4.5 Article

Isolation of three glucaric acids from Leonurus japonicus Houtt. by using high-speed countercurrent chromatography combined with semi-preparative high-performance liquid chromatography

期刊

JOURNAL OF SEPARATION SCIENCE
卷 45, 期 13, 页码 2140-2147

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jssc.202100876

关键词

glucaric acids; high-speed countercurrent chromatography; Leonurus japonicus Houtt; Semi-preparative high-performance liquid chromatography

资金

  1. National Natural Science Foundation of China [81973285]

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In this study, three glucaric acids were successfully isolated and purified from Leonurus japonicus Houtt. using a combination of high-speed countercurrent chromatography and semi-preparative high-performance liquid chromatography. Cation exchange resin chromatography was applied to remove alkaloids and enrich the glucaric acid fractions. The obtained compounds were identified as 2-syringyl glucaric acid, 2,4-disyringyl glucaric acid, and 3,4-disyringyl glucaric acid, with the latter being reported for the first time.
The isomerism of glucaric acids and the complexity of the composition of Leonurus japonicus Houtt. increased the difficulty of the separation of glucaric acids from the herb. In the present study, three glucaric acids were isolated from Leonurus japonicus Houtt. by using high-speed countercurrent chromatography combined with semi-preparative high-performance liquid chromatography. Cation exchange resin chromatography was applied to remove the alkaloids and enrich the glucaric acid fractions. Preliminary separation of the glucaric acid extract by high-speed countercurrent chromatography was carried out at 45celcius by using an optimized solvent system of ethyl acetate/n-butanol/formic acid/water (1:1:0.01:2, v/v/v/v) with satisfied stationary phase retention and separation factor. The semi-preparative high-performance liquid chromatography was used for further separation and purification of the target fractions, and three monomeric compounds were obtained with purities of 90.0%, 91.0%, and 95.3%. Ultraviolet spectroscopy, nuclear magnetic resonance spectroscopy, and mass spectrometry were employed to identify their structures, which were assigned as 2-syringyl glucaric acid, 2,4-disyringyl glucaric acid, and 3,4-disyringyl glucaric acid, respectively, and 2,4-disyringyl glucaric acid was reported for the first time.

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