Quantum particles on graphenic systems. Part 1. roadmap for semiconductor based graphenes

Advances in green nano-technologies is the main field under which the present paper series is firstly envisaged; therefore, advanced, research-progressive nano-science is aimed to shorten the distance from fundamental concepts to applications, devices and their implementations. It however would gather both physics and chemistry fundamental and applicative fields in dealing with solar/black body radiation as well as with new materials based on inorganic-organic hybrids, composites and electron quantum features (excitons, bondons, diffusion, electrical circuits, semiconductors, quantum dots, etc.). Such research is therefore equally highly necessary for both communities (physical engineering and chemical engineering) enlightening the dedicated international forums on quantum-dots based solar cells, as well as for giving further impetus to this new field of photovoltaics by gathering active international scientists in solar energy. The present paper offers a review on the progresses regarding the application of defective graphene and other defect-doped carbon nanostructures in the construction of solar cells devices towards introducing the semiconductor based graphenes. Competitiveness and eco-ecological aspects of such projects are also considered in a resumed scientific and innovative research.     

Measuring markers of liver function using a micropatterned paper device designed for blood from a fingerstick

This paper describes a paper-based microfluidic device that measures two enzymatic markers of liver function (alkaline phosphatase, ALP, and aspartate aminotransferase, AST) and total serum protein. A device consists of four components: (i) a top plastic sheet, (ii) a filter membrane, (iii) a patterned paper chip containing the reagents necessary for analysis, and (iv) a bottom plastic sheet. The device performs both the sample preparation (separating blood plasma from erythrocytes) and the assays; it also enables both qualitative and quantitative analysis of data. The data obtained from the paper-microfluidic devices show standard deviations in calibration runs and "spiked" standards that are acceptable for routine clinical use. This device illustrates a type of test useable for a range of assays in resource-poor settings.     

Magnetic levitation as a platform for competitive protein-ligand binding assays

This paper describes a method based on magnetic levitation (MagLev) that is capable of indirectly measuring the binding of unlabeled ligands to unlabeled protein. We demonstrate this method by measuring the affinity of unlabeled bovine carbonic anhydrase (BCA) for a variety of ligands (most of which are benzene sulfonamide derivatives). This method utilizes porous gel beads that are functionalized with a common aryl sulfonamide ligand. The beads are incubated with BCA and allowed to reach an equilibrium state in which the majority of the immobilized ligands are bound to BCA. Since the beads are less dense than the protein, protein binding to the bead increases the overall density of the bead. This change in density can be monitored using MagLev. Transferring the beads to a solution containing no protein creates a situation where net protein efflux from the bead is thermodynamically favorable. The rate at which protein leaves the bead for the solution can be calculated from the rate at which the levitation height of the bead changes. If another small molecule ligand of BCA is dissolved in the solution, the rate of protein efflux is accelerated significantly. This paper develops a reaction-diffusion (RD) model to explain both this observation, and the physical-organic chemistry that underlies it. Using this model, we calculate the dissociation constants of several unlabeled ligands from BCA, using plots of levitation height versus time. Notably, although this method requires no electricity, and only a single piece of inexpensive equipment, it can measure accurately the binding of unlabeled proteins to small molecules over a wide range of dissociation constants (K(d) values within the range from ~10 nM to 100 μM are measured easily). Assays performed using this method generally can be completed within a relatively short time period (20 min-2 h). A deficiency of this system is that it is not, in its present form, applicable to proteins with molecular weight greater than approximately 65 kDa.     

Use of effect pigments for quality enhancement of offset printed specialty papers

Nowadays, effect pigments are widely used in many printing industries. The colorful effects produced by light scattering of these types of pigments add an additional value to the prints and enhances the overall quality of color appearance. The aim of this study was to investigate the quality enhancement of printed specialty papers with various effect pigments in combination with offset inks. Four different effect pigments were used (one luster pigment‐EP1, two interference pigments‐EP2, EP3, and one multicolor pigment‐EP4) as well as two types of paper substrates (film synthetic paper and wood‐free paper). The effect pigments were overprinted on dried CMYK offset prints on both paper substrates. The following analysis were performed: scanning electron microscopy analysis of effect pigment particles, contact angles of papers and offset prints, Fourier transform infrared spectrocopy (FTIR), principal components analysis (principal components analysis (PCA)), and flop index analysis of overprinted effect pigments, and paper and print gloss. The results of the experiment indicate that effect pigments behaved differently on different printing substrates. From the FTIR and PCA, it was found that the different composition of effect pigments differently influence the behavior of these particles on the final prints. Effect pigments overprinted on offset CMYK inks on both paper substrates enhance print gloss, except interference pigment EP2 on film synthetic paper. It was also found that the ink color has the most pronounced influence on flop index, followed by the papertype and the type of effect pigment. Higher flop index was obtained at wood‐free paper, especially by overprinted pigment EP2. © 2012 Wiley Periodicals, Inc. Col Res Appl, 38, 168–176, 2013.     

The Role of PI3K/AKT and MAPK Signaling Pathways in Erythropoietin Signalization

Erythropoietin (EPO) is a glycoprotein cytokine known for its pleiotropic effects on various types of cells and tissues. EPO and its receptor EPOR trigger signaling cascades JAK2/STAT5, MAPK, and PI3K/AKT that are interconnected and irreplaceable for cell survival. In this article, we describe the role of the MAPK and PI3K/AKT signaling pathways during red blood cell formation as well as in non-hematopoietic tissues and tumor cells. Although the central framework of these pathways is similar for most of cell types, there are some stage-specific, tissue, and cell-lineage differences. We summarize the current state of research in this field, highlight the novel members of EPO-induced PI3K and MAPK signaling, and in this respect also the differences between erythroid and non-erythroid cells.