色谱 ›› 2026, Vol. 44 ›› Issue (4): 403-412.DOI: 10.3724/SP.J.1123.2025.02014

• 研究论文 • 上一篇    下一篇

固相支撑液液萃取结合超高效液相色谱-串联质谱快速检测牧草中10种麦角生物碱毒素

任彩霞, 王晓敏, 盛万里, 韩祎陟, 张春艳, 郑书展*()   

  1. 呼和浩特海关技术中心,内蒙古 呼和浩特 010020
  • 收稿日期:2025-02-25 出版日期:2026-04-08 发布日期:2026-04-13
  • 通讯作者: * E-mail:zhengshuzhan@163.com.
  • 基金资助:
    海关总署科研项目(2022HK122);海关总署科研项目(2023HK082)

Determination of ergot alkaloids toxins in forage grass by ultra performance liquid chromatography-tandem mass spectrometry coupled with solid-phase supported liquid-liquid extraction

REN Caixia, WANG Xiaomin, SHENG Wanli, HAN Yizhi, ZHANG Chunyan, ZHENG Shuzhan*()   

  1. Technical Center of Hohhot Customs,Hohhot 010020,China
  • Received:2025-02-25 Online:2026-04-08 Published:2026-04-13
  • Supported by:
    Scientific Research Project of General Administration of Customs(2022HK122);Scientific Research Project of General Administration of Customs(2023HK082)

摘要:

基于固相支撑液液萃取技术和超高效液相色谱-串联质谱法,建立了一种快速、灵敏检测牧草中10种麦角生物碱毒素的方法。牧草样品使用含1%甲酸的乙腈充分提取,取1.0 mL提取溶剂过固相支撑液液萃取柱净化,乙酸乙酯洗脱,浓缩后复溶为待测液。使用Acquity UPLC BEH C18色谱柱(100 mm×2.1 mm,1.7 μm)分离,以0.25 mmol/L乙酸铵溶液(含0.5%甲酸)和乙腈(含0.5%甲酸)为流动相进行梯度洗脱。采用电喷雾电离正离子(ESI+)扫描和多反应监测(MRM)方式检测,基质标准曲线外标法定量分析。结果显示,10种麦角生物碱毒素在各自线性范围内线性关系良好(r2>0.995),在苜蓿、羊草、燕麦、玉米青贮等牧草中10种麦角生物碱毒素的检出限为0.1~2.3 μg/kg,定量限为0.4~7.3 μg/kg,方法的总体平均回收率为66.3%~116.7%,总体相对标准偏差小于9.9%,方法基质效应较低,净化效果明显,具有操作简单、结果准确、干扰少的特点,适用于牧草中麦角生物碱毒素的同步筛查和确证检测,可为监控牧草品质提供技术支持,同时拓展了固相支撑液液萃取技术在毒素检测领域的应用。

关键词: 麦角生物碱毒素, 牧草, 固相支撑液液萃取, 超高效液相色谱-串联质谱

Abstract:

Toxic alkaloids, especially ergot alkaloid toxins, present in forage grass and pose serious health hazards to humans and livestock. Hence, a method for simultaneously detecting these dangerous plant toxins is needed. This study established a rapid method for detecting ten ergot alkaloid toxins using solid-phase supported liquid-liquid extraction technology combined with ultra performance liquid chromatography-tandem mass spectrometry. Forage samples were extracted with 8.0 mL of acetonitrile containing 1% formic acid. The extraction mixture was vortexed and then centrifuged at 8 000 r/min for 5 min, after which 1.0 mL of the supernatant was mixed with 3.0 mL of water and vortexed for 0.5 min. The entire mixture was transferred to a solid-phase supported liquid-liquid extraction column and allowed to stand for 10 min. The column was eluted with 6.0 mL of ethyl acetate and the collected eluate was evaporated under nitrogen at temperatures below 40 ℃. The residue was dissolved in 1 mL of acetonitrile-water (1∶3, volume ratio, containing 0.5% formic acid), and separated using an Acquity UPLC BEH C18 column (100 mm×2.1 mm, 1.7 μm). A solution of 0.5% formic acid in water containing 0.25 mmol/L ammonium acetate was used as mobile phase A, while 0.5% formic acid in acetonitrile was used as mobile phase B. The following gradient elution program was used: 0-1.0 min, 90%B; 1.0-5.0 min, 90%B-75%B; 5.0-10 min, 75%B-50%B; 10-12 min, 50%B-10%B; 12-14 min, 10%B; 14-16 min, 10%B-90%B. Ten ergot alkaloid toxins (including three pairs of isomers: ergocornine, ergocristine, ergocristinine, ergocryptine, and ergocryptinine) were effectively separated following gradient elution. Positive electrospray-ionization mode and multiple reaction monitoring (MRM) scanning was used for detection, with an external standard curve used for quantification purposes. The ten ergot alkaloid toxins exhibited good linear relationships within their respective linear ranges (r2>0.995). Alfalfa, Leymus chinensis, oats, and silage corn exhibited LODs of 0.1–2.3 μg/kg for the ten ergot alkaloid toxins, with LOQs of 0.4–7.3 μg/kg. The developed method exhibited overall recovery rates of between 66.3% and 116.7%, with relative standard deviations of less than 9.9%. The matrix effect mainly manifested itself in the form of matrix suppression, with silage corn exhibiting a significantly stronger matrix effect than the other three types of forage. Silage corn exhibited a strong matrix effect in more than 50% of samples, while alfalfa, oats, and Leymus chinensis showed relatively low matrix effects, with more than 63% being weak. The developed method is simple to operate, provides accurate results, and exhibits minimal interference; hence, it is suitable for simultaneously screening and confirming ergot alkaloid toxins in forage, thereby providing technical support for monitoring forage quality, while also expanding the applicability of solid-phase supported liquid-liquid extraction technology in the toxin-detection field.

Key words: ergot alkaloid toxins, forage grass, solid-phase supported liquid-liquid extraction, ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)

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