Effects of Muscle Fatigue and Recovery on Complexity of Surface Electromyography of Biceps Brachii

This study aimed to investigate the degree of regularity of surface electromyography (sEMG) signals during muscle fatigue during dynamic contractions and muscle recovery after cupping therapy. To the best of our knowledge, this is the first study assessing both muscle fatigue and muscle recovery using a nonlinear method. Twelve healthy participants were recruited to perform biceps curls at 75% of the 10 repetitions maximum under four conditions: immediately and 24 h after cupping therapy (−300 mmHg pressure), as well as after sham control (no negative pressure). Cupping therapy or sham control was assigned to each participant according to a pre-determined counter-balanced order and applied to the participant’s biceps brachii for 5 min. The degree of regularity of the sEMG signal during the first, second, and last 10 repetitions (Reps) of biceps curls was quantified using a modified sample entropy (E_ms) algorithm. When exercise was performed immediately or 24 h after sham control, E_ms of the sEMG signal showed a significant decrease from the first to second 10 Reps; when exercise was performed immediately after cupping therapy, E_ms also showed a significant decrease from the first to second 10 Reps but its relative change was significantly smaller compared to the condition of exercise immediately after sham control. When exercise was performed 24 h after cupping therapy, E_ms did not show a significant decrease, while its relative change was significantly smaller compared to the condition of exercise 24 h after sham control. These results indicated that the degree of regularity of sEMG signals quantified by E_ms is capable of assessing muscle fatigue and the effect of cupping therapy. Moreover, this measure seems to be more sensitive to muscle fatigue and could yield more consistent results compared to the traditional linear measures.     

热解与气相色谱-质谱联用技术在烟草分析中的应用

应用热解与气相色谱 质谱联用技术 (Py GC/MS) ,在无氧条件下对部分国产卷烟样品进行了热解成分分析。定性定量分析结果表明 ,该方法有较好重复性 (相对标准偏差 <3% ) ;不同卷烟样品 ,具有不同的热解成分构成 ;部分烟草香味物和有害物的含量因样品不同 ,而变化幅度较大。该方法可为推测热解机理 ,设计低害卷烟 ,选择适宜的烟草添加剂 ,提供技术支撑     

London 两个方程等价性与临界态形成动力学

C. P. Bean基于K. Mendelssohn海绵模型建立了非理想Ⅱ类超导体临界态理论, 从而形成了硬超导体电磁理论的重要基础之一.然而近年来基于涡旋动力学理论的发展,逐步形成了临界态动力学研究课题.涡旋运动导致宏观波函数的相滑移,和局域的Joule热等强烈非线性效应是形成自组织临界态物理基础.根据实验观测,磁通进入样品的前锋为线性分布,但其解析理论还在发展中.本文论述了在超导体的零电阻和完全抗磁性的实验基础上建立起来的London第一和第二方程本质上的等价性,并结合London理论与Anderson磁通热激活理论讨论了临界态形成动力学,给出了Slab样品中的电场、电流和磁通密度分布,定量解释了实验观察到的现象.     

Benefits of Innovative and Fully Water-Compatible Stationary Phases of Thin-Film Microextraction (TFME) Blades

Octadecyl (C₁₈) groups are arguably the most popular ligands used for preparation of solid phase microextraction (SPME) devices. However, conventional C₁₈-bonded silica particles are not fully compatible with the nearly 100% aqueous composition of typical biological samples (e.g., plasma, saliva, or urine). This study presents the first evaluation of thin-film SPME devices coated with special water-compatible C₁₈-bonded particles. Device performance was assessed by extracting a mixture of 30 model compounds that exhibited various chemical structures and properties, such as hydrophobicity. Additionally, nine unique compositions of desorption solvents were tested. Thin-film SPME devices coated with C₁₈-bonded silica particles with polar end-capping groups (10 µm) were compared with conventional trimethylsilane end-capped C₁₈-bonded silica particles of various sizes (5, 10, and 45 µm) and characteristics. Polar end-capped particles provided the best extraction efficacy and were characterized by the strongest correlations between the efficacy of the extraction process and the hydrophobicity of the analytes. The results suggest that the original features of octadecyl ligands are best preserved in aqueous conditions by polar end-capped particles, unlike with conventional trimethylsilane end-capped particles that are currently used to prepare SPME devices. The benefits associated with this improved type of coating encourage further implementation of microextractraction as greener alternative to the traditional sample preparation methods.     

Electrokinetic sample injection for high‐sensitivity CZE (part 2): Improving the quantitative repeatability and application of electrokinetic supercharging‐CZE to the detection of atmospheric electrolytes

Electrokinetic supercharging (EKS) is defined as a technique that combines electrokinetic sample injection with transient ITP. Quantitative repeatability of EKS‐CZE and the other CE methods using electrokinetic sample injection process is usually inferior in comparison with the CE methods using hydrodynamic or hydrostatic injection. This is due to some effects, such as the temperature change and the convection of the sample solution in the reservoir, as well as the change of the distance between an electrode and a capillary end (D_ec). In particular, we have found that the D_ec change might most seriously affect the repeatability, especially when the electrode is a thin Pt wire that could be unintentionally bent during sampling. By using a Teflon spacer to fix D_ec to 1.1 mm, the RSD of peak area (n=5) was decreased from 20 to 3.4% in EKS‐CZE for several metal cations. This D_ec dependence of the sample amount injected was supported by computer simulation using CFD‐ACE+ software. The improved repeatability (down to 5.1% at n=5, averaged RSD for Co²⁺, Li⁺, Ni²⁺, Zn²⁺ and Pb²⁺) was also experimentally attained by increasing the D_ec to ca. 20 mm, which was also effective to obtain high sensitivity. Since the temperature and the convection effects on the repeatability are comparatively small in a proper laboratory environment, these effects were estimated from the EKS‐CZE experiments using conditions such as warming and agitating the sample solution during EKS process. Finally, EKS‐CZE was applied to the detection of ions from atmospheric electrolytes in high‐purity water exposed to ambient air for 2 h. The microgram per liter levels of anions (chloride, sulfate, nitrate, formate, acetate and lactate) and cations (ammonium, calcium, sodium and magnesium) could be detected using conventional UV detector.     

Development of a novel high volume band compression injector for the analysis of complex samples like toxaphene pesticide

A new type of injector has been developed for gas chromatographic analysis. The injector has high volume and band compression (HVBC) capabilities useful for the analysis of complex samples. The injector consists essentially of a packed liner operated at room temperature while a narrow heated zone is used to axially scan the liner selectively desorbing the compounds of interest. The scanning speed, distance and temperature of the zone are precisely controlled. The liner is connected to an interface which can vent the solvent or any undesirable compounds, and transfer the analytes to an analytical column for separation and quantification. The injector is designed to be compatible with injection volumes from 1 to more than 250microL. At a low sample volume of 1microL, the injector has competitive performances compared to those of the "on-column" and "split/splitless" injectors for the fatty acid methyl esters and toxaphene compounds tested. For higher volumes, the system produces a linear response according to the injected volume. In this explorative study, the maximum volume injected seems to be limited by the saturation of the chromatographic system instead of being defined by the design of the injector. The HVBC injector can also be used to conduct "in situ" pretreatment of the sample before its transfer to the analytical column. For instance, a toxaphene sample was successively fractionated, using the HVBC injector, in six sub-fractions characterized by simpler chromatograms than the chromatogram of the original mixture. Finally, the ability of the HVBC injector to "freeze" the separation in time allowing the analyst to complete the analysis at a later time is also discussed.     

International comparison of the determination of cadmium and lead in herb: the Comité Consultatif pour la Quantité de Matière (CCQM) pilot study CCQM-P97

A Comité Consultatif pour la Quantité de Matière (CCQM) inter-laboratory comparison program, CCQM-P97, for the analysis of cadmium and lead in Herba Demodii Styracifolii was organized by the Hong Kong Government Laboratory. The objective of the program was to establish comparability of trace metals analysis in herbal matrices amongst the participating national metrology institutes. The arithmetic mean values of the 13 participants were 0.3186 mg kg⁻¹ (RSD = 11.3%) and 1.650 mg kg⁻¹ (RSD = 11.0%) for cadmium and lead, respectively. The participants using double-isotope dilution mass spectrometry technique for their quantification were found to provide similar mean values to those of non-isotope dilution mass spectrometry users. The observation indicated that trace metal analysis in herbal matrices was not method-dependent, but the use of the highest metrological IDMS approach gave a better precision than other routine calibration methods.     

化学蒸气发生-四通道原子荧光光谱法同时测定水样中的痕量砷、锑、硒和汞

应用自行设计的化学蒸气发生-四通道无色散原子荧光光谱仪,建立了同时测定水样中As、Sb、Se、Hg的新方法.在实验中优化了四元素同时化学蒸气发生条件和测定的最佳工作参数.在样品预处理阶段用HCl将Se6+还原为Se4+,然后用质量浓度5 g/L硫脲将As5+和Sb5+还原为As3+和Sb3+.在最佳条件下,方法对As、Sb、Se、Hg的检出限分别为0.05、0.03、0.05、0.01 ng/mL(3d);RSD分别为0.42%、0.74%、0.97%、1.0%(对5 ng/mL As、Sb、Se和0.5ng/mL Hg混合标准,n=7).用所建立的方法对不同类型水样中的As、Sb、Se、Hg进行了同时测定,测定结果与用标准方法测定所得结果之间无明显差异,各元素的加标回收率在93%～105%.     

KMnO_4-鲁米诺体系测定苯唑西林钠

基于苯唑西林钠对碱性介质中KMnO4-鲁米诺体系化学发光的增强作用,建立了流动注射化学发光法测定苯唑西林钠的新方法.在最佳的实验务件下,苯唑西林钠的质量浓度与化学发光强度成正比,线性范围为0.01～20μg/mL,检出限(3σ)为1.0 ng/mL,对1.0μg/mL苯唑西林钠进行了11次平行测定,其相对标准偏差为2.4%.     

条件样本函数极值中$\gamma^2$的估计方法

本文对条件样本函数极值中$\gamma^2$的估计进行了探讨,给出了$\gamma^2$估计的一种新方法------自助法,并对所得到的统计量的性质进行了分析.