Discontinuous reactions in melt-spun Cu–10 at. %Co alloys and their effect on magnetic anisotropy

The occurrence of discontinuous reactions under isothermal annealing of melt-spun Cu–10 at. % Co alloys, consisting of ribbons (20 µm thick) with columnar grains in the as-solidified state, has been investigated. The microstructure of the ribbons for different annealing temperatures (723–923 K) and annealing times (5–60 min) was determined by transmission electron microscopy, including analysis by energy-dispersive X-ray spectroscopy. Magnetic properties at room temperature were measured by means of hysteresis curve measurements in a vibrating sample magnetometer. Different types of microstructure were observed within grains and at grain boundaries. The spinodal decomposition microstructure was observed during the early stages of annealing for all annealing temperatures. Spherical precipitates grew from the modulated structure at a later stage, forming homogenous distributions throughout the grains. Heterogeneous distributions of incoherent precipitates formed at T > 873 K. As result of discontinuous precipitation, all grain boundaries exhibited arrays of rod-like Co precipitates with diameters and inter-rod spacing of few nanometers. The coarsening of discontinuous precipitates is attributed to a grain boundary-controlled phenomenon, called discontinuous coarsening (DC). The columnar morphology of the grains in the as-solidified alloy was connected with Co rods that were primarily oriented along the ribbon plane. This structure is connected with magnetic anisotropy, which is later weakened by DC. These results elucidate the unusual magnetic behavior of melt-spun Cu–Co alloys and provide a key to understanding their higher magnetoresistance in comparison with other heterogeneous systems.     

Boson Gas in a Periodic Array of Tubes

We report the thermodynamic properties of an ideal boson gas confined in an infinite periodic array of channels modeled by two, mutually perpendicular, Kronig-Penney delta-potentials. The particle’s motion is hindered in the x–y directions, allowing tunneling of particles through the walls, while no confinement along the z direction is considered. It is shown that there exists a finite Bose-Einstein condensation (BEC) critical temperature T _c that decreases monotonically from the 3D ideal boson gas (IBG) value T ₀ as the strength of confinement P ₀ is increased while keeping the channel’s cross section, a _x a _y constant. In contrast, T _c is a non-monotonic function of the cross-section area for fixed P ₀. In addition to the BEC cusp, the specific heat exhibits a set of maxima and minima. The minimum located at the highest temperature is a clear signal of the confinement effect which occurs when the boson wavelength is twice the cross-section side size. This confinement is amplified when the wall strength is increased until a dimensional crossover from 3D to 1D is produced. Some of these features in the specific heat obtained from this simple model can be related, qualitatively, to at least two different experimental situations: ⁴He adsorbed within the interstitial channels of a bundle of carbon nanotubes and superconductor-multistrand-wires Nb₃Sn.     

Multiplexed Biosensing Diagnostic Platforms Detecting Autoantibodies to Tumor-Associated Antigens from Exosomes Released by CRC Cells and Tissue Samples Showed High Diagnostic Ability for Colorectal Cancer

Colorectal cancer (CRC) is the second leading cause of cancer-related death worldwide. The five-year survival rate of CRC patients depends on the stage at diagnosis, being higher than 80% when CRC is diagnosed in the early stages but lower than 10% when CRC is diagnosed in advanced stages. Autoantibodies against specific CRC autoantigens (tumor-associated antigens (TAAs)) in the sera of patients have been widely demonstrated to aid in early diagnosis. Thus, we herein aim to identify autoantigens target of autoantibodies specific to CRC that possess a significant ability to discriminate between CRC patients and healthy individuals by means of liquid biopsy. To that end, we examined the protein content of the exosomes released by five CRC cell lines and tissue samples from CRC patients by means of immunoprecipitation coupled with mass spectrometry analysis. A total of 103 proteins were identified as potential autoantigens specific to CRC. After bioinformatics and meta-analysis, we selected 15 proteins that are more likely to be actual CRC autoantigens in order to evaluate their role in CRC prognosis by Western blot (WB) and immunohistochemistry (IHC). We found dysregulation at the protein level for 11 of these proteins in both tissue and plasma exosome samples from patients, along with an association of nine of these proteins with CRC prognosis. After validation, all but one showed a statistically significant high diagnostic ability to distinguish CRC patients and individuals with premalignant lesions from healthy individuals, either by luminescence Halotag-based beads, or by a multiplexed biosensing platform involving the use of magnetic microcarriers as solid support modified with covalently immobilized Halotag fusion proteins constructed for CRC detection. Taken together, our results highlight the usefulness of the approach defined here to identify the TAAs specific to chronic diseases; they also demonstrate that the measurement of autoantibody levels in plasma against the TAAs identified here could be integrated into a point-of-care (POC) device for CRC detection with high diagnostic ability.