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凝胶渗透色谱净化系统与气相色谱-串联质谱法检测5种食品中14种有机磷和7种拟除虫菊酯类农药残留
引用本文:刘国平,黄诚,薛荣旋,周日东,卢丽明. 凝胶渗透色谱净化系统与气相色谱-串联质谱法检测5种食品中14种有机磷和7种拟除虫菊酯类农药残留[J]. 中国食品卫生杂志, 2014, 26(4): 366-372
作者姓名:刘国平  黄诚  薛荣旋  周日东  卢丽明
作者单位:中山市疾病预防控制中心,广东 中山 528403;中山市疾病预防控制中心,广东 中山 528403;中山市疾病预防控制中心,广东 中山 528403;中山市疾病预防控制中心,广东 中山 528403;中山市疾病预防控制中心,广东 中山 528403
基金项目:中山市科技计划项目(20132A064)
摘    要:建立GPC与GC-MS/MS测定5种食品中14种有机磷和7种拟除虫菊酯类农药残留的方法,初步分析GPC净化技术及MS/MS分析技术在食品农药多残留分析的优势。方法 用GPC作为样品前处理方法,处理韭菜、大白菜、辣椒、猪肉、鱼肉五种食品,用 GC-MS/MS检测并进行定性、定量分析。结果 GPC与GC-MS-MS检测食品中14种有机磷和7种拟除虫菊酯类农药方法的线性相关系数r>0.995,定量限为0.002~0.034 mg/kg,对韭菜、猪肉样品按0.05、0.10、0.20 mg/kg三组水平加标测试,方法精密度RSD%为2.9~10.2%,回收率为78.6~108.3%。结论 本方法检测样品范围广、灵敏度高、定性可靠、定量准确,适合多种类食品中农药多残留分析。

关 键 词:凝胶渗透色谱净化系统   气相色谱-串联质谱法   农药残留   食品污染物   有机磷   拟除虫菊酯
收稿时间:2014-03-31

Determination of 14 organophosphorus pesticides and 7 pyrethroids pesticides in five kinds of food by GPC and GC-MS/MS
LIU Guo-ping,HUANG Cheng,XUE Rong-xuan,ZHOU Ri-dong and LU Li-ming. Determination of 14 organophosphorus pesticides and 7 pyrethroids pesticides in five kinds of food by GPC and GC-MS/MS[J]. Chinese Journal of Food Hygiene, 2014, 26(4): 366-372
Authors:LIU Guo-ping  HUANG Cheng  XUE Rong-xuan  ZHOU Ri-dong  LU Li-ming
Affiliation:Zhongshan Center for Disease Control and Prevention,Guangdong Zhongshan 528403,China;Zhongshan Center for Disease Control and Prevention,Guangdong Zhongshan 528403,China;Zhongshan Center for Disease Control and Prevention,Guangdong Zhongshan 528403,China;Zhongshan Center for Disease Control and Prevention,Guangdong Zhongshan 528403,China;Zhongshan Center for Disease Control and Prevention,Guangdong Zhongshan 528403,China
Abstract:To establish a method for determining 14 organophosphorus pesticides(OPs) and 7 pyrethroids pesticides (PPs) in 5 kinds of food by GPC and GC-MS/MS, and find the advantages of GPC and GC-MS/MS in analyzing pesticide residues in food.MethodsFive kinds of food including leeks, Chinese cabbage, pepper, pork and fish were pretreated with GPC, and the samples were analyzed qualitatively and quantitatively by GC-MS/MS. ResultsThe linear correlation coefficients of 14 OPs and 7 PPs were above 0.995. The limit of quantification was in the range of 0.002-0.034 mg/kg. The relative standard deviation (RSD) was 2.9-10.2%, and the rates of recovery were 78.6-108.3% for leek and pork samples spiked with 0.05,0.10 and 0.20 mg/kg of 14 OPs and 7 PPs. ConclusionThe method was widely used, highly sensitive, reliable, accurate, and suitable for analysis of pesticide residues in many kinds of food.
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