Antioxidant activities ofPandanus amaryllifoliusleavesextractedunderfour designed extractionconditions
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Creator Natthaphon Thatsanasuwan, Warangkana Srichamnong, Chaowanee Chupeerach, Wantanee Kriengsinyos and Uthaiwan Suttisansanee
Title Antioxidant activities ofPandanus amaryllifoliusleavesextractedunderfour designed extractionconditions
Publisher Faculty of Agro-Industry
Publication Year 2558
Journal Title Food and Applied Bioscience
Journal Vol. 3
Journal No. 2
Page no. 130-136
Keyword antioxidantactivity, ferric reducing antioxidant power (FRAP), bioactive compounds, Pandanus amaryllifolius
URL Website www.tci-thaijo.org/index.php/fabjournal
Website title www.tci-thaijo.org/index.php/fabjournal/article/view/78185
ISSN 2286-8615
Abstract Pandanus amaryllifolius is a tropical plant in Pandanaceae family, which customarily used for food coloring and flavoring. Leaves of P.amaryllifoliusprovidea rich source of essentials oil, carotenoid, vitamin E and other bioactive compounds suchas antioxidants.High quantity of total phenolic compounds (TPC) and antioxidants (as being detected by 2,2-diphenyl-1-picry hydrazyl radical (DPPH) and linoleic acid peroxidation methods)were previously reported. Nevertheless, limited information on antioxidant activities of P.amaryllifolius leaves regarding extraction conditions is available. Thus, the purpose of this study was to investigate the effect ofextraction conditions ofP.amaryllifoliusleavesregarding its antioxidant activity. Freeze-dried powder of P.amaryllifoliusleaves were extracted under designed extraction conditions including extraction times (15240 minutes), concentrations of aqueous ethanol(0100% v/v), extraction temperatures (3090?C) and solid-to-liquid ratios (1:201:60v/w). The antioxidant activities were measured using ferric reducing antioxidant power (FRAP) method. As results, it was found that the antioxidant activities of P.amaryllifoliusleaves extracted under investigatedexperiments were ranged from 9.5423.16mg trolox equivalent (TE) per 1 g dry weight. The optimized extraction conditions of P.amaryllifoliusleaves were 15 minutes of extraction time, 80% (v/v) aqueous ethanol,and 1:60(v/w) of solid-to-liquidratio, while extraction temperaturewas an insignificant factor for extraction conditions. The information received from this research would support further investigation on optimized of condition for extraction by using response surface methodology and isolation of bioactive compounds from leaves of P.amaryllifolius.
Chiang Mai University

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