沙田柚不同组织部位酚类物质组成及其抗氧化活性研究

摘 要：目的 揭示沙田柚不同部位酚类物质组成和抗氧化活性的差异。方法 提取沙田柚油胞层、白皮层、囊衣和籽中游离酚和结合酚,测定其总酚、总黄酮含量,单体酚组成和抗氧化活性,并采用皮尔森相关性分析确定酚类物质含量与抗氧化活性之间的相关性。结果 沙田柚各部位酚类物质主要以游离酚为主,其总酚、总黄酮含量变幅分别为2.01~13.28 mg GAE/g DW和3.79~15.2 mg RE/g DW,油胞层和白皮层总酚、总黄酮含量均高于囊衣和籽。从沙田柚各部位鉴定出柚皮苷、橙皮素、甜橙黄酮、对羟基苯甲酸、对香豆酸和阿魏酸共6个单体酚,柚皮苷是各部位中最主要的黄酮类化合物且以白皮层中含量最高。沙田柚各部位铁离子还原能力(ferric reducing antioxidant power,FRAP)和氧自由基吸收能力(oxygen radical absorbance capacity, ORAC)变幅分别为7.6336~69.26 mmol TE/g DW和116.9~625.111.69~62.51 μmol TE/g DW,甜橙黄酮是各部位发挥FRAP活性的重要成分,而柚皮苷是各部位发挥ORAC活性的重要成分。结论 沙田柚副产物,尤其是果皮(油胞层和白皮层),是天然酚类物质的来源。     

The antioxidant activity and the composition of free and bound phenolic acids in dough of wheat flour enriched by Boletus edulis after mixing and thermal processing

The porcino is good source of phenolics and has been used to enrich wheat flour. The antioxidant activity and the content and composition of free and bound phenolic acids in the dough of wheat and porcino flour mixture (70:30 w/w) were investigated. The free form in the amount of 1305.76 μg g^?1 was the main part of the phenolic content in the flour mixture. By dough mixing, the content of free phenolics increased by approximately 70%. Further thermal processing decreased the content of both forms of phenolics compared to dough after mixing, but the content of free phenolics of 1764.24 μg g^?1 is still higher than in the flour mixture. The stability of the detected phenolic acids during mixing and thermal processing depended on whether they were in free or bound form. After thermal processing, the total content of detected phenolic acids was 683.31 μg g^?1, indicating that approximately 87% of the total content of phenolic acids detected in flour mixture was retained.     

Chemical composition and biological activities of essential oil and extracts from Ocimum sanctum

The objective of the present research work was to evaluate the antioxidant, antimicrobial and antimalarial activities of essential oil and various extracts from O. sanctum. Gas chromatography-mass spectrometry analysis identified the following major compounds with their quantification as: eugenol (22.0%), β-elemene (19.2%), β-caryophyllene (19.1%), and Germacrene D (5.03%). HPLC analysis of O. sanctum extracts revealed that gallic acid, chlorogenic acid, p-hydroxy benzoic acid, caffeic acid, vanillic acid, p-coumeric acid, sinapic acid, and ferulic acid were the important phenolic acids. The methanol extract exhibited highest level of total phenolic (1.36 g/100 g dry plant material) and total flavonoid (0.67 g/100 g dry plant material) followed by ethanol and n-hexane extracts. The oil and extracts exhibited excellent free radical scavenging potential as measured by 2,2-diphenyl-1-picrylhydrazyl radical free radical-scavenging ability, and antioxidant activity as measured by inhibition of linoleic acid oxidation. Essential oil, n-hexane, methanol, and ethanol extracts exhibited moderate antimalarial potential in term of anti-haem biocrystallization activity. In the resazurin microtitre plate and disc diffusion assays, the essential oil of O. sanctum showed better antibacterial activity than various extracts. The results of the present investigation demonstrated significant (p < 0.05) variations in the antioxidant, antimicrobial, and antimalarial activities of essential oil and extracts from O. sanctum.     

Phenolic acid profiles and antioxidant activities of wheat bran extracts and the effect of hydrolysis conditions

Four different types of wheat bran were extracted and analyzed for phenolic acids using the Folin–Ciocalteu method and HPLC. The extracts and their hydrolysis products were also evaluated for their antioxidant activities. The total phenolic content of the red wheat bran was higher than that of the white wheat. We found that the majority of the phenolic acids existed in a bound form in wheat bran. These phenolic acids can be released by hydrolyzing the bran under alkaline or acidic conditions; however, the former was more efficient in the release of free phenolic acids than the latter. Ferulic, vanillic, and syringic acids were the major individual phenolic acids in the studied wheat bran. The main portion of the total ferulic acid was from alkaline hydrolysis. The alkaline hydrolysable fractions had greater antioxidant activities, while the acid hydrolysable fractions showed lower activities in both the red and white bran. The antioxidant activity of bran extract was stronger than that of free phenolic acids.     

Polyphenolic content and antioxidant properties of Moringa oleifera leaf extracts and enzymatic activity of liver from goats supplemented with Moringa oleifera leaves/sunflower seed cake

The study investigated antioxidant potency of Moringa oleifera leaves in different in vitro systems using standard phytochemical methods. The antioxidative effect on the activities of superoxide dismutase (SOD), catalase (CAT), lipid peroxidation (LPO) and reduced glutathione (GSH) were investigated in goats supplemented with M. oleifera (MOL) or sunflower seed cake (SC). The acetone extract had higher concentrations of total flavonoids (295.01 ± 1.89 QE/g) followed by flavonols (132.74 ± 0.83 QE/g), phenolics (120.33 ± 0.76 TE/g) and then proanthocyanidins (32.59 ± 0.50 CE/g) than the aqueous extract. The reducing power of both solvent extracts showed strong antioxidant activity in a concentration dependent manner. The acetone extract depicted higher percentage inhibition against DPPH, ABTS and nitric oxide radicals which were comparable with reference standard antioxidants (vitamin C and BHT). MOL increased the antioxidant activity of GSH (186%), SOD (97.8%) and catalase (0.177%). Lipid peroxidation was significantly reduced by MOL. The present study suggests that M. oleifera could be a potential source of compounds with strong antioxidant potential.     

The phenolic composition and antioxidant capacity of soluble and bound extracts in selected dietary spices and medicinal herbs

Phenolic compounds, commonly found in plant‐based foods, exist in free or bound form. Despite much research on the soluble phenolics in spices and herbs, their bound phenolics have not been intensively investigated. In this study, six common dietary spices and medicinal herbs (Padang cassia, oregano, clove, Chinese cassia, Japanese knotweed and peel of pomegranate) were selected to evaluate and compare their phenolic composition and antioxidant capacity in soluble extracts (SEs) and bound extracts (BEs). Generally, the samples had high total phenolic content and antioxidant capacity, with lower levels in the BEs. From the HPLC results, (+)‐catechin, (?)‐epicatechin, eugenol, cinnamaldehyde and carvacrol were the major phenolic compounds in the SEs, and gallic acid, p‐coumaric acid and ellagic acid in the BEs. Phenolic compounds are likely the major contributors to the antioxidant capacity of these plant samples. Overall, these dietary spices and medicinal herbs can be excellent sources of natural antioxidant phenolics.     

Broccoli seed extracts but not sulforaphane have strong free radical scavenging activities

The abilities of broccoli seed extracts and purified sulforaphane (SF) to scavenge 2,2′‐azinobis [3‐ethylbenzothiazoline‐6‐sulphonate] (ABTS^?+), 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH^?) and superoxide anions were studied. The free radical scavenging activities of broccoli seed extracts had no exact correlation with SF content, indicating that SF was not the main antioxidant component. The broccoli seed extracts were separated by high‐speed countercurrent chromatography to obtain purified SF, which showed dose‐dependent free radical scavenging activities in the DPPH^? and ABTS^?+ assays, but its activities were weaker to those of ascorbic acid. The same trend was observed in the chemiluminescence assay. The results showed that broccoli seed extracts had strong free radical scavenging activities that were not attributable to SF.     

Phenolic profiles and cellular antioxidant activity of longan pulp of 24 representative Chinese cultivars

The phytochemical composition and antioxidant activity of fruits are associated with their health benefits. Longan is a traditional Chinese edible and medicinal fruit, but its varietal differences in phytochemical profiles and antioxidant activity were unknown. Twenty-four longan cultivars from southern China were investigated in this study. Their total phenolic and flavonoid contents in pulp were 22.09–132.47 mg gallic acid equivalents/100 g and 2.48–14.26 mg catechin equivalents/100 g, respectively. The mean contributions of free phenolics and ?avonoids to the total were 82.5% and 94.0%, respectively. Among 10 individual phenolics detected by HPLC, the contents of epicatechin, 4-methylcatechol, chlorogenic, and vanillic acids were relatively higher. The cellular antioxidant activity (CAA) of longan pulp showed significant varietal discrepancies and positive correlation with phenolic and flavonoid contents. Phenolics in longan pulp of 24 cultivars showed lower CAA potential than many other fruits with the CAA qualities from 0.35 to 1.21 µmol quercetin equivalent/100 µmol total phenolics. Longan cultivars were classified into six groups by hierarchical clustering analysis. Six cultivars in group 4 and 6 had higher phytochemical contents and CAA activity.     

Antioxidant activities and total phenolic contents of various extracts from defatted wheat germ

Defatted wheat germ (DWG) is the main by-product of the wheat germ oil extraction process. Its nutritional value has well been accepted. In this study, the antioxidant properties of 30% ethanol, 50% ethanol, 70% ethanol, 100% ethanol, and aqueous extracts of DWG were measured using various in vitro assays. Among the DWGEs (DWG extracts) tested, the 70% ethanol extract showed the best DPPH radical scavenging power while the 100% ethanol extract showed the highest ABTS radical scavenging activity and reducing power. In addition, both the 70% ethanol extract and the 50% ethanol extract exhibited relatively higher antioxidant activity in linoleic acid system. The extracts in question exhibited total phenolic contents ranging from 13.98 to 16.75 mg GAE/g. DWG, as a source of natural antioxidants, can be used to formulate nutraceuticals with potential applications to reducing the level of oxidative stress. The antioxidant potency of the DWG extracts could be the basis for its health promoting potential.     

In vitro evaluation of the antioxidant activities in fruit extracts from citron and blood orange

Consumers are increasingly aware of diet related health problems and therefore demanding natural ingredients which are expected to be safe and health-promoting. Recently, number of studies on health benefits associated with citrus phytochemicals have been demonstrated. In the present study, an attempt has been made to isolate antioxidant fractions from two different citrus species such as Citron (Citrus medica) and blood orange (C. sinensis). Antioxidant fractions were extracted from mature, ripe fruits using five different solvents using a Soxhlet extractor. The total phenolic content of the extracts was determined by Folin–Ciocalteu method. MeOH:water (80:20) extract of citron and acetone extract of blood orange was found to contain maximum phenolics. The dried fractions were screened for their antioxidant activity potential using in vitro model systems such as 1, 1-diphenyl-2-picryl hydrazyl (DPPH), phosphomolybdenum method and as well as by the nitroblue tetrazolium (NBT) reduction test at different concentrations. The MeOH:water (80:20) fraction of citron showed highest radical scavenging activity 42.5%, 77.8% and 92.1% at 250, 500 and 1000 ppm, respectively, while MeOH:water (80:20) fraction of blood orange showed lowest DPPH radical scavenging activity at all the tested concentrations. Furthermore, all the fractions showed remarkable antioxidant capacity by the formation of phosphomolybdenum complex. In addition, superoxide radical scavenging activity was assayed using non-enzymatic (NADH/phenaxine methosulfate) superoxide generating system. All the extracts showed variable radical scavenging activity. The data obtained in the in vitro models clearly establish the antioxidant potency of citrus fruit extracts. However, comprehensive studies need to be conducted to ascertain the in vivo safety of such extracts in experimental animal models. To the best of our knowledge, this is the first report on antioxidant activity of citron and blood orange varieties of citrus fruits.     

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     

Comparing profiles and antioxidant properties of soluble and insoluble phenolics in Perilla frutescens seed flour extracts obtained by different extraction/hydrolysis methods

Cold‐pressed Perilla frutescens seed flour (CP‐PFSF) is a potential source of natural antioxidants. In this study, different methods were used to extract both soluble and insoluble phenolics from CP‐PFSF. Also, the phenolic profiles and antioxidant properties were compared. Results showed that soluble phenolics could be extracted using aqueous‐organic solvents, where 80% acetone resulted in the highest extraction yield and antioxidant activities. Insoluble phenolics remaining in residues could be released by acid or alkaline hydrolysis, where acid hydrolysis provided higher yield and antioxidant activities than alkaline. Soluble and insoluble phenolics could be extracted simultaneously through acid/alkaline hydrolysis, resulting in nearly the same yields for total phenolics. However, the phenolic components and antioxidant activities of extracts varied significantly, depending on the methods. Principal component analysis and correlation analysis revealed that a strategy of 80% acetone with successive acid hydrolysis steps released more rosmarinic acid, which have high antioxidant activities.     

Screening of some Algerian medicinal plants for the phenolic compounds and their antioxidant activity

Since recent times, there is a growing interest in the food industry and in preventive health care for the development and evaluation of natural antioxidants from medicinal plant materials. In the present work we have investigated the antioxidant potency of phenolic compounds of 11 indigenous wild plant species from the Algerian Atlas commonly used in Arab folk medicine for a wide range of conditions. The antioxidant activity of each phenolic extracts has been assessed by using the Trolox Equivalent Antioxidant Capacity (TEAC) as a chemical test, and in a dynamic way by a biological assay based on whole blood resistance to free radical aggression. Of the 11 tested plants, 2 showed prominent antioxidant activity: Anthemis arvensis and Artemisia campestris. These plants had a very high level of Trolox equivalents and induced a strong delay of free radical-induced red blood cells hemolysis compared to antioxidant references. Artemisia campestris was the best inhibitor, its effect was far stronger than that of caffeic acid and was more than three times as high as ascorbic acid and two times higher than α-tocopherol efficiency. HPLC analysis showed a good correlation between the antioxidant activity and hydroxycinnamic derivatives. These preliminary results on the in vitro protection of blood against oxidative stress emphasized the benefit of the phenolic compounds of these medicinal plants. Our results enable us to proceed towards more detailed chemical and pharmacological understanding of these plant materials and show the interest of natural antioxidant in medicinal plants for the prevention of much free radical-mediated pathology.     

Optimisation,characterisation and quantification of phenolic compounds in olive cake

The phenolic compounds in extracts from pressed olive cake were investigated. Free phenolic compounds were extracted from olive cake using methanol. To liberate bound phenolic compounds, the olive cake was subjected to basic and acidic hydrolysis followed by methanol extraction. The individual phenolic compounds and antioxidant activity of the extracts were determined. The highest total phenolic content and antioxidant activity were obtained using methanol extraction for 12 h at 70 °C. The RP-HPLC profiles for full-fat and defatted olive cake showed that protocatechuic acid, hydroxybenzoic acid, sinapic acid, p-coumaric acid, rutin and hesperidin were the predominant free phenolic compounds. Meanwhile, syringic acid, sinapic acid, caffeic acid and protocatechuic acid were the predominant bound phenolic acids. A positive correlation was observed between total phenolic content and antioxidant activity. The results indicated that most of the phenolic compounds in olive products were present in their free forms (75–90% of total phenolic content), while bound phenolic compounds were only a small proportion (10–25%) of total phenolic content.     

Phenolic profile and antioxidant activities of olive mill wastewater

Olive trees play an important role in the Moroccan agro-economy, providing both employment and export revenue. However, the olive oil industry generates large amounts of wastes and wastewaters. The disposal of these polluting by-products is a significant environmental problem that needs an adequate solution. On one hand, the phytotoxic and antimicrobial effects of olive mill wastewaters are mainly due to their phenolic content. The hydrophilic character of the polyphenols results in the major proportion of natural phenols being separated into the water phase during the olive processing. On other hand, the health benefits arising from a diet containing olive oil have been attributed to its richness in phenolic compounds that act as natural antioxidants and are thought to contribute to the prevention of heart diseases and cancers. Olive mill wastewater (OMW) samples have been analysed in terms of their phenolic constituents and antioxidant activities. The total phenolic content, flavonoids, flavanols, and proanthocyanidins were determined. The antioxidant and radical scavenging activity of phenolic extracts and microfiltred samples was evaluated using different tests (iron(II) chelating activity, total antioxidant capacity, DPPH assays and lipid peroxidation test). The obtained results reveal the considerable antioxidant capacity of the OMW, that can be considered as an inexpensive potential source of high added value powerful natural antioxidants comparable to some synthetic antioxidants commonly used in the food industry.     

Comparison of microwave and high-pressure processing on bound phenolic composition and antioxidant activities of sorghum hull

The influence of microwave boiling (MB treated 5, 10 and 15 s was abbreviated as MB5, MB10 and MB15, respectively) and high-pressure boiling (HB processed 10, 20 and 30 min was denoted as HB10, HB20 and HB30, respectively) processing on the composition and content of bound phenolic substances of sorghum hull and their antioxidant capacity were evaluated. Nine bound phenolic profiles were identified by HPLC-ESI-MS/MS, including syringic acid, veratric acid, p-hydroxybenzonic acid, caffeic acid, sinapic alcohol, ascorbic acid, prenylnaringenin and luteolin. Compared with traditional hot water processing (HP treated 10, 30 and 50 min was abbreviated as HP10, HP30 and HP50, respectively), the content of free procyanidins and total phenolics of sorghum hull treated with HB increased by 35.92–58.87% and 6.20–18.70%, respectively. Sorghum hull treated with HB20 possessed the highest ABTS (ABTS radical scavenging capacity) and FRAP (ferric ion reducing antioxidant power) among all treatment groups.     

Characterization of different annatto extracts based on antioxidant and colour properties

Annatto seeds are known as the only natural source of bixin, a carotenoid widely used in the food industry as colourant. Thus, the aim of this study was to obtain annatto extracts with different solvents and use statistical multivariate analysis to correlate the antioxidant and colourant properties of these extracts. According to the Principal Component Analysis, PC1 was associated to colour and PC2 to antioxidant capacity. Extracts with similar polarities were joined together by Cluster Analysis. The annatto extracts obtained with methanol/water and ethanol/water were characterized by their low bixin levels and a soft yellowish colour, whilst those obtained with methanol, ethanol and ethyl acetate showed red colour and higher bixin contents. The best solvent for bixin extraction was ethyl acetate (4.9 mg bixin/g seeds), whereas the highest total phenolic levels were verified in the most polar extracts, achieving maximum of 1.84 gallic acid equivalent/g seeds in the methanol/water extract. On the other hand, the hexane extract showed both low phenolic and bixin contents, as well as low free radical scavenging activity. Taking into consideration the antioxidant and colourant properties, solvents with medium polarity, especially methanol, should be used to obtain functional annatto extracts.