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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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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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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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样品基质对吸附管采样-热脱附-气相色谱-质谱法测定挥发性有机化合物的影响
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作者 董翊 姜阳 +3 位作者 于瑞祥 高艳秋 任逸尘 魏王慧 《理化检验(化学分册)》 北大核心 2025年第2期143-148,共6页
用氮气稀释含有丙酮、异丙醇、正己烷、乙酸乙酯、苯等5种挥发性有机化合物(VOCs)的混合标准气体制备标准吸附管系列,采用热脱附-气相色谱-质谱法测定并绘制工作曲线,以考察空气、二氧化碳、甲醇基质对低、中、高含量上述5种VOCs测定的... 用氮气稀释含有丙酮、异丙醇、正己烷、乙酸乙酯、苯等5种挥发性有机化合物(VOCs)的混合标准气体制备标准吸附管系列,采用热脱附-气相色谱-质谱法测定并绘制工作曲线,以考察空气、二氧化碳、甲醇基质对低、中、高含量上述5种VOCs测定的影响。结果显示:5种VOCs的质量在不同范围内和对应的定量离子的峰面积呈线性关系,检出限(3S/N)为0.0300~1.00 ng,测定值的相对标准偏差(n=7)为2.1%~5.7%;除甲醇基质中低含量丙酮和异丙醇的回收率大于200%外,3种基质中不同含量的5种VOCs的回收率均在90.0%~110%内,推测残留在检测器中的甲醇影响了与甲醇保留时间接近的丙酮和异丙醇的电离,导致离子强度增大,回收率增加。 展开更多
关键词 吸附管采样 热脱附 气相色谱-质谱法 挥发性有机化合物 基质影响 甲醇
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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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液相色谱-串联质谱法测定凉茶中18种非法添加抗病毒药物的含量
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作者 温家欣 何嘉雯 +2 位作者 曹雅静 陈俏 赖宇红 《理化检验(化学分册)》 北大核心 2025年第1期70-76,共7页
提出了液相色谱-串联质谱法测定凉茶中18种非法添加抗病毒药物(盐酸吗啉胍、喷昔洛韦、磷酸奥司他韦、三水合帕拉米韦、扎那米韦、利巴韦林、阿比多尔、法匹拉韦、洛匹那韦、拉尼米韦、盐酸金刚烷胺、盐酸金刚乙胺、玛巴洛沙韦、利托那... 提出了液相色谱-串联质谱法测定凉茶中18种非法添加抗病毒药物(盐酸吗啉胍、喷昔洛韦、磷酸奥司他韦、三水合帕拉米韦、扎那米韦、利巴韦林、阿比多尔、法匹拉韦、洛匹那韦、拉尼米韦、盐酸金刚烷胺、盐酸金刚乙胺、玛巴洛沙韦、利托那韦、阿昔洛韦、更昔洛韦、泛昔洛韦、盐酸伐昔洛韦)含量的方法。取凉茶样品1.0000 g置于50 mL容量瓶中,加入40 mL体积比1∶3的甲醇-乙腈混合溶液,超声30 min,冷却至25℃,用体积比1∶3的甲醇-乙腈混合溶液定容,过0.22μm尼龙滤膜,取滤液待测。以Waters ACQUITY BEH HILIC色谱柱为固定相,以不同体积比的含0.1%(体积分数)乙酸的10 mmol·L^(-1)乙酸铵溶液和含0.1%(体积分数)甲酸的乙腈溶液的混合液为流动相进行梯度洗脱,采用电喷雾离子(ESI)源,在正离子(ESI^(+))扫描模式下进行多反应监测(MRM)模式质谱分析,以基质匹配的混合标准溶液绘制工作曲线。结果表明,18种非法添加抗病毒药物(盐类抗病毒药物以游离态计)的质量浓度在一定范围内与对应的色谱峰面积呈线性关系,检出限(3S/N)为0.005~2.0 mg·kg^(-1)。按照标准加入法进行回收试验,回收率为70.3%~115%,测定值的相对标准偏差(n=6)均小于12%。方法用于387批凉茶分析,有10批凉茶检出金刚烷胺,检出量为0.125~420 mg·kg^(-1),4批凉茶检出吗啉胍,检出量为177~6404 mg·kg^(-1)。 展开更多
关键词 液相色谱-串联质谱法 凉茶 非法添加抗病毒药物 基质匹配
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等/变截面铁摩辛柯梁单元一致质量矩阵分析
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作者 胡连超 张军锋 +3 位作者 杨作杰 耿玉鹏 叶雨山 李杰 《结构工程师》 2025年第1期34-42,共9页
因既有研究对铁摩辛柯梁单元质量矩阵的分析过程缺乏系统介绍,为明确其一致质量矩阵的推导方法,以其所用拉格朗日形函数为基础,基于虚功原理,区分伸缩、扭转、挠曲变形和转角变形这四种运动状态,分别给出了2节点和3节点等截面单元在单... 因既有研究对铁摩辛柯梁单元质量矩阵的分析过程缺乏系统介绍,为明确其一致质量矩阵的推导方法,以其所用拉格朗日形函数为基础,基于虚功原理,区分伸缩、扭转、挠曲变形和转角变形这四种运动状态,分别给出了2节点和3节点等截面单元在单一运动状态下的质量矩阵,并汇总为完整质量矩阵理论表达式,还针对变截面单元给出了有限元计算中的简化计算方法。另外,介绍了铁摩辛柯梁和欧拉梁在形函数层面上的差异,以及铁摩辛柯梁单元在受弯状态下质量矩阵和刚度矩阵分析中的差异。结果表明,拉格朗日形函数作为铁摩辛柯梁各种受力变形的统一表达,尤其是受弯状态下挠曲和转角变形的独立性,使得所有单独受力模式下的质量矩阵形式相同,均可由相应的截面参数配合同一种形函数来表达,并且最终所得单元的完整质量矩阵有更好的解耦性;对于变截面单元,实用计算中采用独立积分并配合高斯分的简化计算方法,由此所得质量矩阵表达式与等截面梁的形式一致,只是采用等效截面参数替换等截面梁的截面参数。 展开更多
关键词 一致质量矩阵 铁摩辛柯梁单元 形函数 独立插值 变截面
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超高效液相色谱−串联质谱法测定织纹螺中河豚毒素的方法优化
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作者 沈晓娜 陈小红 +2 位作者 罗方方 陈慧斌 刘智禹 《渔业研究》 2025年第1期64-73,共10页
【背景】近年来,因食用织纹螺引发的河豚毒素(TTX)中毒事件频发,然而现行国家标准(GB 5009.206-2016)中的液相色谱−串联质谱法(LC-MS/MS)仅适用于河鲀中TTX含量的检测,因此亟需建立一种适用于检测织纹螺中TTX含量的高效、准确的方法。... 【背景】近年来,因食用织纹螺引发的河豚毒素(TTX)中毒事件频发,然而现行国家标准(GB 5009.206-2016)中的液相色谱−串联质谱法(LC-MS/MS)仅适用于河鲀中TTX含量的检测,因此亟需建立一种适用于检测织纹螺中TTX含量的高效、准确的方法。【目的】基于超高效液相色谱−串联质谱法(UPLC-MS/MS)建立一种高效且能准确测定织纹螺中TTX含量的方法。【方法】通过比较不同前处理方法(提取溶液、提取方式、冷冻时间)下TTX回收率的大小,以及不同色谱条件(流动相、进样量)对色谱峰的影响,获得最佳实验条件。此外,采用优化后的方法和现行国家标准方法对采自福建省莆田市和宁德市的织纹螺样品进行测定,以比较该检测方法的准确性和可靠性。【结果】最佳前处理条件:样品首先采用0.1%乙酸溶液60℃超声提取20 min,随后使用80%(体积分数)0.1%乙酸甲醇溶液稀释并在−18℃下冷冻30 min后离心,取上清液过膜后,上机测定;UPLC-MS/MS条件:以含5 mmol·L^(−1)乙酸铵的0.1%甲酸溶液和乙腈为流动相,经Amide-80色谱柱梯度洗脱后,采用电喷雾正离子选择反应监测模式,以基质标准曲线外标法定量。TTX在织纹螺中的基质效应为68.9%,在1~100 ng·mL^(−1)基质标准曲线范围内线性关系良好,线性回归方程相关系数R^(2)>0.99。本方法的检出限和定量限分别为10、25μg·kg^(−1),能同时满足中国和欧洲食品安全委员会对水产品中TTX安全限量值(分别为2200、44μg·kg^(−1))的要求。此外,在3个TTX加标浓度(50、500、4000μg·kg^(−1))下,平均回收率为74.8%~104%,相对标准偏差(RSD)均小于15%(n=6)。分别采用优化后的实验方法和现行国家标准方法对9份织纹螺样品进行检测,2种方法检测的TTX含量范围分别为<0.0250~22.8、0.0120~23.5 mg·kg^(−1),相对偏差为1.51%~14.6%,表明本检测方法准确可靠。【结论】本研究优化建立了一种适用于测定织纹螺中TTX含量的UPLC-MS/MS法,具有前处理简单、快速准确和低成本等特点,为实现织纹螺中TTX含量的快速批量检测奠定良好基础。 展开更多
关键词 织纹螺 河豚毒素 方法优化 超高效液相色谱−串联质谱法 基质效应
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普通铅对LA-ICP-MS磷灰石U-Pb定年结果的影响及校正方法
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作者 罗涛 王瀚林 +2 位作者 朱松柏 卿丽媛 胡兆初 《岩矿测试》 CAS 北大核心 2025年第1期51-62,共12页
磷灰石是火成岩、变质岩和沉积岩中广泛分布的含铀矿物,开展磷灰石U-Pb年代学研究对揭示岩浆演化过程、示踪溯源等方面具有重要意义。激光剥蚀电感耦合等离子体质谱法(LA-ICP-MS)是开展磷灰石U-Pb年龄微区分析的重要手段之一。当前,基... 磷灰石是火成岩、变质岩和沉积岩中广泛分布的含铀矿物,开展磷灰石U-Pb年代学研究对揭示岩浆演化过程、示踪溯源等方面具有重要意义。激光剥蚀电感耦合等离子体质谱法(LA-ICP-MS)是开展磷灰石U-Pb年龄微区分析的重要手段之一。当前,基体匹配磷灰石U-Pb定年矿物标样缺乏和标样中不可避免的普通铅是制约LA-ICP-MS高精度磷灰石U-Pb年龄分析的主要瓶颈。本文对比研究了标样中普通铅对LA-ICP-MS磷灰石U-Pb定年结果的影响,采用含普通铅的磷灰石MAD作外标直接开展U-Pb年龄校正,获得的被测样品年龄会产生显著的系统偏差(最大约6%);采用207Pb法或Tera-Wasserburg图解法先校正标样中普通铅,再利用校正后的数据进行元素分馏和仪器漂移校正则可获得准确的磷灰石U-Pb年龄,与推荐值偏差在2%以内。另一方面,为消除标样中普通铅对分析结果的影响,本文还采用水蒸气辅助激光剥蚀方法,实现以NIST612玻璃作为外标准确分析磷灰石U-Pb年龄,解决了磷灰石U-Pb定年微区分析高质量标样缺乏的难题。本研究通过对标样中普通铅进行预校正或采用非基体匹配分析,建立了高精度LA-ICP-MS磷灰石U-Pb定年新方法,将促进磷灰石U-Pb年代学在地球科学研究中的应用。 展开更多
关键词 激光剥蚀电感耦合等离子体质谱法 磷灰石 U-PB定年 普通铅校正 非基体匹配分析
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2020-2022年广西柳州市工人医院细菌耐药性监测
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作者 李梦薇 韦柳华 +5 位作者 罗国兰 朱虹贞 林盛张 陈丽坤 蒋利君 王海霞 《中国感染与化疗杂志》 北大核心 2025年第2期195-202,共8页
目的 了解2020-2022年连续3年广西柳州市工人医院临床分离菌对常见抗菌药物的耐药性与敏感性。方法 使用VITEK-2 Compact或纸片扩散法或E试验法进行药敏试验,参照CLSI M100 32^(nd) 2022年版药敏折点标准判读结果,采用WHONET 5.6软件进... 目的 了解2020-2022年连续3年广西柳州市工人医院临床分离菌对常见抗菌药物的耐药性与敏感性。方法 使用VITEK-2 Compact或纸片扩散法或E试验法进行药敏试验,参照CLSI M100 32^(nd) 2022年版药敏折点标准判读结果,采用WHONET 5.6软件进行分析。结果 该院共收集到临床分离株26 254株,其中革兰阳性菌27.9%,革兰阴性菌72.1%。甲氧西林耐药葡萄球菌MRSA和MRCNS的检出率分别为20.0%和 72.2%。甲氧西林耐药株(MRSA和MRCNS)对大多数抗菌药物耐药率高于甲氧西林敏感株(MSSA和MSCNS);未发现有万古霉素、利奈唑胺和替加环素的耐药菌株。屎肠球菌对大多常用抗菌药物耐药率普遍高于粪肠球菌,均未发现两者对万古霉素耐药的菌株,但有少数菌株对利奈唑胺耐药。非脑膜炎肺炎链球菌中儿童株和成人株分别为691株和123株;两组菌株中PRSP分别为0.4%和1.6%,但均未发现有中介株。耐碳青霉烯类肺炎克雷伯菌(CRKpn)的检出率三年间分别为1.2%、1.2%、13.8%;而铜绿假单胞菌和鲍曼不动杆菌中耐碳青霉烯类菌株(CRPae 和CRAba)三年间分别为10.7%、17.5%、14.3%和68.4%、75.2%、77.3%。1 269株流感嗜血杆菌中儿童株和成人株各为84.6%和15.4%,两组菌株中β内酰胺酶的检出率分别为39.4%和46.8%;产酶株对氨苄西林耐药,但在不产酶株中已经发现有少数的氨苄西林耐药(BLNAR)株,其检出率为27.0%。结论 该院细菌对抗菌药物的耐药形势严峻,尤其是碳青霉烯类耐药革兰阴性杆菌(CRO)菌株的检出率较高,应加强院感防控措施和临床抗菌药物管理,及CRO的主动筛查。临床应多送检疑似感染部位的标本,在药敏报告发出前首先经验用药,待收到药敏报告后,再根据药敏报告合理选用抗菌药物。 展开更多
关键词 耐药监测 药敏试验 全自动微生物质谱检测仪 碳青霉烯类耐药菌 抗菌药物
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QuEChERS结合GC-MS/MS法测定蕹菜中41种农药残留
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作者 李南 韦盈 +3 位作者 王丹 吴含秀 陈思明 智丽 《现代食品》 2025年第1期183-188,195,共7页
建立测定蕹菜中41种农药残留量的QuEChERS-气相色谱-串联质谱(Gas Chromatography-Tandem Mass Spectrometry,GC-MS/MS)检测方法。蕹菜样品经乙腈提取后,采用QuEChERS方法前处理,以N-丙基乙二胺(N-Propyl Ethylenediamine,PSA)、石墨化... 建立测定蕹菜中41种农药残留量的QuEChERS-气相色谱-串联质谱(Gas Chromatography-Tandem Mass Spectrometry,GC-MS/MS)检测方法。蕹菜样品经乙腈提取后,采用QuEChERS方法前处理,以N-丙基乙二胺(N-Propyl Ethylenediamine,PSA)、石墨化炭黑(Graphitized Carbon Black,GCB)吸附提取液中的干扰组分,提取液经GC-MS/MS多反应监测模式分析测定,匹配基质标准曲线内标法定量。结果表明,采用本研究建立的方法测定41种农药,线性范围为10~500 ng·mL^(-1),相关系数(R^(2))在0.9938~0.9998,线性关系良好,定量限均为0.01 mg·kg^(-1)。在0.010、0.025、0.250 mg·kg^(-1)3个加标水平下的平均加标回收率为62.1%~117.2%,相对标准偏差在0.2%~14.3%(n=6)。所建方法的准确度、精密度均能满足蕹菜中41种农药残留基本定量要求,操作简单、效率高,可用于蕹菜中实际农药残留的检测。 展开更多
关键词 QUECHERS 气相色谱-三重四极杆串联质谱 基质效应
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基体分离-电感耦合等离子体质谱法测定高纯钽中Ni、B含量
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作者 巩琛 黄辉 +3 位作者 张嘉祺 苗世海 李颖 李本涛 《中国无机分析化学》 北大核心 2025年第3期398-405,共8页
针对高纯钽测试过程基体对被测杂质元素干扰的问题,通过将样品湿法消解后经基体分离,消除钽基体对杂质的质谱干扰,建立基体分离-电感耦合等离子体质谱法测定高纯钽中杂质元素含量的方法。考察基体干扰0~1 000 ng/mL、仪器功率0.8~1.4 k... 针对高纯钽测试过程基体对被测杂质元素干扰的问题,通过将样品湿法消解后经基体分离,消除钽基体对杂质的质谱干扰,建立基体分离-电感耦合等离子体质谱法测定高纯钽中杂质元素含量的方法。考察基体干扰0~1 000 ng/mL、仪器功率0.8~1.4 kW、采样深度5~9 mm、等离子体气流量7.5~12 L/min、雾化气流量0.6~1.1 L/min等影响因素的干扰情况,确定了最佳分析条件。结果表明,在基体分离,RF功率1.36 kW、采样深度5 mm、等离子气流量9.0 L/min、雾化气流量0.88 L/min条件下,仪器处于最佳分析测试状态,在此条件下Ni、B的校准曲线方程相关系数均大于0.999,检出限(LOD)分别为0.3、1.2 ng/g,加标回收率在96.0%~105%,样品测试相对标准偏差(RSD)<3%(n=10)。方法检出限低,准确性高,适用于高纯钽中Ni、B杂质元素含量的快速定量测试。 展开更多
关键词 电感耦合等离子体质谱法 高纯钽 基体分离
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食品农药残留的高效液相色谱-质谱联用检测方法优化策略
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作者 黄芳 羊超菠 +1 位作者 韦雪飞 厉畅达 《食品安全导刊》 2025年第1期169-171,共3页
本研究分析了食品农药残留检测中高效液相色谱-质谱联用技术面临的主要挑战,包括检测灵敏度不足、定量准确性受限及复杂基质干扰等问题。通过优化样品前处理方法、改进色谱分离条件、创新质谱检测参数等策略,提出了基质固相分散萃取与... 本研究分析了食品农药残留检测中高效液相色谱-质谱联用技术面临的主要挑战,包括检测灵敏度不足、定量准确性受限及复杂基质干扰等问题。通过优化样品前处理方法、改进色谱分离条件、创新质谱检测参数等策略,提出了基质固相分散萃取与同位素内标法相结合的分析方案,有助于提高农药残留检测的灵敏度和准确度。 展开更多
关键词 液相色谱-质谱联用 农药残留 基质效应
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