OBJECTIVE: The method was established to identify Panax ginseng, P. quinquefolium and P. notoginseng. METHOD: Polaris C18-A analytical column (250 mm x 4.6 mm, 5 microns); acetonitrile-water as gradient eluent, flow rate 1.5 ml.min-1, detective wavelength at 203 nm. RESULT AND CONCLUSION: The fingerprints of P. ginseng, P. quinquefolium and P. notoginseng were obtained, and all ginsenosides were analyzed perfectly. The peak height ratio of ginsenoside Rg1 and ginsenoside Re was a suitable character to differentiate the three species from each other.
OBJECTIVE: The method was established to identify Panax ginseng, P. quinquefolium and P. notoginseng. METHOD: Polaris C18-A analytical column (250 mm x 4.6 mm, 5 microns); acetonitrile-water as gradient eluent, flow rate 1.5 ml.min-1, detective wavelength at 203 nm. RESULT AND CONCLUSION: The fingerprints of P. ginseng, P. quinquefolium and P. notoginseng were obtained, and all ginsenosides were analyzed perfectly. The peak height ratio of ginsenoside Rg1 and ginsenoside Re was a suitable character to differentiate the three species from each other.