Antioxidant activity of evening primrose phenolics in sunflower and rapeseed oils

Crude ethanol/ethyl acetate extracts of industrial evening primrose (Oenothera biennis L.) seed meal were separated into six fractions using the Sephadex LH‐20 column chromatography and 96% aqueous ethanol as a mobile phase. Their antioxidant activities were tested in sunflower and rapeseed oils by using an Oxidograph apparatus at a temperature of 110 °C. Only the fractions III and IV displayed a pronounced antioxidant activity while the other fractions were either inactive or even pro‐oxidative. The active fractions contained phenolic acids and their esters; gallic acid, methyl and ethyl gallates, protocatechuic acid and its methyl ester were identified by GC/MS. Catechin was present, too, but exhibited only moderate antioxidant activity in sunflower oil.     

Effect of Greek sage and summer savory extracts on vegetable oil thermal stability

The effect of ethanol and acetone extracts obtained from Greek sage (Salvia fruticosa) and summer savory (Satureja hortensis L.) on the thermal stability of vegetable oils heated at frying temperature (180 °C) was studied. Virgin olive oil (VOO), refined olive oil (ROO), sunflower oil (SO), and a commercial oil blend suitable for frying (BL), enriched with each extract obtained from the two plant materials at a concentration of 3 g/kg oil, were heated at 180 °C for 10 h. Changes during heating were assessed by quantification of total polar materials and determination of p‐anisidine values. The acetone extract obtained from Greek sage showed a better inhibitory effect against thermal oxidation of heated refined oils (BL, ROO, SO) than the respective ethanol extract, although the latter was found to have a relatively higher total phenol content. Both summer savory extracts effectively retarded the thermal oxidation reactions during oil heating, showing a more pronounced effect than the Greek sage acetone extract. The activity of the acetone extract obtained from summer savory was stronger (SO, BL) or similar (ROO, VOO) to that of the summer savory ethanol extract, although the latter was found to have a higher total phenol content.     

Antioxidant capacity of rapeseed meal and rapeseed oils enriched with meal extract

Response surface methodology (RSM) was used to evaluate the quantitative effects of two independent variables: solvent polarity and temperature of the extraction process on the antioxidant capacity (AC) and total phenolics content (TPC) in meal rapeseed extracts. The mean AC and TPC results for meal ranged between 1181–9974 µmol TE/100 g and 73.8–814 mg sinapic acid/100 g of meal. The experimental results of AC and TPC were close to the predicted values calculated from the polynomial response surface models equations (R² = 0.9758 and 0.9603, respectively). The effect of solvent polarity on AC and TPC in the examined extracts was about 3.6 and 2.6 times greater, respectively, than the effect of processing temperature. The predicted optimum solvent polarity of ε = 78.3 and 63.8, and temperature of 89.4 and 74.2°C resulted in an AC of 10 014 µmol TE/100 g and TPC of 863 mg SAE/100 g meal, respectively. The phenolic profile of rapeseed meal was determined by an HPLC method. The main phenolics in rapeseed meal were sinapine and sinapic acid. Refined rapeseed oils were fortified with an extract – rich in polyphenols – obtained from rapeseed meal. The supplemented rapeseed oil had higher AC and TPC than the refined oil without addition of meal extracts. However, AC and TPC in the enriched oils decreased during storage. The TPC in the studied meal extracts and rapeseed oils correlated significantly (p<0.0000001) positively with their AC (R² = 0.9387). Practical applications: Many bioactive compounds extracted from rapeseed meal provide health benefits and have antioxidative properties. Therefore, it seems worth to consider the application of antioxidants extracted from the rapeseed meal for the production of rapeseed oils with potent AC. Moreover, antioxidants extracted from the rapeseed meal were added to refined rapeseed oil in order to enhance its AC. AC was then tested by FRAP assay. FRAP method is based on the reduction of the ferric tripyridyltriazine (Fe³⁺‐TPTZ) complex to the ferrous tripyridyltriazine (Fe²⁺‐TPTZ), and it is simple, fast, low cost, and robust method. FRAP method does not require specialized equipment and can be performed using automated, semi‐automatic, or manual methods. Therefore the proposed FRAP method can be employed by the fat industry laboratories to asses the AC of rapeseed oils and meal.     

Antioxidant activity of tea extracts in lipids and correlation with polyphenol content

The present study examined the antioxidative activity of water and ethanol extracts of green and black tea leaves against the oxidation of heated sunflower oil and lard. Oxidation was conducted at 110 °C in the Rancimat test. Total polyphenols and catechin contents in tea extracts were measured. The research showed that the total polyphenol content in green and black tea leaves was 205.2 and 148.7 mg/g, respectively. In tea leaves extracts, it ranged between 245.9 mg/g and 837.7 mg/g and depended on the extraction solvent and the kind of tea used (p <0.001). The highest polyphenol content was observed in samples extracted with 95% ethanol, lower contents were found with the use of water. Results showed that the highest antioxidant activity, measured as an induction period, with 1000 ppm green tea ethanol extract, was comparable to á‐tocopherol activity in sunflower oil. In lard, the longest induction period was measured with 500 and 1000 ppm of green tea ethanol extract. Other tea extract concentrations were significantly less active. Statistical analysis of the tea extract antioxidant activity in lipids in the Rancimat test showed an essential influence of the catechin contents. Further statistical analysis also showed an influence of (?)‐epicatechin gallate (ECG), (?)‐epicatechin (EC), and (+)‐catechin (C) contents in the tea extracts on the antioxidant activity in lipids. It was stated that the antioxidant activity was higher in tea extracts containing high levels of ECG, EC, and C.     

核桃仁抗氧化活性研究

采用清除二苯代苦味肼基(DPPH)自由基、清除[2,2′-连氨-(3-乙基苯并噻唑啉-6-磺酸)二氨盐](ABTS)自由基及铁离子还原/抗氧化能力(FRAP)测定法,对核桃仁提取物进行抗氧化活性评价,并与阳性对照没食子酸丙酯(PG)、丁基羟基茴香醚(BHA)和二丁基羟基甲苯(BHT)进行比较。在核桃仁提取物中,乙酸乙酯提取物清除DPPH和ABTS自由基的能力(IC50值分别为1.58 mg/L和1.69 mg/L)强于BHA(IC50值分别为3.43 mg/L和1.72 mg/L)和BHT(IC50值分别为18.79 mg/L和6.04 mg/L),弱于PG(IC50值分别为0.86 mg/L和0.66 mg/L);乙酸乙酯提取物还原Fe3+的能力最强〔FRAP值为(13212.99±55.35)μmol TE/g〕,强于PG〔FRAP值为(10617.75±138.38)μmol TE/g〕、BHA〔FRAP值为(7383.10±121.08)μmol TE/g〕和BHT〔FRAP值为(1748.49±3.46)μmol TE/g〕;核桃仁正丁醇提取物清除DPPH和ABTS自由基的能力(IC50值分别为4.94和1.90 mg/L)以及还原Fe3+的能力〔FRAP值为(2299.99±27.68)μmol TE/g〕强于BHT。结果表明,核桃仁乙酸乙酯和正丁醇提取物都具有很好的抗氧化活性,且乙酸乙酯提取物活性强于正丁醇提取物。     

Lipid oxidation inhibiting capacities of blackseed essential oil and rosemary extract

Lipid oxidation is the main deterioration process that occurs in vegetable oils containing lipid molecules with polyunsaturation. The aim of the present study was to investigate the possible effects of blackseed (Nigella sativa L.) essential oil (BEO) and rosemary (Rosmarinus officinalis L.) extract (RE) on stabilization of sunflower oil under accelerated storage conditions. RE was obtained by soxhlet extraction using methanol, whereas BEO was hydrodistilled from the blackseed extract obtained by extraction using petroleum ether (b.p. 40–60°C). The results indicate that both extracts stabilize sunflower oil to a certain extent, the extent being greater with RE than with BEO based on measurements of peroxide value, p‐anisidine value, amount of nonoxidized linoleic acid in saponified oil samples by HPLC‐DAD, concentration of conjugated diene hydroperoxide, and UV light absorption. The oil stabilizing effect of BEO against lipid oxidation, especially at concentrations of 0.06 and 0.1 g/100 g oil was found to increase as the temperature increased, according to principal component analysis results. Based on its strong lipid oxidation inhibiting capacity, RE can be used as a potential natural extract for stabilizing sunflower oil against oxidation. BEO, at carefully selected concentrations, can be suggested as an alternative supplement of plant origin for improving oil stabilization. Practical applications: Sunflower oil is a widely used vegetable oil for cooking and frying, and has a high linoleic acid content of about 40–70%. Here we show that sunflower oil can be stabilized by adding rosemary and blackseed extracts. The treatment can be useful especially in applications which require heating the oil to high temperatures.     

Influence of Zataria multiflora Boiss. essential oil on oxidative stability of sunflower oil

In this study, the influence of the application of 0.025%, 0.05% and 0.075% of Zataria multiflora Boiss. essential oil (EO) on oxidative stability of sunflower oil was examined and the EO was compared to butylated hydroxyanisole (BHA) and butylated hydroxytoluene (BHT) during storage at 37°C and 47°C. The main components of EO were identified as carvacrol (45.6%), p‐cymene (18.1%) and thymol (16.3%). Peroxide value (PV), anisidine value (AnV) and thiobarbituric acid (TBA) value measurement in sunflower oil showed that all concentrations of EO had a lower antioxidant effect in comparison to BHA and BHT. Samples supplemented with EO concentration of 0.075% were the most stable during storage at both temperatures (p<0.05). Furthermore, Totox value, antioxidant activity (AA), stabilization factor (F) and antioxidant power (AOP) determination confirmed efficacy of this EO as antioxidant in sunflower oil. EO also was able to reduce the stable 2,2‐diphenyl‐1‐picrylhydrazyl free radical (DPPH ^. ) with a 50% inhibition concentration (IC₅₀) of 34.3 ± 0.8 µg/mL. The results indicate that EO could be used as a natural antioxidant in oils for food uses.     

Analysis of carotenoids and vitamin E in selected oilseeds,press cakes and oils

Carotenoids and vitamin E in oils from the market – 6 rapeseed and 6 sunflower oils, half of each cold pressed and refined – and in the oils of rape, sunflower, flax and safflower as well as the respective seeds and press cakes from a local oil mill were quantified by HPLC. Furthermore, a photometric determination of carotenoid content was tested and checked against the chromatographic method. In the cold pressed oils minor amounts of xanthophylls (all‐E)‐lutein and (all‐E)‐zeaxanthin were determined. With exception of traces of (all‐E)‐β‐carotene in cold‐pressed rapeseed oil this provitamin A active compound did not occur. Cold pressed rapeseed oils contained 0.5–1.5 mg total carotenoids/100 g which was manifold the content of the further oils. Vitamin E was found in all vegetable oils at plant‐typic tocopherol patterns. The photometric determination of carotenoids resulted in significantly higher concentrations compared to the HPLC. This overestimation bases on the carotenoid pattern which was validated by comparison with known high‐carotenoid materials, i.e. maize flour with an abundant amount of xanthophylls and carrots with an abundant amount of carotenes.     

Oregano flavonoids as lipid antioxidants

Oregano (Origanum vulgare L.) leaves were successively extracted with hexane, ethyl ether, ethyl acetate and ethanol. The ethanol extract was reextracted in a separatory funnel with petroleum ether, ethyl ether, ethyl acetate and butanol. The ethyl ether layer was the most effective in stabilizing lard against oxidation, with activity equal to butylated hydroxytoluene. It also showed antioxidant activity when tested on vegetable oils under storage or frying conditions. The main antioxidant factors isolated from the ethyl ether layer consisted of flavonoids. Chromatographic and spectrophotometric analysis demonstrated the presence of the flavone apigenin, the flavanone, eriodictyol and the dihydroflavonols, dihydrokaempferol and dihydroquercetin.     

Antioxidant Capacity of Rapeseed Extracts Obtained by Conventional and Ultrasound‐Assisted Extraction

Ultrasound‐assisted extraction (UAE) and conventional solid–liquid extraction were applied to extract total antioxidants from two rapeseed varieties. The antioxidant capacities (AC) of winter and spring rapeseed cultivars were determined by four different analytical methods: ferric reducing antioxidant power (FRAP), cupric reducing antioxidant capacity (CUPRAC), 2,2′‐diphenyl‐1‐picrylhydrazyl (DPPH), 2,2′‐azino‐bis‐3‐ethylbenzothiazoline‐6‐sulfonic acid (ABTS). The average AC of the studied rapeseed cultivars ranged between 4.21–10.03 mmol Trolox (TE)/100 g, 7.82–10.61 mmol TE/100 g, 8.11–51.59 mmol TE/100 g, 22.48–43.13 mmol TE/100 g for FRAP, CUPRAC, DPPH and ABTS methods, respectively. There are positive correlations between total phenolics (TPC = 804–1625 mg sinapic acid (SA)/100 g) and AC of the studied rapeseed extracts (r = 0.2650–0.9931). Results of the principal component analysis (PCA) indicate that there are differences between the total amounts of antioxidants in rapeseed samples extracted by different extraction techniques. Rapeseed extracts obtained after 18 min of ultrasonication revealed the highest content of total antioxidants. The UAE is a very useful, efficient and rapid technique of oilseed samples preparation for determination of AC by different analytical methods.     

Synthesis of two modified carotenoids and their behavior during light exposure

Two modified carotenoids, β‐6‐hydroxy‐2, 5, 7, 8‐tetramethyl‐chromane carboxylic acid β‐apo‐8'‐carotenoate (Caro‐Trolox) and 3, 5‐di‐tert‐butyl‐4‐hydroxy benzoic acid β‐apo‐8'‐carotenoate (Caro‐BHT) were synthesized by esterification of β‐apo‐8'‐carotenol with Trolox and with 3, 5‐di‐tert‐butyl‐4‐hydroxy benzoic acid, respectively. Their activity under light exposure was examined comparatively to that of Trolox, α‐tocopherol, β‐carotene, β‐apo‐8'‐carotenoic acid (CA} and ethyl β‐apo‐8'‐carotenoate. The substrate used was purified sunflower oil. In the absence of a photosensitizer (240 W/m² , 25 °C) Caro‐Trolox (200 mg/kg) behaved as an antioxidant and was quite stable (1/5 of the initial amount remained after 2‐wk storage). Caro‐BHT (200 mg/kg) showed no antioxidant activity and was quite unstable (it was destroyed within 7 d). In the presence of 5 mg/kg chlorophyll α (12000 lx, 25 °C) similar observations were made. The activity of Caro‐Trolox was concentration‐dependent. At a 100‐mg/kg level of addition its activity was similar to that of the mixture of α‐t_copherol (100 mg/kg) and β‐carotene (10 mg/kg). Its performance at the 10‐mg/kg level was slightly better than that of the other carotenoids. The antioxidant behavior of the modified carotenoids was attributed to the presence of the phenolic moiety as supported by the results of the 1, 1‐diphenyl‐2‐picrylhydrazyl test (e.g. EC₅₀ after 15 min: 26.2, Caro‐Trolox; 35.8, Caro‐BHT; 122, CA; 22.3, Trolox).     

Antioxidant activity of extracts from six different Sudanese plant materials

Methanolic extracts obtained by manual solvent extraction (MSE) and accelerated solvent extraction (ASE) of different Sudanese plant materials (Sclerocarya birrea leaves, Salvadora persica bark and leaves, Combretum hartmannianum leaves, Guiera senegalensis leaves and roots) were investigated for their antioxidant activity. There was no significant difference between the two extraction methods (p < 0.01) regarding the total amount of phenolic compounds expressed as gallic acid equivalents (GAE) (52.6–166.7 mg GAE/g total extractable compounds for MSE and 53.1–169.3 mg GAE/g for ASE). In comparison to a control without extract, the extracts were remarkably effective in the β‐carotene bleaching method, whereas the effectiveness was half or less in comparison to Trolox as standard antioxidant. Also using the 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) method antioxidant activity could be shown in comparison to a control, however, the extracts were less effective than Trolox. No significant difference was found between the two extraction methods. The increase of the peroxide value of sunflower oil during storage at 70°C was markedly lower after addition of the extracts in comparison to the control, but in the Rancimat test (120°C) the extracts showed only a small stabilization factor (F = 0.9–1.4) especially in comparison to Trolox (F = 5.8).     

Pro-Oxidant Effects of β-Carotene During Thermal Oxidation of Edible Oils

β-Carotene is one of the most important fat soluble pigments with well-known antioxidant and pro-vitamin A activity. It is used in industries as a food colorant and a source of vitamin A. The thermal induced degradation during processing of wide varieties of carotenoid-rich foods leads to color and properties losses. The thermal stability of edible oils is thus of great importance to food manufacturers. Corn oil, rapeseed, and sunflower oils were fortified with 50–300 μg/g of β-carotene and oxidized using a Rancimat apparatus (air flow rate 20 L/h) at 110 °C for 14 h. β-Carotene degradation was measured using high performance thin layer chromatography and confirmed by HPLC–DAD–MS. Triacylglycerols and polar compounds (PC) were determined using LC–ESI–MS. Results showed that most of the β-carotene was degraded during the first 5 h of the thermal oxidation. It was found that the addition of β-carotene produces significant effects (P < 0.05) on the peroxide index, free fatty acid values and radical scavenging activity of the three oils. Triacylglycerols containing high amounts of oleic acid show higher stability toward thermal oxidation and β-carotene treatment. Among the oils, rapeseed oil was the most stable oil in terms of the formation of polar compounds (PC), followed by corn oil, while sunflower oil was more prone to oxidation and thus higher amounts of PC were formed.     

Modified ferrous oxidation‐xylenol orange method to determine lipid hydroperoxides in fried snacks

A modified ferrous oxidation‐xylenol orange (FOX) method was adapted to measure lipid hydroperoxides (LHP) in lipid extracts from snack foods fried in vegetable oils. First, a methanol‐based FOX reaction medium was assayed, but this became turbid upon addition of the lipid extracts dissolved in ethanol. To avoid the precipitation of lipids, the polarity of the reaction medium was reduced by lowering its water content and by replacing the methanol as the basis of the medium for less polar solvents. Some of the solvents used instead of methanol yielded a lower FOX reaction response. Of the reaction media assayed, the one based on dichloromethane/ethanol (3:2, vol/vol) was not turbid at high lipid extract concentrations (assayed at up to 25 mg of lipid extract/mL reaction medium) and provided the same response level as the methanol‐based medium. Thus, this FOX method shows high sensitivity and is particularly useful for lipid extracts with low LHP content. This method was also successfully applied to edible oils. Solvents such as 2‐propanol, ethyl acetate and butanol were discarded, because they easily produce hydroperoxides, which interfere in the FOX reaction. Xylenol orange preparations from a number of suppliers were tested, and some differences affecting the sensitivity of the reaction were observed.     

Antioxidant activity of crude tannins of canola and rapeseed hulls

The antioxidant activity of crude tannins of canola and rapeseed hulls was evaluated by β-carotene-linoleate, α,α-diphenyl-β-picrylhydrazyl (DPPH) radical, and reducing power assays. Crude tannins were extracted from three samples of Cyclone canola (high-tannin) hulls and Kolner, Ligaret, and Leo Polish rapeseed (low-tannin) hulls with 70% (vol/vol) acetone. The total phenolic content in crude tannin extracts ranged between 128 and 296 mg of sinapic acid equivalents per 1 g of extract. The ultraviolet spectra of methanolic solution of canola extracts showed two absorption maxima (282 and 309 nm), whereas those of rapeseed extracts exhibited a single maximum (326 nm). Crude tannins isolated from canola hulls exerted significantly (P<0.025) greater antioxidant activity than those from rapeseed in all three assays. The scavenging effect of all crude tannins, at a dose of 1 mg, on the DPPH radical ranged from 35.2 to 50.5%. The reducing power of Cyclone canola hull extracts on potassium ferricyanide was significantly (P≤0.0025) greater than that of rapeseed hull extracts, and the observed data correlated well (r=0.966; P=0.002) with the total content of phenolics present.     

Chemical Analysis of Polyphenols with Antioxidant Capacity from Pinus durangensis Bark

The most active phenolics in Pinus durangensis residual bark were identified and evaluated following a chromatographic fractionation. Bark powder was defatted with hexane, and a crude extract (CE) was obtained by extraction with aqueous acetone (67%). A liquid partition with ethyl acetate was performed to produce an organic extract (OE), which was subsequently purified by column chromatography (Toyopearl HW-40F, methanol), resulting in ten fractions (MF1 to MF10) and an oligomeric fraction eluted with acetone 67% (OLF). Subfraction MF6-1 was obtained by a second chromatographic purification of MF6. Extraction yields, total phenolics, flavonoids, and flavanols contents were determined in CE and OE. The antioxidant activity of bark extracts was measured by DPPH and ABTS assays at 100 µg/mL, expressed in percentage, median effective concentration (IC₅₀), and TEAC (mM). Also the low density lipoprotein inhibition was evaluated. Identification of major phenolics was carried out by HPLCESI–MS and HPLC–DAD instruments. Bioactive taxifolin (dihydroquercetin), dihydromyricetin, myricetin, quercetin, pinomyricetin (myricetin-methoxy), pinoquercetin (quercetin-methoxy), trimeric, and tetrameric procyanidins were detected and identified in P. durangensis bark extracts. Polyphenols found are similar to those contained in Pycnogenol and other Pinus species.     

粘毛蓼的抗氧化活性

用清除二苯代苦味酰基(DPPH)自由基、清除[2,2′-连氨-(3-乙基苯并噻唑啉-6-磺酸)二氨盐](ABTS)自由基和铁离子还原/抗氧化能力(FRAP)测定法,对粘毛蓼体外总抗氧化活性进行了评价,结果与6-羟基-2,5,7,8-四甲基苯并二氢吡喃-2-羧酸(Trolox)及阳性对照丁基羟基茴香醚(BHA)、二丁基羟基甲苯(BHT)比较发现,粘毛蓼提取物有很好的体外抗氧化活性。乙酸乙酯提取物清除DPPH自由基(IC50=7.89 mg/L)的能力比BHT清除能力(IC50=18.71 mg/L)强,比BHA(IC50=3.20 mg/L)清除能力略弱;清除ABTS自由基能力(IC50=6.67 mg/L)比BHT(IC50=7.72 mg/L)清除能力强,比BHA(IC50=1.88 mg/L)清除能力弱;还原Fe3+的能力〔FRAP=(1362.55±47.22)μmol TE/g〕比BHT〔FRAP=(1581.68±97.41)μmol TE/g〕略低。在3种提取物中,乙酸乙酯提取物具有最高的抗氧化能力,甲醇提取物次之。3种方法中,DPPH方法和ABTS方法相关性最高(R=0.993)。     

Extraction of low-molar-mass phenolics and lipophilic compounds from Pinus pinaster wood with compressed CO2

Near-supercritical and supercritical CO₂ was used to extract low-molar-mass phenolics and lipophilic compounds from Pinus pinaster wood. Extraction of samples containing sapwood and knotwood was carried out at 10⿿25 MPa and 30⿿50 °C to assess the influence of the operational conditions on the yields of total extracts and phenolics, as well as on the radical scavenging capacity of extracts. The use of ethanol as a co-solvent increased both the extraction yields and the concentration of phenolics in extracts. Operating under selected conditions (25 MPa, 50 °C, 10% ethanol), the extraction yield accounted for 4.1 wt% of the oven-dry wood. The extracts contained up to 7.6 g of phenolic compounds (measured as gallic acid equivalents) per 100 g extract, and showed one third of the radical scavenging capacity of Trolox. Native resin acids accounted for about 24 g per 100 g extracts, whereas flavonoids, lignans, stilbenes and juvabiones were found at lower proportions.     

Stabilization of Camelina Oil with Synthetic and Natural Antioxidants

Camelina oil was found to have a much lower Oil Stability Index and higher p-anisidine rates in the oven storage test than either rapeseed or sunflower oils. Stabilization of camelina oil was evaluated with 21 food grade synthetic and natural antioxidants and antioxidant formulations, using both the Oil Stability Index (OSI) and the oven storage test. The Oil Stability Index of camelina oil was able to be increased above that of rapeseed oil with TBHQ and its formulation with citric acid, and above that of sunflower oil with EGC, EGCG, carnosic acid, propyl gallate, rosemary extract with ascorbyl palmitate or with gallic acid. para-Hydroxyphenols were found to be more effective than ortho-hydroxyphenols and monohydroxyphenols had no significant effect on the OSI. Good correlation (R ² = 0.96) was found between the stabilizing effect of ortho-hydroxyphenols and the molarity of the phenyl hydroxyl groups per weight of antioxidant. The oven storage test carried out with six of the evaluated antioxidants indicated that p-anisidine rates of camelina oil stabilized with commercial formulations of TBHQ with citric acid or rosemary extract with ascorbyl palmitate were about the same as that of sunflower oil, an almost 90% rate reduction when compared to camelina oil. Accordingly, camelina oils stabilized with TBHQ/citric acid and rosemary extract/ascorbyl palmitate formulations were more stable than rapeseed and sunflower oils, respectively in terms of OSI induction times and p-anisidine rates.     

Oxidation Rates of Triacylglycerol and Ethyl Ester Fish Oils

Fish oil is available primarily as triacylglycerols (TAG) or ethyl esters (EE). Anecdotal evidence suggests that TAG have superior bioavailability and oxidative stability compared to EE. In this work, peroxide value (PV) and p‐anisidine value (AV) were used to monitor oxidation in commercially available TAG and EE fish oils incubated at temperatures from 5 to 60 °C. Pseudo first‐order kinetics were assumed and rate constants were calculated for each temperature. At all temperatures, the rates of oxidation were higher for EE oils than TAG oils. For PV and AV measured in both oils, non‐linear Arrhenius models were plotted, generating activation energies that ranged from 7 to 103 and 2 to 159 kJ/mol for PV and AV, respectively. Although TAG were more resistant to oxidation than EE, they had lower activation energies (E_a) at ≤15 °C for reactions measured with PV and AV. The E_a for EE was negative at temperatures ≥45 °C, indicating that reaction rate was influenced by factors in addition to temperature.