Quantitative detection of singlet O2 by cavity-enhanced absorption

A method for the practical determination of the absolute concentration of single (a1delta(g)) oxygen is discussed. The method is based on sensitive off-axis integrated-cavity-output spectroscopy (ICOS). Off-axis ICOS allows narrowband, continuous-wave lasers to be used in conjunction with optical cavities to record sensitive absorption measurements. The details of the method as well as spectroscopic data confirming the first observation of the (1, 0) band of the b1sigma(g)(+) - a1delta(g) Noxon system are presented. The absolute transition probabilities for the b1sigma(g)(+) - a1delta(g) Noxon system, which are not known precisely from experiments, are determined by quantum chemistry theory.     

Effect of pressure on the magneto-optical properties of bcc and bct iron

We have studied the effect of pressure on the electronic structure of bcc and bct iron within the local spin density approximation (LSDA) for the electronic exchange and correlation. We report calculations of the magneto-optical properties of ferromagnetic iron in the bcc and bct phases using the full potential linearized augmented plane wave (FPLAPW) method as implemented in the WIEN2K code. In both phases, we find two prominent minima in Kerr rotation. In bcc phase, both the calculated Kerr minima shift towards higher energies with increase in pressure while in bct phase, the low energy minimum in Kerr rotation spectra 2 eV becomes less pronounced and the minimum at 7 eV moves towards higher energies on increasing pressure.     

Effects of thermal energy deposition on material ejection in poly(methyl methacrylate)

The effects of absorption of 7.9 and 5.0 eV photons by the polymer poly(methyl methacrylate) are studied using molecular dynamics simulations. By rapidly depositing a critical amount of thermal energy in the surface region (greater than 0.03 eV Å⁻³), a pressure wave is formed which causes spallation of the substrate. If there is only one photon absorbed per monomer unit of the polymer, the 7.9 eV photons can supply sufficient energy density to initiate ejection.     

Synthesis of high molecular weight polymer nanoparticles by [Cp2ZrCl2] catalyzed emulsion polymerization

An early transition metal metallocene compound, Cp₂ZrCl₂, with an anionic surfactant, sodium n‐dodecyl sulfate (SDS) as emulsifier and NaBPh₄ as cocatalyst has been found to be an effective catalytic system for polymerization and copolymerization of monomers like styrene and methyl methacrylate in aqueous medium. The diameters of the latex particles were found to be in between 20 and 40 nm. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

A New Chromogenic Spray Reagent for Detection and Identification of Monocrotophos

JPC – Journal of Planar Chromatography – Modern TLC - Sensitive and selective detection of monocrotophos after TLC is possible by use of vanillin as reagent. The product from alkaline...     

A comparative study on thermoresponsive magnetic nanohydrogels: role of surface-engineered magnetic nanoparticles

A comparative study of thermoresponsive poly(N-isopropylacrylamide)(PNIPAAm)-chitosan (CS)-based magnetic nanohydrogels (MNHGs) encapsulating functionalized Fe₃O₄ nanoparticles (NPs) in terms of the parameters governing their suitability for real hyperthermia is reported. Iron oxide NPs functionalized with (a) citric acid (CA-Fe₃O₄), (b) ethylenediamine (Amine-Fe₃O₄) and (c) dimercaptosuccininc (DMSA-Fe₃O₄) have been synthesized and their encapsulation into MNHGs was obtained through physical encapsulation method. The structural characterizations of synthesized materials include X-ray diffraction, FT-IR, TGA, ICP-AES and X-ray photoelectron spectroscopy (XPS). Encapsulation of the functionalized NPs into MNHGs were observed in TEM micrographs, while SEM and AFM micrographs confirmed their spherical morphology (~250–300 nm). Lower critical solution temperature (LCST) variation was measured by UV–visible spectrophotometer and differential scanning calorimetry (DSC). MNHGs exhibited sufficient magnetization and heating ability for hyperthermia. Typically, hydrogels containing CA-Fe₃O₄ (50 mg/ml) raised the temperature of the medium to 43 °C, a suitable dose for in vivo application in tumor-bearing mice.     

Thin-Layer Chromatographic Detection of Selected Pyrethroids with p-Benzoquinone Reagent

JPC – Journal of Planar Chromatography – Modern TLC - Cypermethrin is frequently encountered in poisoning cases in India. In TLC, the compound can be detected by spraying the plate with...     

A Rapid and Simple UPLC-MS–MS based Simultaneous Determination of the Medicinally Important E- and Z-Guggulsterone from Oleogum-Resins of Naturally Occurring Commiphora wightii Plants

A fast and simple method for simultaneous detection and quantification of the medicinally important E- and Z-guggulsterone from raw oleogum-resin of Commiphora wightii by UPLC was developed. Both E- and Z-guggulsterone were extracted from naturally occurring resin samples using ethyl acetate and methanol. Chromatographic separation of the analytes and their respective standards were performed on an Acquity UPLC BEH C₁₈ column followed by UV as well as a triple quadrupole detector in positive ionization mode. A linear gradient elution profile followed; mobile phase consisted of acetonitrile and 2 mM ammonium acetate in water. The method was validated over a range of 6.25 to 100 ng mL⁻¹ for both the guggulsterones. The calibration curves were linear with correlation coefficients of 0.9998 for E-guggulsterone and 0.9999 for Z-guggulsterone. The LOD and LOQ were 1.65 and 5.02 ng mL⁻¹ for E-guggulsterone and 2.57 and 7.79 ng mL⁻¹ for Z-guggulsterone respectively. The average recovery of E-guggulsterone (104.63%) and Z-guggulsterone (104.33%) achieved from spiked samples were consistent and reproducible. The intra- and inter-day assay precision of the analytes over the entire concentration range was less than 2%. The developed method required only 6 min to complete a run including 1 min to equilibrate the system and hence suitable for high throughput applications. Efficiency, reliability and accuracy of the developed method were evaluated by analyzing resin sample from different C. wightii populations. The result of this study offers improvement in terms of speed and sensitivity as compared to previously reported methods.

     

On‐line 2D‐LC‐ESI/MS/MS determination of rifaximin in rat serum

A highly sensitive and selective on‐line two‐dimensional reversed‐phase liquid chromatography/electrospray ionization–tandem mass spectrometry (2D‐LC‐ESI/MS/MS) method was developed and validated to determine rifaximin in rat serum by direct injection. The 2D‐LC‐ESI/MS/MS system consisted of a restricted access media column for trapping proteins as the first dimension and a Waters C₁₈ column as second dimension using 0.1% aqueous acetic acid:acetonitrile as mobile phase in a gradient elution mode. Rifampacin was used as an internal standard. The linear dynamic range was 0.5–10 ng/mL (r² > 0.998). Acceptable precision and accuracy were obtained over the calibration range. The assay was successfully used in analysis of rat serum to support pharmacokinetic studies. Copyright © 2009 John Wiley & Sons, Ltd.