West China School of Public Health, Sichuan University, Chengdu, China.
School of Public Health, Xi'an Jiaotong University Health Science Center, Xi'an, China.
J Sep Sci. 2018 Apr;41(8):1829-1838. doi: 10.1002/jssc.201701393. Epub 2018 Feb 1.
An efficient ultrasound-assisted saponification was developed for simultaneous determination of vitamin E isomers in vegetable oil by high-performance liquid chromatography with fluorescence detection. The samples were saponified ultrasonically with potassium hydroxide solution for only 7 min, then the analytes were extracted with ether. Vitamin E isomers were separated on a C column at 25°C with a mobile phase of methanol/acetonitrile (81:19, v/v) at a flow rate of 0.8 mL/min. Fluorescence detection was operated at 290 nm of excitation wavelength and 327 nm of emission wavelength. Under the optimized conditions, good linearities over the range of 0.001-8.00 μg/mL (r > 0.999) were obtained. Mean recoveries of the method were 88.0-106%, with intra- and interday RSDs less than 11.8 and 12.8%, respectively. The detection limits and quantification limits of the method were 0.30-1.8 and 1.0-6.1 μg/kg, respectively. The recoveries of this method were much higher than that of the quick, easy, cheap, effective, rugged, and safe method and direct dilution method, but were similar to those of hot saponification. This proposed method provides reliable, simple, and rapid quantification of vitamin E isomers in vegetable oils. Five kinds of vegetable oils were analyzed, the quantification results were within the ranges reported by other authors.
一种高效的超声辅助皂化法被开发用于通过高效液相色谱法与荧光检测同时测定植物油中的维生素 E 异构体。样品仅用氢氧化钾溶液超声皂化 7 分钟,然后用乙醚萃取分析物。维生素 E 异构体在 C 柱上于 25°C 下,以甲醇/乙腈(81:19,v/v)为流动相,流速为 0.8 mL/min 进行分离。荧光检测的激发波长为 290nm,发射波长为 327nm。在优化条件下,该方法在 0.001-8.00μg/mL 的范围内具有良好的线性关系(r>0.999)。该方法的平均回收率为 88.0-106%,日内和日间 RSD 分别小于 11.8%和 12.8%。该方法的检测限和定量限分别为 0.30-1.8 和 1.0-6.1μg/kg。该方法的回收率明显高于快速、简单、廉价、有效、坚固、安全法和直接稀释法,但与热皂化法相似。该方法为植物油中维生素 E 异构体的可靠、简单、快速定量提供了依据。对 5 种植物油进行了分析,定量结果在其他作者报道的范围内。