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高效液相色谱法测定食品中维生素K_(1)和维生素K_(2)的含量 被引量:6
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作者 孔凡华 郭倩 +5 位作者 白沙沙 徐佳佳 李东 王竹 张雪松 崔亚娟 《食品工业科技》 CAS 北大核心 2021年第4期226-231,共6页
建立高效液相色谱-荧光检测法(HPLC-FLD)测定食品中维生素K1和维生素K2含量的分析方法。方法:配方奶粉、酸奶、纳豆冻干粉和鸡胗冻干粉经酶解、异丙醇分散、正己烷萃取、旋转蒸发复溶后,使用Thermo Acclaim^(TM)120C18色谱柱(150 mm... 建立高效液相色谱-荧光检测法(HPLC-FLD)测定食品中维生素K1和维生素K2含量的分析方法。方法:配方奶粉、酸奶、纳豆冻干粉和鸡胗冻干粉经酶解、异丙醇分散、正己烷萃取、旋转蒸发复溶后,使用Thermo Acclaim^(TM)120C18色谱柱(150 mm×4.6 mm,5μm)分离,锌粉还原柱(50 mm×4.6 mm)衍生,以900 mL甲醇:100 mL四氢呋喃(含冰醋酸0.3 mL,氯化锌1.5 g,无水乙酸钠0.5 g)为流动相,激发波长为243 nm,发射波长为430 nm,分离维生素K 1(Vitamin K 1,VK 1)、四烯甲萘醌(menaquinone-4,MK-4)、七烯甲萘醌(menaquinone-7,MK-7)和九烯甲萘醌(menaquinone-9,MK-9)。结果:VK 1、MK-4、MK-7和MK-9在20~1000μg/L范围内与峰面积有良好线性关系。配方奶粉、酸奶、纳豆冻干粉和鸡胗冻干粉中VK1、MK-4、MK-7、MK-9含量的相对标准偏差(RSD)均小于5%,表明精密度好。配方奶粉、酸奶和纳豆冻干粉不同水平加标回收率分别为85.0%~107.8%、85.8%~109.6%、85.1%~102.7%,回收率的RSD均小于5%,表明回收率高,相对标准偏差小。结论:实验建立的方法重复性好、准确度高,可以精准定量食品中维生素K_(1)和维生素K_(2)的含量。 展开更多
关键词 高效液相色谱-荧光检测法(HPLC-FLD) 维生素K_(1)(VK_(1)) 维生素K_(2)(VK_(2)) 四烯甲萘醌(mk-4) 七烯甲萘醌(mk-7) 九烯甲萘醌(mk-9)
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Simultaneous Determination of Content of VK_(1) and VK_(2) in Milk and Dairy Products by High Performance Liquid Chromatography
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作者 Huili GONG Guoxia DUAN +3 位作者 Lijun LIU Shuo TANG Cuizhi LI Zhiyong LU 《Asian Agricultural Research》 2022年第7期63-68,71,共7页
[Objectives]To make simultaneous determination of vitamin K_(1)(VK_(1))and vitamin K_(2)(VK_(2),mainly MK-4,MK-7 and MK-9)in milk and dairy products.[Methods]A high performance liquid chromatographic method was develo... [Objectives]To make simultaneous determination of vitamin K_(1)(VK_(1))and vitamin K_(2)(VK_(2),mainly MK-4,MK-7 and MK-9)in milk and dairy products.[Methods]A high performance liquid chromatographic method was developed for the simultaneous determination of vitamin K_(1)(VK_(1))and vitamin K_(2)(VK_(2),mainly MK-4,MK-7 and MK-9)in milk and dairy products.After enzymatic digestion,the samples were extracted with hexane for VK_(1),MK-4,MK-7 and MK-9,subjected to gradient elution at excitation wavelength 243 nm and emission wavelength 430 nm,detected by high performance liquid chromatography with fluorescence detector and quantified by external standard method.[Results]The linearity of VK_(1),MK-4,MK-7 and MK-9 was good in the concentration range of 2.5-1000 ng/mL with the correlation coefficients greater than 0.999;The relative standard deviations(RSD)of VK_(1),MK-4,MK-7 and MK-9 in milk powder,liquid milk and yogurt were 1.32%-5.05%,1.10%-2.48% and 2.20%-3.47%,respectively;the recovery rates of VK_(1),MK-4,MK-7 and MK-9 at different levels in milk powder,liquid milk and yogurt were 81.1%-108%,81.8%-103%and 82.1%-99.2%,respectively.[Conclusions]The method is rapid,accurate,reproducible and capable of simultaneous determination of VK_(1),MK-4,MK-7 and MK-9. 展开更多
关键词 High performance liquid chromatography(HPLC) Vitamin K_(1) Vitamin K_(2) mk-4 mk-7 mk-9
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