Preprint / Version 1

Anti-tumor and antioxidant activity of kaempferol-3-O-alpha-L-rhamnoside (Afzelin) isolated from Pithecellobium dulce leaves

Authors

  • Masuma Akter Department of Pharmacy, Faculty of Science, University of Rajshahi, Rajshahi, 6205 Bangladesh
  • Mst Parvin Department of Pharmacy, Faculty of Science, University of Rajshahi, Rajshahi, 6205 Bangladesh
  • Md Hasan Department of Pharmacy, Faculty of Science, University of Rajshahi, Rajshahi, 6205 Bangladesh
  • Md Rahman Department of Pharmacy, Faculty of Science, University of Rajshahi, Rajshahi, 6205 Bangladesh
  • Md Islam Department of Pharmacy, Faculty of Science, University of Rajshahi, Rajshahi, 6205 Bangladesh

Keywords:

Antioxidant, Anti-tumor, EAF, NMR analysis, AAPH, EAC cell

Abstract

Pithecellobium dulce (Roxb.), an evergreen medium-sized, spiny tree which have vast nutritional values and widely used in ayurvedic medicines and home remedies. The plant has also been a rich source of biologically active compounds. The present study was designed to isolate pure compound from ethyl acetate fraction of methanol extract of leaves and to know the efficacy as antioxidant as well as its anti-tumor activity on Ehrlich ascites carcinoma cell (EAC).  Methods The leaves were extracted with methanol and fractionated with different solvents. The isolation of the compound was carried out by column chromatography from ethyl acetate fraction (EAF) and structure was revealed by 1H-NMR and 13C NMR. The antioxidant activity was investigated by the scavenging of 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radicals as well as the inhibition of oxidative damage of pUC19 plasmid DNA, hemolysis and lipid peroxidation induced by a water-soluble free radical initiator 2,2’-azo (2-asmidinopropane) dihydrochloride (AAPH) in human erythrocytes. In vivo anti-tumor activity of the compound was also evaluated by determining the viable tumor cell count, hematological profiles of experimental mice along with observing morphological changes of EAC cells by fluorescence microscope. Results The isolated compound kaempferol-3-O-alpha-L-rhamnoside effectively inhibited AAPH induced oxidation in DNA and human erythrocyte model and lipid per oxidation as well as a stronger DPPH radical scavenging activity. In anti-tumor assay, at a dose of 50 mg/kg body weight exhibit about 70.89 ± 6.62% EAC cell growth inhibition, whereas standard anticancer drug vincristine showed 77.84 ± 6.69% growth inhibition. Conclusion The compound may have a great importance as a therapeutic agent in preventing oxidative damage of biomolecules and therapeutic use in chemotherapy. Supplementary Information The online version contains supplementary material available at 10.1186/s12906-022-03633-x. Keywords: Antioxidant, Anti-tumor, EAF, NMR analysis, AAPH, EAC cell