Spinodal decomposition of binary mixtures with composition-dependent heat conductivities

Spinodal decomposition of a very viscous binary mixture is simulated, assuming that the fluid is bounded by two walls that are instantaneously quenched below the critical temperature. As usual, the mixture phase separates by forming dendritic structures whose size grows with time. While in conventional spinodal decomposition the morphology of the mixture is isotropic, here we show that, when the two components of the mixture have different heat conductivities, the configuration of the mixture may become anisotropic, depending on whether heat propagates slower or faster than mass. Specifically, for large heat conductivity differences, when the Lewis number is small, dendrites tend to align parallel to the isothermal lines; when it is large, dendrites progressively align perpendicular to the isothermal lines. This behavior can be explained observing that the morphology of the mixture is the result of two competing effects: on one hand, the mixture phase separates as soon as its temperature reaches its critical value and therefore it tends to follow the isothermal lines; on the other hand, the system tend to maximize heat transport, and therefore dendrites tend to span between the two quenched walls, i.e. perpendicular to the isothermal lines. This explanation is confirmed showing that when the imposed temperature difference between the side walls (and therefore the heat flux at equilibrium as well) is increased, dendrites tend to align across the walls more and more.     

The puzzling afterglow of GRB 050721: a rebrightening seen in the optical but not in the X-ray

We present here the analysis of the early and late multiwavelength afterglow emission, as observed by Swift a small robotic telescope and very large telescope (VLT). We compare early observations with late afterglow observations obtained with Swift and the VLT and we observe an intense rebrightening in the optical band at about 1 day after the burst, which is not present in the X-ray band. The lack of detection in X-ray of such a strong rebrightening at lower energies may be described with a variable external density profile. In such a scenario, the combined X-ray and optical observations allow us to derive that the matter density located at approximately 1017 cm from the burst is approximately a factor of 10 higher than in the inner region. This is the first time in which a rebrightening has been observed in the optical afterglow of a gamma-ray burst that is clearly absent in the X-ray afterglow.     

Cell Contact with Endothelial Cells Favors the In Vitro Maintenance of Human Chronic Myeloid Leukemia Stem and Progenitor Cells

Chronic Myeloid Leukemia (CML) originates in a leukemic stem cell that resides in the bone marrow microenvironment, where they coexist with cellular and non-cellular elements. The vascular microenvironment has been identified as an important element in CML development since an increase in the vascularization has been suggested to be related with poor prognosis; also, using murine models, it has been reported that bone marrow endothelium can regulate the quiescence and proliferation of leukemic stem and progenitor cells. This observation, however, has not been evaluated in primary human cells. In this report, we used a co-culture of primitive (progenitor and stem) CML cells with endothelial colony forming cells (ECFC) as an in vitro model to evaluate the effects of the vascular microenvironment in the leukemic hematopoiesis. Our results show that this interaction allows the in vitro maintenance of primitive CML cells through an inflammatory microenvironment able to regulate the proliferation of progenitor cells and the permanence in a quiescent state of leukemic stem cells.     

A Combinatorial Virtual Screening Approach Driving the Synthesis of 2,4-Thiazolidinedione-Based Molecules as New Dual mPGES-1/5-LO Inhibitors

Dual inhibition of microsomal prostaglandin E₂ synthase-1 (mPGES-1) and 5-lipoxygenase (5-LO), two key enzymes involved in pro-inflammatory eicosanoid biosynthesis, represents a new strategy for treating inflammatory disorders. Herein we report the discovery of 2,4-thiazolidinedione-based mPGES-1/5-LO dual inhibitors following a multidisciplinary protocol, involving virtual combinatorial screening, chemical synthesis, and validation of the biological activities for the selected compounds. Following the multicomponent-based chemical route for the decoration of the 2,4-thiazolidinedione core, a large library of virtual compounds was built (∼2.0×10⁴ items) and submitted to virtual screening. Nine selected molecules were synthesized and biologically evaluated, disclosing among them four compounds able to reduce the activity of both enzymes in the mid- and low- micromolar range of activities. These results are of interest for further expanding the chemical diversity around the 2,4-thiazolidinedione central core, facilitating the identification of novel anti-inflammatory agents endowed with a promising and safer pharmacological profile.     

Improved batch fuzzy learning vector quantization for image compression

In this paper, we develop a batch fuzzy learning vector quantization algorithm that attempts to solve certain problems related to the implementation of fuzzy clustering in image compression. The algorithm’s structure encompasses two basic components. First, a modified objective function of the fuzzy c-means method is reformulated and then is minimized by means of an iterative gradient-descent procedure. Second, the overall training procedure is equipped with a systematic strategy for the transition from fuzzy mode, where each training vector is assigned to more than one codebook vectors, to crisp mode, where each training vector is assigned to only one codebook vector. The algorithm is fast and easy to implement. Finally, the simulation results show that the method is efficient and appears to be insensitive to the selection of the fuzziness parameter.     

Schedule-induced kinesic and taxic behavioral stereotypy in the pigeon.

Two experiments explored the functional character of 2 schedule-induced interim behaviors (pacing and retreat) and 1 terminal behavior (keypecking) that developed on fixed-time (FT) schedules of food delivery with a keylight that increased in brightness throughout the interstimulus interval. In Experiment 1, this ramp procedure was compared with a less discriminable ramp, and FT and Random Time (RT) procedures without a signal. Decreased discriminability expanded keypecking in the trial. The FT schedule eliminated only keypecking and the RT procedure eliminated keypecking and retreat while pacing remained. In Experiment 2, predictive and unpredictive ramps were added to the RT procedure. The data suggest that schedule-induced stereotypy can be divided into kinesic stereotypy (pacing), which arises from repeated reinforcer presentations, and taxic stereotypy, which is tied to an increase (keypecking) or decrease (retreat) in the momentary probability of reinforcement. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

A novel tri-functional antibody fusion protein with improved pharmacokinetic properties generated by fusing a bispecific single-chain diabody with an albumin-binding domain from streptococcal protein G

The therapeutic application of small recombinant antibody molecules is often limited by a short serum half-life. In order to improve the pharmacokinetic properties, we have investigated a strategy utilizing fusion with an albumin-binding domain (ABD) from streptococcal protein G. This strategy was applied to a bispecific single-chain diabody (scDb CEACD3) developed for the retargeting of cytotoxic T cells to CEA-expressing tumor cells. This novel tri-functional fusion protein (scDb-ABD) was expressed in mammalian cells and recognized both antigens as well as human and mouse serum albumin. scDb-ABD was capable to retarget T cells to CEA-expressing target cells in vitro and to activate the effector cells as measured by stimulation of IL-2 release. Although activity was reduced 3-fold compared with scDb and further reduced 4-fold in the presences of human serum albumin, this assay demonstrated that scDb-ABD is active when exposed to all three antigens. Compared with scDb, the circulation time of scDb-ABD in mice was prolonged 5- to 6-fold similar to a previously described scDb-HSA fusion protein. This strategy, which adds only a small protein domain (46 amino acids) and which utilizes high-affinity, non-covalent albumin interaction, should be broadly applicable to improve serum half-lives of small recombinant antibody molecules.