Investigation of Cytotoxic Compounds in Ethyl Acetate and Chloroform Extracts of Nigella sativa by Sulforhodamine-B Assay-Guided Fractionation
Commenced in January 2007
Frequency: Monthly
Edition: International
Paper Count: 33122
Investigation of Cytotoxic Compounds in Ethyl Acetate and Chloroform Extracts of Nigella sativa by Sulforhodamine-B Assay-Guided Fractionation

Authors: Harshani Uggallage, Kapila D. Dissanayaka

Abstract:

A Sulforhodamine-B assay-guided fractionation on Nigella sativa seeds was conducted to determine the presence of cytotoxic compounds against human hepatoma (HepG2) cells. Initially, a freeze-dried sample of Nigella sativa seeds was sequentially extracted into solvents of increasing polarities. Crude extracts from the sequential extraction of Nigella sativa seeds in chloroform and ethyl acetate showed the highest cytotoxicity. The combined mixture of these two extracts was subjected to bioassay guided fractionation using a modified Kupchan method of partitioning, followed by Sephadex® LH-20 chromatography. This chromatographic separation process resulted in a column fraction with a convincing IC50 (half-maximal inhibitory concentration) value of 13.07 µg/ml, which is considerable for developing therapeutic drug leads against human hepatoma. Reversed phase High-Performance Liquid Chromatography (HPLC) was finally conducted for the same column fraction and the result indicates the presence of one or several main cytotoxic compounds against human HepG2 cells.

Keywords: Cytotoxic compounds, half-maximal inhibitory concentration, high-performance liquid chromatography, human HepG2 cells, Nigella sativa seeds, Sulforhodamine-B assay-guided fractionation.

Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 450

References:


[1] J. M. Pezzuto, “Plant-derived anticancer agents,” Biochemical Pharmacology, vol. 53, pp. 121-133, 1997.
[2] C. Y. Wang, X. Y. Bai, and C. H. Wang, “Traditional Chinese Medicine: A Treasured Natural Resource of Anticancer Drug Research and Development” The American Journal of Chinese Medicine, vol. 42, pp. 543-559, 2014.
[3] S. Iddamaldeniya, N. Wickramasinghe, I. Thabrew, N. Ratnatunge, and M. Thammitiyagodage, “Protection against diethylnitrosoamine-induced hepatocarcinogenesis by an indigenous medicine comprised of Nigella sativa, Hemidesmus indicus and Smilax glabra: a preliminary study,” Carcinogenesis, vol. 2, pp. 1-6, 2003.
[4] M. I. Thabrew, R. R. Mitry, M. A. Morsy, and R. D. Hughes, “Cytotoxic effects of a decoction of Nigella sativa, Hemidesmus indicus and Smilax glabra on human hepatoma HepG2 cells,” Life Sciences, vol. 77, pp. 1319-1330, 2005.
[5] S. R. Samarakoon, I. Thabrew, P. B. Galhena, D. De Silva, and K. H. Tennekoon, “A comparison of the cytotoxic potential of standardized aqueous and ethanolic extracts of a polyherbal mixture comprised of Nigella sativa (seeds), Hemidesmus indicus (roots) and Smilax glabra (rhizome),” Pharmacognosy research, vol. 2, pp. 335-342, 2010.
[6] M. T. Donato, A. Lahoz, J. V. Castell, and M. J. Gómez-Lechón, “Cell lines: a tool for in vitro drug metabolism studies,” Current Drug Metabolism, vol. 9, pp. 1-11, 2008.
[7] R. R. Mitry, C. E. Sarraf, R. Havlík, and N. A. Habib, “Detection of adenovirus and initiation of apoptosis in hepatocellular carcinoma cells after Ad-p53 treatment,” Hepatology, vol. 31, pp. 885-889, 2000.
[8] H. Jork, W. Funk, W. Fischer, H. Wimmer and D. T. Burns, “Thin-layer chromatography. Reagents and detection methods. Physical and chemical detection methods” VCH, Weinheim, (ISBN 3-527-27834-6), vol. 1, pp. 128-132, 1990.
[9] A. E. Cohen, and A. P. J. Fields, “The cat that caught the canary: what to do with single-molecule trapping,” ACS Nano, vol.57, pp. 5296-5299, 2011.
[10] B. Schuler, “Single-molecule FRET of protein structure and dynamics - a primer,” Journal of Nanobiotechnology, vol. 11, S2, 2013.
[11] K. D. Dissanayaka, B. K. Canfield and L. M. Davis, “Three-dimensional feedback-driven trapping of a single nanoparticle or molecule in aqueous solution with a confocal fluorescence microscope,” Optics Express, vol. 27, pp. 29759-29769, 2019.