Effect of solvents in extracting polyphenols and antioxidants of selected raw vegetables

Thirty-seven raw vegetables were extracted using four solvent systems: 70% acetone, 70% ethanol, 70% methanol, and distilled water. The extracts were tested for their total phenolic content, total flavonoid content and antioxidant activities (using diphenylpicryl-hydrazyl (DPPH) and ferric reducing antioxidant power (FRAP) assays). The results revealed the effect of different extracting solvents in altering the quantitative analyses of all vegetables and 70% acetone was identified as the most efficient solvent for extracting polyphenolic antioxidants from the vegetables. The highest total phenolic content and total flavonoid content were obtained from 70% acetone extract of Portulaca oleracea (138.2 ± 2.1 mg GAE/g dw basis) and 70% methanol extract of Cosmos caudatus (27.7 ± 1.0 mg QE/g dw basis), respectively. The 70% acetone extract of Etlingera elatior with moderate amount of total phenolic content exhibited the highest antioxidant activity in both assays. The correlation analyses within 37 different extracts of each solvent extraction demonstrated weak to moderate relationships between all the studied parameters. The highest r value of 0.7139 (p < 0.001) was determined between total phenolic contents and FRAP values of the 70% methanol extracts. Meanwhile, a wide range of correlation coefficients was derived from correlation analyses within four different extracts of each vegetable, with the highest relationship between total phenolic contents and FRAP values for the extracts of Coriandrum sativum (r = 0.9998, p < 0.001).     

Antioxidant compounds and antioxidant activity in acerola (Malpighia emarginata DC.) fruits and derivatives

Acerola (Malpighia emarginata DC.) is a wild plant from Central America. This fruit is well known as an excellent food source of vitamin C, and it also contains phytochemicals such as carotenoids and polyphenols. The present work evaluates the antioxidant capacity of hydrophilic extracts of acerola pulps and juices by 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), ORAC and 1,1-diphenyl-2-picrylhydrazyl (DPPH) methods. Antioxidant activity values obtained for acerola juice were higher than those reported for other fruit juices particularly rich in polyphenols such as strawberry, grape and apple juices, among others. Vitamin C, total phenol index (TPI), total anthocyanins and polyphenolic compounds by high performance liquid chromatography (HPLC), as main factors responsible for antioxidant activity, were determined. Contents in total ascorbic acid ranged from 6.32 to 9.20 g kg⁻¹ of pulp and 9.44 to 17.97 g L⁻¹ of juice. Five different polyphenolic compounds were identified in the samples by means of HPLC and diode-array detection: chlorogenic acid, (−)-epigallocatechin gallate, (−)-epicatechin, procyanidin B1 and rutin, being the two last predominant. By means of solid phase extraction (SPE) three soluble polyphenolic fractions (phenolic acids, anthocyanins and flavonoids) were separated from the different sample extracts, and their respective antioxidant activities calculated. Among them, phenolic acids are the main contributors to the antioxidant activity.     

Phenolic and antioxidant composition of cider

Forty-four Asturian ciders were analysed for total phenolic content, phenolic profiles, and antioxidant capacity by the FRAP and the DPPH radical assays. The Folin index of ciders ranged between 446 and 1180 mg gallic acid/L. The phenolic profile of Asturian cider is mainly constituted by phenolic acids, flavan-3-ols, volatile phenols and dihydrochalcones. The methods to determine the antioxidant activity of ciders were optimised in terms of suitable reaction times, within-day and between-day repeatability. Thus, time courses of ciders in the DPPH and the FRAP assays were performed. Mean values for antioxidant activity of cider, expressed in ascorbic acid equivalents were 2.9 mM (as determined by the DPPH assay). When the FRAP assay was used, the antioxidant capacity of cider increased with the reaction time from 3.8 mM (4 min) to 5.4 mM (40 min). Multivariate approaches based on phenolic composition can be useful to predict the antioxidant capacity of cider. Folin index and flavanols and hydrocaffeic acid contents were the best predictors for antioxidant activity.     

Phenolic compounds and antioxidant activity of Spanish commercial grape juices

Evaluation of the antioxidant activity of components of the diet is important in order to establish healthy consumption patterns. Data are reported here on the antioxidant activity (FRAP and ABTS), of 20 commercial grape juices and 10 typical Spanish wines and on their content of total phenolic compounds, anthocyanins, flavonoids and 10 individual phenolic compounds (flavanols, benzoic acids and cinnamic acids, measured by HPLC-UV). Red grape juices had a significantly higher (p < 0.05) concentration of total phenols (1177 vs. 744 mg gallic acid/L), flavonoids (98 vs. 63 mg catechin/L) and a higher antioxidant activity (9.16 vs. 2.83 meq Trolox/L) in comparison to white grape juices. In comparison to the white wines, white grape juices contained more total phenols (744 vs. 286 mg gallic acid/L) and flavonoids (63 vs. 29 mg catechin/L) and evidenced higher antioxidant activity (p < 0.05). In comparison to the red wines, a lower content of total phenols (286 vs. 2358 mg gallic acid/L) and flavonoids (228 vs. 29 mg catechin/L) and an absence of anthocyanins were observed in the white wines, which are therefore less antioxidant. Although a two-fold higher concentration of antioxidant compounds was found in red wines than in red grape juices, the latter may be a good option for all age groups because of the absence of alcohol and the potentially beneficial health effects of their phenolic composition and elevated antioxidant activity.     

Phenolic composition and antioxidant capacity of bacaba-de-leque (Oenocarpus distichus Mart.) genotypes

Phenolic compound composition and antioxidant capacity of four Oenocarpus distichus Mart. (bacaba-de-leque) genotypes were determined. In order to set the parameters for phenolic compound extraction, the effect of methanol concentration and extraction time on the reducing power of the extracts was evaluated using the surface response methodology. The optimal conditions were: a 60:40 methanol:water (v/v) solution and 11 min of extraction. Extracts were analyzed by ultra-high performance liquid chromatography with diode array detection and by ultra-high performance liquid chromatography coupled to mass spectrometry. Eleven substances were identified, of which six were quantified. Rutin was the major compound in bacaba-de-leque genotypes (15.2–56.8 μg.g⁻¹) followed by epicatechin (15.5–21.2 μg.g⁻¹). The Black-03 genotype had the highest amounts of all phenolic compounds and the highest antioxidant capacity by DPPH and ORAC assays, indicating that this genotype may be selected in breeding programs to obtain cultivars with higher phenolic compound contents and antioxidant capacity. Moreover, the results indicated that bacaba-de-leque has great potential as a novel supplier of phenolic acids and flavonoids to human diet, with levels comparable to or higher than other fruits belonging to the same family, such as açaí.     

Antioxidant activity and phenolic content in three lupin species

Total phenolic compounds, phenolic acids and flavonoid contents and antioxidant activities were measured in extracts from seeds of Lupinus albus, Lupinus luteus and Lupinus angustifolius cultivars. The total phenolic compound contents varied from 491.51 to 731.14 mg/100 g d.m. for cvs. Butan (L. albus) and Parys (L. luteus), respectively. Protocatechuic acid was the most abundant in seeds of yellow lupin (up to 73.60 mg/kg d.m.), whereas p-hydroxybenzoic acid in narrow-leaf lupin (about 43 mg/kg d.m.). The HPLC (high performance liquid chromatography) analysis revealed two dominant flavonoid compounds, which were identified by HPLC/MSⁿ to be apigenin-6,8-di-C-β-glucopyranoside and apigenin 7-O-β-apiofuranosyl-6,8-di-C-β-glucopyranoside. The highest content of the apigenin glycosides was recorded in yellow lupin while the lowest in white lupin. A positive correlation between the content of the analyzed compounds and the antioxidant activity measured by 2,2′-diphenyl-1-picrylhydrazyl (DPPH) method was established, but no such relation was found using the radical-trapping antioxidant parameter (TRAP) method. Modification of the peroxyl radical-trapping potential of lupin extracts by formation of phenoxyl radicals is suggested.     

Effects of soaking conditions on the antioxidant potentials of oolong tea

The antioxidant properties of water extracts of oolong tea (Commercial name: Fenghuangdancong) prepared using different soaking temperatures and times were investigated. The yield of powdered extract ranged from 6.7% at 80 °C for 3 min soaking to 22.7% at 100 °C for 10-min soaking. Oolong tea extracts reduced peroxidation of peanut oil and delayed the time of POV20 (peroxide value). Among these soaking treatments, soaking for 10 min in 100 °C water produced extracts with the greatest ability to inhibit the peroxidation of peanut oil. As well, the SC50 (scavenging-percentage) of the α, α-diphenyl-β-picrylhydrazyl radical (DPPH radical) was 0.119 mL of oolong tea extract using 3-min soaking at 100 °C, which is closed to the SC50 of 0.109 mL (2 mg/mL) for vitamin C. The DPPH radical scavenging activity of oolong tea extracts increased with increasing temperature of the soaking water indicating greater extraction of antioxidant compounds. In addition, inhibition of oxidation of peanut oil and DPPH radical scavenging activity by water extract of oolong tea was associated with polyphenol concentrations. Sensory assessment, found that the water extract of oolong tea using 3-min soaking at 95 °C had the strongest aroma and sweetness attributes.     

Antioxidant activity and phenolic content of fresh and dry nuts with or without the seed coat

Total antioxidant activities based on ABTS free radical scavenging activity and phenolic content of fresh or dry hazelnuts, walnuts and pistachios assayed with their seed coats changed between 3063 and 11,076 μmol trolox equivalents/100 g d.w. and 256 and 755 mg gallic acid equivalents/100 g d.w., respectively. The walnuts used in this study showed the highest antioxidant activity, followed by pistachios and hazelnuts. The removal of seed coat reduced the total antioxidant activity of hazelnuts, walnuts and pistachios almost 36, 90 and 55%, respectively. The total antioxidant activities of investigated fresh and dry nuts are not considerably different. However, phenolic content and antioxidant activity in hydrophilic and ethanolic fractions obtained by successive extraction of nuts showed some variation. The antioxidant activity in 1-serving portion of fresh or dry walnuts is equivalent to that in almost 2-serving portions of black tea, and 1.2–1.7-serving portions of green and Earl Grey tea. One-serving portions of dry hazelnuts and fresh or dry pistachios contained antioxidant activity equivalent to that in 0.7–1-serving portions of black tea. The antioxidant activity measurements correlated with phenolic content (r² = 0.70). This study showed the potential of using fresh or dry nuts to develop functional foods with high antioxidant activity.     

Antioxidant activity of methanolic extract of emblica fruit (Phyllanthus emblica L.) from six regions in China

The phenolic contents of methanolic extracts of emblica (Phyllanthus emblica L.) fruit from six regions in China were measured in this work. The antioxidant activities of these extracts were also evaluated. Total phenolic content was ranged from 81.5 to 120.9 mg gallic acid equivalents (GAE)/g and the flavonoid content was varied from 20.3 to 38.7 mg quecetin equivalents (QE)/g, while proanthocyanidin content was ranged from 3.7 to 18.7 mg catechin equivalents (CE)/g. Among all the methanolic extracts analyzed, the Huizhou sample exhibited a significantly higher phenolic content than other samples (P<0.05). The antioxidant activities were evaluated by in vitro experiments using scavenging assays of 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals, hydroxyl radicals, and superoxide anion radicals, chelating ability of ferrous ion, reducing power, and inhibition capability of Fe (II)-induced lipid peroxidation, respectively. The Huizhou sample was found to have the strongest antioxidant activities in scavenging DPPH radicals, superoxide anion radicals, and had the highest reducing power, while the Chuxiong sample showed the best performance in chelating iron and inhibiting lipid peroxidation. Furthermore, the Chuxiong sample exhibited a stronger inhibition activity of the hydroxyl radicals compared with other samples. The high correlation coefficient was existed between the phenolic content and superoxide anion radical scavenging activity, but no significant correlation was found between the former and hydroxyl radical scavenging activity. Methanolic extracts of emblica fruit from some selected regions exhibited stronger antioxidant activities compared to those of the commercial compounds (quercetin and BHA). It might be considered as a potential plant source of antioxidants.     

Radical scavenging,antioxidant and metal chelating activities of Annona cherimola Mill. (cherimoya) peel and pulp in relation to their total phenolic and total flavonoid contents

This study aimed to evaluate the total phenolic and flavonoid content, radical scavenging activity (by DPPH and ABTS tests) and antioxidant capacity (by β-carotene bleaching test) of Annona cherimola (cherimoya) fruits cultivated in Italy for human consumption. The metal chelating activity and ferric reducing power were also determined. A. cherimola peel and pulp were characterized by a total phenolic content of 14.6 and 12.6 mg chlorogenic acid equivalents/100 g fresh weight, respectively. A similar trend was observed with flavonoid content. Both extracts exhibited high antioxidant activity through different mechanisms of action. In particular, peel extract demonstrated the strongest free radical scavenging activity with an IC₅₀ value of 57.7 μg/mL. The same extract was more effective in preventing β-carotene oxidation (IC₅₀ value of 63.5 μg/mL after 60 min) and showed higher chelating ability (IC₅₀ value of 79.6 μg/mL) than pulp extract. This work demonstrated the high quality of cherimoya fruits cultivated in Italy, and recommends the peel of this fruit product that may be of interest from a functional point of view as a major source of natural antioxidants.     

Determination of free and bound phenolics using HPLC-DAD,antioxidant activity and in vitro digestibility of Eragrostis tef

White and brown Eragrostis tef were assessed for total flavonoid and phenolic content, HPLC profile of the most common phenolics and antioxidant activity including both free and bound phenolics. Antioxidant activity was evaluated in correlation with free and bound phenolics and in vitro digestibility was determined. Content of flavonoids (0.52–1.02 mg RE/g) and phenolics (0.90–1.42 mg GAE/g) as well as antioxidant activity (1.70–4.37 μmol TEAC/g using ABTS method) was higher in free phenolic fraction. Correlation showed that bound flavonoids were not significant contributors to antioxidant activity (R² = 0.4513 and 0.4893, respectively). The main free phenolics in brown teff were trans-p-coumaric, protocatechuic, ferulic and gallic acids, while the major free phenolics in white teff were rutin, protocatechuic and ferulic acids. The main bound phenolics in brown teff were ferulic and gallic acids, quercetin and catechin, in white teff ferulic acid, rutin, catechin and quercetin. Cooked teff showed very high level of in vitro organic matter digestibility (80.5–85.1%), whereas brown teff was significantly more digestible than white teff (P < 0.05).     

Evaluation of the mutagenicity and antimutagenicity of extracts from oat,buckwheat and wheat bran in the Salmonella/microsome assay

This study examined the mutagenic and antimutagenic activities of the DMSO extracts from the oat, buckwheat and wheat bran, which are good sources of polyphenols with antioxidant and anticarcinogenic properties. Extracts from buckwheat and wheat bran showed no mutagenic activity. Oat extract showed slight mutagenic effect in Salmonella typhimurium TA102. The antimutagenic activities against direct-acting (3-(5-nitro-2-furyl)acrylic acid, 2-nitrofluorene, hydrogen peroxide) and indirect-acting (aflatoxin B1) mutagens were also investigated using Ames test with S. typhimurium TA98, TA100 and TA102. Cereal extracts exhibit concentration-dependent protective antigenotoxic activity against all used mutagens. The total phenolic content in studied cereal extracts expressed as gallic acid equivalent increases in the order: buckwheat < wheat bran < oat. Total flavonoid content expressed as rutin equivalent increases in the order: oat < wheat bran < buckwheat.     

Characterization of phenolics,betacyanins and antioxidant activities of the seed,leaf, sprout,flower and stalk extracts of three Amaranthus species

Hydrophilic extracts from different parts including leaves, stalks, seeds, flowers and sprouts of 3 Amaranthus species (Amaranthus hypochondriacus, Amaranthus caudatus and Amaranthus cruentus) were characterized for their phytochemical profiles including the phenolics and betacyanins by UHPLC and LC–ESI–MS, and their antioxidant activities by FRAP and ORAC assays. The main betacyanins in Amaranthus samples were identified to be amaranthine and isoamaranthine. Eleven phenolic compounds (gallic acid, protocatechuic acid, chlorogenic acid, gentistic acid, 2,4-dihydroxybenzoic acid, ferulic acid, salicylic acid, rutin, ellagic acid, kaempferol-3-rutinoside and quercetin) were identified in the extracts of different parts of Amaranthus. The total phenolic content (TPC) ranged from 1.04 to 14.94 mg GAE/g DW; the total flavonoid content (TFC) ranged from 0.27 to 11.40 mg CAE/g DW; while the total betalain content (TBC) ranged from 0.07 to 20.93 mg/100 g DW. FRAP values ranged from 0.63 to 62.21 μmol AAE/g DW and ORAC ranged from 30.67 to 451.37 μmol TE/g DW. The leaves of Amaranthus showed the highest TPC, TFC, TBC, FRAP and ORAC values; while the seeds and stalks the lowest. There was a strong correlation between TPC, TBC, TFC and the antioxidant activity. The result suggests that all parts of the Amaranthus plant can be a good source of antioxidants.     

In vitro antioxidant activities of Stevia rebaudiana leaves and callus

Leaf extract of Stevia rebaudiana promotes effects on certain physiological systems such as the cardiovascular and renal and influences hypertension and hyperglycemia. Since these activities may be correlated with the presence of antioxidant compounds, leaf and callus extracts of Stevia rebaudiana were evaluated for their total phenols, flavonoids content and total antioxidant capacity. Total phenols and flavonoids were analyzed according to the Folin–Ciocalteu method and total antioxidant activity of water and methanolic extracts of stevia leaves and callus was assessed by ferric reducing/antioxidant power (FRAP) assay as well as 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. The total phenolic compounds were found to be 25.18 mg/g for stevia leaves and 35.86 mg/g for callus on dry weight basis. The flavonoids content was found to be 21.73 and 31.99 mg/g in the leaf and callus, respectively. The total antioxidant activity was expressed as mg equivalent of gallic acid, ascorbic acid, BHA and trolox per gram on dry weight basis. Total antioxidant activity found was ranged from 9.66 to 38.24 mg and 11.03 to 36.40 mg equivalent to different standards in water and methanolic extract of stevia leaves, respectively. In case of stevia callus, it was found to be 9.44 to 37.36 mg for water extract and 10.14 to 34.37 mg equivalent to standards for methanolic extract. The concentrations required for 50% inhibition (IC₅₀) of DPPH radicals were 11.04, 41.04 and 57.14 μg/mL for gallic acid, trolox and butylated hydroxyanisole (BHA), respectively. The percent inhibition of DPPH radical of various extracts of stevia leaves and callus found were ranged from 33.17% to 56.82%. The highest percent of inhibition was observed in methanolic extract of callus.     

Identification and quantification of phenolic compounds responsible for the antioxidant activity of sweet potatoes with different flesh colours using high performance thin layer chromatography (HPTLC)

The objectives of the present study were to develop a simple high performance thin layer chromatography (HPTLC)-based protocol: (i) to allow high-throughput profiling of phenolic compounds of microwaved roots from 295 sweet potato varieties and breeding lines, (ii) to quantify the content of anthocyanins and caffeoylquinic acid (CQA) derivatives, and (iii) to determine their respective contributions to the antioxidant activity of sweet potato methanolic extracts using the DPPH test. Analysed accessions were separated into three groups: white-fleshed (n = 100), orange-fleshed (n = 64) and purple-fleshed (n = 131). Purple-fleshed accessions presented the highest mean CQA content. After DPPH treatment and transmittance scanning of the plate at 517 nm, the most active free radical scavengers were found to be the four CQAs (CGA, 3,4-, 4,5- and 3,5-diCQA) while the anthocyanins were found to be less active. The total antioxidant capacity of the sweet potato methanolic extracts was mostly linked to total CQAs content. This method can now be used for fast routine analysis and selection of sweet potato breeding clones.     

Total phenolic compounds and antioxidant potential of Hedychium spicatum Buch. Ham. ex D. Don in west Himalaya,India

Total phenolic compounds and antioxidant potential of Hedychium spicatum were analyzed for 16 different natural populations located in Uttarakhand (west Himalaya) for promotion as health or medicinal food. Total phenolic compounds varied among populations from 4.70 mg gallic acid equivalent (GAE) to 2.84 mg GAE/g dry weight. Three in vitro antioxidant assays, i.e. azinobisethylbenzothiazoline-6-sulphonic acid radical scavenging (ABTS) assay, diphenyl-2-picrylhydrazyl (DPPH) assay and ferric reducing antioxidant power (FRAP) assay, showed significant (p < 0.05) differences across populations. ABTS assay showed highest values of antioxidant potential ranging from 2.581 mM ascorbic acid equivalent (AAE) per 100 g to 1.91 mM AAE per 100 g dry weight, followed by FRAP assay (1.921–0.6635 mM AAE per 100 g). Lowest values were observed for DPPH assay, which varied from 0.549 to 1.059 mM AAE per 100 g dry weight. All assays (ABTS, DPPH and FRAP) showed significant (p < 0.05) correlation with total phenolic compounds. Total phenolic compounds showed a significant relationship (p < 0.05) to altitude.     

Sweet cherry phytochemicals: Identification and characterization by HPLC-DAD/ESI-MS in six sweet-cherry cultivars grown in Valle del Jerte (Spain)

Individual anthocyanin pigments and phenolic compounds were isolated, identified and quantified in six different sweet-cherry cultivars (Prunus avium L.) grown in Valle del Jerte area (Spain). An extractive-chromatographic method has been optimized for one-step extraction and simultaneous determination of all the studied components by HPLC/DAD-MS. The highest levels of phytochemicals were found in the autochthonous sweet-cherry cultivars that belong to the Protected Designation of Origin (POD) Cereza del Jerte. Van cultivar showed the lowest level of anthocyanin pigments and phenolic compounds. The most abundant anthocyanin pigment in all the studied cultivars was cyanidin-3-rutinoside (105 mg/100 g fresh weight (fwt) in Pico Negro sweet-cherry cultivar). The most abundant phenolic compound was the flavanol p-coumaroylquinic acid (130 mg/100 g fwt in Pico Negro sweet-cherry cultivar). In addition, chemical attributes (antioxidant activity, soluble solid content and pH) were also evaluated.     

Survey of antioxidant capacity and nutritional quality of selected edible and medicinal fruit plants in Hong Kong

Twenty-two samples (including fruits, pulp, peel, or seeds) from 13 edible and medicinal fruit plant species selected in Hong Kong were investigated for their antioxidant capacity, nutritional quality and phenolic profiles. Significant variation existed among the tested samples in all the antioxidant and nutritional parameters. Proanthocyanidins, flavonoids and phenolic acids were identified as major categories of phenolic compounds in these samples. Whole fruits of Hong Kong gordonia exhibited the strongest antioxidant capacity (213.4 mmol trolox/100 g DW) and had the second highest content of carotenoids. Seeds of Annona squamosa possessed the highest contents of total protein, fat and amino acids (17.6, 37.2 and 14.4%, respectively). Most peel and some seeds contained high levels of phenolics, carotenoids and vitamin C, which contributed to their strong antioxidant activity. Some of the fruits, peel or seeds from these Hong Kong plants can be a potential resource of functional components and nutraceuticals.     

Bioactive compounds and antioxidant activity of gamma irradiated sun dried apricots (Prunus armeniaca L.)

The phenolics from both control and irradiated (3.0 kGy) dried apricots of Halman variety were identified and quantified by HPLC method using external standards. HPLC analysis revealed the presence of seventeen phenolic acids and eight flavonoids in dried apricots. Among the phenolic acids, ten were hydroxybenzoic acid derivatives (HBA), six hydroxycinnamic acid derivatives (HCA) and the one was present as ellagic acid. The most abundant flavonoids present in dried apricots were apigenin followed by quercetin and catechin. The results of the antioxidant activity as determined by DPPH radical scavenging, ferric reducing ability power (FRAP) and β-carotene bleaching assay revealed significant (p ≤ 0.05) decrease in EC₅₀ values and corresponding increase in antioxidant profile and activity due to irradiation, in addition to its effect in overcoming quarantine barriers. Irradiation decreased the EC₅₀ values by 19.1%, 13.6%, and 16.1% respectively with respect to control for DPPH, FRAP and β-carotene assays.     

Evaluation of antioxidant activities of phenolic compounds from two extra virgin olive oils

The aim of this work was to investigate the antioxidant properties of two varieties of olive oil (Chétoui and Chemlali), and to study the protective effect of phenolic extract (PE) from these varieties against low density lipoprotein (LDL) oxidation in vitro. Antioxidant activities were examined as well, using different radical scavenging assays: radical scavenging activity by DPPH, and total antioxidant status by ABTS. The antioxidant effect of the oils on human LDL was evaluated by measuring levels of conjugated dienes and polyunsaturated fatty acids. Chemlali oil was less rich in total phenols (158 mg/kg) than Chétoui oil (395 mg/kg) (p < 0.05). The highest antioxidant activity was attributed to Chétoui oil (78.56% vs. 37.23% of DPPH and 2.42 vs. 0.61 mmol Trolox/kg; p < 0.05). Chétoui PE had a significantly greater inhibitory effect on LDL oxidation than Chemlali PE (lag time = 116 ± 6.05 min vs. 64 ± 11.31 min at 0.3 mg/l of PE respectively; p < 0.05). The differences in quantity and quality of the studied oils influenced their biological activities and they could provide beneficial effects in cardiovascular disease by inhibiting LDL oxidation.