Direct growth of sub-micron diamond structures

Abstract

By employing optical and electron beam lithography, micrometer and sub-micrometer wide polymer structures were fabricated on a diamond nano-particle layer. After selective removal of the diamond nano-particles (seeds) in the buffer oxide etchant, all samples were exposed to microwave plasma-assisted chemical vapor deposition. Well-defined diamond channels (in widths from 5 μm down to 250 nm) were realized. The advantages and limitations of the wet treatment process and the lithographical polymer application as a masking material are discussed in this study.     

The carbonization of thin polyaniline films

Polyaniline films on silicon and ceramic supports were prepared in situ during the oxidative polymerization of aniline. The films were heated up to 500 °C in an inert nitrogen atmosphere. The changes in molecular structure during the carbonization have been studied by infrared spectroscopy and Raman scattering using 514, 633 and 785 nm laser excitation lines. The transformation from polyaniline salt to the base form has been detected above 100 °C. The conversion to nitrogen-containing carbon-like material followed above 200 °C. The molecular structure of the films produced during heating to 500 °C contains crosslinked phenazine-like and oxidized quinonoid units. The aniline oligomers deposited on the support in the early stages of aniline oxidation are stable during heating as it has been observed by resonance Raman scattering using 785 nm laser excitation line. The water contact angles changed after carbonization, and the films became more hydrophilic as carbonization progressed.     

Poly(2-oxazoline) hydrogels by photoinduced thiol-ene “click” reaction using different dithiol crosslinkers

Fabrication of a library of biocompatible hydrogels by photoinduced thiol-ene “click” reaction is described. The hydrogels are based on two different statistical copolymers consisting of 2-butenyl-2-oxazoline (EnOx) with either 2-methyl-2-oxazoline (MeOx) or 2-ethyl-2-oxazoline (EtOx). Crosslinking is achieved via pendant vinyl groups of EnOx in the copolymers with selected dithiol crosslinkers, namely dithiothreitol, 1,3-propanedithiol, 1,6-hexanedithiol, and 1,9-nonanedithiol by thiol-ene photocoupling. On the basis of different polarity and flexibility of particular dithiols and three different molar ratios to double bonds, it is possible to control swelling and mechanical characteristics of resulting hydrogels. Biocompatibility of all hydrogel types is verified by determination of toxicity of hydrogel extracts and contact direct toxicity towards mice 3T3 fibroblast cell line. The resulting low toxicity of all prepared hydrogels predetermines its utilization in biomedicine.     

The interaction of thin polyaniline films with various H‐phosphonates: Spectroscopy and quantum chemical calculations

The conducting form of polyaniline (PANI) is formed by doping of non‐conducting PANI base usually by protonic acids. An alternative way of doping, consisting in an interaction via hydrogen bonding, has been previously proven for H‐phosphonates. In this study, PANI base films are exposed to various H‐phosphonates, changes in the structure of the films are analyzed by ultraviolet–visible, infrared, and Raman spectroscopies and spectroscopic data are compared with quantum chemical calculations. According to our results, the interaction of the PANI base films with H‐phosphonates is realized by hydrogen bonding between the imine nitrogen of PANI and the hydroxy group of the H‐phosphonate tautomeric form, i.e., phosphite. This is in the contrast to the PANI powders doped with H‐phosphonates where both interacting phosphite and non‐interacting H‐phosphonate forms were observed. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46728.     

Performance of a Retrofitted Medieval Stone Bridge under a Severe Flood

The very long absence of floods with a return period of more than about 100 years in the Vltava river basin dulled the vigilance of the state administration and self-government bodies. Flood safety measures were mostly related to once-in-a-hundred-years floods. When planning the engineering works before major repairs to the medieval Stone Bridge in Písek in the 1990s, an unpleasant but justified question was raised—what would happen to the Stone Bridge if an extremely powerful 500-year return period flood were to occur? The following case study deals with this question and provides a definitive answer to it. Works were carried out on the Stone Bridge, which was just a few years later exposed to the catastrophic flood that occurred in Bohemia in 2002.     

Alkyl Xylosides: Physico‐Chemical Properties and Influence on Environmental Bacteria Cells

A group of four selected non‐ionic surfactants based on carbohydrates, namely octyl d ‐xyloside (C₈X), nonyl d ‐xyloside (C₉X), decyl d ‐xyloside (C₁₀X) and dodecyl d ‐xyloside (C₁₂X), have been investigated to accomplish a better understanding of their physico‐chemical properties as well as biological activities. The surface‐active properties, such as critical micelle concentration (CMC), emulsion and foam stability, the impact of the compounds on cell surface hydrophobicity and cell membrane permeability together with their toxicity on the selected bacterial strains have been determined as well. The studied group of surfactants showed high surface‐active properties allowing a decrease in the surface tension to values below 25 mN m^?1 for dodecyl d ‐xyloside at the CMC. The investigated compounds did not have any toxic influence on two Pseudomonas bacterial strains at concentrations below 25 mg L^?1. The studied long‐chain alkyl xylosides influenced both the cell inner membrane permeability and the cell surface hydrophobicity. Furthermore, the alkyl chain length, as well as the surfactant concentration, had a significant impact on the modifications of the cell surface properties. The tested non‐ionic surfactants exhibited strong surface‐active properties accompanied by the significant influence on growth and properties of Pseudomonas bacteria cells.     

In-house validation of an ELISA method for screening of semicarbazide in eggs

An enzyme-linked immunosorbent assay (ELISA) method is described for the semi-quantitative determination of semicarbazide (SEM), the marker residue for the banned nitrofuran drug, nitrofurazone, in chicken eggs. The sample homogenate is subjected to acid hydrolysis and derivatisation with o-nitrobenzaldehyde, followed by ethyl acetate/hexane extraction and detection by ELISA. The ELISA procedure has been validated using 0.3, 1.0 and 3 microg kg(-1) of SEM in fortified samples. Detection capability (CC(ss)) was based on the acceptance of 5% false compliant results for a given concentration level according to Commission Decision 2002/657/EC and was determined to be 0.3 microg kg(-1) with a respective limit of detection of 0.13 microg kg(-1). A validated LC-MS/MS method was used for the analysis of incurred egg samples and the results compared with ELISA. A good correlation between the results obtained from ELISA and LC-MS/MS within the concentration range 0.12-20.3 microg kg(-1) was observed in samples collected from chickens fed with a medicated ration of nitrofurazone (r = 0.992, n = 14). Validated ELISA enabled reliable monitoring of SEM levels in eggs collected from incurred chickens over a 90-day period.     

Effect of 1-Ethyl-3-methylimidazolium Tetrafluoroborate and Acetate Ionic Liquids on Stability and Amyloid Aggregation of Lysozyme

Amyloid fibrils draw attention as potential novel biomaterials due to their high stability, strength, elasticity or resistance against degradation. Therefore, the controlled and fast fibrillization process is of great interest, which raises the demand for effective tools capable of regulating amyloid fibrillization. Ionic liquids (ILs) were identified as effective modulators of amyloid aggregation. The present work is focused on the study of the effect of 1-ethyl-3-methyl imidazolium-based ILs with kosmotropic anion acetate (EMIM-ac) and chaotropic cation tetrafluoroborate (EMIM-BF₄) on the kinetics of lysozyme amyloid aggregation and morphology of formed fibrils using fluorescence and CD spectroscopy, differential scanning calorimetry, AFM with statistical image analysis and docking calculations. We have found that both ILs decrease the thermal stability of lysozyme and significantly accelerate amyloid fibrillization in a dose-dependent manner at concentrations of 0.5%, 1% and 5% (v/v) in conditions and time-frames when no fibrils are formed in ILs-free solvent. The effect of EMIM-BF₄ is more prominent than EMIM-ac due to the different specific interactions of the anionic part with the protein surface. Although both ILs induced formation of amyloid fibrils with typical needle-like morphology, a higher variability of fibril morphology consisting of a different number of intertwining protofilaments was identified for EMIM-BF_4.