Eco‐friendly ionic liquid assisted capillary electrophoresis and α‐acid glycoprotein‐assisted liquid chromatography for simultaneous determination of anticancer drugs in human fluids

In the current work, two eco‐friendly analytical methods based on capillary electrophoresis (CE) and reversed phase liquid chromatography (RPLC) were developed for simultaneous determination of the most commonly used anticancer drugs for Hodgkin's disease: methotrexate (MTX), vinblastine, chlorambucil and dacarbazine. A background electrolyte (BGE) of 12.5 mmol/L phosphate buffer at pH 7.4 and 0.1 µmol/L 1‐butyl‐3‐methyl imidazolium bromide (BMImBr) ionic liquid (IL) was used for CE measurements at 250 nm detection wavelength, 20 kV applied voltage and 25 °C. The rinsing protocol was significantly improved to reduce the adsorption of IL on the interior surface of capillary. Moreover, RPLC method was developed on α‐1‐acid glycoprotein (AGP) column. Mobile phase was 10 mmol/L phosphate buffer at pH 6.0 (100% v/v) and flow rate at 0.1 mL/min. As AGP is a chiral column, it was successfully separated l ‐MTX from its enantiomer impurity d ‐MTX. Good linearity of quantitative analysis was achieved with coefficients of determinations (r²) >0.995. The stability of drugs measurements was investigated with adequate recoveries up to 24 h storage time under ambient temperature. The limits of detection were <50 and 90 ng/mL by CE and RPLC, respectively. The using of short‐chain IL as an additive in BGE achieved 600‐fold sensitivity enhancement compared with conventional Capillary Zone Electrophoresis (CZE). Therefore, for the first time, the proposed methods were successfully applied to determine simultaneously the analytes in human plasma and urine samples at clinically relevant concentrations with fast and simple pretreatments. Developed IL‐assisted CE and RPLC methods were also applied to measure MTX levels in patients’ samples over time. Copyright © 2014 John Wiley & Sons, Ltd.     

Separation and analysis of triazine herbcide residues by capillary electrophoresis

Triazines are widely used in agriculture around the world as selective pre‐ and post‐emergence herbicides for the control of broad leaf and grassy weeds. With high toxicity and persistence, triazines can contaminate the environment and crops, so the development of rapid and sensitive methods for the determination of different triazines is necessary. Capillary electrophoresis comprises a group of techniques used to separate chemical mixtures. Analytical separation is based on different electrophoretic mobilities. This review focuses on the analysis of triazine herbicides with different modes of capillary electrophoresis, including capillary zone electrophoresis, micellar electrokinetic capillary electrophoresis, capillary electrochromatography and nonaqueous capillary electrophoresis. Determinations of triazines in various matrices such as surface water, groundwater, vegetables, soil and grains are emphasized. Copyright © 2014 John Wiley & Sons, Ltd.     

Periodicity and convergence for xn+1=|xn−xn−1|

Each solution {x_n} of the equation in the title is either eventually periodic with period 3 or else, it converges to zero—which case occurs depends on whether the ratio of the initial values of {x_n} is rational or irrational. Further, the sequence of ratios {x_n/x_n−1} satisfies a first-order difference equation that has periodic orbits of all integer periods except 3. p-cycles for each p≠3 are explicitly determined in terms of the Fibonacci numbers. In spite of the non-existence of period 3, the unique positive fixed point of the first-order equation is shown to be a snap-back repeller so the irrational ratios behave chaotically.     

Spectrophotometric and AAS determination of trace amounts of cobalt after preconcentration by using alpha-benzilmonoxime-microcrystalline naphthalene.

The formed cobalt-a-benzilmonoxime complex was adsorbed onto microcrystalline naphthalene. Then it was determined by zero and first derivative spectrophotometry and by atomic absorption spectrophotometry (AAS) after dissolving into chloroform and methylisobutylketone (MIBK), respectively. Under optimum conditions, cobalt in the range of 1.0 - 20.0, 0.4 - 30.0 and 2.5 - 50.0 microg could be determined by spectrophotometry, first derivative spectrophotometry and AAS method, respectively. By the method, a preconcentration factor equal to approximately 30 for cobalt was obtained. The effect of diverse ions on the determination of 5.0 microg cobalt was also studied. The method was successfully applied to some pharmaceuticals and synthetic alloy samples.     

Convergence analysis of perturbed hemivariational inequalities

We consider the rate of convergence for a class of perturbed hemivariational inequalities in reflexive Banach Spaces. Our results can be viewed as an extension and refinement of some previous known results in this area.     

Time Asymptotic Behaviour for a One-Velocity Transport Operator with Maxwell Boundary Condition

This paper is concerned with the spectral analysis of a one-velocity transport operator with Maxwell boundary condition in L ₁-space. After a detailed spectral analysis it is shown that the associated Cauchy problem is governed by a C ₀-semigroup. Next, we discuss the irreducibility of the transport semigroup. In particular, we show that the transport semigroup is irreducible. Finally, a spectral decomposition of the solutions into an asymptotic term and a transient one which will be estimated for smooth initial data is given.     

Sur l'existence des opérateurs d'onde pour l'équation de Wigner dans les espaces L2,pExistence of wave operators for the Wigner equation in L2,p spaces

Basing on the formalism established by Markovich, we show the completeness of wave operators for the Wigner equation in L². In the second part, using estimations proved by Castella and Perthame on the one hand, and the L^p→L^q estimations for the Schrödinger group on the other hand, we prove the existence of the wave operators in L^2,p spaces. To cite this article: H. Emamirad, P. Rogeon, C. R. Acad. Sci. Paris, Ser. I 334 (2002) 811–816.     

Sorption of cesium from aqueous waste solution on a SuperLigÒ644 resin

Summary The removal of cesium from aqueous waste solution was investigated in a column setup using a relatively coarse SuperLig^ò644 resin. The bed volume (BV=140) at the onset of breakthrough surpassed the design requirement of 100 BV at 50% breakthrough, and also corresponds to 99.96% cesium removal. Cesium elution with 0.5M HNO₃was satisfactory with a peak BV of 2.5. The elution BV for C/C₀=0.01 was 10, which is less than the target of 15 BV. The percent of sorbed cesium eluted was 99.88%. Further, the BV of the various solutions used for the supporting process steps was sufficient.     

On Surfaces of Finite Chen — Type

We investigate some relations concerning the first and the second Beltrami operators corresponding to the fundamental forms I, II, III of a surface in the Euclidean space E³ and we study surfaces which are of finite type in the sense of B.-Y. Chen with respect to the fundamental forms II and III.