2000
DOI: 10.1093/chromsci/38.6.229
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High-Performance Liquid Chromatographic Analysis of Saponin Compounds in Bupleurum falcatum

Abstract: A mixture of saponin compounds (saikosaponin c, a, and d) in the 70% ethanol extract of a powdered sample of Bupleuri radix are analyzed by an Inertsil ODS-3 C(18) column at a flow rate of 1.0 mL/min and detection wavelength of 203 nm. Well resolved chromatograms of saikosaponin c, a, and d are obtained with a gradient elution of acetonitrile-water from 40:60 (v/v) to 50:50 (v/v). The total time required for a single analysis is approximately 20 min. Calibration curves for saikosaponin c, a, and d are linear u… Show more

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Cited by 42 publications
(22 citation statements)
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“…The programmed gradient elution using acetonitrile-water from 40:60 (v/v) to 50:50 (v/v) in 10 min at a flow rate of 1.0 mL/min and detection wavelength of 203 nm were used (Park et al, 2000). For the analysis of baicalin, baicalein and glycyrrhizic acid, the elution solution consisted of (A) 25 mM NaH 2 PO 4 (pH 2.5) and (B) acetonitrile.…”
Section: Analysis Of Saikosaponins Baicalin Baicalein and Glycyrrhmentioning
confidence: 99%
“…The programmed gradient elution using acetonitrile-water from 40:60 (v/v) to 50:50 (v/v) in 10 min at a flow rate of 1.0 mL/min and detection wavelength of 203 nm were used (Park et al, 2000). For the analysis of baicalin, baicalein and glycyrrhizic acid, the elution solution consisted of (A) 25 mM NaH 2 PO 4 (pH 2.5) and (B) acetonitrile.…”
Section: Analysis Of Saikosaponins Baicalin Baicalein and Glycyrrhmentioning
confidence: 99%
“…Most studies on Bupleurum have mainly focused on component analysis, pharmacology, chemical structure, and clinical applications (Tan et al 2008; Kanazawa et al 1990; Guo et al 1996; Ebata et al 1996; Park et al 2000). Consequently, the saikosaponin biosynthetic pathway and site in Bupleurum are unknown, although some studies have reported the cloning of critical gene fragments and gene regulation in the triterpene biosynthetic pathway of Bupleurum (Kim et al 2006; Kim et al 2011; Dong et al 2011; Sui et al 2010).…”
Section: Introductionmentioning
confidence: 99%
“…Based on studies on the chemical characterization of the constituent herbs of SST [17,[49][50][51][52][53], it is assumed that the S-fraction contains various classes of compounds with different polarity and structure (i.e., flavonoids, triterpenes, saccharides, amino acids). Therefore, subsequent fractionations of the S-fraction are performed based on either the polarity or the structural properties of compounds.…”
Section: Separation Of Various Classes Of Compounds From the S-fractimentioning
confidence: 99%