Functionalised Anodised Aluminium Oxide as a Biocidal Agent

In this article, we describe the antimicrobial properties of a new composite based on anodic aluminium oxide (AAO) membranes containing propyl-copper-phosphonate units arranged at a predetermined density inside the AAO channels. The samples were prepared with four concentrations of copper ions and tested as antimicrobial drug on four different strains of Escherichia coli (K12, R2, R3 and R4). For comparison, the same strains were tested with three types of antibiotics using the minimal inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) tests. Moreover, DNA was isolated from the analysed bacteria which was additionally digested with formamidopyrimidine-DNA glycosylase (Fpg) protein from the group of repair glycosases. These enzymes are markers of modified oxidised bases in nucleic acids produced during oxidative stress in cells. Preliminary cellular studies, MIC and MBC tests and digestion with Fpg protein after modification of bacterial DNA suggest that these compounds may have greater potential as antibacterial agents than antibiotics such as ciprofloxacin, bleomycin and cloxacillin. The described composites are highly specific for the analysed model Escherichia coli strains and may be used in the future as new substitutes for commonly used antibiotics in clinical and nosocomial infections in the progressing pandemic era. The results show much stronger antibacterial properties of the functionalised membranes on the action of bacterial membranes in comparison to the antibiotics in the Fpg digestion experiment. This is most likely due to the strong induction of oxidative stress in the cell through the breakdown of the analysed bacterial DNA. We have also observed that the intermolecular distances between the functional units play an important role for the antimicrobial properties of the used material. Hence, we utilised the idea of the 2D solvent to tailor them.     

Regional differences in price levels across the European Union and their implications for its regional policy

Although regional price levels should be accounted for in any analysis of well-being in regions, the European Union fails to reflect them because they are not currently available for most EU member states. To fill this gap, we estimate regional price levels for all EU regions on the basis of available regional price level data from six EU countries. Once socio-economic indicators are recalculated using our estimates, substantially higher differences in living standards emerge. These results also have important implications for the European cohesion policy, with 9% of regions currently misclassified as a consequence of regional price levels not being used.     

Transition between two solid-solutions: Effective and easy way for fine Ce1−xGdxO2−x/2 powders preparation

Ceria, pure or doped, is an important electrolyte material in solid oxide fuel cells, catalysts, and plutonium surrogates. Even though ceria is a widely studied material, its coprecipitation with the most common doping element, gadolinium, remains mostly overlooked. Here, we present a comprehensive study of gadolinium–cerium oxalates prepared by coprecipitation of gadolinium (III) and cerium (III) salts by oxalic acid under different reaction conditions and element ratios. For this purpose, we assessed the effects of basic precipitation conditions on the final oxalate size, shape, and conversion into the corresponding oxides. The results showed that coprecipitation with oxalic acid yields and ideal solid solution, which translates into the oxides. This low-cost and straightforward synthetic route provides then high-quality solid solutions of Ge–Gd in the oxide lattice. Thus, this approach has a high industrialization potential, with significant advantages over hydrolysis or hydrothermal techniques.     

The impact of glycated pea proteins on bacterial adhesion

Adhesion is one of the bacterial strategies indispensable for colonization of the small intestine. Food components reaching the small intestine, are not only digested and absorbed there, but may also influence the microorganisms colonizing the mentioned region. In this way, nutrients, particularly the ones the enzymatic degradation of which is hindered, acquire the ability to modify the adhesive potential of the autochthonic microorganisms. The glycated food proteins are noteworthy here for they often undergo relevant structural and functional alterations. Such proteins tend to display a lowered susceptibility to enzymatic degradation and thus may act as modulators of both metabolic activity and adhesive potential of bacteria adhered to the intestinal cells. For that reason, this study aimed at establishing the impact of the glycated pea proteins on adhesion of the bacteria from the genera: Lactobacillus, Enterococcus, and Escherichia, which are typical for the human small intestine.     

Study on the new bone cement based on calcium sulfate and Mg,CO3 doped hydroxyapatite

In order to improve some features of bone substitutes the new self-setting composite-type implant material based on Mg²⁺/CO₃^2? co-substituted hydroxyapatite (Mg-CHA) and calcium sulfate hemihydrate (CSH) was developed. Synthetic hydroxyapatites doped with small amounts of additives found in natural bone (e.g. Mg²⁺ and CO₃^2?) are regarded as promising components of calcium phosphate bone cements (CPCs). The CPCs, now available on the market, due to low resorption rate are too stable to permit material degradation and are slowly replaced by the newly formed bone. To improve cement resorption we used calcium sulfate which is a well-known biodegradable and biocompatible bone defect filler. Combining properties of Mg-CHA and CSH allowed developing a new, promising, easy shapeable implant material with high potential for bone regeneration.     

Determination of Thermal-Diffusivity Dependence on Temperature of Transparent Samples by Thermal Wave Method

The use of a typical measuring cryostat with a standard temperature controller was proposed for investigation of the temperature dependence of the thermal diffusivity of transparent samples. The basic idea is to use the cryostat heater to control the mean sample temperature and to generate the thermal wave in it, simultaneously. Because of the relatively high thermal inertia of the system, the measurements are carried out at frequencies not exceeding 50 mHz. The periodic temperature disturbance in the sample was detected optically by the use of the mirage effect. The proposed method was used for determination of the thermal diffusivity of yttrium aluminum garnet single crystals in a temperature range from 20 °C to 200 °C.     

Hydrophilic polycarbonate chips for generation of oil-in-water (O/W) and water-in-oil-in-water (W/O/W) emulsions

Modification of the surfaces of polycarbonate (PC) with the use of a solution of tin (II) chloride renders them hydrophilic. The surface draping is stable against exposure to water and to alcohols. Exposure to alkanes reduces but does not diminish the effect. The method is compatible—in using the same solvent and temperature—with the hydrophobic modification of PC (Jankowski et al. in Lab Chip 11:1151–1156, 2011). The combination of these methods makes it possible to generate single and multiple monodisperse emulsions with the use of flow-focusing junctions in systems made in PC—a material that is suitable for fabrication of multilayer, high-throughput microfluidic devices.     

Shaping Luminescent Properties of Yb3+ and Ho3+ Co‐Doped Upconverting Core–Shell β‐NaYF4 Nanoparticles by Dopant Distribution and Spacing

At the core of luminescence color and lifetime tuning of rare earth doped upconverting nanoparticles (UCNPs), is the understanding of the impact of the particle architecture for commonly used sensitizer (S) and activator (A) ions. In this respect, a series of core@shell NaYF₄ UCNPs doped with Yb³⁺ and Ho³⁺ ions are presented here, where the same dopant concentrations are distributed in different particle architectures following the scheme: YbHo core and YbHo@…, …@YbHo, Yb@Ho, Ho@Yb, YbHo@Yb, and Yb@YbHo core–shell NPs. As revealed by quantitative steady‐state and time‐resolved luminescence studies, the relative spatial distribution of the A and S ions in the UCNPs and their protection from surface quenching has a critical impact on their luminescence characteristics. Although the increased amount of Yb³⁺ ions boosts UCNP performance by amplifying the absorption, the Yb³⁺ ions can also efficiently dissipate the energy stored in the material through energy migration to the surface, thereby reducing the overall energy transfer efficiency to the activator ions. The results provide yet another proof that UC phosphor chemistry combined with materials engineering through intentional core@shell structures may help to fine‐tune the luminescence features of UCNPs for their specific future applications in biosensing, bioimaging, photovoltaics, and display technologies.