食品科学 ›› 2021, Vol. 42 ›› Issue (8): 214-220.doi: 10.7506/spkx1002-6630-20200331-455

• 成分分析 • 上一篇    下一篇

超声辅助浊点萃取-液相色谱-串联质谱法测定蔬菜中天然VK同系物

李凯龙,陈同强,徐文泱,李涛,王亮亮,王芳,孙桂芳   

  1. (食品安全监测与预警湖南省重点实验室,湖南省食品质量监督检验研究院,湖南 长沙 410111)
  • 出版日期:2021-04-25 发布日期:2021-05-14
  • 基金资助:
    湖南省科技创新计划项目(2019SK2121);湖南省创新型省份建设专项(2019TP1058)

Ultrasonic Assisted Cloud Point Extraction Combined with Liquid Chromatography-Tandem Mass Spectrometry for the Determination of Natural Vitamin K Homologues in Vegetables

LI Kailong, CHEN Tongqiang, XU Wenyang, LI Tao, WANG Liangliang, WANG Fang, SUN Guifang   

  1. (Hunan Key Laboratory of Food Safety Monitoring and Early Warning,Hunan Institute of Food Quality Supervision Inspection and Research, Changsha 410111, China)
  • Online:2021-04-25 Published:2021-05-14

摘要: 通过优化超声辅助提取和微波辅助浊点萃取方法,建立超声辅助浊点萃取-液相色谱-串联三重四极杆质谱法同时测定蔬菜中天然VK同系物叶绿醌(phylloquinone,PK)和四烯甲萘醌(menaquinone-4,MK-4)的检测方法。蔬菜样品经乙腈超声辅助提取分离出分析物,并通过微波辅助浊点萃取,以甲酸铵溶液-甲醇作为流动相梯度洗脱,采用电喷雾离子源正离子多反应监测模式测定,外标法定量。结果显示,超声辅助浊点萃取的优化条件为1.5?g样品加入乙腈体积2?mL、超声提取、提取液中氯化钠添加量0.15?g、萃取溶剂采用Triton?X-45、萃取溶剂体积50?μL。2?种VK同系物PK和MK在1.0~500.0?ng/mL范围线性良好,相关系数均大于0.997?0,PK和MK的方法检出限分别为1.0?ng/g和0.8?ng/g。加标含量为40、80、120?ng/g的PK和MK加标回收率在94.5%~106.2%范围内,方法日间和日内重复性相对标准偏差不大于10%,根茎类蔬菜中未检出天然VK,而绿叶蔬菜均仅检测到PK,含量在96.2~1?704.5?ng/g之间,其中菠菜中PK含量最高。

关键词: 浊点萃取;液相色谱-串联质谱;蔬菜;VK

Abstract: In this study, an ultrasonic-assisted cloud point extraction combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS) with a triple quadrupole (QqQ) mass detector method was developed and optimized for determining the natural vitamin K homologues phylloquinone (PK) and menaquinone-4 (MK) in vegetables. The analytes were isolated from vegetable samples by ultrasound-assisted extraction using acetonitrile as the extraction solvent followed by microwave-assisted cloud point extraction with Triton X-45, chromatographed by gradient elution using ammonium formate solution-methanol as the mobile phase, detected using an electrospray ionization source in the positive ion mode (ESI+) with multiple reaction monitoring (MRM), and quantified by the external standard method. The results showed that the optimized conditions for ultrasonic-assisted cloud point extraction were as follows: 1.5 g of the sample was ultrasonically extracted with 2 mL of acetonitrile, and the extract was re-extracted with 50 μL of Triton X-45 after adding 0.15 g of sodium chloride to it. Good linearity was achieved for the two vitamin K homologues in the range of 1.0–500.0 ng/mL with correlation coefficients of greater than 0.997 0. The limits of detection (LODs) were 1.0 ng/g and 0.8 ng/g for PK and MK, respectively. The recoveries for samples spiked at three concentration levels of 40, 80 and 120 ng/g ranged from 94.5% to 106.2%, and the relative standard deviations (RSDs) of inter-day and intra-day precision were less than 10%. No natural vitamin K was detected in the root and stem vegetables. Only PK was detected in the leafy vegetable samples analyzed at levels in the range of 96.2–1 704.5 ng/g, with the highest value being observed in spinach.

Key words: cloud point extraction; liquid chromatography-tandem mass spectrometry; vegetables; vitamins K

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