2006
DOI: 10.1016/j.foodchem.2004.12.015
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Evaluation of antioxidant property of extract and fractions obtained from a red alga, Polysiphonia urceolata

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Cited by 532 publications
(333 citation statements)
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“…Another important matter is that ABTS + can be dissolved in aqueous and organic media, in which the antioxidant activity can be measured, due to the hydrophilic and lipophilic nature of the compounds, those existed in the plant cells. In contrast, DPPH has been used extensively as a free radical to evaluate reducing substances (Cotelle et al 1996) and is a useful reagent for investigating the free radical scavenging activities of polyphenol compounds (Duan et al 2006). Many researchers have reported positive correlation between free radical scavenging activity.…”
Section: Introductionmentioning
confidence: 99%
“…Another important matter is that ABTS + can be dissolved in aqueous and organic media, in which the antioxidant activity can be measured, due to the hydrophilic and lipophilic nature of the compounds, those existed in the plant cells. In contrast, DPPH has been used extensively as a free radical to evaluate reducing substances (Cotelle et al 1996) and is a useful reagent for investigating the free radical scavenging activities of polyphenol compounds (Duan et al 2006). Many researchers have reported positive correlation between free radical scavenging activity.…”
Section: Introductionmentioning
confidence: 99%
“…DPPH, superoxide anion radical scavenging activity assays are most commonly accepted ones which have been used in the present investigation [46,47] . DPPH has been used extensively as a free radical to evaluate reducing substances and is a useful reagent for investigating the free radical scavenging activities of compounds [48] . The use of the DPPH radical provides an easy, rapid and convenient method to evaluate the antioxidant and radical scavengers [49,50] .…”
Section: Discussionmentioning
confidence: 99%
“…Scavenging effects on DPPH radicals Scavenging effects of the extracts on DPPH radicals were determined according to Duan et al (2006). Hundred microliters of various concentrations of tea extracts was mixed with 2900 μl DPPH solution (120 μM) in ethanol and incubated at 37˚C for 30 min in the dark.…”
Section: Methodsmentioning
confidence: 99%