Antidiabetic properties and mechanism of action of Gynura procumbens water extract in streptozotocin-induced diabetic rats

Gynura procumbens (Lour.) Merr (family Compositae) is cultivated in Southeast Asia, especially Indonesia, Malaysia and Thailand, for medicinal purposes. This study evaluated the in vivo hypoglycemic properties of the water extract of G. procumbens following 14 days of treatment and in vitro in RIN-5F cells. Glucose absorption from the intestines and its glucose uptake in abdominal skeletal muscle were assessed. The antidiabetic effect of water extract of G. procumbens leaves was investigated in streptozotocin-induced diabetic rats. The intraperitoneal glucose tolerance test (IPGTT) was performed in diabetic rats treated with G. procumbens water extract for 14 days. In the IPGTT, blood was collected for insulin and blood glucose measurement. After the IPGTT, the pancreases were collected for immunohistochemical study of β-cells of the islets of Langerhans. The possible antidiabetic mechanisms of G. procumbens were assessed through in vitro RIN-5F cell study, intestinal glucose absorption and glucose uptake by muscle. The results showed that G. procumbens significantly decreased blood glucose levels after 14 days of treatment and improved outcome of the IPGTT. However, G. procumbens did not show a significant effect on insulin level either in the in vivo test or the in vitro RIN-5F cell culture study. G. procumbens also showed minimal effects on β-cells of the islets of Langerhans in the pancreas. However, G. procumbens only significantly increased glucose uptake by muscle tissues. From the findings we can conclude that G. procumbens water extract exerted its hypoglycemic effect by promoting glucose uptake by muscles.     

Synthesis and Characterization of Iron Oxide Nanoparticles by Solid State Chemical Reaction Method

The iron oxide nanoparticles were synthesized by solid state chemical reaction method. The synthesized powders were characterized by XRD, SEM, EDAX and TG-DTA techniques. An average grain size of 10–20 nm for Maghemite and 80–85 nm for Hematite was calculated using XRD line broadening and SEM. The effect of different parameters such as annealing temperature, milling time, Fe⁺³:Fe⁺² concentration ratio have been investigated on the particle size and phase formation. Heat treatment of the produced powders in which Fe⁺³:Fe⁺² ratio equal to 2:1, resulted in tetragonal (Maghemite) and rombohedral (Hematite) structures at 300 and 600 °C, respectively. It was found that by changing Fe⁺³:Fe⁺² ratios from 2:1 to 1:2, hematite phase and from 2:1 to 1:1, Maghemite phase were formed at 300 °C. In addition with increasing milling time, the iron oxide particle size decreases, but there was no changing in the kind of phase.     

SmI2-mediated radical cyclizations directed by a C-Si bond

The use of a silicon stereocontrol element in cyclobutanol and cyclopentanol-forming cyclizations mediated by SmI(2) results in excellent diastereocontrol. The C-Si bond in the products of cyclization provides a versatile handle for further manipulation. An asymmetric route to cyclization substrates involving copper-catalyzed silyl transfer has also been developed.     

Fabrication, characterization and measurement of thermal conductivity of Fe3O4 nanofluids

Magnetite Fe₃O₄ nanoparticles were synthesized by a co-precipitation method at different pH values. The products were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and transmission electronic microscopy. Their magnetic properties were evaluated on a vibrating sample magnetometer. The results show that the shape of the particles is cubic and they are superparamagnetic at room temperature. Magnetic nanofluids were prepared by dispersing the Fe₃O₄ nanoparticles in water as a base fluid in the presence of tetramethyl ammonium hydroxide as a dispersant. The thermal conductivity of the nanofluids was measured as a function of volume fraction and temperature. The results show that the thermal conductivity ratio of the nanofluids increases with increase in temperature and volume fraction. The highest enhancement of thermal conductivity was 11.5% in the nanofluid of 3 vol% of nanoparticles at 40 °C. The experimental results were also compared with the theoretical models.     

Optical band gap and refractive index dispersion parameters of As x Se70Te30−x (0≤x≤30 at.%) amorphous films

Amorphous As _x Se₇₀Te_30?x thin films with (0≤x≤30 at.%) were deposited onto glass substrates by using thermal evaporation method. The transmission spectra T(λ) of the films at normal incidence were measured in the wavelength range 400–2500 nm. A straightforward analysis proposed by Swanepoel based on the use of the maxima and minima of the interference fringes has been used to drive the film thickness, d, the complex index of refraction, n, and the extinction coefficient, k. The dispersion of the refractive index is discussed in terms of the single-oscillator Wemple and DiDomenico model (WDD). Increasing As content is found to affect the refractive index and the extinction coefficient of the As _x Se₇₀Te_30?x films. With increasing As content the optical band gap increases while the refractive index decreases. The optical absorption is due to allowed indirect transition. The chemical bond approach has been applied successfully to interpret the increase of the optical gap with increasing As content.     

Improvements of physical and mechanical properties of electron beam irradiation—crosslinked EVA foams

In this work, ethylene–vinyl acetate (EVA) copolymer foams were prepared and crosslinked by using high‐energy electron beam (e‐beam) radiation (10 MeV). The effect of parameters such as irradiation dose, the contents of foaming agent, radiation activator, and radiation sensitizer on improvement of physical and mechanical properties of the EVA foamed samples were investigated. The foams were obtained through a four‐step process of melt mixing, forming, crosslinking, and foaming. During the melt mixing process EVA was compounded with different amounts of azodicarbonamide (ADCA) as a blowing agent, zinc oxide (ZnO) as a radiation activator, and trimethylol propane‐trimethacrylate (TMPTMA) as a radiation sensitizer. The samples were compression molded into flat sheets at low temperature (110°C) and were then radiation‐crosslinked by 20–80 kGy e‐beam. Finally, the crosslinked samples were converted to foams by a high temperature (210°C) compression molding process. The foamed samples were analyzed in terms of gel content, density, compression molding set, tensile properties, and micro‐structural features. It was found that an increase in absorbed radiation dosage increases crosslink density, elasticity, percentage recovery, tensile strength, and compression properties of the EVA foams. Due to the increased recovery the percentage of compression set was reduced. Similarly increasing the TMPTMA content in the formulation increased the crosslink density and the resulting mechanical properties. Contrary to these findings, addition of ADCA led to the formation of extra gases which in turn reduced the crosslink density, and resulted in the deterioration of the mechanical properties and hence an increase in the compression set. However, addition of ZnO and TMPTMA led to the formation of smaller and more uniform cell size with improved mechanical properties. Copyright © 2008 John Wiley & Sons, Ltd.     

Synthesis and spectroscopic studies of the charge transfer complexes of 2- and 3-aminopyridine

The interactions of the electron donors 2-aminopyridine (2APY) and 3-aminopyridine (3APY) with the π-acceptors tetracyanoethylene (TCNE), 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ), 2-chloro-1,3,5-trinitrobenzene (picryl chloride, PC), and 2,3,5,6-tetrachloro-1,4-benzoquinone (chloranil) were studied spectrophotometrically in chloroform at room temperature. The electronic and infrared spectra of the formed molecular charge transfer (CT) complexes were recorded. Photometric titration showed that the stoichiometries of the reactions were fixed and depended on the nature of both the donor and the acceptor. The molecular structures of the CT-complexes were, however, independent of the position of the amino group on the pyridine ring and were formulated as [(APY)(TCNE)], [(APY)(DDQ)], [(APY)(PC)], and [(APY) (chloranil)]. The formation constants (K_CT), charge transfer energy (E_CT) and molar extinction coefficients (_CT) of the formed CT-complexes were obtained.     

Electrocatalytic reduction of NAD+ at glassy carbon electrode modified with single-walled carbon nanotubes and Ru(III) complexes

A simple procedure was developed to prepare a glassy carbon electrode modified with carbon nanotubes and Ruthenium (III) complexes. First, 25 μl of dimethyl sulfoxide–carbon nanotubes solutions (0.4 mg/ml) was cast on the surface of the glassy carbon electrode and dried in air to form a carbon nanotube film at the electrode surface. Then, the glassy carbon/carbon nanotube-modified electrode was immersed into a Ruthenium (III) complex solution (direct deposition) for a short period of time (10–20 s for multiwalled carbon nanotubes and 20–40 s for single-walled carbon nanotubes). The cyclic voltammograms of the modified electrode in aqueous solution shows a pair of well-defined, stable, and nearly reversible redox couple, Ru(III)/Ru(II), with surface-confined characteristics. The attractive mechanical and electrical characteristics of carbon nanostructures and unique properties and reactivity of Ru complexes are combined. The transfer coefficient (α), heterogeneous electron transfer rate constants (k _s), and surface concentrations (Γ) for the glassy carbon/single-walled carbon nanotubes/Ru(III) complex-, glassy carbon/multiwalled carbon nanotubes/Ru(III) complex-, and glassy carbon/Ru(III) complex-modified electrodes were calculated using the cyclic voltammetry technique. The modified electrodes showed excellent catalytic activity, fast response time, and high sensitivity toward the reduction of nicotinamide adenine dinucleotide in phosphate buffer solutions at a pH range of 4–8. The catalytic cathodic current depends on the nicotinamide adenine dinucleotide concentration. In the presence of alcohol dehydrogenase, the modified electrode exhibited a response to addition of acetaldehyde. Therefore, the main product of nicotinamide adenine dinucleotide electroreduction at the Ru(III) complex/carbon nanotube-modified electrode was the enzymatically active NADH. The purposed sensor can be used for acetaldehyde determination.     

New formulae for higher order derivatives and applications

We present new formulae (the Slevinsky–Safouhi formulae I and II) for the analytical development of higher order derivatives. These formulae, which are analytic and exact, represent the kth derivative as a discrete sum of only k+1 terms. Involved in the expression for the kth derivative are coefficients of the terms in the summation. These coefficients can be computed recursively and they are not subject to any computational instability. As examples of applications, we develop higher order derivatives of Legendre functions, Chebyshev polynomials of the first kind, Hermite functions and Bessel functions. We also show the general classes of functions to which our new formula is applicable and show how our formula can be applied to certain classes of differential equations. We also presented an application of the formulae of higher order derivatives combined with extrapolation methods in the numerical integration of spherical Bessel integral functions.     

Control of chaos in atomic force microscopes using delayed feedback based on entropy minimization

Active chaos control of a tapping mode atomic force microscope (AFM) model via delayed feedback method is presented. The feedback gain is obtained and adapted according to a minimum entropy (ME) algorithm. In this method, stabilizing an unstable fixed point of the system Poincare map is achieved by minimizing the entropy of points distribution on the Poincare section. Simulation results show the feasibility of the proposed method in applying the delayed feedback technique for chaos control of an AFM system.