食品科学 ›› 2012, Vol. 33 ›› Issue (20): 289-293.

• 分析检测 • 上一篇    下一篇

果蔬中复硝酚盐残留量检测方法的建立

李 立1,张禧庆2,张 攀2,池连学2,娄喜山2,付 建2   

  1. 1.中国检验检疫科学研究院 2.烟台杰科检测服务有限公司
  • 收稿日期:2011-09-06 修回日期:2012-09-07 出版日期:2012-10-25 发布日期:2012-11-09
  • 通讯作者: 李立 E-mail:ytciqli@163.com

Determination of Nitrophenol Residues in Fruits and Vegetables

  • Received:2011-09-06 Revised:2012-09-07 Online:2012-10-25 Published:2012-11-09

摘要: 建立了固相萃取-气相色谱-电子捕获检测水果蔬菜中复硝酚盐残留量的方法,样品经甲醇-水-磷酸体系提取,HLB固相萃取柱净化,乙酸酐衍生,气相色谱-电子捕获检测器测定,外标法定量,液相色谱-质谱定性。结果表明,在0.01~1.0mg/L范围内线性良好,方法定量限为0.01mg/kg。对草莓、苹果、番茄、马铃薯、菠菜、茄子6种水果蔬菜进行3个水平(0.01、0.02、0.05mg/kg)的添加回收,回收率在81.0%~106.6%之间,相对标准偏差3.9%~8.1%,该方法可靠、稳定,可满足水果蔬菜中复硝酚盐残留检测与确证的需要。

关键词: 气相色谱-电子捕获, 固相萃取, 复硝酚盐, 水果蔬菜, 液相色谱-质谱

Abstract: A solid-phase extraction coupled with gas chromatography method was developed for the determination of nitrophenol residues in fruits and vegetables. Samples were extracted with methanol-water-H3PO4. The crude extract was purified on HLB solid-phase extraction column, derivatized with acetic anhydride, and re-extracted with n-hexane. The derivatives were determined and confirmed by gas chromatography-election capture detector (GC-ECD). The established method was linear in the range of 0.01–1.0 mg/L. The limit of quantification (LOQ) was 0.01 mg/kg. The recovery rates were in the range of 81.0%–106.6% across three spiked levels (0.01, 0.02 mg/kg and 0.05 mg/kg) in six fruits and vegetables (strawberry, apple, tomato, potato, spinach and aubergine), and the relative standard deviations (RSD) were in the range of 3.9%–8.1%. This method is reliable, stable and suitable for the determination of nitrophenol residue in fruits and vegetables.

Key words: GC-ECD, solid-phase extraction (SPE), sodium nitrophenolates, fruits and vegetables, LC-MS/MS

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