高效液相色谱法测定黄酒中苯甲酸、山梨酸和糖精钠含量

目的建立高效液相色谱法测定黄酒中苯甲酸、山梨酸和糖精钠的分析方法。方法样品经称取、加热、定容,利用高效液相色谱法检测,甲醇水混合溶液作为流动相,PDA检测器检测,苯甲酸、山梨酸和糖精钠的检测波长为230nm。结果苯甲酸和山梨酸在0.05~0.30 mg/mL、糖精钠在0.0025~0.0125mg/mL时,都具有良好的线性关系,相关系数(r)均0.999。苯甲酸、山梨酸和糖精钠的LOD分别为1.8、1.2、0.1g/kg,LOQ分别为5.4、3.6、0.3mg/kg。平均加标回收率为95.1%~96.4%,RSD为2.6%~3.8%。50份黄酒样品中,苯甲酸检出有19份,检出率为38.0%,检测结果范围为0.0025~1.48g/kg;山梨酸检出有6份,检出率为12.0%,检测结果范围为0.028~0.44g/kg;糖精钠检出有24份,检出率为48.0%,检测结果范围为0.005~0.73g/kg。结论该方法灵敏度高,回收率高,检测限低,符合分析要求,适合黄酒中苯甲酸、山梨酸和糖精钠的检测要求。     

State of the art of bioimplants manufacturing: part I

Bioimplants are becoming increasingly important in the modern society due to the fact of an aging population and associated issues of osteoporosis and osteoarthritis. The manufacturing of bioimplants involves an understanding of both mechanical engineering and biomedical science to produce biocompatible products with adequate lifespans. A suitable selection of materials is the prerequisite for a long-term and reliable service of the bioimplants, which relies highly on the comprehensive understanding of the material properties. In this paper, most biomaterials used for bioimplants are reviewed. The typical manufacturing processes are discussed in order to provide a perspective on the development of manufacturing fundamentals and latest technologies. The review also contains a discussion on the current measurement and evaluation constraints of the finished bioimplant products. Potential future research areas are presented at the end of this paper. The full text can be downloaded at https://link.springer.com/article/10.1007/s40436-017-0207-4     

The Effect of Isosaponarin Derived from Wasabi Leaves on Glutamate Release in Rat Synaptosomes and Its Underlying Mechanism

Excessive glutamate release is known to be involved in the pathogenesis of neurological diseases, and suppression of glutamate release from nerve terminals is considered to be a treatment strategy. In this study, we investigated whether isosaponarin, a flavone glycoside isolated from wasabi leaves, could affect glutamate release in rat cerebral cortex nerve terminals (synaptosomes). The release of glutamate was evoked by the K⁺ channel blocker 4-aminopyridine (4-AP) and measured by an online enzyme-coupled fluorimetric assay. Isosaponarin produced a concentration-dependent inhibition of 4-AP-evoked glutamate release with a half-maximum inhibition of release value of 22 μM. The inhibition caused by isosaponarin was prevented by eliminating extracellular Ca²⁺ or by using bafilomycin A1, an inhibitor of synaptic vesicle exocytosis. Isosaponarin decreased intrasynaptosomal rises in Ca²⁺ levels that were induced by 4-AP, without affecting the synaptosomal membrane potential. The isosaponarin-induced inhibition of glutamate release was significantly prevented in synaptosomes that were pretreated with a combination of the calcium channel blockers ω-conotoxin GVIA (N-type) and ω-agatoxin IVA (P/Q-types). The protein kinase C (PKC) pan-inhibitor GF109203X and the Ca²⁺-dependent PKC inhibitor Go6976 abolished the inhibition of glutamate release by isosaponarin, while the Ca²⁺-independent PKC inhibitor rottlerin did not show any effect. The results from immunoblotting assays also showed that isosaponarin lowered PKC, PKCα, synaptosomal-associated protein of 25 kDa (SNAP-25), and myristoylated alanine-rich C-kinase substrate (MARCKS) phosphorylation induced by 4-AP. In addition, FM1-43-labeled synaptic vesicles in synaptosomes showed that treatment with isosaponarin resulted in an attenuation of the 4-AP-induced decrease in fluorescence intensity that is consistent with glutamate release. Transmission electron microscopy of synaptosomes also provided evidence that isosaponarin altered the number of synaptic vesicles. These results indicate that isosaponarin suppresses the Ca²⁺-dependent PKC/SNAP-25 and MARCKS pathways in synaptosomes, causing a decrease in the number of available synaptic vesicles, which inhibits vesicular glutamate release from synaptosomes.     

Cross-stream migration of nonspherical particles in second-order fluid flows: Effect of flow profiles

We investigate the cross-stream migration of spheroidal particles in a weakly viscoelastic fluid under various unbound parabolic flows (circular and elliptic tube flow, as well as 2D slit flow). The viscoelastic fluid investigated is a second-order fluid under the co-rotational limit. Our theory finds that the different flow profiles do not significantly alter the migration speed of particles toward the flow centerline, but drastically alter their orientation dynamics. At long times, prolate particles align along the flow direction in a circular tube flow, but undergo log-rolling in a 2D slit flow. We explain the origin of these orientation dynamics, and explain why such behavior can give rise to a similar cross-stream migration velocity. We lastly examine particle motion in an unbound elliptic tube flow with unequal velocity curvature in the two lateral directions. We quantify the conditions under which the long-time particle orientation changes from log-rolling to flow-alignment.     

Polarization-insensitive 3D conformal-skin metasurface cloak

Electromagnetic metasurface cloaks provide an alternative paradigm toward rendering arbitrarily shaped scatterers invisible. Most transformation-optics (TO) clo...     

An Anthranilate Derivative Inhibits Glutamate Release and Glutamate Excitotoxicity in Rats

The neurotransmitter glutamate plays an essential role in excitatory neurotransmission; however, excessive amounts of glutamate lead to excitotoxicity, which is the most common pathogenic feature of numerous brain disorders. This study aimed to investigate the role of butyl 2-[2-(2-fluorophenyl)acetamido]benzoate (HFP034), a synthesized anthranilate derivative, in the central glutamatergic system. We used rat cerebro-cortical synaptosomes to examine the effect of HFP034 on glutamate release. In addition, we used a rat model of kainic acid (KA)-induced glutamate excitotoxicity to evaluate the neuroprotective potential of HFP034. We showed that HFP034 inhibits 4-aminopyridine (4-AP)-induced glutamate release from synaptosomes, and this inhibition was absent in the absence of extracellular calcium. HFP034-mediated inhibition of glutamate release was associated with decreased 4-AP-evoked Ca²⁺ level elevation and had no effect on synaptosomal membrane potential. The inhibitory effect of HFP034 on evoked glutamate release was suppressed by blocking P/Q-type Ca²⁺ channels and protein kinase C (PKC). Furthermore, HFP034 inhibited the phosphorylation of PKC and its substrate, myristoylated alanine-rich C kinase substrate (MARCKS) in synaptosomes. We also observed that HFP034 pretreatment reduced neuronal death, glutamate concentration, glial activation, and the levels of endoplasmic reticulum stress-related proteins, calpains, glucose-regulated protein 78 (GRP 78), C/EBP homologous protein (CHOP), and caspase-12 in the hippocampus of KA-injected rats. We conclude that HFP034 is a neuroprotective agent that prevents glutamate excitotoxicity, and we suggest that this effect involves inhibition of presynaptic glutamate release through the suppression of P/Q-type Ca²⁺ channels and PKC/MARCKS pathways.     

Multi-extremum-modified response basis model for nonlinear response prediction of dynamic turbine blisk

For the nonlinear dynamic analyses of complex mechanical components, it is necessary to apply efficient modeling framework to reduce computational burden. The accurate surrogate model for approximating the nonlinear responses of several failures is a vital issue to provide robust and safe design conditions in complex engineering applications. In this paper, two different Modified multi-extremum Response Surface basis Models (MRSM) are proposed for dynamic nonlinear responses of failure capacities for turbine blisk responses. The proposed MRSM is established using two regression processes including regressed the input variables by linear or exponential basis functions in first calibrating phase and regressed the second-order polynomial basis function using inputs data provided by first stage in second calibrating procedure. A sensitivity analysis using MRSM is proposed to consider the variation of input variables on the nonlinear responses. In the sensitivity analysis procedure, the effects of input variables are evaluated using the calibrating results given from the first regressed process. To evaluate the performance of the proposed MRSM, three multi-extremum failure modes including radial deformation of compressor blisk, maximum strain, and stress of compressor blade and disk are considered. the prediction of MRSM of nonlinear responses for Thermal-fluid–structure system with dynamical nonlinear finite-element analyses is compared with response surface method (RSM) and artificial neural network (ANN). The predicted results of modeling approaches showed that the sensitivity analysis based on MRSM accurately provided the effective degree for input variables. The gas temperature has the highest effects on nonlinear responses of turbine blisk which is followed by angular speed and material density. The MRSM combined with basic exponential function performs better than other models, while the MRSM coupled with linear function is more accurate than ANN and RSM. The proposed MRSM models have illustrated the accurate and efficient framework for approximating dynamic structural analysis of complex components.

     

Genome-Wide Discovery of miRNAs with Differential Expression Patterns in Responses to Salinity in the Two Contrasting Wheat Cultivars

Salinity is a serious environmental issue. It has a substantial effect on crop yield, as many crop species are sensitive to salinity due to climate change, and it impact is continuing to increase. Plant microRNAs (miRNAs) contribute to salinity stress response in bread wheat. However, the underlying molecular mechanisms by which miRNAs confer salt tolerance in wheat are unclear. We conducted a genome-wide discovery study using Illumina high throughput sequencing and comprehensive in silico analysis to obtain insight into the underlying mechanisms by which small RNAs confer tolerance to salinity in roots of two contrasting wheat cvv., namely Suntop (salt-tolerant) and Sunmate (salt-sensitive). A total of 191 microRNAs were identified in both cultivars, consisting of 110 known miRNAs and 81 novel miRNAs; 181 miRNAs were shared between the two cultivars. The known miRNAs belonged to 35 families consisted of 23 conserved and 12 unique families. Salinity stress induced 43 and 75 miRNAs in Suntop and Sunmate, respectively. Among them, 14 and 29 known and novel miRNAs were expressed in Suntop and 37 and 38 in Sunmate. In silico analysis revealed 861 putative target mRNAs for the 75 known miRNAs and 52 putative target mRNAs for the 15 candidate novel miRNAs. Furthermore, seven miRNAs including tae-miR156, tae-miR160, tae-miR171a-b, tae-miR319, tae-miR159a-b, tae-miR9657 and novel-mir59 that regulate auxin responsive-factor, SPL, SCL6, PCF5, R2R3 MYB, and CBL-CIPK, respectively, were predicted to contribute to salt tolerance in Suntop. This information helps further our understanding of how the molecular mechanisms of salt tolerance are mediated by miRNAs and may facilitate the genetic improvement of wheat cultivars.     

The study on the shrink-fit multi-ring flywheel with fall-off function

Structural integrity of the flywheel of reactor coolant pump is important for safe operation of a nuclear power plant.A shrink-fit multi-ring flywheel is designed with a fall-off function,i.e.,it will separate from the shaft at a designed fall-off rotation speed,which is determined by the assembly process and the gravity.However,the two factors are ignored in the analytical method based on the Lame's equation.In this work,we conducted fall-off experiments to analyze the two factors and used the experimental data to verify the validity of the analytical method and the finite element method (FEM).The results show that FEM performs better than the analytical method in designing the falloff function of the flywheel,though FEM cannot successfully predict the strain variation with the rotational speed.