Antioxidant and Antisteatotic Activities of a New Fucoidan Extracted from Ferula hermonis Roots Harvested on Lebanese Mountains

Fucoidan is a fucose-rich sulfated polysaccharide with attractive therapeutic potential due to a variety of biological activities, including antioxidant action. Fucoidan is typically found in the cell wall of marine brown algae, but extra-algal sources have also been discovered. In the present work, for the first time we extracted a water soluble fucoidan fraction from the roots of the terrestrial shrub Ferula hermonis. This fucoidan fraction was termed FUFe, and contained fucose, glucose, sulfate, smaller amounts of monosaccharides such as galactose and mannose, and a minor quantity of proteins. FUFe structural features were investigated by FTIR, ¹H NMR and ¹³C NMR spectroscopy. The antioxidant property of FUFe was measured by DPPH, ABTS and FRAP assays, which revealed a high radical scavenging capacity that was confirmed in in vitro cellular models. In hepatic and endothelial cells, 50 μg/mL FUFe could reduce ROS production induced by intracellular lipid accumulation. Moreover, in hepatic cells FUFe exhibited a significant antisteatotic action, being able to reduce intracellular triglyceride content and to regulate the expression of key genes of hepatic lipid metabolism. Altogether, our results candidate FUFe as a possible bioactive compound against fatty liver disease and related vascular damage.     

Kinetics of Oxidative Cracking of n-Hexane to Light Olefins using Lattice Oxygen of a VOx/SrO-γAl2O3 Catalyst

The kinetics of oxidative cracking of n-hexane to light olefins using the lattice oxygen of VO_x/SrO-γAl₂O₃ catalysts has been investigated. Kinetic experiments were conducted in a CREC Riser Simulator (CERC: Chemical Reactor Engineering Center), which mimics fluidized bed reactors. The catalyst's performance is partly attributed to the moderate interaction between active VO_x species and the SrO-γAl₂O₃ support. This moderate interaction serves to control the release of lattice oxygen to curtail deep oxidation. The incorporation of basic SrO component in the support also helped to moderate the catalyst's acidity to checkmate excessive cracking. Langmuir-Hinshelwood model was applied to formulate the rate equations. The intrinsic kinetic parameters were obtained by fitting the experimental data to the kinetic model using a nonlinear regression algorithm at a 95% confidence interval, implemented in MATLAB. n-Hexane transforms to olefins at a specific reaction rate of 1.33 mol/gcat.s and activation energy of 119.2 kJ/mol. These values when compared with other duplets (i. e., ki° and E_A) for paraffins to olefins, show that indeed olefins are stable products of the oxidative conversion of n-hexane over VO_x/SrO-γAl₂O₃ under a fluidized bed condition. Values of activation energy for all CO_x formation routes indicate that intermediate paraffins are likely to be cracked to form CH₄ than to be converted directly to CO_x. On the other hand, olefins may transform partly, and directly to CO_x (E₉=9.65 kJ/mol) than to form CH₄ (E₈=89.1 kJ/mol) in the presence of excess lattice oxygen. Overall, olefins appear to be stable to deep oxidation due to the role of SrO in controlling the amount of lattice oxygen of the catalyst at the reaction temperature.     

In vitro drug release characteristic and cytotoxic activity of silibinin-loaded single walled carbon nanotubes functionalized with biocompatible polymers

In this paper, we demonstrate the preparation of silibinin-loaded carbon nanotubes (SWSB) with surface coating agents via non-covalent approach as an effective drug delivery system. The resulting surface-coated SWSB nanocomposites are extensively characterized by Fourier transform infrared (FTIR) and Raman spectroscopies, ultraviolet–visible (UV–Vis) spectrometry and field emission scanning electron microscopy (FESEM). The FTIR and Raman studies show that an additional layer is formed by these coating agents in the prepared nanocomposites during the coating treatment and these results are confirmed by FESEM. Drug loading and release profiles of the coated SWSB nanocomposites in phosphate buffered saline solution at pH 7.4 is evaluated by UV–Vis spectrometry. The in vitro results indicate that the surface-modified nanocomposites, with SB loading of 45 wt%, altered the initial burst and thus, resulted in a more prolonged and sustained release of SB. In addition, these nanocomposites exhibit a pseudo-second-order release kinetic which was driven by the ion exchange between the ionized SWSB and the anions in the release medium. The cytotoxicity effect of the resulting nanocomposites on normal mouse fibroblast cells is evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. It is observed that the surfactant and polymer coating improved the biocompatibility of the SWSB nanocomposites significantly, which deem further exploitation for their application as potential anticancer drug delivery system.     

Quantile regression with group lasso for classification

Applications of regression models for binary response are very common and models specific to these problems are widely used. Quantile regression for binary response data has recently attracted attention and regularized quantile regression methods have been proposed for high dimensional problems. When the predictors have a natural group structure, such as in the case of categorical predictors converted into dummy variables, then a group lasso penalty is used in regularized methods. In this paper, we present a Bayesian Gibbs sampling procedure to estimate the parameters of a quantile regression model under a group lasso penalty for classification problems with a binary response. Simulated and real data show a good performance of the proposed method in comparison to mean-based approaches and to quantile-based approaches which do not exploit the group structure of the predictors.     

Asymptotic behavior of a generalized Cahn–Hilliard equation with a mass source

We consider in this article a generalized Cahn–Hilliard equation with mass source (nonlinear reaction term) which has applications in biology. We are interested in the well-posedness and the study of the asymptotic behavior of the solutions (and, more precisely, the existence of finite-dimensional attractors). We first consider the usual Dirichlet boundary conditions and then Neumann boundary conditions. The latter require additional assumptions on the mass source term to obtain the dissipativity. Indeed, otherwise, the order parameter u can blow up in finite time. We also give numerical simulations which confirm the theoretical results.     

Retrieving the time-dependent thermal conductivity of an orthotropic rectangular conductor

The aim of this paper is to determine the thermal properties of an orthotropic planar structure characterized by the thermal conductivity tensor in the coordinate system of the main directions (Oxy) being diagonal. In particular, we consider retrieving the time-dependent thermal conductivity components of an orthotropic rectangular conductor from nonlocal overspecified heat flux conditions. Since only boundary measurements are considered, this inverse formulation belongs to the desirable approach of non-destructive testing of materials. The unique solvability of this inverse coefficient problem is proved based on the Schauder fixed point theorem and the theory of Volterra integral equations of the second kind. Furthermore, the numerical reconstruction based on a nonlinear least-squares minimization is performed using the MATLAB optimization toolbox routine lsqnonlin. Numerical results are presented and discussed in order to illustrate the performance of the inversion for orthotropic parameter identification.     

Part III: Study of Tissue Distribution and Retention

The tissue distribution of colloidal zirconyl phosphate-P₃₂ and its retention following i.m and i.v. injection in mice were studied. About 63 per cent of the i.m. injected P₃₂ activity was retained at the site of injection after 5 days, suggesting the use of the colloid in the local treatment of tumours. The deposition of the colloid in bone and liver after i.v. injection presented zirconyl phosphateP₃₂ as useful in the radiotherapy of bone and liver disease.     

Synthesis and characterization of [4-(2,4-dichlorophenoxybutyrate)-zinc layered hydroxide] nanohybrid

A new layered organic–inorganic nanohybrid material in which an agrochemical, 4-(2,4-dichlorophenoxy)butyrate (DPBA) is intercalated into inorganic interlayers of zinc layered hydroxide (ZLH) was synthesized by direct reaction of aqueous DPBA solution with zinc oxide. The resulting nanohybrid is composed of the organic moieties, DPBA sandwiched between ZLH inorganic interlayers. The nanohybrid afforded well ordered crystalline layered structure, a basal spacing of 29.6 Å, 23.5% carbon (w/w) and 47.9% (w/w) loading of DPBA. FTIR study shows that the absorption bands of the resulting nanohybrid composed the FTIR characteristics of both the DPBA and ZLH which further confirmed the intercalation episode. The intercalated organic moiety in the form of nanohybrid is thermally more stable than its sodium salt. Scanning electron micrograph shows the ZnO precursor has very fine granular structure and transformed into a flake-like when the nanohybrid is formed. This work shows that the nanohybrid of DPBA-ZLH can be synthesized using simple, direct reaction of ZnO and DPBA under aqueous environment for the formation of a new generation of agrochemical.     

Macrocyclic Systems Containing 2,6,9-Trioxabicyclo[3.3.1]-nona-3,7-dienes as Chiral Spacer Groups: Synthesis,Stereochemical Features and Preliminary Complexation Properties

Novel 2:2-macrocycles bearing bridged concave 2,6,9-trioxabicyclo[3.3.1]nona-3,7-dienes as chiral spacer units were obtained by cyclocondensation reaction of the chiral bisacid chloride and the corresponding diols, while use of methylene diamines instead of diols afforded 1:1 macrocycles only. Applying the same, but now template-assisted, experimental procedure to the reaction of the bisacid chloride with triethylene glycol brought about a significant increase in yield as well as a suitable simplification of the work-up during preparation and separation of the corresponding 1:1 as well as 2:2 macrocycles, when compared to results reported previously. HPLC separation on chiral columns revealed the presence of diastereoisomers [R,R(S,S)- and R,S-(meso)-forms] for all 2:2 macrocycles, which was further evidenced by the CD spectrum of one of those species as an example. Preliminary ESI-MS experiments indicated strong complexation abilities of the sulphur-containing ligand towards Ag(I), Cu(II) and Au(III) ions.