Numerical stability analysis of submerged slopes subject to rapid sedimentation processes

In this paper, the stability of infinitely long submerged slopes subject to rapid sedimentation processes is theoretically/numerically investigated. In particular, rapid deposition is considered as a potential triggering factor for static liquefaction in inclined loose sand layers. The corresponding initial boundary value problem is numerically analysed by employing a one-dimensional finite difference scheme in conjunction with two distinct versions of the same constitutive model—elasto-plastic and elasto-viscoplastic (EV). The EV approach is shown to be the most suitable for describing the onset of liquefaction phenomena, since its mathematical well-posedness and numerical stability are never lost. The results of parametric analyses for both homogeneous and inhomogeneous strata are critically discussed in the light of some case history data concerning natural and anthropic sedimentation processes.     

A sinapic acid–calix[4]arene hybrid selectively binds Pb over Hg and Cd

The binding affinity for Pb²⁺, Cd²⁺ and Hg²⁺ of the sinapic acid–calix[4]arene hybrid 2, having four sinapyl pendants at the upper rim, has been investigated via an UV–Vis study. Compound 2 has better complexing ability than the monomeric p-phenetidine derivative 1. This highlights that the clustering of sinapyl units in a basket-like structure, dictated by the calixarene scaffold, greatly enhances the complexing properties. Ligand 2 forms complexes even with Hg²⁺, which is not complexed by 1 at all; the complexes formed by 2 with Pb²⁺ and Cd²⁺ are much stronger than the analogous complexes formed by 1. The UV–Vis investigation shows that the hybrid 2 markedly favors Pb²⁺ over Cd²⁺ and Hg²⁺. Information on the structural properties of the complex species was obtained by ¹H NMR spectroscopy. NMR data show that all three metal ions are placed into the cavity consisting of the calixarene scaffold and the sinapyl pendants, though their binding affects the coordinating regions to a different extent.     

A microcalorimetric enzymatic method for trehalose determination in food

As trehalose is a glucose font and also an additive in food, a new reliable method for trehalose determination is proposed. The analytical method uses an isothermal microcalorimeter, directly relates the analyte concentration with the heat variation of the enzymatic decomposition of trehalose into two glucose molecules. The enzymatic reaction is performed inside the calorimeter in the presence of trehalase enzyme immobilized on amino activated glass beads. Through the calibration curve, the trehalose quantity in some food samples (mushrooms and honey) has been determined. The calorimetric procedure was compared to a previously identified methodology based on an amperometric biosensor.     

DNA interaction of platinum(II) complexes with 1,10-phenanthroline and extended phenanthrolines

The interaction with DNA of the platinum(II) square planar complexes [Pt(N-N)(py)(2)](2+) (N-N = 1,10-phenanthroline (phen), dipyrido[3,2-d:2',3'-f]quinoxaline (dpq), dipyrido[3,2-a:2',3'-c]phenazine (dppz), benzodipyrido[b:3,2-h:2'3'-f]phenazine (bdppz)) has been investigated by means of absorption, circular and linear dichroism spectroscopy, DNA melting, and viscosity. In the presence of excess [DNA] all the complexes intercalate to the double helix. For those with the most extended phenanthrolines the binding mode depends on the [DNA]/[complex] ratio (q); at low q values the substances bind externally to DNA probably self-aggregating along the double helix. When the DNA concentration is large enough, the aggregate breaks up and the complex intercalates within the nucleobases. The complexes self-aggregate, without added DNA, in the presence of a large salt concentration.     

On the Influence of the Kinetic Energy¶on the Stability of Equilibria¶of Natural Lagrangian Systems

Natural Lagrangian systems (T,Π) on R ² described by the equation are considered, where is a positive definite quadratic form in and Π(q) has a critical point at 0. It is constructively proved that there exist a C ^∞ potential energy Π and two C ^∞ kinetic energies T and such that the equilibrium q(t)≡ 0 is stable for the system (T,Π) and unstable for the system . Equivalently, it is established that for C ^∞ natural systems the kinetic energy can influence the stability. In the analytic category this is not true. Accepted: October 20, 1999     

A Silver Monochrome “Concetto spaziale” by Lucio Fontana: A Spectroscopic Non- and Micro-Invasive Investigation of Materials

In several of his artworks, for instance the Venezie cycle, Fontana employed metallic paints; previous investigations on such materials highlighted the use of different synthetic binders and of thick paint layers below the metal one, having different colours to change the visual perception of the metallic surface. In the present work, a monochrome silver “Concetto spaziale” by the Italo–Argentine artist belonging to a private collection recently gifted to the museum of the Church of San Fedele in Milano, Italy, was investigated to deepen the knowledge of this particular group of Fontana’s paintings. The artwork was initially visually inspected in visible and ultraviolet (UV) light. Subsequently, a non-invasive spectroscopic investigation was performed by X-ray fluorescence (XRF), reflection Fourier-transform infrared (FTIR) and Raman spectroscopy. A minute fragment of silver-coloured paint was taken from the reverse of the painting, near the cut edge, and examined by scanning electron microscopy coupled with energy dispersive X-ray analysis (SEM-EDX) and micro-Fourier-transform Raman (FT-Raman) spectroscopy. The analytical data made it possible to identify the composition of the metallic paint layer and of the underlying dark one, both from the point of view of the pigments and of the binders used, also highlighting the potential of the non-invasive and micro-invasive methods adopted in the investigation.     

The Small Molecule PPARγ Agonist GL516 Induces Feeding-Stimulatory Effects in Hypothalamus Cells Hypo-E22 and Isolated Hypothalami

PPARγ agonists are implicated in the regulation of diabetes and metabolic syndrome and have therapeutic potential in brain disorders. PPARγ modulates appetite through its central effects, especially on the hypothalamic arcuate nucleus (ARC). Previous studies demonstrated that the small molecule GL516 is a PPARγ agonist able to reduce oxidative stress and apoptosis with a potential neuroprotective role. Herein, we investigated the effects of GL516, in vitro and ex vivo, on the levels of hypothalamic dopamine (DA) and serotonin (5-HT). The gene expressions of neuropeptide Y, CART, AgRP, and POMC, which play master roles in the neuroendocrine regulation of feeding behavior and energy balance, were also evaluated. HypoE22 cells were treated with H₂O₂ (300 μM) for 2 h e 30’ and with different concentrations of GL516 (1 nM-100 µM). The cell viability was evaluated after 24 and 48 h of culturing using the MTT test. DA and 5-HT levels in the HypoE22 cell supernatants were analyzed through HPLC; an ex vivo study on isolated hypothalamic specimens challenged with scalar concentrations of GL516 (1–100 µM) and with pioglitazone (10 µM) was carried out. The gene expressions of CART, NPY, AgRP, and POMC were also determined by a quantitative real-time PCR. The results obtained showed that GL516 was able to reduce DA and 5-HT turnover; moreover, it was effective in stimulating NPY and AgRP gene expressions with a concomitant reduction in CART and POMC gene expressions. These results highlight the capability of GL516 to modulate neuropeptide pathways deeply involved in appetite control suggesting an orexigenic effect. These findings emphasize the potential use of GL516 as a promising candidate for therapeutical applications in neurodegenerative diseases associated with the reduction in food intake and stimulation of catabolic pathways.     

Lyotropic mesomorphism of alkyl esters of acyl-L-carnitines

The lyotropic polymorphism of a series of alkyl esters of acyl-L-carnitine has been studied by optical polarizing microscopy and X-ray diffraction. The different structures observed as a function of concentration and temperature have been characterized and their topology determined. As a result, two different phase sequence patterns have been detected: esters of normal alcohols bearing an alkyl chain of 6 or more carbon atoms in the acyl substituent display only a lamellar phase, while compounds which bear a relatively short alkyl chain (4 or less carbon atoms) show in addition non-lamellar type I hexagonal and cubic Q²³⁰ phases. From the analysis of the areas-per-molecule at the polar/apolar interface, the ability of the compounds investigated to form not only non-lamellar phases, but also direct micelles in isotropic solution has been related to the structural characteristics of the molecules. Curved, convex interfaces (in micelles and in non-lamellar phases) are possible only for the most polar acylcarnitines which have a relatively short alkyl chain, so that they behave like single chain surfactants; the most paraffinic derivatives, which have a relatively long alkyl chain, are effective double chain surfactants and then generate only quasi-planar interfaces.