Synthesis of Benzophenones and in vitro Evaluation of Their Anticancer Potential in Breast and Prostate Cancer Cells

Breast and prostate cancers are frequently treated with chemotherapy. Several novel chemicals are being reported for this purpose, particularly synthetic and natural benzophenones. This work reports the synthesis of substituted 2-hydroxybenzophenones through 1,4-conjugate addition/intramolecular cycloaddition/dehydration of nitromethane on key intermediate chromones. Structures were extensively studied by means of 2D NMR spectroscopy and single-crystal XRD. Their cytotoxicity was evaluated in vitro in two breast cancer cell lines (MDA-MB-231 and T47-D) and one prostate cancer cell line (PC3). The most potent compound exhibited good cytotoxic effects against the three cancer cell lines (IC₅₀ values ranging from 12.09 to 26.49 μm ) and induced cell-cycle retardation only on prostate cancer cells, which suggested that it might exert cell-type-specific effects.     

Bacteroides fragilis enterotoxin cleaves the zonula adherens protein, E-cadherin

Strains of Bacteroides fragilis associated with diarrheal disease (enterotoxigenic B. fragilis) produce a 20-kDa zinc-dependent metalloprotease toxin (B. fragilis enterotoxin; BFT) that reversibly stimulates chloride secretion and alters tight junctional function in polarized intestinal epithelial cells. BFT alters cellular morphology and physiology most potently and rapidly when placed on the basolateral membrane of epithelial cells, suggesting that the cellular substrate for BFT may be present on this membrane. Herein, we demonstrate that BFT specifically cleaves within 1 min the extracellular domain of the zonula adherens protein, E-cadherin. Cleavage of E-cadherin by BFT is ATP-independent and essential to the morphologic and physiologic activity of BFT. However, the morphologic changes occurring in response to BFT are dependent on target-cell ATP. E-cadherin is shown here to be a cellular substrate for a bacterial toxin and represents the identification of a mechanism of action, cell-surface proteolytic activity, for a bacterial toxin.     

Carbon segregation and inclusions effects on surface fracture morphology of a 12% chromium stainless steel

Martensitic 12% chromium stainless steel is generally used for the manufacture of water vapour turbine blades. This material, under these environmental conditions, develops fatigue corrosion with failure as a result of the segregation of certain constituent elements such as phosphorus (P) and sulphur (S),^[1–3] or the presence of some types of inclusions.^[2–4] To be able to understand and explain these phenomena, in situ characterization of the fractured surfaces were performed for two types of samples: steel 1 as manufactured turbine material whose fracture mode is intergranular and steel 2 issued from last stage turbine blades after 100 000 h service at 40 °C whose fracture mode is transgranular. The techniques used for characterization were scanning electron microscopy (SEM) coupled with the x-ray analysis by energy dispersive spectroscopy (EDS), and auger electron spectroscopy (AES). The Auger results enabled the understanding of the brittle to ductile transition for the material by showing the simultaneous diffusion of carbon from grain boundaries (GB) to grains (G) and chromium from G to GB. Furthermore, the heavy segregation of phosphorus at the GBs could explain the intergranular crack rupture traces observed in steel 2. SEM observations coupled with EDS analysis showed the presence of different types of non-metallic inclusions such as silicon-based complex inclusions and manganese sulfides (MnS). The presence of silicon-based complex inclusions at GB could explain the intergranular fracture mode previously reported. The characterization of the fracture appearance suggests also that MnS inclusions can act as nucleation sites for secondary microcracks at the GB level that were observed after service.     

Buoyancy effects on gaseous slip flow in a vertical rectangular microchannel

Consideration is given to the buoyancy effects on the fully developed gaseous slip flow in a vertical rectangular microduct. Two different cases of the thermal boundary conditions are considered, namely uniform temperature at two facing duct walls with different temperatures and adiabatic other walls (case A) and uniform heat flux at two walls and uniform temperature at other walls (case B). The rarefaction effects are treated using the first-order slip boundary conditions. By means of finite Fourier transform method, analytical solutions are obtained for the velocity and temperature distributions as well as the Poiseuille number. Furthermore, the threshold value of the mixed convection parameter to start the flow reversal is evaluated. The results show that the Poiseuille number of case A is an increasing function of the mixed convection parameter and a decreasing function of the channel aspect ratio, whereas its functionality on the Knudsen number is not monotonic. For case B, the Poiseuille number is decreased by increasing each of the mixed convection parameter, the Knudsen number, and the channel aspect ratio.     

Bending-stretching analysis of thick functionally graded micro-plates using higher-order shear and normal deformable plate theory

In the present article, higher-order shear and normal deformable plate theory together with modified couple stress theory are developed to study the bending analysis of thick functionally graded rectangular micro-plates. One material length scale parameter is used for capturing the size effects. Utilizing the variational approach and also a principle of virtual displacement, a new form of equilibrium equations and the corresponding boundary conditions are derived. It is assumed that material properties vary through the thickness according to the power law function. Finally, an analytical solution for the bending problem of a simply supported FG rectangular micro-plate is presented.     

Dehydrogenation kinetics and modeling studies of MgH2 enhanced by NbF5 catalyst using constant pressure thermodynamic forces

In this research, the effect of NbF₅ as an additive on the hydrogen desorption kinetics of MgH₂ was investigated and compared to TiH₂, Mg₂Ni and Nb₂O₅ catalysts. The kinetics measurements were done using a method in which the ratio of the equilibrium plateau pressure to the opposing pressure was the same for all the reactions. The data showed NbF₅ to be vastly superior to the other catalysts for improving the desorption kinetics of MgH₂. The rates of desorption were found to be in the order NbF₅ ? Nb₂O₅ > Mg₂Ni > TiH₂ > Pure MgH₂. Kinetic modeling measurements showed that chemical reaction at the phase boundary to be the likely process controlling the reaction rates. TPD analyses showed the mixture with NbF₅ has the lowest desorption temperature although it was accompanied with some weight penalty.     

Cellular polypropylene‐based piezoelectric films

Cellular polypropylene‐calcium carbonate based piezoelectric films were obtained using biaxial stretching and gas‐mediated inflation followed by a corona discharge treatment using home‐made devices. The obtained results revealed a cellular structure that develops at the interface between the solid particles and the polymer matrix and the final piezoelectric coefficient was found to depend both on the gas pressure profile and on time. The inflation step gives better results when the gas pressure is increased in stepwise manner allowing the gas to adequately intrude the cavities and maintain the required pressure. The overall results are discussed in terms of processing conditions and in terms of the developed microstructure. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Dithiocarbamate as an efficient intermediate for the synthesis of 2-(alkylthio)thiazol-4(5H)-ones

An effective approach for the synthesis of 2-(alkylthio)thiazol-4(5H)-ones from alkyl dithiocarbamates and chloroacetyl chloride in the presence of NaHCO₃ has been developed. Good to excellent yields of products, simple reaction conditions and general applicability are the most important advantages of this protocol.     

Pure Hydrogen and Propylene Coproduction in Catalytic Membrane Reactor-Assisted Propane Dehydrogenation

Propane dehydrogenation on a commercial Pt-Sn/Al₂O₃ catalyst in a Pd-Ag membrane reactor is considered. A mathematical model is developed to evaluate the performance of the catalytic membrane reactor for the process of propane dehydrogenation. Design and operating conditions are systematically evaluated for key performance metrics such as propane conversion, propylene selectivity, hydrogen selectivity, and hydrogen recovery under different operating conditions. The results confirm that the high performance of the membrane reactor is related to the continuous removal of hydrogen from the reaction zone to shift the reaction equilibrium towards the formation of more propylene and hydrogen.