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钩藤药材的特征图谱建立、化学模式识别分析及其与不同基原、
混伪品的鉴别
Δ
何雨晴 1, 2, 3, 4* ,陈盛君 2, 3, 4 # ,周海琴 2, 3, 4 ,钱 润 2, 3, 4 ,顾 超 2, 3, 4 ,谢思梅 1, 2, 3, 4 ,文红梅(1.南京中医药大学药学
1
院,南京 210023;2.江阴天江药业有限公司技术中心,江苏 江阴 214434;3.江苏省中药配方颗粒制备与质量
控制关键技术重点实验室,江苏 江阴 214434;4.江苏省中药配方颗粒工程技术中心,江苏 江阴 214434)
中图分类号 R917 文献标志码 A 文章编号 1001-0408(2024)05-0566-06
DOI 10.6039/j.issn.1001-0408.2024.05.10
摘 要 目的 建立不同产地钩藤药材超高效液相色谱(UPLC)特征图谱,并进行化学模式识别分析,同时对钩藤不同基原样品及
其混伪品进行鉴别。方法 采用UPLC法建立43批不同产地钩藤药材的特征图谱,结合聚类分析及主成分分析对其进行质量分
析,然后对钩藤不同基原样品及其混伪品进行鉴别。结果 建立了钩藤药材UPLC特征图谱,标定了13个共有峰,并指认峰2为儿
茶素、峰3为绿原酸、峰4为隐绿原酸、峰7为异绿原酸B、峰8为异去氢钩藤碱、峰9为异钩藤碱、峰10为去氢钩藤碱、峰11为异绿
原酸C、峰12为钩藤碱和峰13为喜果苷。通过聚类分析可将43批钩藤药材按照产地分为5类。进一步通过主成分分析发现,江
西、湖南产钩藤药材主成分综合得分较高,为0.264~2.904分。通过特征图谱可将钩藤不同基原样品及其混伪品进行有效区分。
结论 建立的UPLC特征图谱可用于钩藤药材的质量控制,且本研究发现江西、湖南产钩藤药材质量较优。
关键词 钩藤;超高液相色谱;不同基原;聚类分析;主成分分析;真伪鉴别
Establishment of specific chromatogram, chemical pattern recognition analysis and identification with
different origins and counterfeit products of Uncariae Ramulus Cum Uncis
HE Yuqing 1, 2, 3, 4 ,CHEN Shengjun 2, 3, 4 ,ZHOU Haiqin 2, 3, 4 ,QIAN Run 2, 3, 4 ,GU Chao 2, 3, 4 ,XIE Simei 1, 2, 3, 4 ,WEN
Hongmei(1. School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China;2. Jiangyin
1
Tianjiang Pharmaceutical Co., Ltd. Technical Center, Jiangsu Jiangyin 214434, China;3. Key Laboratory of
Key Technologies for Preparation and Quality Control of Traditional Chinese Medicine Formula Granules in
Jiangsu Province, Jiangsu Jiangyin 214434,China;4. Jiangsu Provincial Traditional Chinese Medicine Formula
Granule Engineering Technology Center, Jiangsu Jiangyin 214434, China)
ABSTRACT OBJECTIVE To establish the ultra-high liquid chromatography (UPLC) characteristic spectrum of Uncariae
Ramulus Cum Uncis from different producing areas, to conduct chemical pattern recognition analysis, and to identify the medicinal
materials of their different origins and counterfeit products. METHODS UPLC method was adopted to establish the characteristic
spectra of 43 batches of Uncariae Ramulus Cum Uncis from different origins; cluster analysis combined with principal component
analysis were used to analyze their quality; Uncariae Ramulus Cum Uncis from different origins and counterfeit products were
identified. RESULTS UPLC specific spectrum of Uncariae Ramulus Cum Uncis was established, and 13 common peaks were
calibrated; peak 2 was identified as catechin, peak 3 as chlorogenic acid, peak 4 as cryptochlorogenic acid, peak 7 as
isochlorogenic acid B, peak 8 as isodehydroguotenine, peak 9 as isooguotenine, peak 10 as dehydroguotenine, peak 11 as
isochlorogenic acid C, peak 12 as goutenine, and peak 13 as camptothecin. Through cluster analysis, the medicinal materials of 43
batches of Uncariae Ramulus Cum Uncis could be divided into 5 categories according to their different origins. Further principal
component analysis revealed that the principal component comprehensive scores of Uncariae Ramulus Cum Uncis produced in
Jiangxi and Hunan were relatively high, ranging from 0.264 to 2.904. The specific chromatogram could effectively distinguish
among the different origins and their counterfeit products of Uncariae Ramulus Cum Uncis. CONCLUSIONS The established
UPLC specific chromatogram can be used for quality control of Uncariae Ramulus Cum Uncis, and the study found that the quality
of Uncariae Ramulus Cum Uncis from Jiangxi and Hunan
Δ 基金项目 江苏省科技成果转化专项(No.BA2021018) provinces is relatively good.
*第一作者 硕士研究生。研究方向:中药制药技术与产品研发。
E-mail:1367259523@qq.com KEYWORDS Uncariae Ramulus Cum Uncis; ultra-high
# 通信作者 主任药师,硕士生导师,博士。研究方向:中药配方颗 liquid chromatography; different origins; cluster analysis;
粒及经典名方研究开发。E-mail:chensj@tianjiang.com principal component analysis; authenticity identification
· 566 · China Pharmacy 2024 Vol. 35 No. 5 中国药房 2024年第35卷第5期