Direct analysis of copper-base alloys using laser ablation techniques is an increasingly common procedure in cultural heritage studies. However, main discussions remain focused on the possibility of using non-matrix m...Direct analysis of copper-base alloys using laser ablation techniques is an increasingly common procedure in cultural heritage studies. However, main discussions remain focused on the possibility of using non-matrix matched external reference materials. To evaluate the occurrence of matrix effects during in situ microanalysis of copper-base materials, using near infrared femtosecond laser ablation techniques (NIR fs-LA-ICP-MS), two bronzes, i.e., (Sn-Zn)-ternary and (Sn)-binary copper-matrix reference materials, as well as a reference synthetic glass (NIST-SRM-610) have been analyzed. The results have been compared to data obtained on a sulfide-matrix reference material. Similar values in relative sensitivity averages of 63Cu, 118Sn and 66Zn, as well as in 118Sn/63Cu and 66Zn/63Cu ratios were obtained, for all analyzed matrix types, i.e., copper-base-, silicate-, and sulfide-reference materials. Consequently, it is possible to determinate major and minor element concentrations in copper alloys, i.e., Cu, Sn and Zn, using silicate and sulfide reference materials as external calibrators, without any matrix effect and over a wide range of concentrations (from wt.% to ppm). Equally, Cu, Sn and Zn concentrations can be precisely determined in sulfides using homogeneous alloys (reference) materials as an external calibrator. Thus, it is possible to determine Cu, Sn and Zn in copper-base materials and their ore minerals, mostly sulfides, in a single analytical session, without requiring specific external calibrators for each matrix type. In contrast, immiscible elements in copper matrix, such as Pb and Fe show notable differences in their relative sensitivity values and ratios for different matrix-materials analyzed, implying that matrix-matched external calibrations remain to be applied for their trace quantification.展开更多
应用电感耦合等离子体质谱法(ICP-MS)测定地球化学样品中痕量银时,受到相对地球化学丰度高的Nb,Zr,Y等元素的离子化合物干扰严重,样品不经富集分离,银的测试结果偏差非常大。本研究以负载二苯硫脲泡塑选择性富集Au和Ag,实现了Au和Ag与...应用电感耦合等离子体质谱法(ICP-MS)测定地球化学样品中痕量银时,受到相对地球化学丰度高的Nb,Zr,Y等元素的离子化合物干扰严重,样品不经富集分离,银的测试结果偏差非常大。本研究以负载二苯硫脲泡塑选择性富集Au和Ag,实现了Au和Ag与其它干扰元素的分离,建立了负载二苯硫脲泡塑富集、硫脲解脱-ICP-MS同时测定痕量Au和Ag的新方法。方法采用王水(1∶1)封闭消解矿样,补加水量50 m L,振荡时间和吸附温度分别为25 min和20℃,Au和Ag的方法检出限分别为0.02和0.007μg/g。使用本方法对8个国家一级标准物质中Au和Ag的检测结果与标准值基本相符,确证了方法的可行性。展开更多
A method of analysis trace element chloride in cleaning products by Inductively Coupled Plasma-Mass Sepctrometry (ICPMS) was studied. It has good precision (RSD<5%). The LOD is 0.06 μg/L (n=7). The recovery is 93....A method of analysis trace element chloride in cleaning products by Inductively Coupled Plasma-Mass Sepctrometry (ICPMS) was studied. It has good precision (RSD<5%). The LOD is 0.06 μg/L (n=7). The recovery is 93.7%-110.0%.展开更多
In this paper,the determination of six heavy metal ions (arsenic,lead,cadmium,chromium,mercury and nickel) in the Chinese Herb by inductively coupled plasma-mass spectrometry (ICP-MS) was studied.The samples were dige...In this paper,the determination of six heavy metal ions (arsenic,lead,cadmium,chromium,mercury and nickel) in the Chinese Herb by inductively coupled plasma-mass spectrometry (ICP-MS) was studied.The samples were digested by nitric acid and hydrogen peroxide in a microwave oven.The Sc,Y,In,Bi were added as internal standards to eliminate the matrix interferences.The results show that most of the relative standard deviations of these trace elements were below 3.5%,the standard recoveries of these elements were in the range of 91%-107%,and the detection limits were in the range of 0.001-0.006 μg·L-1. This method is accurate,rapid,convenience,and can be applied to the determination of arsenic,lead,cadmium,chromium,mercury and nickel in Chinese Herb with good results.展开更多
Objective The aim of this survey was to investigate the level of contamination of the most consumed foods in China with 26 rare earth elements （REEs）, and to provide the basic data for establishing and revising food...Objective The aim of this survey was to investigate the level of contamination of the most consumed foods in China with 26 rare earth elements （REEs）, and to provide the basic data for establishing and revising food safety standards for REEs. Methods Sixteen REEs in foods were measured by inductively coupled plasma-mass spectrometry （ICP-MS） in the labs of the Centers for Disease Control and Prevention of four provinces and two municipalities, during 2009-2020. Results 2 231 samples were analyzed and 29 221 concentration data of 16 REEs were collected. The REEs levels in the investigated foods varied significantly. The concentrations of cerium （Ce）, dysprosium （Dy）, yttrium （Y）, lanthanum （La）, and neodymium （Nd） were relatively high, while the remaining eleven REEs were at low levels. The mean values of total rare earth element oxides （REOs） in cereals, fresh vegetables, fresh aquatic products, fresh meats and eggs varied from 0.052 mg/kg to 0.337 mg/kg. Conclusion 16 REEs in the major foods were at very low contamination levels in the investigated regions.展开更多
AIM： To evaluate the bioequivalence of ranitidine and bismuth derived from two compound preparations. METHODS： The bioavailability was measured in 20 healthy male Chinese volunteers following a single oral dose （eq...AIM： To evaluate the bioequivalence of ranitidine and bismuth derived from two compound preparations. METHODS： The bioavailability was measured in 20 healthy male Chinese volunteers following a single oral dose （equivalent to 200 mg of ranitidine and 220 mg of bismuth） of the test or reference products in the fasting state. Then blood samples were collected for 24 h. Plasma concentrations of ranitidine and bismuth were analyzed by high-performance liquid chromatography and inductively coupled plasma-mass spectrometry （ICPMS）, respectively. The non-compartmental method was used for pharmacokinetic analysis. Log-transformed Cmax, AUC（0-t） and AUC（0-∞） were tested for bioequivalence using ANOVA and Schuirmann two-one sided t-test. Tmax was analyzed by Wilcoxon＇s test. RESULTS： Various pharmacokinetic parameters of ranitidine derived from the two compound preparations, including Cmax, AUC（0-t）, AUC（0-∞）, Tmax and T1/2, were nearly consistent with previous observations. These parameters derived from test and reference drug were as follows： Cmax（0.67 ± 0.21 vs 0.68 ± 0.22 mg/L）, AUC（0-t）（3.1 ± 0.6 vs 3.0 ± 0.7 mg/L per hour）, AUC（0-∞）（3.3 ± 0.6 vs 3.2 ± 0.8 mg/L per hour）, Tmax （2.3 ± 0.9 VS 2.1 ± 0.9 h） and T1/2 （2.8 ± 0.3 vs 3.1 ± 0.4 h）. In addition, double-peak absorption profiles of ranitidine were found in some Chinese volunteers. For bismuth, those parameters derived from test and reference drug were as follows： Cmax （11.80 ± 7.36 vs 11.40 ± 6.55 μg/L）, AUC（0-t） （46.65 ± 16.97 vs 47.03 ± 21.49 μg/L per hour）, Tmax （0.50 ± 0.20 vs 0.50 ± 0.20 h） and T1/2 （10.2 ± 2.3 vs 13.0 ± 6.9 h）. Ninety percent of confidence intervals for the test/reference ratio of Cmax, AUC（0-t） and AUC（0-∞） derived from both ranitidine and bismuth were found within the bioequivalence acceptable range of 80%-125%. No significant difference was found in Tmax derived from both ranitidine and bismuth. CONCLUSION： The two compound preparations are bioequivalent and may be prescribed interchangeably.展开更多
文摘Direct analysis of copper-base alloys using laser ablation techniques is an increasingly common procedure in cultural heritage studies. However, main discussions remain focused on the possibility of using non-matrix matched external reference materials. To evaluate the occurrence of matrix effects during in situ microanalysis of copper-base materials, using near infrared femtosecond laser ablation techniques (NIR fs-LA-ICP-MS), two bronzes, i.e., (Sn-Zn)-ternary and (Sn)-binary copper-matrix reference materials, as well as a reference synthetic glass (NIST-SRM-610) have been analyzed. The results have been compared to data obtained on a sulfide-matrix reference material. Similar values in relative sensitivity averages of 63Cu, 118Sn and 66Zn, as well as in 118Sn/63Cu and 66Zn/63Cu ratios were obtained, for all analyzed matrix types, i.e., copper-base-, silicate-, and sulfide-reference materials. Consequently, it is possible to determinate major and minor element concentrations in copper alloys, i.e., Cu, Sn and Zn, using silicate and sulfide reference materials as external calibrators, without any matrix effect and over a wide range of concentrations (from wt.% to ppm). Equally, Cu, Sn and Zn concentrations can be precisely determined in sulfides using homogeneous alloys (reference) materials as an external calibrator. Thus, it is possible to determine Cu, Sn and Zn in copper-base materials and their ore minerals, mostly sulfides, in a single analytical session, without requiring specific external calibrators for each matrix type. In contrast, immiscible elements in copper matrix, such as Pb and Fe show notable differences in their relative sensitivity values and ratios for different matrix-materials analyzed, implying that matrix-matched external calibrations remain to be applied for their trace quantification.
文摘应用电感耦合等离子体质谱法(ICP-MS)测定地球化学样品中痕量银时,受到相对地球化学丰度高的Nb,Zr,Y等元素的离子化合物干扰严重,样品不经富集分离,银的测试结果偏差非常大。本研究以负载二苯硫脲泡塑选择性富集Au和Ag,实现了Au和Ag与其它干扰元素的分离,建立了负载二苯硫脲泡塑富集、硫脲解脱-ICP-MS同时测定痕量Au和Ag的新方法。方法采用王水(1∶1)封闭消解矿样,补加水量50 m L,振荡时间和吸附温度分别为25 min和20℃,Au和Ag的方法检出限分别为0.02和0.007μg/g。使用本方法对8个国家一级标准物质中Au和Ag的检测结果与标准值基本相符,确证了方法的可行性。
文摘A method of analysis trace element chloride in cleaning products by Inductively Coupled Plasma-Mass Sepctrometry (ICPMS) was studied. It has good precision (RSD<5%). The LOD is 0.06 μg/L (n=7). The recovery is 93.7%-110.0%.
文摘In this paper,the determination of six heavy metal ions (arsenic,lead,cadmium,chromium,mercury and nickel) in the Chinese Herb by inductively coupled plasma-mass spectrometry (ICP-MS) was studied.The samples were digested by nitric acid and hydrogen peroxide in a microwave oven.The Sc,Y,In,Bi were added as internal standards to eliminate the matrix interferences.The results show that most of the relative standard deviations of these trace elements were below 3.5%,the standard recoveries of these elements were in the range of 91%-107%,and the detection limits were in the range of 0.001-0.006 μg·L-1. This method is accurate,rapid,convenience,and can be applied to the determination of arsenic,lead,cadmium,chromium,mercury and nickel in Chinese Herb with good results.
文摘Objective The aim of this survey was to investigate the level of contamination of the most consumed foods in China with 26 rare earth elements （REEs）, and to provide the basic data for establishing and revising food safety standards for REEs. Methods Sixteen REEs in foods were measured by inductively coupled plasma-mass spectrometry （ICP-MS） in the labs of the Centers for Disease Control and Prevention of four provinces and two municipalities, during 2009-2020. Results 2 231 samples were analyzed and 29 221 concentration data of 16 REEs were collected. The REEs levels in the investigated foods varied significantly. The concentrations of cerium （Ce）, dysprosium （Dy）, yttrium （Y）, lanthanum （La）, and neodymium （Nd） were relatively high, while the remaining eleven REEs were at low levels. The mean values of total rare earth element oxides （REOs） in cereals, fresh vegetables, fresh aquatic products, fresh meats and eggs varied from 0.052 mg/kg to 0.337 mg/kg. Conclusion 16 REEs in the major foods were at very low contamination levels in the investigated regions.
文摘AIM： To evaluate the bioequivalence of ranitidine and bismuth derived from two compound preparations. METHODS： The bioavailability was measured in 20 healthy male Chinese volunteers following a single oral dose （equivalent to 200 mg of ranitidine and 220 mg of bismuth） of the test or reference products in the fasting state. Then blood samples were collected for 24 h. Plasma concentrations of ranitidine and bismuth were analyzed by high-performance liquid chromatography and inductively coupled plasma-mass spectrometry （ICPMS）, respectively. The non-compartmental method was used for pharmacokinetic analysis. Log-transformed Cmax, AUC（0-t） and AUC（0-∞） were tested for bioequivalence using ANOVA and Schuirmann two-one sided t-test. Tmax was analyzed by Wilcoxon＇s test. RESULTS： Various pharmacokinetic parameters of ranitidine derived from the two compound preparations, including Cmax, AUC（0-t）, AUC（0-∞）, Tmax and T1/2, were nearly consistent with previous observations. These parameters derived from test and reference drug were as follows： Cmax（0.67 ± 0.21 vs 0.68 ± 0.22 mg/L）, AUC（0-t）（3.1 ± 0.6 vs 3.0 ± 0.7 mg/L per hour）, AUC（0-∞）（3.3 ± 0.6 vs 3.2 ± 0.8 mg/L per hour）, Tmax （2.3 ± 0.9 VS 2.1 ± 0.9 h） and T1/2 （2.8 ± 0.3 vs 3.1 ± 0.4 h）. In addition, double-peak absorption profiles of ranitidine were found in some Chinese volunteers. For bismuth, those parameters derived from test and reference drug were as follows： Cmax （11.80 ± 7.36 vs 11.40 ± 6.55 μg/L）, AUC（0-t） （46.65 ± 16.97 vs 47.03 ± 21.49 μg/L per hour）, Tmax （0.50 ± 0.20 vs 0.50 ± 0.20 h） and T1/2 （10.2 ± 2.3 vs 13.0 ± 6.9 h）. Ninety percent of confidence intervals for the test/reference ratio of Cmax, AUC（0-t） and AUC（0-∞） derived from both ranitidine and bismuth were found within the bioequivalence acceptable range of 80%-125%. No significant difference was found in Tmax derived from both ranitidine and bismuth. CONCLUSION： The two compound preparations are bioequivalent and may be prescribed interchangeably.
