potential antioxidant anthraquinones isolated from rheum emodi showing nematicidal activity against meloidogyne incognita

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ID: 240381
2014
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Ranked #131 of 215 articles by views in british journal of psychology (london, england : 1953)

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Abstract
Antioxidant and nematicidal properties were evaluated for R. emodi extractives which are extracted by standardizing and adopting accelerated solvent extraction (ASE) method along with traditional Soxhlet extraction. The extracted material was separated using flash chromatography and the separation conditions and solvents were standardized for the extracted plant constituents. The purity was detected by using analytical reverse phase high pressure liquid chromatography (HPLC). LC-MS/MS detection in the direct infusion mode of the isolated, purified products afforded four anthraquinones, characterized by their infrared spectra (IR) and 1H spectra as chrysophanol, physcion, emodin, and aloe-emodin. Five antraquinone glucoside derivatives and piceatannol-3-O-β-d-glucopyranoside have also been detected from the extracted product. During in vitro evaluation the antioxidant potential of methanolic crude extract (CE1) was the highest, followed by ethyl acetate crude extract (CE2) and chloroform extract (CE3) in DPPH radical scavenging activity. The CE1 also demonstrated outstanding nematicidal activity as compared with other extracts, pure anthraquinones, and even positive control azadirachtin. The study conclusively demonstrated the antioxidant potential of R. emodi extracts and also its ability in extenuating the Meloidogyne incognita (root-knot nematode). The bioassay results can be extrapolated to actual field condition and clinical studies.
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tripathi2014journalpotential Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Brijesh Tripathi;Rohit Bhatia;Alka Pandey;Jitender Gaur;Gautam Chawala;Suresh Walia;Eun Ha Choi;Pankaj Attri
Journal british journal of psychology (london, england : 1953)
Year 2014
DOI
10.1155/2014/652526
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