刘景凡,孙聪,梁少华.高效液相色谱法测定玉米植物甾醇中 豆甾醇、菜油甾醇和β-谷甾醇[J].中国油脂,2025,50(6):.[LIU Jingfan, SUN Cong, LIANG Shaohua.Determination of stigmasterol, campesterol and β-sitosterol in corn sterols by high performance liquid chromatography[J].China Oils and Fats,2025,50(6):.]
高效液相色谱法测定玉米植物甾醇中 豆甾醇、菜油甾醇和β-谷甾醇
Determination of stigmasterol, campesterol and β-sitosterol in corn sterols by high performance liquid chromatography
  
DOI:10.19902/j.cnki.zgyz.1003-7969.240202
中文关键词:  玉米植物甾醇  豆甾醇  菜油甾醇  β-谷甾醇  高效液相色谱
英文关键词:corn sterols  stigmasterol  campesterol  β-sitosterol  HPLC
基金项目:国家“十三五”重点研发基金资助项目(2018YFD0401100)
作者单位
刘景凡,孙聪,梁少华 (河南工业大学 粮油食品学院郑州 450001) 
Author NameAffiliation
LIU Jingfan, SUN Cong, LIANG Shaohua (College of Food Science and Engineering, Henan University of Technology Zhengzhou 450001, China) 
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中文摘要:
      旨在为玉米植物甾醇的实际生产或深度开发利用奠定基础,建立了一种同时测定玉米植物甾醇中豆甾醇、菜油甾醇和β-谷甾醇的高效液相色谱检测方法。采用Waters Symmetry C18色谱柱(4.6 mm×250 mm,5 μm),二极管阵列检测器,检测波长205 nm,甲醇-水(体积比92∶ 8)为流动相进行检测,外标法进行定量。结果表明:3种甾醇单体在125~2 000 μg/mL质量浓度范围内线性关系良好,检出限均不大于0.07 μg/mL;3种甾醇单体的峰面积和保留时间的相对标准偏差(RSD)在仪器精密度实验中介于0.24%~1.23%,在样品重复性实验中介于0.61%~2.38%,在日内稳定性实验中介于0.13%~2.92%,在日间稳定性实验中介于0.67%~3.43%;3种甾醇单体的加标回收率在76.86%~105.74%之间,RSD均小于5%。综上,该方法具有灵敏度高、准确性好、操作简便、稳定性好的特点,可实现玉米植物甾醇中豆甾醇、菜油甾醇和β-谷甾醇的定量分析。
英文摘要:
      Aiming to lay the foundation for the actual production or deep exploitation and utilization of corn sterols, a high performance liquid chromatography (HPLC) method was established for the simultaneous determination of stigmasterol, campesterol and β-sitosterol in corn sterols. The separation was performed on a Waters Symmetry C18 column (4.6 mm×250 mm, 5 μm) with a diode array detector at a detection wavelength of 205 nm, and methanol-water (volume ratio 92∶ 8) as the mobile phase, and the analytes was quantified by external standard method. The results showed that the linearity of the three sterol monomers was good in the range of 125-2 000 μg/mL, and the detection limits were not more than 0.07 μg/mL for all of them. The relative standard deviations (RSD) of the peak area and retention time of the three sterol monomers ranged from 0.24% to 1.23% in the instrumental precision experiments, from 0.61% to 2.38% in the sample reproducibility experiments, from 0.13% to 2.92% in the intra-day stability experiments, and from 0.67% to 3.43% in the inter-day stability experiments. The recoveries of the three sterol monomers ranged from 76.86% to 105.74%, and the RSD were less than 5%. In conclusion, the method is characterized by high sensitivity, good accuracy, easy operation and good stability, and can realize the quantitative analysis of stigmasterol, campesterol and β-sitosterol in corn sterols.
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