Rapid determination of lactulose in milk by microdialysis and biosensors

A simple and rapid flow system for the determination of lactulose in milk samples was developed. It is based on the hydrolysis of lactulose to galactose and fructose by the enzyme beta-galactosidase immobilised in a reactor. The amount of fructose produced was measured with an electrochemical biosensor based on the fructose dehydrogenase enzyme, K3[Fe(CN)6] as mediator and a platinum based electrochemical transducer. Parameters such as the enzyme immobilisation in the reactor and under the electrode surface, the lifetime of the beta-galactosidase reactor and of the dehydrogenase biosensor and the flow parameters were studied and optimised. Fructose was determined in the range 1 x 10(-6)-5 x 10(-3) mol l-1 with an RSD of about 2% and a detection limit of 5 x 10(-7) mol l-1. The use of a microdialysis probe as the sampling system permitted the direct measurement of lactulose in milk samples without pre-treatment in the range 1 x 10(-5)-5 x 10(-3) mol l-1. The sensitivity of the procedure allowed pasteurised, UHT and in-container sterilised milk to be distinguished.     

Cu(II) adsorption by halloysites intercalated with sodium acetate

Intercalated halloysites with sodium acetate at various contact time were prepared. The resulting materials were characterised by X-ray powder diffraction, Fourier transformed infrared spectroscopy, scanning electronic microscopy, and specific surface area evaluation. The modified halloysites were employed as Cu(II) adsorbents from aqueous solutions. Various parameters were studied through the batch method. Kinetic data, equilibrium isotherms, and thermodynamic parameters were evaluated by considering several models. The fraction of halloysite intercalated with sodium acetate remained low, up to 7 days, then linearly increased with contact time. Thirty days were required to achieve a ratio of 91%. For this sample, a proliferation of small tubes (nanotubes) was evidenced. The best results were achieved with the pseudo-second-order kinetic model associated with intraparticle diffusion and with the Redlich-Peterson isotherm, for the equilibrium data. The thermodynamic data show that adsorption would be spontaneous at low temperatures, of exothermic nature, resulting in an adsorbate-adsorbent system much more ordered. The insertion of CH(3)COONa into halloysite significantly affects the Cu(II) adsorption. The magnitude in enhancement of copper adsorption on solid phase thus depends on the content of the carboxylic functional groups, which increases with the insertion of CH(3)COONa into the halloysitic matrix. The involved mechanism is quite complex. It implies electrostatic considerations and a cationic exchange process. The most intercalated sample was found to be very effective as adsorbent of copper(II) from aqueous solutions.     

A construction of new exact periodic wave and solitary wave solutions for the 2D Ginzburg–Landau equation

Using a uniform algebraic method, new exact solitary wave solutions and periodic wave solutions for 2D Ginzburg–Landau equation are obtained. Moreover, three-dimensional and two-dimensional graphics of some solutions have been plotted.     

Radiochemical and biological characteristics of radioactive iodine labeled indomethacin for imaging of inflammation

Summary Indomethacin was successfully labeled with ¹²⁵I. This labeling reaction was carried out via electrophilic substitution of hydrogen atom with the iodonium atom I⁺. The reaction was found to be strongly dependent on pH of the reaction medium. At neutral pH value, 7 the labeling yield was maximum. This may be due to the good solubility of indomethacin, good protonation and good working of the oxidizing agent at this pH value. Towards the acidic pH value, the yield decreased and towards the alkaline pH value the yield decreased due to the decomposition of the indomethacin. The labeling reaction is very fast but needs five minutes for completion. The produced ¹²⁵I-indomethacin was found stable in-vivo as the thyroid gland uptake did not exceed 2%. Labeled indomethacin shows a good localization in inflamed muscle, either septic or sterile. It excretes mainly via liver and to some extent via kidney. The imaging must be carried out at 24-hour post injection, after that time, the background activity has cleared and the activity is concentrated in the target site.     

Permeability identification of a weakly permeable partially saturated porous rock

The present paper deals with the determination of permeability in partially saturated conditions for weakly permeable porous continua such as argillites or deep clayey formations. The permeability can be deduced from measurements of transient weight loss of a sample submitted to a laboratory drying test: a decrease of relative humidity is imposed by saline solution in an hermetic chamber. Assumptions of constant gas pressure equal to atmospheric pressure and of negligible Fickean diffusive transport of vapour are adopted. The only transport phenomenon taken into account inside the sample is the Darcean advective transport of the water liquid. The forward problem is solved by following two modelling approaches: a linear one and a nonlinear one. The parameter identification procedure is based upon the solution of corresponding inverse problems. In the two cases, the Levenberg–Marquardt algorithm has been used for the minimization problem. In the linear approach, the solution of the forward problem is explicit. In the non linear approach, finite volume method for the spatial discretization combined with a Newton–Raphson algorithm has been used to solve the non linear forward problem. The identification method enables variations of permeability and capillary capacity to be estimated. Comparisons between linear and non linear approaches show that the first one is useful to give mean values and order of magnitude of permeability and capacity. A more complete information is deduced from the non linear approach as variations of equivalent capacity and permeability during a test are significant in most cases. The analysis of the obtained results shows that the basic modelling assumption of constant gas pressure inside the sample would not be relevant for lower range of relative humidities and liquid permeability than those investigated.     

Carbon Black‐Modified Electrodes as Sensitive Tools for the Electrochemical Detection of Nitrite and Nitrate

Both screen‐printed electrodes modified with a dispersion of carbon black (CB) and solid paste electrodes prepared using a nanostructured CB were developed and characterized. Indeed, increasing the peak currents and/or their shifting to negative potentials were observed, exhibiting efficient electrocatalytic activity towards nitrite oxidation with high sensitivity and low detection limit. Solid carbon paste electrodes (SCPEs) and solid carbon black paste electrodes (SCBPEs) were challenged in amperometric mode with nitrite since detection limit reached is 65 and 5 nM respectively. Nitrate was first reduced to nitrite in reductor column, then detected on SCBPEs. Nitrate and nitrite were determined in real samples.     

BIOLOGICALLY ACTIVE THIONES DERIVED FROM PYRIDAZINONES

Abstract

A number of pyridazin-3-thione (II), some hydrazinopyridazine derivatives (III) and its Schiff base (IV) have been prepared. α-(3-thiopyridazinyl)-β-aroylpropionic acids (VI) have also been synthesised. Structural evidences are discussed. The antibacterial activity of these compounds has been studied.     

Liquid–liquid extraction of thorium(IV) by fatty acids: a comparative study

In this paper, extractants that have the potential to be sustainably regenerated, are proposed for thorium(IV) removal from nitrate aqueous phases. These extractants are oleic (OA), palmitic (PA) and lauric (LA) acids. The advantages of using these acids are their sustainability, their biocompatibility and their non-toxicity, this makes these simpler and greener compared to other extractants (organophosphorus, azote derivatives, macrocyclic crown, etc…) used for metal extraction. These acids were applied as chelating agent for Th(IV) liquid–liquid extraction. The extractions were carried out in chloroform as an organic phase through the formation of thorium–OA, thorium–PA and thorium–LA complexes. The synergistic extraction of Th(IV) with these extractants in the presence of tributhylphosphine (TBP) has been investigated. The effect of different variables, such as time contact, pH of the aqueous phase, concentration of fatty acid, TBP addition on fatty acids, ionic strength and temperature, is reported. The results showed that the extraction kinetics using LA and OA were fast than with PA. The KNO₃ addition does not seem to highly influence the extraction yield, and no important synergy effect was noticed in the presence of TPB. Thermodynamic data for Th(IV) solvent extraction are also reported in this paper.