Coupling frontal elution paper chromatography with desorption corona beam ionization mass spectrometry for rapid analysis of chlorphenamine in herbal medicines and dietary supplements

We developed a convenient method by coupling frontal elution paper chromatography with desorption corona beam ionization mass spectrometry (DCBI-MS) for rapid determination of chlorphenamine added in herbal medicines or dietary supplements. In this method, the ethanol extract of the herbal products was spotted directly onto an isosceles triangular filter paper sheet, and then the paper sheet was developed under strong elution condition with the sample zone migrating at the solvent front. The analyte was finally condensed at the V-shaped tip which could then be placed under the visible plasma beam of DCBI for ionization. The overall procedure took less than 5 min. The frontal elution paper chromatography on a triangular plate used in this work improved the signal intensity of chlorphenamine by 30-fold due to the analyte condensing at the tip and the reduction of the background suppression. Furthermore, the paper sheet also functioned as a filter in the analysis of solid or powder samples, which can increase the analytical throughput by omitting the step of centrifugation. The proposed method in current study was successfully applied in the determination of chlorphenamine in herbal medicines. Chlorphenamine was detected in four of the twelve types of herbal medicines examined in this study. The limit of detection was 200 ng/mL (2.0 ng absolute) in full-scan positive-ion mode and the linear range was from 5.0 μg/mL to 50 μg/mL with satisfactory linear coefficient (R(2) (the square of the correlation coefficient)=0.895). Good reproducibility was achieved with relative standard deviations (RSDs) less than 15.0% and the recoveries of chlorphenamine ranged from 84.3 to 90.6%.     

Chaos in the Fractional Order Generalized Lorenz Canonical Form

A fractional-order generalized Lorenz system is constructed and numerically investigated. Chaotic behavior existing in the fractional-order generalized Lorenz system is found. The numerical simulations and interesting figures are performed.     

一个电张弛振子中的瞬态激变

报道一例映孔导致激变后发生的奇异排斥子的拓扑突变.这种突变以其分数维的突变为标志 ,并引起激变后长混沌瞬态运动行为的突变,因而应该具有基础理论和实践上的重要意义. 关键词：激变奇异排斥子混沌瞬态     

采用密度泛函理论与分子动力学对聚甲基丙烯酸甲酯双折射性的理论计算

双折射性是各种光学材料的重要性能之一,具有高双折射率的光学材料在诸多研究及工业领域的应用越来越广泛.然而,作为常用的光学薄膜及光波导材料之一的聚合物材料的双折射性通常却很弱,只能通过实验对其双折射率进行大致的表征,缺乏对其双折射率的系统性理论计算,从而限制了提高聚合物双折射性的研究.本文建立了从聚合物的单体分子结构到多分子链的系统性的双折射率理论计算方法,并借助此方法研究了导致聚合物弱双折射性的限制因素.以聚甲基丙烯酸甲酯(PMMA)为研究对象,运用密度泛函理论研究了其本征双折射率,这里的本征双折射率是指分子链完全取向时其单体单元的双折射率.计算结果表明其本征双折射率高达0.0738左右,并且通过计算给出了PMMA单体单元的平均双折射率色散曲线.采用分子动力学方法研究了该聚合物(包含20个分子链)的材料双折射率.理论计算结果表明,尽管该聚合物具有较大的本征双折射率,但是由于聚合物中分子链取向度极低,聚合物材料最终表现出来的双折射率只有0.00052.本文建立的研究方法及研究结果为研究增强聚合物材料双折射性提供了理论依据.     

一维生物芯片蛋白质检测技术平台

本文提出和构建了一种新型的生物芯片平台技术,这种芯片平台技术将微流控芯片[1～3]与基于高通量并行分析方法的生物芯片[4]原理相结合,发展成基于微流控串行分析技术的一维生物芯片.这种芯片设计的优势在于不仅试样用量极微,自动化程度高,不易污染,而且有望在"芯片实验室"上实现将单细胞水平上的基因、蛋白表达谱分析.     

Time Discretization Schemes for an Integro-Differential Equation of Parabolic Type

1.IntroductionWeconsiderthetimediscretizationoftheequationwhereAisanunboundedpositivedefiniteselfadjointoperatorwithdensedomainD(A)inaHilbertspaceHandBisanotheroperatorwithdomainD(B)DD(A),Thekernelb(t,s)isassumedtobeasmoothreaJ-vaJuedfunctionofbothtandsforoSsStandf(t)EHisasmoothfunction-ThistrpeofproblemoccursinaPplicationssuchasheatconductioninmaterialwithmemorycompressiollofporthviscoelasticmedia,nuclearreactordynamics,etc.ThenumericaJsolutionbymeansofspatialdiscretizationbyfinitedif…     

Synthesis and Characterization of Poly(Diallyldimethylammonium Chloride-g-Acrylamide)

Graft copolymers of poly(diallyldimethylammonium chloride), (poly-DADMAC), with acrylamide were synthesized using a ceric salt/nitric acid initiation system. The effects of concentration of initiator, monomer, and substrates were studied. Copolymers were characterized by viscometry and size-exclusion chromatography. The highest molecular weight ( M _w ) of graft copolymer obtained was 1.70 × 10⁶. The compositions of copolymers are dependent upon the ratios of the concentration of monomer to the concentration of substrate. The highest content of DADMAC monomer unit in the copolymer was 33 wt%.     

Use of isotope mass probes for metabolic analysis of the jasmonate biosynthetic pathway

In order to quantitatively study the jasmonate biosynthetic pathway, we chemically synthesized a pair of isotope mass probes and established a labeling protocol. The pair of mass probes used in our work were ω-bromoacetonylpyridinium bromide (BPB) and d(5)-ω-bromoacetonylpyridinium bromide (d(5)-BPB), which contain carboxylic acid reactive groups, isotopically labeled groups and permanent positive charges. High performance liquid chromatography (HPLC) and electrospray ionization quadrupole-time of flight mass spectrometry (ESI-QTOF-MS) were used for the detection of labeled standard mixtures and plant samples. In comparison to negative mode electrospray ionization detection of unlabeled analytes, the ESI signal of reverse charge labeled compounds was shown to improve by 20- to 80-fold. Accurate relative quantification was achieved as no isotopic effects of the different isotope labeled phytohormones during RP/SCX mixed-mode liquid chromatographic separation were observed. A data analysis method was established for analyzing metabolic pathways using our labeling strategy. We then applied our method and examined the jasmonate biosynthetic pathway of rice under salt stress and the premature senescence mutant. Here we found that under salt stress conditions, rice showed up-regulation in (13S)-hydroperoxyoctadecatrienoic acid (HOPT), cis-(+)-12-oxophytodienoic acid (OPDA), 3-oxo-2-(2'-pentenyl)-cyclopentane-1-octanoic acid (OPC-8) and jasmonoyl-valine (JA-Val) levels, while α-linolenic acid (LA) and jasmonic acid (JA) showed down-regulation, and three components (HPOT, OPC-8 and JA-Val) were accumulated. The premature senescence mutant showed up-regulation in all major components of the jasmonate biosynthetic pathway with the exception of LA, and an accumulation of HPOT, OPC-6 and JA-Val. This study demonstrates that our chemical stable isotope labeling strategy can be used as a powerful tool for metabolic pathway analysis of phytohormones in plants.     

Electron beam density imaging system at Beam study using a portable slit the Shanghai Electron Ion Trap

In this work, a portable slit imaging system is developed to study both the electron beam diameter and the profile of the newly developed Shanghai Electron Beam Ion Trap （Shanghai EBIT）. Images are detected by a charge coupled device （CCD） sensitive to both X rays and longer wavelength photons （up to visible）. Large scale ray tracings were conducted for correcting the image broadening effects caused by the finite slit width and the finite width of the CCD pixels. A numerical de-convolution method was developed to analyse and reconstruct the electron beam density distribution in the EBIT. As an example of the measured beam diameter and current density, the FWHM （full width at half maximum） diameter of the electron beam at 81 keV and 120 mA is found to be 76.2 μm and the density 2.00 × 10^3 A.cm-2, under a magnetic field of 3 T, including all corrections.