4.6 Article

Fast determination of saikosaponins in Bupleurum by rapid resolution liquid chromatography with evaporative light scattering detection

期刊

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpba.2009.01.011

关键词

Rapid resolution liquid chromatography (RRLC); Evaporative light scattering detection (ELSD); Saikosaponins; Bupleurum; Radix bupleuri

资金

  1. Changjiang Scholars and Innovative Research Team in University (PCSIRT)
  2. NCET Foundation [30725045]
  3. National 863 Program [2006AA02Z338]
  4. China Postdoctoral Science Foundation [20070410711]
  5. 973 program [2007CB507400]
  6. Shanghai Leading Academic Discipline [B906]
  7. China International Science and Technology Cooperation [2007DFC31030]
  8. Scientific Foundation of Shanghai China [07DZ19728, 06DZ19717, 06DZI9005]

向作者/读者索取更多资源

A rapid resolution liquid chromatography coupled with evaporative light scattering detection method was established for simultaneous determination of six saikosaponins, namely saikosaponin a, saikosaponin c. saikosaponin cl, 6 ''-O-acetylsaikosaponin a. 3 ''-O-acetylsaikosaponin d and 6 ''-O-acetylsaikosaponin d in Bupleurum. The analysis was performed by using an Agilent Zorbax SB-C18 column (1.8 mu m, 3.0 mm x 50 min i.d.) at gradient elution of water and acetonitrile, and the saikosaponins were well separated within 12 min, which provided about a fourfold reduction in analysis time by comparing a conventional high performance liquid chromatography method. Owing to their low ultraviolet absorption, the saikosaponins were detected by evaporative light scattering. The standard curves to quantify the saikosaponins were constructed by the log-log plot, which showed good linearity with the correlation coefficients exceeding 0.9954. The detection limits and quantification limits ranged in 8.38-25.00 mu g/mL and 25.13-45.00 mu g/mL, respectively. Satisfactory intra-day and inter-day precisions were achieved with the relative standard deviation (R.S.D.) less than 6.58%, and the average recoveries obtained were in the range of 96.9-100.4%. In addition, MeOH-1.0% (v/v) pyridine was found to be the best the extraction solvent when compared to MeOH and MeOH-1.0% (v/v) ammonia water. A total of 23 samples of roots of Bupleurum from different species or locations were examined with this analytical method, and their chemical profiles provided information for the chemotaxonomic investigation. The results demonstrated that the analytical method is highly effective for the quality evaluation of Bupleurum species. (C) 2009 Elsevier B.V. All rights reserved.

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