Journal of Applied Science and Engineering

Published by Tamkang University Press

1.30

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2.10

CiteScore

Ming-Ren S. Fuh  1 and Hung-Jian Lin1

1Department of Chemistry Soochow University Taipei, Taiwan 111, R.O.C.


 

Received: December 18, 2002
Accepted: January 17, 2003
Publication Date: March 1, 2003

Download Citation: ||https://doi.org/10.6180/jase.2003.6.1.04  


ABSTRACT


Liquid chromatography-electrospray-mass spectrometry (LC-ES -MS) was employed to analyze five biologically active components (sennoside A and B, rhein, emodin and aloe-emodin) in rhubarb. The separation was achieved on a C18 column using gradient elution. Negative ion detection mode was utilized for ES-MS detection. For sennosides, [M-H]− and a fragmented ion (m/z = 386) were detected. In addition to [M-H]− , [M-COOH]− was observed for rhein. Only one major ion, [M-H]− , was determined for aloe-emodin and emodin. A post-column splitter was employed to enhance the sensitivity of sennoside measurement. Extracted ion monitoring was applied for quantitative analysis. Satisfactory linearity (r2 = 0.99) of each compound was determined. In addition, the content of these five active components in various rhubarb samples were examined by this newly developed LC-ES-MS.


Keywords: LC-MS, Chinese Herbal Medicine, Sennoside


REFERENCES


  1. [1] Okabe, H.; Matsuo, K.; Nishioka, I. Chem Pharm. Bull. 1973, 87, 1254.
  2. [2] Oshio, H.; Imai, S.; Fujioka, S.; Sugawara, T.; Miyamaoto, M.; Tsukui, M. Chem. Pharm. Bull. 1974, 22, 823.
  3. [3] Hsu, H.-Y.; Chen, Y P.; Hsu, S.-J.; Chen, C.-C.; Chang, H.-C. Chin. Mater. Medica – A Concise Guide; Modern Drug Press, Taipei, Taiwan, 1985.
  4. [4] Oshio, H.; Naruse, Y.; Tsukui, M. Chem. Pharm. Bull. 1978, 26, 2458.
  5. [5] Kobashi, K.; Nishimura, T.; Kusaka, M.; Hottori, M.; Namba, T. Planta Med. 1980, 40, 225.
  6. [6] Oshima, Y.; Takahashi K. Chromatogr. J. 1983, 258, 292.
  7. [7] Takahashi, K.; Kaizuka, H.; Oshima, Y. Chromatogr. J. 1983, 258, 522.
  8. [8] Sagara, K.; Oshima, Y.; Yoshida, T. Chromatogr. J. 1987, 403, 253
  9. [9] Kashiwada, Y.; Nonaka, G.; Nishioka, I. Chem. Pharm. Bull. 1989, 37, 999.
  10. [10] Sheu, S. J.; Lu, S. J. Chromatogr. A. 1995, 704, 518.
  11. [11] Zong, Y. Y.; Che, C. T. J. of Natural Products 1995, 58, 577.
  12. [12] Harting, C.; Storm, T.; Jekel, M. J. Chromatogr. A 1999, 854, 163.
  13. [13] Bogusz, M. J.; Kruger, K. D.; Maier, R. D. J. Anal. Toxicol. 2000, 24, 77.
  14. [14] Fuh, M. R.; Tai, Y. L.; W. H. T. Pan J. Chromatogr. B 2001, 752, 107.
  15. [15] Leitner, A.; Zollner, P.; W Lindner J. Chromatogr. A 2001, 939, 49. [16] Fuh, M. R.; Chia, K. J. Talanta 2002, 56, 663.
  16. [17] API-Electrospray LC/MS System User’s Guide, 1994; Chapter 4.
  17. [18] Hopfgartner, G.; Bean, K.; Henion, J.; Henry, R. J. Chromatogr. 1993, 647, 51.
  18. [19] Fuh, M. S.; Lu, K. T. 213th Amer. Chem. Soc. National Meeting, San Francisco, CA, U.S.A. 13-18 April 1997.