Antioxidant properties of durian fruit as influenced by ripening

The antioxidant properties of durian (Durio zibethinus Murr., cv. Mon Thong) at different stages of ripening were investigated using fluorometry, UV spectroscopy, and HPLC/DAD analyses. Total polyphenols, flavonoids, anthocyanins and flavanols in ripe durian were significantly higher (p < 0.05) than in mature and overripe fruits. Free polyphenols and flavonoids were at lower levels than hydrolyzed ones. Caffeic acid and quercetin were the dominant antioxidant substances in ripe durian. In these fruits, methanol extracts contained a relatively high capacity of 74.9 ± 7.1% inhibition using β-carotene-linoleic acid assay. Ferric-reducing/antioxidant power (FRAP) and cupric-reducing antioxidant capacity (CUPRAC) assays supported this finding. The correlation coefficients between polyphenols and antioxidant capacities of durian samples with all applied assays were about 0.98. In conclusion, the bioactivity of ripe durian was high and the total polyphenols were the main contributors to the overall antioxidant capacity.     

Quality of nectarine and peach nectars as affected by lye-peeling and storage

This study was focused on nectarine and peach nectars, with the aim to evaluate different quality indices at the time of production and to devise a predictive model for quality variation during storage at 23 and 37 °C. Nectars were produced from the Elegant Lady and Redhaven peach varieties and from the Stark Red Gold nectarine variety, from both peeled and unpeeled fruits. The effects of processing on antioxidant contents, antioxidant activity and colour were evaluated. At the time of production, β-carotene ranged from 0.52 to 0.79 mg/kg, hydroxycinnamic acids (chlorogenic and neochlorogenic) from 34 to 73 mg/kg, catechin from 0 to 24 mg/kg, quercetin 3-O-glycosides from 3.9 to 12.7 mg/kg, and cyanidin 3-O-glucoside from 0 to 9.4 mg/kg. Within the same variety, carotenoid and phenolic contents were lower in the nectars obtained from peeled fruits than in those obtained from unpeeled fruits. However, as ascorbic acid was adjusted to a level of 300 mg/kg during blending, which is far higher than the observed levels of phenolics and carotenoids, it mainly accounted for nectar radical-scavenging activity towards the 2,2-diphenyl-1-(2,4,6-trinitrophenyl)hydrazyl radical, which on average was 1.8 mmoles Trolox equivalents/kg. The colour of nectars was improved by processing lye-peeled fruits at room temperature, whatever the variety used; i.e., this process decreased the redness index, a^∗, and increased the lightness index, L^∗, and yellowness index, b^∗, with respect to the traditional process.     

Effect of ripeness and postharvest storage on the evolution of colour and anthocyanins in cherries (Prunus avium L.)

The relationship between colour parameters and anthocyanins of four sweet cherry cultivars, Burlat, Saco, Summit and Van was studied. The colour (L^∗, a^∗, b^∗, chroma and hue angle parameters) and anthocyanins were analysed during two different years at two different ripening stages (partially ripe, and ripe, respectively). The cherries were analysed at harvest and after storage at 1.5 ± 0.5 °C and 15 ± 5 °C for 30 and 6 days, respectively. The colour was measured by tristimulus colourimetry (CIELAB system) directly on the fruits, while anthocyanins were quantified by HPLC-DAD analysis on methanolic extracts of freeze-dried samples of the fresh cherries and on the differently stored cherries. L^∗, chroma, and hue angle values were always lower for the ripe than for the partially ripe cherries. All of the cultivars were found to contain cyanidin-3-rutinoside and cyanidin-3-glucoside as the major anthocyanins. The total anthocyanin content in fruits of the different cultivars varied in the order Burlat > Saco > Van > Summit. The concentration of anthocyanins increased at both temperatures of storage in both ripe and partially ripe cherries, but the extent of increase varied among cultivars. Cherries stored at 15 ± 5 °C showed higher reduction of L^∗, chroma and hue angle than fruits stored at 1.5 ± 0.5 °C. L^∗, a^∗, b^∗, chroma and hue angle correlated negatively (P < 0.001) with the total anthocyanins levels, but not with the total phenols. These results show that chromatic functions of chroma and hue correlate closely with the evolution of colour and anthocyanins levels during storage of sweet cherries and indicate that colour measurements can be used to monitor pigment evolution and anthocyanin contents of cherries (and vice versa).     

Evaluation of the antioxidant and cytoprotective properties of the exotic fruit Annona cherimola Mill. (Annonaceae)

Cherimoya is a tropical and subtropical native exotic fruit which has become an important crop due to its tasty flavor, high pulp content, nutritional value and potential use in folk medicine.In this study the pulp of ripe fruits were extracted using three organic solvents (ethanol, methanol and dimethyl formammide) and analyzed for the total phenols, antioxidants power and cytoprotective activity on lymphocyte tert-butyl hydroperoxide treated. Also, potential antiperoxidative activity of each extract has been performed. Organic extracts from cherimoya pulp had powerful antioxidant and ferric reducing power activities and, among the extracts, the dimethyl formammide one showed the highest scavenging activity towards DPPH, ABTS⁺, O₂⁻ radical and FRAP assay, while the ethanol one showed the highest activity against lipid peroxidation induced by tert-butyl hydroperoxide. Extract protective activities were also evaluated in isolated human peripheral blood lymphocytes exposed to 250 ??M tert-butyl hydroperoxide. The results showed that all the extracts could significantly enhance cell survival and clearly decrease the release of lactate dehydrogenase, with data almost superimposable for all the tested samples. Moreover RP-HPLC-DAD-ITMS analysis reveals the presence of flavanols and procyanidins (dimers and trimers). These results highlight cherimoya extracts' strong antioxidant properties, remarkable decrease of lipid peroxidation and cytoprotective effects against strong oxidant, supporting their suitable employment as bioactive elements in cosmetic, pharmaceutical and food processing industries.     

Increase of Antioxidant Activity of Tomato Juice Upon Functionalisation with Vegetable Byproduct Extracts

Phenolic-enriched extracts from blanched artichoke (BA), artichoke blanching waters (ABW), cauliflower (CA), carrot (CR), celery (CE) and onion (ON) byproducts were used to ‘functionalise’ tomato juice. The antioxidant activity of functional tomato juice significantly increased over control juice according to a set of in vitro antioxidant assays (i.e. inhibition of lipid peroxidation determined by the ferric thiocyanate method and scavenging of both ABTS^•+ and DPPH^• free radicals). A trained sensory evaluation panel determined the maximal allowed byproduct extract concentration in the functionalisation of tomato juice without modifying its natural sensory properties (mg extract/mL tomato juice): 2.5, 5, 10, 10, 10 and 20 for CA, ON, BA, ABW, CE and CR, respectively. The maximum antioxidant activity (within consumers' acceptance limits and measured by the ABTS^•+ method) was increased 5.4-, 3.4-, 2.5-, 1.7-, 1.5- and 0.6-fold over the control when functional tomato juice was assayed after modification with ABW, BA, CR, ON, CE and CA, respectively. A serving of functional tomato juice (250 mL) containing vegetable extracts (within consumers' acceptance limits) provides an additional intake of phenolic compounds which can range from 22 mg (when functionalised with CA extract) to 300 mg (with BA extract). In the light of the above investigations, the use of vegetable byproducts could be useful for developing a functional tomato juice with potentially increased health-promoting properties.     

Stability of the total antioxidant capacity and total polyphenol content of 23 commercially available vegetable juices before and after in vitro digestion measured by FRAP, DPPH, ABTS and Folin-Ciocalteu methods

Vegetables are known to contain a wide variety of antioxidants which may provide protection against the development of a number of disease states. Recently there has been a large increase in the number of vegetable juices which have become commercially available. The objective of the present study was to analyse the total antioxidant capacity of 23 commercially available vegetable juices [via Ferric Reducing Antioxidant Power (FRAP), 2, 2-diphenyl-1-picrylhydrazyl (DPPH), 2, 2-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS⁺) and Folin-Ciocalteu Reagent (FCR) for total polyphenols] and to determine the stability of the antioxidant capacity following an in vitro digestion procedure using the same methods. All 23 juices were significant sources of antioxidants both in terms of total antioxidant capacity and total polyphenols, although results varied considerably between the juices [1369-9500 ??mol/L (FRAP), 57.8-100% inhibition of DPPH, 10.9-90.7% inhibition of ABTS⁺ and 449-3025 ??g ferulic acid equivalents/mL for FCR]. Beetroot juice displayed the highest level of total antioxidants and total polyphenols compared to the other juices which were analysed (tomato, carrot, mixed vegetable, mixed fruit and vegetable). The antioxidant capacity of the juices remained high throughout the in vitro digestion.     

Antioxidant stability of small fruits in postharvest storage at room and refrigerator temperatures

Strawberries (Fragaria ananassa), raspberries (Rubus idaeus) and red currants (Ribes rubrum), as well as two drupes, cherries (Prunus avium), and sour cherries (Prunus cerasus), were subjected to two storage temperatures (4 °C and 25 °C) and phytochemicals concentrations (total phenols, flavonoids and anthocyanins) as well as antioxidant capacity (DPPH, ABTS and FRAP assays) were monitored until the fruit visually spoiled. Red currants and strawberries exhibited the highest initial total phenol (TP) contents (322.40 ± 5.56 and 335.47 ± 6.12 mg GAE/100 g FW, respectively) and maintained the highest TP contents throughout storage at both temperatures. Storage of at 25 °C as opposed to 4 °C, facilitated faster spoilage of analyzed fruits. In addition, most fruits stored at 4 °C, exhibited slightly higher antioxidant activity values at the end of storage according to all three antioxidant activity assays as opposed to fruits stored at 25 °C. The dynamic evolution of antioxidant capacity at both temperatures reflected the transient changes in phytochemical composition of small fruits in storage.     

Antioxidant and free radical scavenging potential of Achillea santolina extracts

The antioxidative activities of hydroalcoholic extract of Achillea santolina were investigated employing various established in vitro systems including total antioxidant activity in linoleic acid emulsion system, 1,1-diphenyl-2-picrylhydrazyl (DPPH), superoxide and hydroxyl radicals scavenging, reducing power, and inhibitory effect on protein oxidation as well as the inhibition of Fe²⁺/ascorbate induced lipid peroxidation in rat liver homogenate. Total phenolic and flavonoid content of A. santolina extract (ASE) was also determined by a colorimetric method. The results revealed that ASE has notable inhibitory activity on peroxides formation in linoleic acid emulsion system along with concentration-dependent quenching of DPPH and superoxide radicals. Furthermore, the extract showed both nonsite-specific (Fe²⁺ + H₂O₂ + EDTA) and site-specific (Fe²⁺ + H₂O₂) hydroxyl radical scavenging suggesting potent hydroxyl radical scavenging and chelating ability for iron ions in deoxyribose degradation model. A linear correlation between ASE and the reducing power was also observed (r² = 0.9981). ASE prevents thiobarbituric acid reactive substances formation in Fe²⁺/ascorbate induced lipid peroxidation in rat liver tissue in a dose-dependent manner. Moreover, free radical induced protein oxidation was suppressed significantly by the addition of ASE over a range of concentration. These results clearly demonstrated that A. santolina extract possess a marked antioxidant activity.     

Radical scavenging and reducing properties of extracts of cashew shoots (Anacardium occidentale)

The total phenolic content and antioxidant activities of methanol, hexane and ethyl acetate extracts of the shoots of Anacardium occidentale were measured. Total phenolic content was assessed by the Folin–Ciocalteau assay whereas antioxidant activities were assessed by measuring the ability of the extracts to scavenge the ABTS^·+ and DPPH^· radicals, superoxide anion radicals and nitric oxide radicals as well as their ability to reduce ferric ions. Results indicated that the methanol extract of A. occidentale was the most potent reducing agent and radical-scavengers compared to the other two extracts. The ethyl acetate extract exhibited some antioxidant activities whereas the hexane extract is the least reactive. The order of the antioxidant potency of the plant extract is methanol > ethyl acetate > hexane. The methanol extract contained more than 7 fold of total phenolic content compared to the hexane and ethyl acetate extracts indicating the likely possibility that the observed antioxidant activities were partly contributed by the phenolics. The results suggest that the shoots of A. occidentale are a source of natural antioxidants.     

Antioxidant activities of Sideritis congesta Davis et Huber-Morath and Sideritis arguta Boiss et Heldr: Identification of free flavonoids and cinnamic acid derivatives

Different solvent extracts of endemic Sideritis (Labiatae) species, Sideritis congesta Davis et Huber-Morath and Sideritis arguta Boiss et Heldr, were analyzed for free flavonoids (quercetin, apigenin, myricetin and kaempferol) and cinnamic acid derivatives (rosmarinic acid, ferulic acid, caffeic acid, p-coumaric acid and chlorogenic acid) using HPLC-DAD. All the phenolics were quantified in acid-hydrolyzed extracts, except rosmarinic acid, chlorogenic acid and myricetin which were quantified in raw samples. Antioxidant activities of extracts of these two plants and many of their components in pure form were evaluated based on DPPH^. and ABTS^.+ assays. In general, S. arguta extracts displayed higher antioxidant activity than S. congesta extracts possibly due to their richness in antioxidant components of strong activity. Acetone extract of S. arguta, with its strikingly high TEAC value of 3.2 mM trolox and low IC₅₀ value of 38.3 ??g/mL showed the highest antioxidant potency among all extracts. ??-tocopherol, the positive control, displayed IC₅₀ and TEAC values of 33.8 ??g/mL and 2.9 mM trolox, respectively. No direct correlation was found between antioxidant activities and total phenolic contents of the plant extracts studied.     

Molecular Mass and Solubility Changes in Pectins during Storage of Satsuma Mandarin Fruits (Citrus unshiu Marc.)

Soluble pectins in satsuma mandarin fruits stored at 5°C were investigated by High Performance Gel Filtration chromatography. Pectins isolated from the flavedo, albedo, membranes and juice sacs were separated into four fractions. The hydrochloric acid soluble pectin fraction in each part was the highest and decreased slightly while the water-soluble pectin increased slightly. The avergae molecular weights of the fractionated soluble pectins in juice sacs were nearly constant but those in flavedo, albedo and membranes decreased as storage time increased. The ratios of higher molecular weight of water soluble and ammonium oxalate-soluble pectins in all the four parts and those of hydrochloric acid soluble pectin in flavedo and membranes decreased as ratios of lower molecular weight fractions increased.