4.2 Article

Evaluation of Antioxidant Activity of Picrorhiza kurroa (Leaves) Extracts

Journal

INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 75, Issue 3, Pages 324-329

Publisher

INDIAN PHARMACEUTICAL ASSOC
DOI: 10.4103/0250-474X.117438

Keywords

Picrorhiza kurroa; leaves; HPLC; antioxidant activity; DPPH; ABTS

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Picrorhiza kurroa is a well-known herb in Ayurvedic medicine. Although it shows antioxidant, antiinflammatory and immunomodulatory activities, it is most valued for its hepatoprotective effect. The rhizomes are widely used against indigestion problems since ancient times due to improper digestive secretions. Aim of this study was to explore antioxidant study of P. kurroa leaves for a new source of naturally occurring antioxidants. Two pure compounds, luteolin-5-O-glucopyranoside (1) and picein (2) were isolated from butanol extract through column chromatography. Different extracts of P. kurroa leaves (ethanol, ethyl acetate, butanol) were quantified for isolated compound (2) by high-performance liquid chromatography. All the extracts and isolated compounds were evaluated for its antioxidant activity using two assays, 2,2-diphenyl-1-picrylhydrazyl radical and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonicacid) assay. The linear detection range was 1.56-200 mu g/ml for picein. The limit of detection and limit of quantification for picein were 2.34 and 7.81 mu g/ml, respectively. Butanol and ethyl acetate extract showed greater antioxidant activity as compare to ethanol extract. Compound 1 and ascorbic acid showed nearly similar antioxidant activity where as 2 showed no activity at standard concentration. The IC50 values for 2,2-diphenyl-1-picrylhydrazyl radical and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) assay for ascorbic acid, compound 1, ethanol extract and its different fractions (ethyl acetate and butanol) were found to be 0.81, 1.04, 67.48, 39.58, 37.12 and 2.59, 4.02, 48.36, 33.24, 29.48 mu g, respectively.

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