Xu Shuangjiao, Liu Liangliang, Wang Yanqin, Zhou Dayun, Kuang Meng, Fang Dan, Yang Weihua, Wei Shoujun, Xiao Aiping, Ma Lei
State Key Laboratory of Cotton Biology, Institute of Cotton Research of CAAS, Anyang, China.
Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, Changsha, China.
J Sep Sci. 2016 Aug;39(16):3205-11. doi: 10.1002/jssc.201600434. Epub 2016 Jul 28.
A simple, rapid, organic-solvent- and sample-saving pretreatment technique, called dispersive liquid-liquid microextraction, was developed for the determination of six synthetic phenolic antioxidants from edible oils before high-performance liquid chromatography with diode array detection. The entire procedure was composed of a two-step microextraction and a centrifugal process and could be finished in about 5 min, only consuming only 25 mg of sample and 1 mL of the organic solvent for each extraction. The influences of several important parameters on the microextraction efficiency were thoroughly investigated. Recovery assays for oil samples were spiked at three concentration levels, 50, 100 and 200 mg/kg, and provided recoveries in the 86.3-102.5% range with a relative standard deviation below 3.5%. The intra-day and inter-day precisions for the analysis were less than 3.8%. The proposed method was successfully applied for the determination of synthetic phenolic antioxidants in different oil samples, and satisfactory results were obtained. Thus, the developed method represents a viable alternative for the quality control of synthetic phenolic antioxidant concentrations in edible oils.
一种简单、快速、节省有机溶剂和样品的预处理技术——分散液液微萃取,被开发用于在高效液相色谱-二极管阵列检测之前测定食用油中的六种合成酚类抗氧化剂。整个过程由两步微萃取和一个离心过程组成,大约5分钟即可完成,每次萃取仅消耗25毫克样品和1毫升有机溶剂。深入研究了几个重要参数对微萃取效率的影响。对油样进行加标回收试验,加标浓度为50、100和200毫克/千克三个水平,回收率在86.3-102.5%范围内,相对标准偏差低于3.5%。分析的日内和日间精密度均小于3.8%。该方法成功应用于不同油样中合成酚类抗氧化剂的测定,获得了满意的结果。因此,所开发的方法是食用油中合成酚类抗氧化剂浓度质量控制的一种可行替代方法。