Background: Phytochemicals are well known to have many important pharmaceutical properties. Heritiera fomes grows in low saline environments. The present study was initiated to explore the biologically beneficial properties of H. fomes. Methods: The crude extracts of H. fomes were extracted in acetone by orbital shaker and concentrated using rota evaporator. Total flavonoid content and Total phenolic content were estimated spectrophotometrically and the in-vitro antioxidant capacity was estimated by DPPH (2,2-diphenyl-1-picrylhydrazyl), Ferric Reducing Antioxidant Power (FRAP) and Hydrogen peroxide (H 2 O 2 ) Scavenging Assays. Anti-microbial activity was determined by Disc diffusion method. Results: Phytochemical screening of acetone extract of H. fomes showed the presence of major classes of phytochemicals like alkaloids, glycosides, flavonoids, saponins, carbohydrates, phenols and sterols in considerable quantity. The total amount of phenolic and flavonoid content was found to be 75.3 mg GAE/g dry weight and 61.3 mg QE/g dry weight respectively. Antioxidant activity of plant extract determined by using different assays like H 2 O 2 radical scavenging, DPPH and FRAP. A positive correlation between all the pairs of antioxidant assays was observed. Further, antimicrobial activity against various pathogens was evaluated by disc diffusion method where the zone of inhibitions were found to be in range from 5± 0.35 to 12 ± 0.50 mm. Conclusion: The study concludes that the plant Heritiera fomes has its effect in scavenging free radicals and has a potential to be a power antioxidant. Several in-vitro studies possess significant antioxidant, antimicrobial activities. The present study plays an important tool for new drug discovery.
Objective: The objective of the present study was to evaluate synergistic growth inhibitory effect of a flavonol, kaempferol in combination with chemotherapeutic drugs doxorubicin or cisplatin.
Methods:The anti-proliferative activities of kaempferol, doxorubicin and cisplatin on human colorectal cancer cells (HCT-15) and human breast cancer (MDA MB 231) were analyzed by 3-(4,5-dimehylthiaol-2-yl)-2,5-diphenyltetraolium bromide (MTT) assay. Further, combinational studies were performed in both the cell lines to evaluate the interaction of drugs with kaempferol. The combination index (CI) method was used to assess the synergism of kaempferol with doxorubicin or cisplatin. Finally, morphological alterations associated with apoptosis were examined under fluorescent microscope.Results: All compounds showed dose-dependent growth inhibition in both HCT-15 and MDA MB 231 cells. The phytochemical kaempferol showed fifty percent inhibitory concentrations (IC50) at 120±3.2 µg/ml and 64±1.2 µg/ml on HCT-15 and MDA MB 231 respectively. IC50 concentrations of doxorubicin and cisplatin on both the cell lines were achieved at 49.6±0.5 µg/ml, 25.4±2.9 µg/ml and 44±1.8 µg/ml, 40.6±0.8 µg/ml respectively. Further, in vitro therapeutic effect (IC50) of doxorubicin and cisplatin in terms of cell growth inhibition on HCT-15 cells were achieved at their onefifth (10±0.83 µg/ml) and half (10±1.34 µg/ml) concentrations respectively when they were combined with 30 µg/ml of kaempferol individually. Simultaneously, on MDA-MB 231 cell line, the IC50 concentrations were reduced to 18±1.22 µg/ml and 15±1.87 µg/ml respectively i
Conclusion:The study reveals the prominent synergism between the phytochemical, kaempferol and chemotherapeutic drugs doxorubicin or cisplatin which helps in elevating the therapeutic efficacy of drugs.n combination with 32 µg/ml of kaempferol. The combinational index studies revealed the synergistic association of kaempferol with doxorubicin and cisplatin individually in each cell line. The fluorescence imaging studies strongly supported the synergistic association between kaempferol and doxorubicin or cisplatin by confirming significant apoptotic cell death in both the cell lines which was ~3 fold higher than each agent alone.
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