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African Journal of Biotechnology

     
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  Afr. J. Biotechnol.

  Vol. 9 No. 8

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  Search Pubmed for articles by:

  Eid EEM
  Abdullah R

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African Journal of Biotechnology Vol. 9 (8), pp. 1260-1265, 22 February 2010

ISSN 1684-5315  © 2010 Academic Journals  

 

 

Full Length Research Paper

 

Validated high performance liquid chromatographic (HPLC) method for analysis of zerumbone in plasma

 

Eltayeb Elamin M. Eid1, Ahmad Bustamam Abdul1*, Adel S. Al-Zubairi1,4, Mohamed Aspollah Sukari2 and Rasedee Abdullah3

 

1Laboratory of Cancer Research MAKNA-UPM, Institute of Bioscience, University Putra Malaysia, 43400 Serdang, Selangor DE, Malaysia.

2Department of Chemistry, Faculty of Science, University Putra Malaysia, 43400 Serdang, Selangor DE, Malaysia.

3Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, University Putra Malaysia, 43400, Serdang, Selangor DE, Malaysia.

4Department of Biochemistry and Molecular Biology, Faculty of Medicine and Health Sciences, University of Sana’a, Sana’a, Yemen.

 

*Corresponding author. E-mail: ahmadbstmm@yahoo.com or adelalzubairi@hotmail.com. Tel: +603-89462124 Fax: +603-89462101.

 

Accepted 11 November, 2009

 

   Abstract

 

Zerumbone (ZER) is a sesquiterpene derived from Zingiber zerumbet smith, family Zingiberaceae. It has been shown to possess anti-cancer and apoptosis-inducing properties against various human tumour cells as well as in vivo against a number of induced malignancies in mice. In this study a simple, specific and accurate high performance liquid chromatographic method for determination of ZER in micro-volumes human plasma (| 1.5 ml) was developed and validated. ZER and its analogue α-Humulene as internal standard were easy recovered by simple one step plasma protein precipitation using acetonitrile and separated in isocratic mobile phase, on reverse phase-C18 column. The effluent was monitored by Photodiode Array (PDA) detector and at a flow rate of 1.0 ml/min. The linearity of proposed method was 2 – 15 µg/ml. The intra-day and inter-day coefficient of variation and percent error values of the method were less than 15% and mean recovery was more than 90% for both ZER and α-Humulene. This method was found to be precise, specific, accurate and robust for detection and analysis of ZER in human plasma.

 

Key words: ZER, humulene, HPLC, human plasma.

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