Publikationen

An attempt has been made to develop a new metallic glass (MG) that combines high hardness with wear resistance. Refractory metallic films of W33Ni32B35 (at.%) have been deposited on stainless steel and Si substrates by dc magnetron sputtering. The alloy films are glassy, have a high crystallization temperature of 873 °C and rank among the very hard metallic materials (∼24 GPa). Importantly, this MG also shows excellent wear resistance, approaching that of standard tribological materials like TiN and hence it represents one of the most wear-resistant known metallic materials. Based on its unique combination of high strength and low elastic modulus, other potential applications are also discussed.

Copper kills bacteria rapidly by a mechanism that is not yet fully resolved. The antibacterial property of copper has raised interest in its use in hospitals, in place of plastic or stainless steel. On the latter surfaces, bacteria can survive for days or even weeks. Copper surfaces could thus provide a powerful accessory measure to curb nosocomial infections. We here investigated the effect of the copper surface structure on the efficiency of contact killing of Escherichia coli, an aspect which so far has received very little attention. It was shown that electroplated copper surfaces killed bacteria more rapidly than either polished copper or native rolled copper. The release of ionic copper was also more rapid from electroplated copper compared to the other materials. Scanning electron microscopy revealed that the bacteria nudged into the grooves between the copper grains of deposited copper. The findings suggest that, in terms of contact killing, more efficient copper surfaces can be engineered.

The focus of this study was to fabricate and investigate the mechanical behavior of porous poly(para-phenylene) (PPP) for potential use as a load-bearing orthopedic biomaterial. PPPs are known to have exceptional mechanical properties due to their aromatic backbone; however, the manufacturing and properties of PPP porous structures have not been previously investigated. Tailored porous structures with either small (150–250 µm) or large (420–500 µm) pore sizes were manufactured using a powder-sintering/salt-leaching technique. Porosities were systematically varied using 50 vol.% to 90 vol.%. Micro-computed tomography (µCT) and scanning electron microscopy (SEM) were used to verify an open-cell structure and investigate pore morphology of the scaffolds. Uniaxial mechanical behavior of solid and porous PPP samples was characterized through tensile and compressive testing. Both modulus and strength decreased with increasing porosity and matched well with foam theory. Porous scaffolds showed a significant decrease in strain-to-failure (< 4%) under tensile loading and experienced linear elasticity, plastic deformation, and densification under compressive loading. Over the size ranges tested, pore size did not significantly influence the mechanical behavior of the scaffolds on a consistent basis. These results are discussed in regards to use of porous PPP for orthopedic applications and a prototype porous interbody fusion cage is presented.

The remarkable ability of some plants and animals to cling strongly to substrates despite relatively weak interfacial bonds has important implications for the development of synthetic adhesives. Here, we examine the origins of large detachment forces using a thin elastomer tape adhered to a glass slide via van der Waals interactions, which serves as a model system for geckos, mussels and ivy. The forces required for peeling of the tape are shown to be a strong function of the angle of peeling, which is a consequence of frictional sliding at the edge of attachment that serves to dissipate energy that would otherwise drive detachment. Experiments and theory demonstrate that proper accounting for frictional sliding leads to an inferred work of adhesion of only approximately 0.5 J m-2 (defined for purely normal separations) for all load orientations. This starkly contrasts with the interface energies inferred using conventional interface fracture models that assume pure sticking behaviour, which are considerably larger and shown to depend not only on the mode-mixity, but also on the magnitude of the mode-I stress intensity factor. The implications for developing frameworks to predict detachment forces in the presence of interface sliding are briefly discussed.

An analytical model is provided for the peeling of a tape from a surface to which it adheres through cohesive tractions. The tape is considered to be a membrane without bending stiffness and is initially attached everywhere to a flat rigid surface. The tape is assumed to deform in plane strain, and finite deformations in the form of elastic strains are accounted for. The cohesive tractions are taken to be uniform when the tape is within a critical interaction distance from the substrate and then to fall immediately to zero once this critical interaction distance is exceeded. When the distance between the tape and the substrate is zero, repulsive and attractive tractions balance to zero; in this segment, sliding of the tape relative to the substrate is forbidden when we pull the tape up somewhere in the middle, though we permit such sliding when the tape is peeled from one end. In the cohesive zone and where the tape is detached, the interaction of the tape with the substrate is frictionless. Results are given for the force to peel a neo-Hookean tape at any angle up to vertical when one end of it is pulled away from the substrate, as well as for scenarios when the tape is lifted somewhere in the middle to form a V shape being pulled away from the substrate.

In recent times, the relevance of an accurate diagnosis of attention-deficit/hyperactivity disorder (ADHD) in adults has been the focus of several studies. No longer considered a pathology exclusive to children and adolescents, and taking into account its social implications, developing enhanced support tools for the current diagnostic procedure becomes a priority. Here we present a method for the objective assessment of ADHD in adults using chirp-evoked, paired auditory late responses (ALRs) combined with a two-dimensional ALR denoising scheme to extract correlates of intracortical inhibition. Our method allows for an effective single-sweep denoising, thus requiring less trials to obtain recognizable physiological features, useful as pointers of cortical impairment. Results allow an optimized diagnosis, reduction of data loss and acquisition time; moreover, they do not account exclusively for critical elements within clinical evaluations, but also allow studying the pathophysiology of the condition by providing objective information regarding impaired cortical functions.

Superparamagnetic iron oxide nanoparticles (SPION) are widely used both clinically and experimentally for diverse in vivo applications, such as contrast enhancement in magnetic resonance imaging, hyperthermia and drug delivery. Biomedical applications require particles to have defined physical and chemical properties, and to be stable in biological media. Despite a suggested low cytotoxic action, adverse reactions of SPION in concentrations relevant for biomedical use have not yet been studied in sufficient detail. In the present work we employed Endorem®, dextran-stabilized SPION approved as an intravenous contrast agent, and compared its action to a set of other nanoparticles with potential for magnetic resonance imaging applications. SPION in concentrations relevant for in vivo applications were rapidly taken up by endothelial cells and exhibited no direct cytotoxicity. Electric cell impedance sensing measurements demonstrated that SPION, but not BaSO4/Gd nanoparticles, impaired endothelial integrity, as was confirmed by increased intercellular gap formation in endothelial monolayers. These structural changes induced the subcellular translocation and inhibition of the cytoprotective and anti-atherosclerotic enzyme endothelial NO-synthase and reduced NO production. Lipopolysaccharide-induced inflammatory NO production of macrophages was not affected by SPION. In conclusion, our data suggest that SPION might substantially alter endothelial integrity and function at therapeutically relevant doses, which are not cytotoxic.

Endotoxin contaminations of engineered nanomaterials can be responsible for observed biological responses, especially for misleading results in in vitro test systems, as well as in vivo studies. Therefore, endotoxin testing of nanomaterials is necessary to benchmark their influence on cells. Here, we tested the traditional Limulus amebocyte lysate gel clot assay for the detection of endotoxins in nanoparticle suspensions with a focus on possible interference of the particles with the test system. We systematically investigated the effects of nanomaterials made of, or covered by, the same material. Different types of bare or PEGylated silica nanoparticles, as well as iron oxide-silica core shell nanoparticles, were tested. Detailed inhibition/enhancement controls revealed enhanced activity in the Limulus coagulation cascade for all particles with bare silica surface. In comparison, PEGylation led to a lower degree of enhancement. These results indicate that the protein-particle interactions are the basis for the observed inhibition and enhancement effects. The enhancement activity of a particle type was positively related to the calculated particle surface area. For most silica particles tested, a dilution of the sample within the maximum valid dilution was sufficient to overcome non-valid enhancement, enabling semi-quantification of the endotoxin contamination.

Investigating the safety of nanoparticles is essential for many fields of their applications, in particular for consumer products, food and medicines. The conventional dye and fluorescence-based cytotoxicity assays are limited by the interference of such readouts with nanomaterials. This holds in particular when nanomaterials have been fluorescently labelled for other purposes, for example, confocal microscopy. Moreover, most of these assays are invasive, that is, typically involve irreversible changes or destruction of cells and hence only allowing one endpoint measurement. Therefore, a non-invasive method for the detection of cytotoxicity was developed which is based on the automated online monitoring of the oxygen concentration in solution (SensorDish® Reader). Fluorescently labelled silica nanoparticles with different sizes and surface modifications were used as model systems to explore this novel assay. Thereby, the SensorDish® Reader allows a life documentation of the cellular behaviour and clarifies that size, time, concentration and surface modification of nanoparticles affect cellular viability.

The supermolecular morphology of injection-molded SiO2/polypropylene (PP) nanocomposites was investigated via thin sections analyzed under polarized light and the systematic development of an appropriate etching technique, which allowed the study of the supermolecular morphologies with light microscopy (LM) and high-resolution field emission scanning electron microscopy (FESEM). In parallel, information regarding the dispersion, distribution state, and morphology of SiO2 particles was investigated via transmission electron microscopy (TEM) and scanning electron microscopy (SEM) of the ion-polished and fractured surfaces of SiO2-filled PP. The TEM/SEM results demonstrated an almost homogeneous dispersion and distribution of SiO2 particle agglomerates in the PP matrix. With polarized transmitting LM, reflecting LM, and FESEM, the spherulitic structure of the nanocomposites could be visualized to obtain information on the nanoparticle influence on the crystallization and structural behavior. The size and size distribution of the spherulites analyzed with transmitting light (thin sections) and reflecting light (etched specimens) showed an excellent correlation. With increasing filler loading, the mean size of the spherulites decrease as did the degree of crystallinity. This was a clear indication that the particles acted as nucleation agents and, on the other hand, hindered the arrangement of the molecules during the crystallization. As a result, the particles were most likely located in three areas: the center of the spherulites, the areas between the highly crystalline branches, and the spherulite boundaries.