Antioxidant,Antibacterial, and Antiproliferative Activities of Free and Bound Phenolics from Peel and Flesh of Fuji Apple

This study was conducted to investigate the antioxidant, antibacterial, and antiproliferative activities of flesh free (FF), flesh bound (FB), peel free (PF), and peel bound (PB) phenolics from Fuji apple. The PB, which had highest total phenolic contents (126.15 ± 2.41 mg/100 g wet weight) and lowest total carbohydrate contents (34.68 ± 2.78 mg/100 g wet weight), showed the strongest 2,2’‐azinobis‐(3‐ethylbenthiazoline‐6‐sulphonate) (ABTS) radical scavenging activity (EC₅₀ = 0.36 ± 0.02 mg/mL), 1,1‐diphenyl‐2‐picryhydrazyl (DPPH) radical scavenging activity (EC₅₀ = 0.26 ± 0.01 mg/mL), and ferric reducing antioxidant power (Ferric reducing antioxidant power; EC₅₀ = 0.19 ± 0.02 mg/mL) compared with those of FF, FB, and PF. The PB also showed the strongest antibacterial activities on Escherichia coli, Staphylococcus aureus, and Listeria monocytogenes and it also showed the highest antiproliferative effects on Caco‐2 human colonic cancer cell (EC₅₀ = 1.44 ± 0.01 mg/mL) and Hela human cervical cell (EC₅₀ = 2.81 ± 0.01 mg/mL). Both free and bound phenolics from Fuji apple showed good antioxidant, antibacterial, and antiproliferative activities in our study, and bound phenolics had significantly higher activities compared with those of free phenolics.     

Comparison of Antioxidant Activity of Barley (Hordeum vulgare L.) and Malt Extracts with the Content of Free Phenolic Compounds Measured by High Performance Liquid Chromatography Coupled with CoulArray Detector

Hot water (45°C) extracts of ten barley varieties and their corresponding malts were analyzed in terms of antioxidant activity. The ferric reducing antioxidant power (FRAP) and radical scavenging activity (ABTS), ranged from 0.23‐0.45 mg GAE/g_dw for malt and 0.12‐0.25 mg GAE/g_dw for barley. The hull‐less malt KM 1910 was the variety with the best antioxidant properties, whereas the highest antioxidant capacity for barley was detected for the variety Merlin. A significant positive correlation between the methods FRAP, ABTS and ITT was found (p < 0.01). The influence of fertilization (20 kg N/ha) on barley antioxidant capacity was studied. The results obtained suggest that the impact of fertilization was not evident and that it depends significantly on barley genotype. The total polyphenol content, as measured according to Folin‐Ciocalteu's method, ranged from 0.6‐2.9 mg GAE/g_dw and correlated positively with all the antioxidant methods used (p < 0.01). Free phenolic compounds were measured by HPLC with a CoulArray detector. The dominant phenolic compound was ferulic acid and its content ranged from 12.5–21.9 and 7.8–56.1 μg/g_dw for barley and malt, respectively. The content of catechin ranged from 11.0–17.0 μg/g_dw in barley and 0.9–12.1 μg/g_dw in malt.     

酿造啤酒大麦发芽前后多酚组分变化及抗氧化活性

以8?种酿造啤酒大麦及麦芽为原料,分别提取游离酚和结合酚,分析多酚组分变化,并测定其抗氧化活性。结果显示,啤酒大麦发芽前后多酚含量及组分均有显著变化,大麦发芽后总酚含量普遍高于发芽前,其中,Hindmarsh发芽后总酚增加率最高;阿魏酸、荭草素含量在发芽过程中显著增加（P＜0.05）。Hindmarsh游离没食子酸、香草醛与阿魏酸增加率最高;Metcalf结合阿魏酸与荭草素增加率最高。体外抗氧化结果表明,相比发芽前,麦芽多酚清除1,1-二苯基-2-三硝基苯肼（1,1-diphenyl-2-picrylhydrazyl,DPPH）自由基能力及氧自由基吸收能力普遍增强,其中,Scope麦芽游离酚清除DPPH自由基能力最强,Baudin麦芽结合酚的氧自由基吸收能力最好。     

基于UPLC-Q TOF-MS和HPLC-QQQ-MS技术的赤豆酚类化合物定性、定量分析及其抗氧化能力分析

为深入了解赤豆的营养价值,用80%甲醇溶液提取酚类物质,对提取物中不同存在形态的酚类化合物含量及其抗氧化活性进行测定,并对其80%甲醇提取物中酚类物质进行定性、定量分析。结果表明,赤豆80%甲醇提取物中酚酸含量为3.44 mg/g,黄酮含量为2.50 mg/g,其中3 种存在形式酚类萃取物含量及抗氧化能力不同,糖苷键合态酚酸含量最高,可达1.44 mg/g,游离态黄酮含量最高,可达0.85 mg/g;糖苷键合态亚铁离子还原能力最强,可达15.76 mmol/g,酯键合态1,1-二苯基-2-三硝基苯肼自由基、2,2′-联氮双(3-乙基苯并噻唑啉-6-磺酸)阳离子自由基清除能力最强;80%甲醇提取物通过超高效液相色谱串联四极杆飞行时间质谱仪定性分析,初步鉴定出25 种化合物,包括3 种有机酸、6 种酚酸、16 种黄酮;高效液相色谱串联三重四极杆质谱联用仪定量分析可得,芦丁（327.40 μg/g）、儿茶素类（210.70 μg/g）含量丰富。     

苦荞麸皮多酚抑制人结肠癌细胞Caco-2增殖活性研究

研究了产自重庆酉阳的苦荞(Fagopyrum tartaricum L.Gaerth,FG1)麸皮和四川西昌的苦荞(Fagopyyrum tartaricum L.Gaerth,FG2)麸皮中酚类化合物的含量、抗氧化和抗增殖活性。结果表明:FG1和FG2 2种苦荞麸皮总酚含量分别为(26.40±0.41)和(27.00±0.72)mg GAE/g DW,且游离态是其酚类化合物的主要存在形式(约占其总酚含量的93%);2种苦荞麸皮酚提取物均表现出一定的抗氧化性,并且FG2的抗氧化能力强于FG1(P0.05),FG1和FG2的DPPH自由基清除能力总IC50值分别为(39.56±2.76)和(24.69±0.33)μg·mL~(-1);还原力总EC_(50)值分别为(97.92±1.4)和(73.18±4.32)μg·mL~(-1);在抗增殖试验中,与对照组相比,FG1和FG2游离酚提取物均能明显抑制人结肠癌细胞Caco-2增殖(P0.05)。然而,在不产生细胞毒性的浓度范围内,其结合酚提取物却表现出极弱的抗增殖作用。     

青钱柳叶活性成分的抗氧化活性及UPLC-QTOF-MS/MS分析

利用96孔板法测定青钱柳叶不同溶剂(水、70%乙醇、乙酸乙酯和正己烷)提取物中总酚、总黄酮含量及抗氧化活性(DPPH自由基清除能力、还原能力、总抗氧化能力),考察酚类物质含量与抗氧化活性的相关性,并采用超高效液相色谱-四极杆飞行时间串联质谱(ultra performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spetrometry,UPLC-QTOF-MS/MS)分析提取物中主要活性成分。结果表明:不同提取物中总酚、总黄酮含量及抗氧化活性存在显著性差异且70%乙醇溶液提取物表现出最高的总酚(219.01 mg GAE/g)、总黄酮含量(7.23 mg CE/g)及最强的DPPH自由基清除能力(35.46 mg TE/g)和还原能力(1.89 mmol Fe SO_4/g);总酚、总黄酮含量与DPPH自由基清除能力、还原能力之间呈正相关,与总抗氧化能力呈显著负相关,表明多酚类物质是青钱柳中主要的抗氧化剂。UPLC-QTOF-MS/MS分析70%乙醇溶液提取物并初步鉴定出22种化合物,包括2种有机酸、4种酚酸、5种黄酮、8种三萜皂苷类和3种酯类,其中酚酸和黄酮类化合物是主要的抗氧化活性成分,有机酸、三萜皂苷及酯类化合物可能是潜在的抗氧化活性成分。     

海菜花结合酚的组成、抗氧化活性及其对DNA损伤的保护作用

采用福林-酚法、亚硝酸钠-氯化铝法分别测定海菜花花、茎、叶中结合酚总酚及黄酮含量,采用高效液相色谱(HPLC)分析结合酚的组成,并研究其抗氧化活性及其对过氧自由基(ROO·)介导的DNA损伤保护作用.结果表明,海菜花结合酚总酚含量为209.72～366.35 mg GAE/g提取物(Extract),黄酮含量为156....     

薏米中多酚化合物的分离纯化及抗氧化活性分析

利用葡聚糖凝胶将薏米中两类多酚类物质进行分离纯化,从而得到6个不同的组分。采用Folin-Ciocalteu法测定该6个组分总酚含量,采用氧自由基吸收能力(oxygen radical absorbance capacity,ORAC)、过氧化氢自由基清除能力(peroxyl radical scavenging capacity,PSC)和细胞内抗氧化能力(cellular antioxidant activity assay,CAA)分析法测定所得6个组分抗氧化能力。在所得的6个组分中选择抗氧化活性最强的3个组分进行半制备,可制得4种薏米多酚纯化物,并测定其4种纯化物的抗氧化活性。结果发现,所分离的6个组分中,薏米中的多酚主要存在于组分2、组分3及组分5中,其总酚含量分别为(30.56±2.25)、(17.40±2.76)、(25.18±1.10)mg GAE/100 g薏米粉末,结合型酚类化合物占薏米总酚含量1/3以上。组分2、组分3及组分5薏米多酚的抗氧化能力较强。经过半制备液相得到的4种多酚纯化物质分别为N_1,N_5-双(对香豆酰)亚精胺、对香豆酸、阿魏酸及芦丁,其中N_1,N_5-双(对香豆酰)亚精胺为游离型多酚的主要物质,而阿魏酸为结合型多酚的主要物质,但在游离型多酚中也有少许存在。4种酚类化合物均具有强抗氧化活性,是薏米中多酚类物质发挥抗氧化作用的主要活性成分。     

Antioxidant and antigenotoxic effect of dairy products supplemented with red ginseng extract

The purpose of this study was to evaluate the antioxidant and antigenotoxic effect of dairy products milk (M) and yogurt (Y) after the addition of 2% red ginseng extract to milk (RM) and to yogurt (RY). Total phenolic content, total flavonoid content, 2,2-diphenyl-1-picrylhydrazyl radical scavenging activity, oxygen radical absorbance capacity, and total radical trapping antioxidant potential were determined in the samples. Furthermore, antigenotoxic effect of samples was measured, using comet assay in human leukocytes. Total phenolic content and total flavonoid content of RM [38.3 ± 0.8 mg of gallic acid equivalents (GAE)/100 g, 23.6 ± 0.1 mg of quercetin equivalents (QE)/100 g] and RY (41.1 ± 0.9 mg of GAE/100 g, 18.7 ± 0.1 mg of QE/100 g), respectively, were higher than those of M (6.31 ± 0.2 mg of GAE/100 g, 10.4 ± 0.1 mg of QE/100 g) and Y (8.1 ± 0.9 mg of GAE/100 g, 8.4 ± 0.2 mg of QE/100 g), respectively. The 2,2-diphenyl-1-picrylhydrazyl radical scavenging activity and oxygen radical absorbance capacity values increased significantly after the addition of 2% red ginseng in both. Additionally, the total radical trapping antioxidant potential in RM (787.7 ± 7.0 μg/mL) was lower than in M (2074.0 ± 28.4 μg/mL). The H₂O₂-induced DNA damage in RY (0.1 ± 0.0 mg/mL) was less than the damage in Y (0.4 ± 0.0 mg/mL), but we found no significant difference between M and RM. This study indicates that supplementation with red ginseng can fortify the antioxidant and antigenotoxic effects of dairy products effectively.     

Determination of oil palm fruit phenolic compounds and their antioxidant activities using spectrophotometric methods

There is scarce information on the phenolics of oil palm fruits (Elaeis guineensis). In this study, phenolics were extracted from oil palm fruits and analysed using spectrophotometry for information on the different types of palm phenolics and their antioxidative activities. Analyses of the total phenolic content (TPC), total flavonoid content (TFC), o‐diphenols index, hydroxycinnamic acid index, flavonols index and phenol index showed ranges between 5.64 and 83.97 g L^?1 gallic acid equivalent (GAE), 0.31–7.53 g L^?1 catechin equivalent, 4.90–93.20 g L^?1 GAE, 23.74–77.46 g L^?1 ferulic acid equivalent, 3.62–95.33 g L^?1 rutin equivalent and 15.90–247.22 g L^?1 GAE, respectively. The antioxidant assay, 2,2‐diphenyl‐2‐picrylhydrazyl radical scavenging assay, showed antioxidative activities in all the extracts with results ranging from 4.41 to 61.98 g L^?1 trolox equivalent. The high antioxidant activities of the oil palm fruit phenolics were also found to increase with increasing TPC and TFC.     

Antioxidant Properties and Phenolic Composition of Greek Propolis Extracts

This study was undertaken to determine the total phenols, total flavonoids, and major phenolic compounds in the polar (methanol, 80% methanol, and aqueous) extracts of propolis collected from the Greek mainland (West Macedonia) and the Greek island, Rhodes. The antioxidant properties of the propolis extracts were also evaluated by using free 2,2^′-diphenyl-1-picrylhydrazyl radical scavenging assay and ferric reducing antioxidant power assay. The results showed that propolis from West Macedonia was found to be the strongest radical scavenger and ferric reducing agent (mean IC₅₀ 0.179 and 0.009 mg/ml, respectively). Methanol (mean IC₅₀ 0.181 mg/ml) and 80% methanol extracts (mean IC₅₀ 0.138 mg/ml) of propolis from West Macedonia showed higher radical scavenging activity than the synthetic antioxidant butylated hydroxytoluene (mean IC₅₀ 0.207 mg/ml), while exhibiting similar levels of reducing activity (IC₅₀ 0.0099 mg/ml and 0.0085 mg/ml, respectively) with flavonol quercetin (mean IC₅₀ 0.0101 mg/ml). In addition, analysis by high performance liquid chromatography showed that West Macedonia propolis, contained the highest amount of phenolic compounds: phenolic acids (caffeic acid, caffeic acid phenethylester, ferulic acid, p-coumaric acid) and flavonoids (quercetin, galangin, luteolin, apigenin). Caffeic acid (0.639–4.172 mg/g propolis) and galangin (1.317–8.551 mg/g propolis) were found to be the predominant phenolic compounds in these propolis extracts.     

Phenolic acid composition and antioxidant properties of Malaysian honeys

Abstract: The phenolic acid and flavonoid contents of Malaysian Tualang, Gelam, and Borneo tropical honeys were compared to those of Manuka honey. Ferric reducing/antioxidant power assay (FRAP) and the 1,1‐diphenyl‐2‐picryl‐hydrazyl (DPPH) radical‐scavenging activities were also quantified. All honey extracts exhibited high phenolic contents (15.21 ± 0.51– 42.23 ± 0.64 mg/kg), flavonoid contents (11.52 ± 0.27– 25.31 ± 0.37 mg/kg), FRAP values (892.15 ± 4.97– 363.38 ± 10.57 μM Fe[II]/kg), and high IC₅₀ of DPPH radical‐scavenging activities (5.24 ± 0.40– 17.51 ± 0.51 mg/mL). Total of 6 phenolic acids (gallic, syringic, benzoic, trans‐cinnamic, p‐coumaric, and caffeic acids) and 5 flavonoids (catechin, kaempferol, naringenin, luteolin, and apigenin) were identified. Among the Malaysian honey samples, Tualang honey had the highest contents of phenolics, and flavonoids, and DPPH radical‐scavenging activities. We conclude that among Malaysian honey samples, Tualang honey is the richest in phenolic acids, and flavonoid compounds, which have strong free radical‐scavenging activities.     

In vitro evaluation of the antioxidant activities in the differentially processed seeds from underutilized legume, Bauhinia vahlii Wight & Arn

Antioxidant potential and total phenolics content of 70% acetone extracts of the raw and processed seeds of Bauhinia vahlii were evaluated. The extract of raw seeds contained higher levels of total phenolics (30.8 g/100 g) and tannins (19.6 g/100 g) compared to dry heated and soaking followed by autoclaving seed extracts. Extracts were screened for antioxidant and free radical scavenging activities using various chemical and in vitro model systems. In all the models, except DPPH radical scavenging activity, the extract from raw seeds manifested the strongest antioxidant activity than that from processed seeds. In β-carotene/linoleic acid emulsion system and superoxide scavenging activity, the raw seed extract registered more activity when compared to the standards (butylated hydroxyanisole and α-tocopherol). Whereas, the extract from dry heated seed exhibited higher DPPH^· scavenging activity (IC₅₀ 70.77 μg/mL) than the raw seeds (IC₅₀ 74.4 μg/mL). This study has to some extent validated the antioxidant potential of the seeds of B. vahlii.     

Antioxidant capacity, phenolic content, and polysaccharide content of Lentinus edodes grown in whey permeate-based submerged culture

ABSTRACT:  Total antioxidant capacity (TAC), phenolic content, and crude water-soluble polysaccharide (WSP) were determined for Lentinus edodes mycelia grown on both whey permeate (WP)-based medium with lactose content of 4.5% and controlled medium, and harvested after 5, 10, 15, or 20 d of fermentation at 25 °C. Both methanol extracts and water extracts of L. edodes in this study were found to exhibit high free radical scavenging capacity. The harvesting time was found to contribute to most of the variability in the free radical scavenging capacity. High levels of antioxidant capacities (0.28 ± 0.03 and 0.29 ± 0.06 mmol TAE/g dry weight for methanol and water extracts, respectively) were observed in mycelia grown on whey permeate and harvested on day 10. Harvesting time and the type of media can interact to alter the chemical content of mycelia. Mycelia grown in whey permeate had greater ( P < 0.05) WSP than mycelia grown in the synthetic media. High levels of WSP (4.1 × 10²± 71 mg polysaccharide/g dried mycelia) were found in mycelia grown in whey permeate and harvested on day 10. Whey permeate grown mycelia had phenolic compounds ranging from 4.2 ± 0.1 to 8.0 ± 0.8 mg GAE/g dried mycelia. The overall means of total phenolic contents of mycelia grown in whey permeate were 5.9 ± 0.5 and 6.2 ± 0.6 mg GAE/g dried mycelia for methanol and water extracts, respectively.     

不同产地尖顶羊肚菌多酚组成及抗氧化活性研究

为研究不同产地羊肚菌多酚的抗氧化活性及组成,以3 种不同产地（云南、西藏、新疆）尖顶羊肚菌为原料,提取羊肚菌游离酚和结合酚,测定其1,1-二苯基-2-三硝基苯肼（1,1-diphenyl-2-picrylhydrazyl,DPPH）自由基清除能力、还原力、2,2’-联苯-二（3-乙基-苯并噻唑-6-磺酸）二铵盐（2,2’-azinobis-（3-ethylbenzthiazoline-6-sulphonate）,ABTS）自由基清除能力和抗氧化能力指数（oxygen radical absorbance capacity,ORAC）值,并通过高效液相色谱（high performance liquid chromatography,HPLC）分析其组分。结果表明,3 种尖顶羊肚菌平均总酚含量为5.958 mg GAE/g,游离酚约为结合酚的25 倍;云南尖顶羊肚菌游离酚、结合酚含量最高（（6.157±0.192）、（0.250±0.018） mg GAE/g）,西藏尖顶羊肚菌游离酚、结合酚含量最低（（4.928±0.045）、（0.188±0.026） mg GAE/g）。3 种尖顶羊肚菌多酚组分主要为酚酸和黄酮,组成较一致,但含量差异显著。体外抗氧化结果表明：3 种尖顶羊肚菌多酚均具有一定的抗氧化活性,其中对DPPH自由基的清除能力最强;西藏尖顶羊肚菌多酚的DPPH自由基清除能力和还原力最强;新疆尖顶羊肚菌多酚的ABTS＋·清除能力最强,ORAC值也最高。     

Antioxidant activity and proline content of leaf extracts from Dorystoechas hastata

Dorystoechas hastata (D. hastata) is a monotypic plant endemic to Antalya province of Turkey. D. hastata leaves are used to make a tea locally called “çalba tea”. Diethyl ether (E), ethanol (A), and water (W) were used for the sequential preparation of extracts from dried D. hastata leaves. A hot water extract (S) was also prepared by directly boiling the powdered plant in water. The antioxidant activities of the extracts were tested by ferric thiocyanate (FTC) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging methods. E extract exhibited the greatest antioxidant activity with FTC method, whereas S extract exhibited the lowest IC₅₀ value (6.17 ± 0.53 μg/ml) for DPPH radical scavenging activity. Total phenolic contents of the extracts were estimated by Folin–Ciocalteu method and S extract was found to contain the highest amount (554.17 ± 20.83 mg GAE/g extract) of phenolics. Extract A contained highest flavonoid content and there was a inverse linear correlation (R² = 0.926) between IC₅₀ values for DPPH radical scavenging activity and flavonoid contents of all extracts. Reducing power of extracts increased in a concentration-dependent manner. S extract was found to possess higher reducing power than equivalent amount of ascorbic acid at 20 and 25 μg/ml concentrations. Linear correlation between reducing power and concentration of E, A, and W extracts (R² > 0.95) was observed. A, W, and S extracts contained relatively high levels of proline. The results presented suggest that D. hastata may provide a natural source of antioxidants and proline.     

不同花色芸豆种皮酚类化合物组成及抗氧化活性

利用化学萃取法提取7种不同花色芸豆种皮的自由态、结合态酚类化合物,分析其总酚、总黄酮、总花青素和酚类化合物组成,同时利用1,1-二苯基-2-三硝基苯肼(1,1-diphenyl-2-picrylhydrazyl,DPPH)法、2,2’-联氮双-(3-乙基苯并噻唑林-6-磺酸)二胺盐(2,2’-azinobis (3-ethylbenzothi azoline-6-sulfonic acid) ammonium salt,ABTS)法和铁离子还原法测定提取物的抗氧化活性。结果表明:7种芸豆种皮中总酚含量为0.76～48.73 mg/g,总黄酮含量为2.93～201.2 mg/g,总花青素含量为0～2.57 mg/g。黑芸豆种皮的总酚、总花青素最高,红花芸豆种皮的总黄酮最高;没食子酸、绿原酸、儿茶素、3,4-二羟基苯甲酸和对羟基苯甲酸是芸豆种皮中的主要酚类化合物,槲皮素只存在红芸豆种皮中(48.64μg/g),对香豆酸在白花芸豆种皮中最高(65.40μg/g);黑色芸豆皮的抗氧化能力最强(DPPH自由基清除能力、ABTS阳离子自由基清除能力、铁离子还原能力以每克干基中所含Trolox当量表...     

Nutritional composition and antioxidant activity in hazelnut shells from US‐grown cultivars

The hard shell of a hazelnut is a major waste of the hazelnut industry. The chemical composition, phenolic compounds (total phenolics, tannins and condensed tannins), antioxidant activity (DPPH and ABTS free‐radical scavenging assays), and the relationships between phenolic compounds and antioxidant activities of the hazelnut shells from twelve US grown cultivars were investigated to for potential commercial development. Crude fibre accounted for over 85% of total carbohydrate. The shells contained high concentrations of phenolic compounds. Concentrations of phenolic constituents and ABTS^?+ ‐scavenging capacities were significantly higher (P > 0.05) in the Oregon cultivars than their Nebraska counterparts. There were significant positive correlations between ABTS^?+ scavenging capacities and the phenolic compounds, whereas DPPH^? ‐scavenging capacity demonstrated a weak negative correlation with ABTS^?+ scavenging capacity and the phenolics. The results suggest that hazelnut hard shell may serve as a potential source of natural antioxidants for food applications.     

大花罗布麻不同部位酚类物质含量及其抗氧化活性比较研究

目的：比较大花罗布麻根、茎、叶、花4 个部位中游离态和结合态酚类物质的含量和抗氧化活性的差异,并分析含量与抗氧化活性之间的相关性。方法：采用Folin-Ciocalteu法、NaNO2-Al(NO3)3法分析罗布麻的根、茎、叶、花4 个部位的游离态和结合态总多酚、总黄酮含量,采用DPPH自由基清除能力、ABTS+·清除能力和铁离子还原能力3 种方法评价其体外抗氧化能力差异。结果：大花罗布麻总酚含量次序为：叶＞根＞花＞茎,各样品间存在显著性差异（P＜0.05）。各部位游离酚、结合酚和总多酚含量分别介于3 560.19～6 273.23、13.45～22.01和3 582.2～6 286.68 mg GAE/100 g干质量,其游离态多酚占总酚含量百分比平均为99.60%;游离态黄酮、结合态黄酮和总黄酮含量分别介于1 080.30～2 488.21、9.69～28.59、1 106.81～2 516.80 mg RE/100 g 干质量,其游离态黄酮占总黄酮含量的百分比平均为98.64%。大花罗布麻叶提取物清除DPPH 自由基、ABTS+·能力和总还原力最强,抗氧化活性与总酚含量之间具有良好的线性关系（r＞0.950 0）。结论：大花罗布麻各部位中含有较丰富的酚类物质,具有较强的抗氧化活性。     

Antioxidant Properties of Free,Soluble Ester and Insoluble‐Bound Phenolic Compounds in Different Barley Varieties and Corresponding Malts

Ten different barley cultivars and their corresponding malts were used to obtain different fractions. Phenolics extracted belonged to free, soluble esters and insoluble‐bound fractions. Total phenolic content (TPC) of the free fraction, as measured according to the Folin‐Ciocalteu method, ranged from 37.7 to 167.2 mg gallic acid equiv/kg of dried material (GAE/kg_dw) for barley and between 34.1 and 72.3 mg GAE/kg_dw for malt. The bound phenolic content ranged from 210.3 to 320.5 and between 81.1 and 234.9 mg GAE/kg_dw for barley and malt, respectively. The contribution of bound phenolics to the TPC was significantly higher than that of free and esterified fractions. Catechin and ferulic acid, quantified by high performance liquid chromatography with diode array detector (HPLC‐DAD), were the most abundant phenolics in the free and bound fractions, respectively. The p‐coumaric acid content was lower in hulless genotypes, as compared to hulled genotypes, showing that it is mainly concentrated in the hull. The antioxidant activities of the phenolic fractions were investigated using the radical scavenging assay (DPPH) and ferricyanide reducing power. The bound phenolics demonstrated a significantly higher antioxidant capacity compared to the free and esterified phenolics. During the malting process, a significant decrease of the bound phenolics was observed with a corresponding increase of the esterified fraction.