Sensitive profiling of biogenic amines in human urine by capillary electrophoresis with field amplified sample injection

In order to monitor biogenic amines in human urine, a method based on field‐amplified sample injection combined with capillary electrophoresis and direct UV absorption detection was developed. Dopamine, tyramine, tryptamine, serotonin and epinephrine were effectively separated and identified in human urine samples, and detection limits were 0.072, 0.010, 0.027, 0.010 and 0.120 µmol/L, respectively. Detection limits comparable to laser‐induced fluorescence detection or solid phase extraction combined with capillary electrophoresis were achieved. Parameters affecting electrophoretic system detection sensitivity were investigated. Optimal separation conditions were obtained using as background electrolyte a pH 6.5 mixture of 2‐(morpholino)ethanesulfonic acid 20 mmol/L and 30 mmol/L phosphate buffer, containing 0.05% hydroxypropylcellulose and 10% v/v methanol. Injections of the sample solution were performed by applying a voltage of 12 kV for 50 s. Recovery and accuracy ranged between 89.4 and 94.9%, and 89 and 112%, respectively. The method was successfully applied on actual urine samples (from a healthy volunteer): target bioamine content was consistent with endogenous levels reported in the literature. The proposed method is simple, fast and inexpensive and can be conveniently employed in work‐related stress studies. The affordability and noninvasive sampling of the method allow epidemiological studies on large number of exposed persons to be performed. Copyright © 2013 John Wiley & Sons, Ltd.     

The FEL SASE operation, bunch compression and the beam heater

We discuss the conditions required for an optimal SASE FEL operation when bunch compression techniques are exploited to enhance the bunch peak current. We discuss the case of velocity bunching and magnetic bunch compression. With reference to the latter technique we provide a quantitative estimate of the amount of laser heater power necessary to suppress the micro-bunching instability without creating any problem to the SASE dynamics.     

光谱线宽与中心波长可同时调谐的高功率光纤激光实现3 kW输出

光谱灵活可调的高功率光纤激光在光谱合束、光声光谱检测和非线性频率变换等方面具有独特优势,近年来受到国内外研究人员的广泛关注。基于光谱灵活可调的超荧光光纤种子源,通过主振荡功率放大器结构实现了光谱中心波长1065～1085 nm可调谐、3 dB线宽2.4～13.8 nm可调谐的3 kW光纤激光输出。

     

高功率光纤激光器中ASE噪声的测量方法（英）

高峰值功率脉冲光纤激光器在激光雷达系统中有着广泛的应用。然而,光纤激光器中放大自发辐射噪声（ASE）严重影响了系统的探测性能。提出一种测量高峰值功率脉冲光纤激光器中ASE噪声的方法。在该方法中,首先对高峰值功率的激光脉冲衰减,然后在时域分别测量和计算ASE噪声和激光脉冲的相对能量。给出了光纤激光器在驱动电流分别为6 A,7 A和8 A时衰减后的ASE噪声廓线以及ASE噪声占激光脉冲能量的比例。     

Field-amplified on-line sample stacking for determination of carnosine-related peptides by capillary electrophoresis

An on-line sample stacking method, namely field-amplified sample injection, has been developed for the separation and determination of carnosine, anserine, and homocarnosine by capillary electrophoresis. Using electrokinetic injection, about 130- to 160-fold improvement of sensitivity was achieved without loss of separation efficiency when compared to conventional sample injection. For conventional injection, the samples were dissolved in running buffer and then hydrodynamically injected for 10 s (3.45 kPa). Various parameters affecting separation and sample stacking were optimized. Under optimum conditions, linear responses were obtained over two orders of magnitude and the detection limits (defined as S/N = 3) of carnosine, anserine, and homocarnosine were 1.5 x 10(-8) to 1.6 x 10(-8) mol/L.     

Advances of a capillary electrophoretic on-line concentration technique: Electrokinetic supercharging

After comparing with electrokinetic injection (EKI) and transient isotachophoresis (t-ITP), the principles of electrokinetic supercharging (EKS) were introduced. Thereafter, the advances and applications of EKS in capillary electrophoresis were intorduced in the following aspects: EKI setups, t-ITP setups, capillary electrophoresis (CE) separation, and real sample analysis. The factors that limit its application are discussed, and the future development of EKS is also prospected.     

Field‐amplified sample injection in capillary zone electrophoresis for the pharmacokinetic research of trace risperidone and its major metabolite 9‐hydroxyrisperidone in beagle dogs

This article describes a method for the simultaneous quantitation of risperidone and its major metabolite, 9‐hydroxyrisperidone, in beagle dog plasma by field‐amplified sample injection in capillary zone electrophoresis. The separation was carried out at 25°C in a 48 cm × 75 µm fused‐silica capillary with an applied voltage of 20 kV using 60 mM NaH₂PO₄ buffer (pH 3.6). The detection wavelength was 280 nm. Clean‐up and preconcentration of plasma samples were conducted by 96‐well formatted liquid‐liquid extraction. In this study, this stacking technique provided a sensitivity enhancement of approximately 158 to 188 fold compared with the same sample without stacking. The method was suitably validated with respect to stability, specificity, linearity, lower limit of quantitation, accuracy, precision, and extraction recovery. Calibration curves exhibited good linearity (r² > 0.995) over a wide concentration range of 2.5 to 200 ng/mL for both risperidone and 9‐hydroxyrisperidone. The intra‐ and interday precisions at the three quality control levels were less than 11.40%. The intra‐ and interday accuracies ranged from 87.90 to 107.17% for risperidone and from 88.43 to 105.92% for 9‐hydroxyrisperidone. All validation data were within the required limits. In conclusion, the method developed was successfully applied to pharmacokinetic studies of risperidone and 9‐hydroxyrisperidone in beagle dogs.     

空间多点抽运双包层光纤激光器的数值分析:典型三点抽运情形

利用数值模拟对在空间不同三点设立抽运点的几种典型抽运条件下包含放大自发发射的掺Yb光纤高功率激光器特性进行了分析，结果表明，即使不考虑抽运光的腔镜反射，对于不同的三点抽运情形，也存在不同的激光分配及功率分布特点。     

Alq/DCM薄膜中的放大自发发射

自从在以 8-羟基喹啉铝 (Alq)掺杂小分子激光染料 DCM为激活介质的波导结构中 [1] ,光泵浦下观察到激光现象以来 ,这种以高效发光有机半导体材料代替以往的溶胶、凝胶或透明聚合物材料来稀释激光染料的方法 ,引起了人们广泛的关注和巨大的兴趣。因为 Alq的发射谱和 DCM的激发谱有很大的重叠 ,所以经光泵浦后的 Alq∶ DCM薄膜中处于激发态的 Alq分子很容易与附近的 DCM分子形成能量迁移[1] ,从而其发射谱表现为 DCM的荧光谱 ,而不是 Alq和 DCM的荧光谱的简单叠加。由于材料的发射谱相对于激发谱红移很大 ,所以很大程度上降低了材料…     

Ratiometric DNA Walking Machine for Accurate and Amplified Bioassay

DNA walking machines opened new avenues for the biosensing and demonstrated great success in the past few years. Since DNA machines are mainly nonequilibrium systems driven by dynamic interactions, the matrix effects on DNA machines is a bottleneck and more intricate than common DNA-mediated assays, especially for complicated physiological samples. Herein, to realize an accurate and reliable quantitative machine, a ratiometric DNA walking machine was developed in human serums and cell lysates based on the elemental isotope ratio measurement. The target DNA-triggered walking machine converted and amplified biological signals into mass spectrometric signal ratios (¹⁹⁷Au/¹¹⁵In) via a burnt-bridge mechanism. Under the optimized conditions, the limit of detection (LOD, 3σ) was 8 fM for target DNA, with a dynamic linear range of 0.05–0.7 pM. The ratiometric DNA walking machine was directly applied in human serum samples with satisfactory recoveries of 94 to 105 %, demonstrating an excellent stability and a high accuracy. Combining the aptamer-based specific recognition, the proposed DNA machine is expected to be a versatile platform for other targets, such as small biomolecules and proteins.