两轴周视光电跟踪天际线焦平面像的解析表达

鉴于动基座周视光电跟踪系统的基座俯仰和横滚角会造成天际线在红外焦平面阵列上所成的像不再与反射镜面俯仰轴在焦平面阵列上的投影平行,建立了动基座两轴周视光电跟踪系统的五自由度数学模型。重构了包含目标信息的天际平面在大地坐标系下的方程,推导得出了天际线在焦平面阵列上成像的解析表达式,并将其与反射镜面俯仰轴在焦平面阵列上的投影表达式进行了对比。天际线焦平面阵列成像的解析表达式可为目标可测、天际线不可测情况下,沿像的方向向量及其正交方向进行方位、俯仰补偿及目标方位解算提供理论前提。     

Application of d-SPE before SPE and HPLC-FLD to Analyze Bisphenols in Human Breast Milk Samples

In this study, we propose a simple, cost-effective, and sensitive high-performance liquid chromatography with fluorescence detection (HPLC-FLD) for the simultaneous determination of seven bisphenols (bisphenol F (BPF), bisphenol E (BPE), bisphenol B (BPB), BADGE (bisphenol A diglycidyl ether), BADGE∙2H₂O, BADGE∙H₂O, BADGE∙2HCl) in human breast milk samples. The dispersive solid phase extraction (d-SPE) coupled with solid phase extraction (SPE) procedure performed well for the majority of the analytes with recoveries in the range 57–88% and relative standard deviations (RSD%) of less than 9.4%. During the d-SPE stage, no significant matrix effect was observed thanks to the application of different pairs of salts such as zirconium-dioxide-based sorbents (Z-Sep or Z-Sep +) and primary secondary amine (PSA) or QuEChERS Enhanced Matrix Removal-Lipid (EMR-Lipid) and PSA. The method limits of quantification (mLOQs) for all investigated analytes were set at satisfactory low values in the range 171.89–235.11 ng mL⁻¹. Analyte concentrations were determined as the average value from human breast milk matrix samples. The results show that the d-SPE/SPE procedure, especially with the application of EMR-Lipid and PSA, could be used for further bisphenol analyses in human breast milk samples.     

基于神经元电响应的人体热舒适性评价理论

本文提出一种利用神经元电响应频率定量评价人体热舒适性的理论方法和准则。利用Hodgkin-Huxley方程和Pennes生物传热方程描述皮下神经元在瞬态温度场下的电响应特性,并研究了环境温度、对流换热系数,血液灌注率和组织导热率等参数对它的影响,结果表明神经元动作电位频率在等效温度发生0.1℃时就会发生明显变化,可以组合多个环境和热物性参数评价人体热舒适性。     

基因重组糖蛋白-人尿激酶原糖基化修饰的质谱测定

酶法结合生物质谱技术测定了基因重组糖蛋白-人尿激酶原(rhProUK)的N-糖含量、唾液酸含量分别为9％和5％。糖蛋白／肽先经Con A凝集素亲和富集,肽：N-糖苷酶F(PNGaseF)对N-糖基化位点进行特异性质量标记,然后利用Lc-MS/MS技术测定出N-糖基化位点在第302位天冬酰胺残基上。     

激光打靶数字延时信号完整性的研究

针对高速数字电路设计中遇到的信号完整性问题,本文给出了激光打靶装置中高速数字电路延时分配原理.根据传输线理论,提出端接迹线最大匹配长度值限定法,结合PCB设计,可避免端接失配反射.由电学理论,建模串扰的产生及消除串扰的端接方式.通过对噪声电流I和瞬态负载电流IL复合干扰分析,采取了相应的抑制方法.打靶实验表明,对保证延时信号的完整性是有效的.     

ICP-AES法测定古代车师人肋骨中的痕量元素

近几十年来 ,古代人群的食谱研究已经成为现代科技考古学的一个重要组成部分 ,也是当前国际科技考古学研究领域的一项前沿性课题。人类骨骼的微量元素分析为重建古代居民的食谱提供了大量信息。本文用硝酸 盐酸消解样品 ,采用电感耦合等离子发射光谱仪 (ICP AES) ,在选定的最佳条件下 ,对新疆地区古代车师人肋骨中的Sr,Zn ,Ca ,Cu ,Mg,Fe ,Ba ,Mn等 8种痕量元素进行了测定 ,该方法采用一次溶样 ,多元素同时测定 ,回收率为 87 4 %～ 1 0 6 6 %之间。相对标准偏差为 0 5 %～ 3 3%。该方法简单 ,快捷可靠 ,适用于古代骨样品的测定 ,结果令人满意。其结果为考古学和人类学的研究提供了科学的依据。同时考察了不同酸度对分析结果的影响和共存元素间的相互干扰 ,此外还进行了精密度实验。     

CPLD在红外密集度光电立靶测试系统中的抗干扰的应用

通过对光电靶原理的分析,证明了弹丸所引起的光电靶输出信号与声波、蚊虫等所引起的光电靶输出信号是不同的。在此基础上,提出了一种利用CPLD(complexprogrammablelogicdevice)器件实现抗干扰电路的方法。仿真分析和应用结果表明:该电路能有效地抑制声波和蚊虫等带来的干扰,明显地提高了电路的抗干扰能力,保证了测试结果的可靠性和精确性。     

Highly sensitive method for the determination of omeprazole in human plasma by liquid chromatography-electrospray ionization tandem mass spectrometry: application to a clinical pharmacokinetic study

A highly sensitive, rapid assay method has been developed and validated for the estimation of omeprazole (OPZ) in human plasma with liquid chromatography coupled to tandem mass spectrometry with electrospray ionization in the positive-ion mode. The assay procedure involves alkalinization of plasma followed by simple liquid-liquid extraction of OPZ and lansoprazole (internal standard, IS) from human plasma with acetonitrile. Chromatographic separation was achieved with 0.01 M ammonium acetate:acetonitrile (40:60, v/v) at a flow rate of 0.25 mL/min on an Inertsil ODS 3 column with a total run time 2.5 min. The MS/MS ion transitions monitored were 346.1 --> 198.1 for OPZ and 370.1 --> 252.1 for IS. Method validation and clinical sample analysis were performed as per FDA guidelines and the results met the acceptance criteria. The lower limit of quantitation achieved was 0.05 ng/mL and the linearity was observed from 0.05 to 10.0 ng/mL. The intra-day and inter-day precisions were in the ranges 2.09-8.56 and 5.29-8.19%, respectively. This novel method has been applied to a pharmacokinetic study of OPZ in humans.     

Calix[4]arenes as Molecular Platforms for Magnetic Resonance Imaging (MRI) Contrast Agents

The novel amphipilic conjugate of a calix[4]arene with four Gd–1,4,7,10‐ tetra(carboxymethyl)‐1,4,7,10‐tetraazacyclododecane (DOTA) chelates has potential as a magnetic resonance imaging contrast agent, both in its monomeric and in its micellar form. The system, illustrated here with its nuclear magnetic relaxation profile, shows good relaxivities, thanks to its high rigidity.

     

Sensitive DNA biosensor improved by Luteolin copper(II) as indicator based on silver nanoparticles and carbon nanotubes modified electrode

A novel and sensitive electrochemical DNA biosensor has been developed for the detection of DNA hybridization. The biosensor was proposed by using copper(II) complex of Luteolin C₃₀H₁₈CuO₁₂ (CuL₂) as an electroactive indicator based on silver nanoparticles and multi-walled carbon nanotubes (Ag/MWCNTs) modified glassy carbon electrode (GCE). In this method, the 4-aminobenzoic acid (4-ABA) and Ag nanoparticles were covalently grafted on MWCNTs to form Ag/4-ABA/MWCNTs. The proposed method dramatically increased DNA attachment quantity and complementary ssDNA detection sensitivity for its large surface area and good charge-transport characteristics. DNA hybridization detection was performed using CuL₂ as an electroactive indicator. The CuL₂ was synthesized and characterized using elemental analysis (EA) and IR spectroscopy. Cyclic voltammetry (CV) and fluorescence spectroscopy were used to investigate the interaction between CuL₂ and ds-oligonucleotides (dsDNA). It was revealed that CuL₂ presented high electrochemical activity on GCE, and it could be intercalated into the double helices of dsDNA. The target ssDNA of the human hepatitis B virus (HBV) was quantified in a linear range from 3.23 × 10⁻¹² to 5.31 × 10⁻⁹ M (r = 0.9983). A detection limit of 6.46 × 10⁻¹³ M (3σ, n = 11) was achieved.