Effectiveness of combined use of verapamil and adenosine triphosphate in experimental animals

A wide application of ATP to abolish reciprocal paroxysmal tachycardia is limited by frequent and adverse effects of the drug. Experiments on 49 rats have revealed that successive intravenous injections of verapamil and ATP have a more pronounced and prolonged action than the drugs alone. It is assumed that decreased pacemaker activity of sinus nodal cells and reduced atrioventricular conduction ("binodal dysfunction") are as a result of drug calcium channel block in the cellular membranes of myocytes. Potentiation of the pharmacological action of the drugs in question may be used in the clinical setting to lower an ATP dose and to reduce the incidence of adverse effects.     

Surface morphology and optical properties of porphyrin/Au and Au/porphyrin/Au systems

Porphyrin/Au and Au/porphyrin/Au systems were prepared by vacuum evaporation and vacuum sputtering onto glass substrate. The surface morphology of as-prepared systems and those subjected to annealing at 160°C was studied by optical microscopy, atomic force microscopy, and scanning electron microscopy techniques. Absorption and luminescence spectra of as-prepared and annealed samples were measured. Annealing leads to disintegration of the initially continuous gold layer and formation of gold nanoclusters. An amplification of Soret band magnitude was observed on the Au/meso-tetraphenyl porphyrin (TPP) system in comparison with mere TPP. Additional enhancement of luminescence was observed after the sample annealing. In the case of sandwich Au/porphyrin/Au structure, suppression of one of the two porphyrins’ luminescence maxima and sufficient enhancement of the second one were observed.     

Premium quality renewable diesel fuel by hydroprocessing of sunflower oil

Hydroprocessing of neat sunflower oil was carried out at 360-420 °C and 18 MPa over a commercial hydrocracking catalyst in a bench scale fixed bed reactor. In the studied experimental range, products consisted exclusively of hydrocarbons that differed significantly in composition. While the concentration of n-alkanes exceeded 67 wt.% in the reaction products collected at 360 °C, it decreased to just 20 wt.% in the product obtained at 420 °C. Consequently, the fuel properties of the latter product were very similar to those of standard (petroleum-derived) diesel fuel. Particularly, it exhibited excellent low-temperature properties (cloud point −11 °C; CFPP −14 °C). Reaction products obtained at 400 and 420 °C were blended into petroleum-derived diesel fuel in three concentration levels ranging from 10 to 50 wt.% and the fuel properties of these mixtures were evaluated. Diesel fuel mixtures containing the product of sunflower oil hydrocracking at 420 °C showed very good low-temperature properties including cloud point (−8 °C) and CFPP (−15 °C) that was further lowered to −25 °C due to addition of flow improvers.     

"Soft and rigid" dithiols and Au nanoparticles grafting on plasma-treated polyethyleneterephthalate

ABSTRACT: Surface of polyethyleneterephthalate (PET) was modified by plasma discharge and subsequently grafted with dithiols (1, 2-ethanedithiol (ED) or 4, 4'-biphenyldithiol) to create the thiol (-SH) groups on polymer surface. This "short" dithiols are expected to be fixed via one of -SH groups to radicals created by the plasma treatment on the PET surface. "Free" -SH groups are allowed to interact with Au nanoparticles. X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and electrokinetic analysis (EA, zeta potential) were used for the characterization of surface chemistry of the modified PET. Surface morphology and roughness of the modified PET were studied by atomic force microscopy (AFM). The results from XPS, FTIR, EA and AFM show that the Au nanoparticles are grafted on the modified surface only in the case of biphenyldithiol pretreatment. The possible explanation is that the "flexible" molecule of ethanedithiol is bounded to the activated PET surface with both -SH groups. On the contrary, the "rigid" molecule of biphenyldithiol is bounded via only one -SH group to the modified PET surface and the second one remains "free" for the consecutive chemical reaction with Au nanoparticle. The gold nanoparticles are distributed relatively homogenously over the polymer surface.     

Mathematical modeling of AC electroosmosis in microfluidic and nanofluidic chips using equilibrium and non-equilibrium approaches

AC electroosmotic micropumps are suggested to be powerful tools for electrolyte dosing in various micro- and nanofluidic systems. In this paper, we compare two modeling approaches for studying the AC electroosmosis in the following micro and nanochannel systems: (i) a traveling-wave AC pump with a spatially continuous wave of electric potential applied on a planar boundary, (ii) a traveling-wave AC pump with a wave of electric potential applied on a set of discrete planar electrodes, and (iii) an AC pump with a set of non-planar electrodes. The equilibrium approach is based on the use of capacitor–resistor boundary conditions for electric potential and the slip boundary conditions for velocity at electrode surfaces. The non-equilibrium approach uses the mathematical model based on the Poisson equation and the non-slip boundary conditions. We have observed discrepancies between the predictions given by the both models and then we have identified their possible reasons. The comparison of the equilibrium and non-equilibrium results further showed three important actualities: (a) how the equilibrium model overestimates or underestimates the net velocity, (b) how the velocity maxima in the frequency characteristics can be shifted, if the equilibrium model assumptions are not satisfied, (c) the parametric region where the equilibrium model is applicable. Because the data are obtained in a dimensionless form, they can be exploited for AC electroosmotic studies. We discuss the limitations of the equilibrium and non-equilibrium models and compare selected predictions with available experimental data.     

Investigation of purified sulfate turpentine on engine performance and exhaust emission

This study deals with an experimental work that aims to examine effects of purified sulfate turpentine obtained from a kraft pulp mill in Turkey on an engine performance and exhaust emissions of a spark ignition engine. Three fuel samples are used to test the performance and emission of a 1300 cc engine manufactured by TOFA?. They are pure gasoline with 98-octane number and two other gasoline-turpentine fuel samples obtained by blending gasoline with turpentine in ratios of 5% and 10% on basis of total mass of the fuel. The thermophysical properties of the fuels are acquired by density, viscosity, flash and fire points, sulphur content, heating value and distillation tests. The experimental results showed that the turpentine has a positive effect on the engine performance parameters, such as brake power, thermal efficiency, mean effective pressure and specific fuel consumption. The turpentine also increases pollutant NO_x, unburned hydrocarbon contents and exhaust temperature, but it decreases CO concentration in the exhaust. It is observed that utilization of the sulfate turpentine alone is not viable and it needs to be used as an additive into gasoline to some extent, thereby providing a viable alternative to pure gasoline.     

Hydrogenation of phenylacetylene and 3-phenylpropyne using Rh(diene) complexes under homogeneous and heterogeneous conditions

Hydrogenation of phenylacetylene (PA) and 3-phenylpropyne (PP) was carried out using [Rh(diene)Cl]₂ complexes (diene is hexadiene (HD), cycloocta-1,5-diene (COD), norborna-2,5-diene (NBD)) in their immobilized forms and compared with hydrogenation in homogeneous arrangement. Immobilization brings significant increase of the catalytic activity and product selectivity in the step-wise hydrogenation to corresponding vinyl-resp. allyl-benzenes. Diene-ligand effect was apparent in PA hydrogenation; the product selectivity decreased in order Rh(HD) > Rh(NBD) > Rh(COD) and catalytic activity decreased in order Rh(HD) > Rh(COD) > Rh(NBD).     

The synthesis of N-derivatives of 3-aminoperylene and their absorption and fluorescence properties

N-Acetyl and N-triazinyl 3-aminoperylenes were prepared. N-(4,6-Dichloro-1,3,5-triazin-2-yl)-3-aminoperylene was synthesized by the condensation of 3-aminoperylene with cyanuric chloride; other N-triazinyl derivatives were prepared by the successive substitution of chlorine atoms with methoxy or aniline groups. The structure and purity of the compounds were confirmed by elemental analysis, NMR spectroscopy and mass spectrometry. The UV/vis absorption, fluorescence and excitation spectra as well as the fluorescence quantum yields for the compounds were measured in dibutyl ether, 1,4-dioxane, ethyl acetate and acetonitrile; fluorescence lifetimes were measured in ethyl acetate and dimethyl sulfoxide. The influences of both the character of the N-substituent and the solvent polarity upon the spectra and quantum yields are discussed.     

Surface properties of poly(ethylene terephthalate) foils of different thicknesses

Surface properties of commercially available poly(ethylene terephthalate) (PET) foils of different thicknesses (3, 13, 23, 50, and 100 μm) were characterized using different analytical methods. Surface roughness and morphology were determined by atomic force microscopy, goniometry was used for determination of contact angle (wettability of surface) and electrokinetical analysis (zeta potential) for characterization of surface polarity and conductivity. X-ray photoelectron spectroscopy was used for characterization of PET surface chemistry. Infrared spectroscopy and differential scanning calorimetry (DSC) were used for determination of crystallinity portion. By DSC analysis, it was confirmed that the crystallinity portion depends on the foil thickness. Most important result of this study is that the surface properties of PET foils depend not only on the foil thickness but also on the foil side under study. This finding may be of importance for future experiments performed on PET foils and for their application in tissue engineering or microelectronics.     

Non-natural aglycones of glycopeptide antibiotics of the vancomycin group. Synthesis and antibacterial activity

A new approach for the modification of the heptapeptide core of glycopeptide antibiotics was proposed based on the replacement of amino acid residues in positions 1 and 3 in teicoplanin aglycone and in position 1 in the eremomycin aglycone. Six novel nonnatural aglycones of the vancomycin type were obtained. Compounds derived from the teicoplanin aglycone exhibited in vitro activity against Gram-positive bacteria, and two of them were also active against the vancomycin-resistant enterococci.