Investigation of Matrix Effects on the Determination of Carbadox and Olaquindox in Feed by LC–MS/MS

A comprehensive survey of matrix effects on the LC–MS/MS analysis of the banned antibiotic growth promoters carbadox and olaquindox in feed was carried out. Various factors of sample preparation procedure and measurement were systematically investigated by pre- and post-extraction addition and postcolumn infusion experiments. In general, strong signal suppression up to 70 % for carbadox and up to 90 % for olaquindox was observed when using different extraction solvents and techniques as well as different chromatographic conditions. Reduction of matrix effects was achieved by SPE clean-up and dilution of sample extracts. Nevertheless, matrix effect profiles determined by postcolumn infusion revealed, that reduction of signal suppression at a respective retention time cannot guarantee improvement of the methods performance. If high variability of matrix effects is present along the chromatographic run, accuracy might decrease despite reduced signal suppression. Besides method parameters, different feedingstuffs were investigated and showed similar matrix effects.

     

Nonlinear kinetic Sunyaev-Zeldovich effect

We derive fully nonlinear expressions for temperature fluctuations from the kinetic Sunyaev-Zeldovich (SZ) effect, the scattering of cosmic microwave background photons off hot electrons in bulk motion. Our result reproduces the Ostriker-Vishniac effect to second order in perturbation theory but contains nonlinear corrections to the electron velocities and densities that were neglected previously. We use the recently developed halo model for nonlinear gravitational clustering to compute the nonlinear kinetic SZ power spectrum, which dominates the primary anisotropy on small angular scales.     

Synchronous, dual-wavelength, injection-seeded amplification of 5-ns pulses in a flash-lamp-pumped Ti:sapphire laser

The outputs of two cw diode lasers are coupled into a flash-lamp-pumped Ti:sapphire laser cavity for regenerative amplification. Slices of each seed beam are simultaneously trapped in the cavity and amplified for approximately 33 round trips. The output is a 4.7-ns pulse, the total pulse energy is 110 mJ, and linewidths are only 50% greater than the Fourier-transform limit. The timing jitter between the pulses at the two wavelengths is less than +/-75 ps , and their relative energy is controlled by adjustment of the seed power of the cw diode lasers. Gain competition between the two frequencies does not lead to instabilities.     

Processes involving fragmentation functions beyond the leading order in QCD

We point out that the electron propagator, calculated from a truncated Johnson-Baker-Willey equation, suffers from the following defects: lack of renormalizability gauge dependence of the electron electromagnetic mass, as well as unacceptable analytic structure.     

Highly efficient blue-light generation from a compact, diode-pumped femtosecond laser by use of a periodically poled KTP waveguide crystal

We present a simplified, potentially portable, and highly efficient blue-light source from a periodically poled KTP waveguide crystal with a compact femtosecond Cr:LiSAF laser. This light source generates 5.6 mW of blue average output power at 424 nm with 27 mW of incident fundamental in a single-pass extracavity arrangement at room temperature. The overall system efficiency of electrical power to blue light is 0.5%, and the internal second-harmonic generation conversion efficiency is as high as 37%. The slope efficiency of 5.5% pJ(-1) at low pulse energies is, to our knowledge, the highest slope efficiency yet reported for frequency conversion into the blue spectral region.     

Evaluation of sulfur, selenium and tellurium catalysts with antioxidant potential

Oxidative stress is implicated, either directly or indirectly, in the pathology of a range of human diseases. As a consequence, the development of efficient antioxidants for medical use has become increasingly important. We have synthesised a range of structurally related organo-sulfur, -selenium and -tellurium agents and demonstrated that a combination of electrochemical methodology, in vitro assays and cell culture tests can be used to rationalise the antioxidant activity of these catalytic agents. Based on its exceptionally low anodic oxidation potential (Epa) and high activity against the representative oxidative stressors tert-butyl hydroperoxide and peroxynitrite, 4,4'-dihydroxydiphenyltelluride is predicted to be a potent antioxidant. This compound exhibits a correspondingly high activity with a remarkably low IC50 value of 20 nM, when tested in PC12 cell culture using a bioassay indicative of the early stages of Alzheimer's disease.     

Anodic oxidation of a tetrasubstituted cyclooctatetraene. Multiple carbon-carbon bond cleavage and aromatization

Anodic oxidation of 1,2-,5,6-bis[trimethylene]cyclooctaetraene in methanol affords as the major product a substance formed by a complex sequence of carbon-carbon bond cleavages and concomitant aromatization.     

Experimental and computed absolute redox potentials of polycyclic aromatic hydrocarbons are highly linearly correlated over a wide range of structures and potentials

A more rigorous theoretical treatment of methods previously used to correlate computed energy values with experimental redox potentials, combined with the availability of well-developed computational solvation methods, results in a shift away from computing ionization potentials/electron affinities in favor of computing absolute reduction potentials. Seventy-nine literature redox potentials measured under comparable conditions from 51 alternant and nonalternant polycyclic aromatic hydrocarbons are linearly correlated with their absolute reduction potentials computed by density functional theory (B3LYP/6-31+G(d)) with SMD/IEF-PCM solvation. The resulting correlation is very strong (R(2) = 0.9981, MAD = 0.056 eV). When extrapolated to the x-intercept, the correlation results in an estimate of 5.17 ± 0.01 eV for the absolute potential of the ferrocene-ferrocenium redox couple in acetonitrile at 25 °C, indicating that this simple method can be used reliably for both calculating absolute redox potentials and for predicting relative redox potentials. When oxidation and reduction data are evaluated separately, the overall MAD value is improved by 50% to 0.028 eV, which improves relative potential predictions, but the computed values do not extrapolate to a reasonable estimate of the absolute potential of the ferrocene-ferrocenium ion reference.