陈 东,范 赛,沙博郁,赵 榕,吴国华.超高效液相色谱-串联质谱法测定茶叶中高氯酸盐[J].食品安全质量检测学报,2018,9(4):925-929
超高效液相色谱-串联质谱法测定茶叶中高氯酸盐
Determination of perchlorate in tea by ultra performance liquid chromatography tandem mass spectrometry
投稿时间:2018-01-17  修订日期:2018-01-30
DOI:
中文关键词:  高氯酸盐  同位素内标法  茶叶  超高效液相色谱-串联质谱法
英文关键词:perchlorate  isotopic internal standard method  tea  ultra performance liquid chromatography tandem mass spectrometry
基金项目:
作者单位
陈 东 北京市疾病预防控制中心, 北京市预防医学研究中心 
范 赛 北京市疾病预防控制中心, 北京市预防医学研究中心 
沙博郁 北京市疾病预防控制中心, 北京市预防医学研究中心 
赵 榕 北京市疾病预防控制中心, 北京市预防医学研究中心 
吴国华 北京市疾病预防控制中心, 北京市预防医学研究中心 
AuthorInstitution
CHEN Dong Beijing Center for Disease Prevention and Control, Beijing Center for Preventive Medicine Research 
FAN Sai Beijing Center for Disease Prevention and Control, Beijing Center for Preventive Medicine Research 
SHA Bo-Yu Beijing Center for Disease Prevention and Control, Beijing Center for Preventive Medicine Research 
ZHAO Rong Beijing Center for Disease Prevention and Control, Beijing Center for Preventive Medicine Research 
WU Guo-Hua Beijing Center for Disease Prevention and Control, Beijing Center for Preventive Medicine Research 
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中文摘要:
      目的 建立一种使用同位素内标法定量测定茶叶中高氯酸盐的超高效液相色谱-串联质谱法(ultra performance liquid chromatography tandem mass spectrometry, UPLC-MS/MS)。方法 茶叶样品经0.2%乙酸提取, 高速离心, 上清液用石墨炭黑柱净化, 再经Thermo Acclaim TRINITY P1色谱柱分离, 串联质谱法检测, 内标法定量。结果 高氯酸盐在0.25~50.0 μg/L 范围内线性关系良好, 相关系数(r)为0.9991。加标浓度为0.05~0.80 mg/kg时, 方法的平均回收率分别为在94.6%~110.2%, 相对标准偏差为1.8%~9.6%。结论 本方法前处理简单、灵敏度高、准确、可靠, 适用于茶叶中高氯酸盐的测定。
英文摘要:
      Objective To establish a method for determination of perchlorate in tea by ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) based on isotopic internal standard method. Methods The perchlorate residue in tea was extracted with 0.2% acetic acid, and then centrifuged. The supernatant was cleaned-up with Carb SPE. The separation of perchlorate was carried out on a Thermo Acclaim TRINITY P1 column, and the detection was performed with tandem mass spectrometry with internal standard method for quantification. Results The calibration curve was linear in the concentration range of 0.25~50.0 μg/L (r=0.9991). The average recoveries at the spiked levels of 0.05~0.80 mg/kg were 94.6%~110.2% and the relative standard deviations (RSDs) were 1.8%~9.6%, respectively. Conclusion This method is simple, sensitive, accurate and reliable, which is suitable for the determination of perchlorate in tea.
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