网络办公自动化的设计与实现——以辽宁科技学院网络办公平台为例

阐述了网络办公平台的发展现状及研究意义,讨论了网络办公平台系统的设计与实现,最后对该系统进行了应用分析.开发平台采用JSP技术,后台采用Oracle数据库,该系统的设计与实现为高校校园办公、科研和教学提供了高效的现代化管理手段.     

基于参数微扰法精确计算铍离子Be2+和硼离子B3+的基态能量

建立含有屏蔽参数σ的铍离子Be~(2+)(z=4)和硼离子B~(3+)(z=5)的哈密顿方程.以有效核电荷数为z*=z-σ的类氢原子基态1s和激发态ns(n=2,3,…)组合的双电子波函数,作为铍离子Be~(2+)和硼离子B~(3+)的基态近似波函数.应用参数微扰法确定铍离子Be~(2+)的屏蔽参数σ=0.56350197和硼离子B~(3+)的屏蔽参数σ=0.525070444,应用参数微扰法计算铍离子Be~(2+)三级近似基态能量和硼离子B~(3+)四级近似基态能量的理论值与实验值的误差为ΔE≈10~(-4)~10~(-5)a.u..     

单片机在计算机散热系统中的研究

单片机在检测和控制系统中有着广泛的应用,温度是系统经常需要测量、控制、保持的一个量。本文的温度测量和控制系统主要由DSl8820温度传感器和AT89C51单片机组成,计算机散热系统主要有风扇和水盒来完成。     

山西省环境保护局办公自动化系统的设计

通过对“山西省环境保护局办公自动化系统”设计的介绍，探讨了办公自动化系统应用Iternet技术在Intranet网络环境下实现的方法。     

Vxworks基于S3C44B0X处理器的中断处理设计

嵌入式微处理器和嵌入式实时操作系统是嵌入式系统的两大核心技术。详细分析了wind River公司的嵌入式实时操作系统Vxworks中断处理机制,并针对Vxworks中断处理机制对于SAMSUNG公司ARM7微处理器芯片S3C44B0X的特殊性,给出了Vxworks基于S3C44B0X处理器的中断实现。     

N-Butyrylated Hyaluronic Acid Achieves Anti-Inflammatory Effects In Vitro and in Adjuvant-Induced Immune Activation in Rats

Previously synthesized N-butyrylated hyaluronic acid (BHA) provides anti-inflammatory effects in rat models of acute gouty arthritis and hyperuricemia. However, the mechanism of action remains to be elucidated. Herein, the anti-inflammatory and antioxidative activities of BHA and the targeted signaling pathways were explored with LPS-induced RAW264.7 and an adjuvant-induced inflammation in a rat model. Results indicated that BHA inhibited the generation of pro-inflammatory cytokines TNFα, IL-1β and IL-6, reduced ROS production and down-regulated JAK1-STAT1/3 signaling pathways in LPS-induced RAW264.7. In vivo, BHA alleviated paw and joint swelling, decreased inflammatory cell infiltration in paw tissues, suppressed gene expressions of p38 and p65, down-regulated the NF-κB and MAPK signaling pathways and reduced protein levels of TNFα, IL-1β and IL-6 in joint tissues of arthritis rats. This study demonstrated the pivotal role of BHA in anti-inflammation and anti-oxidation, suggesting the potential clinical value of BHA in the prevention of inflammatory arthritis and is worthy for development as a new pharmacological treatment.     

Anti-Inflammatory Effects of Spiramycin in LPS-Activated RAW 264.7 Macrophages

Drug repurposing is a simple concept with a long history, and is a paradigm shift that can significantly reduce the costs and accelerate the process of bringing a new small-molecule drug into clinical practice. We attempted to uncover a new application of spiramycin, an old medication that was classically prescribed for toxoplasmosis and various other soft-tissue infections; specifically, we initiated a study on the anti-inflammatory capacity of spiramycin. For this purpose, we used murine macrophage RAW 264.7 as a model for this experiment and investigated the anti-inflammatory effects of spiramycin by inhibiting the production of pro-inflammatory mediators and cytokines. In the present study, we demonstrated that spiramycin significantly decreased nitric oxide (NO), interleukin (IL)-1β, and IL-6 levels in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. Spiramycin also inhibited the expression of NO synthase (iNOS), potentially explaining the spiramycin-induced decrease in NO production. In addition, spiramycin inhibited the phosphorylation of mitogen-activated protein kinases (MAPKs); extracellular signal-regulated kinase (ERK) and c-Jun N terminal kinase (JNK) as well as the inactivation and subsequent nuclear translocation of nuclear factor κB (NF-κB). This indicated that spiramycin attenuates macrophages’ secretion of IL-6, IL-1β, and NO, inducing iNOS expression via the inhibition of the NF-κB and MAPK signaling pathways. Finally, we tested the potential application of spiramycin as a topical material by human skin primary irritation tests. It was performed on the normal skin (upper back) of 31 volunteers to determine whether 100 μM and μM of spiramycin had irritation or sensitization potential. In these assays, spiramycin did not induce any adverse reactions. In conclusion, our results demonstrate that spiramycin can effectively attenuate the activation of macrophages, suggesting that spiramycin could be a potential candidate for drug repositioning as a topical anti-inflammatory agent.     

分光光度法测定碱性无汞电池中铟的含量

研究了在硫酸介质中,非离子型表面活性剂PVA存在下,乙基罗丹明B络阳离子与InI4^-络阴离子所形成的离子缔合物分散在水相中,形成了胶束增溶显色体系,缔合物的最大吸收波长位于602nm处,方法的表观摩尔吸光系数为ε’602=1．58×10^5L·mol^-1·cm^-1,铟含量在0-11μg／10mL范围内服从比尔定律,用于碱性无汞电池样品中铟的测定,相对标准偏差为1．9％（n=4）,加标回收率为95％-107％,比对实验结果吻合．     

基于UML与Struts的客户合同管理子系统设计与实现

运用基于UML的面向对象开发方法以及Struts体系结构,对B／S模式的某港口物流系统中客户与合同管理信息系统进行了分析、设计与实现．分析了客户与合同管理的信息需求,利用Rational Rose对系统进行建模,给出了系统模型和实现的总体类图,并予实现．     

Amphotericin B and Curcumin Co-Loaded Porous Microparticles as a Sustained Release System against Candida albicans

Amphotericin B (AMB) is an antifungal drug used for serious fungal infections. However, AMB has adverse reactions such as nephrotoxicity, which limit the clinical application of AMB alone or in combination with other antifungal drugs. Nano or micro drug delivery systems (DDS) have been proven to be effective in reducing the toxic and side effects of drugs. Further, the combination of AMB with other compounds with antifungal activity, such as curcumin (CM), may enhance the synergistic effects. Herein, AMB and CM were co-loaded into porous poly (lactic-co-glycolic acid) (PLGA) microparticles (MPs) to prepare AMB/CM-PLGA MPs. The AMB/CM-PLGA MPs showed a remarkably reduced hemolysis (62.2 ± 0.6%) compared to AMB (80.9 ± 1.1%). The nephrotoxicity of AMB/CM-PLGA MPs is significantly lower than that of AMB. In vitro, AMB/CM-PLGA MPs had better inhibitory effects on the adhesion and biofilm formation of Candida albicans compared with AMB. Experiments on mice infected with C. albicans showed that AMB/CM-PLGA MPs have a better therapeutic effect than AMB in vivo. In summary, AMB/CM-PLGA MPs may be a novel and promising therapeutic candidate for fungal infection.