Antioxidant activity of novel indole derivatives and protection of the myocardial damage in rabbits

Novel indole derivatives containing a triazole moiety (1a-d, 2a-c) were synthesized as lead compounds with interesting pharmacological profiles. Their antioxidant activity was investigated on in vitro non-enzymatic rat hepatic microsomal lipid peroxidation. All compounds showed significant effect in the above assay. The effect depended mainly on the attachment position of the triazole moiety on the indole nucleus. The most potent antioxidant derivatives la, 1c and 1d were tested for their protective ability against the oxidative damage of the myocardium after ischemia-reperfusion, in male rabbits which were subjected to 30 min regional ischemia followed by reperfusion. The tested antioxidant compounds 1a, 1c and 1d were continuously infused for 30 min starting at 10th min of ischemia and lasted at 10th min of reperfusion. The concentration of malondialdehyde (MDA, a marker of lipid peroxidation) and hemodynamic parameters (blood pressure and heart rate) were measured in the baseline, at 20th min of the sustained ischemia, 1st and 20th min of reperfusion. It was found that the examined compounds la, 1c and 1d reduced significantly the level of MDA in rabbits under ischemia-reperfusion and proved to be promising substances for further evaluation of anti-ischemic properties.     

Oxidative cycloaddition of 1,1,3,3-tetramethyldisiloxane to alkynes catalyzed by supported gold nanoparticles

Gold nanoparticles supported on TiO(2) (0.1-1% mol) catalyze at room temperature and at extremely mild conditions the unprecedented oxidative cycloaddition of 1,1,3,3-tetramethyldisiloxane to alkynes, forming substituted 2,5-dihydro-1,2,5-oxadisiloles, with concomitant evolution of hydrogen gas. For the majority of the substrates, the yields are exceptional (up to 99%). The reaction proceeds at room temperature, tolerates a variety of functional groups, and can be performed in several solvents.     

Anti-Ageing Potential of S. euboea Heldr. Phenolics

In recent years, the use of Sideritis species as bioactive agents is increasing exponentially. The present study aimed to investigate the chemical constituents, as well as the anti-ageing potential of the cultivated Sideritis euboea Heldr. The chemical fingerprinting of the ethyl acetate residue of this plant was studied using 1D and 2D-NMR spectra. Isomeric compounds belonging to acylated flavone derivatives and phenylethanoid glycosides were detected in the early stage of the experimental process through 2D-NMR techniques. Overall, thirty-three known compounds were isolated and identified. Some of them are reported for the first time not only in S. euboea, but also in genus Sideritis L. The anti-ageing effect of the ethyl acetate residue and the isolated specialized products was assessed as anti-hyaluronidase activity. In silico docking simulation revealed the interactions of the isolated compounds with hyaluronidase. Furthermore, the in vitro study on the inhibition of hyaluronidase unveiled the potent inhibitory properties of ethyl acetate residue and apigenin 7-O-β-d-glucopyranoside. Though, the isomers of apigenin 7-O-p-coumaroyl-glucosides and also the 4′-methyl-hypolaetin 7-O-[6′′′-O-acetyl-β-d-allopyranosyl]-(1→2)-β-d-glucopyranoside exerted moderate hyaluronidase inhibition. This research represents the first study to report on the anti-hyaluronidase activity of Sideritis species, confirming its anti-inflammatory, cytotoxic and anti-ageing effects and its importance as an agent for cosmetic formulations as also anticancer potential.     

Byzantine wall paintings from Kastoria, northern Greece: spectroscopic study of pigments and efflorescing salts

This study concerns the investigation of pigments and efflorescence phenomena on the wall paintings of Kastoria, a rural, non-metropolitan Byzantine town. A large number of representative samples were collected from the murals of three churches, dated to post-Byzantine era (14th-17th c. AD). The identified pigments for the red colour were hematite (Fe2O3), cinnabar (HgS) and minium (Pb3O4), while brown and yellow colours were attributed to mixtures of ochres (Fe-oxides and hydroxides) and lime. The utilization of admixtures of iron, lead and mercury compounds was also attested in order to render specific tones on the painted surfaces. Black and dark blue hues were prepared using black carbon and Mn in some cases. Grey colours were assigned to a mixture of black carbon and lime. Green colour is rather attributed to admixtures of Fe-rich minerals and lime and not to the commonly used green earths. Baryte (BaSO4) was also evidenced as a filler or extender. Phosphorous was detected and connected to proteinaceous material and Mo and Sb were traced which are probably affiliated to Fe-oxides. Regarding efflorescing salts, the determined compounds are: calcite, dolomite, gypsum, halite, nitratine, natron and mirabilite, all of which are related to temperature and humidity changes and moisture fluctuations inside the wall paintings.     

Reaction of hydrosilanes with alkynes catalyzed by gold nanoparticles supported on TiO2

Gold nanoparticles supported on TiO₂ (0.8–1.4 mol %) catalyze the β-(E) regioselective hydrosilylation of a variety of functionalized terminal alkynes with alkylhydrosilanes in 1,2-dichloroethane (70 °C). The product yields are excellent, and the reaction times relatively short, while almost equimolar amounts of alkynes and hydrosilanes can be used. Minor side-products in up to 35% relative yield of cis-oxidative (dehydrogenative) disilylation, an unprecedented reaction pathway, are formed in the cases of the less hindered hydrosilanes and alkynes. Triethoxysilane reacts faster and affords apart from β-(E) addition products, minor α-hydrosilylation regio-isomers in upto 15% relative yield. Internal alkynes are generally less reactive or even unreactive. It is proposed that cationic Au(I) species stabilized by the support are the reactive catalytic sites, forming in the presence of hydrosilanes either silyl–Au(III)–H (hydrosilylation pathway) or Au(III)–disilyl species (dehydrogenative disilylation pathway). Regarding the mechanism of hydrosilylation, kinetic experiments are in agreement with silyl carbometallation of the triple bond in the rate determining step of the reaction.     

Initial stages of oxidation of a precipitation-hardening (PH) steel

The oxidation of a precipitation-hardening (PH) steels is a rather unexplored area. In this study an attempt is made to estimate the oxidation mechanism and the kinetics that take place up to 850 °C. For this purpose specimens of the material under examination were isothermally heated at 725, 775, 800, 825, and 850 °C for 12 h in O₂ atmosphere. The as-treated samples were examined with SEM and XRD, while kinetics were based on thermogravimetric (TG) results. From this examination it was deduced that the oxidation of this steel is accomplished at minimum three steps, following the changes of the scale morphology and the kinetics. After 850 °C although that the oxidation rate increases, the scale morphology does not change. From the calculations of the rate constant k _p and the activation energy for the phenomena below 850 °C, it was deduced that the oxidation phenomena during this stage provides another barrier to the deterioration of the ferrous material.     

Thermal,mineralogical and spectroscopic study of plasters from three post-Byzantine churches from Kastoria (northern Greece)

Several plaster samples were collected from the wall paintings of post-Byzantine monuments from Kastoria town, northern Greece. They were analysed mainly by simultaneous thermal analysis (TG-DTG/DTA) and X-ray diffraction and supplementary by electron microscope (ESEM-EDX) and Raman spectroscopy. Whitish and dark plaster layers were evident in most cases. Calcite, micas, and quartz were the dominant minerals, while dolomite, gypsum, and feldspar were detected as minor phases in most of the samples. Hydromagnesite and chlinochlore were also determined in a few samples. The utilisation of the results for chronological purposes (i.e. for assignment of different painting periods) was also suggested and the presence of dolomite and hydromagnesite could be characteristic for the provenance of the raw material. Gypsum was regarded mainly as a weathering product due to sulfation process, and secondly as a binding material of the plaster. The thermoanalytical results are in good agreement with the mineralogical data. The white plasters are categorized as hydraulic lime mortars, while the dark ones as natural pozzolanic mortars. Calcite and gypsum correlates well with their respective mass losses at certain temperature ranges and their Raman spectra are clearly detected. ESEM-EDX revealed fine calcareous components with aluminolisilicate aggregates and the application of the fresco technique either as a multi-layer or a single-layer plaster. The deterioration caused by salts (gypsum, halite, and nitratine) and micro-organisms was also determined. The detrimental effect of the salt crystallization and dissolution was also confirmed using the so-called Peltier-stage experiment.