基于分形矩的印刷体藏文特征提取方法

基于现有的藏文字丁特征提取方法——图像投影法和方向线素法，运用分形矩理论，提出了一种基于分形矩的藏文字符特征提取方法．用该方法提取的特征有效地反映了藏文字丁的局部和全局特征，减少了图像中像素位置变化给识别部分带来的负面影响．该方法在一定程度上克服了藏文字丁极多而造成的误识率高的缺点，并且解决了由于特征向量雏数较多造成的运算速度慢的问题．     

动态多值背景下的概念格在网络中的应用

针对搜索引擎检索网站信息存在的一些问题—信息资源相对丰富而知识比较匮乏,文中提出动态背景下的概念格,用于抽取网络信息资源中潜在的有价值的知识。基于web文本的信息特性是不断变化的,在处理过程中,先把动态多值背景转化为静态多值背景,然后在转化成单值背景。在利用概念格的hasse图抽取隐藏在网络信息资源中潜在的有价值的知识。     

超声波提取扁蓄总黄酮及测定

目的:从扁蓄中提取总黄酮并测定其含量.方法:选择乙醇为溶剂,用超声波技术从扁蓄中提取黄酮类物质,并对所提取的黄酮类物质进行验证,用分光光度法测定含量.结果:测得样品中总黄酮的平均含量为1.88%,平均回收率为100.95%.结论:运用超声波法从扁蓄中可以提取出黄酮类物质,加快提取速度,提高提取效率.     

一种基于网页特征提取的网站全文搜索系统的设计与实现

给出了一种针对目标网站的全文搜索系统的程序框架图，介绍了其工作原理及实现过程．在全文信息数据库的建立过程中，针对HTML文档的特点，提出了网页特征信息提取技术，有效地减少了信息存储量．最后，给出了应用结果．     

中国榛属植物DNA提取与SSR初步分析

为了探讨适合中国榛属植物基因组DNA的提取方法,分析榛属植物的遗传多样性,本实验以榛属植物的叶片为试材,通过对Doyle和Doyle方法的改良,摸索出适于中国榛属植物基因组DNA提取的方法,并以核酸产量、纯度、片断分布情况等指标来评价,获得高质量基因组DNA;同时应用4对欧榛SSR引物对中国榛属植物进行了跨种转移,并对具有商业潜力的平榛、毛榛和川榛3个种的遗传多样性进行了初步评价,4对引物从3个种的29个样本中扩增出33个等位基因,位点拥有的等位基因数量在6~12个之间,位点平均等位基因数为8.38.上述结果表明SSR是用于榛属种间育种、品种鉴定以及种间遗传图构建的有力工具.     

Determination of metoserpate,buquinolate, and diclofenac in pork,eggs, and milk using liquid chromatography–tandem mass spectrometry

In this work, a method was developed for the simultaneous determination of residual metoserpate, buquinolate and diclofenac in pork, milk, and eggs. Samples were extracted with 0.1% formic acid in acetonitrile, defatted with n‐hexane, and filtered prior to analysis using liquid chromatography–tandem mass spectrometry. The analytes were separated on a C₁₈ column using 0.1% acetic acid and methanol as the mobile phase. The matrix‐matched calibration curves showed good linearity over a concentration range of 5–50 ng/g with coefficients of determination (R²) ≥0.991. The intra‐ and inter‐day accuracies (expressed as recovery percentage values) calculated using three spiking levels (5, 10, and 20 μg/kg) were 80–108.65 and 74.06–107.15%, respectively, and the precisions (expressed as relative standard deviation) were 2.86–13.67 and 0.05–11.74%, respectively, for the tested drugs determined in various matrices. The limits of quantification (1 and 2 μg/kg) were below the uniform residual level (0.01 mg/kg) set for compounds that have no specific maximum residue limit (MRL). The developed method was tested using market samples and none of the target analytes was detected in any of the samples. The validated method proved to be practicable for detection of the tested analytes in pork, milk, and eggs.     

HPLC method development and validation of cytotoxic agent phenyl‐heptatriyne in Bidens pilosa with ultrasonic‐assisted cloud point extraction and preconcentration

Extraction and pre‐concentration of a bioactive marker compound, phenyl‐1,3,5‐heptatriyne from Bidens pilosa, prior to HPLC has been demonstrated using both organic and ecofriendly solvents. Non‐ionic surfactants, viz. Triton X‐100, Triton X‐114 and Genapol X‐80, were used for extraction. No back‐extraction or liquid chromatographic steps were required to remove the target phytochemical from the surfactant‐rich extractant phase. The optimized cloud point extraction procedure has been shown to be a potentially useful methodology for the preconcentration of the target analyte, with a preconcentration factor of 4–99. Moreover, the method is simple, sensitive, rapid and consumes lesser solvent than traditional methods. An isocratic chromatographic separation and quantitation was accomplished on a C₁₈ column with acetonitrile–acidified aqueous as mobile phase at a flow rate of 1.0 mL/min, UV detection at 254 nm and specificity with photo diode‐array detector (PDA) and MS. Under the optimum experimental conditions recovery was satisfactory (99.18–100.33%) without interference from the surfactant. The method seems to be reliable with intraday precision and interday precision below 2.0%. Good linearity was obtained in the working range from 7.5 to 30 µg/mL with correlation coefficient >0.99. The limits of detection and quantitation were 1.84 and 6.13 µg/mL, respectively. The method was validated following international guidelines and successfully applied for quantitative assays of cytotoxic compound phenyl‐1,3,5‐heptatriyne in Bidens pilosa. Copyright © 2010 John Wiley & Sons, Ltd.     

Pervaporation in chemical analysis

Unlike thermal processes such as distillation, pervaporation relies on the relative rates of solute permeation through a membrane and is a combination of evaporation and gas diffusion. The analytical pervaporation systems consist of a membrane module suitable for liquid sample introduction and a vacuum (or a sweeping gas) on the permeate side. It has been used in a wide range of applications including the analysis of various organic and inorganic compounds, and sample concentration. It has been directly interfaced with gas chromatography, spectrophotometry, capillary electrophoresis, electrochemical detectors, liquid chromatography, and mass spectrometry. A wide range of liquids, slurries, and solids samples has been analyzed using these techniques. This review highlights the basic principles of the pervaporation and the state of its current development as applied to analytical chemistry.     

萃提技术在皂素生产中的应用

天然产物的提取是一个复杂的过程。当溶剂加入到植物原料中时，在溶剂的扩散和渗透作用下，渗透至原料的内部，将原料中可溶性物质进行溶解，从而造成内部及其吸附溶剂和外部溶剂的浓度不一致，存在一定的化学势差，它付之间不断地进行交换，直至它们的化学势趋于一致，内外溶液的浓度达到一种动态平衡，此时原料、吸附溶液和外部溶液的浓度基本保持衡定，溶济提取达到最大效能［１，５］．将该溶液滤出，破坏它们之间的平衡，重新加入新的溶剂促使它们之间进行新的交换，建立一种新的平衡体系，并不断地破坏它们，从而不断地将原料中的成分…     

Development of new extraction method based on liquid–liquid–liquid extraction followed by dispersive liquid–liquid microextraction for extraction of three tricyclic antidepressants in plasma samples

In the present study, a new extraction method based on a three–phase system, liquid–liquid–liquid extraction, followed by dispersive liquid–liquid microextraction has been developed and validated for the extraction and preconcentration of three commonly prescribed tricyclic antidepressant drugs – amitriptyline, imipramine, and clomipramine – in human plasma prior to their analysis by gas chromatography–flame ionization detection. The three phases were an aqueous phase (plasma), acetonitrile and n–hexane. The extraction mechanism was based on the different affinities of components of the biological sample (lipids, fatty acids, pharmaceuticals, inorganic ions, etc.) toward each of the phases. This provided high selectivity toward the analytes since most interferences were transferred into n–hexane. In this procedure, a homogeneous solution of the aqueous phase (plasma) and acetonitrile (water–soluble extraction solvent) was broken by adding sodium sulfate (as a phase separating agent) and the analytes were extracted into the fine droplets of the formed acetonitrile. Next, acetonitrile phase was mixed with 1,2–dibromoethane (as a preconcentration solvent at microliter level) and then the microextraction procedure mentioned above was performed for further enrichment of the analytes. Under the optimum extraction conditions, limits of detection and lower limits of quantification for the analytes were obtained in the ranges of 0.001–0.003 and 0.003–0.010 μg mL⁻¹, respectively. The obtained extraction recoveries were in the range of 79–98%. Intra– and inter–day precisions were < 7.5%. The validated method was successfully applied for determination of the selected drugs in human plasma samples obtained from the patients who received them.