史俊文,刘凤芝.免疫亲和柱净化-高效液相色谱-三重串联四级杆质谱法测定食用植物油中的黄曲霉毒素B1[J].中国油脂,2014,39(5):.[SHI Junwen,LIU Fengzhi.Determination of aflatoxin B1 in edible vegetable oil by immunoaffinity column purification and HPLC-MS/MS[J].China Oils and Fats,2014,39(5):.]
免疫亲和柱净化-高效液相色谱-三重串联四级杆质谱法测定食用植物油中的黄曲霉毒素B1
Determination of aflatoxin B1 in edible vegetable oil by immunoaffinity column purification and HPLC-MS/MS
  
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中文关键词:  免疫亲和柱净化  高效液相色谱-三重串联四级杆质谱法  黄曲霉毒素B1  食用植物油
英文关键词:immunoaffinity column purification  HPLC-MS/MS  aflatoxin B1  edible vegetable oil
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史俊文  
刘凤芝  
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中文摘要:
      建立了免疫亲和柱净化-高效液相色谱-三重串联四级杆质谱法测定食用植物油中黄曲霉毒素B1的方法。采用70%甲醇水溶液提取食用植物油中黄曲霉毒素B1,提取液经过滤、免疫亲和柱净化后,上高效液相色谱-三重串联四级杆质谱仪进行测定。结果表明,黄曲霉毒素B1在0.2~10 ng/mL范围内方程线性关系良好,方法检出限(S/N=3)为0.05 μg/kg, 定量限(S/N=10)为0.2 μg/kg,平均加标回收率在83.0%~94.8%之间,相对标准偏差小于7.8%。
英文摘要:
      Immunoaffinity column purification and HPLC-MS/MS method was established to determine aflatoxin B1 in edible vegetable oil. Aflatoxin B1 was extracted from edible vegetable oil by 70% of methanol,then the extract was filtered and purified by immunoaffinity column before being injected into HPLC-MS/MS to determine aflatoxin B1. The results showed that calibration curve presented good linear relationship when the mass concentration of aflatoxin B1 ranged from 0.2 ng/mL to 10 ng/mL;the limit of detection(S/N=3) and the limit of quantification(S/N=10) of the method were 0.05 μg/kg and 0.2 μg/kg respectively,the average recovery of standard addition was in the range of 83.0%-94.8%, and the relative standard deviation was less than 7.8%.
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