食品科学 ›› 2019, Vol. 40 ›› Issue (12): 237-244.doi: 10.7506/spkx1002-6630-20181112-126

• 成分分析 • 上一篇    下一篇

高效液相色谱-串联质谱联用法与高效液相色谱法同步测定白玉菇麦角固醇和VD2方法比较

徐明芳1,沈林燕1,杨云舒2,傅利军2,孙 勇2,*,王洋洋1,彭 璐1,黄晓晶1,李 彦1   

  1. 1.暨南大学生命科学技术学院,广东 广州 510632;2.北京食品科学研究院,北京 100068
  • 出版日期:2019-06-25 发布日期:2019-06-28
  • 基金资助:
    广东省科技计划项目(2015A010107006);“十三五”国家重点研发计划重点专项(2018YFD0400202)

Comparison of HPLC-MS/MS and HPLC for the Synchronous Determination of Ergosterol and VD2 in White Hypsizygus marmoreus

XU Mingfang1, SHEN Linyan1, YANG Yunshu2, FU Lijun2, SUN Yong2,*, WANG Yangyang1, PENG Lu1, HUANG Xiaojing1, LI Yan1   

  1. 1. College of Life Science and Technology, Jinan University, Guangzhou 510632, China; 2. Beijing Academy of Food Science, Beijing 100068, China
  • Online:2019-06-25 Published:2019-06-28

摘要: 建立高效液相色谱-串联质谱(high performance liquid chromatography-tandem mass spectrometry,HPLCMS/MS)联用法与HPLC法同步检测白玉菇样品中麦角固醇和VD2含量方法,经方法学评价确定两种检测方法的线性范围、灵敏度与精确性。通过对经醇碱皂化回流法提取样品中麦角固醇和VD2的分析验证,阐述两种检测方法的差异性,为白玉菇有效生物活性成分与相关产品的质量检测和对白玉菇中麦角固醇与VD2之间转化关系的研究提供技术支持。HPLC-MS/MS法中,采用色谱分离柱Agilent SB-C8 Rapid Res柱(2.1 mm×50 mm,3.5 μm)及在优化的色谱条件下,麦角固醇与VD2之间色谱峰保留时间分别为4.303 min和4.22 min。电喷雾离子源正离子模式下采用多反应选择离子监测模式,分别选择m/z 379.3/125.3与m/z 397.3/125.3离子对麦角固醇与VD2进行定量,结果表明麦角固醇在0.15~6 mg/L、VD2在0.01~1 mg/L范围内与峰面积线性关系良好,平均加标回收率分别为93.51%、90.56%,日内和日间相对标准偏差均小于7%。HPLC法采用COSMOSIL Column 5C18-MS-II(4.6 mm×250 mm,5 μm)柱分离体系,麦角固醇和VD2色谱峰保留时间分别为12.891 min和9.919 min,方法学评价结果显示,麦角固醇在15~750 mg/L、VD2在0.5~50 mg/L范围内与峰面积线性关系良好,两者的平均回收率分别为98.51%、94.05%,日内和日间相对标准偏差均小于1%。采集的样品采用HPLC-MS/MS联用法和HPLC法分别检测实验结果有一定的差异,与HPLC法相比,HPLC-MS/MS联用法具有快速检测时间短、检出限低、更灵敏的优势。

关键词: 高效液相色谱-串联质谱(HPLC-MS/MS)联用法, 高效液相色谱(HPLC)法, 麦角固醇, VD2, 同步检测, 白玉菇

Abstract: A high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method and a high performance liquid chromatography (HPLC) method were established to simultaneously detect the contents of ergosterol and VD2 in white Hypsizygus marmoreus and methodological evaluation was performed to determine the linearity range, sensitivity and accuracy of the two detection methods under optimized detection parameters. The differences between the two detection methods in qualitative and quantitative analysis of ergosterol and VD2 extracted from samples by alcohol-alkali saponification reflux method were verified in order to provide technical support for the detection of effective bioactive components and the study of the conversion between ergosterol and VD2 in white H. marmoreus. In the HPLC-MS/MS method, the chromatographic peak retention times of ergosterol and VD2 were 4.303 min and 4.22 min, respectively, under optimized chromatographic conditions using Agilent SB-C8 Rapid Res column (2.1 mm × 50 mm, 3.5 μm) as the separation column. Ergosterol and VD2 were quantified by selecting m/z 379.3/125.3 and 397.3/125.3 as ion pairs under the multi-reaction monitoring (MRM) mode using an electrospray ionization (ESI) source operating in the positive ion mode. The results showed that the concentration and peak area presented a good linear relationship for ergosterol and VD2 in the range of 0.15–6 mg/L and 0.01–1 mg/L, respectively. The average recoveries of ergosterol and VD2 from spiked samples were 93.51% and 90.56%, respectively, and the relative standard deviations (RSDs) of intra-day and inter-day differences were both less than 7%. In the HPLC method, the peak retention times of ergosterol and VD2 were 12.891 min and 9.919 min, respectively, under optimized separation conditions on a COSMOSIL 5C18-MS-II column (4.6 mm × 250 mm, 5 μm) . The methodology evaluation results of HPLC showed a good linear relationship between concentration and peak area for ergosterol and VD2 in the range of 15–750 and 0.5–50 mg/L, respectively. The average recoveries of ergosterol and VD2 from spiked samples were 98.51% and 94.05%, respectively, and the RSDs of intraday and inter-day differences were lower than 1%. Some differences existed between the two methods. Compared with HPLC, the HPLC-MS/MS method established in this research exhibited the advantages of short detection time, low detection limit and high sensitivity.

Key words: liquid chromatography-tandem mass spectrometry (HPLC-MS/MS), high performance liquid chromatography (HPLC), ergosterol, VD2, synchronous detection, white Hypsizygus marmoreus

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