African Journal of
Pharmacy and Pharmacology

  • Abbreviation: Afr. J. Pharm. Pharmacol.
  • Language: English
  • ISSN: 1996-0816
  • DOI: 10.5897/AJPP
  • Start Year: 2007
  • Published Articles: 2279

Full Length Research Paper

Anti-oxidant and cytotoxic activities of Cassia nodosa Buch.-Ham. ex Roxb. and some of its pure constituents

Suzy A. El-Sherbeni*
  • Suzy A. El-Sherbeni*
  • Department of Pharmacognosy, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
  • Google Scholar
Souzan M.I. Moustafa
  • Souzan M.I. Moustafa
  • Department of Pharmacognosy, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
  • Google Scholar
Abdel-Rahim S. Ibrahim
  • Abdel-Rahim S. Ibrahim
  • Department of Pharmacognosy, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
  • Google Scholar
Kamilia A. El Seoud
  • Kamilia A. El Seoud
  • Department of Pharmacognosy, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
  • Google Scholar
Farid A. Badria
  • Farid A. Badria
  • Department of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.
  • Google Scholar


  •  Received: 30 December 2013
  •  Accepted: 03 May 2014
  •  Published: 08 June 2014

Abstract

Cassia nodosa Buch.-Ham. ex Roxb. is an ornamental plant which belongs to the family Fabaceae. It does not have the appropriate phytochemical and biological investigation. This was the first time to investigate anti-oxidant and cytotoxic activity of Cassia nodosa flowers, leaves, stem bark methanolic extracts and their fractions (petroleum ether, methylene chloride, ethyl acetate and n-butanol). Besides, some pure constituents isolated from C. nodosa were assessed as anti-oxidant and cytotoxic agents. Remarkable results were obtained specially for stem bark methanolic extract as a strong cytotoxic agent against MCF-7 and VERO cell lines. Chrysophanol (IV) displayed the highest activity as anti-oxidant (anti-hemolytic and DNA protective agent). Anti-oxidant activity of it was higher than ascorbic acid which was the positive control. This was the first time to isolate Kaempferol-3-O-α-L-rhamnopyranosyl (1→2)-β-D-glucoside (I) from ethyl acetate fraction of leaves. Isolation of 4,5-dihydroxyanthraquinone-2-carboxylic acid (rhein) (III) and 1,8-dihydroxy-3-methyl anthraquinone (chrysophanol) (IV) was achieved from methylene chloride fraction of flowers and stem bark, respectively. Kaempferol 3-O-α-L- rhamnoside (II) was isolated from ethyl acetate fraction of leaves besides compound (I).

 

Key words: Cassia nodosa, erythrocyte hemolysis, 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid)  (ABTS) assay, bleomycin, cytotoxic, kaempferol rhamnosyl glucoside, kaempferol rhamnoside, rhein, chrysophanol.