Microdetermination of Xanthates

Summary A rapid, convenient and accurate method for the determination of xanthates has been developed. N-bromosuccinimide has been used to displace iodine from potassium iodide which in turn oxidizes xanthate to dixanthogen. The p_H 4 is optimum for the determination. The maximum relative standard deviation is 6% in the case of ethyl potassium xanthate when a 0.5 mg sample was taken.

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Zusammenfassung Ein genaues Verfahren zur raschen Bestimmung von Xanthat wurde entwickelt. N-Bromsuccinimid dient zur Freisetzung von Jod aus KJ; Jod oxydiert Xanthat zu Dixanthogen. Das optimale p_H für die Bestimmung ist 4. Die größte relative Standardabweichung ist 6% bei einer Einwaage von 0,5 mg Kaliumäthylxanthat.

     

Ion population fraction calculations using improved screened hydrogenic model with l-splitting

Ion population fraction(IPF) calculations are very important to understand the radiative spectrum emitted from the hot dense matter. IPF calculations require detailed knowledge of all the ions and correlation interactions between the electrons of an ion which are present in a plasma environment. The average atom models, e.g., screened hydrogenic model with l-splitting(SHML), now have the capabilities for such calculations and are becoming more popular for in line plasma calculations. In our previous work [Ali A, Shabbir Naz G, Shahzad M S, Kouser R, Rehman A and Nasim M H 2018 High Energy Density Phys. 26 48], we have improved the continuum lowering model and included the exchange and correlation effects in SHML. This study presents the calculation of IPF using classical theory of fluctuation for our improved screened hydrogenic model with l-splitting(I-SHML) under local thermodynamic equilibrium conditions for iron and aluminum plasma over a wide range of densities and temperatures. We have compared our results with other models and have found a very good agreement among them.     

An improved method of synthesis of N-protected L-amino acids as their benzoxymethyl esters

An improved method for the synthesis of L-amino acids as their benzoxymethyl esters has been reported. All the synthesized compounds were characterized by (1)H NMR, EI-MS and IR spectroscopic methods.     

One-step in-syringe dispersive liquid–liquid microextraction and GC-FID determination of trace amounts of di(2-ethylhexyl) phthalate and its metabolite in human urine samples

Di(2-ethylhexyl) phthalate (DEHP) is used as plasticizer in polyvinylchloride (PVC) plastics. Its metabolites and the parent phthalates are considered toxic. As the DEHP plasticizers are not chemically bound to PVC, they can migrate, evaporate or be leached into indoor air and atmosphere, foodstuff, and other materials. We have reported a novel, easy and available analytical method for the determination of DEHP and its metabolite, mono(2-ethylhexyl) phthalate (MEHP) in human urine samples by the in-syringe dispersive liquid–liquid microextraction method coupled with gas chromatography with flame ionization detector. The limits of detection and precision (RSD) were 2.5 μg/L and 1.4% for DEHP and 1.1 μg/L and 3.0% for MEHP, respectively. This method could be utilized for routine monitoring of the trace DEHP and MEHP in urine of human exposure to plasticizers.     

Electrocatalytic determination of chlorpromazine drug using Alizarin Red S as a mediator on the glassy carbon electrode

The anodic oxidation of chlorpromazine (CPZ) has been studied on a glassy carbon electrode by electrocatalytic effect of Alizarin Red S (ARS) as a homogenous mediator in universal buffer (pH = 2). The linear sweep voltammetry (LSV) studies showed that the catalytic current of this system depends on the concentration of CPZ. The magnitude of the peak current for ARS increased severely in the presence of CPZ, and proportional to CPZ concentration. The catalytic peak current was linearly dependent on CPZ concentration in the ranges of 10–500 μM and the detection limit was 5.16 μM by LSV. The diffusion coefficient of CPZ was estimated using chronoamperometry. The method also was used for estimation of catalytic rate constant at catalytic reaction between ARS and CPZ. The influences of potentially interfering substances on the current response of the system were examined. The importance of technique is because of its ability to electrocatalytic determination of CPZ with ARS as homogenous electrocatalyst, while it does not need to be prepared as for the modified electrode. The method was successfully applied for analysis of CPZ in solid pharmaceutical formulations.     

Nigella sativa extract as a potent antioxidant for petrochemical-induced oxidative stress

Various beneficial properties has been attributed to Nigella sativa, including its antioxidant potential. Previously, it was reported that supercritical fluid extraction (SFE) could be used to obtain N. sativa extract rich in antioxidants. In the present study, N. sativa extracts prepared using the previously optimized SFE as well as the traditional Soxhlet extraction approaches were analyzed for various known antioxidants. N. sativa extracts were found to prevent protein carbonyl formation as well as depletion of intracellular glutathione (GSH) in fibroblasts exposed to toluene. Furthermore, partially purified SFE and Soxhlet fractions could prevent loss of hepatic GSH in toluene-induced oxidative stressed Wistar rats as well as in L929 fibroblasts. The results showed that SFE-produced N. sativa extract is richer in antioxidants than the Soxhlet approach. It was also shown using preparative silica gel and reverse phase chromatography that different fractions of SFE-extracted or Soxhlet-extracted N. sativa had different levels of protective effects with regards to GSH depletion in vivo as well as in cell culture. Although fractions rich in thymoquinone were found to be most potent in terms of antioxidant capacity, the data indicates that the protective effects of N. sativa may not only be due to thymoquinone, but perhaps other antioxidants.     

MnZnFe nanoparticles for self-controlled magnetic hyperthermia

Manganese zinc iron magnetic nanoparticles were synthesized by a co-precipitation method for application as hyperthermia inducing agents. The structure, morphology and magnetic properties of the nanoparticles are characterized using scanning electron microscopy, X-ray diffraction, and a superconducting quantum interference device. The magnetic properties being investigated include Curie temperature, saturation magnetization, remnant magnetization, coercive field, and hysteresis. The study showed that adjusting the Mn contribution to the particles contributed to the adjustment of all magnetic properties of the complex.     

Synthesis,in vitro $$\alpha $$-glucosidase inhibitory activity,and in silico study of ( E)-thiosemicarbazones and ( E)-2-(2-(arylmethylene)hydrazinyl)-4-arylthiazole derivatives

This study is focused on the identification of thiazole-based inhibitors for the \(\alpha \)-glucosidase enzyme. For that purpose, (E)-2-(2-(arylmethylene)hydrazinyl)-4-arylthiazole derivatives were synthesized in two steps and characterized by various spectroscopic techniques. All derivatives and intermediates were evaluated for their in vitro \(\alpha \)-glucosidase inhibitory activity. Thiosemicarbazones 20 and 35, and cyclized thiazole derivatives 2, 5–11, 13, 15, 21–24, 27–31, and 36–37 showed significant inhibitory potential in the range of \(\hbox {IC}_{50}=6.2\pm 0.19\)–\(43.6\pm 0.23~\upmu \hbox {M}\) as compared to standard acarbose (\(\hbox {IC}_{50}=37.7\pm 0.19~\upmu \hbox {M}\)). A molecular modeling study was carried out to understand the binding interactions of compounds with the active site of enzyme.