Self-powered Pt/a-Ga2O3/ITO vertical Schottky junction solar-blind photodetector with excellent detection performance.

Self-powered solar-blind photodetectors (PDs) are promising for military and civilian applications owing to convenient operation, easy preparation, and weak-light sensitivity. In the present study, the solar-blind deep-ultraviolet (DUV) photodetector based on amorphous Ga2O3 (a-Ga2O3) and with a simple vertical stack structure is proposed by applying the low-cost magnetron sputtering technology. By tuning the thickness of the amorphous Ga2O3 layer, the device exhibits excellent detection performance. Under 3 V reverse bias, the photodetector achieves a high responsivity of 671A/W, a high detectivity of 2.21 × 1015 Jones, and a fast response time of 27/11 ms. More extraordinary, with the help of the built-in electric field at the interface, the device achieves an excellent performance in detection when self-powered, with an ultrahigh responsivity of 3.69 A/W and a fast response time of 2.6/6.6 ms under 254 nm light illumination. These results demonstrate its superior performance to most of the self-powered Schottky junction UV photodetectors reported to date. Finally, the Pt/a-Ga2O3/ITO Schottky junction photodiode detector is verified as a good performer in imaging, indicating its applicability in such fields as artificial intelligence, machine vision, and solar-blind imaging.

Simultaneous electrochemical degradation of tetracycline and metronidazole through a high-efficiency and low-energy-consumption advanced oxidation process.

With the increasing complexity of water environment pollution, it is becoming ever more practical to study the simultaneous removal of multiple pollutants in water. Electrochemical advanced oxidation technology is considered to be one of the most promising green approaches for the degradation of organic pollutants. Herein, Ti3+ and oxygen vacancies (VO) self-doped TiO2-x nanotube array electrodes are employed to investigate the simultaneous degradation and an energy consumption assessment for the effective removal of the antibiotics tetracycline (TC) and metronidazole (MNZ). The electrocatalytic performance of the nanotube arrays prepared at different reduction times is significantly different. The electrochemical reduction of TiO2 nanotube arrays for 10 min presents the best degradation performance for TC and MNZ. When a mixed solution of TC and MNZ is simultaneously degraded, the removal rate of TC (50 mg L-1) and MNZ (50 mg L-1) within 3 h reaches 100%, while the chemical oxygen demand (COD) removal rate is 79.1%. The energy consumption is significantly reduced compared to the degradation of a single substance. Simultaneously, the current utilization rate of the electrochemical degradation system is also significantly improved, with a specific energy consumption of only 85.78 kWh kg-1 and an average current efficiency that can reach 20.2%.

[Clinical Efficacy of High Dose Methotrexate, Temozolomide and Rituximab in the Treatment of Patients with Primary Central Nervous System Lymphoma].

OBJECTIVE: To investigate the clinical efficacy of high dose methotrexate (HD-MTX), temozolomide (TMZ), and rituximab (R) in the treatment of patients with primary central nervous system lymphoma (PCNSL). METHODS: Clinical data of patients with PCNSL diagnosed and treated in Guangdong Provincial People's Hospital from February 2010 to May 2017 were collected. First, patients were given 6-8 cycles of MTX (3.5 g/m2) for induction treatment, and then 12 cycles of TMZ (150 mg/m2) for maintenance treatment. The day before induction treatment, patients were given rituximab 375 mg/m2 according to their economic status. A retrospective cohort study was performed on patients receiving HD-MTX+TMZ or HD-MTX+TMZ+R to analyze the efficacy and survival. RESULTS: There were 42 patients enrolled in the study, 17 cases in HD-MTX+TMZ group and 25 cases in HD-MTX+TMZ+R group. The median PFS and OS times in HD-MTX+TMZ+R group were 56.7 months and N/A, respectively, while, 7.3 months and 34.7 months in HD-MTX+TMZ group, respectively. In addition, there was no significant difference in median survival between patients who received TMZ maintenance therapy and those who were only actively monitored. During the induction period, all the patients had grade 1-2 nausea and vomiting, while in the consolidation treatment period, no grade 3/4 toxicity was observed. CONCLUSION: The combination of HD-MTX+TMZ+R in the treatment of PCNSL patients shows a definite short-term effect, which can increase the survival rate of the patients. The side effects are mild, and the patients can generally tolerate.

Electrochemically reduced phytic acid-doped TiO2 nanotubes for the efficient electrochemical degradation of toxic pollutants.

Element-doped TiO2 nanotube arrays (TNAs) with optimized active sites provide an effective approach for significantly improving electrocatalytic performance. The challenges in such construction mainly include selection of green dopant and control of active sites. Herein, we present phytic acid as a phosphorus source for P-doped TNAs. An oxygen vacancy (Ov) and P co-doped TNAs (P-TiO2-y) was prepared as an electrochemical oxidation anode. P-TiO2-y exhibits excellent degradation activity due to the formation of Ti-O-P bonds and generation of Ov. P-doping was beneficial in improving the oxygen evolution potential of the electrode, which would be benefit for electrocatalytic degradation of pollutants. Using the P-TiO2-y anode with a current density of 10 mA/cm2 for tetracycline degradation, after a 3 h treatment, the removal rate, chemical oxygen demand and total organic carbon removal rates were 100%, 90.32% and 76.60%, respectively. The P-TiO2-y also has excellent degradation performance for phenol, hydroquinone, p-nitrophenol and metronidazole.

Nanosilver and protonated carbon nitride co-coated carbon cloth fibers based non-enzymatic electrochemical sensor for determination of carcinogenic nitrite.

A novel electrochemical nitrite (NaNO2) sensor was fabricated by combining nanosilver with protonated carbon nitride (H-C3N4) supported on carbon cloth (CC). H-C3N4 was distributed uniformly on the CC surface, providing more active sites for the electrocatalytic active center (nanosilver). CC as a substrate improved the H-C3N4 conductivity and provided the sensor with a flexible feature. The strong synergistic effect between CC, H-C3N4, and nanosilver can exert a significant electrocatalytic performance on the flexible sensor. The Ag/H-C3N4/CC flexible sensor electrode did not consume much more time to polish the surface of traditional electrodes, and possessed a high sensitivity of 0.85537 µA/mg, a wide linear response range that spanned 5 to 1000 µM, a low detection limit of 0.216 µM (S/N = 3), and high selectivity for nitrite in the presence of common organic and inorganic interfering species (such as CaCl2, NaCl, MgCl2, NaNO3, glucose, urea, and p-nitrophenol). The Ag/H-C3N4/CC flexible sensor can be used for sample detection of nitrite as it has a strong anti-interference ability, good reproducibility, repeatability, and long-term stability. The Ag/H-C3N4/CC sensor is a promising alternative electrode to traditional ones such as ITO, gold or glassy carbon electrodes.

Angiopep-2 conjugated nanoparticles loaded with doxorubicin for the treatment of primary central nervous system lymphoma.

Primary central nervous system lymphoma (PCNSL) is a rare brain tumor. Its therapeutic efficacy is much lower than that of traditional lymphoma, largely due to the presence of the blood-brain barrier (BBB), which hinders the effective drug delivery and deposition on the disease site. Angiopep-2 (ANG) can target low-density lipoprotein receptor-related protein (LRP) on the surface of brain capillary endothelial cells (BCECs) and exhibits high BBB transport capability. In this study, we designed an ANG conjugated poly(ethylene glycol)-b-poly(ε-caprolactone) (PEG-b-PCL) (APP) nanoparticle to deliver doxorubicin (DOX) for the treatment of PCNSL. Our data indicated that the targeted APP nanoparticles showed significantly increased cellular uptake by BCECs compared with the control nanoparticles. In the intracranial SU-DHL-2-LUC lymphoma xenograft mice model, APP enhanced drug deposition in tumor tissues, and DOX-loaded APP (APP@DOX) exhibited a better therapeutic effect than free DOX and nontargeted PP@DOX, which significantly prolonged the survival time of mice.

Electrochemical Actuators Based on Two-Dimensional Ti3C2Tx (MXene).

Electrochemical actuators are devices that convert electrical energy into mechanical energy via electrochemical processes. They are used in soft robotics, artificial muscles, micropumps, sensors, and other fields. The design of flexible and stable electrode materials remains a major challenge. MXenes, an emerging family of 2D materials, have found applications in energy storage. Here, we report an actuator device using MXene (Ti3C2Tx) as a flexible electrode material. The electrode in 1 M H2SO4 electrolyte exhibits a curvature change up to 0.083 mm-1 and strain of 0.29%. Meanwhile, the MXene-based actuator with a symmetric configuration separated by gel electrolyte (PVA-H2SO4) has curvature and strain changes up to 0.038 mm-1 and 0.26% with excellent retention after 10,000 cycles. In situ X-ray diffraction analysis demonstrates that the actuation mechanism is due to the expansion and shrinkage of the interlayer spacing of MXenes. This research shows promise of this new family of materials for electrochemical actuators.

Phenotypic and genetic evidence for ecological speciation of Aquilegia japonica and A. oxysepala.

Natural selection is thought to be a driving force that can cause the evolution of reproductive isolation. The genus Aquilegia is a model system to address how natural selection promotes the process of speciation. Morphological differences between A. oxysepala, A. japonica and their hybrids were quantified for two vegetative (plant height and leaf area) and three floral morphological (sepal area, corolla length and diameter) traits. We also evaluated the genetic variability of the two species and their hybrids based on two chloroplast (1225 bp), four nuclear (5811 bp) genes and 15 microsatellites. Our results revealed that differentiation of A. japonica and A. oxysepala at the ecological and morphological levels also involved divergence at the genetic level. In addition, the analysis of nucleotide variation patterns showed that the two species possessed numerous fixation sites at nuclear genes gAA4, gA7 and gAA12. Furthermore, we found that all of the phenotypic hybrids also showed a genetically admixed ancestry. These findings suggest that natural selection has indeed facilitated the formation of distinct genetic variation patterns in the two Aquilegia species and habitat adaptation has been driving the ecologically based evolution of reproductive isolation.

Cellular responses to electrospun membranes made from blends of PLLGA with PEG and PLLGA-b-PEG.

Control of cellular responses is crucial for the use of electrospun membranes in biomedical applications, including tissue engineering or biomedical devices. However, it is still unclear whether adhesion and proliferation of fibroblasts is stimulated or inhibited on polyethylene glycol (PEG)-modified electrospun membranes. In this study, poly(L-lactide-co-glycolide) (PLLGA)-PEG copolymer and pure PEG were blended with PLLGA, and then electrospun onto nonwoven membranes. The effects of blending of PLLGA-PEG or pure PEG on the adsorption of proteins, and further on the adhesion and proliferation of L929 fibroblasts on the electrospun membranes were investigated. Addition of PLLGA-PEG or PEG significantly improved the hydrophilicity of the electrospun membranes. Pure PEG had no obvious effects on the growth of L929 fibroblasts; in contrast, PLLGA-PEG significantly inhibited the adsorption of proteins and the proliferations of the cells on the electrospun membranes. In response to diminished protein adsorption, mRNA expression of genes related to cell adhesion and migration was up-regulated. The limited effects of pure PEG were probably caused by its preferential dissolution, whereas membrane-confined PLLGA-PEG displayed excellent performance on the inhibition of protein adsorption and cell proliferation.

Genomic and EST microsatellite markers for Aquilegia flabellata and cross-amplification in A. oxysepala (Ranunculaceae).

PREMISE OF THE STUDY: The goal of this study was to identify genomic and expressed sequence tag (EST)-derived microsatellite markers from the species Aquilegia flabellata and assess their transferability in A. oxysepala. METHODS AND RESULTS: Eleven genomic and nine EST-derived microsatellite loci were characterized in A. flabellata. These microsatellite primers amplified 66 alleles in all 20 loci. The observed heterozygosity (H(O)) for each population ranged from 0.00 to 0.94. CONCLUSIONS: All of the 20 loci were successfully amplified in A. oxysepala. These genomic and EST-derived microsatellite markers will be useful in further genetic structure, speciation, and adaptive evolution studies.

[A comparative study of early degradation of PLLA and PLGA rods at various sites in rabbit].

This study was designed to assess the effect of implantation site and environment on early in vivo degradation behaviors of poly(L-lactide) (PLLA) and poly(L-lactide-co-glycolide) (PLGA) copolymer. The rods were implanted at two sites in each of 24 New Zealand White rabbits. The first site was within the suprapatellar bursa of the joint cavities (JC) and the second site was in the opposite condyles of femurs (CF). Three rabbits of each group underwent explantation of rods after 4, 8, 12, and 16 weeks. At each interval, measures were taken to evaluate the molecular weight, shear strength, weight loss and thermal properties of PLLA and PLGA. It was found that PLGA degraded slightly faster than PLLA. After 16 weeks, PLLA's initial inherent viscosity of 4.6 decreased to about 3.4 in both implantation sites while that of PLGA decreased from 4.6 to about 2.2. Both PLGA and PLLA showed enough shear strength retention in 16 weeks (> or = 53MPa) within 16 weeks. Autocatalysis mechanism was confirmed by the fact of accelerated weight loss of PLGA after 8 weeks and of PLLA after 12 weeks. The results revealed that PLGA could be a promising candidate material as a replacement of PLLA in internal fixation of bone fractures, and no significant difference of early in vivo degradation behaviors between PLLA and PLGA was observed in regard to different implantation sites in 16 weeks.