食品科学 ›› 2025, Vol. 46 ›› Issue (8): 259-266.doi: 10.7506/spkx1002-6630-20241031-206

• 成分分析 • 上一篇    下一篇

质谱导向高效液相色谱一测多评测定葛根提取物中异黄酮的相对含量

农金梅,韩默,吴四清,李立兵,邓后勤   

  1. (1.湖南农业大学食品科学技术学院,湖南?长沙 410128;2.湖南九维生物医药有限公司,湖南?长沙 410125)
  • 出版日期:2025-04-25 发布日期:2025-04-09

Determination of Relative Contents of Isoflavones in Radix Puerariae Extract by Mass Spectrometry Guided High Performance Liquid Chromatography Using Quantitative Analysis of Multi-component with Single Marker

NONG Jinmei, HAN Mo, WU Siqing, LI Libing, DENG Houqin   

  1. (1. College of Food Science and Technology, Hunan Agricultural University, Changsha 410128, China;2. Hunan Jiuwei Biopharmaceutical Co. Ltd., Changsha 410125, China)
  • Online:2025-04-25 Published:2025-04-09

摘要: 建立一种质谱(mass spectrometry,MS)定性鉴别结合高效液相色谱(high performance liquid chromatography,HPLC)法定量分析,并以葛根素为单一外标物的一测多评测定葛根提取物中多种异黄酮类成分相对含量的方法,为保健食品中提取物原料的综合评价提供参考。使用EcoPak C18 Plus色谱柱(4.6 mm×150 mm,5 μm),以中药材葛根饮片为对照样优化的色谱条件为:流动相体系0.1%氨水溶液(pH 7.5)-乙腈-甲醇(梯度洗脱),进样体积10 μL,检测波长250 nm,柱温(35±0.2)℃,流速0.8 mL/min;MS条件为电喷雾离子源,全离子扫描,负离子模式检测,扫描范围m/z 200~1 000,电喷雾电压12 000 psi,离子源温度为600 ℃,载气为氮气。结果表明,葛根饮片中异黄酮化合物的分离度良好,高效液相色谱-紫外(high performance liquid chromatography-ultra violet,HPLC-UV)检测中21 个色谱峰重复性较好(相对标准偏差(relative standard deviation,RSD)<0.7%);MS的21 个离子流峰的保留时间重复性良好(RSD<1.0%),且两者的保留时间可相对应。结合文献研究鉴定了18 个葛根异黄酮化合物发现葛根素质量浓度在0.052~500 μg/mL线性范围内线性关系良好(R2=0.999 2),检出限为0.015 µg/mL(信噪比≥3),同时以葛根素为参照,相对定量了18 种葛根异黄酮化合物的含量。植物提取物成分复杂,以质谱定性鉴别具有用量少、操作简单、快速准确的特点,本研究方法可更低成本、方便快捷的综合评价提取物的品质,为葛根类药食同源物质在保健食品开发和应用提供参考。

关键词: 高效液相色谱-质谱法;葛根;异黄酮;一测多评

Abstract: This study developed a method for the qualitative and quantitative analysis of isoflavones in Radix Puerariae extract using mass spectrometry (MS) and high performance liquid chromatography (HPLC). The relative contents of various kinds of isoflavones in the extract were determined using the quantitative analysis of multi-component with single marker (QAMS) method with puerarin as a single external standard. Chromatography was accomplished using a EcoPak C18 Plus column (4.6 mm × 150 mm, 5 μm). Using Radix Puerariae slices as control, the optimized chromatographic conditions were determined as follows: elution with a mobile phase consisting of 0.1% ammonia solution (pH 7.5), acetonitrile and methanol at a flow rate of 0.8 mL/min, an injection volume of 10 μL, column temperature of (35 ± 0.2) ℃, and detection wavelength of 250 nm. The MS conditions were set as follows: electrospray ionization source (ESI), full scan mode, negative ion mode detection, scan range of m/z 200–1 000, electrospray voltage of 12 000 psi, ion source temperature of 600 ℃, and nitrogen as carrier gas. The results showed that the separation of isoflavone compounds from Radix Puerariae slices was good, and 21 peaks were obtained with good reproducibility by HPLC with an ultra violet (HPLC-UV) (relative standard deviations (RSD) < 0.7%). The retention time reproducibility of 21 ion current peaks in MS was good (RSD < 1.0%), and the retention times of the chromatographic and ion current peaks were matched with each other. Totally 18 isoflavones were identified based on relevant literature. Good linearity was observed within the puerarin range of 0.052–500 μg/mL (R2 = 0.999 2), and the detection limit was 0.015 µg/mL (RSN ≥ 3). Furthermore, using puerarin as a reference standard, the contents of the 18 isoflavone compounds were relatively quantified. MS is useful for qualitative identification of plant extracts, which has complex composition, with the advantages of low consumption of materials, simple operation, rapidity and accurate results. The method proposed in this study can comprehensively evaluate the quality of extracts at a lower cost and conveniently, providing a reference for the development and application of Radix Puerariae as both an edible and medicinal material in health foods.

Key words: high performance liquid chromatography-mass spectrometry; Radix Puerariae; isoflavones; quantitative analysis of multi-components with single marker

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