4.5 Article

Anti-inflammatory bioactive equivalence of combinatorial components β-carboline alkaloids identified in Arenaria kansuensis by two-dimensional chromatography and solid-phase extraction coupled with liquid-liquid extraction enrichment technology

期刊

JOURNAL OF SEPARATION SCIENCE
卷 40, 期 14, 页码 2895-2905

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jssc.201700144

关键词

Arenaria kansuensis; bioactive equivalence of combinatorial components; liquid-liquid extraction; solid-phase extraction; two-dimensional chromatography

资金

  1. West Light Foundation of The Chinese Academy of Sciences for Doctors
  2. Natural Science Foundation of Qinghai Province [2015-ZJ-927Q]
  3. Science and Technology Major Project of Qinghai Province, China [2014-GX-A3A]
  4. Strategic network planning project of biological resources service from Chinese academy of science [ZSTH-027]
  5. Significant Science & Technological Project of Qinghai Province [2014-GX-A3A-01]

向作者/读者索取更多资源

Bioactive equivalent combinatorial components play a critical role in herbal medicines. However, how to discover and enrich them efficiently is a question for herbal pharmaceuticals researchers. In our work, a novel two-dimensional reversed-phase/hydrophilic interaction high-performance liquid chromatography method was established to perform real-time components trapping and combining for preparation and isolation of coeluting components. Arenaria kansuensis was taken as an example, and solid-phase extraction coupled with liquid-liquid extraction as a simple and efficient method for enriching trace components, reversed phase column coupled with hydrophilic interaction liquid chromatography XAmide column as two-dimensional chromatography technology for isolation and preparation of coeluting constituents, enzyme-linked immune-sorbent assay as bio-guided assay, and anti-inflammatory bioactivity evaluation for bioactive constituents. A combination of 12 beta-carboline alkaloidswas identified as anti-inflammatory bioactive equivalent combinatorial components from A. kansuensis, which accounts for 1.9% w/w of original A. kansuensis. This work answers the key question of which are real anti-inflammatory components from A. kansuensis and provides a fast and efficient approach for discovering and enriching trace beta-carboline alkaloids from herbal medicines for the first time. More importantly, the discovery of bioactive equivalent combinatorial components could improve the quality control of herbal products and inspire a herbal medicine based on combinatorial therapeutics.

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