运用Actigraph GT3X三轴加速度传感器测量成年及老年男性人群步行的信效度研究

评价Actigraph GT3X三轴加速度传感器测量中国男性人群典型体力互动信效度,开发基于中国人群步行活动模式的GT3X三轴加速度传感器能耗推算方程。方法受试对象包括青年组(21.92±1.14岁),老年组(55.5±4.52岁)。受试者佩戴GT3X三轴加速度传感器,在跑台上分别完成3km/h(慢走)、4.5km/h(正常步行)、4.5km/h10%(上坡步行)、6km/h(快走)以及7.5km/h(慢跑)速度的走跑运动各5min。受试者佩戴COSMED K4b2便携式代谢测试仪,并将GT3X三轴加速度传感器佩戴于髋部,同步采集心肺功能仪及加速度传感器数据。结果根据受试对象4种无坡度走跑运动推导出线性方程MET=0.000653*counts(Axis1)+2.345521以及线性方程MET=0.000689*counts(VM)+1.640721,但其相关系数不高;GT3X+三轴加速度传感器记录上坡步行(4.5km/h10%)运动与无坡度运动(4.5km/h)相比,三轴counts及VM均显示有差异性(P<0.05),但counts增加率远低于MET增加率;GT3X+三轴加速度传感器两次重复测试,pearson值高,即离散程度低。结论本研究推导垂直轴(Axis1)、三轴矢量和(VM)的线性方程,为中度相关,误差值较大,且上坡运动时的GT3X+三轴加速度传感器记录counts值与MET值呈非线性相关,提示Actigraph GT3X三轴加速度传感器能耗推算方程可根据不同运动方式、运动强度推算相对应方程;Actigraph GT3X三轴加速度传感器测量我国成年及老年男性人群步行活动其信度较高。     

专利风险评价指标体系构建及关键指标国际比较

 从经济安全的角度，基于专利价值链理论，构建了一套专利风险评估指标体系，用于衡量一个国家或地区在专利活动中遭遇风险的程度。利用专利基本活动中的4个关键指标，即专利质量水平、专利转化能力、专利纠纷风险程度和专利贸易国际地位，对美国、日本、韩国、德国和中国进行比较分析，得出2006-2015年，中国的专利发展“快而不高”“大而不强”，但与其他专利强国相比，在专利价值链关键环节的竞争中，中国不占优势，甚至存在较为严重的风险，尤其专利使用费逆差越来越大，对国家经济安全存在一定程度的威胁。     

盐酸伊达比星杂质A的合成工艺优化及其高效液相分析

通过对盐酸伊达比星脱羟基杂质A的合成研究，为盐酸伊达比星的质控标准提供参考。以盐酸伊达比星为起始原料，经过4步反应得到脱羟基杂质A。本文提供了盐酸伊达比星杂质A的制备方法以及高效液相色谱分析方法，为杂质含量控制提供了依据。该工艺可以稳定、快速制备高纯度脱羟基杂质A，制备总收率为57.20%，纯度为57.20%，其结构经¹H NMR， ¹³C NMR和MS(ESI)表征。     

Comprehensive Profiling by Non-targeted Stable Isotope Tracing Capillary Electrophoresis-Mass Spectrometry: A New Tool Complementing Metabolomic Analyses of Polar Metabolites

Mass spectrometry (MS) driven metabolomics is a frequently used tool in various areas of life sciences; however, the analysis of polar metabolites is less commonly included. In general, metabolomic analyses lead to the detection of the total amount of all covered metabolites. This is currently a major limitation with respect to metabolites showing high turnover rates, but no changes in their concentration. Such metabolites and pathways could be crucial metabolic nodes (e.g., potential drug targets in cancer metabolism). A stable-isotope tracing capillary electrophoresis–mass spectrometry (CE-MS) metabolomic approach was developed to cover both polar metabolites and isotopologues in a non-targeted way. An in-house developed software enables high throughput processing of complex multidimensional data. The practicability is demonstrated analyzing [U-¹³C]-glucose exposed prostate cancer and non-cancer cells. This CE-MS-driven analytical strategy complements polar metabolite profiles through isotopologue labeling patterns, thereby improving not only the metabolomic coverage, but also the understanding of metabolism.     

Boundedness of semilinear Duffing equations at resonance in a critical situation

In this paper, we propose a sufficient and necessary condition for the boundedness of all the solutions for the equation $\ddot{x}+n^{2}x+g(x)=p(t)$ with the critical situation that $|{\int }_0^{2\pi }p(t)e^{?int}dt|=2|g(+\infty )?g(?\infty )|$ on g and p, where $n\in {\mathbb{N}}^{+}$, $p(t)$ is periodic and $g(x)$ is bounded.     

Convergence of the viscosity solution of non-autonomous Hamilton-Jacobi equations

In this paper,we investigate the non-autonomous Hamilton-Jacobi equation ■ where H is 1-periodic with respect to t and M is a compact Riemannian manifold without boundary.We obtain the viscosity solution denoted by T_(t_0)~tφ(x) and show T_(t_0)~tφ(x) converges uniformly to a time-periodic viscosity solution u~*(x,t) of ?_tu+H(t,x,?_xu,u)=0.     

Finite-time boundedness of uncertain Hamiltonian systems via sliding mode control approach

Nonlinear Dynamics - This paper seeks to address the problem of finite-time stabilization for a class of uncertain Hamiltonian systems via sliding mode control approach. A novel sliding function in...     

Origins of Boosted Charge Storage on Heteroatom-Doped Carbons

Although tremendous efforts have been devoted to understanding the origin of boosted charge storage on heteroatom-doped carbons, none of the present studies has shown a whole landscape. Herein, by both experimental evidence and theoretical simulation, it is demonstrated that heteroatom doping not only results in a broadened operating voltage, but also successfully promotes the specific capacitance in aqueous supercapacitors. In particular, the electrolyte cations adsorbed on heteroatom-doped carbon can effectively inhibit hydrogen evolution reaction, a key step of water decomposition during the charging process, which broadens the voltage window of aqueous electrolytes even beyond the thermodynamic limit of water (1.23 V). Furthermore, the reduced adsorption energy of heteroatom-doped carbon consequently leads to more stored cations on the heteroatom-doped carbon surface, thus yielding a boosted charge storage performance.