静平,胥璐,马志勇,鲍蕾,于冰,丛海林,吕宁,吴振兴,梁成珠,汪纪波.高效液相色谱法检测粮谷及其制品中六种A, B型单端孢霉烯族真菌毒素[J].食品安全质量检测学报,2012,3(2):106-111
高效液相色谱法检测粮谷及其制品中六种A, B型单端孢霉烯族真菌毒素
Determination of six type A and type B trichothecenes by high performance liquid chromatography-tandem mass spectrometry
  
DOI:
中文关键词:  A,B型单端孢霉烯族真菌毒素  高效液相色谱?串联质谱  粮谷及其制品
英文关键词:type a and type b trichothecenes  high performance liquid chromatography-tandem mass spectrometry  grain and grain-products
基金项目:山东出入境检验检疫局科研基金资助项目(SK200652), 国家自然科学基金资助项目(21105125)
作者单位
静平 山东出入境检验检疫局食品农产品中心 
胥璐 青岛大学化学化工与环境学院 
马志勇 青岛大学化学化工与环境学院 
鲍蕾 山东出入境检验检疫局食品农产品中心 
于冰 青岛大学化学化工与环境学院 
丛海林 青岛大学化学化工与环境学院 
吕宁 山东出入境检验检疫局食品农产品中心 
吴振兴 山东出入境检验检疫局食品农产品中心 
梁成珠 山东出入境检验检疫局食品农产品中心 
汪纪波 罗氏医疗器械有限公司 
AuthorInstitution
JING Ping Food and Agricultural Testing Agency of Shangdong Entry-Exit Inspection and Quarantine Bureau 
XU Lu Chemical Engineering and Environment, Qingdao University 
MA Zhi-Yong Chemical Engineering and Environment, Qingdao University 
BAO Lei Food and Agricultural Testing Agency of Shangdong Entry-Exit Inspection and Quarantine Bureau 
YU Bing Chemical Engineering and Environment, Qingdao University 
CONG Hai-Lin Chemical Engineering and Environment, Qingdao University 
LV Ning Food and Agricultural Testing Agency of Shangdong Entry-Exit Inspection and Quarantine Bureau 
WU Zheng-Xing Food and Agricultural Testing Agency of Shangdong Entry-Exit Inspection and Quarantine Bureau 
LIANG Cheng-Zhu Food and Agricultural Testing Agency of Shangdong Entry-Exit Inspection and Quarantine Bureau 
WANG Ji-Bo Roche Diagnostics Limited 
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中文摘要:
      目的 建立粮谷及其制品中六种A,B型单端孢霉烯族真菌毒素的高效液相色谱?串联质谱分析方法。方法 样品经乙腈?水溶液(84︰16, V/V)提取, MycoSep?226或MycoSep?227多功能柱净化, Waters Atlantis dC18色谱柱分离, 串联四极杆质谱多反应离子监测模式检测。结果 6种真菌毒素在各自的线性范围内线性关系良好, 相关系数均不低于0.996, 定量下限为0.1~20 μg/kg, 低、中、高3个加标水平下平均回收率为60.1%~123%, 相对标准偏差为7.5%~19.8% 。结论 该方法具有前处理简单、净化效果好、灵敏度高的优点, 适用于复杂基质样品中A,B型单端孢霉烯族真菌毒素残留的确证和定量检测。
英文摘要:
      Objective To establish a method for the simultaneous determination of six type A and type B trichothecenes by high performance liquid chromatography-tandem mass spectrometry. Method The homogenized sample was extracted by 84% acetonitrile-water solution (V/V) and further purified by MycoSep?226 or MycoSep?227. The target compounds were separated by waters Atlantis dC18column and detected by MS/MS system with eletrospray ionization (ESI) under multiple reaction monitoring (MRM) mode. Results It was shown that the high correlation coefficients (r≥0.996) of six mycotoxins were obtained within their respective linear ranges. The LOQ for the six compounds ranged from 0.1~20 μg/kg. The mean recoveries ranged from 60.1%~123% with the relative standard deviations of 7.5%~19.8%. Conclusion This method was suitable for the identification and quantification of multi-component mycotoxin contaminants in complex matrixes with advantages of simple pretreatment, good purification and high sensitivity.
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