湖北农业科学 ›› 2026, Vol. 65 ›› Issue (4): 219-224.doi: 10.14088/j.cnki.issn0439-8114.2026.04.033

• 检测分析 • 上一篇    下一篇

黄芪多糖中痕量单糖及酚酸类杂质的UPLC-MS/MS同步检测方法学研究

石中琪, 姚芳芳, 陈瑞义, 朱斌, 屈琴   

  1. 巴中市产品质量检验检测中心,四川 巴中 636000
  • 收稿日期:2025-11-10 出版日期:2026-04-25 发布日期:2026-05-06
  • 通讯作者: 屈 琴(1982-),女,四川巴中人,副主任药师,硕士,主要从事药品质量控制研究,(电话)15351421957(电子信箱)9223408@qq.com。
  • 作者简介:石中琪(1988-),男,四川巴中人,主管中药师,主要从事药品质量控制研究,(电话)18095001188(电子信箱)568750720@qq.com。
  • 基金资助:
    四川省药品监督管理局科技计划项目(2025012)

Study on the synchronous detection methodology of trace monosaccharides and phenolic acid impurities in Astragalus polysaccharides by UPLC-MS/MS

SHI Zhong-qi, YAO Fang-fang, CHEN Rui-yi, ZHU Bin, QU Qin   

  1. Bazhong Product Quality Inspection and Testing Center, Bazhong 636000, Sichuan,China
  • Received:2025-11-10 Published:2026-04-25 Online:2026-05-06

摘要: 黄芪多糖(APS)作为重要中药活性成分,其生产过程中残留的单糖、酚酸等杂质严重影响药物安全性与有效性,为控制其质量,旨在建立一种同步检测APS中痕量单糖及酚酸类杂质的分析方法。建立基于超高效液相色谱-串联质谱(UPLC-MS/MS)的多维检测方法,采用亲水相互作用色谱(HILIC)优化梯度洗脱程序(乙腈-5 mmol/L甲酸铵,pH 4.5),结合三重四极杆质谱多反应监测模式(MRM),实现单糖类(葡萄糖、半乳糖)和酚酸类(原儿茶酸、咖啡酸)杂质的精准分离与定量。方法学验证表明,目标物检出限为0.03~0.08 ng/mL,线性范围0.2~50 ng/mL(R2≥0.999 3),回收率93.7%~104.1%,精密度RSD≤5.5%。实际样品检测显示3批APS总杂质含量(4.5~5.2 μg/g)符合药典标准。该方法突破了传统分析技术瓶颈,为中药多糖类成分的“成分-杂质”双标质量控制体系提供关键技术支撑。

关键词: 超高效液相色谱-串联质谱(UPLC-MS/MS), 黄芪多糖(APS), 杂质分析, 质量控制

Abstract: Astragalus polysaccharides (APS), as an important active component of traditional Chinese medicine, have impurities such as monosaccharides and phenolic acids remaining during its production process, which seriously affect the safety and efficacy of the drug. In order to control its quality, this study aimed to establish an analytical method for the simultaneous detection of trace monosaccharides and phenolic acids impurities in APS. A multi-dimensional detection method based on ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. The gradient elution program (acetonitrile -5 mmol/L ammonium formate, pH 4.5) was optimized by hydrophilic interaction chromatography (HILIC), and combined with the multi-reaction monitoring mode (MRM) of triple quadrupole mass spectrometry,the precise separation and quantification of monosaccharides (glucose, galactose) and phenolic acid (protocatechuic acid, caffeic acid) impurities were achieved. Methodological validation indicated that the detection limit of the target substance was 0.03-0.08 ng/mL, the linear range was 0.2-50 ng/mL (R2≥0.999 3), the recovery rate was 93.7%-104.1%, and the precision RSD was ≤5.5%. The actual sample tests showed that the total impurity content (4.5-5.2 μg/g) of the three batches of APS met the pharmacopoeia standards. This method broke through the bottleneck of traditional analytical techniques and provided key technical support for the "component-impurity" dual-standard quality control system of polysaccharide components in traditional Chinese medicine.

Key words: ultra-performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS), Astragalus polysaccharides(APS), impurity analysis, quality control

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