张凤云,高川#,刘芹,杨彩霞,牛军.固相萃取-气相色谱法测定猪肉中敌敌畏残留[J].食品安全质量检测学报,2018,9(14):3670-3674
固相萃取-气相色谱法测定猪肉中敌敌畏残留
Determination of dichlorvos in pork by solid phase extraction-gas chromatography
投稿时间:2018-05-30  修订日期:2018-05-30
DOI:
中文关键词:  固相萃取-气相色谱法  猪肉样品  敌敌畏
英文关键词:solid phase extraction-gas chromatography  poke  dichlorvos
基金项目:
作者单位
张凤云 正大食品(襄阳)有限公司品质检控中心 
高川# 正大食品(襄阳)有限公司品质检控中心 
刘芹 正大食品(襄阳)有限公司品质检控中心 
杨彩霞 正大食品(襄阳)有限公司品质检控中心 
牛军 正大食品(襄阳)有限公司品质检控中心 
AuthorInstitution
ZHANG Feng-Yun C.P.Food(xiangyang)Co.,Ltd. 
GAO Chuan C.P.Food(xiangyang)Co.,Ltd 
LIU Qin Quality Control Center, C.P. Food (Xiangyang) Co., Ltd. 
YANG Cai-Xia Quality Control Center, C.P. Food (Xiangyang) Co., Ltd. 
NIU Jun Quality Control Center, C.P. Food (Xiangyang) Co., Ltd. 
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中文摘要:
      目的 建立固相萃取-气相色谱法(gas chromatography, GC)测定猪肉中敌敌畏残留量的方法。方法 猪肉样品中残留敌敌畏经过丙酮和二氯甲烷(4:3, V:V)提取后, 经过水浴30 ℃旋转蒸发浓缩。浓缩液由丙酮和二氯甲烷(1:1, V:V)复溶后再由石墨化碳黑/氨基Carbon/NH2(500 mg/500 mg/6 mL)双层固相萃取小柱进行净化处理, 收集净化液再次经过30 ℃旋转蒸发浓缩, 最后浓缩液经由岛津弱极性毛细管柱SH-RTX-5分离, 通过磷滤光片的火焰光度检测器检测, 采用外标法定量。结果 敌敌畏在11 min内完全出峰, 在0.2~1 μg/mL范围内线性关系良好, 相关系数r2为0.9997, 在20、50、100 μg/kg加标水平下, 回收率为100%~120%, 相对标准偏差(relative standard deviation, RSD)为2.60%。结论 该方法准确、灵敏、快速, 具有稳定性强、重现性好等优点, 并且能有效消除基质效应, 适合猪肉样品中的敌敌畏残留量的测定。
英文摘要:
      Objective To establish a method for determination of dichlorvos in pork by solid phase extraction-gas chromatography (GC). Method Dichlorvos residues in pork were extracted by acetone and dichloromethane (4:3, V:V) and then concentrated by rotary evaporation with 30 ℃ water bath. The concentrated solution was reconstituted with acetone and dichloromethane (1:1, V:V) and then purified by graphitized carbon black/amino (500 mg/500 mg/6 mL) double-layer solid-phase extraction cartridge. The purified solution was reconcentrated by rotary evaporation at 30 ℃. The concentrated solution was separated by shimadzu SH-RTX-5 weak polar capillary column, detected by a flame photometric detector of a phosphorus filter, and quantified by external standard method. Result The dichlorvos could be detected within 11 min and had good linearity in the range of 0.2-1 μg/mL, and the correlation coefficient r2 was 0.9997. The recoveries were 100%-120% with 3 spiked levels of 20, 50, and 100 μg/kg. The relative standard deviation (RSD) was 2.60% (n=6). Conclusion This method is accurate, sensitive, rapid, stable, reproducible, and can effectively eliminate the matrix effect, which is suitable for the determination of dichlorvos residues in pork samples.
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