| 引用本文: | 毛菊华,陈张金,方洁,潘俊杰,吴查青,程科军.基于UPLC-MS/MS快速测定中药材中6种鞣质类成分[J].中国现代应用药学,2021,38(9):1055-1059. |
| MAO Juhua,CHEN Zhangjin,FANG Jie,PAN Junjie,WU Chaqing,CHENG Kejun.Rapid Determination of Six Tannins in Chinese Medicinal Materials Based on UPLC-MS/MS[J].Chin J Mod Appl Pharm(中国现代应用药学),2021,38(9):1055-1059. |
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| 摘要: |
| 目的 建立快速测定中药材中没食子酸、没食子酸甲酯、没食子酸乙酯、鞣花酸、3，3’-O-二甲基鞣花酸、柯里拉京6种鞣质类成分的超高效液相色谱串联质谱（UPLC-MS/MS）分析方法。方法 采用Agilent RRHD Eclipse Plus C18色谱柱（2.1 mm×50 mm，1.8 μm），流动相为甲醇-0.1%甲酸水溶液，梯度洗脱，流速0.3 mL·min-1，柱温40℃，进样量1 μL；三重四级杆质谱，采用电喷雾离子源、负离子模式，通过多重反应监测模式对15种中药材中6种鞣质类成分进行定量分析。结果 6种成分在各自浓度范围内线性关系良好（r>0.999），没食子酸、没食子酸甲酯、没食子酸乙酯、鞣花酸、3，3’-O-二甲基鞣花酸、柯里拉京的加样回收率分别为99.8%，98.3%，100.1%，100.3%，100.7%，99.2%，RSD值分别为1.11%，2.23%，1.07%，1.34%，1.64%，1.24%。15种中药材中均含一定量的没食子酸和没食子酸乙酯，且以五倍子中含量最高；鞣花酸含量以覆盆子根最高；另外3种成分不均匀分布于各药材中。结论 所建立的方法稳定、快速、灵敏度高，适用于含有上述6种鞣质类成分中药材的定量分析。 |
| 关键词: 中药材 没食子酸甲酯 没食子酸乙酯 3,3'-O-二甲基鞣花酸 柯里拉京 鞣质 UPLC-MS/MS |
| DOI：10.13748/j.cnki.issn1007-7693.2021.09.006 |
| 分类号:R284.1 |
| 基金项目:丽水市科技计划项目（2020zdhz01，2019GYX08）；中国民族医药学会科研项目（2017KYXM-M244-11） |
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| Rapid Determination of Six Tannins in Chinese Medicinal Materials Based on UPLC-MS/MS |
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MAO Juhua1, CHEN Zhangjin1, FANG Jie2, PAN Junjie2, WU Chaqing1, CHENG Kejun2
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1.Lishui Institute for Quality Inspection and Testing, Lishui 323000, China;2.Lishui Academy of Agricultural and Forestry Sciences, Lishui 323000, China
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| Abstract: |
| OBJECTIVE To develop an UPLC-MS/MS method for rapidly qualitative and quantitative determination of six tannins(gallic acid, methyl gallate, ethyl gallate, ellagic acid, 3,3'-Di-O-methylellagic acid, coriagin) in Chinese medicinal materials. METHODS An Agilent RRHD Eclipse Plus C18 column(2.1 mm×50 mm, 1.8 μm) with a gradient elution of methanol and 0.1%formic acid in water at a flow rate of 0.3 mL·min-1, the column temperature was 40℃, and the injection volume was 1 μL. Triple quadrupole mass spectrometry with electrospray ion source and negative ion mode was used to quantitatively analyze 6 tannins in 15 kinds of Chinese herbal medicines by multiple reaction monitoring mode. RESULTS Good linear relationship(r>0.999) were observed in the test ranges for 6 compounds, and the average recoveries of gallic acid, methyl gallate, ethyl gallate, ellagic acid, 3,3'-Di-O-methylellagic acid, coriagin were 99.8%(RSD=1.11%), 98.3%(RSD=2.23%), 100.1%(RSD=1.07%), 100.3%(RSD=1.34%), 100.7%(RSD=1.64%), 99.2%(RSD=1.24%), respectively. The gallic acid and ethyl gallate were detected in all 15 kinds of Chinese medicinal materials, and the content in Chinese gallnut was the maximum; the content of ellagic acid in Rubi Radix et Rhizoma was the highest; another 3 compounds were distributed in above drugs non-uniformly. CONCLUSION The established method is stable, rapid, sensitive, it can be used for the quantitative analysis of above six tannins in Chinese medicinal materials. |
| Key words: Chinese medicinal materials methyl gallate ethyl gallate 3,3’-Di-O-methylellagic acid coriagin tannins UPLC-MS/MS |
