Thermal-Disrupting Interface Mitigates Intercellular Cohesion Loss for Accurate Topical Antibacterial Therapy

Bacterial infections remain a leading threat to global health because of the misuse of antibiotics and the rise in drug-resistant pathogens. Although several strategies such as photothermal therapy and magneto-thermal therapy can suppress bacterial infections, excessive heat often damages host cells and lengthens the healing time. Here, a localized thermal managing strategy, thermal-disrupting interface induced mitigation (TRIM), is reported, to minimize intercellular cohesion loss for accurate antibacterial therapy. The TRIM dressing film is composed of alternative microscale arrangement of heat-responsive hydrogel regions and mechanical support regions, which enables the surface microtopography to have a significant effect on disrupting bacterial colonization upon infrared irradiation. The regulation of the interfacial contact to the attached skin confines the produced heat and minimizes the risk of skin damage during thermoablation. Quantitative mechanobiology studies demonstrate the TRIM dressing film with a critical dimension for surface features plays a critical role in maintaining intercellular cohesion of the epidermis during photothermal therapy. Finally, endowing wound dressing with the TRIM effect via in vivo studies in S. aureus infected mice demonstrates a promising strategy for mitigating the side effects of photothermal therapy against a wide spectrum of bacterial infections, promoting future biointerface design for antibacterial therapy.     

Designing Champion Nanostructures of Tungsten Dichalcogenides for Electrocatalytic Hydrogen Evolution

Fine-tuning strain and vacancies in 2H-phase transition-metal dichalcogenides, although extremely challenging, is crucial for activating the inert basal plane for boosting the hydrogen evolution reaction (HER). Here, atomically curved 2H-WS₂ nanosheets with precisely tunable strain and sulfur vacancies (S-vacancies) along with rich edge sites are synthesized via a one-step approach by harnessing geometric constraints. The approach is based on the confined epitaxy growth of WS₂ in ordered mesoporous graphene derived from nanocrystal superlattices. The spherical curvature imposed by the graphitic mesopores enables the generation of uniform strain and S-vacancies in the as-grown WS₂ nanosheets, and simultaneous manipulation of these two key parameters can be realized by simply adjusting the pore size. In addition, the formation of unique mesoporous WS₂@graphene van der Waals heterostructures ensures the ready access of active sites. Fine-tuning the WS₂ layer number, strain, and S-vacancies enables arguably the best-performing HER 2H-WS₂ electrocatalysts ever reported. Density functional theory calculations indicate that compared with strain, S-vacancies play a more critical role in enhancing the HER activity.     

垂直水平联合自流排渗在银山矿业尾矿库降渗工程中的应用

为解决江西铜业集团银山矿业尾矿库安全检查中发现的坝体浸润线超高问题，保证坝体稳定性，结合尾矿库现场实际情况，在充分分析不同排渗方式特点的基础上，提出采用垂直水平联合自流排渗方式，并制定了经济合理可行的技术方案。通过浸润线观测数据表明:在落实排渗方案以后，坝体浸润线有明显的下降，坝体局部渗水、沼泽化现象有明显改观，有效地保证了坝体稳定性。     

FeCrAl不锈钢包壳管挤压及退火工艺优化

利用光学显微镜、扫描电镜、电子背散射衍射和万能拉伸试验机等对FeCrAl合金包壳管挤压前后的微观组织、析出相及退火后的微观组织、析出相、再结晶及力学性能进行了研究。结果表明:Nb含量对FeCrAl合金中第二相的析出影响显著,高Nb含量下Laves相的析出温度和析出数量均大大提高;降低挤压温度有助于FeCrAl合金管坯中形成细小弥散第二相;随着退火温度升高,细小弥散相的析出数量呈现先增多后减少的趋势;在相同退火工艺下,800 ℃热挤压管坯的室温力学性能比950 ℃热挤压管坯的室温力学性能要更加优异。     

A Dual Inhibitor of DYRK1A and GSK3β for β-Cell Proliferation: Aminopyrazine Derivative GNF4877

Loss of β-cell mass and function can lead to insufficient insulin levels and ultimately to hyperglycemia and diabetes mellitus. The mainstream treatment approach involves regulation of insulin levels; however, approaches intended to increase β-cell mass are less developed. Promoting β-cell proliferation with low-molecular-weight inhibitors of dual-specificity tyrosine-regulated kinase 1A (DYRK1A) offers the potential to treat diabetes with oral therapies by restoring β-cell mass, insulin content and glycemic control. GNF4877, a potent dual inhibitor of DYRK1A and glycogen synthase kinase 3β (GSK3β) was previously reported to induce primary human β-cell proliferation in vitro and in vivo. Herein, we describe the lead optimization that lead to the identification of GNF4877 from an aminopyrazine hit identified in a phenotypic high-throughput screening campaign measuring β-cell proliferation.     

Carborane and cyanine conjugated galactose targeted amphiphilic copolymers for potential near infrared imaging-guided boron neutron capture therapy (BNCT)

Near infrared fluorescent galactose targeted glycopolymer containing m-carborane has been synthesized through ring open and atom transfer radical polymerization, followed by post-functionalization with a cyanine NIR dye. The copolymer could self-assemble into micelles which work as a potential agent for imaging-guided boron neutron capture therapy. The NIR micelles revealed no cytotoxicity for HepG2 cells. An enhanced and fast endocytosis due to the specific interaction between the HepG2 cells and the glycopolymer could be traced by fluorescence microscopy, and the bioimaging makes it possible to trace the nanoparticles and provides information where and when the neutron irradiation should be triggered.     

Optimization of C/TiCx duplex diffusion barrier coatings for SiCf/Ti composites based on interfacial structure evolution exploration

Introducing a carbon single coating is a popular method used to protect SiC_f/Ti composites from severe interface reactions. However, carbon coatings lose their protective effect on SiC fibres at high temperature, even after a short period time. As such, given the strong demand for high temperature applications in aeronautics and astronautics a more coating which is more effective at high temperatures is desirable. In order to improve the high temperature interfacial stability of SiC_f/Ti composites, a C/TiC_x duplex coating system with different C contents in TiC_x was introduced to explore the protection of fibres at 1200?°C for 1?h. The results show that the C/quasi-stoichiometric TiC coating system protects the SiC fibres most effectively. Based on insights from the evolution of the interface structure, TiC_x has been identified as an interfacial reaction product from the C single coating, exhibiting a gradient in C content and grain size, which is different from a deposited TiC layer with a well-distributed composition and structure. The different coating structure gives rise to different ability to resist C diffusion at high temperatures, in which poor resistance ability appears in TiC_x interfacial reaction layer coming from C single coating due to short-circuit diffusion in C-rich fine-grained TiC layer and fast intracrystalline diffusion trigged by amounts of vacancies in sub-stoichiometric coarse-grained TiC layer. Therefore, C/quasi-stoichiometric TiC duplex coatings with a thick, coarse-grained quasi-stoichiometric TiC layer could effectively inhibit C diffusion by comparison to C single coatings, and is more effective than C/rich-carbon TiC duplex coatings due to the existence of short-circuit diffusion in the latter. As such, C/quasi-stoichiometric TiC duplex coatings appear to be an optimal diffusion barrier for SiC_f/Ti composites at high temperature.     

焊缝表面缺陷激光扫描三维重构测量

为检测工件焊缝表面缺陷，采用点激光位移传感测距法和数据拟合技术进行焊缝表面缺陷检测试验研究. 首先采集缺陷表面轮廓数据点，利用高斯滤波对原始数据降噪处理. 再对处理后的数据点进行Delaunay三角剖分，使散乱点连接并结合其空间坐标重构出缺陷的三维模型. 结果表明，基于点激光位移传感测距技术及焊缝表面缺陷三维重构方法可以准确判断焊缝成形情况.     

Rare earth element cerium substituted Ca–Si–Mg system bioceramics: From mechanism to mechanical and degradation properties

Cerium (Ce)-substituted diopsides (CaMgSi₂O₆) with enhanced mechanical strength and bioactivity were fabricated by precipitation method, followed by annealing at 1000 °C for 4 h. The mineralogical, morphological, in vitro biomineralization, degradation, and mechanical properties were investigated in order to assess the factors and mechanisms affecting the resultant properties. The X-ray diffractometer results showed that the onset of substitutional solid solubility in 0.25 mol Ce would result in new phase formation (cerium dioxide [CeO₂], and magnesium silicate [MgSiO₃]) further causing lattice instability. With increasing Ce dopant levels to 1.00 mol, the initial CaMgSi₂O₆ phase was completely replaced by new phases. The field-emission scanning electron microscopy results indicated that the 0.25 mol Ce had the best biomineralization performance in vitro, while less hydroxyapatite precipitates were found with further increasing Ce dopant levels, suggesting the new phases led to the hindrance of precipitates. The weight loss values indicated that the high dissolution rate of ions in the matrix was observed in the pure sample, while the high readsorption rate of ions in the simulated body fluid (SBF) occurred with increasing Ce dopant levels. The pH value and the inductively coupled plasma-mass spectrometer results suggested that the release of Ca and Mg ions controlled the pH value. The mechanical strength of matrices before SBF immersion was related to the phase transformation, the elastic modulus of CeO₂ and CaMgSi₂O₆, and the release of Mg ions, while the mechanical strength of matrices after SBF immersion was dominated by the structure of matrices.