Separation and Determination of the Major Active Components in Tibetan Folk Medicinal Species Swertia franchetiana by HPLC with DAD

Abstract

A sensitive and specific reversed‐phase high performance liquid chromatography (RP‐HPLC) method with diode array detection (DAD) was established for the quantitative determination of the nine active components, namely, swertiamarin (SWM, 1), mangiferin (MA, 2), gentipicroside (GE, 3), sweroside (SWO, 4), isoorientin (IS, 5), swertisin (SWS, 6), swertianolin (SWN, 7), 7‐O‐[α‐L‐rhamnopyranosyl‐ 1→2)‐β‐D‐xylopyranosyl]‐1,8‐dihydroxy‐3‐methoxyxanthone (RX, 8), and bellidifolin (BE, 9) used as the external standard, in Tibetan folk medicinal species Swertia franchetiana. Based on the baseline chromatographic separation of most components from the methanolic extract of Swertia franchetiana on a reversed‐phase Eclipse XDB‐C8 column with water‐acetonitrile‐formic acid as mobile phase, the nine components were identified by comparison with standard samples and qualified by using the external standard method with DAD at 254 nm. The correlation coefficients of all the calibration curves were found to be higher than 0.9980. The relative standard deviations (RSDs) of the peak areas and retention times for the nine standards were less than 2.07% and 2.86%, respectively.

Keywords:

• Swertiamarin
• Gentipicroside
• Sweroside
• Swertianolin
• Bellidifolin
• Swertia franchetiana

Acknowledgment

Support for this research was provided by the Chinese Academy of Sciences (the Talent Cultivation Plan “Hope of the West China” and the Knowledge Innovation Program).