2005
DOI: 10.1016/j.foodchem.2004.04.016
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Antioxidative activities of water extract and ethanol extract from field horsetail (tsukushi) Equisetum arvense L

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Cited by 84 publications
(57 citation statements)
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“…DPPH assay was performed according to the procedure as reported by Gyamfi et al (1999). ABTS radical cation (Re et al, 1999), phosphomolybdenum method (Prieto et al, 1999), β-carotenelinoleate (Sun and Ho, 2005), superoxide radical scavenging activity (Nishikimi et al, 1972), hydroxyl radicals (Nagai et al, 2005), hydrogen peroxide (Ruch et al, 1989) and the chelating ability of ferrous ions by various fractions were estimated by the method of Dinis et al (1994). After % activity of free radical inhibition, IC50 of various assays was determined using Graph pad software.…”
mentioning
confidence: 99%
“…DPPH assay was performed according to the procedure as reported by Gyamfi et al (1999). ABTS radical cation (Re et al, 1999), phosphomolybdenum method (Prieto et al, 1999), β-carotenelinoleate (Sun and Ho, 2005), superoxide radical scavenging activity (Nishikimi et al, 1972), hydroxyl radicals (Nagai et al, 2005), hydrogen peroxide (Ruch et al, 1989) and the chelating ability of ferrous ions by various fractions were estimated by the method of Dinis et al (1994). After % activity of free radical inhibition, IC50 of various assays was determined using Graph pad software.…”
mentioning
confidence: 99%
“…Field horsetail was rich in vitamins C and E. and contained high levels of copper and zinc. These were essential elements, for superoxide dismutase to act against active oxygen species [78]. The antioxidative activity of different horsetail (Equisetum arvense) extracts was studied by the electron spin resonance spectroscopy-spin trapping method.…”
Section: Pharmacological Effectsmentioning
confidence: 99%
“…The lipid peroxidation control (without plant extract) chromogen, test samples included with increased concentrations of the extract (20-100 lg/mL) resulted chromogen were measured at 532 nm. 2-Deoxy ribose sugar protection property of the MEAIL from hydroxyl radicals was analysed using Deoxy ribose method described by Nagai et al (2005). The source of hydroxyl radical was Fenton's reagent, the amount of 2-Deoxy ribose sugar was 10 mM (150 lL) and the extract concentrations ranging from 20-100 lg/mL were used against hydroxyl radicals.…”
Section: Lipid Peroxidation and 2-deoxy Ribose Sugar Damage Mitigationmentioning
confidence: 99%