Identification of phenolics in the fruit of emblica (Phyllanthus emblica L.) and their antioxidant activities

An activity-directed fractionation and purification process was used to identify the antioxidative components of emblica fruit. Dried fruit of emblica was extracted with methanol and then partitioned by ethyl ether, ethyl acetate, butanol and water. The ethyl acetate fraction showed the strongest 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity among four fractions. The ethyl acetate fraction was then subjected to separation and purification using Sephadex LH-20 chromatography and reverse-phase high-performance liquid chromatography (HPLC). Six compounds were identified to be geraniin (1), quercetin 3-β-d-glucopyranoside (2), kaempferol 3-β-d-glucopyranoside (3), isocorilagin (4), quercetin (5), and kaempferol (6), respectively, by spectral methods, ¹H and ¹³C nuclear magnetic resonance (NMR) spectroscopy, ultraviolet–visible (UV–Vis) spectrophotometry and mass spectroscopy (MS), and comparison with literatures. Compounds 2–4 and 6 were identified from emblica fruit for the first time. Furthermore, the antioxidant activities of purified compounds were screened for their antioxidative potential using lipid peroxidation and DPPH systems. All the purified compounds showed strong antioxidant and radical scavenging activities. Amongst, geraniin showed the highest antioxidant activity (4.7 and 65.7 μM of IC₅₀ values for DPPH and lipid peroxidation assay, respectively) than other purified compounds.     

Structural identification of isomallotusinin and other phenolics in Phyllanthus emblica L. fruit hull

The air-dried fruit hull of Phyllanthus emblica L. was extracted with 95% ethanol, and then the extract was partitioned by diethyl ether and ethyl acetate (EA). The EA fraction was then subjected to separation and purification using silica gel and Sephadex LH-20 column chromatography repeatedly to obtain five hydrolysable tannins. They were identified as mucic acid 1,4-lactone 3-o-gallate (C1), isocorilagin (C2), chebulanin (C3), chebulagic acid (C4) and isomallotusinin (C5) using mass spectrometry and nuclear magnetic resonance (NMR) spectrometry. Isomallotusinin and chebulanin were identified from emblica dried fruit hull for the first time, and isomallotusinin was the first time identified from Phyllanthus. Furthermore, the antioxidant abilities of these hydrolysable tannins were investigated using DPPH and ABTS⁺ radical scavenging systems. All hydrolysable tannins showed strong DPPH and ABTS⁺ radical scavenging activities. Isomallotusinin and chebulagic acid exhibited the highest antioxidant activity compared to other purified compounds tested.     

Antioxidant and Anti‐inflammatory Activities of Methanol Extracts of Tremella fuciformis and Its Major Phenolic Acids

Methanol extract subfractions of the edible white jelly mushroom (Tremella fuciformis), were assessed for the following antioxidant properties: ABTS⁺ radical scavenging activity, 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) radical scavenging activity, and inhibitory activity of human low‐density lipoprotein (LDL) oxidation. Among the subfractions tested, the chloroform subfraction exhibited the strongest antioxidant activity, with the highest total phenolic content (66.31 μg CAE/mg extract) and flavonoids content (5.12 μg QE/mg extract). The ABTS⁺ radical scavenging activity of the chloroform subfraction was 7.89 μmol trolox/mg extract, which was the highest among all subfractions. This subfraction also showed the highest DPPH radical scavenging activity and inhibitory activity of LDL oxidation. In addition, the chloroform subfraction demonstrated anti‐inflammatory activity through inhibition of nitric oxide production and inducible nitric oxide synthase expression in RAW 264.7 cells. Major phenolic acids from the mushroom extract were identified as 4‐hydroxybenzoic acid (323 mg/kg dry weight of mushroom), gentisic acid (174 mg/kg dry weight of mushroom), and 4‐coumaric acid (30 mg/kg dry weight of mushroom).     

HPLC测定余甘子茶中3种多酚成分及抗氧化活性研究

福林酚法测定五个产地的余甘子茶中总多酚(TP)的含量,高效液相色谱法(High performance liquid chromatography,HPLC)分析没食子酸(GA)、柯里拉京(CO)、鞣花酸(EA)的含量,并对其抗氧化活性进行研究。结果表明:TP含量最高的是凉山的余甘子茶,其值为228 mg/g;漳州的余甘子茶中GA、CO、EA含量最高,分别为5.00、28.76、4.30 mg/g;在抗氧化活性研究中,昆明的余甘子茶提取液总还原能力较高,但凉山的余甘子茶提取液对DPPH自由基(DPPH·)和羟自由基(·OH)清除能力较好,EC₅₀分别为7.46 μg/mL和0.44 mg/mL,其对自发性肝脂质氧化抑制能力好于其它产地。相比较而言,凉山产地的余甘子茶作为开发天然抗氧化剂更具优势。     

Effect of hot acidic fructose solution on caramelisation intermediates including colour,hydroxymethylfurfural and antioxidative activity changes

Fructose model solutions of various concentrations were adjusted to pH 3.0, then incubated at 75, 85, and 95 °C, respectively, for studying the reaction kinetics of colour development, hydroxymethylfurfural (HMF) production, and antioxidative activities change in the caramelisation reaction. Results showed that colour development, HMF production, DPPH radical scavenging activity and ABTS^·+ radical scavenging activity in the system increased linearly with a first-ordered kinetics on fructose concentration. Their values of Q₁₀ were 1.87, 4.48, 2.06, and 2.24, and activation energies were 66, 160, 77, and 86 kJ/mol, respectively.     

Activity guided isolation of antioxidants from the leaves of Ricinus communis L.

An activity-guided isolation and purification process was used to identify the DPPH (l,l-diphenyl-2-picrylhydrazyl) free radical scavenging components of the food plant (Ricinus communis L.) of Eri silkworm. Dry leaves of R. communis L. were extracted with different solvents and tested for their antioxidant activity against DPPH^•. The MeOH:water (8:2) extract showed strong DPPH radical-scavenging activity, and was subjected to column chromatography over silica gel. Gallic acid, quercetin, gentisic acid, rutin, epicatechin and ellagic acid were isolated as active components and characterised by different spectroscopic techniques.     

Total phenolic content and antioxidant capacity of extracts obtained from six important fruit residues

The extracts from kinnow peel, kinnow seeds, litchi pericarp, litchi seeds, grape seeds, and banana peel were screened for total phenolic content (TPC), trolox equivalent antioxidant capacity (TEAC), 1,1 diphenyl-2-picryl hydrazyl (DPPH) radical scavenging activity, as well as reducing power. Kinnow peel extract exhibited the highest reducing power, TEAC, and DPPH free radical scavenging activity, whereas, the phenolic content of 37.4 mg GAE/g-dw was highest for grape seed extract. Banana peel extract with a low TPC showed the lowest reducing power, TEAC as well as DPPH free radical scavenging activity among the fruit residue extracts examined in the present study. Correlation analysis between the reducing power and DPPH radical scavenging ability; reducing power and ABTS radical scavenging activity; and ABTS and DPPH radical scavenging abilities showed a high degree of correlation (r² = 0.85-0.91). However, r² of 0.36, 0.66, and 0.49 between TPC and DPPH radical scavenging activity; TPC and reducing power; and TPC and ABTS radical scavenging ability, respectively, indicated that some non-phenolic compounds also contributed to the total antioxidant activity in fruit residue extracts examined in this study. To the best of our knowledge, this is the first paper presenting comprehensive data on TPC, reducing power, and antioxidant activity for the six fruit residues. This study demonstrated that kinnow peel, litchi pericarp, litchi seeds, and grape seeds, can serve as potential sources of antioxidants for use in food and pharmaceutical industry.     

Antioxidant and antimicrobial activities of Polygonum cognatum Meissn extracts

The antioxidant activities, reducing powers, 2,2‐diphenyl‐l‐picrylhydrazyl (DPPH) radical‐scavenging activities, total phenolic compound contents and antimicrobial activities of ether, ethanol and hot water extracts of Polygonum cognatum Meissn were studied in vitro. The highest antioxidant activity was found in the water extract. However, there were no statistically significant differences among 15 µg ml^?1 extract‐containing samples in linoleic acid emulsion (0.02 M , pH 7.0) during 120 h of incubation (P > 0.05). The reducing power of the water extract was the highest, but its reducing power was markedly lower than that of ascorbic acid. The highest DPPH radical‐scavenging activity was found in the water extract, with 50% DPPH radical scavenging at a concentration of 100 µg ml^?1 dried water extract, while at the same concentration of dried ethanol extract the value was 12%. Surprisingly, no DPPH radical‐scavenging activity was observed in the ether extract. The concentrations of phenolic compounds found were 0.48, 0.50 and 0.01 µg ml^?1 gallic acid equivalent in 10 µg ml^?1 water, ethanol and ether extracts respectively. The ether and ethanol extracts showed antimicrobial activity against Staphylococcus aureus and Bacillus subtilis. The water extract did not show antimicrobial activity against the studied micro‐organisms. © 2002 Society of Chemical Industry     

Antioxidant activity of extracts from the fruiting bodies of Agrocybe aegerita var. alba

Antioxidant activity of the methanol crude extract and its fractions, isolated by liquid–liquid partition, from the fruiting bodies of Agrocybe aegerita, an edible mushroom, was evaluated by scavenging activity of 2,2^′-azinobis-(3-ethylbenzthiazoline-6-sulphonic acid) radical cation (ABTS⁺) and inhibition of lipid peroxidation of rat brain homogenate. The ethyl acetate (EA) fraction, which showed the most potent antioxidant activity in the above two assays, was further fractionated by a Sephadex LH-20 column into four subfractions (EA1–EA4). EA3 exhibited the strongest radical-scavenging activity in the ABTS⁺ and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical and showed a similar extent of in vitro inhibition of human LDL oxidation to caffeic acid. Significant correlation was found between the total phenolic content and the antioxidant activity (p<0.01) in the EA fraction and its subfractions.     

Effect of roasting on the radical scavenging activity of cocoa beans

The free-radical scavenging activity of cocoa samples subjected to different roasting treatments has been determined. The samples (raw, pre-roasted and roasted) were separated into four molecular weight fractions per sample (>30, 30–10, 10–5, and <5 kDa). The free-radical scavenging activity was determined with the DPPH^• (1,1-dipheny-2-picrylhydrazyl), and ABTS^•+ [2,2’-azinobis (3-ethylbenzothiazoline-6-sulfonic acid)] free-radical scavenging assays for all samples. Both tests were compared in terms of sensitivity and measurement precision, at different reaction times. Comparing the results from each test, the free-radical scavenging activity trends were similar for each fraction but with notable differences in the sensitivity of the assays. Analysis of the concentration of reducing substances, such as water soluble phenolics, melanoidins, carbohydrates, etc, in these fractions by the photometric Folin–Ciocalteu assay, showed a similar pattern to the free-radical scavenging activity trend. Moreover, this comparison showed that there were significantly (P < 0.05) more reducing substances and free-radical scavenging activity in the 10–5 kDa roasted cocoa bean fraction.     

Assessment of phenolic profile of Turkish honeys

In this study, phenolic profile and antioxidant activity of 60 Turkish honey samples of nineteen different floral origins were evaluated by ultra-performance liquid chromatography with electrospray ionization coupled to tandem mass spectrometry, providing the identification of 32 phenolic compounds. Thyme (1051.58 mg/kg), pine (994.18 mg/kg), carob (935.03 mg/kg), eucalyptus (814.46 mg/kg), rhododendron (680.71 mg/kg), heather (562.59 mg/kg), cedar (561.83 mg/kg), and euphorbia (501.64 mg/kg) present significantly high phenolic content. Moreover ferulic, homogentisic, gentisic, syringic, 3,4-dihydroxybenzoic, caffeic, vanillic, p-coumaric, 4-hydroxy benzoic, and trans-2-hydroxy cinnamic acids were the most abundant of the determined compounds. The antioxidant activities of the honeys were evaluated by β-carotene-linoleic acid inhibition, DPPH free radical scavenging activity and ABTS⁺ cation radical scavenging activity which were measured as IC₅₀: 10.87 – 48.23 µg/mL, SC₅₀: 54.33 – 99.40 µg/mL and SC₅₀: 10.33 – 41.20 µg/mL, respectively. Phenolic compounds are considered antioxidant constituents, and they could be stated as components that account for antioxidant activity in Turkish honeys.     

Kinetics of fructose on the Maillard brown colour development,pH change and antioxidative activity development in model fructose/glycine systems

Model fructose/glycine systems with fructose concentration between 0.035 and 0.28 m were incubated at temperature 45–90 °C for investigating the effects of fructose and temperature on the brown colour development, pH change and the antioxidative activity developments of Maillard reaction. The result showed that effects of fructose followed logarithm‐order kinetics on brown colour and DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) radical scavenging activity (S_DPPH) development, and first‐order kinetics on system pH decrease. However, the effect of fructose on ABTS·⁺ (2,2′‐azino‐bis[3‐ethylbenzthiazoline‐6‐sulphonic acid]) radical scavenging activity (S_ABTS) development was first order at 60–90 °C and logarithm order at 45 °C, which revealed the mutual synergistic interaction of concentration with temperature on S_ABTS development. Activation energy for S_DPPH development was lower than that for S_ABTS development, revealing that DPPH radical was more vulnerable than ABTS·⁺ radical to fructose/glycine MRPs at low temperature. But the relative vulnerability would invert at high temperature, as the Q₁₀ value for S_DPPH development was lower than that for S_ABTS development.     

Antioxidant properties of different fractions of Vitex negundo Linn.

Vitex negundo Linn. (VN), belonging to family Verbenaceae, is an aromatic shrub distributed throughout India. In the ayurvedic system of medicine it is used as a drug of choice to manage pain, inflammation and other related diseases. It contains many polyphenolic compounds, terpenoids, glycosidic iridoids and alkaloids. Since polyphenolic compounds have high antioxidant potential, the antioxidant potency of V. negundo was investigated by employing various established in vitro systems, such as 2,2′-azino-bis 3-ethyl benzothiazoline-6-sulfuric acid (ABTS^∗+)/Lipid Peroxides (LPO)/Superoxide/Hydroxyl radical scavenging and iron ion chelation. Total antioxidant capacity was determined by the assay based on the preformed radical monocation ABTS^∗+. Lipid peroxidation was assessed in terms of thiobarbituric acid reactive substances by using egg yolk homogenates as lipid rich media. Superoxide radical scavenging assay was based on the riboflavin-light-Nitro blue tetrazolium (NBT) system. Hydroxyl radical trapping potential was determined by evaluating hydroxyl radical induced deoxyribose degradation using the thiobarbituric acid method. In order to assess the metal chelation properties, hydroxyl radical induced deoxyribose degradation was evaluated in the absence of Ethylenediamine tetra acetic acid (EDTA). All the polar fractions significantly showed trapping of free radicals, and thereby inhibition of lipid peroxidation, and also chelated the iron ion. Interestingly, the hexane fraction did not show any activity against superoxides radicals and it had minimum trapping potential for other free radical (FR) species also. Thus, it may be concluded that the polar fractions of VN possess potent antioxidant properties, which may be mediated through direct trapping of the free radicals and also through metal chelation. Therefore its reported anti-inflammatory properties, could be through the down regulation of the free radical mediated pathway of inflammation.     

Antioxidant properties of dried product of ‘haba-nori’, an edible brown alga, Petalonia binghamiae (J. Agaradh) Vinogradova

Dried ‘haba-nori’ Petalonia binghamiae, a brown alga, is a traditional food in the fisheries towns in Japan. To determine the antioxidant properties of the dried P. binghamiae, assays for antioxidant activities, including ferrous-reducing power, ferrous ion chelating, 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging and scavenging of a superoxide anion radical-generated by non-enzymatic system were tested in this study. A water extract solution contained total phenols at about 75 μmol phloroglucinol equivalents/g dry sample and showed strong antioxidant activities in the reducing power, DPPH radical and superoxide anion radical scavenging assays. The antioxidant activities were detected in high-molecular (>100 kDa), 10–30 kDa, and low-molecular (<5 kDa) fractions and were correlated with, not only phenolic compounds, but also brown compounds. The radical- scavenging activities were increased by heat treatment at 121 °C for 1 h. These results suggest that P. binghamiae is both a useful seafood and a healthy food with antioxidant activity.     

Polyphenol contents and in vitro antioxidant activities of lyophilised aqueous extract of kiwifruit (Actinidia deliciosa)

The aim of this study was to determine the antioxidant potency and total phenolic and flavonoid contents of kiwifruit (Actinidia deliciosa) in vitro by analysing the radical scavenging activity of lyophilised water extract from kiwifruit (LEK) for 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS), 1,1-diphenyl-2-picryl-hydrazyl (DPPH), N,N-dimethyl-p-phenylenediamine (DMPD), and superoxide anion radical (O₂⁻) as well as the total reducing power by FRAP and CUPRAC assays and the metal chelating activities. LEK showed efficient radical scavenging activity with DPPH, ABTS, DMPD, and O₂⁻ radicals; ferric (Fe³⁺) and cupric (Cu²⁺) ion reducing power and metal chelating activities. Moreover, the amounts of phenolic compounds, such as caffeic acid, ferulic acid, syringic acid, ellagic acid, catechol, pyrogallol, p-hydroxy benzoic acid, vanillin, p-coumaric acid, gallic acid, quercetin, ??-tocopherol and ascorbic acid, in LEK were quantified by LC-MS-MS. The results show that pyrogallol (2070.0 mg/kg LEK) is the main phenolic compound responsible for the antioxidant and radical scavenging activities of LEK. Finally, total phenolic and flavonoid contents were determined as gallic acid (GAE) and quercetin equivalents (QE). The GAE and QE values in LEK were 16.67 ± 2.83 ??g GAE/mg and 12.95 ± 0.52 ??g QE/mg, respectively. The results suggest that consumption of kiwifruit (A. deliciosa) can be beneficial effects due to its antioxidant properties.     

Phenolics from hull of Garcinia mangostana fruit and their antioxidant activities

The air-dried fruit hulls of Garcinia mangostana Linn. were extracted with 70% MeOH, and then partitioned into the n-BuOH fractions. Furthermore, three major phenolic components related to their antioxidant activities were purified by silica gel column chromatography and Sephadex LH-20 and then identified as P₁ (1,3,6,7-tetrahydroxy-2,8-(3-methyl-2-butenyl)), P₂ [1,3,6-trihydroxy-7-methoxy-2,8-(3-methyl-2-butenyl) xanthone] and P₃ (epicatechin) using UV–visible spectrophotometry, IR spectrophotometry and NMR spectroscopy, respectively. The antioxidant activities of three major phenolics were evaluated using different tests, including the free radical scavenging capability and total antioxidant activity in a linoleic acid peroxidation. These three phenolic compounds exhibited different antioxidant activities in these antioxidant tests. The hydroxyl radical and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging capabilities and the activity against linoleic acid peroxidation of P₁ were greater than those of P₂ and P₃, while the superoxide anion radical scavenging activity of P₃ was greater than that of P₁, but was close to that of P₂ or α-tocopherol. An activity-guided isolation and purification process was used to identify the components showing the strong DPPH radical scavenging activity from G. mangostana Linn.     

植物油的不同组分DPPH自由基清除能力及其与微量有益成分含量的相关性

研究评估13种常见植物油的极性组分、非极性组分和全油样品的DPPH自由基清除能力,并将DPPH自由基清除能力与生育酚、多酚、植物甾醇等微量有益成分含量进行相关性分析。结果表明:橄榄油、芝麻油、小麦胚芽油和米糠油极性组分的DPPH自由基清除能力高于其他植物油,均大于200μmol TE/100 g;植物油非极性组分的DPPH自由基清除能力在10.53~553.20μmol TE/100 g之间,小麦胚芽油和米糠油的清除能力较高;植物油全油的DPPH自由基清除效果比非极性组分的略高;植物油非极性组分、植物油全油的DPPH自由基清除能力与生育酚含量、β-谷甾醇含量、菜油甾醇含量呈显著相关(P0.01);植物油极性组分的DPPH自由基清除能力则与多酚含量呈显著相关(P0.05)。