Determination of lewisite metabolite 2-chlorovinylarsonous acid in urine by use of dispersive derivatization liquid-liquid microextraction followed by gas chromatography–mass spectrometry

The purpose of this study was to develop a sensitive and simple method, based on dispersive derivatization liquid-liquid microextraction–gas chromatography–mass spectrometry (DDLLME–GC–MS) in scanning and selected-ion-monitoring (SIM) modes, for detection of 2-chlorovinylarsonous acid (CVAA) as a hydrolysis product and urinary metabolite of lewisite in urine samples. Chloroform (65 μL), methanol (500 μL), and ethanedithiol (10 μL) were used as extraction solvent, dispersive solvent, and derivatizing reagent, respectively. Critical conditions of the proposed method were optimized. The nucleophilic reactions of dithiol and monothiol compounds with CVAA were also studied using a competitive method. In view of the high affinity of trivalent arsenic for sulfhydryl groups, the interaction between CVAA and bis(2-chlorovinyl)arsonous acid (BCVAA) and free cysteine (Cys) was also investigated using liquid chromatography–electrospray ionization mass spectrometry (LC–ESI-MS). The interference of Cys, present in human urine, with the detection of CVAA was evaluated using dithiol and monothiol chemicals as derivatization agents. The developed method provided a preconcentration factor of 250, and limits of detection of 0.015 and 0.30 μg L^?1 in SIM and scanning modes, respectively. The calibration curves were linear over the concentration range of 1–400 μg L^?1 in full-scan mode. The relative standard deviation (RSD) values were calculated to be 5.5 and 3.2 % at concentrations of 20 and 100 μg L^?1, respectively. Collision-induced dissociation studies of the major electron-impact (EI) ions were performed to confirm the proposed fragment structure of CVAA-dithiols derivatives. Results indicated that the developed method for analysis of CVAA is suitable not only for verification of human exposure to lewisite, but also for quantification of CVAA in urine samples.

Fabrication of polyaniline‐coated halloysite nanotubes by in situ chemical polymerization as a solid‐phase microextraction coating for the analysis of volatile organic compounds in aqueous solutions

We have synthesized an organic–inorganic polyaniline–halloysite nanotube composite by an in situ polymerization method. This nanocomposite is immobilized on a stainless‐steel wire and can be used as a fiber coating for solid‐phase microextraction. It was found that our new solid‐phase microextraction fiber is an excellent adsorbent for the extraction of some volatile organic compounds in aqueous samples in combination with gas chromatography and mass spectrometry. The coating can be prepared easily, is mechanically stable, and exhibits relatively high thermal stability. It is capable of extracting phenolic compounds from water samples. Following thermal desorption, the phenols were quantified by gas chromatography with mass spectrometry. The effects of extraction temperature, extraction time, sample ionic strength, stirring rate, pH, desorption temperature and desorption time were studied. Under optimal conditions, the repeatability for one fiber (n = 5), expressed as the relative standard deviation, is between 6.2 and 9.1%. The detection limits range from 0.005 to 4 ng/mL. The method offers the advantage of being simple to use, with a shorter analysis time, lower cost of equipment and higher thermal stability of the fiber in comparison to conventional methods of analysis.     

Hydrogen-bonded liquid-crystalline complexes of polyester containing a pyridyl moiety with 4-(alkoxy)benzoic acid

Novel hydrogen-bonded polyester complexes from mesogenic 4-(butyloxy)benzoic acid (2a), 4-(octyloxy)benzoic acid (2b), 4-(dodecyloxy)benzoic acid (2c) and 4-(tetradecyloxy)benzoic acid (2d) as the hydrogen bond donors and a polyester (3) based on 2,6-pyridine dicarboxylic acid as the hydrogen bond acceptor were prepared by the melt method. The association by hydrogen bonding was confirmed by means of FTIR. The components were miscible up to 0.1 mole ratio of 2d and 2c versus the polyester repeat unit. The limiting mole ratio for 2b and 2a to 3 were 0.2 and 0.4, respectively. Phase separation in the supramolecular complexes occurred above these limiting values and a two phase system consisting of a polyester supramolecular complex and 4-(alkyloxy)benzoic acid was formed. This was due to weak hydrogen bonding between the low molecular acid (especially the acid with longer terminal alkoxy group) and pyridyl unit of polyester in comparison with thermodynamically more favorable dimerization of acid molecules. The liquid crystalline behavior of these supramolecular polymeric complexes was confirmed by differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). It was found that 2a exhibits no mesomorphism when mixed with polyester. However, among the other acid derivatives, 2b exhibited stable mesogenic complexes.     

Framework‐Substituted Bismuth Zeolite‐P: Synthesis and Characterization

Bismuth‐modified zeolite‐P (Bi‐ZP) was synthesized by hydrothermal methods during the phase transformation of analcime to zeolite‐P. The evolution of phase transformation of pure analcime to Bi‐ZP was investigated. The results showed that bismuth atoms were incorporated into the framework of the microporous zeolite‐P. The effect of various Bi/Al (0–3) and Si/Bi (1–5) mole ratios on the synthesis of bismuth modified zeolite were studied by X‐ray diffraction (XRD) technique and FT‐IR spectroscopy. Evolution of the growth process of Bi‐ZP spheres was carried out at different time intervals with XRD patterns and FE‐SEM images. The energy dispersive X‐ray (EDX) spectrum indicated the existence of bismuth atoms in the synthesized Bi‐ZP. Framework substitutions of bismuth were evidenced by a set of complementary characterizations such as diffusive reflectance UV/Vis (DRS) and Raman spectroscopy on the synthesized Bi‐ZP (Si/Bi = 1).     

Power absorbed during whole-body fore-and-aft vibration: Effects of sitting posture,backrest, and footrest

Although the discomfort or injury associated with whole-body vibration cannot be predicted directly from the power absorbed during exposure to vibration, the absorbed power may contribute to understanding of the biodynamics involved in such responses. From measurements of force and acceleration at the seat, the feet, and the backrest, the power absorbed at these three locations was calculated for subjects sitting in four postures (feet hanging, maximum thigh contact, average thigh contact, and minimum thigh contact) both with and without a rigid vertical backrest while exposed to four magnitudes (0.125, 0.25, 0.625, and 1.25 m s^?2 rms) of random fore-and-aft vibration. The power absorbed by the body at the supporting seat surface when there was no backrest showed a peak around 1 Hz and another peak between 3 and 4 Hz. Supporting the back with the backrest decreased the power absorbed at the seat at low frequencies but increased the power absorbed at high frequencies. Foot support influenced both the magnitude and the frequency of the peaks in the absorbed power spectra as well as the total absorbed power. The measurements of absorbed power are consistent with backrests being beneficial during exposure to low frequency fore-and-aft vibration but detrimental with high frequency fore-and-aft vibration.     

The Effect of Rainbow Trout (Oncorhynchus mykiss) Collagen Incorporated with Exo-Polysaccharides Derived from Rhodotorula mucilaginosa sp. on Burn Healing

Burn is one of the physically debilitating injuries that can be potentially fatal; therefore, providing appropriate coverage in order to reduce possible mortality risk and accelerate wound healing is mandatory. In this study, collagen/exo-polysaccharide (Col/EPS 1–3%) scaffolds are synthesized from rainbow trout (Oncorhynchus mykiss) skins incorporated with Rhodotorula mucilaginosa sp. GUMS16, respectively, for promoting Grade 3 burn wound healing. Physicochemical characterizations and, consequently, biological properties of the Col/EPS scaffolds are tested. The results show that the presence of EPS does not affect the minimum porosity dimensions, while raising the EPS amount significantly reduces the maximum porosity dimensions. Thermogravimetric analysis (TGA), FTIR, and tensile property results confirm the successful incorporation of the EPS into Col scaffolds. Furthermore,the biological results show that the increasing EPS does not affect Col biodegradability and cell viability, and the use of Col/EPS 1% on rat models displays a faster healing rate. Finally, histopathological examination reveals that the Col/EPS 1% treatment accelerates wound healing, through greater re-epithelialization and dermal remodeling, more abundant fibroblast cells and Col accumulation. These findings suggest that Col/EPS 1% promotes dermal wound healing via antioxidant and anti-inflammatory activities, which can be a potential medical process in the treatment of burn wounds.