Selectively Promoting or Preventing Osteoblast Growth on Titanium Functionalized with Polyelectrolyte Multilayers

Titanium plays an important role in medical applications, such as hip joint implants or fixation plates. These implants must perform differently depending on their clinical application. In particular, the osseointegrative properties required of the implant vary with clinical application. The present work is aimed at the functionalization of titanium surface using polyelectrolyte multilayers consisting of natural biopolymers and testing their cell adhesive properties with respect to the osseointegration capacity. Multilayered coatings were created from chitosan (Chi), hyaluronic acid (HA), and gelatine (Gel) through layer‐by‐layer deposition. Cell adhesion, proliferation, and viability were tested in vitro with the human osteoblast cell line CAL‐72 at timescales up to 7 d. Two multilayer coatings consisting of alternated chitosan/gelatin or chitosan/hyaluronic acid layers with the outmost layer of gelatin (Chi/Gel) or hyaluronic acid (Chi/HA), respectively, were tested. The experimental results showed that surfaces functionalized with Chi/Gel and Chi/HA multilayers demonstrated a good initial adhesion of osteoblasts. After 4 d culturing, osteoblast cells were almost completely detached from the substrates functionalized with Chi/HA multilayers. In contrast to Chi/HA, the proliferation of osteoblasts on substrates with Chi/Gel multilayer coatings was statistically significantly higher compared to the control titanium. We have shown that the growth of osteoblasts can be enhanced or completely prevented on a titanium surface functionalized with polyelectrolyte multilayers consisting of natural biopolymers, as desired. Both multilayer coatings, Chi/Gel and Chi/HA, have potential for applications in the field of titanium implants, where rapid osseointegration is essential, and/or where no ingrowth of the implant is desired, respectively.     

Controlling single-molecule conductance through lateral coupling of π orbitals

In recent years, various single-molecule electronic components have been demonstrated. However, it remains difficult to predict accurately the conductance of a single molecule and to control the lateral coupling between the π orbitals of the molecule and the orbitals of the electrodes attached to it. This lateral coupling is well known to cause broadening and shifting of the energy levels of the molecule; this, in turn, is expected to greatly modify the conductance of an electrode-molecule-electrode junction. Here, we demonstrate a new method, based on lateral coupling, to mechanically and reversibly control the conductance of a single-molecule junction by mechanically modulating the angle between a single pentaphenylene molecule bridged between two metal electrodes. Changing the angle of the molecule from a highly tilted state to an orientation nearly perpendicular to the electrodes changes the conductance by an order of magnitude, which is in qualitative agreement with theoretical models of molecular π-orbital coupling to a metal electrode. The lateral coupling is also directly measured by applying a fast mechanical perturbation in the horizontal plane, thus ruling out changes in the contact geometry or molecular conformation as the source for the conductance change.     

Self-standing crystalline TiO2 nanotubes/CNTs heterojunction membrane: synthesis and characterization

In the present study, we report for the first time synthesis of TiO(2) nanotubes/CNTs heterojunction membrane. Chemical vapor deposition (CVD) of CNTs at 650 °C in a mixture of H(2)/He atmosphere led to in situ detachment of the anodically fabricated TiO(2) nanotube layers from the Ti substrate underneath. Morphological and structural evolution of TiO(2) nanotubes after CNTs deposition were investigated by field- emission scanning electron microscopy (FESEM), glancing angle X-ray diffraction (GAXRD), and X-ray photoelectron spectroscopy (XPS) analyses.     

The oxygen evolution reaction on platinum,iridium, ruthenium and their alloys at 80°C in acid solutions

Kinetic parametes were determined for the oxygen evolution reaction on 50–50 atom percent alloys of RuIr, RuPt, and IrPt and compared with results obtained using ruthenium, iridium, platinum, and RuO₂/TiO₂ electrodes. The potentiostatic studies were made on oxide covered electrodes at 80°C in both 1.0 M H₂SO₄ and 1.0 M CF₃SO₃H. Cyclic voltammetric studies showed that while these noble metals and alloys are about equally effective as electrocatalysts for the hydrogen evolution reaction, striking differences in activity are found for the oxygen evolution reaction. The order of electrocatalytic activity towards oxygen evolution in H₂SO₄ is Ru > RuIr alloy ～ RuO₂/TiO₂ ～ Ir > IrPt alloy > RuPt alloy > Pt. The type of acid used had very little effect on the kinetic parameters. The lower electrocatalytic activities when platinum is present is probably due to the formation of a platinum oxide film. The dual barrier model is used to interpret the results for the electrodes containing platinum. The best electrocatalysts for oxygen evolution in acid solutions consist of noble metals which form oxide films (RuO₂, IrO₂) possessing metallic characteristics.     

Zur kontinuierlichen kontrolle der viskositätszahl bei der herstellung von polymeren auf schneckenmaschinen

In polymer production inherent viscosity as a characteristic key of product quality should be as uniform as possible. For many polymers exists a close connection between inherent viscosity and melt viscosity. For the case of producing polymers in extruder reactors and putting them out through a nozzle, a linear relationship is developed between the inherent viscosity on the one side and the temperature and the pressure of the mass before the nozzle, the hourly throughput and the temperature of the nozzle on the other side. A simple physical model supports this relationship which is useful for control purposes and which obviates the installation of process viscosimeters.     

Polarized FTIR photoacoustic spectroscopy on blends of thermoplastic poly(ether‐urethanes) with modified polypropylenes

Polarized Fourier transform infrared (FTIR) transmission and attenuated total reflection (ATR) spectroscopy are well‐known powerful tools to determine the orientation function of polymer materials. Both methods demand a special sample preparation. In our present studies, we used polarized FTIR photoacoustic spectroscopy (PAS) to determine the orientation function of real products from polymer processing without special preparation. We compare the results with those obtained with polarized FTIR transmission spectroscopy. It is demonstrated that polarized FTIR–PAS is useful to describe differences in the orientational behavior of hard and soft segments of thermoplastic poly(ether‐urethane) in different elongated blends with common polypropylene and polypropylene grafted with maleic anhydride. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 75: 1194–1204, 2000     

Polychalcones Based on Carbazole-derived Building Blocks: Synthesis by Acetylative Polycondensation

A new carbazole-based soluble polychalcone, poly(9-dodecyl-6-acryloylcarbazole-3,β-diyl), has been synthesized by acetylation of 3-formyl-9-dodecyl-carbazole followed by in situ polycondensation of the acetylated intermediate; it has been characterized by means of nuclear magnetic resonance spectroscopy. The acetylative polycondensation of N-substituted 3-formyl-carbazoles has been shown to provide a promising approach to the synthesis of low band gap polymers via acid-induced quaternization of the nitrogen atoms in the carb-azole moieties of the resulting polychalcone to form a conjugated azoquinoid structure. © of SCI.