4.2 Article

Simultaneous Determination of Chlorogenic Acid, Caffeic Acid, Alantolactone and Isoalantolactone in Inula helenium by HPLC

Journal

JOURNAL OF CHROMATOGRAPHIC SCIENCE
Volume 53, Issue 4, Pages 526-530

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/chromsci/bmu079

Keywords

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Funding

  1. Health Department of Hebei Province [20110173]
  2. Department of Hebei Education [Z2011304]
  3. Key Project of Hebei North University
  4. Youth Foundation of Hebei North University [Q2013029]
  5. Syngenta Ltd. [20013-Hebei Medical University-Syngenta-04]
  6. National Natural Science Foundation of China [81302664, 81072551, 81241101]

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A rapid and sensitive high-performance liquid chromatographic (HPLC) method was developed for the simultaneous separation and determination of chlorogenic acid, caffeic acid, alantolactone and isoalantolactone in Inula helenium. The HPLC separation was performed on an Elite Hypersil C-18 column (200 x 4.6 mm i.d., 5 mu m particle size) with a gradient elution of solvent A (acetonitrile) and solvent B (0.1% phosphoric acid in water) at a flow rate of 1.0mL/min. Detection was monitored at 225 nm. The recovery of chlorogenic acid ranged from 95.6 to 107.7%, the recovery of caffeic acid ranged from 95.4 to 104.2%, the recovery of alantolactone ranged from 95.8 to 100.8% and the recovery of isoalantolactone ranged from 96.5 to 102.3%. The retention times for chlorogenic acid, caffeic acid, alantolactone and isoalantolactone were 5.2, 7.1, 25.6 and 26.6 min with the limits of detection of 0.069, 0.021, 0.039 and 0.051 mu g/mL, respectively. Relative standard deviation for the intra-day and inter-day was <= 2.5%. The validated method is reliable for the routine control of these four compounds in I. helenium.

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