贾彦博,陆吉琛,朱蓓,林舒忆,洪春来.高效液相色谱-电感耦合等离子体质谱联用法测定东海乌参样品中的二价汞、甲基汞、乙基汞和苯基汞[J].食品安全质量检测学报,2016,7(11):4609-4613
高效液相色谱-电感耦合等离子体质谱联用法测定东海乌参样品中的二价汞、甲基汞、乙基汞和苯基汞
Determination of bivalent mercury, methyl-mercury, ethyl-mercury and phenyl-mercury in Acaudina leucoprocta by high performance liquid chromatography-inductively coupled plasma-mass spectrometry
投稿时间:2016-05-13  修订日期:2016-11-14
DOI:
中文关键词:  高效液相色谱-电感耦合等离子体质谱法  二价汞  甲基汞  乙基汞  苯基汞  东海乌参
英文关键词:high performance liquid chromatography-inductively coupled plasma-mass spectrometry  bivalent mercury  methyl-mercury  ethyl-mercury  phenyl-mercury  Acaudina leucoprocta
基金项目:浙江省公益性技术应用研究(分析测试)项目 (2013C37058)
作者单位
贾彦博 杭州市食品药品检验研究院 
陆吉琛 杭州市食品药品检验研究院 
朱蓓 杭州市食品药品检验研究院 
林舒忆 杭州市食品药品检验研究院 
洪春来 浙江省农业科学院环境资源与土壤肥料研究所 
AuthorInstitution
JIA Yan-Bo Hangzhou Institute for Food and Drug Control 
LU Ji-Chen Hangzhou Institute for Food and Drug Control 
ZHU Bei Hangzhou Institute for Food and Drug Control 
LIN Shu-Yi Hangzhou Institute for Food and Drug Control 
HONG Chun-Lai Institute of Environment, Resource Soil and Fertilizer, Zhejiang Academy of Agricultural Sciences 
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中文摘要:
      目的 建立高效液相色谱-电感耦合等离子体质谱法(high performance liquid chromatography-inductively coupled plasma-mass spectrometry, HPLC-ICP-MS)测定东海乌参样品中的二价汞、甲基汞、乙基汞和苯基汞4种汞形态的含量。方法 样品经25%KOH微波萃取1 h, 采用Agilent Zorbax Plus C18色谱柱分离, 以10 mmol/L醋酸铵+0.12%L-半胱氨酸缓冲盐及2%甲醇作为流动相进行梯度洗脱, 采用ICP-MS进行检测。结果 二价汞、甲基汞、乙基汞和苯基汞在10 min内完成分离, 检出限分别为0.8、0.2、0.2和0.8 ng/mL; 在0.10、0.20和0.40 mg/kg 3个加标水平下, 4种汞化合物的回收率为78.1%~105.8%, 相对标准偏差为5.3%~8.2%。结论 本方法简便、快速、准确, 可适用于汞形态的分析。
英文摘要:
      Objective To establish a method for determination of 4 kinds of mercury speciation including bivalent mercury, methl-mercury, ethyl-mercury and phenyl-mercury in Acaudina leucoprocta by high performance liquid chromatography-inductively coupled plasma-mass spectrometry (HPLC-ICP-MS). Methods After microwave extraction with 25% potassium hydroxide (KOH) for 1 h, the sample was separated by Agilent Zorbax Plus C18 column with the mobile phase of 10 mmol/L ammonium acetate/0.12% L-cysteine/methanol for gradient elution and then detected by ICP-MS. Results Bivalent mercury, methl-mercury, ethyl-mercury and phenyl-mercury could be separated within 10 min. The detect limits were 0.8, 0.2, 0.2 and 0.8 ng/mL, respectively. The recoveries of 4 kinds of mercury speciation spiked at 3 levels of 0.10, 0.20 and 0.40 mg/kg were ranged from 78.1% to 105.8% with the relative standard deviations of 5.3%~8.2%. Conclusion The developed method is simple, rapid and accurate, which can be used for determination of mercury speciation.
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