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) |
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Author | Institution |
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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