Mo–Si–B alloys for ultra-high-temperature space and ground applications: liquid-assisted fabrication under various temperature and time conditions

Journal of Materials Science - Boron-doped molybdenum silicides have been already recognized as attractive candidates for space and ground ultra-high-temperature applications far beyond limits of...     

Effect of Ti,Nb, and Ti + Nb Coatings on the Bond Strength-Structure Relationship in Al/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Joints

There is a growing interest in metal-ceramic bonding for wide range of applications in electronic devices and high technology industry for fabrication of metal matrix composites and bonding of ceramic components to metals. The object of the work was to study the effect of Ti, Nb, and Ti + Nb thin films deposited by PVD method on alumina substrates on structure and bond strength properties of Al/Al₂O₃ joints. The joints were fabricated using the results of a wetting experiment and the sessile drop method at a temperature of 1223 K in a vacuum of 0.2 MPa for 30 min of contact. The structure of the metal/ceramic interface was investigated using scanning electron microscopy. The elemental distribution at the metal-ceramic interface was analyzed using energy dispersive x-ray spectroscopy. Transmission electron microscopy was also used to investigate some aspects of the metal/ceramic interface. The bond strength properties of joints were measured using shear test. The shear strength results demonstrated significant improvement of shear strength of Al/Al₂O₃ joints due to the application of Ti + Nb thin film on alumina substrate. Microstructural investigations of the interface indicated that Al/coating/Al₂O₃ couples have diffusion transition interface which influences the strengthening of these joints. A conclusion could be drawn that the presence of thin film layers changes the character of interaction and leads to the formation of new reaction products in the bonding layer.     

Resveratrol Affects Insulin Signaling in Type 2 Diabetic Goto-Kakizaki Rats

Resveratrol is a biologically active diphenolic compound exerting multiple beneficial effects in the organism, including anti-diabetic properties. This action is, however, not fully elucidated. In the present study, we examined effects of resveratrol on some parameters related to insulin signaling, and also on diabetes-associated dysregulation in Goto-Kakizaki (GK) rats with congenital type 2 diabetes. Resveratrol was given at the dose of 20 mg/kg b.w. for 10 weeks. It was shown that the expression and phosphorylation levels of insulin receptor in the skeletal muscle of GK rats were significantly decreased, compared with control animals. However, these changes were totally prevented by resveratrol. Liver expression of the insulin receptor was also reduced, but in this case, resveratrol was ineffective. Resveratrol was also demonstrated to significantly influence parameters of insulin binding (dissociation constant and binding capacity) in the skeletal muscle and liver. Moreover, it was shown that the expression levels of proteins related to intracellular glucose transport (GLUT4 and TUG) in adipose tissue of GK rats were significantly decreased. However, treatment with resveratrol completely abolished these changes. Resveratrol was found to induce normalization of TUG expression in the skeletal muscle. Blood levels of insulin and GIP were elevated, whereas proinsulin and GLP-1 diminished in GK rats. However, concentrations of these hormones were not affected by resveratrol. These results indicate that resveratrol partially ameliorates diabetes-associated dysregulation in GK rats. The most relevant finding covers the normalization of the insulin receptor expression in the skeletal muscle and also GLUT4 and TUG in adipose tissue.     

Novel Dual PI3K/mTOR Inhibitor,Apitolisib (GDC-0980), Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells

Deregulated PI3K/AKT/mTOR signalling commonly exists in glioblastoma, making this axis an attractive target for therapeutic manipulation. Given that activation of PI3K/AKT/mTOR promotes tumour growth, metastasis, and resistance to anticancer therapies, mTOR inhibitors show promise in the treatment of cancer. The aim of this study was to investigate the underlying mechanism of novel dual PI3K/mTOR inhibitor, Apitolisib (GDC-0980), in A-172 and U-118-MG GBM tumour cell line suppression. It has been demonstrated that GDC-0980 induces time- and dose-dependent cytotoxicity and apoptosis in investigated glioma cell lines. In our study, the strongest induction of apoptosis was exhibited in the A-172 line after 48 h of incubation with 20 µM GDC-0980, where we observed 46.47% of apoptotic cells. In conclusion, we first discovered that dual PI3K/mTOR blockade by GDC-0980 markedly suppressed survival of human GBM cells and induced apoptosis, independent of the ER stress-mediated DR5 activation. We suggest that GDC-0980, by exerting an inhibitory effect on PERK expression, may thus block its inhibitory effect on protein synthesis, leading to intensification of translation, and this may result in an increase in apoptosis. On the other hand, CHOP stimulates protein synthesis and increases apoptosis. These findings suggest that GDC-0980 may be a candidate for further evaluation as a chemotherapeutic agent for anti-GBM therapy.     

Compensated MOSFET devices

The turn-on and conduction mechanisms of a p-channel compensated MOSFET are discussed. Depending on the implantation and back-bias conditions, two distinct modes of operation occur, each with its own characteristic threshold voltage and conductance relations. In addition, major factors influencing punch-through and the associated subthreshold characteristics have been taken into account. The effect of inversion in the compensating p-layer on the gate capacitance is shown. Experimental data verify the theoretical results presented. Consequences of typical device properties for CMOS modelling are discussed.     

The Preliminary Study on the Proapoptotic Effect of Reduced Graphene Oxide in Breast Cancer Cell Lines

Breast cancer is the most common cancer diagnosed in women, however traditional therapies have several side effects. This has led to an urgent need to explore novel drug approaches to treatment strategies such as graphene-based nanomaterials such as reduced graphene oxide (rGO). It was noticed as a potential drug due to its target selectivity, easy functionalisation, chemisensitisation, and high drug-loading capacity. rGO is widely used in many fields, including biological and biomedical, due to its unique physicochemical properties. However, the possible mechanisms of rGO toxicity remain unclear. In this paper, we present findings on the cytotoxic and antiproliferative effects of rGO and its ability to induce oxidative stress and apoptosis of breast cancer cell lines. We indicate that rGO induced time- and dose-dependent cytotoxicity in MDA-MB-231 and ZR-75-1 cell lines, but not in T-47D, MCF-7, Hs 578T cell lines. In rGO-treated MDA-MB-231 and ZR-75-1 cell lines, we noticed increased induction of apoptosis and necrosis. In addition, rGO has been found to cause oxidative stress, reduce proliferation, and induce structural changes in breast cancer cells. Taken together, these studies provide new insight into the mechanism of oxidative stress and apoptosis in breast cancer cells.     

The Effect of the Simultaneous Operation of Two Metal Ions on Soluble and Immobilized Peroxidase

Changes in the activity of peroxidase (EC 1.11.1.7) were compared under the influence of two simultaneously present metal ions, one of which deactivates most enzymes (mercury or cadmium) while the other possesses stimulating properties (magnesium, manganese or calcium). A possibility of a considerable increase in peroxidase activity (50–200%) was found in the presence of the ions of manganese, magnesium or calcium, in spite of the presence of ions known to possess toxic properties (mercury or cadmium). An enzyme immobilization method was employed in order to determine the kind of protein functional groups (COOH or NH₂) involved in the processes of peroxidase activity changes due to the presence of metal ions. It was found that by immobilizing peroxidase by free amino groups of the enzyme, one achieves a considerable decrease in the toxic effect of mercury or cadmium, and a higher increase in peroxidase activity in the presence of manganese, magnesium or calcium. © 1997 SCI.     

The Pro-Apoptotic Effect of Silica Nanoparticles Depends on Their Size and Dose,as Well as the Type of Glioblastoma Cells

Despite intensive investigations, nanoparticle-induced cellular damage is an important problem that has not been fully elucidated yet. Here, we report that silica nanoparticles (SiNPs) demonstrated anticancer influence on glioblastoma cells by the induction of apoptosis or necrosis. These effects are highly cell type-specific, as well as dependent on the size and dose of applied nanoparticles. Exposure of LN-18 and LBC3 cells to different sizes of SiNPs—7 nm, 5–15 nm, or 10–20 nm—at dosages, ranging from 12.5 to 1000 µg/mL, for 24 and 48 h reduced the viability of these cells. Treatment of LN-18 and LBC3 cells with 7 nm or 10–20 nm SiNPs at doses ≥50 µg/mL caused a strong induction of apoptosis, which is connected with an increase of intracellular reactive oxygen species (ROS) production. The 5–15 nm SiNPs exhibited distinct behavior comparing to silica nanoparticles of other studied sizes. In contrast to LBC3, in LN-18 cells exposed to 5–15 nm SiNPs we did not observe any effect on apoptosis. These nanoparticles exerted only strong necrosis, which was connected with a reduction in ROS generation. This suggests that SiNPs can trigger different cellular/molecular effects, depending on the exposure conditions, the size and dose of nanoparticles, and cell type of glioblastoma.