Molecularly imprinted macroporous polymer monolithic layers for L-phenylalanine recognition in complex biological fluids

In present work, the development of macroporous monolithic layers bearing the artificial recognition sites toward L-phenylalanine has been carried out. The set of macroporous poly(2-aminoethyl methacrylate-co-2-hydroxyethyl methacrylate-co-ethylene glycol dimethacrylate) materials with average pore size ranged in 340–1200 nm was synthesized. The applicability of Hildebrand's and Hansen's theories for the prediction of polymer compatibility with porogenic solvents was evaluated. The dependences of average pore size on theoretically calculated parameters were plotted. The linear trend detected for Hansen's theory has indicated the high suitability of this approach to select appropriate porogens. The synthesized monolithic MIP layers were tested toward the ability to rebind phenylalanine-derivative in microarray format. The influence of such factors as average pore size of the material, the concentration of template molecule in polymerization mixture, interaction time of analyte with its imprinted sites on binding efficiency were studied. The developed materials demonstrated good analyte rebinding from buffer solution with recognition factors 2.5–3.4 depending on the MIP sample. The comparable rebinding efficiency was also detected when the analysis was carried using complex biological media. The selectivity of phenylalanine binding from the equimolar mixture of structural analogues was 81.9% for free amino acid and 91.2% for labeled one.     

Lignite oxidative desulphurization: notice 3—process technological aspects and application of products

International Journal of Coal Science & Technology - The study reviews the process of oxidative desulphurization of high-sulphur Ukrainian lignite, which was performed by coal treatment using...     

Design and Synthesis of Polycyclic Imidazole‐Containing N‐ Heterocycles based on C?H Activation/Cyclization Reactions

A new strategy for the synthesis of polycyclic imidazole‐containing N‐heterocycles, based on the two general synthetic ways, namely the Pd(II)‐catalyzed intramolecular arylation via CH/C Hal and CH/CH coupling reactions, was developed. The method proposed here enables the synthesis of many fused N‐heterocycles containing purine, 1‐deazapurines and benzimidazole structural units.     

Digital replicas of historical skirts

Abstract

Digitisation of historical costumes is an actual multidisciplinary area of research that uses science-based methods of reconstruction in virtual reality. The main aim of this study was to create a method for generating numerical replicas of skirts of the late 1850?s and the1860s. We applied two-dimensional and three-dimensional software to parameterise all the elements of the skirts and recreate them layer by layer. Computer modelling allowed us to gain insight into the interrelation between the parameters of cage crinolines, skirt construction and the behaviour of textile materials on the crinoline’s surface. A replica of a historical costume was generated and the similarity between the historical prototype and its replica was proved. The application of computer graphics tools for the reconstruction of the visible and invisible elements of historical costumes can advance their scientific study. The reconstructions can be an effective instrument for teaching, enriching museum collections and producing online presentations.     

Guiding Cell Network Assembly using Shape-Morphing Hydrogels

Forces and relative movement between cells and extracellular matrix (ECM) are crucial to the self-organization of tissues during development. However, the spatial range over which these dynamics can be controlled in engineering approaches is limited, impeding progress toward the construction of large, structurally mature tissues. Herein, shape-morphing materials called “kinomorphs” that rationally control the shape and size of multicellular networks are described. Kinomorphs are sheets of ECM that change their shape, size, and density depending on patterns of cell contractility within them. It is shown that these changes can manipulate structure-forming behaviors of epithelial cells in many spatial locations at once. Kinomorphs are built using a new photolithographic technology to pattern single cells into ECM sheets that are >10× larger than previously described. These patterns are designed to partially mimic the branch geometry of the embryonic kidney epithelial network. Origami-inspired simulations are then used to predict changes in kinomorph shapes. Last, kinomorph dynamics are shown to provide a centimeter-scale program that sets specific spatial locations in which ≈50 µm-diameter epithelial tubules form by cell coalescence and structural maturation. The kinomorphs may significantly advance organ-scale tissue construction by extending the spatial range of cell self-organization in emerging model systems such as organoids.     

Thermodynamic Description of the Ti-Al-O System Based on Experimental Data

Phase equilibria of the TiO₂-Al₂O₃ system were investigated experimentally using XRD, SEM/EDX and DTA methods. Temperature stability limits of the aluminum titanate (Al₂TiO₅) were detected. The thermodynamic parameters of the liquid phase as well as solid solution phases were assessed by CALPHAD approach using obtained experimental results. The thermodynamic data for the Ti-Al, Al-O and Ti-O systems and available experimental data for the Ti-Al-O system were critically evaluated and optimized to develop database of the Ti-Al-O system.