Functional Properties of Polyurethane Ureteral Stents with PLGA and Papaverine Hydrochloride Coating.

Despite the obvious benefits of using ureteral stents to drain the ureters, there is also a risk of complications from 80-90%. The presence of a foreign body in the human body causes disturbances in its proper functioning. It can lead to biofilm formation on the stent surface, which may favor the development of urinary tract infections or the formation of encrustation, as well as stent fragmentation, complicating its subsequent removal. In this work, the effect of the polymeric coating containing the active substance-papaverine hydrochloride on the functional properties of ureteral stents significant for clinical practice were assessed. Methods: The most commonly clinically used polyurethane ureteral Double-J stent was selected for the study. Using the dip-coating method, the surface of the stent was coated with a poly(D,L-lactide-glycolide) (PLGA) coating containing the papaverine hydrochloride (PAP). In particular, strength properties, retention strength of the stent ends, dynamic frictional force, and the fluoroscopic visibility of the stent during X-ray imaging were determined. Results: The analysis of the test results indicates the usefulness of a biodegradable polymer coating containing the active substance for the modification of the surface of polyurethane ureteral stents. The stents coated with PLGA+PAP coating compared to polyurethane stents are characterized by more favorable strength properties, the smaller value of the dynamic frictional force, without reducing the fluoroscopic visibility.

Toxicity of the Zinc Oxide and Vermiculite/Zinc Oxide Nanomaterials.

Nanomaterials and nanocomposite materials on the base of zinc oxide (ZnO) are being produced and applied in our daily life at a rapid pace mainly as additives to the different polymer materials. The antibacterial behaviors of ZnO nanoparticles are intensively studied but related health and environmental toxicity assessments are lagging behind. The aim of this work was evaluated the toxic effect of self-synthesized samples (ZnO nanoparticles, vermiculite/ZnO nanocomposite) and one commercial sample of the ZnO nanoparticles, to induce oxidative stress via lipid peroxidation. This ability is one of the indicators of material toxicity. The toxicity results were compared with the results of titanium dioxide nanoparticles as a validated toxic standard. The effect of the major nanoparticles properties as particle and crystallite size, shape, specific phase and composition were evaluated using the dynamic laser diffraction, scanning electron microscopy and X-ray diffraction analysis. The attention was also focused on the influence of the vermiculite (as matrix of nanocomposite samples) and temperature of the nanostructured materials preparation. All samples containing vermiculite are not able to induce peroxidation of lipids in comparison to TiO2 nanoparticles. However, samples of ZnO nanoparticles demonstrate the ability to induce oxidative stress via lipid peroxidation, which decreases with the increasing temperature of preparation and for commercial ZnO was higher than for prepared ZnO nanoparticles.

Hybrid Antibacterial Nanocomposites Based on the Vermiculite/Zinc Oxide-Chlorhexidine.

The hybrid nanocomposite materials based on the vermiculite/zinc oxide-chlorhexidine were prepared in two steps. In the first step the vermiculite/zinc oxide nanocomposite was prepared by the mechanochemical method followed by a heat treatment at 650 °C for 90 min. In the second step the chlorhexidine dihydrochloride was intercalated to the vermiculite/zinc oxide nanocomposite in weight ratio 1:1, 1:2, 1:4, 2:1 and 4:1 (wt%) thereby vermiculite/zinc oxide-chlorhexidine nanocomposites were prepared. Phase analysis, crystal structure, phase transformation, chemical composition and particle size of the prepared hybrid nanocomposite materials were using X-ray diffraction methods, energy dispersive X-ray fluorescence spectroscopy, carbon phase analysis, Fourier transforms infrared spectroscopy and particle size analysis. Antibacterial activity of hybrid nanocomposite materials was investigated on Gram negative (E. coli, P. aeruginos.) and the Gram positive (S. aureus, E. faecalis) bacterial strain and against yeast Candida a. by finding the minimum inhibitory concentration. The hybrid nanocomposite materials exhibit high antibacterial activity after 30 minutes with a long-lasting effect persisting up to 5 days. Dependence of the zinc oxide and chlorhexidine concentration in vermiculite structure on the antibacterial activity was observed.

Synthesis and Antimicrobial Activity of Polyethylene/Chlorhexidine/Vermiculite Nanocomposites.

The set of polyethylene/clay nanocomposites with increasing amount of antimicrobial nanofiller (3, 6 and 10 wt%) was prepared by melt compounding procedure. The antimicrobial drug chlorhexidine diacetate was loaded into natural clay mineral vermiculite and also to its monoionic sodium form and then these organoclay nanofillers were incorporated into polymeric matrix. The structure of prepared organoclays and nanocomposites was studied by X-ray diffraction analysis and Fourier transforms infrared spectroscopy. Further thermal properties of polyethylene/clay nanocomposites were investigated by thermogravimetric analysis and the surface roughness was evaluated by atomic force microscopy. Finally, organoclays and polyethylene/clay nanocomposites were tested for antimicrobial activity against bacterial strains Staphylococcus aureus, Escherichia coli and yeast Candida albicans. Prepared samples showed a very good antimicrobial activity with long lasting effect. In the case of polyethylene/clay nanocomposites we observed some differences in antimicrobial action between two used antimicrobial nanofillers. These results suggested great potential of using the polymer/clay nanocomposites in the wide range of antimicrobial applications.

Microstructure and Electrochemical Behavior of TiO2 Nanotubes Coated on Titanium-Based Substrate Before and After Thermal Treatment.

The comparative study of the structure and electrochemical properties of TiO2 layers on the surfaces of commercially pure titanium and Ti6Al4V alloy were performed. The TiO2 surface layers produced by anodization in ethylene glycol-based electrolyte solution using Power Supply MCS-3204 MANSON at 20 V or 40 V for 60 minutes were formed on the titanium substrates by simultaneous surface oxidation and controlled dissolving of oxide film due the fluorine ions. The SEM and X-ray diffraction analyses were performed to determine the properties of the anodized layers before and after heat treatment at 500 °C for 120 minutes. The as-anodized TiO2 nanotubes exhibited an amorphous structure. An anatase phase appeared in annealed nanotube layers of both Ti based substrates. The corrosion behavior in simulated physiological solution was compared for not anodized, anodized and anodized heat treated conditions of both titanium surfaces. The results of the electrochemical measurements corresponded to the microstructure and treatment condition. The porous feature of the anodizing layers on Ti6Al4V substrate led to lower corrosion resistance that increased after the heat treatment.

Investigation of Geometric Properties of Modified Titanium White by Fluidisation for Use in the Process of Transport, Handling, Processing and Storage.

The present article deals with investigation of geometric properties of surface modified titanium white with the help of silica oxide by various methods of shape and size identification of clusters made by processing by fluidisation. For the purpose of the investigation of geometric properties the artificially made titanium oxide (titanium white) was processed by fluidisation with a defined percentage of silica oxide additive. The selected additive was represented by hydrophilic pyrogenic silica (micronised silica oxide), known under commercial name Aerosil 200, Aerosil R972 and hydrophilic pyrogenic metal oxide Aeroxide P25. The investigation began by image acquisition of the individual additives and the titanium white with scanning electron microscope and continued by investigation of clusters created by fluidisation in a vertical fluidisation cell using state-of-the-art methods of particle size identification analysis. The research was oriented toward the area of mutual impact of particles in the titanium white clusters with particles of additives.

Micronization of Ibuprofen Particles Using Supercritical Fluid Technology.

Most of drugs are only slightly soluble in the circulatory system of the human body. This reduces the efficiency of their use and that is why new ways how to increase their solubility are investigated. One way to improve the solubility of the drug is to reduce its particle size. Conventional techniques such as crushing or grinding usually do not guarantee a narrow particle size distribution, which is required for pharmaceuticals. Application of supercritical fluids, especially of supercritical CO2, seems to be convenient method for the preparation of pharmaceuticals submicron particles or nanoparticles. The method enables the preparation of particles in a narrow size distribution and at the same time it does not leave any unwanted residues of solvents or other chemicals. The aim of this work is the micronization of ibuprofen particles using the supercritical fluid and characterization of formed products. The micronization of the particles was done using commercially available device Spe-ed SFE-4 in rapid expansion of supercritical solution mode. The applied temperatures and pressures were 308.15 K and 313.15 K and 200, 250 and 300 bar. The prepared particles were characterized using methods of X-ray diffraction, infrared spectroscopy, particle size distribution, scanning electron microscopy and tests of dissolution and permeability. Mean particles size was reduced from 180 µm (original ibuprofen) to 2.8-7.3 µm of the processed samples. The dissolution test confirmed better solubility and the permeability of newly formed particles improved.

Determination of Oxidative Potential Caused by Brake Wear Debris in Non-Cellular Systems.

Wear debris from automotive brake systems represents a major source of non-exhaust emissions from road traffic and its production increases with number of cars worldwide. However, impact of brake wear debris on the environment and organisms is still not clear. One of the most possible ways by which these particles may affect living organisms is oxidative stress. Production of reactive oxidative species may cause damage of basic cell components, lipids, proteins, etc. Aim of this study is to perform characterization of airborne and nonairborne fractions of brake wear debris generated during standard dynamometer tests and evaluation of its potential to induce oxidative stress via lipid peroxidation and carbonylation of proteins in non-cellular system. Elemental and phase composition were determined by scanning electron microscopy, Raman microspectroscopy, and X-ray powder diffraction analysis. Carbon in amorphous form and graphite, copper, and iron in form of oxides were identified as major components in both studied fractions. Characteristic size of studied wear particles was evaluated by dynamic light scattering. Both airborne and nonairborne samples showed ability to induce oxidative stress which results from determination of carbonylated proteins.

Effects of Foliar Application of ZnO Nanoparticles on Lentil Production, Stress Level and Nutritional Seed Quality under Field Conditions.

Nanotechnology offers new opportunities for the development of novel materials and strategies that improve technology and industry. This applies especially to agriculture, and our previous field studies have indicated that zinc oxide nanoparticles provide promising nano-fertilizer dispersion in sustainable agriculture. However, little is known about the precise ZnO-NP effects on legumes. Herein, 1 mg·L-1 ZnO-NP spray was dispersed on lentil plants to establish the direct NP effects on lentil production, seed nutritional quality, and stress response under field conditions. Although ZnO-NP exposure positively affected yield, thousand-seed weight and the number of pods per plant, there was no statistically significant difference in nutrient and anti-nutrient content in treated and untreated plant seeds. In contrast, the lentil water stress level was affected, and the stress response resulted in statistically significant changes in stomatal conductance, crop water stress index, and plant temperature. Foliar application of low ZnO-NP concentrations therefore proved promising in increasing crop production under field conditions, and this confirms ZnO-NP use as a viable strategy for sustainable agriculture.

Phytosynthesis of Ag, ZnO and ZrO2 Nanoparticles Using Linden: Changes in Their Physical-Chemical Nature Over Time.

Bionanotechnology provides many new methods and protocols in nanomaterial preparation. One of these special new chemical methods is phytosynthesis. The application of biological processes in living organisms such as bacteria, fungi and higher plants contributes to rapid and easy formation of metallic nanoparticles. These nanoparticles present a promising future in heterogeneous catalysis and medicine, and here we focus on phytosynthesis of Ag, ZnO and ZrO2 nanoparticles using leachate from the linden plant. Nanoparticle activity in liquid is an important aspect of their behavior, and we investigated nanoparticles ζ-potential and monitored their particle size by dynamic light scattering during the period of three months. Transmission electron microscopy then determined shape and morphology, with results confirming their spherical shape and average size in tens and hundreds of nanometers. The amount of metals was estimated in tens of mg L-1 and the different nanoparticle sizes obtained by dynamic light scattering and transmission electron microscopy are discussed. The nanoparticles were tested against 4 human pathogens using minimum inhibitory concentration to investigate their antimicrobial potential. Only Ag nanoparticles provided antibacterial properties against Escherichia coli and Pseudomonas aeruginosa; with the remaining nanoparticles having no antibacterial effect on the four tested pathogens. All studied phenomena are related to nanoparticle concentration and their surface charge, and therefore ζ-potential and other physical and chemical properties are important in ascertaining positive and negative aspects of metallic nanoparticles in future applications and related research.