2010
DOI: 10.1016/j.foodchem.2010.01.028
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Antioxidant activity of devil’s claw cell biomass and its active constituents

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Cited by 31 publications
(20 citation statements)
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“…Prior to the experiments reported here the callus culture was supported on Linsmayer and Skoog medium (LS; Linsmayer & Skoog, 1965) with 0.2 mg/l 2,4-dichlorophenoxyacetic acid, while the hairy root culture was supported on Murashige and Skoog medium (MS; Murashige & Skoog, 1962), in both cases supplemented with 30 g/l sucrose and solidified by plant agar (5.5 g/l, Duchefa, The Netherlands). The maintenance conditions for these cultures, and the preparation and inoculation of the cell suspension and hairy root cultures are described elsewhere (Georgiev, Heinrich, Kerns, Pavlov, & Bley, 2006;Georgiev et al, 2010). In the experiments the cell suspension culture and hairy roots were cultured submerged on a shaker (110 rpm), at 26°C, in the dark.…”
Section: Devil's Claw In Vitro Systemsmentioning
confidence: 99%
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“…Prior to the experiments reported here the callus culture was supported on Linsmayer and Skoog medium (LS; Linsmayer & Skoog, 1965) with 0.2 mg/l 2,4-dichlorophenoxyacetic acid, while the hairy root culture was supported on Murashige and Skoog medium (MS; Murashige & Skoog, 1962), in both cases supplemented with 30 g/l sucrose and solidified by plant agar (5.5 g/l, Duchefa, The Netherlands). The maintenance conditions for these cultures, and the preparation and inoculation of the cell suspension and hairy root cultures are described elsewhere (Georgiev, Heinrich, Kerns, Pavlov, & Bley, 2006;Georgiev et al, 2010). In the experiments the cell suspension culture and hairy roots were cultured submerged on a shaker (110 rpm), at 26°C, in the dark.…”
Section: Devil's Claw In Vitro Systemsmentioning
confidence: 99%
“…To evaluate the anti-inflammatory effects we applied a scheme for isolating the bioactive metabolites, involving low pressure chromatographic separation, as described by Georgiev et al (2010). Portions (50 g) of the freeze-dried suspension cell biomass and hairy roots were individually homogenised with sea sand using a mortar and pestle, then extracted by incubation in pure MeOH for 48 h. The resulting extracts from the cell biomass and hairy roots, designated fractions CME-CB and CME-HR, respectively, were filtered and the solvent and volatile components were evaporated in vacuo, leaving dry residues of 23.4 and 20.13 g, respectively.…”
Section: Extraction and Sample Preparationmentioning
confidence: 99%
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“…1;Georgiev et al 2010;Gyurkovska et al 2010) and hairy root cultures Homova et al 2010). The present study has been undertaken to evaluate the biosynthetic potential of H. procumbens cell suspensions, batchcultivated in shake-flasks, and to compare them as potential sources for commercial production of bioactive secondary metabolites to hairy root cultures of the same species.…”
Section: Introductionmentioning
confidence: 99%
“…Previous chemical and pharmacological studies have preliminarily confirmed that phenylpropanoid glycosides, iridoid glycosides and flavonoids are the main chemical constituents and active substances of this plant [4,5]. These kinds of compounds play an important role in human health owing to their antioxidant activities [6][7][8]. Therefore, the development of convenient and efficient methods to screen and separate antioxidant active substances with higher activity and safety from this plant is highly desirable.…”
Section: Introductionmentioning
confidence: 99%