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Bi-large Neutrino Mixing See-Saw Mass Matrix with Texture Zeros and Leptogenesis
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作者 CHAO Wei HE Xiao-Gang LI Xue-Qian 《Communications in Theoretical Physics》 SCIE CAS CSCD 2006年第6期1073-1084,共12页
We study constraints on neutrino properties for a class of bi-large mixing See-Saw mass matrices with texture zeros and with the related Dirac neutrino mass matrix to be proportional to a diagonal matrix of the form d... We study constraints on neutrino properties for a class of bi-large mixing See-Saw mass matrices with texture zeros and with the related Dirac neutrino mass matrix to be proportional to a diagonal matrix of the form diag (e, 1, 1). Texture zeros may occur in the light (class a)) or in the heavy (class b)) neutrino mass matrices. Each of these two classes has 5 different forms which can produce non-trivial three generation mixing with at least one texture zero. We tind that two types of texture zero mass matrices in both class a and class b can be consistent with present data on neutrino masses and mixing. None of the neutrinos can have zero masses and the lightest of the light neutrinos has a mass larger than about 0.046 eV for class a and 0.0027 eV for class b. In these models although the CK.M CP violating phase vanishes, the non-zero Majorana phases can exist and can play an important role in producing the observed baryon asymmetry in our universe through leptogenesis mechanism. The requirement of producing the observed baryon asymmetry can further distinguish different models and also restrict the See-Saw scale to be in the range of 10^12- 10^15 GeV. We also discuss RG effects on V^13. 展开更多
关键词 NEUTRINO neutrino mass matrix neutrino masses and mixing bi-large mixing matrix
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An Upper Bound on the Higgs Self-Coupling and Higgs Boson Mass from the Positivity Condition of the Mass Matrix
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作者 Partha Pratim Pal 《Journal of Modern Physics》 2015年第4期369-373,共5页
The actual value of Higgs boson mass is difficult to determine theoretically due to lack of knowledge on the exact value of Higgs self coupling constant l. The purpose of this paper is to obtain an upper bound on the ... The actual value of Higgs boson mass is difficult to determine theoretically due to lack of knowledge on the exact value of Higgs self coupling constant l. The purpose of this paper is to obtain an upper bound on the Higgs mass in the Standard Model on the basis of one-loop effective potential in the ’t Hooft-Landau gauge and MS scheme. The condition of positivity of mass matrix at ф?= ф0 (where ф0 is the absolute minimum of the effective potential) of the scalar field gives an upper bound on the Higgs self coupling as l ≤ 0.881. This condition yields an upper bound on the Higgs mass as mH ≤ 229.48 GeV. 展开更多
关键词 ONE-LOOP Effective Potential Standard Model mass matrix HIGGS BOSON mass
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The Majorana neutrino mass matrix indicated by the current data
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作者 ZHANG XinYi MA BoQiang 《Science China(Physics,Mechanics & Astronomy)》 SCIE EI CAS CSCD 2015年第7期36-48,共13页
The Majorana neutrino mass matrix combines information from the neutrino masses and the leptonic mixing in the flavor basis. Its invariance under some transformation matrices indicates the existence of certain residua... The Majorana neutrino mass matrix combines information from the neutrino masses and the leptonic mixing in the flavor basis. Its invariance under some transformation matrices indicates the existence of certain residual symmetry. We offer an intuitive display of the structure of the Majorana neutrino mass matrix, using the whole set of the oscillation data. The structure is revealed depending on the lightest neutrino mass. We find that there are three regions with distinct characteristics of structure. A group effect and the μ-T exchange symmetry are observed. Six types of texture non-zeros are shown. Implications for flavor models are discussed. 展开更多
关键词 NEUTRINO Majorana mass matrix oscillation data
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ELASTO-PLASTIC STIFFNESS MATRIX OF ROCK MASS ELEMENT WITH SOFT CLAY STRATA AND ITS APPLICATION
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作者 Li,Zhenzi Sun,Zongqi Central-South University of Technology,Changsha,Hunan,410083,China 《中国有色金属学会会刊:英文版》 CSCD 1993年第2期15-17,共3页
The fault element is used to handle soft clay strata in a rock mass.The formulas or clasto-plastic stiffnessmatrix for the fault element are derived using the constitutive relationship between plastic increment stress... The fault element is used to handle soft clay strata in a rock mass.The formulas or clasto-plastic stiffnessmatrix for the fault element are derived using the constitutive relationship between plastic increment stress andstrain.A numerical example of a circular tunnel with soft clay strata in the rock medium are examined. 展开更多
关键词 rock mass clement FAULT clasto-plastic STIFFNESS matrix
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用于夹层梁静动力及屈曲分析的新型组合结构单元
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作者 林建平 陈昆 +2 位作者 潘剑超 王冠楠 冯倩 《浙江大学学报(工学版)》 EI CAS CSCD 北大核心 2024年第3期518-528,共11页
推导出新型组合结构单元,用于考虑界面滑移的3层部分作用夹层组合梁的静动力及屈曲特性分析.基于铁木辛柯梁理论,建立考虑夹层梁部分作用效应的能量原理.针对其受力特性,在节点位移、横截面转角和界面滑移插值时均采用含内部自由度的高... 推导出新型组合结构单元,用于考虑界面滑移的3层部分作用夹层组合梁的静动力及屈曲特性分析.基于铁木辛柯梁理论,建立考虑夹层梁部分作用效应的能量原理.针对其受力特性,在节点位移、横截面转角和界面滑移插值时均采用含内部自由度的高阶插值函数,以解决含界面有限元数值分析中常遇到的“滑移锁定”现象.通过变分原理得到夹层梁的刚度矩阵、质量矩阵以及几何刚度矩阵的显示表达式.基于MATLAB编译相应夹层结构的有限元程序并验证其准确性.对不同截面3层夹层组合梁进行不同荷载条件和边界条件下的静动力及屈曲特性分析,并探讨不同夹层组合梁跨高比和不同界面抗剪连接刚度下的计算结果及其误差的变化规律.所推导的显示表达式新型组合结构单元计算效率高,并便于推广应用于其他有限元程序或商业软件子程序中. 展开更多
关键词 夹层组合梁 部分作用 静动力分析 刚度矩阵 质量矩阵 铁木辛柯梁理论
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考虑剪切变形的欧拉梁单元一致质量矩阵
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作者 张军锋 胡连超 +2 位作者 吴靖江 耿玉鹏 李杰 《郑州大学学报(工学版)》 CAS 北大核心 2024年第5期128-134,共7页
为明确考虑剪切变形的欧拉梁单元一致质量矩阵推导方法,以形函数为基础,基于虚功原理,区分伸缩、扭转以及是否考虑剪切变形的弯曲受力状态,给出了欧拉梁单元一致质量矩阵表达式。研究表明:不考虑剪切变形时,欧拉梁受弯状态的一致质量分... 为明确考虑剪切变形的欧拉梁单元一致质量矩阵推导方法,以形函数为基础,基于虚功原理,区分伸缩、扭转以及是否考虑剪切变形的弯曲受力状态,给出了欧拉梁单元一致质量矩阵表达式。研究表明:不考虑剪切变形时,欧拉梁受弯状态的一致质量分析中一般不计单元上微元体水平方向的惯性力,此时仅需弯曲变形引发的竖向位移形函数即可;考虑剪切变形时,则需计入水平方向的惯性力,且同时需要完整的竖向位移形函数和纯弯曲转角位移形函数;对于变截面欧拉梁单元,其一致质量矩阵表达式过于复杂,可在等截面梁的基础上,根据元素位置对矩阵元素匹配左右端或平均截面面积及截面极惯性矩近似给出实用的质量矩阵表达式;考虑剪切变形时,欧拉梁的刚度矩阵亦可经竖向位移和纯弯曲转角位移形函数计算得到,这一过程与使用纯弯曲竖向位移和纯剪切竖向位移形函数的过程在本质上是一致的。 展开更多
关键词 一致质量矩阵 欧拉梁单元 形函数 剪切变形 变截面
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六自由度运动模拟平台设计与分析
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作者 魏国 余潇 +2 位作者 赵益 贺廿六 李绍民 《兵工自动化》 北大核心 2024年第6期31-35,60,共6页
针对实际道路测试周期长、成本高、容易受到恶劣天气影响等问题,设计一种能够用于车载光电跟踪系统进行模拟试验的六自由度摇摆台。模拟扰动测试,通过六自由度摇摆台提供扰动;对六自由度摇摆台进行结构设计、运动及频率特性分析。结果表... 针对实际道路测试周期长、成本高、容易受到恶劣天气影响等问题,设计一种能够用于车载光电跟踪系统进行模拟试验的六自由度摇摆台。模拟扰动测试,通过六自由度摇摆台提供扰动;对六自由度摇摆台进行结构设计、运动及频率特性分析。结果表明,该摇摆台能够推导其固有频率与机构刚度矩阵和质量矩阵的关系。 展开更多
关键词 六自由度摇摆台 频率特性 质量矩阵 刚度矩阵
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埃尔米特梁单元的分块对角与高阶质量矩阵
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作者 王东东 吴振宇 侯松阳 《计算力学学报》 CAS CSCD 北大核心 2024年第1期178-185,共8页
埃尔米特梁单元常用的集中质量矩阵,是由挠度自由度对应的一致质量矩阵元素通过行求和或节点积分构造.然而,数值结果表明该集中质量矩阵在求解包含自由端的梁振动问题时,会出现频率精度掉阶现象.本文首先从保障质量矩阵最优收敛性的数... 埃尔米特梁单元常用的集中质量矩阵,是由挠度自由度对应的一致质量矩阵元素通过行求和或节点积分构造.然而,数值结果表明该集中质量矩阵在求解包含自由端的梁振动问题时,会出现频率精度掉阶现象.本文首先从保障质量矩阵最优收敛性的数值积分精度出发,分别针对三次和五次梁单元,发展了质量矩阵的梯度增强节点积分方案.利用梯度增强节点积分方案,可以得到具有分块对角形式的单元质量矩阵,而其组装的整体质量矩阵除边界节点外仍然呈现对角形式.对于两种单元,其分块对角质量矩阵分别具有4阶最优精度和6阶次优精度.再者,将标准一致质量矩阵和具有同阶精度的梯度增强节点积分质量矩阵进行优化组合,建立了具有超收敛特性的高阶质量矩阵.最后,通过数值算例系统验证了三次和五次单元的分块对角与高阶质量矩阵的频率计算精度. 展开更多
关键词 埃尔米特梁单元 振动频率 集中质量矩阵 分块对角质量矩阵 高阶质量矩阵
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Analysis of Single Nucleotide Polymorphism in Human Paraoxonase 1 Gene(Q192R) with Matrix-assisted Laser Desorption/Ionization Time-of-flight Mass Spectrometry 被引量:1
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作者 SUN Ya-dong SUN Shu-chen +2 位作者 WANG Zhi YANG Yang ZHANG Jin 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2006年第3期394-396,共3页
Introduction Single nucleotide polymorphisms (SNPs) are the most abundant DNA markers in the human genome occurring at a frequency of one in every 500--1000 nucleotides. A variety of methods have been used for the ... Introduction Single nucleotide polymorphisms (SNPs) are the most abundant DNA markers in the human genome occurring at a frequency of one in every 500--1000 nucleotides. A variety of methods have been used for the analysis of single nucleotide polymorphisms, including restriction fragment length polymorphism (RFLP), direct sequencing by using laser-induced fluorescence detectionTM, fluorescence energy transfer, MALDI-TOF MS combined with primer extension or invasive cleavage, and fluorescence polarization. During the past two decades, mass spectrometry has become a very popular tool in the analysis of biomolecules and is perfectly suited to the analysis of single nucleotide polymorphisms (SNPs) due to its speed, low cost, and accuracy. In this work, we used MALDI TOF mass spectrometry to detect the fragments of restriction endonuclease hydrolysis of PCR products flanking a SNP located at paraoxonase 1(Q192R). Compared with electrophoresis, this method requires less time of analysis and possess a higher accuracy. 展开更多
关键词 Single nucleotide polymorphism Human paraoxonase 1 gene matrix-assisted laser desorption/ionizationtime-of-flight mass spectrometry
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UHAS-MIDA Software Package: Mass Isotopomer Distribution Analysis-Applying the Inverse Matrix for the Determination of Stable Isotopes of Chromium Distribution during Red Blood Cell Labelling
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作者 Daniel A. Abaye Emmanuel B. Odoom +3 位作者 Ernest Y. Boateng Irene A. Agbo John-Bosco Diekuu Samuel Agana 《Journal of Data Analysis and Information Processing》 2022年第2期142-154,共13页
Clinical assessment of fluid volume status in children during malaria can be taxing and often inaccurate. During malaria, changes in fluid volume are rather multifarious and estimating this parameter, especially in si... Clinical assessment of fluid volume status in children during malaria can be taxing and often inaccurate. During malaria, changes in fluid volume are rather multifarious and estimating this parameter, especially in sick children is very challenging for clinicians who frequently rely on indices such as long capillary refill times, tachycardia, central venous pressure and decreased urine volume as guides. Here, we present the UHAS-MIDA, an open-source software tool that calculates the red blood cell (RBC) concentration and blood volume during malaria in children determined using a stable isotope of chromium (<sup>53</sup>Cr as the label) by gas chromatography-mass spectrometry in selective ion monitoring (GC/MS-SIM) analysis. A key component involves the determination of the compositions of the most abundant naturally occurring isotopes of Cr (<sup>50</sup>Cr, <sup>52</sup>Cr, <sup>53</sup>Cr), and converting the proportions into a 3 × 3 matrix. To estimate unknown proportions of chromium isotopic mixtures from the measured abundances of three ions, an inverse matrix was calculated. The inverse together with several inputs is then used to calculate the corrected MS ion abundances. Thus, we constructed the software tool UHAS- MIDA using HTML, CSS/Bootstrap, JavaScript, and PHP scripting languages. The tool enables the user to efficiently determine RBC concentration and fluid volume. The source code, binary packages and associated materials for UHAS-MIDA are freely available at https://github.com/bentil078/Abaye-et-al_UHASmida 展开更多
关键词 mass Isotopomer Distribution Analysis Inverse matrix GC/MS Chromium Stable Isotopes Blood Volume Red Blood Cell mass
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高效液相色谱-质谱法测定淡水鱼中地西泮
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作者 林涛 蔡苇 +5 位作者 王志飞 普家云 李金峰 陈兴连 刘宏程 刘振环 《化学分析计量》 CAS 2024年第9期28-32,共5页
建立高效液相色谱-质谱法测定淡水鱼中地西泮。样品用乙腈提取,采用Florisil填料和氨基填料净化,当Florisil填料和氨基填料的质量比为2∶3时,能够有效地吸附淡水鱼基质中的脂肪、脂质和蛋白质等杂质,降低基质效应,提高质谱响应的信噪比... 建立高效液相色谱-质谱法测定淡水鱼中地西泮。样品用乙腈提取,采用Florisil填料和氨基填料净化,当Florisil填料和氨基填料的质量比为2∶3时,能够有效地吸附淡水鱼基质中的脂肪、脂质和蛋白质等杂质,降低基质效应,提高质谱响应的信噪比。地西泮的质量浓度在0.05~20 ng/mL范围内与色谱峰面积线性关系良好,相关系数为0.9996,检出限为0.15μg/kg,定量限为0.5μg/kg。空白样品加标回收率为84.2%~95.5%,测定结果的相对标准偏差为5.25%~6.83%(n=6)。该方法快速准确,基质效应小,能够满足水产品中地西泮的测定要求。 展开更多
关键词 高效液相色谱-质谱法 淡水鱼 地西泮 基质效应
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Effect of Sample Matrix on Radial and Axial Profiles of Ion Abundance in Inductively Coupled Plasma Mass Spectrometry
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作者 Clarisse Mariet Francine Carrot Mélanie Moskura 《American Journal of Analytical Chemistry》 2011年第7期739-751,共13页
In inductively coupled plasma mass spectrometry (ICP-MS) analysis, only a few options are available to deal with non-spectroscopic interferences. Considering that diluting the sample is impractical for traces analysis... In inductively coupled plasma mass spectrometry (ICP-MS) analysis, only a few options are available to deal with non-spectroscopic interferences. Considering that diluting the sample is impractical for traces analysis, other alternatives must be employed. Traditionally, the method of standard additions is used to correct the matrix effect but it is a time consuming method. Others methods involves separation techniques. Another way to overcome matrix interferences is to understand the mechanism involved and adjust plasma viewing conditions to reduce or eliminate the effect. In this study, the effect of various concomitant elements in ICP-MS was assessed by measuring the distribution of selected singly charged analyte ions (Al, V, Cr, Mn, Ni, Co, Cu, Zn, As, In, Ba, La, Ce, Pb), doubly charged ions (La, Ce, Ba and Pb) and oxides ions (BaO) in the presence of concomitant elements spanning a mass range from 23 (Na) to 133 (Cs) u.m.a. and different ionization energies. Concomitant elements are alkali metals, alkaline earth metals and Si. Analyte ion suppression was observed while moving the ICP across and away from the sampling interface with or without a single concomitant element. Matrix effect measures were realised, firstly, to highlight the relation between the signal extinction of an analyte and the masse of the concomitant element, and secondly to highlight the relation between the removal of the analyte signal and the first ionization energy of the element of matrix. A dependence upon both the mass of the matrix element and the mass of the analyte was observed. The suppression seems increased with increasing matrix element mass and decreased with increasing analyte mass. The effect of the mass of the matrix element was the more significant of the two factors. If space-charge effects were found to be significant for matrix elements of much lower mass, it seems diffusion also played an active part for heavier matrix elements. Finally, some evidence was found for a shift in ion-atom equilibrium for dications and for energy demand regarding oxides. 展开更多
关键词 matrix Effects Easily Ionized Elements Inductively Coupled Plasma mass SPECTROMETRY Spatial PROFILING
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A novel sample preparation method of matrix-assisted laser desorption/ionization time of flight mass spectrometry for polystyrene
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作者 Shu Zhang Zhen Wen Zhao +3 位作者 Lei Xiong Bin Xin Wei Hua Hu Shao Xiang Xiong 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第6期718-721,共4页
A novel sample preparation method of matrix-assisted laser desorption/ionization mass spectrometry for polystyrene was reported. Compared to the conventional dried-droplet method, the efficiency of ionization and sign... A novel sample preparation method of matrix-assisted laser desorption/ionization mass spectrometry for polystyrene was reported. Compared to the conventional dried-droplet method, the efficiency of ionization and signal intensity of mass spectra were improved. The mechanism was also analyzed. 展开更多
关键词 POLYSTYRENE matrix-assisted laser desorption/ionization time of flight mass spectrometry Three-layer method
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New Kinetic Computerized Model for Multicomponent Mass Transfer in Bi-Functional Matrix of NanoComposites
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作者 Anatoliy Kalinitchev 《Advances in Nanoparticles》 2013年第2期191-203,共13页
The aim of this theoretical investigation is the description of the multicomponent mass transfer process in the Nano- Composites (NC)—novel materials with the bi-functional matrix. The new theoretical NC Model is ass... The aim of this theoretical investigation is the description of the multicomponent mass transfer process in the Nano- Composites (NC)—novel materials with the bi-functional matrix. The new theoretical NC Model is assigned for the modern theoretical investigations of the multicomponent mass transfer kinetics in the bi-functional NC materials. This NC Model for the multicomponent mass transfer in the bi-functional NC matrix includes into the consideration the proposed key conception—two co-existing routes: I—chemical reactions onto the active NC centers-sites, and II—diffusion mass transfer inside the bi-functional NC matrix. All the results are presented in the terms of the additional key concept: propagating multicomponent concentration waves (W+) in the NC matrix. The used W+ concept for the description of the multicomponent NC mass transfer kinetics give the clear interpretation of the computerized results. The mass transfer process in the NC matrix has been described theoretically by computerized simulation. The results of the calculations are new and illustrated by author’s animations showing visually the propagation of the multicomponent concentration waves (W) inside the various NC matrixes: r-beads, cylindrical ro-fibers, or planar L-membranes. Two variants of modeling for mass transfer diffusion kinetics in the bi-functional NC matrixes with one (Variant 1), or two (Variant 2) dissociation-association reactions at the active nano-sites (R0) are considered theoretically. 展开更多
关键词 NANOCOMPOSITES mass Transfer Concentration Waves Diffusion MULTICOMPONENT Kinetics Bi-Functional matrix Active Nano-Sites
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MicrobMatcher: a microbial comparison software based on matrix-assisted laser desorption/ionization with time-of-flight mass spectrometry
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作者 Yizhen Fu Feng Liu Yalu Ye 《Journal of Biomedical Science and Engineering》 2011年第5期403-409,共7页
Matrix-assisted Laser Desorption/Ionization with Time-of-flight Mass Spectrometry (MALDI-TOFMS) was investigated as a method for the rapid identifica-tion of species. Current demand in microbial identi-fication is how... Matrix-assisted Laser Desorption/Ionization with Time-of-flight Mass Spectrometry (MALDI-TOFMS) was investigated as a method for the rapid identifica-tion of species. Current demand in microbial identi-fication is how to compare unknown strains to the known one quickly, semi-automatically and accurately. In this paper, we present a software tool that allows flexibly microbial matching in a user-friendly way, by letting the users to customize comparison parameters including: in vitro transcription enzyme, mass tolerance,minimum fragment length, intensity threshold and corresponding weights. We provide three spectral scoring functions to compute the affin-ity between the species. Therefore, the precision of microbial comparison increases. To test and verify this tool, we employed experimental spectral data based on MALDI-TOFMS and the gene sequences of E.coli and Salmonella. This software is written in Java for cross-platform intention. 展开更多
关键词 MICROBIAL Comparison matrix-Assisted Laser Desorption/Ionization with TIME-OF-FLIGHT mass SPECTROMETRY
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ICP-QQQ-MS法分析婴幼儿谷物辅助食品中镉含量的干扰及其校正 被引量:1
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作者 蔡玮 赵博 +4 位作者 赵少雷 陈欢欢 李潇 逯海 韦超 《食品科学》 EI CAS CSCD 北大核心 2024年第14期234-239,共6页
建立三重串联四极杆电感耦合等离子体质谱(inductively coupled plasma triple quadrupole mass spectrometry,ICP-QQQ-MS)法测定婴幼儿谷物辅助食品中镉(Cd)含量的方法。研究单四极杆氦气碰撞模式(SQ-He)、串联四极杆氦气碰撞模式(QQQ-... 建立三重串联四极杆电感耦合等离子体质谱(inductively coupled plasma triple quadrupole mass spectrometry,ICP-QQQ-MS)法测定婴幼儿谷物辅助食品中镉(Cd)含量的方法。研究单四极杆氦气碰撞模式(SQ-He)、串联四极杆氦气碰撞模式(QQQ-He)、串联四极杆氧气反应模式(QQQ-O_(2))3种碰撞/反应模式下质谱测量中存在的各类干扰,并进行逐一分析、消除。结果显示,抗基体、抗氧化物和多原子离子干扰能力均为QQQ-O_(2)>QQQ-He>SQ-He,采用QQQ-O_(2)模式联合标准加入法可获得更为准确的干扰消除效果。通过引入干扰校正方程,有效解决由于同量异位素锡(Sn)干扰导致的Cd同位素丰度比与天然丰度比不一致问题。QQQ-O_(2)模式下同位素稀释质谱法与标准加入法测量Cd的结果等效一致,证明婴幼儿谷物辅助食品中Cd测量时受到的基体效应和质谱干扰被有效消除。所建方法为使用ICP-QQQ-MS准确测定复杂基体样品中Cd提供重要参考。 展开更多
关键词 三重串联四极杆电感耦合等离子体质谱 质谱干扰 同位素稀释质谱 基体效应
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气相色谱—串联质谱法测定六类茶叶中11种农药的基质效应
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作者 孙羽婕 陈璐 +2 位作者 王顾希 樊东生 李椤颢 《山东化工》 CAS 2024年第11期122-125,130,共5页
采用气相色谱—串联质谱结合QuEChERS前处理方法在三个不同质量浓度(0.010,0.040,0.16 mg/L)下对六类茶叶中11种农药的基质效应进行考察比较。结果表明:11种农药在六类茶叶中均呈增强基质效应,以增强强基质效应为主。绿茶基质效应范围... 采用气相色谱—串联质谱结合QuEChERS前处理方法在三个不同质量浓度(0.010,0.040,0.16 mg/L)下对六类茶叶中11种农药的基质效应进行考察比较。结果表明:11种农药在六类茶叶中均呈增强基质效应,以增强强基质效应为主。绿茶基质效应范围区间为101.02%~232.28%;花茶基质效应范围区间为108.14%~269.60%;红茶基质效应范围区间为124.41%~311.67%;白茶基质效应范围区间为127.62%~299.09%;黑茶基质效应范围区间为120.23%~318.22%;乌龙茶基质效应范围区间为131.84%~336.03%。六类茶叶11种农药的RSD值均小于10%,表明不同浓度的茶叶基质溶液对供试的农药具有相似的基质效应。在对茶叶农残含量进行检测时,建议选用对应的基质标对目标物进行定量检测,同时在样品前处理时对试样进行多次净化,以保证定量结果的准确度。 展开更多
关键词 茶叶 农药残留 基质效应 气相色谱—串联质谱
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基于响应面法的基质固相分散萃取土壤中有机磷阻燃剂
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作者 王俊霞 徐思婕 +4 位作者 孙悦莹 雷慧慧 程媛媛 王学东 张占恩 《色谱》 CSCD 北大核心 2024年第1期64-74,共11页
有机磷阻燃剂(OPFRs)被广泛添加于商业品和日用品中,由于具有环境持久性、生物富集性和潜在毒性,已成为一种新兴的持久性有机污染物。因此需要建立能准确定量环境中OPFRs的检测方法。该文基于基质固相分散萃取(MSPD),结合气相色谱-串联... 有机磷阻燃剂(OPFRs)被广泛添加于商业品和日用品中,由于具有环境持久性、生物富集性和潜在毒性,已成为一种新兴的持久性有机污染物。因此需要建立能准确定量环境中OPFRs的检测方法。该文基于基质固相分散萃取(MSPD),结合气相色谱-串联质谱(GC-MS/MS)法测定土壤中10种有机磷阻燃剂,筛选对OPFRs具有高选择性的吸附剂,最终确定MSPD最佳萃取条件。该文基于单因素分析法考察了常见吸附剂(C18、PSA、Florisil、石墨化炭黑(GCB)和多壁碳纳米管(MWCNT))及其用量、洗脱溶剂及其体积、研磨时间对OPFRs萃取效率的影响。在此结果基础上,进一步利用响应面法(RSM)考察了3个关键因素(吸附剂用量、洗脱剂用量和研磨时间)以及交互作用对OPFRs萃取效率的影响。最终确定最优条件:吸附剂GCB,用量0.3 g;洗脱溶剂乙酸乙酯,用量10 mL;研磨时间5 min,此时10种OPFR的萃取效率为87.5%。在GC-MS/MS的多反应监测模式(MRM)下,以13C-PCB208为内标物进行定量。10种OPFRs在6个浓度梯度下,获得较好的线性,相关系数大于0.998。该方法的LOD和LOQ分别为0.006~0.161 ng/g和0.020~0.531 ng/g。在最佳条件下,加标土壤中OPFRs的加标回收率为70.4%~115.4%,相对标准偏差(RSD)为0.7%~6.7%。将该方法用于苏州不同功能土壤中OPFRs的含量测定,结果表明电子厂和汽修厂土壤中OPFRs总含量显著高于稻田土和校园土,电子厂和汽修厂土壤中主要污染物为磷酸三(2-氯异丙基)酯(TCIPP)、三苯基氧化膦(TPPO)、磷酸三(2-氯乙基)酯(TCEP)和磷酸三(1,3-二氯-2-丙基)酯(TDCPP),它们在电子厂土壤中含量分别为5.30、4.44、4.54、4.20 ng/g,在汽修厂土壤中的含量分别2.70、3.93、7.60、5.04 ng/g。目前关于TPPO的土壤污染报道较少,该研究在苏州工业区土壤中检出了高浓度TPPO污染。该方法成功用于土壤中10种OPFRs的检测。 展开更多
关键词 气相色谱-串联质谱 基质固相分散萃取 响应面法 有机磷阻燃剂 土壤
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Novel Approach for Quantitative Measurement of Matrix Metalloprotease-1 (MMP1) in Human Breast Cancer Cells Using Mass Spectrometry
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作者 Ming Fa Kathleen Hoch +3 位作者 Xuejun Fan William P. Dubinsky Zhiqiang An Ningyan Zhang 《Journal of Analytical Sciences, Methods and Instrumentation》 2013年第1期54-61,共8页
Identification and quantification of low abundance growth factors and regulators in complex biological samples still present a challenging task in analytical biochemistry. Immunoassays are often used for such purpose ... Identification and quantification of low abundance growth factors and regulators in complex biological samples still present a challenging task in analytical biochemistry. Immunoassays are often used for such purpose but immunoassays face limitation of both availability and qualities of antibody reagents that are necessary for development of immune assays. With genomics data base available, mass spectrometry (MS) can analyze protein tryptic peptides directly for quantitative determination of proteins. In this study, we report a method for detection of matrix metalloproteinase 1 (MMP1), an important extracellular matrix modulator, in human breast cancer cells by quadrupole time-of-flight (Q-TOF) MS. Absolute quantification of MMP1 was conducted using the selected reaction monitoring (SRM) on a triple quadrupole (Triple-Quad) MS via transitions selected from MMP1 tryptic peptides using non isotope labeled MMP1 protein as a titration standard. In comparison with immune based assay, this MS method showed picogram level sensitivity for quantitative determination of MMP1 intotal cell lysates. Our results demonstrated the feasibility of absolute quantification of low abundance proteins using label-free protein standard by mass spectrometry. Therefore, this method provides not only advantages of high sensitivity but also cost saving in comparison with the commonly used mass spectrometry that currently employs isotype labeled proteins for quantitative analysis. 展开更多
关键词 matrix Metalloprotease-1 (MMP1) SKBR3 BREAST Cancer Cells mass SPECTROMETRY Selected Reaction Monitoring ABSOLUTE Quantification
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高盐食品基质中砷含量的测定 被引量:2
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作者 戴瑞平 刘花梅 +6 位作者 舒露 唐丽君 黎申英 李彪 张梅玲 刘涛 黄宗兰 《现代食品科技》 CAS 北大核心 2024年第4期321-330,共10页
建立了一种基体匹配-动态反应池-电感耦合等离子体质谱法测定高盐食品基质中砷含量的方法,以解决高盐基体对砷测定的质谱干扰和基体干扰。研究电感耦合等离子体质谱法与氢化物发生原子荧光光谱法测定食品中总砷的技术要点,通过分析前处... 建立了一种基体匹配-动态反应池-电感耦合等离子体质谱法测定高盐食品基质中砷含量的方法,以解决高盐基体对砷测定的质谱干扰和基体干扰。研究电感耦合等离子体质谱法与氢化物发生原子荧光光谱法测定食品中总砷的技术要点,通过分析前处理消解方式、有机基质、氯含量和内标校正元素等对砷含量测定的影响,建立了高盐食品基质中砷含量的测定方法。实验结果表明,微波消解法并不太适用于氢化物发生原子荧光光谱法测定食品中总砷,有机基质和氯分别会对砷的质谱测定信号产生增敏效应和质谱干扰,74Ge比72Ge更适合作为电感耦合等离子体质谱法测定食品中总砷的内标元素。建立的检测方法定量限0.010 mg/kg,高盐基体中砷在0.010、0.025、0.20、0.50 mg/kg添加水平的回收率为91.50%~110.80%,相对标准偏差范围为0.76%~7.22%。本法和参照法对样品分析结果统计值均大于t0.90,10(1.81,双边),测定结果存在显著性差异,对实际样品测定结果表明动能歧视测定模式并不太适用于高盐食品基质样品中总砷的测定。该方法准确可靠,能用于高盐和高基体食品中砷含量的测定分析。 展开更多
关键词 高盐食品基质 氢化物发生原子荧光光谱法 电感耦合等离子体质谱法 基体匹配
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