Assessment of Surface Treatment Degree of Steel Sheets in the Bonding Process

The aim of the paper is to determine the influence of the surface treatment on the adhesive properties of steel sheet surfaces and the strength of the adhesive joints of steel sheets. The paper also aims to assess the degree of steel sheets’ surface treatment in the bonding process. Due to the many methods of surface treatment and types of materials, the assessment of the surface treatment method is extremely important in adhesive processes. Two variants of the surface treatment were used: without a paint coating and with a paint coating, divided into two groups (without degreasing and with degreasing). Additionally, in the case of the analysis of the steel samples without the paint coating, mechanical treatment was applied. Two-component epoxy adhesive, prepared on the basis of bisphenol A and a polyamide curing agent, was used to prepare the single-lap adhesive joints of the steel sheets. The tests determined: (i) the adhesive properties of the steel sheets’ surface based on the measurement of the contact angle of polar and apolar liquids (including wettability, work of adhesion, and surface free energy), (ii) surface roughness parameters (PN EN ISO 4287), and (iii) mechanical properties (load capacity and shear strength) of the steel sheets’ adhesive joints (EN DIN 1465). Contact angle measurements of the steel sheet surfaces showed that the polar liquid better reflects the obtained strength results of the analyzed adhesive joints than the apolar liquid. Furthermore, better wettability of the surface of steel sheets with both polar and apolar liquids was obtained for samples whose surface was subjected to degreasing. It can also be concluded that the wettability of the surface can be used as one of the indicators of the degree of the surface treatment for the bonding process.     

Controlled release of dexamethasone from PLGA microspheres embedded within polyacid-containing PVA hydrogels

The development of zero-order release systems capable of delivering drug(s) over extended periods of time is deemed necessary for a variety of biomedical applications. We hereby describe a simple, yet versatile, delivery platform based on physically cross-linked poly(vinyl alcohol) (PVA) microgels (cross-linked via repetitive freeze/thaw cycling) containing entrapped dexamethasone-loaded poly(lactic-co-glycolic acid) (PLGA) microspheres for controlled delivery over a 1-month period. The incorporation of polyacids, such as humic acids, Nafion, and poly(acrylic acid), was found to be crucial for attaining approximately zero-order release kinetics, releasing 60% to 75% of dexamethasone within 1 month. Microspheres alone entrapped in the PVA hydrogel resulted in negligible drug release during the 1-month period of investigation. On the basis of a comprehensive evaluation of the structure-property relationships of these hydrogel/microsphere composites, in conjunction with their in vitro release performance, it was concluded that these polyacids segregate on the PLGA microsphere surfaces and thereby result in localized acidity. These surface-associated polyacids appear to cause acid-assisted hydrolysis to occur from the surface inwards. Such systems show potential for a variety of localized controlled drug delivery applications such as coatings for implantable devices.     

Nerve growth factor (NGF) promotes angiogenesis in the quail chorioallantoic membrane.

Angiogenesis, the formation of new blood vessels, is tightly regulated by growth factors, such as vascular endothelial growth factor (VEGF) and fibroblast growth factor (FGF). The authors hypothesize that nerve growth factor (NGF), a well known neurotrophin, may play a direct angiogenic role. To test this hypothesis, the authors measured the effects of NGF on the natural vascularization of the quail chorioallantoic membrane (CAM). The angiogenic effect of NGF was compared to that of human recombinant VEGF165 (rhVEGF) and basic FGF (rhbFGF). In comparison to phosphate-buffered saline-treated controls, NGFs from different biological sources (mouse, viper, and cobra) increased the rate of angiogenesis in a dose-dependent fashion from 0.5 to 5 microg. For quantitative morphometry, grayscale images of the blood vessels end points of the CAM arteries were binarized for visualization and skeletonized for quantization by fractal analysis. In mouse NGF-treated embryos the fractal dimension (Df), indicative of arterial vessel length and density, increased to 1.266 +/- 0.021 compared to 1.131 +/- 0.018 (p < .001) for control embryos. This effect was similar to that of 0.5 microg rhVEGF (1.290 +/- 0.021, p < .001) and 1.5 microg rhbFGF (1.264 +/- 0.028, p < .001). The mouse NGF-induced angiogenic effect was blocked by 1 microM K252a (1.149 +/- 0.018, p < .001), an antagonist of the NGF/trkA receptor, but not by 1 microM SU-5416 (1.263 +/- 0.029, p < .001), the VEGF/Flk1 receptor antagonist, indicating a direct, selective angiogenic effect of NGF via quail embryo trkA receptor activation. These results confirm previous observations that NGF has angiogenic activity and suggest that this neurotrophin may also play an important role in the cardiovascular system, besides its well-known effects in the nervous system. The angiogenic properties of NGF may be beneficial in engineering new blood vessels and for developing novel antiangiogenesis therapies for cancer.     

Upper respiratory colonization by Streptococcus pneumoniae in healthy pre-school children in south-east Poland

Objective

Carriage of Streptococcus pneumoniae in upper respiratory tract of healthy children is a major factor in the horizontal transmission of pneumococcal strains, especially between children attending day-care centers and may be also the source of infection in other individuals. During 8-month prospective study including 3 seasons (autumn, winter, spring), we determined risk factors for S. pneumoniae colonization in general and colonization at 2 or 3 time points in healthy pre-school children, including penicillin non-susceptible likewise multidrug resistant strains.

Methods

Pneumococcal cultures were obtained from 311 children aged 3–5. Finally, a total of 342 isolates were identified. Resistance of pneumococcal isolates was determined and information about potential risk factors were obtained from questionnaires.

Results

A total of 72.4% children were colonized by pneumococci at least once, including 8.4% children colonized at 3 time points, 25.4% children – twice and 38.6% children – only once. Penicillin non-susceptible pneumococcal colonization was found in 36.3% children at least once while multidrug-resistant pneumococcal colonization in 34.1% children. Of the 10.9% and 10.6% children were colonized at 2 or 3 time points by penicillin non-sussceptible and multidrug-resistant isolates, respectively. Pneumococcal colonization (in general or by non-susceptible to penicillin isolates) was independently associated with day care attendance, having no siblings, frequent respiratory tract infections and higher number of antibiotic courses. Children attending day care center, with frequent respiratory tract infections, exposed to tobacco smoke were prone to colonization by multidrug-resistant isolates. Risk of colonization at 2 or 3 time points by pneumococcal isolates, including penicillin-nonsusceptible isolates, was associated with age and day care attendance while multidrug-resistant pneumococcal colonization was found to be significantly higher in children aged 3, with frequent respiratory tract infections and higher number of antibiotic courses.

Conclusion

These results indicate high rate of upper respiratory colonization by S. pneumoniae in healthy preschool children in Poland, including colonization by penicillin non-susceptible and multidrug-resistant pneumococci.     

Temporally Controlled Ultrasonication‐Mediated Atom Transfer Radical Polymerization in Miniemulsion

Due to the increasing requirement for more environmentally and industrially relevant approaches in macromolecules synthesis, ultrasonication‐mediated atom transfer radical polymerization (sono‐ATRP) in miniemulsion media is applied for the first time to obtain precisely defined poly(n‐butyl acrylate) (PBA) and poly(methyl methacrylate) (PMMA) homopolymers, and poly(n‐butyl acrylate)‐block‐poly(tert‐butyl acrylate) (PBA‐b‐PtBA) and poly(n‐butyl acrylate)‐block‐poly(butyl acrylate) (PBA‐b‐PBA) copolymers. It is demonstrated in the reaction setup with strongly hydrophilic catalyst copper(II) bromide/tris(2‐pyridylmethyl)amine (Cu^IIBr₂/TPMA) responsible for two principal mechanisms – interfacial and ion‐pair catalysis reflecting single‐catalyst approach. This solution turns out to be an excellent tool in controlled preparation of well‐defined polymers with narrow molecular weight distribution (up to Ð = 1.28) and preserves chain‐end functionality (DCF = 0.02% to 0.32%). Temporal control over the polymer chain growth is successfully conducted by turning the ultrasonication on/off. Taking into consideration long OFF stage (92.5 h) during ultrasonication‐induced polymerization in miniemulsion, synthesis is efficiently reinitiated without any influence on controlled characteristics maintaining the precise structure of received PBA homopolymers, confirmed by narrow molecular weight distribution (Ð = 1.26) and high retention of chain‐end functionality (DCF = 0.01%). This procedure constitutes an excellent simple and eco‐friendly approach in preparation of functional polymeric materials.     

Ca²(+) /calmodulin-dependent protein kinase II mediates the octopamine-induced increase in sensitivity in spider VS-3 mechanosensory neurons

G-protein-coupled octopamine (OA) receptors mediate their effects by Ca2(+) signaling or adjusting intracellular cAMP levels. Depending on OA concentration and cell type, activation of OA receptors in excitable cells triggers excitatory or inhibitory effects, but the mechanisms by which Ca2(+) or cAMP mediates these effects are not well understood. We investigated signaling mechanisms that are potentially activated by OA, and OA effects on excitability and frequency sensitivity in mechanosensory neurons innervating the VS-3 slit sensilla on the patella of the spider Cupiennius salei. These neurons are directly innervated by octopaminergic efferents, and possess OA receptors that were immunoreactive to an antibody against an OA receptor highly expressed in mushroom bodies. OA application enhanced VS-3 neuron sensitivity, especially at high stimulation frequencies. This enhancement lasted for at least 1 h after OA application. Changes in sensitivity were also detected when the Ca2(+) ionophore ionomycin or the cAMP analog 8-Br-cAMP was applied. However, the cAMP pathway was unlikely to mediate the OA effect, as the protein kinase A inhibitor RP-cAMPS did not diminish this effect. In contrast, the OA-induced sensitivity enhancement was significantly reduced by KN-62, an inhibitor of Ca2(+) /calmodulin-dependent protein kinase II (CaMKII), and by the Ca2(+) chelator BAPTA-AM. OA depolarized the neurons by 3.8 mV from resting potential, well below the threshold for opening of voltage-activated Ca2(+) channels. OA also reduced the amplitudes of voltage-activated K(+) currents. We propose that OA receptors in VS-3 neurons activate inositol 1,4,5-trisphosphate, leading to Ca2(+) release from intracellular stores. The Ca2(+) surge switches on CaMKII, which modulates voltage-activated K(+) channels, resulting in persistent enhancement in excitability.     

Application of Screening Methods,Shape Signatures and Engineered Biosensors in Early Drug Discovery Process

Purpose  

In this study, two unreported estrogen antagonists were identified using a combination of computational screening and a simple bacterial estrogen sensor.     

Increased BDNF Levels in Long-term Bipolar Disorder Patients

IntroductionBipolar disorder (BD) is a prevalent, chronic and progressive illness. There is a growing body of evidence indicating that brain-derived neurotrophic factor (BDNF) plays an important role in the pathophysiology of BD.ObjectiveThe aim of this study was to evaluate BDNF plasma levels in BD patients with long term illness in comparison with controls.Methods87 BD type I patients and 58 controls matched by age, gender and education level were enrolled in this study. All subjects were assessed by the Mini-International Neuropsychiatric Interview and the patients by the Young Mania Rating Scale and the Hamilton Depression Rating Scale. The plasma levels of BDNF were measured by ELISA.ResultsOn average, patients had suffered from BD for 23.4 years. In comparison with controls, BD patients with mania presented a 1.90-fold increase in BDNF plasma levels (p = .001), while BD patients in remission presented a 1.64-fold increase in BDNF plasma levels (p = .03). BDNF plasma levels were not influenced by age, length of illness or current medications.ConclusionsThe present study suggests that long-term BD patients exhibit increased circulating levels of BDNF.