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      Optimal Binary Solvent Extraction System for Phenolic Antioxidants from Mengkudu ( Morinda citrifolia) Fruit

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          Abstract

          Antioxidants have been widely used in the food industry to enhance product quality by preventing oxidation of susceptible substances. This work was carried out to maximise the recovery of total phenolic content (TPC), total flavonoid content (TFC), 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical-scavenging capacity and 2,2′-diphenyl-1-picrylhydrazyl (DPPH) radical-scavenging capacity from Morinda citrifolia fruit via modification of the ethanol concentration, extraction time and extraction temperature at minimal processing cost. The optimised conditions yielded values of 881.57 ± 17.74 mg GAE/100 g DW for TPC, 552.53 ± 34.16 mg CE/100 g DW for TFC, 799.20 ± 2.97 µmol TEAC/100 g DW for ABTS and 2,317.01 ± 18.13 µmol TEAC/100 g DW for DPPH were 75% ethanol, 40 min of time and 57 °C. The four responses did not differ significantly ( p > 0.05) from predicted values, indicating that models obtained are suitable to the optimisation of extraction conditions for phenolics from M. citrifolia. The relative amounts of flavonoids were 0.784 ± 0.01 mg quercetin/g of extract and 1.021 ± 0.04 mg rutin/g of extract. On the basis of the results obtained, M. citrifolia extract can be used as a valuable bioactive source of natural antioxidants.

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          Structure-radical scavenging activity relationships of phenolic compounds from traditional Chinese medicinal plants.

          Traditional Chinese medicinal plants associated with anticancer contain a wide variety of natural phenolic compounds with various structural features and possessing widely differing antioxidant activity. The structure-radical scavenging activity relationships of a large number of representative phenolic compounds (e.g., flavanols, flavonols, chalcones, flavones, flavanones, isoflavones, tannins, stilbenes, curcuminoids, phenolic acids, coumarins, lignans, and quinones) identified in the traditional Chinese medicinal plants were evaluated using the improved ABTS*+ and DPPH methods. Different categories of tested phenolics showed significant mean differences in radical scavenging activity. Tannins demonstrated the strongest activity, while most quinones, isoflavones, and lignans tested showed the weakest activity. This study confirmed that the number and position of hydroxyl groups and the related glycosylation and other substitutions largely determined radical scavenging activity of the tested phenolic compounds. The differences in radical scavenging activity were attributed to structural differences in hydroxylation, glycosylation and methoxylation. The ortho-dihydroxy groups were the most important structural feature of high activity for all tested phenolic compounds. Other structural features played a modified role in enhancing or reducing the activity. Within each class of phenolic compounds, the structure-activity relationship was elucidated and discussed. This study reveals the structure-activity relationships of a large series of representative natural phenolic compounds more systematically and fully than previous work. Structure-radical scavenging activity relationships of some natural phenolics identified in the medicinal plants were evaluated for the first time.
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            Systematic evaluation of natural phenolic antioxidants from 133 Indian medicinal plants

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              Antioxidant properties in vitro and total phenolic contents in methanol extracts from medicinal plants

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                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                14 June 2013
                June 2013
                : 18
                : 6
                : 7004-7022
                Affiliations
                [1 ]School of Hospitality, Tourism and Culinary Arts, KDU University College, Jalan SS 22/41, Damansara Jaya, 47400 Petaling Jaya, Selangor, Malaysia; E-Mail: yy.thoo@ 123456kdu.edu.my
                [2 ]Department of Food Technology, Faculty of Food Science & Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia; E-Mail: hkheng@ 123456hotmail.com
                [3 ]Department of Food Science, Faculty of Food Science & Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia; E-Mail: faridah@ 123456food.upm.edu.my
                [4 ]Department of Bioprocess Technology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia; E-Mail: omlai@ 123456biotech.upm.edu.my
                [5 ]Department of Food Science and Nutrition, Faculty of Applied Sciences, UCSI University, No.1, Jalan Menara Gading, UCSI Heights, Cheras 56000, Kuala Lumpur, Malaysia; E-Mail: cwho@ 123456ucsiuniversity.edu.my
                Author notes
                [* ] Author to whom correspondence should be addressed; E-Mail: tancp@ 123456putra.upm.edu.my ; Tel.: +603-8946-8418; Fax: +603-8942-3552.
                Article
                molecules-18-07004
                10.3390/molecules18067004
                6270242
                23771061
                c72a5f1c-717e-4062-b7aa-40d544b1682b
                © 2013 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 24 April 2013
                : 26 May 2013
                : 09 June 2013
                Categories
                Article

                mengkudu (morinda citrifolia),total phenolic content (tpc),total flavonoid content (tfc),2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (abts) radical-scavenging capacity,2,2′-diphenyl-1-picrylhydrazyl (dpph) radical-scavenging capacity

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