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A preparative high-speed counter-current chromatography (HSCCC) method was developed for the isolation of the major iridoid glycosides from the stem bark of Catalpa ovata (Bignoniaceae). A biphasic solvent system comprising EtOAc/BuOH/water (10:1:10, v/v) was selected as the optimal condition for purification, leading to the isolation of catalposide (1, 3.9 mg, 98.1% purity) and 6-O-trans-feruloyl catalpol (2, 12.2 mg, 99.2% purity) from 100 mg of a 70% EtOH crude extract. The structures of the isolates were identified by the ¹H- and ¹³C-NMR spectroscopy and HR-MS, and their purities were determined by HPLC-ELSD analysis. As 6-O-trans-feruloyl catalpol (2) has recently been proposed as a promising therapeutic agent for liver regeneration, the optimized HSCCC conditions may serve as an efficient preparative strategy for this bioactive compound.
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Hwang et al. (2026) studied this question.
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