Jin Jing, Chen Jiping, Tian Yuzeng, Zou Lili, Wang Longxing, Li Fang
Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Se Pu. 2013 Jun;31(6):556-60. doi: 10.3724/sp.j.1123.2012.12036.
On the basis of the source of illegal cooking oil (heated vegetable oil and animal oil) and the important referents reflecting their sources, namely, undecanoic acid and 13-methyl-tetradecanoic acid connected to the glyceride, their corresponding ramifications in edible oil were detected with internal standard method. The sensitivity and selectivity of this method were improved by the on-line cleanup and preconcentration. The detection limits of the method were 0.070 mg/kg for undecanoic acid and 0.006 mg/kg for 13-methyl-tetradecanoic acid. Additionally, most of the normal vegetable oils have lower levels of both fatty acids than illegal cooking oils. It was suggested to evaluate the quality of edible oils to some extent on the basis of the contents of undecanoic acid and 13-methyl-tetradecanoic acid.
基于非法食用油(加热植物油和动物油)的来源以及反映其来源的重要指标,即与甘油酯相连的十一烷酸和13-甲基十四烷酸,采用内标法检测它们在食用油中的相应衍生物。通过在线净化和预浓缩提高了该方法的灵敏度和选择性。该方法对十一烷酸的检出限为0.070mg/kg,对13-甲基十四烷酸的检出限为0.006mg/kg。此外,大多数正常植物油中这两种脂肪酸的含量均低于非法食用油。建议根据十一烷酸和13-甲基十四烷酸的含量在一定程度上评估食用油的质量。