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Extraction and Determination of Vitamin K1 in Foods by Ultrasound-Assisted Extraction, SPE, and LC-MS/MS.
Xu, Yueqing; Zhang, Liangxiao; Yang, Ruinan; Yu, Xu; Yu, Li; Ma, Fei; Li, Hui; Wang, Xiupin; Li, Peiwu.
  • Xu Y; Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Wuhan 430062, China.
  • Zhang L; Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture and Rural Affairs, Wuhan 430062, China.
  • Yang R; Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Wuhan 430062, China.
  • Yu X; Laboratory of Quality and Safety Risk Assessment for Oilseed Products (Wuhan), Ministry of Agriculture and Rural Affairs, Wuhan 430062, China.
  • Yu L; Quality Inspection and Test Center for Oilseed Products, Ministry of Agriculture and Rural Affairs, Wuhan 430062, China.
  • Ma F; Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Wuhan 430062, China.
  • Li H; Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture and Rural Affairs, Wuhan 430062, China.
  • Wang X; Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Wuhan 430062, China.
  • Li P; Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture and Rural Affairs, Wuhan 430062, China.
Molecules ; 25(4)2020 Feb 14.
Article en En | MEDLINE | ID: mdl-32075057
ABSTRACT
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 170 (g/mL), extraction temperature of 50 °C, extraction power of 700 W, extraction time of 50 min, material-wash fluid ratio of 160 (g/mL), and 8 mL of hexane/anhydrous ether (973, 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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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vitamina K 1 / Ondas Ultrasónicas / Análisis de los Alimentos Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vitamina K 1 / Ondas Ultrasónicas / Análisis de los Alimentos Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article