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Rapid determination of polyprenylated xanthones in gamboge resin of Garcinia hanburyi by HPLC

✍ Scribed by Jing-Zheng Song; Yue-Keung Yip; Quan-Bin Han; Chun-Feng Qiao; Hong-Xi Xu


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
492 KB
Volume
30
Category
Article
ISSN
1615-9306

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✦ Synopsis


Abstract

A rapid ion‐pair HPLC method was developed and validated for the determination of eight polyprenylated xanthones including three pairs of epimers, namely morellic acid (MA), 30‐hydroxygambogic acid (HGA), 30‐hydroxyepigambogic acid (HEGA), isogambogic acid (IGA), epiisogambogic acid (EIGA), gambogenic acid (GNA), gambogic acid (GA), and epigambogic acid (EGA), in gamboge resin of Garcinia hanburyi. The separation was performed on a narrow bore C~8~ column with isocratic elution using a mixture of methanol‐ACN‐40 mM KH~2~PO~4~ buffer (37.5 : 37.5 : 25 v/v/v, containing 0.1% tetradecyltrimethylammonium bromide). The newly developed method was used to determine the contents of the eight compounds present in the gamboge. Results showed that GA and EGA are the dominant components of gamboge. The content ratio of each epimer pair remained constant, indicating that the content ratio of epimers can be used as a specific characteristic for the quality control of gamboge.


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