Scientific publications

Frictional heating is common during the dry sliding of polymers against steel, which further makes it complex to understand the friction and wear performance of polymers at high temperature. Towards the goal of addressing the tribological response of polymers to such combined temperatures, the counter steel was heated crossing the glass transition (150 °C) of polyetheretherketone (PEEK), and tribological tests were conducted during temperature ramping or at constant counterbody temperatures. With increasing temperature, different friction responses were revealed depending on the variation manner of temperature (sliding during ramping or at controlled counterbody temperature). Even so, counterbody temperature around PEEK’s glass transition defined a transition, from which distinct friction and wear of PEEK was exhibited. Based on real-time analysis of temperature in the counterbody and PEEK near to the sliding interface, the completion between frictional and external heating is discussed. In combination with worn surface characterization, this also helped understand the mechanisms behind such kind of tribological response to temperatures.

A computationally lean model for the coarse-grained description of contact mechanics of hydrogels is proposed and characterized. It consists of a simple bead-spring model for the interaction within a chain, potentials describing the interaction between monomers and mold or confining walls, and a coarse-grained potential reflecting the solvent-mediated effective repulsion between non-bonded monomers. Moreover, crosslinking only takes place after the polymers have equilibrated in their mold. As such, the model is able to reflect the density, solvent quality, and the mold hydrophobicity that existed during the crosslinking of the polymers. Finally, such produced hydrogels are exposed to sinusoidal indenters. The simulations reveal a wavevector-dependent effective modulus E∗(q) with the following properties: (i) stiffening under mechanical pressure, and a sensitivity of E∗(q) on (ii) the degree of crosslinking at large wavelengths, (iii) the solvent quality, and (iv) the hydrophobicity of the mold in which the polymers were crosslinked. Finally, the simulations provide evidence that the elastic heterogeneity inherent to hydrogels can suffice to pin a compressed hydrogel to a microscopically frictionless wall that is undulated at a mesoscopic length scale. Although the model and simulations of this feasibility study are only two-dimensional, its generalization to three dimensions can be achieved in a straightforward fashion.

Event related potentials (ERPs) represent a noninvasive means for studying sensory and cognitive processes that occur in response to particular stimuli. Here we report on a phase measure for estimating single trial interaction of late somatosensory potentials (LSPs) following a tribological well defined mechanical stimulation of the human fingertip. Stimuli are presented via a programmable Braille-display with actively switchable pins which was slid along the apex of the passive fingertip, i.e., the fingertip rested stationarily in a finger holding system with circular opening at the bottom. The event was the raising and the lowering of either one, three or five lines of pins. Differences were identified by measures based on instantaneous phase synchronization to the stimuli across trials, in particular the wavelet phase synchronization stability (WPSS) measure for single trial sequences of LSPs. In particular, we show that the higher the friction the stronger and more localized the induced phase coherency is. We concluded that the WPSS analysis of single sequences of LSPs represents a reliable method which allows for the quantification of brain responses upon distinct tactile stimuli.

The tribological properties of poly (ether ether ketone) (PEEK) were investigated at different length scales in order to elucidate commonalities and differences in friction and wear. To achieve this goal, the PEEK/steel tribo-system was studied by block-on-ring, block-on-disc, cone-on-disc, and cylinder-on-disc tests as well as by asperity scratching. For better comparability, asperities were prepared from the counter-body steel of the macroscopic experiments. Friction and wear properties were compared on the basis of the pv level. Friction coefficients in macro sliding can be related to the interfacial shear strength in asperity scratching by material's yield pressure. The study confirms that friction and wear of PEEK at different scales can be correlated, despite differences of characteristic velocity and pressure in different experiments.

A model for the contact area of a single asperity sliding in a groove after repeated cycles is presented. Based only on the asperity geometry and on data from friction experiments, the model predicts the area of the asymmetric elliptical contact of the asperity sliding in its own groove. It thus allows to determine the shear stress of the steel–polymer couple in the relevant geometry without need for further microscopy of indenter or groove. The model was validated by experiments with an indenter manufactured from slide bearing steel and polyether-ether ketone (PEEK) as substrate. In experiments of 1000 repeated cycles, the contact area was found to vary with varying load and sliding velocity, while the shear stress was 20.5 MPa at a normal pressure of 50–70 MPa, independent of velocity when friction heating is still negligible. Model and experimental confirmation advance single-asperity friction experiments into an efficient method to extract shear stress and contact area for an understanding of sliding friction in metal-polymer contacts.

Intracellular pH sensing with fluorescent nanoparticles is an emerging topic as pH plays several roles in physiology and pathologic processes. Here, nanoparticle-sized pH sensors (diameter far below 50 nm) for fluorescence imaging have been described. Consequently, a fluorescent derivative of pH-sensitive hydroxypyrene with pKa = 6.1 was synthesized and subsequently embedded in core and core–shell silica nanoparticles via a modified Stöber process. The detailed fluorescence spectroscopic characterization of the produced nanoparticles was carried out for retrieving information about the environment within the nanoparticle core. Several steady-state and time-resolved fluorescence spectroscopic methods hint to the screening of the probe molecule from the solvent, but it sustained interactions with hydrogen bonds similar to that of water. The incorporation of the indicator dye in the water-rich silica matrix neither changes the acidity constant nor dramatically slows down the protonation kinetics. However, cladding by another SiO2 shell leads to the partial substitution of water and decelerating the response of the probe molecule toward pH. The sensor is capable of monitoring pH changes in a physiological range by using ratiometric fluorescence excitation with λex = 405 nm and λex = 488 nm, as confirmed by the confocal fluorescence imaging of intracellular nanoparticle uptake.

The intestinal microvasculature (iMV) plays multiple pathogenic roles during chronic inflammatory bowel disease (IBD). The iMV acts as a second line of defense and is, among other factors, crucial for the innate immunity in the gut. It is also the therapeutic location in IBD targeting aggravated leukocyte adhesion processes involving ICAM-1 and E-selectin. Specific targeting is stressed via nanoparticulate drug vehicles. Evaluating the iMV in enterocyte barrier models in vitro could shed light on inflammation and barrier-integrity processes during IBD. Therefore, we generated a barrier model by combining the enterocyte cell line Caco-2 with the microvascular endothelial cell line ISO-HAS-1 on opposite sides of a transwell filter-membrane under culture conditions which mimicked the physiological and inflamed conditions of IBD. The IBD model achieved a significant barrier-disruption, demonstrated via transepithelial-electrical resistance (TER), permeability-coefficient (Papp) and increase of sICAM sE-selectin and IL-8. In addition, the impact of a prospective model drug-vehicle (silica nanoparticles, aSNP) on ongoing inflammation was examined. A decrease of sICAM/sE-selectin was observed after aSNP-exposure to the inflamed endothelium. These findings correlated with a decreased secretion of ICAM/E-selectin bearing exosomes/microvesicles, as evaluated via ELISA. Our findings indicate that aSNP treatment of the inflamed endothelium during IBD may hamper exosomal/microvesicular systemic communication.

AbstractThe effects of engineered nanomaterials on human health are still intensively studied in order to facilitate their safe application. However, relatively little is known how mechanical strain as induced in alveolar epithelial cells by breathing movements modifies biological responses to nanoparticles (NPs). In this study, A549 cells as a model for alveolar epithelial cells were exposed to 25?nm amorphous colloidal silica NPs under dynamic and static culture conditions. Gene array data, qPCR, and ELISA revealed an amplified effect of NPs when cells were mechanically stretched in order to model the physiological mechanical deformation during breathing. In contrast, treatment of cells with either strain or NPs alone only led to minor changes in gene expression or interleukin-8 (IL-8) secretion. Confocal microscopy revealed that stretching does not lead to an increased internalization of NPs, indicating that elevated intracellular NP accumulation is not responsible for the observed effect. Gene expression alterations induced by combined exposure to NPs and mechanical strain showed a high similarity to those known to be induced by TNF-α. This study suggests that the inclusion of mechanical strain into in vitro models of the human lung may have a strong influence on the test results.

Abstract Due to their importance for the outcome of the inflammatory response, the motile myeloid cells are a focus of novel treatment options. The interplay of selectins and their ligands with leukocytes and endothelial cells, which mediate endothelial attachment and transmigration of immune cells, can be modulated by selectin-binding structures. Here, a library of selectin-targeting ligands coupled to either gold, silver, iron oxide nanospheres, or quantum dots of 5–10 nm in size is used to systematically study their impact on immune cell motility. The multivalent presentation of the carbohydrate mimetics results in very low sub-nanomolar binding to L-selectin. Using human primary monocytes, granulocytes, lymphocytes, and macrophages, it is shown that the ligands exhibit only minor effects on uptake, whereas the motility of leukocytes is critically affected as observed in migration assays evaluated by flow cytometry. The carbohydrate mimetic ring structure, sulfation, in particular, and the degree of ligand presentation, are constituents which cohere in this process. Specific carbohydrate ligands can thus selectively regulate leukocyte subsets. These data form the basis for advanced immunotherapy which inhibits the amplification of inflammation by restricting leukocyte influx to injured tissue sites. Furthermore, the targeting ligands may complement existing treatment options for inflammatory diseases.