TY - JOUR
T1 - Antioxidant, Anticancer and Antibacterial Activity of Withania somnifera Aqueous Root Extract
AU - Barnes, DA
AU - Barlow, R
AU - Nigam, P
AU - Owusu-Apenten, Richard
PY - 2015/11/10
Y1 - 2015/11/10
N2 - Aims: To evaluate total antioxidant capacity, anticancer activity and antibacterial effects Withaniasomnifera aqueous-root extracts.Study Design: In vitro study.Place of Study: School of Biomedical Sciences, Ulster University, UK.Methodology: Total antioxidant capacity (TAC) of whole powder and freeze dried W. somniferaaqueous-root extracts was determined using FRAP, DPPH, Folin and ABTS assays. Anticanceractivity was accessed using MDA-MB-231 breast cells and Sulforhodamine B staining for cellviability. Antibacterial activity was by disk diffusion assay with penicillin, amoxicillin andstreptomycin as positive controls.Results: The TAC for W. somnifera extract was 86, 47, 195,or 443 gallic acid equivalents per 100gdry basis (mgGAE/ 100 g) us ing FRAP, DPPH, Folin or ABTS assays, respectively. CorrespondingTAC values for freeze dried W. somnifera aqueous-root extract were, 418, 553, 1898 or, 1770(mgGAE/100 g). W. somnifera aqueous-root extract inhibited MDA-MB-231 cell proliferation in adose-dependent manner with IC50 = 0.19 mg/ml (21 μM GAE). Nil antibacterial effects weredetected for freeze dried W. somnifera extract (0-1 mg/ml) across six species of bacteria tested.Conclusion: Withania somnifera root water extract showed significant antioxidant and anticanceractivity for MDA-MB-231 breast cancer cells but no antibacterial activity under the conditions of this study.
AB - Aims: To evaluate total antioxidant capacity, anticancer activity and antibacterial effects Withaniasomnifera aqueous-root extracts.Study Design: In vitro study.Place of Study: School of Biomedical Sciences, Ulster University, UK.Methodology: Total antioxidant capacity (TAC) of whole powder and freeze dried W. somniferaaqueous-root extracts was determined using FRAP, DPPH, Folin and ABTS assays. Anticanceractivity was accessed using MDA-MB-231 breast cells and Sulforhodamine B staining for cellviability. Antibacterial activity was by disk diffusion assay with penicillin, amoxicillin andstreptomycin as positive controls.Results: The TAC for W. somnifera extract was 86, 47, 195,or 443 gallic acid equivalents per 100gdry basis (mgGAE/ 100 g) us ing FRAP, DPPH, Folin or ABTS assays, respectively. CorrespondingTAC values for freeze dried W. somnifera aqueous-root extract were, 418, 553, 1898 or, 1770(mgGAE/100 g). W. somnifera aqueous-root extract inhibited MDA-MB-231 cell proliferation in adose-dependent manner with IC50 = 0.19 mg/ml (21 μM GAE). Nil antibacterial effects weredetected for freeze dried W. somnifera extract (0-1 mg/ml) across six species of bacteria tested.Conclusion: Withania somnifera root water extract showed significant antioxidant and anticanceractivity for MDA-MB-231 breast cancer cells but no antibacterial activity under the conditions of this study.
KW - Withania somnifera
KW - antioxidant capacity
KW - anticancer
KW - antibacterial.
U2 - 10.9734/JABB/2016/22523
DO - 10.9734/JABB/2016/22523
M3 - Article
SN - 2394-1081
VL - 5
SP - 1
EP - 6
JO - Journal of Advances in Biology and Biotechnology
JF - Journal of Advances in Biology and Biotechnology
IS - 1
ER -