Titanium dioxide nanoparticles catalyzed synthesis of Hantzsch esters and polyhydroquinoline derivatives

1,4-Dihydropyridine and polyhydroquinoline derivatives have been prepared efficiently in a one-pot synthesis via Hantzsch condensation using nanosized titanium dioxide as a heterogeneous catalyst. The present methodology offers several advantages such as excellent yields, short reaction times (30-120 min), environmentally benign, and mild reaction conditions. The catalyst can be readily separated from the reaction products and recovered in excellent purity for direct reuse

Thermoluminescence behavior of KClXBr1−X: in mixed crystals exposed to gamma radiation

In-doped KClXBr1−X (X=1, 0.75, 0.5, 0.25 and 0) mixed crystal has been grown by the Czochralski method. The segregation coefficient of In was studied by the inductively coupled plasma atomic emission spectrometry (ICP-OES). The crystal structure has been determined using X-ray diffraction (XRD) analysis. The thermoluminescence (TL) characterization of KClXBr1−X mixed crystals, exposed to gamma radiation has been performed. The results show the introduction of the dopants ions induced changes in the TL glow curve structure. The TL results suggest that doped KClXBr1−X mixed crystal has good potential active dosimeter applications for gamma ray irradiation

Curcumin: A new candidate for melanoma therapy?

Melanoma remains among the most lethal cancers and, in spite of great attempts that have been made to increase the life span of patients with metastatic disease, durable and complete remissions are rare. Plants and plant extracts have long been used to treat a variety of human conditions; however, in many cases, effective doses of herbal remedies are associated with serious adverse effects. Curcumin is a natural polyphenol that shows a variety of pharmacological activities including anti-cancer effects, and only minimal adverse effects have been reported for this phytochemical. The anti-cancer effects of curcumin are the result of its anti-angiogenic, pro-apoptotic and immunomodulatory properties. At the molecular and cellular level, curcumin can blunt epithelial-to-mesenchymal transition and affect many targets that are involved in melanoma initiation and progression (e.g., BCl2, MAPKS, p21 and some microRNAs). However, curcumin has a low oral bioavailability that may limit its maximal benefits. The emergence of tailored formulations of curcumin and new delivery systems such as nanoparticles, liposomes, micelles and phospholipid complexes has led to the enhancement of curcumin bioavailability. Although in vitro and in vivo studies have demonstrated that curcumin and its analogues can be used as novel therapeutic agents in melanoma, curcumin has not yet been tested against melanoma in clinical practice. In this review, we summarized reported anti-melanoma effects of curcumin as well as studies on new curcumin formulations and delivery systems that show increased bioavailability. Such tailored delivery systems could pave the way for enhancement of the anti-melanoma effects of curcumin. © 2016 UIC

Finite quantum tomography via semidefinite programming

Using the the convex semidefinite programming method and superoperator formalism we obtain the finite quantum tomography of some mixed quantum states such as: qudit tomography, N-qubit tomography, phase tomography and coherent spin state tomography, where that obtained results are in agreement with those of References \cite{schack,Pegg,Barnett,Buzek,Weigert}.Comment: 25 page

Preliminary study of improving reservoir quality of tight gas sands in the near wellbore region by microwave heating

The formation damages, such as water blocking and clay swelling, in tight gas reservoir have been recognized as severe problems impairing gas production. To remedy these damages, formation heat treatment (FHT) was taken as one of the effective measures by some researchers. In this paper, the effects of microwave heating on the petrophysical properties of sandstone samples has been investigated. A modified commercial microwave oven was used to heat the core plugs and aluminum tubes were used to accommodate tight sandstone samples in order to confine them and reduce their contact with air. After microwave heating, any alterations in the porosity, permeability, texture, structure, mineralogy, and pore size distribution of tight sandstones were investigated by a series of lab experiments. By subjecting tight sandstone samples to microwave, the surface temperature of sandstone can be elevated to approximately 400 °C or more. The intense heat is effective in changing the structure, texture and mineralogy of the sandstone. The shrinkage or decomposition of minerals, which are shown by XRD analysis, and generation of micro-fractures created more spaces in the samples.By employing Automated Permeameter, porosity and permeability are found increased after heating. Nuclear Magnetic Resonance (NMR) and CT numbers of all samples after microwave heating indicate the increase of porosity as well. Moreover, the NMR T2 distribution reveals the smaller pores diminished, so the incremental porosity of short NMR T2 decreased. Micro-fractures generated between grains or in grains due to decomposition of some cement minerals and clay shrinkage, so the amplitude of long NMR T2 increased. The fractures are visible both in X-ray CT images and in Scanning Electronic Microscopy (SEM) images. By comparing with NMR T2 distribution data, it is found that the presence of micro-fractures accounts for the increased population of pores with T2 larger than 10 ms. The numerical simulation of microwave heating in the borehole indicates that the microwave heating is effective to raise the temperature of reservoir rock to approximately 900 °C within 1 day and to remove the water within a distance of 25 cm from the borehole wall. The efficiency of microwave heating can be further improved by optimizing the downhole microwave device

Solid-phase extraction followed by dispersive liquid-liquid microextraction for the sensitive determination of ecstasy compounds and amphetamines in biological samples

A novel approach for the determination of ecstasy and amphetamines (3,4-methylenedioxymethylamphetamine (MDMA, Ecstasy), 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxyethylamphetamine (MDEA) and 3,4-methylenedioxypropylamphetamine (MDPA)) in biological samples is presented. The analytes were extracted from the matrix and transferred to a small volume of a high density, water insoluble solvent using solid-phase extraction (SPE) followed by dispersive liquid-liquid microextraction (DLLME). This combination not only resulted in a high enrichment factor, but also it could be used in complex matrices (biological samples). Some important extraction parameters, such as sample solution flow rate, sample pH, type and volume of extraction and disperser solvents as well as the salt addition, were studied and optimized. Under the optimized conditions, the calibration graphs were linear in the range of 0.5-500 µg L-1 and 1.0-500 µg L-1 with detection limits in the range of 0.1-0.3 µg L-1 and 0.2-0.7 µg L-1 in urine and plasma samples, respectively. The results showed that SPE-DLLME is a suitable method for the determination of ecstasy components and amphetamines in biological and water samples. KEY WORDS: Dispersive liquid-liquid microextraction, Solid-phase extraction, Ecstasy compounds, Amphetamines, Gas chromatography, Biological samples Bull. Chem. Soc. Ethiop. 2014, 28(3), 339-348.DOI: http://dx.doi.org/10.4314/bcse.v28i3.

Application of Ultrasound-assisted Emulsification Microextraction followed by Gas Chromatography for Determination of Oxadiazon in Water and Soil Samples

In this study, a simple and efficient ultrasound-assisted emulsification microextraction (USAEME) method combined with gas chromatography (GC) was developed for the preconcentration and determination of oxadiazon in water and soil samples. In this method, fine droplets of toluene were formedand dispersed in the sample with the help of ultrasonic waves which accelerated the formation of a fine cloudy solution without using disperser solvents. Several factors influencing the extraction efficiency, such as the nature and volume of organic solvent, extraction temperature, ionic strength and centrifugation time, were investigated and optimized. Using optimum extraction conditions a detection limit of 0.1 μg L–1 and a good linearity in a calibration range of 0.25–250 μg L–1 were achieved for the analyte in a river water sample. This proposed method was successfully applied to the analysis of oxadiazon in water and soil samples.KEYWORDS Utrasound-assisted emulsification microextraction, oxadiazon, gas chromatography, water samples, soil samples