Zhang Cuiying, Chen Shilin, Dong Liang
Se Pu. 2015 May;33(5):514-21. doi: 10.3724/sp.j.1123.2015.01018.
Ginseng Radix et Rhizoma (GRR, also named as white ginseng), Ginseng Radix et Rhizoma Rubra (GRR Rubra. also named as red ginseng), Ginseng Folium (GF) and Ginseng Rootlet (GR) products from Asian ginseng, one of the well-known Chinese traditional medicine for thousands of years, are now widely used around the world. Thus the comprehensive quality control is of paramount concern basing on the contents of the bioactive ginsenosides. A rapid, sensitive and reliable method of ultra-performance liquid chromatography coupled with a photodiode array detection (UPLC-PAD) was developed for the quantitative analysis of the 12 ginsenosides in the four commercial ginseng products of Asian ginseng. The chromatography was performed on an ACQUITY UPLC™ BEH C18 column using a gradient elution with acetonitrile/water as the mobile phases. Method validation including calibration curves, accuracies, precisions, repeatabilities and recoveries was investigated. The contents of the 12 ginsenosides were determined in 20 GRR, 4 GF, 4 GR and 11 GRR Rubra samples. To evaluate the sample quality. chenometric methods including hierarchical cluster analysis (HCA) and principal components analysis (PCA) were engaged in evaluating the GRR, GRR Rubra, GF and GR products from Asian ginseng. The results showed that HCA and PCA can be considered as the attractive chemometric techniques in situations where high sample throughput and multiple analytes are required.
人参(GRR,也称为白参)、红参(GRR Rubra,也称为红参)、人参叶(GF)和人参须(GR)均源自亚洲人参,作为一种传承数千年的著名中药,目前在世界各地广泛使用。因此,基于生物活性人参皂苷的含量进行全面质量控制至关重要。建立了一种快速、灵敏且可靠的超高效液相色谱-光电二极管阵列检测法(UPLC-PAD),用于定量分析亚洲人参四种商业产品中的12种人参皂苷。色谱分析在ACQUITY UPLC™ BEH C18柱上进行,以乙腈/水为流动相进行梯度洗脱。考察了方法验证,包括校准曲线、准确度、精密度、重复性和回收率。测定了20个GRR、4个GF、4个GR和11个GRR Rubra样品中12种人参皂苷的含量。为了评估样品质量,采用聚类分析(HCA)和主成分分析(PCA)等化学计量学方法对亚洲人参的GRR、GRR Rubra、GF和GR产品进行评价。结果表明,在需要高样品通量和多种分析物的情况下,HCA和PCA可被视为有吸引力的化学计量学技术。