路 杨,刘印平,王丽英,任贝贝,云 鹏,冯 静,常凤启.高效液相色谱-荧光检测法检测植物性食品中14种欧盟优控多环芳烃[J].食品安全质量检测学报,2020,11(18):6594-6600
高效液相色谱-荧光检测法检测植物性食品中14种欧盟优控多环芳烃
Determination of 14 European Union superior controlled polycyclic aromatic hydrocarbons in plant-orgin foods by high performance liquid chromatography- fluorescence detector
投稿时间:2020-05-09  修订日期:2020-09-11
DOI:
中文关键词:  多环芳烃  植物性食品  欧盟  高效液相色谱-荧光检测法
英文关键词:polycyclic aromatic hydrocarbons  plant-orgin foods  European Union  high performance liquid chromatography-fluorescence detector
基金项目:
作者单位
路 杨 河北省疾病预防控制中心 
刘印平 河北省疾病预防控制中心 
王丽英 河北省疾病预防控制中心 
任贝贝 河北省疾病预防控制中心 
云 鹏 河北省疾病预防控制中心 
冯 静 河北省疾病预防控制中心 
常凤启 河北省疾病预防控制中心 
AuthorInstitution
LU Yang Hebei Provincial Center for Disease Control and Prevention 
LIU Yin-Ping Hebei Provincial Center for Disease Control and Prevention 
WANG Li-Ying Hebei Provincial Center for Disease Control and Prevention 
REN Bei-Bei Hebei Provincial Center for Disease Control and Prevention 
YUN Peng Hebei Provincial Center for Disease Control and Prevention 
FENG Jing Hebei Provincial Center for Disease Control and Prevention 
CHANG Feng-Qi Hebei Provincial Center for Disease Control and Prevention 
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中文摘要:
      目的 建立高效液相色谱-荧光检测法测定植物性食品如蔬菜、水果及粮食中多环芳烃含量, 了解河北省内上述食品中14种欧盟优控多环芳烃的实际污染状况。方法 样品经环己烷-乙酸乙酯(1:1, V:V)溶液超声提取后, 浓缩至近干, 经正己烷复溶后通过多环芳烃专用固相萃取柱进行净化处理, 洗脱液经浓缩后用乙腈定容, 采用高效液相色谱-荧光检测法进行检测。结果 14种化合物的线性范围为1.00~18.0 μg/kg; 方法回收率为60.9%~125.4%, 相对标准偏差为2.2%~7.6%; 苯并(c)芴、苯并(a)蒽、?、5-甲基-1,2-苯并菲、苯并(j)荧蒽、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、二苯并(a,e)芘、二苯并(a,i)芘、二苯并(a,h)芘检出限为0.15 μg/kg; 二苯并(a,l)芘、二苯并(a, h)蒽、苯并(g,h,i)苝、茚并(1,2,3-cd)芘检出限为0.30 μg/kg。市售的96份样品中, 检出不同种类不同含量的多环芳烃类化合物, 检出率为51.0%。结论 本方法重现性好, 检测灵敏度高, 可用于水果、蔬菜及粮食中14种多环芳烃的检测。
英文摘要:
      Objective To establish a method for the determination of polycyclic aromatic hydrocarbons (PAHs) in plant-orgin foods including vegetables, fruits and cereal products by high performance liquid chromatography-fluorescence detector(HPLC-FLD), and understand the actual pollution status of the 14 EU-controlled polycyclic aromatic hydrocarbons in the above-mentioned foods in Hebei province. Methods PAHs were extracted by ultrasonic extraction with cyclohexane-ethyl acetate(1:1, V:V), concentrated to nearly dry, redissolved with n-hexane and then purified by special purification column for PAHs. The eluent was concentrated, and the volume was fixed with acetonitrile. The contents of 14 PAHs were determined by HPLC-FLD. Results The linear range of 14 compounds was 1.00?18.0 μg/kg. The recovery rate was 60.9%?125.4%, and the relative standard deviation was 2.2%?7.6%. The detection limits of target compounds such as benzo (c) fluorene, benzo (a) anthracene, chrysene, 5-methyl chrysene, benzo (j) fluoranthene, benzo (b) fluoranthene, benzo (k) fluoranthene, benzo (a) pyrene, dibenzo (a,e) pyrene, dibenzo (a,i) pyrene and dibenzo (a,h) pyrene were 0.15 μg/kg. The detection limits of dibenzo (a,l) pyrene, dibenzo (a,h) fluoranthene, benzo (g,h,i) perylene, indene (1,2,3-cd) pyrene were 0.30 μg/kg. A total of 96 samples were collected, and the pollution of PAHs were detected in various foods on the market, and the detection rate was 51.0%. Conclusion The method has good reproducibility and high sensitivity, and can be used for the determination of 14 PAHs in vegetables, fruits and cereal products.
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