Analysis of the Major Flavonol Glycosides Present in Four Varieties of Onion (Allium cepa) and Changes in Composition Resulting from Autolysis

The major flavonoids of mature onion bulb were confirmed as the 3,4′-O-diglucoside (Qdg) and 4′-O-monoglucoside (Qmg) of quercetin using a combination of chromatographic comparisons, mass spectrometry and nuclear magnetic resonance spectroscopy. These two components account for over 85% of the total flavonoids in three varieties of onion with Qdg as the main component. Quercetin is detected in these long stored onions but only at low levels of less than 2% of the total. The remaining flavonoid fraction (approx 15%) comprises upto 17 different components of which quercetin-3-O-glucoside and isorhamnetin glucoside are prominent members although each contribute less than 1% of the total flavonoid fraction. There are significant differences in the levels of Qdg and Qmg between the four different onion varieties analysed; Qdg varying from 50–1300 mg kg^-1 fresh onion tissue and Qmg from 36–394 mg kg^-1. Maceration of the tissue for the three varieties tested led to a loss of Qdg and the appearance of Qmg and free quercetin. In the variety Rijnsburger 50% of the Qdg was degraded in 5 h and had completely disappeared after 24 h. These changes in Qdg can be quantitatively explained by increases in Qmg and free quercetin. The possible significance of quercetin glycosides in the diet is discussed. © 1997 SCI     

Instrumental texture and flavonoid profile of paste developed from sprouted onion varieties of Indian origin

The effect of sprouting on the instrumental texture, antioxidant activity, and ?avonoid pro?le of the paste prepared from four Indian onion varieties (Punjab White, Punjab Naroya, PRO-6, and Commercial) was studied. The significant (P ? 0.05) effect of sprouting on microstructure, firmness, adhesiveness, gumminess, and chewiness in paste samples from all varieties was observed. There was significant decrease (P ? 0.05) in lightness with consequent significant (P ? 0.05) increase in redness, greenness, and yellowness in paste samples which was due to the increase in anthocyanin content with sprouting. The paste samples from sprouted onion varieties also showed an increase in phenol content, flavonoid content, antioxidant capacity, and DPPH radical scavenging activity. The HPLC analysis revealed an increase in total flavonoids in pastes from PRO-6 and Punjab Naroya varieties. Thus, present study implied that sprouting could be beneficial as it enhanced the functional potential of onion pastes.     

Biochemical characterisation of the seed oils of four safflower (Carthamus tinctorius) varieties grown in north‐eastern of Morocco

The quality of the oil of four safflower varieties, originating from Spain (Rancho), India (Sharda) and Morocco (Cartamar and Cartafri), which were cultivated at the experimental station in Oujda (a semi‐arid region of eastern Morocco) was evaluated through analysis of their phenolic and carotenoid contents. The composition of the phenolic compounds of safflower oil has not yet been documented. Therefore, in this preliminary study, Thirty different phenolic compounds were identified, and significant differences between the oil varieties were observed (P < 0.05). In the seed oil from the Rancho and Sharda safflower varieties, the main phenolic compound was trans‐chalcone, representing 13.45% and 11.8%, respectively, of the total phenolics, whereas in Cartamar and Cartafri oils, naringin accounted for 26.82% and 16.5%, respectively, of the total phenolics. The total carotenoid contents ranged from 1.13 mg kg^?1 (Rancho) to 1.34 mg kg^?1 (Cartamar and Cartafri). We observed that β‐cryptoxanthin (0.31–0.37 mg kg^?1) and β‐carotene (0.3–0.35 mg kg^?1) were the predominant carotenoids in all of the safflower oils that were studied.     

Variations in the phytosterol and tocopherol compositions and the oxidative stability in seed oils from four safflower (Carthamus tinctorius L) varieties grown in north‐eastern Morocco

Phytosterol and tocopherol contents and oxidative stability were evaluated from seeds oils of four safflower (Carthamus tinctorius L) varieties originating from Spain (Rancho), India (Sharda) and Morocco (Cartamar and Cartafri), which were cultivated at the experimental station in Oujda (a semi‐arid region of eastern Morocco). Total phytosterols ranged from 3640 to 4140 mg kg^?1. GC analysis allowed the identification of nine compounds, of which β‐sitosterol was the major component. Total tocopherols ranged from 461.56 to 499.68 mg kg^?1. HPLC analysis allowed the identification of three compounds, α‐tocopherol (99.45%–98.84%), β‐tocopherol (0.94%–0.5%) and γ‐tocopherol (0.21%–0.01%). Oxidative stability study showed that Sharda had the lowest induction period of 2.3 h compared with 7.18, 7 and 6.67 h for Cartafri, Rancho and Cartamar, respectively. Likewise, we established a positive correlation between the oxidative stability and γ‐tocopherol; however, this difference was not significant.     

Quercetin content in stored onions (Allium cepa L.): effects of storage conditions,cultivar, lifting time and nitrogen fertiliser level

Storage experiments with commercial cultivars of onion (Allium cepa L.) were performed at low constant temperature (1°C) and at higher variable temperature (～8°C). Cultivar differences in quercetin glucoside content were significant, but neither nitrogen fertiliser level nor lifting time had more than minor effects at start of storage or after 3 or 5 months of storage. The role of onion size for quercetin glucoside content and composition was inconsistent but seemed to be of minor importance. Irrespective of storage conditions, the content of quercetin glucosides only showed minor reduction and the composition was unchanged. After 5 months of storage, onion sprouting was recorded during a shelf‐life period of 9 weeks at room temperature. Early lifting resulted in onions with low sprouting and good storage abilities without negative effects on quercetin glucoside content. The results suggest that it may be possible to minimise nitrogen fertiliser levels without negative effects on onion yield, quercetin glucoside content or storage capacity. Copyright © 2007 Society of Chemical Industry     

Phenolic compounds,lycopene and antioxidant activity in commercial varieties of tomato (Lycopersicum esculentum)

Nine commercial varieties of tomato (Rambo, Senior, Ramillete, Liso, Pera, Canario, Durina, Daniella and Remate) produced in Spain were analysed for their lycopene content, content of phenolic compounds and antioxidant capacity. The phenolic compounds were characterised as flavonoids (quercetin, kaempferol and naringenin) and hydroxycinnamic acids (caffeic, chlorogenic, ferulic and p‐coumaric acids). Antioxidant activity was measured using the DPPH and ABTS assays. The concentrations of lycopene and the various phenolic compounds as well as the antioxidant activity were significantly influenced by the tomato variety. Quercetin, the most abundant flavonoid, was found in concentrations ranging between 7.19 and 43.59 mg kg^?1 fresh weight, while naringenin levels were lower than 12.55 mg kg^?1. The most abundant hydroxycinnamic acid was chlorogenic acid, with values ranging from 14 to 32 mg kg^?1 fresh weight, followed by caffeic acid, while p‐coumaric and ferulic acids showed similar concentrations lower than 5 mg kg^?1. The highest content of lycopene was found in Ramillete, Pera and Durina (>50 mg kg^?1 fresh weight), while the concentration in the other varieties was between 50 and 30 mg kg^?1, with the exception of Liso (less than 20 mg kg^?1). The antioxidant activity of tomato extracts varied with the tomato variety and the assay method used. Individual compounds found to be significantly related to antioxidant capacity were lycopene and ferulic and caffeic acids, but not quercetin and chlorogenic acid. © 2002 Society of Chemical Industry     

Effects of cultivar,lifting time and nitrogen fertiliser level on quercetin content in onion (Allium cepa L.) at lifting

Commercial cultivars of onion (Allium cepa L.) were grown at Torslunda research station, Sweden with different levels of nitrogen fertiliser and lifted at different growth stages. Soon after lifting, before any drying or curing, tissue from the fleshy edible part of onions was extracted in ethanol and the raw extracts were analysed by high‐performance liquid chromatography without any previous hydrolysis. It was confirmed that the main flavonoid compounds were quercetin monoglucoside and quercetin diglucoside, whereas only trace amounts of quercetin aglycone and other flavonoids were found. The greatest variation in quercetin content, in the range 100–500 mg kg^?1 fresh weight, occurred between years. The concentration of quercetin glucosides in the onions was strongly correlated (R² = 0.98) with the total amount of global radiation in August. Individual onions with fallen leaves had significantly higher concentrations of quercetin glucosides than individuals in the same row with erect leaves. Only minor differences were found between the three cultivars analysed. Higher levels of nitrogen fertiliser had only minor effects on onion yield and size and resulted in lower or equal amounts of quercetin glucosides. Nitrogen leakage from the soil, a potential source of environmental problems, could therefore be minimised by avoiding high nitrogen fertiliser levels with almost no effect on onion flavonol content. Late lifting of onions (80% fallen leaves) resulted in up to 45% higher concentrations of quercetin glucosides compared with early lifting (50% fallen leaves). Copyright © 2006 Society of Chemical Industry     

Qualitative and quantitative analysis of the major phenolic compounds as antioxidants in barley and flaxseed hulls using HPLC/MS/MS

BACKGROUND: Both qualitative and quantitative analyses of the major phenolic compounds in barley and flaxseed hulls were conducted using reverse phase high‐performance liquid chromatography coupled with photodiode array detection and quadrupole time‐of‐flight mass spectrometry. RESULTS: Ferulic acid, p‐coumaric acid, vanillic acid and vanillin were identified and quantified in four barley hull samples. Four ferulate dehydrodimers were also detected. The phenolic compounds of flaxseed hull were distinct from those of barley hull. Three flaxseed hull samples varied significantly (P < 0.05) in their contents of secoisolariciresinol diglucoside (16.38–33.92 g kg^?1), coumaric acid glucoside (35.68–49.22 g kg^?1) and ferulic acid glucoside (5.07–15.23 g kg^?1). The phytochemical profiles of co‐extracts featured the major phenolic compounds from both barley and flaxseed hulls. The total phenolic content and 2,2‐diphenyl‐1‐picrylhydrazyl radical‐scavenging capacity varied significantly (P < 0.05) among different varieties of flaxseed and barley hulls. CONCLUSION: As agricultural by‐products, barley and flaxseed hulls may be utilised as potential sources of functional food ingredients through extraction and concentration of the phytochemicals identified above. Copyright © 2012 Society of Chemical Industry     

In vitro inhibitory effects of cranberry bean (Phaseolus vulgaris L.) extracts on aldose reductase, α‐glucosidase and α‐amylase

The in vitro inhibitory activities of different seed extracts prepared from cranberry bean mutant SA‐05 and its wild‐type variety Hwachia against aldose reductase, α‐glucosidase and α‐amylase were examined. The results indicated that the polyphenolics‐rich extracts obtained using 800 g kg^?1 methanol and 500 g kg^?1 ethanol demonstrated inhibitory activities against aldose reductase (IC₅₀ of 0.36–0.46 mg mL^?1) and α‐glucosidase (IC₅₀ of 1.32–1.94 mg mL^?1). The 500 g kg^?1 ethanol extracts also showed α‐amylase inhibitory activities (IC₅₀ of 70.11–80.22 μg mL^?1). Subsequent extracts, prepared further with NaCl and H₂O from precipitates of 800 g kg^?1 methanol or 500 g kg^?1 ethanol extracts, exhibited potent α‐amylase inhibitory activities (IC₅₀ of 17.68–38.68 μg mL^?1). A combination of 500 g kg^?1 ethanol extraction plus a subsequent H₂O extraction produced highest polyphenolics and α‐amylase inhibitors. The SA‐05 α‐amylase inhibitor extracts showed greater inhibitory activities than that of Hwachia. Thus, cranberry bean mutant SA‐05 is an advantageous choice for producing anti‐hyperglycaemic compounds.     

Comparison of flavonoids profile in sprouts of common buckwheat cultivars and wild tartary buckwheat

In this study, major types of flavonoids in 7‐day sprouts of five common buckwheat cultivars grown in Poland (Hruszowska, Kora, Panda, Luba and Emka) and wild tartary buckwheat were investigated. Results demonstrated that sprouts of common buckwheat cultivars and wild tartary buckwheat contained both known and a newly discovered flavonol: quercetin 3‐O‐galactosyl‐rhamnoside. An exceptionally high content of this flavonoid was found in cotyledons of wild tartary buckwheat (30.79 ± 0.14 mg g^?1 DW), exceeding about 10 times level of rutin (3.16 ± 0.07 mg g^?1 DW). The results are not consistent with the data published so far on the content of flavonoids in sprouts of tartary buckwheat. Higher levels of flavonoids were measured in cotyledons than in hypocotyls with the exception of anthocyanins, which were present in higher amounts in hypocotyls. Cotyledons of common buckwheat sprouts were rich in C‐glycosides of luteolin and apigenin, the total content of which exceeded ca. 5 times the concentration of rutin.     

Assessment of thermo‐oxidative rancidity in sunflower oil and fried potato chips stabilised with oleoresin sage (Salvia officinalis L.) and ascorbyl palmitate by altered triglycerides and electronic nose

Oleoresin sage (Salvia officinalis) (SAG) (200–1500 mg kg^?1), ascorbyl palmitate (AP) (100–300 mg kg^?1) and TBHQ (200 mg kg^?1) were assessed for delaying the thermo‐oxidation in sunflower oil (SO) during 18 h of frying (180 °C). Electronic nose compared the global aroma fingerprints of potato chips fried in oils. The chemical rancidity indices viz., fatty acids, total polar compounds (TPC), altered triglycerides (dimers, polymers, oxidised monomers, diglycerides), free fatty acids, conjugated dienes and induction periods were monitored along with physical indices viz., viscosity and colour. SO_SAG+AP (1309.62 + 270.71 mg kg^?1) outperformed SO_TBHQ by preserving polyunsaturated fatty acids (60.48% vs. 56.23%), retarding TPCs (28.16% vs. 29.91%), triglyceride dimers (90.24 vs. 95.82 mg g^?1) and polymers (25.40 vs. 26.98 mg g^?1) concomitantly extending the oil disposal time (basis 25% TPC) (15.9 vs. 14.7 h). The postfrying viscosity, colour values and global aroma fingerprints of fried chips indicate a close match between SO_SAG+AP and SO_TBHQ.     

Flavonol glycosides and antioxidant capacity of various blackberry and blueberry genotypes determined by high‐performance liquid chromatography/mass spectrometry

Flavonol glycoside composition and content in blueberry and blackberry extracts were determined using a high‐performance liquid chromatographic (HPLC) separation method coupled with photodiode array (PDA) and mass spectrometric (MS) detection. The hydrophilic antioxidant capacities of crude and fractionated flavonol extracts were also determined by the oxygen radical‐absorbing capacity (ORAC_FL) and photochemiluminescence (PCL) assays. Eight flavonols of quercetin and quercetin–sugar conjugates were identified in Kiowa blackberry, namely rutinoside, galactoside, methoxyhexoside, glucoside, pentoside, [6″‐(3‐hydroxy‐3‐methylglutaroyl)]‐β‐galactoside, glucosylpentoside and oxalylpentoside. Thirteen flavonols were detected in Ozarkblue blueberry. Of these, myricetin 3‐hexoside and 12 quercetin–sugar conjugates, namely rutinoside, galactoside, methoxyhexoside, glucoside, pentoside, glucosylpentoside, caffeoylglucoside, oxalylpentoside, rhamnoside, dimethoxyrhamnoside, acetylgalactoside and acetylglucoside, were identified. In Bluecrop blueberry, two additional quercetin–sugar conjugates were identified, namely glucuronide and caffeoylgalactoside. Quercetin glycosides accounted for 75% of total flavonols in the blueberry genotypes. Total flavonol contents ranged from 99 to 150 mg kg^?1 for blackberries and from 192 to 320 mg kg^?1 for blueberries. Quenching of peroxyl and superoxide anion radicals by the flavonol fractions ranged from 1.5 to 2.3 mmol Trolox equivalents (TE) kg^?1 and from 0.5 to 0.7 mmol TE kg^?1 respectively for blackberries and from 2.9 to 5.2 mmol TE kg^?1 and from 0.8 to 1.4 mmol TE kg^?1 respectively for blueberries. The HPLC method allowed for complete separation and identification of flavonols commonly found in blackberries, and blueberries. Our results showed that blueberry and blackberry genotypes varied significantly in flavonol content and antioxidant capacity. Even though total flavonol content did not correlate well with antioxidant capacity, their ability to scavenge peroxyl and superoxide anion radicals was apparent. Copyright © 2005 Society of Chemical Industry     

Cyanogenic potential of fresh and frozen cassava on retail sale in three Irish cities: a snapshot survey

Imported cassava roots can be found on retail sale in several Irish cities and towns. Fresh roots (n = 36 roots) and peeled frozen root pieces (n = 28 packs) were randomly purchased from five retailers in Belfast, Dublin and Limerick and assayed for cyanogenic potential (CNp). Total CNp of fresh root parenchyma varied from 37.5 to 242.9 mg kg^?1 as HCN, dry weight basis – dwb), averaging 104.4 mg kg^?1 HCN (dwb). Total CNp of frozen root parenchyma (n = 28 packs) ranged from 28.5 to 258.6 mg kg^?1 HCN (dwb), averaging 81.7 mg kg^?1 HCN (dwb). Around 78% of fresh roots, and 93% of packs of frozen parenchyma, complied with the Codex Alimentarius definition of ‘sweet’ cassava, but most (86.1% and 64.3%, respectively) exceeded European Union NETTOX recommendations for total CNp. In around one‐third of frozen parenchyma packs, nonglycosidic cyanogens accounted for 83–100% of total CNp. The toxicological implications are briefly discussed.     

Antioxidant potential of protein‐rich serum from farmed swan goose (Anser cygnoides): in vitro and in vivo evaluation of antioxidant effects

As food ingredient, Anser cygnoides is farmed in large scale; however, its blood is underused. The characteristics, stability and antioxidant activities of P owder of farmed C ygnoides S erum (FACSP) were investigated. Results showed that FACSP was protein‐rich and displayed satisfactory antioxidant activities. In vitro analysis indicated that the IC₅₀ values of 2, 2′‐azinobis‐(3‐ethylbenz‐thiazoline‐6‐sulphonate), 1,1‐diphenyl‐2‐picrylhydrazyl and hydroxyl radicals were 1.56, 2.76 and 39.55 mg mL^?1, respectively. In vivo experiment showed that the activity of total superoxide dismutase and content of glutathione of the FACSP‐treated groups were enhanced, and the contents of malondialdehyde and protein carbonyl were decreased. The parameters of 400 and 800 mg kg^?1 bw day^?1 dose groups were equally or approximately to vitamin C. The FACSP shows potential as an antioxidant functional food at a dose of 400 mg kg^?1 bw day^?1.     

Change in Flavonoid Composition and Antioxidative Activity during Fermentation of Onion (Allium cepa L.) by Leuconostoc mesenteroides with Different Salt Concentrations

The aim of this study is to investigate the change in flavonoid composition and antioxidative activity during fermentation of onion (Allium cepa L.) by Leuconostoc mesenteroides with different NaCl concentrations. In order to qualify and quantify the flavonoids during fermentation of onion, 7 flavonoids, [quercetin 3,7‐O‐β‐d ‐diglucopyranoside (Q3,7G), quercetin 3,4′‐O‐β‐d ‐diglucopyranoside (Q3,4′G), quercetin 3‐O‐β‐d ‐glucopyranoside (Q3G), quercetin 4′‐O‐β‐d ‐glucopyranoside (Q4′G), isorhamnetin 3‐O‐β‐d ‐glucopyranoside (IR3G), quercetin (Q), and isorhamnetin (IR)], were isolated and identified from onion. During fermentation, the contents of flavonoid glucosides (Q3,7G, Q3,4′G, Q3G, Q4′G, and IR3G) gradually decreased, whereas the contents of flavonoid aglycones (Q, IR) gradually increased. Decline rates of the flavonoid glucosides increased with the addition of L. mesenteroides. Furthermore, the activity of β‐glucosidase, which is produced by L. mesenteroides, is dose‐dependently inhibited with different NaCl concentrations during fermentation. The presence of L. mesenteroides enhanced the antioxidative activity of onion as demonstrated using the 1,1‐diphenyl‐2‐picrylhydrazyl, 2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulfonic acid), and reducing power assays. The enhancement of antioxidative activity was considered because the content of flavonoid aglycones increased during fermentation. However, the addition of NaCl may decrease the antioxidative activity; we surmise that this phenomenon occurs because of the inhibition of β‐glucosidase by NaCl. Therefore, we conclude that the addition of NaCl may be useful for the regulation of antioxidative activity via the control of β‐glucosidase action, during the fermentation of flavonoid glucoside‐rich foods.     

Effect of supercritical CO2 extraction process parameters on oil yield and pigment content from by‐product hemp cake

This research gives an insight into the possibility of exploiting the one of the food industry's by‐products – pressed hemp cake. The complete recovery of oil from pressed hemp cake was achieved. Residual oil that remained in cake after pressing was extracted with supercritical CO₂ by applying different process parameters. Optimal extraction conditions were determined using response surface methodology. Total pigment contents of the oils obtained were determined. Extraction pressure had the most significant influence on yield and pigment content of extracted hemp cake oil. Depending on the pressure, the chlorophyll a content ranged from 101.11 to 378.28 mg kg^?1 and chlorophyll b from 65.14 to 189.78 mg kg^?1, while total carotene content was in the range from 33.58 to 132.67 mg kg^?1. The remaining oil in pressed hemp cake after supercritical CO₂ extraction was determined to be 0.56 ± 0.08% and the defatted cake was rich in proteins and fibre.     

An improved method for the measurement of 3‐monochloropropanediol esters by matrix solid‐phase dispersion supported liquid–liquid extraction

3‐Monochloropropanediol (3‐MCPD) esters are contaminants produced from the high‐temperature processing of edible oils. The accurate measurement of 3‐MCPD using an easy‐to‐follow and reliable method that uses a readily available instrument is important. Here, we report an acid transesterification heptafluorobutyrylimidazole (HFBI) derivatisation method for the accurate measurement of 3‐MCPD esters in edible oils. We developed a dispersed matrix solid‐phase supported liquid–liquid extraction (DMSP‐SLE) system to remove impurities. Both the transesterification and DMSP‐SLE conditions were optimised. A good linear relationship was obtained within the range of 0.05–10 mg kg^?1 (R² ≥ 0.999) in both blank solvent and an oil sample. The limit of detection was 20.36 μg kg^?1. The average recovery of the 3‐MCPD esters spiked at 0.5, 1.0 and 2.0 mg kg^?1 into a blank oil matrix was in a range from 105.09 ± 2.77% to 120.16 ± 10.88%. The method we developed was further confirmed by performing detection on a Food Analysis Performance Assessment Scheme (FAPAS) sample.     

Hypolipidaemic and antioxidant capacities of polysaccharides obtained from Laminaria japonica by different extraction media in diet‐induced mouse model

This study shows the industrial feasibility of using aqueous methods to produce antioxidative and hypolipidaemic polysaccharides from Laminaria japonica (LJP). Comparison was firstly made among the polysaccharides prepared using different extraction media, that is water alone (LJPW) and citric acid (LJPC), sulphuric acid, hydrochloric acid and phosphoric acid. LJPC enabled the highest extract yield (~11% dry weight), bile salt adsorption rate (~59% dry weight), ABTS radical scavenging activity (IC₅₀ value 1.06 mg mL^?1) and ORAC antioxidant activity (341.87 μmol Trolox g^?1). In animal trial using diet‐induced high‐fat mice, oral administration of LJP produced with citric acid (LJPC) at a high dose (200 mg kg^?1 body mass per day) enabled significantly higher serum HDL‐C, lower LDL‐C/HDL‐C and unaltered LDL‐C, whilst a medium dose (100 mg kg^?1 body mass per day) significantly decreased LDL‐C. Administration of LJP produced with water (200 mg kg^?1 body mass per day) significantly lowered serum LDL‐C. Therefore, LJP may provide dose‐dependent pharmacological and therapeutic effects to combat atherosclerosis through their hyperlipidaemic and antioxidant properties.     

Antioxidant and anti‐hypertensive activity of anthocyanin‐rich extracts from hulless pigmented barley cultivars

Anthocyanin‐rich acetone extracts of barley grain of four hulless pigmented genotypes were investigated to determine their potential as functional food ingredients. The purple barley cultivar contained 11 anthocyanins, whereas only one anthocyanin, peonidin derivative, was observed in blue, black and yellow barley. The total anthocyanin content of pigmented barley genotypes ranged from 3.2 to 678.5 mg kg^?1 in whole grain and from 4.5 to 1654.6 mg kg^?1 in bran. The purple barley bran extract gave the highest DPPH radical scavenging capacity, superoxide radical scavenging capacity and total antioxidant activity. The half maximal inhibitory concentration (IC₅₀) of angiotensin I‐converting enzyme (ACE) of anthocyanin‐rich extract of purple barley grain and bran was 8.77 and 4.54 mg mL^?1, respectively. Purple barley appears to have great potential uses for the promotion of human health and development of nutraceuticals and functional foods.     

Oil content,phenolic profiling and antioxidant potential of Tunisian olive drupes

BACKGROUND: The aim of this work was to investigate the effect of the maturation process of the olive fruit on oil content, phenolic profile and antioxidant activity of four Tunisian cultivars (Zelmati, Chemchali, Chemlali and Chétoui). RESULTS: The average oil content of the studied varieties ranged between 17.50% and 20.25% at the first stage of maturation and from 30.20% to 35% in the last harvest. Qualitative and quantitative analysis of phenolic compounds were carried out using HPLC and LC‐MS/MS. Twenty‐six biophenolic compounds were identified. In all samples, hydroxytyrosol and oleuropein were the major compounds identified while rutin and luteolin 7‐O‐glucoside were the two main flavonoids. The total phenolic content varied from 3.46 to 4.30 g kg^?1 at the first stage of maturation and from 8.71 to 11.52 g kg^?1 of fruit fresh weight at the last maturation phase. Total flavonoid content reached 432.80 mg kg^?1. The antioxidant activity of the extract was evaluated by DPPH and ABTS assays. The IC₅₀ values of the olive extracts ranged from 2.69 to 10.96 µg L^?1 and from 2.15 to 3.03 mmol L^?1 trolox equivalent at the last stage of maturation. CONCLUSION: A relationship between the changes in phenolic content and the physicochemical changes in Tunisian olive fruit during maturation was established. These findings could be used for controlling the production processes and correlating the oil sensorial characteristics to the polyphenolic pattern. Copyright © 2010 Society of Chemical Industry