Journal
PHARMACOGNOSY RESEARCH
Volume 9, Issue 1, Pages 46-50Publisher
PHCOG NET
DOI: 10.4103/0974-8490.199776
Keywords
3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay; 7-deacetoxy-7-oxogedunin; Cytotoxicity; HeLa; MCF-7; Pseudocedrela kotschyi; RD
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Funding
- Medical Education Partnership Initiative in Nigeria (MEPIN) project - Fogarty International Center
- Office of AIDS Research
- National Human Genome Research Institute of the National Institute of Health
- Health Resources and Services Administration (HRSA)
- Office of the U.S. Global AIDS Coordinator [R24TW008878]
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Background: This study determined the cytotoxic effects of root and stem bark extracts, fractions, and isolated compounds derived from Pseudocedrela kotschyi on HeLa, MCF-7, and RD cells. Materials and Methods: The cytotoxic activity was determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide colorimetric assay against three cell lines (RD, HeLa, and MCF 7) at concentrations ranging from 0.01 to 1000 mu g/mL. Isolation of crude saponin was done from the most active ethyl acetate fraction and further purified using vacuum liquid chromatography and preparative thin layer chromatographic techniques. Results: The cytotoxicity assay revealed that the methanol extract from the root bark and the ethyl acetate fraction from the stem bark exhibited marked anticancer activity with IC50 of 87.36 mu g/ml and 21.53 mu g/ml, respectively, on HeLa cancer cell line and 101.51 mu g/mL and 38.46 mu g/mL, respectively, on RD cell line. These values are comparable with that obtained from vinblastine and methotrexate used as standard drugs (IC50 values of 0.01 mu g/mL and 0.05 mu g/mL, respectively). The isolated crude saponins also gave IC50 values of 5.28 mu g/mL and 81.52 mu g/mL against the RD cell lines and IC50 values of 1.05 mu g/mL and 86.8 mu g/mL for the MCF 7 cancer cell lines. PTLC led to the isolation of a compound from the crude saponin which was identified as 7-deacetoxy-7-oxogedunin through spectroscopic analysis and comparison with literature data. Conclusions: P. kotschyi could be considered as a potential source of chemotherapeutic agent. However, further research to determine the exact mechanism of action needs to be carried out.
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