食品科学 ›› 2026, Vol. 47 ›› Issue (1): 205-211.doi: 10.7506/spkx1002-6630-20250804-027

• 成分分析 • 上一篇    

稳定同位素标记衍生化结合LC-MS/MS测定葱属食品中的甾体皂苷元

薛莹,侯月彩,冷安芹,杨志翔,任琳,雍莉   

  1. (1.四川省疾病预防控制中心,四川 成都 610041;2.中国科学院成都生物研究所,四川 成都 610213)
  • 发布日期:2026-02-04
  • 基金资助:
    四川省科技计划项目(2023YFS0398)

Stable Isotope Labeling Derivatization Combined with LC-MS/MS for the Determination of Steroidal Sapogenins in Allium Vegetables

XUE Ying, HOU Yuecai, LENG Anqin, YANG Zhixiang, REN Lin, YONG Li   

  1. (1. Sichuan Center for Disease Control and Prevention, Chengdu 610041, China; 2. Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610213, China)
  • Published:2026-02-04

摘要: 目的:为提高葱属食品中甾体皂苷元(如剑麻皂苷元和菝葜皂苷元)的检测灵敏度和准确度,该研究建立了一种基于稳定同位素标记衍生化结合液相色谱-串联质谱的分析方法。方法:采用D0/D5-吡啶和三氟甲磺酸酐(Tf2O)对甾体皂苷元的3-羟基进行电荷标记衍生化,利用D0和D5同位素衍生物峰面积比进行内标定量。结果:优化后的衍生化反应在室温下10 min即可完成,衍生化产物稳定性良好;方法学验证表明,其线性范围宽(0.5~200 ng/mL,R²>0.999 4),检出限显著降低至0.2 ng/mL(较未衍生化方法降低95%),精密度(日内相对标准偏差(relative standard deviation,RSD)≤4.02%,日间RSD≤4.36%)和加标回收率(95.5%~104.2%)优异。将该方法应用于实际葱属样品分析,成功测定并揭示了大葱、小葱、洋葱和大蒜中剑麻皂苷元与菝葜皂苷元的含量分布特征。结论:该策略通过电荷标记增强电离效率和同位素内标补偿基质效应,为葱属食品中甾体皂苷元的高灵敏、高准确度定量提供了可靠方案,并可为其他低电离效率天然产物的分析提供参考。

关键词: 葱属食物;甾体皂苷元;衍生化;液相色谱-串联质谱;同位素标记

Abstract: Objective: To improve the detection sensitivity and accuracy of steroidal sapogenins (such as tigogenin and sarsasapogenin) in Allium vegetables, this study established an analytical method based on stable isotope labeling derivatization combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS). Methods: The 3-hydroxy group of steroidal sapogenins was derivatized with D0/D5-pyridine and trifluoromethanesulfonic anhydride (Tf2O) for charge labeling, and internal standard quantification was performed using the peak area ratio between D0 and D5 isotope derivatives. Results: The optimized derivatization reaction was completed within 10 minutes at room temperature, and the derivatives showed excellent stability. The proposed method demonstrated a wide linear range (0.5–200 ng/mL) with a coefficient of determination (R²) > 0.999 4, a limit of detection of 0.2 ng/mL (95% lower than that of the non-derivatized method), and excellent precision (intra-day relative standard deviation (RSD) ≤ 4.02%, and inter-day RSD ≤ 4.36%), and satisfactory spiked recoveries (95.5%–104.2%). This method was successfully applied to the analysis of actual Allium samples, revealing the distribution characteristics of tigogenin and sarsasapogenin in green onions, scallions, onions, and garlic. Conclusion: This strategy enhances the ionization efficiency and compensates for matrix effects through charge labeling. It provides a reliable method for the highly sensitive and accurate quantification of steroidal sapogenins in Allium vegetables and can serve as a reference for the analysis of other natural products with poor ionization efficiency.

Key words: Allium vegetables; steroidal sapogenins; derivatization; liquid chromatography-tandem mass spectrometry; isotope labeling

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