Article ID Journal Published Year Pages File Type
2474844 Acta Pharmaceutica Sinica B 2013 10 Pages PDF
Abstract

To identify the chemical differences which lead to the different therapeutic effects of dried rehmannia root (DRR) and prepared rehmannia root (PRR), we compared the chemical composition of decoctions of randomly purchased DRR and PRR using ultra performance liquid chromatography (UPLC) coupled with time-of-flight mass spectrometry and high performance liquid chromatography (HPLC) coupled with evaporative light scattering detection (ELSD) with the aid of multivariate statistical analysis. Both approaches clearly revealed compositional and quantitative differences between DRR and PRR. UPLC-MS data indicated stachyose, rehmaionoside A (or rehmaionoside B), acteoside (or forsythiaside, or isoacteoside), 6-O-coumaroylajugol (or 6-O-E-feruloylajugol, or 6-O-Z-feruloylajugol) as important discriminators between DRR and PRR decoctions. HPLC-ELSD analysis showed that the content of fructose in the decoctions of PRR was about four times greater than that of DRR (P<10−5), while sucrose content in the decoctions of PRR was only about one seventh of that in DRR (P<0.01). Our results suggest that some compounds, such as fructose, stachyose and rehmaionoside, may be responsible for the differing therapeutic effects of DRR and PRR. Furthermore, improvements in quality control for PRR, which is currently lacking in the Chinese Pharmacopoeia, are recommended.

A chemical comparison between the decoctions of randomly purchased dried rehmannia root and prepared rehmannia root using ultra performance liquid chromatography coupled with time-of-flight mass spectrometry and high performance liquid chromatography coupled with evaporative light scattering detection with the aid of multivariate statistical analysis was made in order to identify chemical differences which may explain the therapeutic differences between DRR and PRR .Figure optionsDownload full-size imageDownload as PowerPoint slide

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Health Sciences Pharmacology, Toxicology and Pharmaceutical Science Drug Discovery
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