成分分析

一测多评法测定艾叶中7个黄酮类成分的含量*

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  • 齐齐哈尔大学化学与化学工程学院 黑龙江省工业大麻加工技术创新中心 国家市场监管技术创新中心(工业大麻),齐齐哈尔 161006
第一作者 Tel:(045)22742562;E-mail:ssunliqiu@163.com
** Tel:(045)22742562;E-mail:chou2035@sina.com

收稿日期: 2023-04-26

  网络出版日期: 2024-06-20

基金资助

* 黑龙江省省属高等学校基本科研业务费科研项目(145109512)

Simultaneous determination of seven flavanoids in Artemisiae Argyi Folium by quantitative analysis of multi-components by single marker*

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  • College of Chemistry and Chemical Engineering, Qiqihar University, Heilongjiang Industrial Hemp Processing Technology Innovation Center, Technology Innovation Center of Industrial Hemp for State Market Regulation, Qiqihar 161006, China

Received date: 2023-04-26

  Online published: 2024-06-20

摘要

目的:建立同时测定艾叶中7个黄酮类成分(5-羟基-6,7,3’,4’-四甲氧基黄酮、芹菜素、高车前素、山柰酚、棕矢车菊素、异泽兰黄素、蔓荆子黄素)的一测多评含量测定方法(QAMS法)。方法:采用高效液相色谱法,Agilent ZORBAX SB-C18色谱柱(150 mm×4.6 mm,5 μm),以乙腈-0.2%磷酸水溶液为洗脱流动相,进行梯度洗脱,流速1.0 mL·min-1,检测波长350 nm,柱温30 ℃。以异泽兰黄素为内参物,建立与其他6个黄酮类成分的相对校正因子,并计算7个待测成分的含量,实现一测多评。同时与外标法进行比较,以验证QAMS法的准确性和可行性。结果:在一定的线性范围内,异泽兰黄素与5-羟基-6,7,3’,4’-四甲氧基黄酮、芹菜素、高车前素、山柰酚、棕矢车菊素、蔓荆子黄素的相对校正因子值分别为0.958、1.387、1.000、0.950、0.957、1.297(相对校正因子的RSD<2.0%),并与常规外标一点法比较,20批艾叶中5-羟基-6,7,3’,4’-四甲氧基黄酮、芹菜素、高车前素、山柰酚、棕矢车菊素、异泽兰黄素、蔓荆子黄素的含量测定结果分别为0.031 4~0.623 5、0.000 9~0.092 6、0.020 6~0.170 7、0.011 0~0.184 7、0.011 7~0.864 0、0.253 2~2.555 0、0.015 6~0.250 7 mg·g-1结论:以异泽兰黄素为内参物,建立艾叶中7个黄酮类成分的QAMS法准确、可行,可用于艾叶的定量分析及质量控制。

本文引用格式

孙立秋, 王丹, 赵英楠, 时志春, 李军, 王金兰, 赵明, 张树军 . 一测多评法测定艾叶中7个黄酮类成分的含量*[J]. 药物分析杂志, 2024 , 44(5) : 806 -815 . DOI: 10.16155/j.0254-1793.2024.05.08

Abstract

Objective: To establish a quantitative analysis of multi-components by single marker (QAMS) for simultaneous determination of 7 flavanoids (5-hydroxy-6, 7, 3’, 4’-tetramethoxyflavone, apigenin, hispidulin, kaempferol, jaceosidin, eupatilin and casticin) in Artemisiae Argyi Folium. Methods: The HPLC system consisted of the Agilent ZORBAX SB-C18 column (150 mm×4.6 mm, 5 μm) column with gradient elution of acetonitrile and 0.2% phosphoric acid as the mobile phase at a flow rate of 1.0 mL·min-1, a detection wavelength of 350 nm, and a column temperature of 30 ℃. Eupatilin was selected as the internal reference substance, the relative correction factors between eupatilin and the other 6 flavanoids were established, and the contents of these 7 constituents in samples were calculated to realize QAMS. At the same time, compared with the external standard method to verify the accuracy and feasibility of the QAMS method. Results: Within a certain linear range, the relative correction factors between eupatilin and 5-hydroxy-6, 7, 3’, 4’-tetramethoxyflavone, apigenin, hispidulin, kaempferol, jaceosidin as well as casticin were 0.958, 1.387, 1.000, 0.950, 0.957 and 1.297, respectively (RSDs of RCFs were less than 2.0%). The contents of 5-hydroxy-6, 7, 3’, 4’-tetramethoxyflavone, apigenin, hispidulin, kaempferol, jaceosidin, eupatilin, casticin in 20 batches of Artemisiae Argyi Folium were 0.031 4-0.623 5 mg·g-1, 0.000 9-0.092 6 mg·g-1, 0.020 6-0.170 7 mg·g-1, 0.011 0-0.184 7 mg·g-1, 0.011 7-0.864 0 mg·g-1, 0.253 2-2.555 0 mg·g-1 and 0.015 6-0.250 7 mg·g-1, respectively. Conclusion: Using eupatilin as the internal reference, QAMS method for 7 flavanoids is established. The method is accurate and reliable, and can be used for quality control and quantitative analysis of Artemisiae Argyi Folium.

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