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不同产地九节木根HPLC指纹图谱研究
引用本文:勾玲,张月华,陈玫伶,李彦媚,黄庆华,苏培丽,卢海啸.不同产地九节木根HPLC指纹图谱研究[J].世界科学技术-中医药现代化,2021,23(10):3757-3764.
作者姓名:勾玲  张月华  陈玫伶  李彦媚  黄庆华  苏培丽  卢海啸
作者单位:玉林师范学院生物与制药学院 玉林 537000,玉林师范学院生物与制药学院 玉林 537000,玉林师范学院生物与制药学院 玉林 537000,玉林师范学院生物与制药学院 玉林 537000,玉林师范学院生物与制药学院 玉林 537000,玉林师范学院生物与制药学院 玉林 537000,玉林师范学院生物与制药学院 玉林 537000;玉林师范学院生物与制药学院/广西农产资源化学与生物技术重点实验室 玉林 537000
基金项目:广西自然科学基金委员会面上项目(2015GXNSFAA139103):九节木的抗阿尔茨海默病活性成分研究,负责人:卢海啸。
摘    要:目的 建立九节木根的HPLC指纹图谱,综合比较不同产地的九节木根质量,为九节木根药材质量控制提供参考。方法 采用Kromasil C18 色谱柱(4.6 mm×250 mm,5 μm);以乙腈(A)-0.4%磷酸溶液(B)为流动相,梯度洗脱;检测波长为232 nm;流速为1 mL·min-1;进样量为10 μL。利用“中药色谱指纹图谱相似度评价系统(2004A版)”计算相似度,SPSS21软件进行聚类分析和主成分分析,比较不同产地九节木根样品的指纹图谱。结果 建立九节木根的HPLC指纹图谱,确定了29个共有峰。10批九节木根指纹图谱与对照图谱的相似度为0.922-0.996,10批次样品聚为3类。结论 该研究建立的九节木根指纹图谱具有较高的重现性、稳定性及专属性,为九节木药材的质量控制和评价的依据。

关 键 词:九节木  HPLC  指纹图谱  聚类分析  主成分分析
收稿时间:2020/9/19 0:00:00
修稿时间:2021/10/20 0:00:00

Study on the HPLC Fingerprint of Psychotria rubra Root from Different Regions
Gou Ling,Zhang Yuehu,Chen Meiling,Li Yanmei,Huang Qinghu,Su Peili and Lu Haixiao.Study on the HPLC Fingerprint of Psychotria rubra Root from Different Regions[J].World Science and Technology-Modernization of Traditional Chinese Medicine,2021,23(10):3757-3764.
Authors:Gou Ling  Zhang Yuehu  Chen Meiling  Li Yanmei  Huang Qinghu  Su Peili and Lu Haixiao
Institution:College of Biology and Pharmacy of Yulin Normal University, Yulin 537000, China,College of Biology and Pharmacy of Yulin Normal University, Yulin 537000, China,College of Biology and Pharmacy of Yulin Normal University, Yulin 537000, China,College of Biology and Pharmacy of Yulin Normal University, Yulin 537000, China,College of Biology and Pharmacy of Yulin Normal University, Yulin 537000, China,College of Biology and Pharmacy of Yulin Normal University, Yulin 537000, China,College of Biology and Pharmacy of Yulin Normal University, Yulin 537000, China;Guangxi Key Laboratory of Agricultural Resources Chemistry and Biotechnology of Yulin Normal University, Yulin 537000, China
Abstract:Objective To establish the HPLC fingerprint of root from Psychotria rubra, and comprehensively compare the quality of Psychotria rubra root from different producing areas, so as to provide reference for the quality control of Psychotria rubra root.Methods The chromatographic separation was performed on a Kromasil C18 column (4.6 mm×250 mm, 5 um). The mobile phase was acetonitrile (A) -0.4% phosphoric acid (B) with gradient elution. The detection wavelength was 232 nm, and the flow rate was 1.0 mL·min-1, and injection volume was 10 uL. The fingerprint was compared for similarity by using "Traditional Chinese Medicine Chromatographic Fingerprint Similarity Evaluation System (2004 A)". Cluster analysis and principal component analysis were adopted in SPSS21, and the HPLC chromatograms from Different Regions of Psychotria rubra root were compared.Results The HPLC fingerprint of Psychotria rubra root was established and 29 common peaks were designated. The similarities of 10 batchdes of samples were from 0.922 to 0.996. The 10 batches of samples were clustered into 3 categories.Conclusion The fingerprint of Psychotria rubra root established in this study has high reproducibility, stability and specificity, which is the basis for the quality control and evaluation of Psychotria rubra.
Keywords:Psychotria rubra  HPLC  Fingerprint  Cluster analysis  Principal component analysis
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