超高效液相色谱—串联质谱法同时测定甘草甜素中8种甜味剂
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云南中烟工业有限责任公司技术中心,云南 昆明 650106

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宋春满(1972—),男,云南中烟工业有限责任公司副研究员,博士。E-mail:chunmansong@126.com

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云南大观实验室项目(编号:YNDG202301XL03);云南中烟工业有限责任公司科技计划项目(编号:2023XL03)


Simultaneous determination of eight sweeteners in glycyrrhizin by ultrahigh performance liquid chromatograph-tandem mass spectrometry
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Technology Center, China Tobacco Yunnan Industrial Co., Ltd., Kunming, Yunnan 650106, China

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    摘要:

    目的 建立超高效液相色谱—串联质谱快速分析甘草甜素中8种甜味剂含量的分析方法。方法 甘草甜素样品经20 mL 纯水超声提取30 min后用0.22 μm微孔滤膜过滤,采用Waters HSS T3色谱柱分离,以体积分数0.2%氨水溶液—甲醇梯度洗脱,电喷雾负离子模式下测定,内标法定量。结果 8种甜味剂在0.1~20.0 μg/mL范围内线性关系良好,相关系数均大于0.99,定量限为0.2~1.0 μg/g,样品加标平均回收率为85.8%~103.0%,相对标准偏差为2.4%~4.6%。结论 该方法简便快速,适用于甘草甜素中8种甜味剂含量分析。

    Abstract:

    Objective To establish a method based on ultrahigh performance liquid chromatography-tandem mass spectrometry for rapid determination of eight sweeteners in glycyrrhizin.Methods The sample is ultrasonically extracted with 20 mL pure water for 30 min, passed through 0.22 μm microporous filter membrane, separated through the Waters HSS T3 column, subjected to gradient elution with 0.2% (V/V) ammonia solution-methanol, and detected under the negative mode of electrospray ionization.Results The eight sweeteners showed a good linear relationship between peak area and concentration within the range of 0.1~20.0 μg/mL, with correlation coefficients greater than 0.99. The limits of quantification are within the range of 0.2~1.0 μg/g. The average recoveries of sample spiked are within the range of 85.8%~103.0%, and the relative standard deviations are in the range of 2.4%~4.6%.Conclusion This method is simple, rapid, and suitable for determination of the content of 8 sweeteners in glycyrrhizin.

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何靓,朱玲超,胡瑞林,等.超高效液相色谱—串联质谱法同时测定甘草甜素中8种甜味剂[J].食品与机械,2026,42(8):55-60.
He Liang, Zhu Lingchao, Hu Ruilin, et al. Simultaneous determination of eight sweeteners in glycyrrhizin by ultrahigh performance liquid chromatograph-tandem mass spectrometry[J]. Food & Machinery,2026,42(8):55-60.

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  • 收稿日期:2025-08-04
  • 最后修改日期:2026-02-06
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  • 在线发布日期: 2026-09-22
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