生地黄低聚糖部位的HPLC指纹图谱  

HPLC Fingerprint for Oligosaccharide Site Unprocessed Rehmanniae Radix

作　　者：张杰[1] 刘炯[1] 张萌[1] 于雷[1] 杨云[1] 

机构地区：[1]河南中医学院药学院,郑州450046

出　　处：《中国实验方剂学杂志》2014年第22期41-44,共4页Chinese Journal of Experimental Traditional Medical Formulae

基　　金：国家"十二五"科技支撑计划项目(2011BAIO06B02)

摘　　要：目的:确定生地黄的低聚糖部位HPLC指纹图谱的测定方法,为道地产区生地黄以低聚糖类成分为指标的内在质量控制提供参考。方法:Agilent Zorbax NH2色谱柱(4.6 mm×250 mm,5μm),流动相乙腈-水梯度洗脱,流速1.0 m L·min-1,柱温30℃,进样量20μL,检测器ELSD,漂移管温度90℃,氮气流速3.0 L·min-1,增益量10,采用聚类分析和相似度分析对指纹图谱进行化学模式识别。结果:13批生地黄低聚糖成分的各个色谱峰都得到了有效分离,确定了12个峰的特征指纹图谱,指认了其中的6个峰,样品分为了两类。结论:建立的HPLC指纹图谱可为生地黄以糖类成分为指标的内在质量控制提供依据。Objective： The aim of this paper was to study the HPLC fingerprint for oligosaccharides site in Rehmanniae Radix,and to provide reference for Rehmanniae Radix of the quality control according to the oligosaccharide composition. Method： Analysis was performed on an Agilent Zorbax NH2column（ 4. 6 mm × 250 mm,5 μm）,with the acetonitrile-water as mobile phase in gradient elution mode. The flow rate was set at 1. 0m L·min^-1. The column temperature was maintained at 30 ℃. The injection volume was 20 μL. The detector was ELSD,drift tube temperature was set at 90 ℃,nitrogen flow rate was set at 3. 0 L·min^-1,and the gain volume was 10. Cluster analysis and principal component analysis were used to fingerprint pattern recognition. Result：Various peaks of thirteen batches of samples have been separated,and 12 peaks were identified as characteristic fingerprints in which six peaks were defined. And samples were divided into two categories. Conclusion： The established HPLC fingerprint can provide the basis for the quality control of Rehmanniae Radix.

关 键 词：怀地黄 生地黄 低聚糖 高效液相色谱指纹图谱 

分 类 号：R284.1[医药卫生—中药学]