Zhao Chen-Guang, Li Cun-Yu, Yang Shan, Xu Qi-Long, Zheng Yun-Feng, Wang Yu-Fu, Li Hong-Yang, Peng Guo-Ping
College of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, China.
College of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, China Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization Nanjing 210023, China.
Zhongguo Zhong Yao Za Zhi. 2020 Jul;45(13):3183-3190. doi: 10.19540/j.cnki.cjcmm.20200424.204.
This work is to establish the fingerprint of Astragalus membranaceus var. mongholicus by HPLC-ELSD method, and to analyze the simulated wildness degree of A. membranaceus var. mongholicus in the genuine region of Inner Mongolia, Ningxia and Gansu. Compared with wild A. membranaceus var. mongholicus, the quality differences of A. membranaceus var. mongholicus in the genuine region were analyzed by identification of chromatographic peaks and similarity evaluation, cluster analysis(CA), principal components analysis(PCA) and orthogonal partial least squares discriminant analysis(OPLS-DA). HPLC fingerprints of A. membranaceus var. mongholicus in different genuine regions are established. The qualitative analysis of mass spectrometry identified 18 components. The similarity evaluation shows that the similarity of 32 batches of A. membranaceus var. mongholicus samples was 0.688-0.993. Among them, the similarity of samples in Shanxi, Inner Mongolia, Ningxia is 0.688-0.993, 0.835-0.989, 0.934-0.988, respectively and the similarity of samples in Gansu is 0.729-0.876 except No. 25 sample. The results of CA show that the samples of A. membranaceus var. mongholicus can be grouped into four categories according to the production area except the No. 11 and No. 25 samples. The results of PCA indicate that 32 batches of A. membranaceus var. mongholicus samples can be clustered according to quality and origin, and the quality of A. membranaceus var. mongholicus in Inner Mongolia is the closest to the wild breed. The results of OPLS-DA indicate that there are six components that can distinguish the wild and domestic A. membranaceus var. mongholicus, which are malonylastragaloside Ⅰ, astragaloside Ⅰ, calycosin-7-O-β-D-glycoside-6″-O-malonate, calycosin-7-O-β-D-glycoside, formononetin-7-O-β-D-glycoside-6″-O-malonate, and astrapterocarpan-3-O-β-D-glycoside-6″-O-malonate. The established method can be used to analyze differences between A. membranaceus var. mongholicus origin and planting environment, and can provide references for the protection and replacement of wild A. membranaceus var. mongholicus resources, and the cultivation, processing and production of A. membranaceus var. mongholicus.
本研究旨在采用高效液相色谱 - 蒸发光散射检测法(HPLC - ELSD)建立蒙古黄芪的指纹图谱,并分析内蒙古、宁夏和甘肃道地产区蒙古黄芪的仿野生程度。通过色谱峰鉴定、相似度评价、聚类分析(CA)、主成分分析(PCA)和正交偏最小二乘法判别分析(OPLS - DA),比较野生蒙古黄芪,分析道地产区蒙古黄芪的质量差异。建立了不同道地产区蒙古黄芪的HPLC指纹图谱。质谱定性分析鉴定出18种成分。相似度评价结果显示,32批次蒙古黄芪样品的相似度为0.688 - 0.993。其中,山西、内蒙古、宁夏样品的相似度分别为0.688 - 0.993、0.835 - 0.989、0.934 - 0.988,甘肃样品(除25号样品外)的相似度为0.729 - 0.876。聚类分析结果表明,除11号和25号样品外,蒙古黄芪样品可按产地分为四类。主成分分析结果表明,32批次蒙古黄芪样品可按质量和产地聚类,内蒙古蒙古黄芪的质量最接近野生品种。正交偏最小二乘法判别分析结果表明,有6种成分可区分野生和栽培蒙古黄芪,分别为丙二酰黄芪甲苷Ⅰ、黄芪甲苷Ⅰ、毛蕊异黄酮 - 7 - O - β - D - 葡萄糖苷 - 6″ - O - 丙二酸酯、毛蕊异黄酮 - 7 - O - β - D - 葡萄糖苷、芒柄花素 - 7 - O - β - D - 葡萄糖苷 - 6″ - O - 丙二酸酯和紫云英苷 - 3 - O - β - D - 葡萄糖苷 - 6″ - O - 丙二酸酯。所建立的方法可用于分析蒙古黄芪产地与种植环境之间的差异,为野生蒙古黄芪资源的保护与替代以及蒙古黄芪的栽培、加工和生产提供参考。