Extraction and Determination of Vitamin K1 in Foods by Ultrasound-Assisted Extraction, SPE, and LC-MS/MS

被引:11
作者
Xu, Yueqing [1 ,2 ]
Zhang, Liangxiao [1 ,3 ,4 ]
Yang, Ruinan [1 ,2 ]
Yu, Xu [1 ,2 ]
Yu, Li [1 ,4 ]
Ma, Fei [1 ,3 ]
Li, Hui [1 ,5 ]
Wang, Xiupin [1 ,4 ]
Li, Peiwu [1 ,3 ,4 ,5 ]
机构
[1] Chinese Acad Agr Sci, Oil Crops Res Inst, Wuhan 430062, Peoples R China
[2] Minist Agr & Rural Affairs, Key Lab Biol & Genet Improvement Oil Crops, Wuhan 430062, Peoples R China
[3] Minist Agr & Rural Affairs, Lab Qual & Safety Risk Assessment Oilseed Prod Wu, Wuhan 430062, Peoples R China
[4] Minist Agr & Rural Affairs, Qual Inspect & Test Ctr Oilseed Prod, Wuhan 430062, Peoples R China
[5] Minist Agr & Rural Affairs, Key Lab Detect Mycotoxins, Wuhan 430062, Peoples R China
关键词
ultrasound-assisted extraction; solid-phase extraction; LC-MS/MS; vitamin K-1; foods; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; FLUORESCENCE DETECTION; VEGETABLE-OIL; K HOMOLOGS; PHYLLOQUINONE; MENAQUINONES; QUANTIFICATION; PHYTOSTEROLS; MARGARINES;
D O I
10.3390/molecules25040839
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vitamin K-1 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 K-1 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 vitaminK(1) were material-liquid ratio of 1:70 (g/mL), extraction temperature of 50 degrees 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 K-1 was analyzed on a ZORBAX SB-C18 column (50 mm x 2.1 mm, 1.8 mu m) 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 mu g/kg, respectively. Calibration curve was linear over the range of 10-500 ng/mL (R-2 > 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.
引用
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页数:12
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