The Influence of pH on Complexation Process of Copper(II) Phosphoethanolamine to Pyrimidine Nucleosides

The influence of pH on the complex formation of phosphoethanolamine and pyrimidine nucleosides (uridine, cytidine and thymidine) with copper(II) ions was studied. All investigations were performed in aqueous solution. The overall stability constants of the complexes and non-covalent compounds were obtained using the potentiometric method with computer calculation of the data. Moreover, equilibrium constants of the reaction were determined. The mode of coordination was obtained using spectroscopic methods. Analysis of the potentiometric and spectroscopic data confirmed the involvement and effectiveness of phosphate groups in species formation as well as the influence of pH on the mode of coordination of the investigated biomaterials. In the next step, studied complexes will be applied as potential biomaterials with biological applications.

Potentiometric Study of the Copper(II) Ions Complexation Process with Thiourea in Acidic Medium

Potentiometric titration method was used to study the copper(II) ions complexation process with thiourea in medium containing 1 mol/l of hydrochloric acid at a temperature of 298 K. It was found out that mononuclear (CuTMn) and binuclear (Cu2TMn) complexes were observed in the copper(II) --- thiourea system depending on the copper ions concentration. It was determined that in acid medium with copper(II) ions concentration less than 5 · 10--4 mol/l and mononuclear complexes of the composition are generated in the system, which constant is equal to lg β3 = 11.9. With an increase in the copper(II) ions concentration (CCu+2 > 5 · 10--4 mol/l), binuclear thiourea complex dominates in the system. Stability constant logarithm of the Cu2TM6 composition binuclear complex is equal to 27.5 and was calculated using the modified Leden's method. Based on the constants, complexes existence regions were determined depending on the ratio CTM/CCu+2. With the CTM/CCu+2 ≥ 5 relations, existence of a dominant complex significantly depends on the copper(II) ions concentration. It turned out that fractions of all complex particles were growing with an increase in the copper(II) ions concentration in the system. It was found that stability of thiourea complexes in the CuLi2+, AgLi+, AuLi+ rows was increasing

Recent Development: Enantioselective Extraction in Chiral Separation

This paper discusses the recent development of enantioselective extraction methods. There are several methods in this field. The principles of all of enantioselective extraction methods are presented a focus on twophase extractions, in these methods used a chiral compound that named chiral selector, this compound distinguishes between two chiral isomers in complexation process, then one isomer more captured by chiral selector, and separation processes happen. The chiral selector should dissolve in on phase. In these methods, typical performance data are reported major emphasis on distribution ratio and enantioselectivity value or selectivity factor. In this paper, we introduce types of enantioselective extraction method, and discuss about them with several examples.

Application of Innovative Analytical Modeling for the Physicochemical Analysis of Adsorption Isotherms of Silver Nitrate on Helicenes: Phenomenological Study of the Complexation Process

The interaction between the silver ion and the cyclic aromatic molecules, namely, the helicenes, is the subject of this paper. In fact, a silver complexation system based on quartz crystal microbalance (QCM) sensor with a functional film of helicenes has been designed and developed at four temperatures. The developed system, in which the sensor response reflects the adsorption of the hexahelicene and the heptahelicene, was able to control the complexed mass of silver for each concentration. Experimental outcomes indicated that the quartz crystal coated with heptahelicene is the adequate material for silver adsorption. Then, a theoretical study has been performed through two statistical physics models (SMPG and SMRG) in order to analyze the experimental adsorption isotherms of the two helicenes at the ionic scale. The SMRG model was developed using the real gas law and was satisfactorily applied for the microscopic investigation of the hexahelicene isotherms indicating that the lateral interactions between the adsorbates are responsible of the decrease of the adsorbed quantity at saturation. The interpretation of the two models’ parameters indicated that the adsorption of the two helicenes is an endothermic phenomenon. Interestingly, the heptahelicene is recommended for silver complexation because it shows the highest adsorption energies involving chemical bonds during the complexation process. The SMPG model and the SMRG model also allow prediction of three thermodynamic functions (configurational entropy, Gibbs free enthalpy, and internal energy) which govern the adsorption mechanism of silver on the two helicenes.

Recent Development: Enantio Selective Eextraction in Chiral Separation

This paper discusses the recent development of enantioselective extraction methods. There are several methods in this field. The principles of all of enantioselective extraction methods are presented a focus on twophase extractions, in these methods used a chiral compound that named chiral selector, this compound distinguishes between two chiral isomers in complexation process, then one isomer more captured by chiral selector, and separation processes happen. The chiral selector should dissolve in on phase. In these methods, typical performance data are reported major emphasis on distribution ratio and enantioselectivity value or selectivity factor. In this paper, we introduce types of enantioselective extraction method, and discuss about them with several examples.

MOLECULAR COMPLEXES OF MONOAMMONIUM SALT OF GLYCYRRHIZIC ACID WITH SOME UREA AND THEIR ANTIBIOTIC ACTIVITY

This article reports on obtaining the inclusion compounds of the monoammonium-glycyrrhizin salts with urea, thiourea and methylolthiourea. The compounds were obtained by the liquid phase way, and their structures were characterized by the UV- and IR-Spectroscopic methods. Proceeding from the spectral data, it was concluded that the complexation occurs through the interaction of polar groups of the components. The composition of the complexes was studied using the method of isomolar series. Equilibrium constants and changes in Gibbs free energy of the complexation process were also calculated. The biological activity of complex compounds was studied on the example of fungicidal activity of one of the most common pathogenic fungus Fusarium. The obtained compounds can be used as as fungicides and stimulants in agriculture.

Tragacanth Gum/Chitosan Polyelectrolyte Complexes-Based Hydrogels Enriched with Xanthan Gum as Promising Materials for Buccal Application

Polyelectrolyte complexes based on the electrostatic interactions between the polymers mixed are of increasing importance, therefore, the aim of this study was to develop hydrogels composed of anionic tragacanth gum and cationic chitosan with or without the addition of anionic xanthan gum as carriers for buccal drug delivery. Besides the routine quality tests evaluating the hydrogel’s applicability on the buccal mucosa, different methods directed toward the assessment of the interpolymer complexation process (e.g., turbidity or zeta potential analysis, scanning electron microscopy and Fourier-transform infrared spectroscopy) were employed. The addition of xanthan gum resulted in stronger complexation of chitosan that affected the hydrogel’s characteristics. The formation of a more viscous PEC hydrogel with improved mucoadhesiveness and mechanical strength points out the potential of such polymer combination in the development of buccal drug dosage forms.

A Molecular View of Lipid-mediated Activation Process of Apolipoprotein E

Apolipoprotein E (ApoE) is a major determinant protein of lipid-metabolism and actively participates in lipid transport in plasma and central nervous system. As a part of its lipid-transport activity, low-density-lipid receptor (LDLR) needs to recognise apoE as a ligand. But, all prior evidences point to the fact that the recognition of apoE by LDLR only takes place in presence of lipid molecules which are assumed to play an important role in conformationally activating apoE upon binding. However, the molecular mechanism underlying the complexation process of apoE with lipid molecules and associated lipid-induced conformational change of apoE are currently elusive. Here we capture the spontaneous complexation process of monomeric apoE3 and phospholipid molecules by employing molecular dynamics simulation at multiple resolution. In particular, our multi scale simulations demonstrate a large-scale conformational change of the full-length apoE3, triggered by two-stage apoE-lipid complexation process. At first stage, lipid molecules assemble close to C-terminal domain of the protein and induce a rapid separation of C-terminal domain of monomeric apoE3 from rest of its tertiary fold. In the second and final stage, long-time scale simulation captures a slow on-the-fly lipid-induced inter-helix separation process in N-terminal domain of the protein. The resultant equilibrated complex, as obtained in the current work resembles an ‘open conformation’ of lipid-stabilised apoE, previously hypothesised based on small-angle X-ray scattering experiments. Taken together, the simulations provide a molecular view of kinetic interplay of apoE and lipid complexation multi-stage process leading to conformational changes in protein, potentially making it conducive for recognising LDLR.