Quality evaluation of Panax notoginseng (Burk.) FH Chen using supercritical fluid chromatography-mass spectrometry and chemical pattern recognition

被引:2
|
作者
Mei, Jie [1 ]
Huang, Yang [2 ,3 ,4 ]
Crommen, Jacques [6 ]
Zha, Dingsheng [7 ]
Jiang, Zhengjin [1 ,5 ]
Zhang, Tingting [1 ]
机构
[1] Jinan Univ, Inst Pharmaceut Anal, Coll Pharm, Guangzhou 510632, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Sch Pharmaceut Sci, Guangzhou Municipal & Guangdong Prov Key Lab Mol, NMPA, Guangzhou 511436, Peoples R China
[3] Guangzhou Med Univ, Sch Pharmaceut Sci, State Key Lab Resp Dis, Guangzhou 511436, Peoples R China
[4] Guangzhou Med Univ, Affiliated Hosp 5, Guangzhou 511436, Peoples R China
[5] Jinan Univ, Guangdong Prov Key Lab Pharmacodynam Constituents, Guangzhou 510632, Peoples R China
[6] Univ Liege, Ctr Interdisciplinary Res Med CIRM, Lab Anal Med, Quartier H op, Ave Hippocrate 15, B-4000 Liege, Belgium
[7] Jinan Univ, Affiliated Hosp 1, Dept Orthopaed, Guangzhou 510630, Peoples R China
基金
对外科技合作项目(国际科技项目);
关键词
Panax Notoginseng (Burk) FH Chen; Supercritical fluid chromatography-mass spectrometry; Chemical pattern recognition; Quality evaluation; LIQUID-CHROMATOGRAPHY; L-ASPARAGINASE; SAPONINS; GINSENG;
D O I
10.1016/j.jpba.2022.115029
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An efficient supercritical fluid chromatography-mass spectrometry (SFC-MS) method was developed for the quality evaluation of Panax Notoginseng (Burk) F.H. Chen (P. notoginseng) by combination with chemical pattern recognition (CPR). Design of experiments (DoE) was applied to obtain optimal SFC-MS conditions. Several CPR methods including hierarchical cluster analysis (HCA), principal component analysis (PCA) and partial least squares discriminant analysis (PLS-DA) were employed to establish a classification model based on the peak areas and contents of 12 components in P. notoginseng in order to evaluate the quality difference according to the collecting time (Chunqi and Dongqi) and medicinal parts (fibrous root, rhizome, branch root, and main root). PLS-DA has proved to be a satisfactory method with accurate discrimination of the selected samples. The characteristic variables based on the variable importance in projection (VIP) values were selected using PLS-DA. Three characteristic components (ginsenoside Rg(2), ginsenoside Rg(1), ginsenoside Rb-1) with higher VIP values (>1) were chosen to further build the CPR model. Subsequently, the model was verified by testing another set of samples and the results indicated that the established model was satisfactory. PLS-DA models based on the peak areas of the 12 selected analytes in 30 batches of P. notoginseng could give accurate classification. The obtained results demonstrate that the developed method using SFC-MS and PLS-DA has a great potential for the quality assessment of P. notoginseng.
引用
收藏
页数:8
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