Planta Med 2002; 68(4): 382-384
DOI: 10.1055/s-2002-26745
Letter
© Georg Thieme Verlag Stuttgart · New York

High Performance Liquid Chromatography Analysis of Canthinone Alkaloids from Eurycoma longifolia

Chee-Yan Choo1 , Kit-Lam Chan1
  • 1School of Pharmaceutical Sciences, Universiti Sains Malaysia, Penang, Malaysia
Further Information

Publication History

June 8, 2001

August 22, 2001

Publication Date:
02 May 2002 (online)

Abstract

A reversed phase-high performance liquid chromatography method with a photodiode array detector was developed for the simultaneous determination of three major alkaloids, 9-methoxycanthin-6-one (1), 3-methylcanthin-5,6-dione (2) and its 9-methoxy analogue (3) in Eurycoma longifolia Jack. These alkaloids were easily separated by a gradient elution protocol of 20 - 42 % acetonitrile in 0.1 % acetic acid. Compound 1 showed characteristic absorption at 350 nm only whereas its dione analogues, 2 and 3 displayed strong absorptions at both 350 and 451 nm. The linear calibration ranges were 0.7 - 50 μg mL-1 for 1, 1.5-50 μg mL-1 for 2 and 3.1 -100 μg mL-1 for 3. The recoveries of the three alkaloids were 90.8-101.0 % with relative standard deviations from 0.35 to 6.31 % (n = 3). The limits of detection for all the alkaloids were within the range of 0.35 - 0.7 μg mL-1. This method was successfully applied to the phytochemical analysis of E. longifolia roots obtained from different sources.[]

References

  • 1 Chan K L, O’Neill M J, Phillipson J D, Warhurst D C. Plants as sources of antimalarial drugs. Part 3 Eurycoma longifolia .  Planta Medica. 1986;  52 105-7
  • 2 Kardono L BS, Angerhofer C K, Tsauri S, Padmawinata K, Pezutto J M, Kinghorn D. Cytotoxic and antimalarial constituents of the roots of Eurycoma longifolia .  J. Nat. Prod.. 1991;  54 1360-7
  • 3 Thoi L -V, Suong N -N. Constituents of Eurycoma longifolia, Jack.  J. Org. Chem.. 1970;  35 1104-9
  • 4 Itokawa H, Kishi E, Morita H, Takeya K. Cytotoxic quassinoids and tirucallane-type triterpenes from the woods of Eurycoma longifolia .  Chem. Pharm. Bull.. 1992;  40 1052-5
  • 5 Morita H, Kishi E, Takeya K, Itokawa H, Iitaka Y. Squalene derivatives from Eurycoma longifolia .  Phytochemistry. 1993;  34 765-71
  • 6 Morita H, Kishi E, Takeya K, Itokawa H, Iitaka Y. Biphenylneolignans from wood of Eurycoma longifolia .  Phytochemistry. 1992;  31 3993-5
  • 7 Chan K L, Lee S P, Sam T W, Han B H. A quassinoid glycoside from the roots of Eurycoma longifolia .  Phytochemistry. 1989;  28 2857-9
  • 8 Chan K L, Lee S P, Sam T W, Tan S C, Noguchi H, Sankawa U. 13β,18-Dihydroeurycomano - a quassinoid from Eurycoma longifolia .  Phytochemistry. 1991;  30 3138-41
  • 9 Chan K L, Lee S P, Yuen K H. Antipyretic activity of quassinoids from Eurycoma longifolia, Jacky. In Chemical Prospecting in Malayan Forest. (Ghazally I, Murtedza M, Laily D, eds.) Pelanduk Publications Selangor; 1995: 219-24
  • 10 Tada H, Yasuda F, Otani K, Doteuchi M, Ishara Y, Shiro M. New antiulcer quassinoids from Eurycoma longifolia .  Eur. J. Med. Chem.. 1991;  26 345-9
  • 11 Choo C Y, Nah B K, Ibrahim P, Chan K L. Antimicrobial activity from the chloroform extract of Eurycoma longifolia, Jack. Proceedings: 16th National Seminar on Natural Products. 2000
  • 12 Chan K L, Choo C Y, Morita H, Itokawa H. High performance liquid chromatography in phytochemical analysis of Eurycoma longifolia .  Planta Medica. 1998;  64 741-5
  • 13 Mitsunaga K, Koike K, Tanaka T, Ohkawa Y, Kobayashi Y, Sawaguchi T, Ohmoto T. Canthin-6-one alkaloids from Eurycoma longifolia .  Phytochemistry. 1994;  35 799-802
  • 14 Newall C A, Anderson L A, Phillipson J D. Herbal Medicines (A Guide for Health-care Professionals). The Pharmaceutical Press London; 1996: 5-6

Kit-Lam Chan

School of Pharmaceutical Sciences

Universiti Sains Malaysia

11800 Penang

Malaysia

Fax: +604-6576836

Email: klchan@usm.my