsed current and NaH2PO2 content. The highest hydrogen evolution reaction (HER) activity with the lowest cathodic transfer coefficient α = 0.130 with high J0 = -1.07 mA cm-2 and the largest surface areas without any porosity are observed for the pulsed current deposition. The calculated α has a direct relation with morphology, composition, chemical state and coating thickness defined by the electrodeposition conditions. Here, a general evaluation criterion with practicality in assessment and high accuracy for electrocatalytic reactions applicable to different metallic alloy systems is presented.

On the extraction of MoO x photothermally active nanoparticles by gel filtration from a byproduct of few-layer MoS2 exfoliation.

Gel filtration is a versatile technique employed for biological molecules and nanoparticles, offering their reproducible classification based on size and shape. Colloidal nanoparticles are of significant interest in biomedical applications due to a large number of solution-based bioconjugation procedures. Nevertheless, the inherent polydispersity of the nanoparticles produced by various techniques necessitates the employment of high yield separation and purification techniques. Here we demonstrate the employment of gel filtration on non-stoichiometric plasmonic MoO x nanoparticles, prepared by an oxidation process during liquid-phase exfoliation of few-layer MoS2 nanosheets. This resulted in the separation of two types of MoO x particles, in the form of two different chromatographic fractions. They showed different sizes, morphological and optical properties. The fraction containing smaller particles with diameters of 1-4 nm, exhibited an increased absorbance peak in the near IR region and responded with a significant temperature increase to laser irradiation at the wavelength close to the maximal absorption. The fraction with the larger particles from 3 up to 10 nm, showed weak photoluminescence and a preferred orientation upon the deposition on a planar substrate. However, it had no absorbance in the near IR compared to the former fraction. According to our knowledge, this is the first time that the gel filtration was applied to the separation of molybdenum oxide nanomaterials. This step ensured the isolation of plasmonic MoO x nanoparticles suitable for further bioconjugation and target photothermal treatment.

Selected Electrochemical Properties of 4,4'-((1E,1'E)-((1,2,4-Thiadiazole-3,5-diyl)bis(azaneylylidene))bis(methaneylylidene))bis(N,N-di-p-tolylaniline) towards Perovskite Solar Cells with 14.4% Efficiency.

Planar perovskite solar cells were fabricated on F-doped SnO2 (FTO) coated glass substrates, with 4,4'-((1E,1'E)-((1,2,4-thiadiazole-3,5-diyl)bis(azaneylylidene))bis(methaneylylidene))bis(N,N-di-p-tolylaniline) (bTAThDaz) as hole transport material. This imine was synthesized in one step reaction, starting from commercially available and relatively inexpensive reagents. Electrochemical, optical, electrical, thermal and structural studies including thermal images and current-voltage measurements of the full solar cell devices characterize the imine in details. HOMO-LUMO of bTAThDaz were investigated by cyclic voltammetry (CV) and energy-resolved electrochemical impedance spectroscopy (ER-EIS) and were found at -5.19 eV and -2.52 eV (CV) and at -5.5 eV and -2.3 eV (ER-EIS). The imine exhibited 5% weight loss at 156 °C. The electrical behavior and photovoltaic performance of the perovskite solar cell was examined for FTO/TiO2/perovskite/bTAThDaz/Ag device architecture. Constructed devices exhibited good time and air stability together with quite small effect of hysteresis. The observed solar conversion efficiency was 14.4%.

Size effects of graphene nanoplatelets on the properties of high-density polyethylene nanocomposites: morphological, thermal, electrical, and mechanical characterization.

High-density polyethylene (HDPE)-based nanocomposites incorporating three different types of graphene nanoplatelets (GnPs) were fabricated to investigate the size effects of GnPs in terms of both lateral size and thickness on the morphological, thermal, electrical, and mechanical properties. The results show that the inclusion of GnPs enhance the thermal, electrical, and mechanical properties of HDPE-based nanocomposites regardless of GnP size. Nevertheless, the most significant enhancement of the thermal and electrical conductivities and the lowest electrical percolation threshold were achieved with GnPs of a larger lateral size. This could have been attributed to the fact that the GnPs of larger lateral size exhibited a better dispersion in HDPE and formed conductive pathways easily observable in scanning electron microscope (SEM) images. Our results show that the lateral size of GnPs was a more regulating factor for the above-mentioned nanocomposite properties compared to their thickness. For a given lateral size, thinner GnPs showed significantly higher electrical conductivity and a lower percolation threshold than thicker ones. On the other hand, in terms of thermal conductivity, a remarkable amount of enhancement was observed only above a certain filler concentration. The results demonstrate that GnPs with smaller lateral size and larger thickness lead to lower enhancement of the samples' mechanical properties due to poorer dispersion compared to the others. In addition, the size of the GnPs had no considerable effect on the melting and crystallization properties of the HDPE/GnP nanocomposites.

Thermally Treated Graphene Oxide/Polyacrylonitrile Based Electrospun Carbon Nanofiber Precursor.

Graphene oxide (GO) included polyacrylonitrile (PAN) composite electrospun nanofiber webs were fabricated, and thermal oxidation of PAN/GO composite nanofibers were performed at different temperatures (25, 250, 280, and 300 °C) for different time intervals (0, 1 and 3 h.) to investigate the oxidation process of PAN/GO nanofibers. The thermal oxidation process of PAN has a complex mechanism through the cyclization and dehydrogenation steps. For all oxidized samples, Electrochemical impedance spectroscopy (EIS), X-ray photoelectron spectroscopy (XPS) and Fourier Transform Infrared-Attenuated Total Reflectance (FTIR-ATR) Spectroscopic results were comparatively evaluated to investigate the effect of GO addition onto the nanofiber webs. After heat treatment, change in C1s spectra from virgin PAN to oxidized form was detected and sp² carbon is developed. The presence of GO accelerated the oxidation and development of the final structure. At shorter heat treatment time, less oxidized forms are obtained. The cyclization of nitrile pendant groups of PAN forming polyimine type structure is the main reaction occurs during stabilization. In addition to the imine sequences with three to six units long, the presence of polar groups C═O, OH and COOH in the chains facilitates the initiation of the cyclization process through a nucleophilic attack and accelerates the subsequent oxidative ring closure reactions which these newly formed bonds during thermal oxidation and stabilization steps play an essential role on the carbonization process as an intermediate form of PAN based structures.