Accuracy and precision of natural gas analysis

Summary Calculations of natural gas properties from chromatographic analysis is increasingly popular. An application of the significance of the various sources of error allows the overall uncertainty of the analytical procedure to be evaluated. Presented at the 15th International Symposium on Chromatography, Nürnberg, October 1984     

A comparative study of CE-SDS,SDS-PAGE,and Simple Western—Precision,repeatability, and apparent molecular mass shifts by glycosylation

SDS gel electrophoresis is a commonly used approach for monitoring purity and apparent molecular mass (Mr) of proteins, especially in the field of quality control of biopharmaceutical proteins. The technological installation of CE-SDS as the replacement of the slab gel technique (SDS-PAGE) is still in progress, leading to a continuous improvement of CE-SDS instruments. Various CE-SDS instruments, namely Maurice (CE-SDS/CE-SDS PLUS) and Wes by ProteinSimple as well as the microchip gel electrophoresis system LabChip® GXII Touch™ HT by PerkinElmer were tested for precision and repeatability compared to SDS-PAGE (Bio-Rad). For assessing these quality control parameters, standard model proteins with minor post-translational modifications were used. Overall, it can be concluded that the CE-SDS-based methods are similar to SDS-PAGE with respect to these parameters. Quality characteristics of test systems gain more significance by testing proteins that do not behave like model proteins. Therefore, glycosylated proteins were analyzed to comparatively investigate the influence of glycosylation on Mr determination in the different instruments. In some cases, high deviations were found both among the methods and with regard to reference values. This article provides possible explanations for these findings.     

Precision of micellar electrokinetic capillary chromatography in the determination of seven antibiotics in pharmaceuticals and feedstuffs

Validation of analytical procedures is important for their efficient and reliable application. The International Conference on Harmonisation (ICH), Food and Drug Administration (FDA) and pharmacopoeia guidelines achieved a great deal in harmonising the definitions of the required validation characteristics. It is well known that poor reproducibility limits the practical implementation of capillary electrophoresis (CE). A precision study on four different MEKC methods was performed with 11 samples, containing seven antibiotics, by two analysts, in few days, on two capillary electrophoresis instruments. Five pharmaceutical preparations and three animal feeds were used. Precision was statistically analysed using migration time, peak area and height of each compound, as well as electroosmotic front (EOF). In 25 of 31 cases, the reproducibility of peak area, peak height and migration time was good (<5%). In most cases the reproducibility of peak area was much better than the reproducibility of peak height. The worst reproducibility that we observed was 12.7% for peak height and 7.6% for peak area.     

基于时间偏差补偿的传感器网络时间同步方法

综合考虑了无线传感器网络中节点间时间偏移的来源,为了提高无线传感器网络中时间同步精度,降低能量开销,提出了一种在簇结构中基于偏差补偿的同步方法.该方法在完成簇内节点一次信息交换之后,通过簇头对各节点时间偏差进行有效估计并进行补偿来维持同步时间精度,很好地降低了能量消耗.通过仿真实验,该方法在信息开销和同步精度上体现出良...     

Multiresidue pesticides analysis in soils using modified QuEChERS with disposable pipette extraction and dispersive solid‐phase extraction

QuEChERS original method was modified into a new version for pesticides determination in soils. The QuEChERS method is based on liquid–liquid portioning with ACN and was followed by cleanup step using dispersive SPE and disposable pipette tips. Gas chromatographic separation with MS detection was carried out for pesticides quantification. The method was validated using recovery experiments for 36 multiclass pesticides. Mean reco‐veries of pesticides at each of the four spiking levels between 10–300 μg/kg of soil ranged from 70–120% for 26 pesticides with RSD values less than 15%. The method achieved low limit of detection less than 7.6 μg/kg. Matrix effects were observed for 13 pesticides. Matrix effects were compensated by using matrix‐matched calibration. The method was applied successfully using d‐SPE or DPX in the analysis of the pesticides in soils from organic farming and integrated pest management.     

A Brief Overview of Potential Treatments for Viral Diseases Using Natural Plant Compounds: The Case of SARS-Cov

The COVID-19 pandemic, as well as the more general global increase in viral diseases, has led researchers to look to the plant kingdom as a potential source for antiviral compounds. Since ancient times, herbal medicines have been extensively applied in the treatment and prevention of various infectious diseases in different traditional systems. The purpose of this review is to highlight the potential antiviral activity of plant compounds as effective and reliable agents against viral infections, especially by viruses from the coronavirus group. Various antiviral mechanisms shown by crude plant extracts and plant-derived bioactive compounds are discussed. The understanding of the action mechanisms of complex plant extract and isolated plant-derived compounds will help pave the way towards the combat of this life-threatening disease. Further, molecular docking studies, in silico analyses of extracted compounds, and future prospects are included. The in vitro production of antiviral chemical compounds from plants using molecular pharming is also considered. Notably, hairy root cultures represent a promising and sustainable way to obtain a range of biologically active compounds that may be applied in the development of novel antiviral agents.     

Targeted metabolomics in cultured cells and tissues by mass spectrometry: Method development and validation

Metabolomics is the identification and quantitation of small bio-molecules (metabolites) in biological samples under various environmental and genetic conditions. Mass spectrometry provides the unique opportunity for targeted identification and quantification of known metabolites by selective reaction monitoring (SRM). However, reproducibility of this approach depends on careful consideration of sample preparation, chemical classes, and stability of metabolites to be evaluated. Herein, we introduce and validate a targeted metabolite profiling workflow for cultured cells and tissues by liquid chromatography–triple quadrupole tandem mass spectrometry. The method requires a one-step extraction of water-soluble metabolites and targeted analysis of central metabolites that include glycolysis, amino acids, nucleotides, citric acid cycle, and the hexosamine biosynthetic pathway. The sensitivity, reproducibility and molecular stability of each targeted metabolite were assessed under experimental conditions. Quantitation of metabolites by peak area ratio was linear with a dilution over a 4 fold dynamic range with minimal deviation R² = 0.98. Inter- and intra-day precision with cells and tissues had an average coefficient of variation <15% for cultured cell lines, and somewhat higher for mouse liver tissues. The method applied in triplicate measurements readily distinguished immortalized cells from malignant cells, as well as mouse littermates based on their hepatic metabolic profiles.     

Processing of shot-to-shot raw data to improve precision in laser-induced breakdown spectrometry microprobe

In order to set up the precision limit that can be reached with laser-induced breakdown spectrometry microprobe, a steel sample was scanned by using a 6-µm diameter spot. Besides being close to the limit of the technique, such a spot diameter resulted in a small plasma size that minimized self-absorption effects. To minimize shot noise, Cr and Fe were used as test elements because of their high contents. Scan consisted of 25 successive matrices formed by 5 × 6 shots, i.e. a total of 750 shots. Results were studied as a whole, as well as between matrices and within matrices, to search for inhomogeneity, outliers and drift. Except a few outliers, the main contribution in the experimental RSD was the drift either within a matrix or between matrices. Drift attributed to laser warm up could be compensated for either by using a polynomial fitting or by using the other element. %RSD significantly below 2 were then obtained demonstrating that there is no penalty in terms of precision to perform laser microprobe using a series of single shots.     

Influence of Farming System and Forecrops of Spring Wheat on Protein Content in the Grain and the Physicochemical Properties of Unsonicated and Sonicated Gluten

The potential for enhancing the spring wheat protein content by different cultivation strategies was explored. The influence of ultrasound on the surface and rheological properties of wheat-gluten was also studied. Spring wheat was cultivated over the period of 2018–2020 using two farming systems (conventional and organic) and five forecrops (sugar beet, spring barley, red clover, winter wheat, or oat). The obtained gluten was sonicated using the ultrasonic scrubber. For all organically grown wheat, the protein content was higher than for the conventional one. There was no correlation between the rheological properties of gluten and the protein content in the grain. Gluten derived from organically grown wheat was more elastic than those derived from the conventional one. Sonication enhanced the elasticity of gluten. The sonication effect was influenced by the forecrops. The most elastic gluten after sonication was found for organic barley and sugar beet. The lowest values of tan (delta) were noted for conventional wheat and conventional oat. Cultivation in the monoculture gave gluten with a smaller susceptibility to increase elasticity after sonic treatment. Sonication promoted the cross-linking of protein molecules and induced a more hydrophobic character, which was confirmed by an increment in contact angles (CAs). Most of the organically grown wheat samples showed a lower CA than the conventional ones, which indicated a less hydrophobic character. The gluten surface became rougher with the sonication, regardless of the farming system and applied forecrops. Sonication treatment of gluten proteins rearranged the intermolecular linkages, especially disulfide and hydrophobic bonds, leading to changes in their surface morphology.     

外场多光轴瞄准偏差测试的基准光轴建立方法

提出一种针对外场真实环境下可见光、激光和红外多光轴瞄准系统瞄准偏差测试的基准光轴建立方法.采用精密大地测距、测角技术获得观测仪器站址坐标、基准光轴方向和靶标中心位置,通过对标定靶标上的中心点作测距和测角观测,并对基准光轴方向大气折射和地球曲率引入的误差进行改正,获得基准光轴、激光和红外系统在靶标上的精确位置.理论分析和实际测试结果表明,该方法具有理论严密、测量准确度高、工程上易于实现的优点,在2 km范围内基准光轴误差小于4.5″,完全满足多光谱多光轴动态瞄准偏差测试中基准光轴准确度的要求.