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基于化学计量学和气相色谱法的艾叶及其混伪品蒙古蒿叶差异性特征成分和鉴别规律的研究*

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  • 1.河南省药品医疗器械检验院(河南省疫苗批签中心) 国家药品监督管理局中药材及饮片质量控制重点实验室,郑州 450008;
    2.中国食品药品检定研究院,北京 102629
第一作者 Tel:(0371)65566039;E-mail:878348987@qq.com
**王海波 Tel:(0371)65566577;E-mail:haibowang99@163.com
石 岩 Tel:(010)53852081;E-mail:shiyan@nifdc.org.cn

收稿日期: 2023-08-31

  网络出版日期: 2024-06-20

基金资助

*中国药品监管科学行动计划第二批重点项目(NMPAJGKX-2023-030);河南省科技厅科技攻关项目(222102310110);国家局药品监管科学体系建设重点项目-新技术新方法在中药质量控制中的应用(RS2024Z006-035)

Identification of Artemisiae Argyi Folium and Artemisiae Mongolica Folium based on gas chromatography and chemometric techniques*

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  • 1. Henan Institute for Drug and Medical Device InspectionHenan Vaccine Issuance Center, NMPA Key Laboratory for Quality Control of Traditional Chinese Medicine Chinese Materia Medica and Prepared Slices, Zhengzhou 450008,China;
    2. National Institutes for Food and Drug Control, Beijing 102629, China

Received date: 2023-08-31

  Online published: 2024-06-20

摘要

目的: 以气相色谱和化学计量学技术为化学分析和数据分析手段,研究艾叶及其混伪品蒙古蒿叶的鉴别方法及化学成分分布规律。方法: 采用Agilent HP-5 19091J(30 m×0.32 mm,0.25 μm)色谱柱进行分离,使用氢火焰离子检测器进行检测,建立了气相色谱化学分析方法,指认了其中21个化学成分,使用该法对29批样品进行测定。采用化学计量学相关技术对色谱数据进行相似度分析、相关性分析、聚类分析、主成分分析和正交偏最小二乘判别分析。结果: 色谱峰峰20(母菊薁)、峰3(桉油精)和峰19[(1S,8aα)-十氢-1,4aβ-二甲基-7β-异丙烯基-1-萘酚]是艾叶与蒙古蒿叶的差异特征色谱峰(化学成分),艾叶和蒙古蒿叶样品的峰3与峰20峰面积比值范围分别为54.50~348.39和0.16~0.87,峰19与峰20峰面积比值范围分别为18.55~128.46和0.01~0.14,正品与混伪品之间有巨大差异,可用于艾叶与蒙古蒿叶的鉴别。结论: 本研究得出的艾叶与蒙古蒿叶的差异特征化学成分及其分布规律对艾叶及相关药品的研究和分析具有一定的参考意义。

本文引用格式

张文静, 李海燕, 王晓伟, 王海波, 李向阳, 李桂本, 张红伟, 耿怡玮, 杨元, 石岩 . 基于化学计量学和气相色谱法的艾叶及其混伪品蒙古蒿叶差异性特征成分和鉴别规律的研究*[J]. 药物分析杂志, 2024 , 44(4) : 649 -662 . DOI: 10.16155/j.0254-1793.2024.04.12

Abstract

Objective: To study and establish a method based on gas chromatography and chemometrics techniques for distinguishing Artemisiae Argyi Folium and its adulterants Artemisiae Mongolica Folium. Methods: Gas chromatography method was established with Agilent HP-5 19091J (30 m×0.32 mm, 0.25 μm) as chromatographic column, and hydrogen flame ion detector (FID) as detector. After the chemical composition of 21 chromatographic peaks in the chromatogram were identified, and the peak area data of the 21 chromatographic peaks in 29 batches of samples were determined. Similarity analysis, correlation analysis, cluster analysis, principal component analysis and orthogonal partial least squares-discriminant analysis were applied to analyze the chromatographic data. Results: The results of chemometric analysis indicated that tpeak 20 (chamazulene), peak 3 (1,8-cineole) and peak 19((1S,8aα)-decahydro-1,4aβ-dimethyl-7β-isopropenyl-1-naphthol) were the differential characteristic chromatographic peaks between Artemisiae Argyi Folium and its adulterants Artemisiae Mongolica Folium. The ratios of the peak areas of peak 3 to peak 20 were in the ranges of 54.50-348.39 and 0.16-0.87 respectively, and the ratios of the peak areas of peak 19 to peak 20 were in the ranges of 18.55-128.46 and 0.01-0.14 respectively. These significant differences could be used for the identification of Artemisiae Argyi Folium and its adulterant Artemisiae Mongolica Folium. Conclusion: The research findings can be used for the identification of Artemisiae Argyi Folium and its adulterant Artemisiae Mongolica Folium, and these have certain reference significance for the research and analysis of Artemisiae Argyi Folium and related drugs.

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