Molecules (Feb 2020)

Extraction and Determination of Vitamin K<sub>1</sub> in Foods by Ultrasound-Assisted Extraction, SPE, and LC-MS/MS

  • Yueqing Xu,
  • Liangxiao Zhang,
  • Ruinan Yang,
  • Xu Yu,
  • Li Yu,
  • Fei Ma,
  • Hui Li,
  • Xiupin Wang,
  • Peiwu Li

DOI
https://doi.org/10.3390/molecules25040839
Journal volume & issue
Vol. 25, no. 4
p. 839

Abstract

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Vitamin K1 is one of the important hydrophobic vitamins in fat-containing foods. Traditionally, lipase is employed in the determination of vitamin K1 to remove the lipids, which makes the detection complex, time-consuming, and insensitive. In this study, the determination of vitamin K1 in fat-containing foods was developed based on ultrasound-assisted extraction (UAE), solid-phase extraction (SPE) combined with liquid chromatography−tandem mass spectrometry (LC-MS/MS). The optimal conditions for extraction of vitamin K1 were material−liquid ratio of 1:70 (g/mL), extraction temperature of 50 °C, extraction power of 700 W, extraction time of 50 min, material-wash fluid ratio of 1:60 (g/mL), and 8 mL of hexane/anhydrous ether (97:3, v/v) as the elution solvent. Then, vitamin K1 was analyzed on a ZORBAX SB-C18 column (50 mm × 2.1 mm, 1.8 μm) by gradient elution with water (0.01% formic acid) and methanol (0.01 formic acid + 2.5 mmol/L ammonium formate) as the mobile phase. The limit of detection (LOD) and limit of quantification (LOQ) were 0.05 and 0.16 μg/kg, respectively. Calibration curve was linear over the range of 10−500 ng/mL (R2 > 0.9988). The recoveries at three spiked levels were between 80.9% and 119.1%. The validation and application indicated that the proposed method was simple and sensitive in determination of vitamin K1 in fat-containing foods.

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