This work reports a promising approach to the development of novel self-buffering and biocompatible ionic liquids for biological research in which the anions are derived from biological buffers (Good's buffers, GB). Five Good's buffers (Tricine, TES, CHES, HEPES, and MES) were neutralized with four suitable hydroxide bases (1-ethyl-3-methylimidazolium, tetramethylammonium, tetraethylammonium, and tetrabutylammonium) producing 20 Good's buffer ionic liquids (GB-ILs). The presence of the buffering action of the synthesized GB-ILs was ascertained by measuring their pH-profiles in water. Moreover, a series of mixed GB-ILs with wide buffering ranges were formulated as universal buffers. The impact of GB-ILs on bovine serum albumin (BSA), here used as a model protein, is discussed and compared with more conventional ILs using spectroscopic techniques, such as infrared and dynamic light scattering. They appear to display, in general, a greater stabilizing effect on the protein secondary structure than conventional ILs. A molecular docking study was also carried out to investigate on the binding sites of GB-IL ions to BSA. We further used the QSAR-human serum albumin binding model, log K(HSA), to calculate the binding affinity of some conventional ILs/GB-ILs to HSA. The toxicity of the GB and GB-ILs was additionally evaluated revealing that they are non-toxic against Vitro fischeri. Finally, the GB-ILs were also shown to be able to form aqueous biphasic systems when combined with aqueous solutions of inorganic or organic salts, and we tested their extraction capability for BSA. These systems were able to extract BSA with an outstanding extraction efficiency of 100% in a single step for the GB-IL-rich phase, and, as a result, the use of GB-IL-based ABS for the separation and extraction of other added-value biomolecules is highly encouraging and worthy of further investigation.

Antibodies obtained from egg yolk of immunized hens, immunoglobulin Y (IgY), are an alternative to the most focused mammal antibodies, because they can be obtained in higher titers by less invasive approaches. However, the production cost of high‐quality IgY for large‐scale applications remains higher than that of other drug therapies due to the lack of efficient purification methods. The search for new purification platforms is thus vital. The solution could be liquid–liquid extraction by using aqueous biphasic systems (ABS). Herein, we report the extraction and attempted purification of IgY from chicken egg yolk by using a new ABS composed of polymers and Good’s buffer ionic liquids (GB‐ILs). New self‐buffering and biocompatible ILs based on the cholinium cation and anions derived from Good’s buffers were synthesized and the self‐buffering characteristics and toxicity were characterized. Moreover, when these GB‐ILs are combined with PPG 400 (poly(propylene) glycol with a molecular weight of 400 g mol‐1) to form ABS, extraction efficiencies, of the water‐soluble fraction of proteins, ranging between 79 and 94 % were achieved in a single step. Based on computational investigations, we also demonstrate that the preferential partitioning of IgY for the GB‐IL‐rich phase is dominated by hydrogen‐bonding and van der Waals interactions.

Novel modified Ni/Fe layered double hydroxides with different morphology of spherical-like shape were fabricated via using urea as a ligand and glycerol (Ni/Fe LDH/GL) with Ni:Fe molar ratios of 2:1 by the simplest co-precipitation method. Also, for comparison purposes, Ni/Fe LDH was synthesized to be used as a control one. A suggested interpretation for the morphology change was also given. The materials were characterized by X-ray diffraction (XRD), The Fourier transform infrared (FT-IR) spectroscopy, field emission scanning electron microscopy (FESEM), EDX for elemental analysis, high resolution transmission electron microscopy (HRTEM), Brunauer, Emmett, and Teller (BET) equation, particle size distributions and Zeta potential measurements. In addition, the synthesized materials were used as adsorbents for removal of potassium dichromate from aqueous solutions under various experimental conditions. The adsorption of Cr (VI) was strongly pH dependant and the pH PZC was studied. Kinetic studies were evaluated through different models including, pseudo first and second orders, mixed 1, 2 orders, intra particle diffusion and Avrami models. For adsorption isotherms, twoparameter models (Langmuir, Freundlich and Temkin) and three parameter models (Sips, Langmuir-Freundlich and Tooth) were investigated showing maximum adsorption capacity of 50.43 mg/g and 136.05 mg/g for Ni/Fe LDH and Ni/Fe LDH/GL, respectively. Also, the effect of temperature was investigated at (23, 35, 45, 55 °C) and the thermodynamic parameters (∆H°, ∆S° and ∆G°) were calculated showing exothermic and spontaneous adsorption process. The effect of coexisting anions (cl − , So 4 2− and HPO 4 2−) and humic acid at different concentrations on the removal efficiency of dichromate ions was investigated. Chemical stability and recyclability of these adsorbents were also studied. The intermolecular hydrogen bonds formation between dichromate ion, urea, glycerol, LDH was explored by Monte Carlo simulation This study suggested that the modified Ni/Fe LDH/GL materials were promising nanoadsorbents for efficient potassium dichromate removal. Water is the most precious natural source important for human beings, agriculture, and industrial activities. Recently, water bodies are potentially contaminated and polluted by many hazardous materials such as nuclear and industrial wastes, pharmaceuticals, organic contaminants and heavy metals. Heavy metals like cadmium, zinc, copper, lead, arsenic, mercury and chromium have significant threat to human health due to its potentially toxic effects 1,2. Chromium is one of heavy metals widely used in many industrial processes such as electroplating, dyes, mining, photography, textile and leather 3. Chromium present in water in a trivalent and hexavalent oxidation state, it is established that hexavalent chromium exhibits high toxicity toward living organisms than trivalent chromium which in contrast is a micronutrient 4. Hexavalent chromium is reported as a cause of respiratory cancers 5,6 and mutations and chromosomal dam...

A new range of Good's buffer ionic liquids (GB-ILs), displaying simultaneously the properties of ionic liquids and Good's buffers, were synthesized by combination of Good's buffers anions (MOPSO, BES, TAPSO and CAPSO) and tetrabutylammonium, tetrabutylphosphonium and cholinium cations via an acid-base neutralization reaction. The activity and stability of a lipolytic enzyme from Pseudomonas cepacia in aqueous solutions of these buffers were evaluated and the results show their advantage as media for enzymatic reactions when compared to conventional phosphate buffers. Moreover aqueous biphasic systems (ABS) composed by these GB-ILs and potassium citrate were investigated and shown to be highly effective and selective for the partitioning of the lipolytic enzyme into the GB-IL-rich phase. The results allow the development of an efficient and biocompatible process combining the self-buffering and enzyme-stabilizing properties of the GB-ILs in the reaction step, with the advantages of GB-ILs as extraction solvents in ABS.

In this work, formation in the binary and ternary systems of the Fe III metal ion with gallic acid and glycine was investigated by means of potentiometry, conductometry, polarography, and UV-visible absorption spectroscopy techniques at 25 °C and in I ) 0.10 mol • dm -3 NaNO 3 . The protonation equilibria of gallic acid and glycine were investigated and discussed. The acidity constants of gallic acid and glycine were determined and used for determining the stability constants of the binary and ternary complexes formed in the aqueous medium under the experimental conditions. The ternary complex formation was found to occur in a stepwise manner. The stability constants of these binary and ternary systems were calculated. The concentration distribution of the various complex species in solution was evaluated and discussed. The solid binary [Fe III -gallic acid] and ternary [Fe III -gallic acid-glycine] complexes were synthesized and characterized by elemental analysis, FT-IR, 1 H NMR, and 13 C NMR spectroscopy.