Complexes of Silver(I) Ions and Silver Phosphate Nanoparticles with Hyaluronic Acid and/or Chitosan as Promising Antimicrobial Agents for Vascular Grafts

Polymers are currently widely used to replace a variety of natural materials with respect to their favourable physical and chemical properties, and due to their economic advantage. One of the most important branches of application of polymers is the production of different products for medical use. In this case, it is necessary to face a significant disadvantage of polymer products due to possible and very common colonization of the surface by various microorganisms that can pose a potential danger to the patient. One of the possible solutions is to prepare polymer with antibacterial/antimicrobial properties that is resistant to bacterial colonization. The aim of this study was to contribute to the development of antimicrobial polymeric material ideal for covering vascular implants with subsequent use in transplant surgery. Therefore, the complexes of polymeric substances (hyaluronic acid and chitosan) with silver nitrate or silver phosphate nanoparticles were created, and their effects on gram-positive bacterial culture of Staphylococcus aureus were monitored. Stages of formation of complexes of silver nitrate and silver phosphate nanoparticles with polymeric compounds were characterized using electrochemical and spectrophotometric methods. Furthermore, the antimicrobial activity of complexes was determined using the methods of determination of growth curves and zones of inhibition. The results of this study revealed that the complex of chitosan, with silver phosphate nanoparticles, was the most suitable in order to have an antibacterial effect on bacterial culture of Staphylococcus aureus. Formation of this complex was under way at low concentrations of chitosan. The results of electrochemical determination corresponded with the results of spectrophotometric methods and verified good interaction and formation of the complex. The complex has an outstanding antibacterial effect and this effect was of several orders higher compared to other investigated complexes.     

Electrochemical oxidation of several chlorophenols on diamond electrodes Part I. Reaction mechanism

The electrochemical oxidation of 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol aqueous wastes using boron-doped diamond electrodes was studied. This treatment led to complete mineralization of the wastes regardless of the operating conditions. A simple mechanistic model is consistent with the voltammetric and electrolysis results. According to this model, the electrochemical treatment of chlorophenol aqueous wastes involves the anodic and cathodic release of chlorine followed by the formation of non-chlorinated aromatic intermediates. Subsequent cleavage of the aromatic ring gives rise to non-chlorinated carboxylic acids. Chlorine atoms arising from the hydrodehalogenation of the chlorophenols are converted into more oxidized molecules at the anode. These molecules react with unsaturated C₄ carboxylic acid to finally yield trichloroacetic acid through a haloform reaction. The non-chlorinated organic acids are ultimately oxidized to carbon dioxide and the trichloroacetic acid into carbon dioxide and volatile organo-chlorinated molecules. Both direct and mediated electrochemical oxidation processes are involved in the electrochemical treatment of chlorophenols.     

An integration experience of a software architecture and a monitoring infrastructure to deploy applications with non‐functional requirements in computing grids

Resource management is an important aspect to consider regarding applications that might have different non‐functional or operational requirements, when running in distributed and heterogeneous environments. In this context, it is necessary to provide the means to specify the required resource constraints and an infrastructure that can adapt the applications in light of the changes in resource availability. We adopted a contract‐based approach to describe and maintain parallel applications that have non‐functional requirements in a Computing Grid context, called ZeliGrid. To form the supporting infrastructure we have designed a software architecture that integrates some of the Globus services, the LDAP and the NWS monitoring services. Some modules that map the contract approach into software artifacts were also integrated to this architecture. This paper addresses the architecture and integration issues of our approach, as well as how we put the pieces together highlighting deployment and implementation details, which have to consider diverse aspects such as monitoring, security and dynamic reconfiguration. Copyright © 2010 John Wiley & Sons, Ltd.     

Asymmetric bihomologous crosslinkers for bicomponent gels—The way to strongly increased elastic moduli

2‐Hydroxyethylmethacrylate (HEMA) and acrylamide (AA) have been copolymerized via free radical mechanism, in the presence of 5 mol % of four different crosslinker systems, the symmetric ethylenglycoldimethacrylate (EGDMA), bisacrylamide (BIS), a mixture of EGDMA and BIS, and the asymmetric acrylamideethylenmethacrylate (METAA). The polymerizations have been monitored with a rheometer, exhibiting the gel obtained with the asymmetric METAA, an elastic modulus that is dramatically increased compared with those of the gels prepared with the other three crosslinker systems. A kinetic analysis using the terminal model has been used to build probabilistic surfaces that give information about how the crosslinker is incorporated into the network. This analysis shows a high dissimilarity between the reactions using the asymmetric and the mixture of symmetric crosslinkers, what has been correlated to the difference in modulus. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Rippled and Helical MoS<Subscript>2</Subscript> Nanowire Catalysts: An Aberration Corrected STEM Study

Abstract  

Aberration corrected (C_s) scanning transmission electron microscopy (STEM) has been used for the first time to characterize MoS₂ catalysts (supported on Al₂O₃ substrates) to provide detailed information of its shape and structure. The high-resolution imaging reveals unprecedented morphologies present in the MoS₂ catalyst that have never been observed before with other experimental techniques because of the insufficient image contrast and/or resolution. High angle annular dark field (HAADF)-STEM images shows very clearly that the catalyst is formed by elongated chains with a twisted and helical structure. Based on the HAADF-STEM images, we built three atomic models to illustrate the different morphologies found in the MoS₂ catalyst. The existence of these nanostructures opens the posibility for novel catalyticaly active edge morphologies in MoS₂-based nanocatalysts.     

Experimental design of the kinetic resolution of a key precursor of high‐value bioactive myo‐inositols by an immobilized lipase

BACKGROUND: The response surface methodology was successfully applied to the optimization of the reaction variables for the kinetic resolution of a precursor of high‐value myo‐inositols, ( ± )‐1,2‐O‐isopropylidene‐3,6‐di‐O‐benzyl‐myo‐inositol (( ± )‐1), by Novozym 435. The resolutions were run separately, with two acylating agents, ethyl acetate and vinyl acetate, in a solvent‐free system. The variables analyzed were reaction temperature, substrate concentration, water concentration and enzyme activity. A statistical model was employed for the evaluation of the influence of the variables on conversion and enantiomeric excess (ee). RESULTS: The optimal conditions for this resolution using vinyl acetate as acylating agent were 45 °C, 5 mg mL^?1 of substrate, 71 U of enzyme activity and 0%w/w of water concentration. The high conversion (49.2 %) and ee (>99%) reached in the chemoenzymatic synthesis of acylated product, L‐(?)‐5‐O‐Acetyl‐3,6‐di‐O‐benzyl‐1,2‐O‐isopropylidene‐myo‐inositol, secure the efficient synthesis of the D enantiomorph present in the original racemic mixture (( ± )‐1) as well. CONCLUSIONS: The use of the experimental design strategy was productive, leading to a 14‐fold increase in the productivity of the reaction compared with the non‐optimized conditions. Both derivative L‐(?)‐2 and remaining substrate D‐(+)‐1 were obtained at high ee. © 2012 Society of Chemical Industry     

Effect of mullite additions on the fracture mode of alumina

This work analyses the effect of mullite additions on the fracture mode of alumina. Mullite is proposed as an alternative to SiC for the second phase particles because the thermal expansion mismatch between alumina and mullite is of the same sign and order as that between alumina and SiC. Three alumina–5 vol.% mullite composites formed by alumina matrices with similar average grain sizes in the micrometric range (≈1 μm) and second phase sub-micrometric (50–350 nm) and nanometric mullite (<50 nm) particles located at grain boundaries and triple points were prepared. The fracture mode of the alumina matrix changed from predominantly intergranular to predominantly transgranular. This change became more significant as the size of the sub-micrometric fraction of mullite particles decreased.     

EPD kinetics: A review

The colloidal approach has been studied as an essential step in the tailoring of ceramic nanostructures, but most colloidal processes are limited by the complexity of preparation of highly concentrated and stable suspensions of nanoparticles and their fast ageing. Electrophoretic deposition (EPD) stands out as the most appropriate colloidal process to produce ceramic structures using low solid content sols and suspensions (<1 g/l). This characteristic drastically increases its range of technological applicability to nanoparticle assembly, becoming an alternative to the evaporative coating processes. Modelling of this direct electrically driven assembly process is key for its application to the performance of new materials on length scales of approximately 1–100 nm. In this paper, the key contributions in this field to process control and development of the electrophoretic kinetics equation are summarised.