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中国精品科技期刊2020
邓梦雅, 彭祖茂, 朱丽, 杨俊, 杨世添, 张协光. 高效液相色谱-荧光检测法测定食品中维生素K2的含量[J]. 食品工业科技, 2019, 40(19): 240-244,250. DOI: 10.13386/j.issn1002-0306.2019.19.041
引用本文: 邓梦雅, 彭祖茂, 朱丽, 杨俊, 杨世添, 张协光. 高效液相色谱-荧光检测法测定食品中维生素K2的含量[J]. 食品工业科技, 2019, 40(19): 240-244,250. DOI: 10.13386/j.issn1002-0306.2019.19.041
DENG Meng-ya, PENG Zu-mao, ZHU Li, YANG Jun, YANG Shi-tian, ZHANG Xie-guang. Determination of Vitamin K2 in Food by High Performance Liquid Chromatography with Fluorescence Detection[J]. Science and Technology of Food Industry, 2019, 40(19): 240-244,250. DOI: 10.13386/j.issn1002-0306.2019.19.041
Citation: DENG Meng-ya, PENG Zu-mao, ZHU Li, YANG Jun, YANG Shi-tian, ZHANG Xie-guang. Determination of Vitamin K2 in Food by High Performance Liquid Chromatography with Fluorescence Detection[J]. Science and Technology of Food Industry, 2019, 40(19): 240-244,250. DOI: 10.13386/j.issn1002-0306.2019.19.041

高效液相色谱-荧光检测法测定食品中维生素K2的含量

Determination of Vitamin K2 in Food by High Performance Liquid Chromatography with Fluorescence Detection

  • 摘要: 建立了高效液相色谱-荧光检测法(HPLC-FLD)同时快速分离检测猪肉、猪肝、纯牛奶、酸奶、黄油、鸡蛋、豆豉、纳豆8种食品中2种维生素K2的方法。样品经酶解、皂化、萃取、氮吹复溶处理后,用Agilent ZORBAX SB-C18色谱柱(150 mm×4.6 mm,5 μm)分离,柱后锌粉还原柱(35 mm×4.6 mm)衍生,以甲醇(含有二氯甲烷10%、冰醋酸0.03%、氯化锌1.5 g/L、无水乙酸钠0.5 g/L)为流动相,进入荧光检测器进行检测。结果表明,四烯甲萘醌(Menatetrenone4,MK-4)、七烯甲萘醌(Menatetrenone7,MK-7)在15 min内分离出峰。2种维生素K2在各自的线性范围内关系良好,相关系数r=1.0000。当取样量为2 g,定容2 mL时,MK-4的检出限为0.01 μg/100 g,定量限为0.04 μg/100 g;MK-7的检出限为0.06 μg/100 g,定量限为0.2 μg/100 g。当取样量为10 g,定容2 mL时,MK-4的检出限为0.002 μg/100 g,定量限为0.008 μg/100 g;MK-7的检出限为0.012 μg/100 g,定量限为0.04 μg/100 g。精密度(RSD)均不超过3.56%,回收率为80.6%~95.5%。8种食品中,猪肉、纯牛奶、酸奶、黄油、鸡蛋中仅含有MK-4,其中纯牛奶中含量最低,仅为(0.34±0.02)μg/100 g,鸡蛋中含量最高,达(25.38±0.85)μg/100 g。猪肝、豆豉、纳豆中仅含MK-7,其中猪肝含量较低,为(25.45±0.83)μg/100 g,纳豆中含量最为丰富,高达(923.20±11.45)μg/100 g。该法准确、可靠、高效,可用于食品中维生素K2的高通量检测。

     

    Abstract: A method for simultaneous determination of two kinds of vitamin K2 in 8 kinds of food,including pork,pork liver,pure milk,yogurt,butter,eggs,lobster sauce and natto,by high performance liquid chromatography-fluorescence detector(HPLC-FLD)was developed. After enzymatic hydrolysis,saponification,extraction,nitrogen blowing and resolving treatment,the sample was separated by an Agilent ZORBAX SB-C18column(150 mm×4.6 mm,5 μm)and derivatized with a post-column zinc powder reduction column(35 mm×4.6 mm). Methanol(containing 10% dichloromethane,0.03%glacial acetic acid,1.5 g/L zinc chloride and 0.5 g/L anhydrous sodium acetate)was used as mobile phase for detection by fluorescence detector. Results showed that the chromatographic peaks of menatetrenone 4(MK-4)and menatetrenone7(MK-7)were found within 15 min. A good respective linearity of two kinds of vitamin K2was obtained with the correlation coefficient(r=1.0000).When the sample size was 2 g and the volume was 2 mL,the detection limit of MK-4 was 0.01 μg/100 g and the quantitative limit was 0.04 μg/100 g.The detection limit of MK-7 was 0.06 μg/100 g and the quantitative limit was 0.2 μg/100 g. When the sample size was 10 g and the volume was 2 mL,the detection limit of MK-4 was 0.002 μg/100 g and the quantitative limit was 0.008 μg/100 g.The detection limit of MK-7 was 0.012 μg/100 g and the quantitative limit was 0.04 μg/100 g.The relative standard deviation(RSD)was no more than 3.56%,and the recoveries ranged from 80.6% to 95.5%.Among the 8 kinds of food,pork,pure milk,yogurt,butter and eggs only contained MK-4,among which the content of pure milk was the lowest(0.34±0.02) μg/100 g and the content of egg was the highest(25.38±0.85) μg/100 g.There was only MK-7 in pork liver,lobster sauce and natto,among which the content of pork liver was low(25.45±0.83) μg/100 g and the content of natto was the most abundant,up to(923.20±11.45) μg/100 g.The method is accurate,reliable,efficient,and can be used for high-throughput determination of vitamin K2 in food.

     

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