邢丽红,付树林,彭吉星,孙伟红,郑关超,李兆新,翟毓秀.液相色谱-串联质谱法测定水产品中硝呋索尔 代谢物残留量[J].食品安全质量检测学报,2016,7(9):3615-3622
液相色谱-串联质谱法测定水产品中硝呋索尔 代谢物残留量
Determination of nifursol metabolites in aquatic products by high performance liquid chromatography-tandem mass spectrometry
投稿时间:2016-08-16  修订日期:2016-09-23
DOI:
中文关键词:  硝呋索尔  3,5-二硝基水杨酸肼  水产品  液相色谱-串联质谱法
英文关键词:nifursol  3,5-dinitrosalicylic acid hydrazide  aquatic products  high performance liquid chromatography- tandem mass spectrometry
基金项目:2014农业行业标准制修订项目(2014-430)、国家自然科学基金资助项目(21207162)
作者单位
邢丽红 中国水产科学研究院黄海水产研究所, 农业部水产品质量安全检测与评价重点实验, 农业部水产品质量安全风险评估实验室(青岛) 
付树林 中国水产科学研究院黄海水产研究所, 农业部水产品质量安全检测与评价重点实验, 农业部水产品质量安全风险评估实验室(青岛) 
彭吉星 中国水产科学研究院黄海水产研究所, 农业部水产品质量安全检测与评价重点实验, 农业部水产品质量安全风险评估实验室(青岛) 
孙伟红 中国水产科学研究院黄海水产研究所, 农业部水产品质量安全检测与评价重点实验, 农业部水产品质量安全风险评估实验室(青岛) 
郑关超 中国水产科学研究院黄海水产研究所, 农业部水产品质量安全检测与评价重点实验, 农业部水产品质量安全风险评估实验室(青岛) 
李兆新 中国水产科学研究院黄海水产研究所, 农业部水产品质量安全检测与评价重点实验, 农业部水产品质量安全风险评估实验室(青岛) 
翟毓秀 中国水产科学研究院黄海水产研究所, 农业部水产品质量安全检测与评价重点实验, 农业部水产品质量安全风险评估实验室(青岛) 
AuthorInstitution
XING Li-Hong Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences, Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Quality, Ministry of Agriculture, Laboratory of Quality & Safety Risk Assessment for Aquatic Products (Qingdao), Ministry of Agriculture 
FU Shu-Lin Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences, Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Quality, Ministry of Agriculture, Laboratory of Quality & Safety Risk Assessment for Aquatic Products (Qingdao), Ministry of Agriculture 
PENG Ji-Xing Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences, Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Quality, Ministry of Agriculture, Laboratory of Quality & Safety Risk Assessment for Aquatic Products (Qingdao), Ministry of Agriculture 
SUN Wei-Hong Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences, Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Quality, Ministry of Agriculture, Laboratory of Quality & Safety Risk Assessment for Aquatic Products (Qingdao), Ministry of Agriculture 
ZHENG Guan-Chao Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences, Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Quality, Ministry of Agriculture, Laboratory of Quality & Safety Risk Assessment for Aquatic Products (Qingdao), Ministry of Agriculture 
LI Zhao-Xin Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences, Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Quality, Ministry of Agriculture, Laboratory of Quality & Safety Risk Assessment for Aquatic Products (Qingdao), Ministry of Agriculture 
ZHAI Yu-Xiu Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences, Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Quality, Ministry of Agriculture, Laboratory of Quality & Safety Risk Assessment for Aquatic Products (Qingdao), Ministry of Agriculture 
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中文摘要:
      目的 建立一种采用液相色谱-串联质谱法检测水产品中硝呋索尔代谢物残留量的测定方法。方法 样品中以结合态形式残留的硝呋索尔代谢物3,5-二硝基水杨酸肼(DNSAH)经盐酸水解, 2-硝基苯甲醛衍生, 用乙腈提取, 以电喷雾离子源负离子扫描模式进行质谱分析, 内标法定量。结果 DNSAH在0.2~20 μg/L范围内线性关系良好, 相关系数r2>0.999。DNSAH添加水平为0.50~5.00 μg/kg时, 平均回收率在88.3%~100%之间, 批内和批间变异系数均<15%。DNSAH的检出限为0.20 μg/kg。结论 本方法灵敏、高效、简单、重现性好, 满足水产品中硝呋索尔代谢物残留量的检测。
英文摘要:
      Objective To establish a method for the determination of nifursol metabolites in aquatic products by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Methods The residue of nifursol metabolite of 3,5-dinitrosalicylic acid hydrazide (DNSAH) in sample was hydrolyzed with HCl, and derivatized with nitrobenzaldehyde. Then the analyte was extracted with acetonitrile and then analyzed by HPLC-MS/MS with internal standard method. Electrospray ionization was applied and operated in the negative ion mode. Results The calibration curve had a good linearity between area and the concentration of DNSAH of 0.2~20 μg/L with the correlation coefficient over 0.999. The average recoveries from spiked sample at three concentrations of 0.50, 2.00 and 5.00 μg/kg were ranged from 88.3% to 100% with intra and inter batch relative standard deviations below 15%. The detection limit of DNSAH was 0.20 μg/kg. Conclusion The efficient and simple method can be used to identify and quantify the nifursol metabolites in aquatic products with satisfactory sensitivity and repeatability.
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