Determination on Heavy Metals Content of Achyranthes bidentata Blume. through Inductively Coupled Plasma Mass Spectrometry (ICP-MS)

[Objective] The inductively coupled plasma mass spectrometry(ICP-MS)was constructed to determine the contents of lead,cadmium,mercury and arsenic in Archyranthes bidentata Blume.[Method]Under the optimum operation condition of ICP-MS,the samples were digested by microwave.The element 114In was taken as an internal standard element to compensate body effect and ICP-MS method was used to determine the contents of lead,cadmium,mercury and arsenic.[Result]For the determined elements,the correlation coefficient(r)of standard curve was over 0.9995 and recovery rate was from 96.7% to 106.4% while RSD was less than 11.2%.The result of determination showed that the heavy metal content in Archyranthes bidentata Blume.beyond standard was serious.[Conclusion]The constructed ICP-MS method with simple operation,rapid response,accuracy and high sensitivity in this experiment could be used for quality control of Chinese medicinal materials by detecting heavy metal contents in different Chinese medicinal materials from original places.

Inductively coupled plasma mass spectrometry (ICP-MS) and its application in life sciences

Inductively-coupled plasma mass spectrometry (ICP-MS) has made much progress since its birth in the late 1990s. This paper will give a rather systematic overview on the use of this technique in new devices and technologies related to plasma source, sample-introducing device and detecting spectrometer etc. In this overview, an emphasis will be put on the evaluation of the ICP- MS technique in combination with a series of physical, chemical and biological techniques, such as laser ablation (LA), capillary electrophoresis (CE) and high performance liquid chromatograph (HPLC), along with their representative high accuracy and high sensitivity. Finally, comprehensive and fruitful applications of the ICP-MS and its combinative techniques in the detection of trace metallic elements and isotopes in complex biological and environmental samples will be revealed.

Determination of impurity elements in MnZn ferrites by inductively coupled plasma mass spectrometry

An inductively coupled plasma mass spectrometry(ICP-MS) method was developed for the determination of Na, Mg, Al,K, Ca, Ti, Cr, Co, Ni, Cu, Ga, As, Mo, Ag, Cd and Pb in MnZn ferrites. The sample was digested by HNO3+HCl with microwave digestion followed by dilution with ultrapure water, then the above 16 impurity elements in the solution were analyzed directly by ICP-MS. The impurity elements were introduced by the helium gas or hydrogen gas into the octopole reaction system(ORS) to eliminate the polyatomic interferences caused by the high salty matrixes. The matrix effect was minimized through matrix matching,and Be, Y and Rh were used as internal standard elements. The working parameters of the instrument were optimized. The results show that the method has good precision and high accuracy. The detection limits for the investigated elements are in the range of0.9-37.5 ng/L, the relative standard deviation of each element is within 1.1%-4.8%, and the recovery of each element is 90%-108%.

Uncertainty Evaluation of Simultaneous Determination of Lead, Cadmium and Arsenic in Cosmetics by Inductively Coupled Plasma Mass Spectrometry

This study aimed to evaluate the uncertainty of simultaneous determination of lead(Pb),cadmium(Cd)and arsenic(As)in cosmetics by microwave digestion-inductively coupled plasma mass spectrometry(ICP-MS)with ^72Ge,^115In and ^209Bi as internal standards.According to the method of Safety and Technical Standards for Cosmetics(2015),a mathematical model was established to evaluate the sources and components of uncertainty for the determination of lead,cadmium and arsenic in cosmetics.The results showed that the uncertainties in the determination of lead,cadmium,and arsenic elements in cosmetics were(10.1±0.6)mg/kg,k=2,(4.84±0.28)mg/kg,k=2,(2.04±0.18)mg/kg,k=2,respectively.The main factors that affect the uncertainty of determination results were standard substance,calibration curve,recovery and measurement repeatability.

ICP-MS测定黄豆中26种无机元素

本文利用微波消解对黄豆进行前处理,采用电感耦合等离子体质谱法(Inductively Coupled Plasma Mass Spectrometer,ICP-MS)对消解液中26种元素的含量进行测定,对方法的线性、精密度、准确度及质控样品进行验证。结果表明,各元素标准曲线的相关系数均≥0.9990,线性关系良好,检出限为0.000583~0.453000 mg·kg^(-1),相对标准偏差≤5.513%,加标回收率为77%~113%,说明该方法能准确检测黄豆中无机元素,满足日常监测需求。

ICP-MS法分析过氧化氢、硝酸、硫酸中的金属杂质

Inductively coupled plasma mass spectrometry (ICP-MS) was used to detect trace metal impurities in reagents such as H2O2, HNO3and H2SO4. The limit of detection to metal elements can be down to 2-20 ng/L in H2O2 and HNO3 and 0.1-1.0 ng/L in H2SO4.

ICP-MS测定硼矿区饮用水和尿样中的硼及多种元素

The application of inductively coupled plasma mass spectrometry (ICP-MS) for determination of boron in water and urine samples was described. The detect limit (3σ) was 0.057 μg/L. The precision of the method was less than 2%. Multi-elements including Cr, Cu, Cd, Ba, Sr, Mn, Co, Tl, Li, Pb, Ca, Fe, K, Na, Mg, P, Si and Zn could be measured simultaneously. The method was successfully used in practice.

Determination of Pb, Cr, Ni and Mn in Tap Water of Riyadh Metropolitan City Using ICP-MS after Preconcentration with Multiwalled Carbon Nanotubes

The determination of toxic metals in water using multiwalled carbon nanotubes （MWNTs） as a solid-phase extraction adsorbent prior to their determination by inductively coupled plasma mass spectrometry （ICP-MS） has been investigated. Standard addition method was applied for the calibration using aqueous solutions. Multiwalled carbon nanotubes （MWNTs） absorb these metals at pH 8.0, HNO3 of 1.0 mol-Ll is used for complete elusion of these metals from MWNTs. Previously investigated parameters have been applied for the determination of Pb, Cr, Ni and Mn in tap water samples. Fifteen tap water samples from different locations of Riyadh metropolitan area have been determined by ICP-MS after preconcentration with MWNTs.

Determination of Fe, Cu, and Zn in Water Samples by Microcolumn Packed with Multiwalled Carbon Nanotubes as a Solid Phase Extraction Adsorbent Using ICP-MS

The heavy metals determination in tap water samples using microcolumn packed with multiwalled carbon nanotubes （MWNTs） as a solid-phase extraction adsorbent before to their determination by inductively coupled plasma mass spectrometry （ICP-MS） has been studied. Standard addition method was applied for the calibration using aqueous solutions. The metals ions absorption were achieved by multiwalled carbon nanotubes （MWNTs） at pH 8.0, and then these retained metals on MWNTs column were eluted by 1.0 mol.L^-1 HNO3. The analytical parameters for the determination ofFe, Cu, and Zn in tap water samples which have been investigated previously were applied. Fifteen tap water samples were collected from different locations of Riyadh metropolitan area and then determined the concentration ofFe, Cu, and Zn by ICP-MS after preconcentration with MWNTs. The concentration range for Fe, Cu, and Zn measured （μg/L） in water samples are 23.37-137.91, 2.12-121.36, and 14.43-202.47 respectively. The level of Fe exceeded the limits set by WHO and SASO for drinking water.

A Survey of 16 Rare Earth Elements in the Major Foods in China

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.

Pt-Os同位素系统定年方法研究

Six massive ores in the Jinchuan deposit were dated by Re-Os technique. The Os concentrations and isotopic ratios were determined by N-TIMS, while Re and Pt concentrations were determined by ICP-MS. The samples gave an isochron age of (852±25) Ma with an initial 187Os/188Os ratio of 0.255 ± 0.014. A 7-point Pt-Os isochrone gives an age of (870±38) Ma with an initial 186Os/188Os ratio of 0.119 84±0.000 27.

烟用接装纸质控样品的制备与应用

采用深珠光印字烟用接装纸作为质控样品,用微波消解处理质控样品,以电感耦合等离子体质谱法(ICP–MS)对样品的铬、砷、铅含量进行定值,并进行不确定度评定。利用方差分析评价均匀性,ADF检验评价稳定性。经F检验表明在95%的置信区间,制备的烟用接装纸质控样品均匀性良好;经ADF检验表明,各元素在1%的显著水平下稳定可靠,样品稳定性良好。将烟用接装纸质控样品用于质控,并绘制Levy–Jennings质控图,质控效果良好。

碰撞反应池等离子体质谱测定有机酸盐中杂质元素

建立有机酸盐中Pb、Cd,Cr、As、Fe、Cu、Mn、Co、Ni、Sb等10种杂质元素的微波消解碰撞反应池技术电感耦合等离子体质谱法。通过基体匹配、正确选择测量同位素及内标元素后,有效地克服了因高钙、高钠基体效应带来的测量偏差,极大的消除了多原子离子对待测元素的干扰,使有机酸盐中杂质元素的测试更为准确。方法的检出限为0.015 mg/kg^1.5 mg/kg之间,回收率均在90.0%~110.0%之间,相对标准偏差为2.01%~10.3%。

电感耦合等离子体磁质谱法测定无尘产品中痕量氯

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%.

Distribution and Relationships of Seven Trace Elements （Cr, Fe, Mn, Ni, Co, Cu and Zn） in Freshwater Fish from Five French Fishing Areas

The concentrations of seven essential trace elements in 149 freshwater fish from eight fish species （European eel, bream, common carp, European catfish, roach, perch, pike and pikeperch） from five different French fishing areas from contaminated and control sites were measured by inductively coupled plasma mass spectrometry after microwave digestion under pressure. Differences in the concentration of elements in the muscles of these species were examined and the mean levels were compared for each species with previous French and European studies. The condition factor and the differences between the control and contaminated sites and between predatory and non-predatory groups, with respect to the concentration of these elements, were also studied.

用电感耦合等离子体质谱法测定中草药中的重金属元素

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.

硒化枸杞多糖的制备及其抗氧化性研究

以亚硒酸钠和枸杞多糖为原料合成硒化枸杞多糖,电感耦合等离子体质谱法(ICP-MS)测定其中硒含量为64.42 mg/g。利用紫外-可见光谱、红外光谱两种表征手段,证实了硒化枸杞多糖的合成。采用邻二氮菲-Fe2+氧化法和邻苯三酚自氧化法测定硒化枸杞多糖的抗氧化能力,结果表明,在实验设置的浓度范围内,硒化枸杞多糖的抗氧化能力随着浓度的增加而增加,且高于枸杞多糖。2.0 mg/mL的枸杞多糖和硒化枸杞多糖对超氧阴离子自由基的清除率分别为51.48%和59.34%,对羟自由基的清除率分别为50.23%和56.16%。本实验为进一步研究硒化枸杞多糖作为抗氧化能力较强的食品和药品的可能性奠定了基础。

电感耦合等离子体质谱测定大气铅污染物

Inductively coupled plasma mass spectrometry(ICP-MS) was used to determine the concentration of Pb in atmospheric particulate samples,and the enrichment factor was calculated.The causes of the results were also discussed.

Pharmacokinetics and bioequivalence of ranitidine and bismuth derived from two compound preparations

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.

Multielement determination in orange juice by ICP-MS associated with data mining for the classification of organic samples

The aim of this study was to discriminate organic from conventional orange juice based on chemical elements and data mining applications.A comprehensive sampling of organic and conventional oranges was carried out in Borborema,state of Sao Paulo,Brazil.The fruits of the variety Valencia(Citrus sinensis(L.)Osbeck)budded on Rangpur lime(Citrus limonia Osbeck)were analyzed.Eleven chemical elements were determined in 57 orange samples grown in organic and conventional systems.In order to classify these samples,data mining techniques(Support Vector Machine(SVM)and Multilayer Perceptron(MLP))were combined with feature selection(F-score and chi-squared).SVM with chi-squared had a better performance compared with the other techniques because it reached 93.00% accuracy using only seven chemical components(Cu,Cs,Zn,Al,Mn,Rb and Sr),and correctly classified 96.73% of the samples grown in an organic system.