TY - JOUR
T1 - Antioxidant and cytotoxic activity of stems of Smilax zeylanica in vitro
AU - Uddin, Mohammad Nasir
AU - Ahmed, Taksim
AU - Pathan, Sanzida
AU - Al-Amin, Md Mamun
AU - Rana, Md Sohel
N1 - Publisher Copyright:
© 2015 by De Gruyter 2015.
PY - 2015/9
Y1 - 2015/9
N2 - BACKGROUND: Plant-derived phytochemicals consisting of phenols and flavonoids possess antioxidant properties, eventually rendering a lucrative tool to scavenge reactive oxygen species. This study was carried out to evaluate in vitro antioxidant and cytotoxic potential of methanolic extract and petroleum ether extracts of Smilax zeylanica L. stems.METHODS: Phytochemical screening was done following standard procedures. Antioxidant activity was tested using several in vitro assays, viz., 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay, NO assay, H2O2 assay, CUPRAC assay, FRAP assay and total antioxidant capacity assay. Total phenol and flavonoid contents were determined by colorimetric method. Brine shrimp lethality and MTT cell viability assays were used for cytotoxic potential.RESULTS: Preliminary phytochemical study revealed the presence of flavonoids and glycosides in both extracts. Methanolic extract was found to possess stronger antioxidant potential than petroleum ether extracts in all assays. The IC50 value of methanolic extract was 29.14±0.39 μg/mL, 120.30±3.32 μg/mL and 78.41±5.53 μg/mL in DPPH assay, NO assay and H2O2 assay, respectively. Likewise, total phenol [56.78 mg/g gallic acid (GAE)] and flovonoid [125.69 mg/g quercetin equivalents (QE)] were higher in methanolic extract. In cytotoxicity assays, petroleum ether extract showed stronger activity in both brine shrimp lethality (LC50 2.85±0.13 μg/mL) and MTT cell viability assay (IC50 15.49±1.18 μg/mL).CONCLUSIONS: These findings demonstrate that methanolic extracts could be considered as potential sources of natural antioxidant, whereas petroleum ether extracts could be explored for promising anticancer molecules.
AB - BACKGROUND: Plant-derived phytochemicals consisting of phenols and flavonoids possess antioxidant properties, eventually rendering a lucrative tool to scavenge reactive oxygen species. This study was carried out to evaluate in vitro antioxidant and cytotoxic potential of methanolic extract and petroleum ether extracts of Smilax zeylanica L. stems.METHODS: Phytochemical screening was done following standard procedures. Antioxidant activity was tested using several in vitro assays, viz., 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay, NO assay, H2O2 assay, CUPRAC assay, FRAP assay and total antioxidant capacity assay. Total phenol and flavonoid contents were determined by colorimetric method. Brine shrimp lethality and MTT cell viability assays were used for cytotoxic potential.RESULTS: Preliminary phytochemical study revealed the presence of flavonoids and glycosides in both extracts. Methanolic extract was found to possess stronger antioxidant potential than petroleum ether extracts in all assays. The IC50 value of methanolic extract was 29.14±0.39 μg/mL, 120.30±3.32 μg/mL and 78.41±5.53 μg/mL in DPPH assay, NO assay and H2O2 assay, respectively. Likewise, total phenol [56.78 mg/g gallic acid (GAE)] and flovonoid [125.69 mg/g quercetin equivalents (QE)] were higher in methanolic extract. In cytotoxicity assays, petroleum ether extract showed stronger activity in both brine shrimp lethality (LC50 2.85±0.13 μg/mL) and MTT cell viability assay (IC50 15.49±1.18 μg/mL).CONCLUSIONS: These findings demonstrate that methanolic extracts could be considered as potential sources of natural antioxidant, whereas petroleum ether extracts could be explored for promising anticancer molecules.
KW - Animals
KW - Antioxidants/pharmacology
KW - Artemia/drug effects
KW - Cell Survival/drug effects
KW - Cytotoxins/pharmacology
KW - Flavonoids/pharmacology
KW - Glycosides/pharmacology
KW - Phenols/pharmacology
KW - Plant Extracts/pharmacology
KW - Smilax/chemistry
KW - MCF7
KW - DPPH
KW - MTT
KW - antioxidant activity
KW - Smilax zeylanica
KW - brine shrimp
KW - H O
UR - http://www.scopus.com/inward/record.url?scp=84938235753&partnerID=8YFLogxK
U2 - 10.1515/jbcpp-2014-0114
DO - 10.1515/jbcpp-2014-0114
M3 - Article
C2 - 25901714
SN - 2191-0286
VL - 26
SP - 453
EP - 463
JO - Journal of Basic and Clinical Physiology and Pharmacology
JF - Journal of Basic and Clinical Physiology and Pharmacology
IS - 5
ER -