Label-free determination of picogram quantities of DNA by stripping voltammetry with solid copper amalgam or mercury electrodes in the presence of copper

Highly sensitive label-free techniques of DNA determination are particularly interesting in relation to the present development of the DNA sensors. We show that subnanomolar concentrations (related to monomer content) of unlabeled DNA can be determined using copper solid amalgam electrodes or hanging mercury drop electrodes in the presence of copper. DNA is first treated with acid (e.g., 0.5 M perchloric acid), and the acid-released purine bases are directly determined by the cathodic stripping voltammetry. Volumes of 5-3 microL of acid-treated DNA can easily be analyzed, thus making possible the determination of picogram and subpicogram amounts of DNA corresponding to attomole and subattomole quantities of 1000-base pair DNA. Application of this determination in DNA hybridization detection is demonstrated using surface H for the hybridization (superparamagnetic beads with covalently attached DNA probe) and the mercury electrodes only for the determination of DNA selectively captured at surface H.     

The effect of temperature and oxygen content on the flowing liquid metal corrosion of structural steels in the Pb–Bi eutectic

We performed corrosion tests of 1000 h each on approximately 20 types of structural steels (austenitic, ferritic and martensitic) in convection loops with flowing Pb–Bi at 500, 450 and 400 °C and a temperature gradient of 100 °C. These experiments were performed in liquid Pb–Bi with different oxygen concentrations (from approximately 1 × 10⁻⁶ to 2 × 10⁻⁵ wt.%) to ascertain at what oxygen concentration and up to what temperature the oxygen technology can create protective oxide or spinel layers to reduce or prevent corrosion. The results showed that the structural materials contemplated for building an ADS system, including 9% Cr–1% Mo (W) martensitic steels and similar steels with a higher Si content (2–3%), can be used with their surface unpassivated at up to 450 °C and suffer only minimal corrosion (up to 5 μm/year). At higher temperatures, their surface must be passivated prior to and regularly during the operation; however, no technology to perform such passivation in the presence of Pb–Bi is known that this time. In addition, we measured the impact of various alloying elements, such as Fe, Cr, Ni, Mn, Si, Al and Mo, on the corrosion of such steels and searched for potential ways to passivate their surface or create protective oxide or spinel layers during operation by varying the amount of oxygen in liquid Pb–Bi.     

Gap Junctional Communication via Connexin43 between Purkinje Fibers and Working Myocytes Explains the Epicardial Activation Pattern in the Postnatal Mouse Left Ventricle

The mammalian ventricular myocardium forms a functional syncytium due to flow of electrical current mediated in part by gap junctions localized within intercalated disks. The connexin (Cx) subunit of gap junctions have direct and indirect roles in conduction of electrical impulse from the cardiac pacemaker via the cardiac conduction system (CCS) to working myocytes. Cx43 is the dominant isoform in these channels. We have studied the distribution of Cx43 junctions between the CCS and working myocytes in a transgenic mouse model, which had the His-Purkinje portion of the CCS labeled with green fluorescence protein. The highest number of such connections was found in a region about one-third of ventricular length above the apex, and it correlated with the peak proportion of Purkinje fibers (PFs) to the ventricular myocardium. At this location, on the septal surface of the left ventricle, the insulated left bundle branch split into the uninsulated network of PFs that continued to the free wall anteriorly and posteriorly. The second peak of PF abundance was present in the ventricular apex. Epicardial activation maps correspondingly placed the site of the first activation in the apical region, while some hearts presented more highly located breakthrough sites. Taken together, these results increase our understanding of the physiological pattern of ventricular activation and its morphological underpinning through detailed CCS anatomy and distribution of its gap junctional coupling to the working myocardium.     

Metformin Influence on the Intestinal Microbiota and Organism of Rats with Metabolic Syndrome

Metformin is a first-line drug for DM2 treatment and prevention, but its complex effect on impaired glucose tolerance (IGT), including its influence on myocardial resistance to ischemia-reperfusion injury, is not completely studied. We aimed to evaluate the influence of metformin on the intestinal microbiota (IM), metabolism, and functional and morphological characteristics of myocardium in rats with IGT. IGT was modelled in SPF Wistar rats with a high-fat diet and streptozotocin and nicotinamide injection. Rats were divided into three groups: IGT (without treatment), IGT MET (metformin therapy), and CRL (without IGT induction and treatment). IGT group was characterized by: higher body weight, increased serum glucose and total cholesterol levels, atherogenic coefficient, impairment in the functional parameters of the isolated heart during perfusion, and larger myocardium infarction (MI) size in comparison with the CRL group. IM of IGT rats differed from that of CRL: an increase of Bacteroides, Acinetobacter, Akkermansia, Roseburia, and a decrease of Lactobacillus genera representation. Metformin therapy led to the diminishing of metabolic syndrome (MS) symptoms, which correlated with IM restoration, especially with the growth of Akkermansia spp. and decline of Roseburia populations and their influence on other members of IM. The obtained results allow us to consider from a new point of view the expediency of probiotic A. muciniphila use for MS treatment.     

LaMgAl11O19 synthesis using non-hydrolytic sol-gel methods

Polycrystalline LaMgAl₁₁O₁₉ (LMA) was prepared by four different non-hydrolytic sol-gel methods. From stable solutions, four powder precursors containing an amorphous and nanocrystalline phase with specific reactivity were obtained. The particle size, morphology, thermal behaviour, and phase composition of the powder precursors were studied using DLS, TEM, DSC/TG and XRD. Bulk ceramic samples containing LMA were prepared at 1200?°C for 16?h and examined in terms of phase purity and microstructure using XRD, SEM, and TEM. Raman spectroscopy of pure LMA was used to study the structure in detail. A mechanism of LMA formation and a relation between powder precursor properties and final phase composition is proposed. These findings may be useful for designing modern technologies for fabrication of LMA for optical or protective coating applications.     

Effect of noble metals in the decomposition of nitrous oxide over Fe-ferrierites

The decomposition of nitrous oxide was studied over Fe-ferrierite, Me-ferrierites and Fe/Me-ferrierites (Me: Pt, Rh and Ru). Flow as well as batch experiments were carried out and showed a synergy between Fe and Me ions. Ions of noble metals in Fe-ferrierite increased the catalytic activity in the sequence Pt < Rh ≅ Ru. Addition of NO substantially decreased the decomposition of N₂O over Rh/ferrierite and Ru/ferrierite, but not over bimetallic ferrierites. NO _x species created during the decomposition of nitrous oxide alone as well as with addition of NO, and employment of nitrous oxide labeled with ¹⁸O allowed us to assume a changing decomposition mechanism in the presence of Me ions in Fe-ferrierites.     

Effects of Zirconia on Microstructure and Dielectric Properties of Barium Titanate Ceramics

Dielectric properties and structural characteristics of BaTiO₃ ceramics are significantly influenced by small addition (2 wt%) of ZrO₂. SEM and TEM observations revealed enhanced microstructural uniformity and retarded grain growth depending on sintering temperature. Above 1320°C, Zr diffusion into the BaTiO₃ lattice resulted in a chemical modification of the tetragonal structure and the development of core–shell grains. Below 1320°C, TEM analysis showed ZrO₂ at the grain boundaries as discrete particles (∼0.03μm). X-ray diffraction analysis revealed a decrease in the axial (c/a) ratio with decreasing grain size. A corresponding decrease in the spontaneous polarization, and twinned domain structures, were also observed in the fine-grained ceramics. These samples also showed a flattened permittivity response with temperature and significantly lower losses.     

Relationship of iso‐α‐acid content and endogenous antioxidative potential during storage of lager beer

One of the critical issues regarding the quality of beer is the change in its chemical composition that occurs during storage. Decomposition of iso‐α‐acids results in an undesirable decrease in bitterness as well as a deterioration in the sensory profile of the beer. These changes are caused by the susceptibility of iso‐α‐acids to degradation owing to the influence of reactive oxygen species and light. The aim of this study was to investigate the influence of storage conditions (temperature, light) on the degradation of iso‐α‐acids during aging, with the main focus on monitoring the relationship between the turnover of iso‐α‐acids, the sulphur dioxide content and the antioxidative potential of stored beer as measured by electron spin resonance spectroscopy. In agreement with previous investigations, a significant decrease in the content of bitter compounds (up to 18 % relative to the original level, depending on storage conditions) was observed. A significant decrease in the antioxidant potential of beer was recorded simultaneously and the data confirmed a strong correlation between these parameters. The decline in beer bitterness could become a marker for estimating oxidative damage during storage. Copyright © 2014 The Institute of Brewing & Distilling     

Scintillation properties of Pr3+-doped lutetium and yttrium aluminum garnets: Comparison with Ce3+-doped ones

Scintillation properties of Pr³⁺-doped LuAG and YAG crystals were investigated and compared with those of Ce³⁺-doped ones. The highest L.Y.’s were observed with the longest shaping time 10 μs. They can reach up to ～16,000 ph/MeV or ～23,500 ph/MeV for LuAG:Pr and LuAG:Ce, respectively. Energy resolutions (FWHM) are a bit better with LuAG:Pr than those of LuAG:Ce, e.g. at 662 keV FWHM are around 6% and between 8–12%, respectively. There were observed no large changes in proportionality of Pr³⁺- or Ce³⁺-doped LuAG or YAG crystals but the best proportionality has YAP:Ce crystal. Pr³⁺- or Ce³⁺-doped LuAG crystals exhibit slow decay components in the time range 1.5–3.5 μs while those of YAG ones have shorter decay components between 0.3–1.7 μs.