Generation of quasi-monoenergetic protons from thin multi-ion foils by a combination of laser radiation pressure acceleration and shielded Coulomb repulsion

We study theoretically and numerically the acceleration of protons by a combination of laser radiation pressure acceleration and Coulomb repulsion of carbon ions in a multi-ion thin foil made of carbon and hydrogen. The carbon layer helps to delay the proton layer from disruption due to the Rayleigh–Taylor instability, to maintain the quasi-monoenergetic proton layer and to accelerate it by the electron-shielded Coulomb repulsion for much longer duration than the acceleration time using single-ion hydrogen foils. Particle-in-cell simulations with a normalized peak laser amplitude of a_0 = 5 show a resulting quasi-monoenergetic proton energy of about 70 MeV with the foil made of 90% carbon and 10% hydrogen, in contrast to 10 MeV using a single-ion hydrogen foil. An analytical model is presented to explain quantitatively the proton energy evolution; this model is in agreement with the simulation results. The energy dependence of the quasi-monoenergetic proton beam on the concentration of carbon and hydrogen is also studied

Representation and measurement of the beam health based on one-dimensional model

This paper proposes a method for online structural health evaluation, and analyzes the correlation between online monitoring data and structural health status. On the basis of this analysis, the structural health can be evaluated by using the deviation of the current status from the initially designed status. The health degree index, representation and measurement models are also defined for structural health evaluation in this work. A numerical case study is conducted to validate the related concept and health evaluation model using a beam under pressure loads. The results indicate that the proposed method can effectively represent the structural health status

Efficient inhibition of hepatitis B virus replication by hepatitis delta virus ribozymes delivered by targeting retrovirus

<p>Abstract</p> <p>Background</p> <p>Hepatitis delta virus (HDV) ribozyme is an attractive molecular tool that can specifically recognize and catalyze the self-cleavage of the viral RNA phosphodiester backbone. However, a major obstacle in the medical application of the HDV ribozyme is the lack of specificity in the delivery of the ribozyme to defined target cells.</p> <p>Results</p> <p>The objective of this study was to determine whether retroviral vectors can deliver the HDV ribozyme into the target cells and to elucidate whether HDV ribozyme plays a role in hepatitis B virus (HBV) replication. In our study, the transduction of helper-free pseudotyped retrovirus, which showed a broad host range, in human hepatoma cells was performed under 2 conditions, that is, in the presence of polymerized human serum albumin (pHSA) and in the absence of pHSA. The transduction ability in the presence of pHSA was higher than in the absence of pHSA. Moreover, HBsAg and HBeAg levels after transductions with pHSA were significantly lower than those in the absence of pHSA, thus indicating that the recombinant retrovirus had HBV-specific cleavage activity and targeted HepG2215 cells.</p> <p>Conclusions</p> <p>These data suggest that this system provides a new approach for targeting hepatocytes and has a great potential in gene therapy for HBV infection.</p

Risk factors and management of hyperuricemia after renal transplantation

Hyperuricemia (HUA) is a common complication after renal transplantation. Currently, there is no uniform consensus on factors which increase the risk for and treatment of HUA in renal transplant recipients. The purpose of this review is to summarize current and proposed risk factors and strategies to manage HUA after renal transplantation in order to assist renal function protection and prolong graft survival time

Progress in Electrocatalytic Hydrogen Evolution Based on Monolayer Molybdenum Disulfide

Energy and environmental issues raise higher demands on the development of a sustainable energy system, and the electrocatalytic hydrogen evolution is one of the most important ways to realize this goal. Two-dimensional (2D) materials represented by molybdenum disulfide (MoS2) have been widely investigated as an efficient electrocatalyst for the hydrogen evolution. However, there are still some shortcomings to restrict the efficiency of MoS2 electrocatalyst, such as the limited numbers of active sites, lower intrinsic catalytic activity and poor interlayer conductivity. In this review, the application of monolayer MoS2 and its composites with 0D, 1D, and 2D nanomaterials in the electrocatalytic hydrogen evolution were discussed. On the basis of optimizing the composition and structure, the numbers of active sites, intrinsic catalytic activity, and interlayer conductivity could be significantly enhanced. In the future, the study would focus on the structure, active site, and interface characteristics, as well as the structure-activity relationship and synergetic effect. Then, the enhanced electrocatalytic activity of monolayer MoS2 can be achieved at the macro, nano and atomic levels, respectively. This review provides a new idea for the structural design of two-dimensional electrocatalytic materials. Meanwhile, it is of great significance to promote the study of the structure-activity relationship and mechanism in catalytic reactions