A Phenylacetamide Resveratrol Derivative Exerts Inhibitory Effects on Breast Cancer Cell Growth

Resveratrol (RSV) is a natural compound that displays several pharmacological properties, including anti-cancer actions. However, its clinical application is limited because of its low solubility and bioavailability. Here, the antiproliferative and anti-inflammatory activity of a series of phenylacetamide RSV derivatives has been evaluated in several cancer cell lines. These derivatives contain a monosubstituted aromatic ring that could mimic the RSV phenolic nucleus and a longer flexible chain that could confer a better stability and bioavailability than RSV. Using MTT assay, we demonstrated that most derivatives exerted antiproliferative effects in almost all of the cancer cell lines tested. Among them, derivative 2, that showed greater bioavailability than RSV, was the most active, particularly against estrogen receptor positive (ER+) MCF7 and estrogen receptor negative (ER-) MDA-MB231 breast cancer cell lines. Moreover, we demonstrated that these derivatives, particularly derivative 2, were able to inhibit NO and ROS synthesis and PGE2 secretion in lipopolysaccharide (LPS)-activated U937 human monocytic cells (derived from a histiocytoma). In order to define the molecular mechanisms underlying the antiproliferative effects of derivative 2, we found that it determined cell cycle arrest at the G1 phase, modified the expression of cell cycle regulatory proteins, and ultimately triggered apoptotic cell death in both breast cancer cell lines. Taken together, these results highlight the studied RSV derivatives, particularly derivative 2, as promising tools for the development of new and more bioavailable derivatives useful in the treatment of breast cancer.     

Antioxidant activity,color chromaticity coordinates,and chemical characterization of monofloral honeys from Morocco

The bioprospecting of several monofloral Moroccan honeys was carried out. The antiradical activity expressed as mmol Trolox equivalents/kg of honey and evaluated by 2,2-diphenyl-1-picrylhydrazyl assay, ranged from 0.15 for euphorb honey to 1.08 for citrus honey. The antioxidant activity expressed as mmol Fe²⁺/kg and evaluated by ferric ion reducing antioxidant power assay, ranged from 0.96 for euphorb honey to 4.74 for orange honey. The total phenol content was evaluated by colorimetric assay, while the color attributes were evaluated as transmittance data. Significant Pearson correlation factors were found between total polyphenol amount and antioxidant activity and between color attributes and antioxidant activity. Furthermore the chemical composition of volatile organic compounds was determined. The volatile organic compounds chemical composition of the studied honeys was mainly represented by terpene and benzene derivatives, Maillard reaction products, isoprenoids, and hydrocarbons. The volatiles fingerprint, as well as a targeted high-performance liquid chromatography analysis of the polar components, was used to tentatively confirm the declared botanical origin of the samples studied.     

Photochemical grafting of acrylated azo dyes onto polymeric surfaces. VII. Kinetics and mechanism of dye-sensitized photoinitiation of some diacrylates

Photoinitiated grafting and graft polymerization of liquid mixtures, adsorbed onto polypropylene, polycaprolactam, and poly(ethylene terephthalate) films, containing one of four acryloxy-substituted aromatic diazenes and one of four diacrylate comonomers, in the presence of 1,2-diphenyl-2,2-dimethoxyethanone as photoinitiator, were investigated kinetically at 30 ± 2°C. Irradiation was carried out polychromatically, with impinging photoenergy from 2.1 × 10^?8 to 20.5 × 10^?8 einstein s^?1 cm^?2; in some of the runs the ultraviolet radiation was filtered. The ratio R between the molar concentration of photoinitiator and the sum of concentrations of dye and diacrylate varied between 0.005 and 0.095; the ratio M between the molar concentration of dye and diacrylate varied between 0.005 and 0.046. The moles of dye and diacrylate n initially deposited per unit apparent polymeric surface S varied between 2 and 74 μmol cm^?2. No selective effect was shown by the presence of dyes in the comonomer mixture. The surface density of grafted molecules at the end of the grafting process was not affected by the photoinitiator concentration (for 0.030 < R < 0.095), by diacrylate or dye concentrations, or by the kind of polymer substrate. This parameter, on the contrary, clearly depended on n/S, and linearly up to n/S ? 30 μmol cm^?2. Quantum efficiencies for the two consecutive kinetic processes of grafting and graft polymerization (Φ₁ and Φ₂, respectively) were evaluated. The dependency of Φ₁ on R, as well as of Φ₂ on n/S, are critically discussed on the basis of the proposed mechanism involving grafting of an oligomeric chain (Φ₁ values up to the order of 10²) followed by a step-by-step graft polymerization (Φ₂ limiting values of the order of unity). The sensitizing effect of acryloxy-substituted aromatic diazenes on both Φ₁ and Φ₂ is evidenced.     

Development and evaluation of a virtual campus on Second Life: The case of SecondDMI

Video games and new communication metaphors are quickly changing today’s young people habits. Considering the actual e-learning scenarios, embedded in a fully technological enabled environment it is crucial to take advantage of this kind of capabilities to let learning process gain best results.     

Nanocomposite epoxy coatings containing rare earth ion-doped LaF3 nanoparticles: Film preparation and characterization

New epoxy-based nanostructured materials containing lanthanide ions doped LaF₃ nanoparticles were obtained by cationic UV-induced ring-opening polymerization.The lanthanide Er³⁺ and Yb³⁺ ions were added as dopant to LaF₃ nanoparticles. The synthesized NPs were solubilized into cyclohexene oxide and afterwards dispersed, in the range between 3 and 20 wt.%, into CE as dicycloaliphatic epoxy resin. The cured films were completely transparent and TEM analysis showed the absence of macroscopic agglomeration. The fast UV curing process was shown to be efficient on “freezing” the good nanometric dispersion achieved in the liquid formulations. These new materials could find suitable applications in optical communication and in LASER waveguide direct writing.     

Mechanically Induced Phase Transformation and Surface Segregation in Bismuth-Doped Tetragonal Zirconia

Compact pressure causes a martensitic transformation of partially stabilized tetragonal bismuth-doped ZrO₂ powders to the monoclinic phase. A similar effect is not observed when pelletization, followed by firing, of amorphous bismuth/ZrO₂ is performed. The stress-induced transition has been monitored via X-ray diffractometry, Raman spectroscopy, and Fourier transform infrared reflectivity. Surface bismuth segregation, which involves few ionic planes, has been probed by angle-resolved X-ray photoelectron spectroscopy. The bismuth segregation enthalpy has been evaluated.     

Photosynthetic membranes, 21. Immobilization of catalase by photochemically grafted ultrafiltration membranes

Catalase has been immobilized in membranes prepared by photoinduced grafting onto microporous polymeric supports and its catalytic activity on hydrogen peroxide decomposition has been studied under ultrafiltration conditions by means of a recirculation apparatus. The membranes showed a very good catalytic performance and the enzyme reaction took place exclusively within the membrane structure. Initial reaction rates measured in the temperature range 5 – 35°C as a function of both substrate concentration and enzyme amount immobilized per unit membrane surface indicate that the mechanism of action of catalase is not altered after immobilization.     

A model study for release of plasticizers from polymer films through vapor phase

A model has been applied to release of plasticizers from polymer films through vapor phase, for which the overall rate of release may be generally determined by evaporation of the plasticizer from the surface of the film, and/or by migration to the surface at below saturation in the polymer. The experimental system employed made use of n-butyl formate, diethyl-phthalate, di-n-butylphthalate, and N,n-butylbenzenesulfonamide as model molecules in polycaprolactam films, both with the aims of studying undesirable loss of plasticizers, and of simulating a model able to envisage releasing, at a constant rate, of any desired additive, with relatively high solubility and vapor pressure, to the content of packaging films. Experimental measurements were made (at 298–333 K) by investigating in a suitable cell the permeation of plasticizers both at concentrations below and above the saturation limit. Rate of evaporation of plasticizers from the membrane surface above the saturation limit, measured in this cell, were found to coincide satisfactorily with those calculated by application of the mass transfer theory to evaporation from a stationary liquid into a stirred gas, at a known velocity of gas flowing past the surface. From these latter rates and solubilities, the mass transfer coefficients H for evaporation could be obtained, as well as from experimental time lags the diffusivities D_p through the polymer membrane. In the light of the theoretical model a correlation was found between activation energies of H and evaporation enthalpies of the model molecules.