Oxidative stability of olive oil after food processing and comparison with other vegetable oils

The use of olive oil showed an important protection of meat and potatoes when compared with other vegetable oils, with sunflower oil samples being oxidised after 60 min of processing at 180 °C. Olive oil samples were not oxidised, independently of the olive oil quality used. Shelf life was longer for extra-virgin olive oil containing samples and this fact was positively correlated with their higher phenolic content. The radical-scavenging activity of extra-virgin olive oil was higher than for other olive oil samples and was also positively correlated with the phenolic content of the oil. Seed oil antioxidants showed little capacity in delaying the oxidative degradation of seed oils and meat processed with them. However, tocopherol content and the identity of tocopherols present in the oil were shown to have a more important role in the oxidative stability of seed oils than the fatty acid composition.     

A capacitive technique to assess water content in extra virgin olive oils

The present research investigated the correlations between capacitance and water content of extra virgin olive oils (EVOO). A commercial capacitor probe for radio applications and an LCR meter were used for electric tests in the frequency range from 500 Hz to 512 kHz. Seventeen samples of different EVOO with a moisture content ranging from 178 to 1321 mg/kg oil were selected for study. To assess the influence of moisture only, the oil with the maximum water content was filtered down to 288 mg/kg oil and five samples with intermediate water contents were prepared and submitted to electrical measurements. Subsequently, the capacitance of all 17 EVOO samples was measured at selected frequencies.     

Extra virgin olive oil: A comprehensive review of efforts to ensure its authenticity,traceability, and safety

The growing demand for extra virgin olive oil (EVOO), appreciated for its unique organoleptic properties and health benefits, has led to various fraudulent practices to maximize profits, including dilution with lower value edible oils. The adulterated oils would be of poor nutritional quality, more readily oxidized, and may contain unhealthy substances formed during processing. Nevertheless, the range of available techniques to detect fraud in EVOO production has been growing. Reliable markers of EVOO adulteration include fatty acids and minor components such as sterols, tocopherols, triterpene alcohols, phenolic compounds, phospholipids, volatile compounds, and pigments. Additionally, increasing consumer interest in high-quality EVOO has led to the development of robust scientific methods for its traceability. This review focuses on (i) the usefulness of certain compounds as markers of EVOO adulteration; (ii) the potential health risks of consuming adulterated EVOO; and (iii) reliable methods for the geographical traceability of olive oil. In conclusion, fraudulent production practices need to be detected to preserve the beneficial health effects of EVOO and to avoid the potential risks associated with ingesting substandard oil. In this work, as EVOO certification and regulatory framework limitations have already been extensively reviewed, we focus our attention on biomarkers that guarantee both the authenticity and traceability of oil, and consequently its health properties. When it is unavailable to obtain a high-resolution mass spectrometry full fingerprint, stigmastadienes and the sterolic profile are proposed as reliable markers.     

Phenolic characterization and geographical classification of commercial Arbequina extra-virgin olive oils produced in southern Catalonia

The aim of this work was to characterize Arbequina extra-virgin olive oils (EVOOs) from different locations in southern Catalonia (Spain) in terms of their phenolic profile, to show the classification of oil samples with respect to geographical area. The phenolic compounds present in 32 olive-oil samples were analyzed by a rapid and effective HPLC–ESI-TOF/MS method, and 18 phenolic compounds belonging to different phenolic types were identified. The results showed no qualitative differences in the phenolic fractions among EVOO from different geographical region. However, quantitative differences were observed in a wide number of phenolic compounds. In all olive-oil samples studied, secoiridoids were the most abundant, followed by lignans, phenolic alcohols, and flavonoids, respectively. Multivariate data were analysed by canonical discriminant analyses. Seventeen variables were used without a variable reduction step. Phenolic content of extra-virgin olive oils was found to depend highly on geographical area.     

Effects of olive paste fast preheating on the quality of extra virgin olive oil during storage

The olive paste obtained after crushing was fast preheated under different time/temperature conditions and then malaxed in an industrial oil mill (600 kg Frantoio/Leccino olive blend). Legal parameters (peroxides, free acidity and sensory panel), oil yield, total phenolic content, oxidative stability and phenolic profile were monitored during 12 months of storage of the virgin olive oil (VOO) kept in closed bottles in the dark. A fast preheating not longer than 72 s at 38 °C without malaxation lead to an extra VOO with a shelf-life of at least 12-months, similarly to the traditional EVOO obtained with malaxation. A fast preheating not longer than 72 s at 38 °C followed by 10 min malaxation lead to an EVOO with a ‘mild’ sensory profile and a shelf life of at least 12-months. Thus, the use of a specific designed fast preheater instead or before (a shortened) malaxation allows to obtain an EVOO with a low bitter/pungent attribute from olives which are rich of (sometimes unpleasant) phenolic compounds with the aim to meet the preference of targeted groups of consumers. Time and temperature of fast preheating are the critical parameters of the process.     

Quantification of soybean oil adulteration in extra virgin olive oil using portable raman spectroscopy

Extra virgin olive oil is produced through either a cold press procedure or a centrifugation with no thermal and chemical treatments and it is considered as the best quality oil under the category of olive oils. The superior properties of olive oil due to its rich in phenolic and antioxidant content and its contribution to prevent several health problems has increased the demand for olive oil over the years. Consequently, it is nowadays sold at remarkably higher price than regular vegetable oils in the market. Unfortunately, extra virgin olive oil (EVOO) has been adulterated with other cheap oils due to potential high commercial profit. Even though, there are methods available to detect the adulteration in EVOO (such as chromatographic methods and PCR), alternative simpler and faster methods are being studied. In this study, performance of portable Raman spectroscopy to quantify soybean oil (SO) adulteration [up to 25?% (w/w)] in EVOO has been evaluated. Partial Least Square Regression (PLSR) calibration models were developed and both internally (using cross-validation, leave-one-out approach) and externally (using an independent sample set) validated. The model gave standard error of prediction (SEP) of 1.34?% (w/w) SO in EVOO and correlation coefficient of prediction (rPred) of 0.99. Additionally, the residual predictive deviation (RPD) value calculated for the model was found to be 5.71, indicating that the model was considered as “good” and could be used for routine analysis and quality control applications.     

Use of capillary electrophoresis with UV detection to compare the phenolic profiles of extra‐virgin olive oils belonging to Spanish and Italian PDOs and their relation to sensorial properties

BACKGROUND: There is much interest in foods that belong to Protected Designations of Origin (PDO) because the quality and other essential and exclusive characteristics are guaranteed because of a particular geographical environment. We have used a capillary electrophoretic method for the simple, rapid and simultaneous characterization and quantification of the polyphenolic fraction of extra‐virgin olive oil from different PDOs (18 compounds in less than 7 min). To demonstrate the usefulness of this method, we have analyzed 16 samples of a Spanish PDO and nine other samples belonging to an Italian PDO (n = 5). RESULTS: In this way, it was possible to compare the phenolic profiles of the oils of different zones of the same PDO, as well as the phenolic profiles of Spanish and Italian extra‐virgin olive oils. Univariate statistics were used for differentiating the oils produced in each PDO. Furthermore, the correlations among several of the phenolic compounds present in the extracts of olive oil and its sensorial properties were checked. decarboxylated oleuropein aglycon (DOA) (b) (peak 6) was the compound more related to the bitterness of the oils, Ac Pin (peak number 4) and the unidentified peak with t_mig 4.025 min played an important role in the pungent taste of the oils, and these two latter compounds and the peak 13 seemed to be related to the fruitiness of the oils. CONCLUSIONS: The electrophoretic method described in the current work has the ability to detect and quantify simultaneously 18 phenolic compounds (belonging to five different families) in less than 7 min. This technique could improve the characterization of this polar fraction and determine the geographical origin of olive oils or detect possible ‘PDO markers’. In fact, capillary electrophoresis coupled to statistical analysis enabled discrimination among olive oils belonging to two different PDOs considering eight phenolic compounds present in the extracts, and also identification of the phenolic compounds which could have more influence on several sensory attributes such as bitterness, pungency and fruitiness. Copyright © 2009 Society of Chemical Industry     

Effect of storage on refined and husk olive oils composition: Stabilization by addition of natural antioxidants from Chemlali olive leaves

Two samples of refined olive and husk oils have been analysed in order to evaluate the influence of storage time on their quality. The following parameters were determined: peroxide values, absorption coefficients K270 and K232, Rancimat induction time, sterols and fatty acid contents. Six months storage at 50 °C in the dark revealed a loss in oil stability. This finding was reflected by the greater increase in peroxide value and a decrease of Rancimat induction time and sterol content. The enrichment of refined olive and husk oils with olive leaves and its hydrolysate extract resulted in an appreciable resistance to oxidative deterioration due to its phenolic antioxidants content. Oleuropein and hydroxytyrosol were the major compounds in Chemlali olive leaves extract and hydrolysate solution, respectively. The antiradical activity of leaves extract as well as its hydrolysate solution was evaluated and compared to that of the BHT. The antioxidant activity of the enriched refined olive and husk oils with leaves and hydrolysate extracts at 400 ppm showed that the latter had the highest protective effect against oil oxidation. Oils with added hydrolysate extract had the lower peroxide value and the higher stability measured with a Rancimat method. After six months of storage the induction time increased from 23.3 to 83.5 h for refined olive oil and from 16.6 to 49 h for husk oil. Furthermore, during oil storage, there was no significant variation in fatty acid composition. However, the total sterol concentration of the oils treated with hydrolysate extract increased. The results suggested that hydrolysate and leaves extracts are excellent antioxidants and can serve as substitutes for synthetic antioxidants.     

Extra-Virgin Olive Oil and Cheap Vegetable Oils: Distinction and Detection of Adulteration as Determined by GC and Chemometrics

Refined oils including corn, sunflower, soybean, and palm oils as well as low-quality olive oil such as refined lampante and pomace olive oils are commonly used for extra-virgin olive oil (EVOO) adulteration. Indeed, K ₂₇₀ could be used as a parameter for the detection of EVOO fraud for each type of the studied refined oils, 10 % olive, 4 % pomace olive, 10 % palm, 5 % corn, and 2 % soybean oils. Moreover, the adulteration could also be detected by the increase of the trans fatty acid contents with 10 % pomace olive, 3 % soybean, 3 % sunflower, 2 % corn, and 10 % palm oils. Actually, stigmasta-3,5-diene content is one of the most effective means of detecting refined oils in EVOO at low levels: 2 % olive, 0.4 % pomace olive, 1 % palm, 0.2 % soybean, 0.5 % sunflower, and 0.1 % corn oils. Finally, the application of linear discriminant analysis could represent an alternative and innovative tool for faster and cheaper evaluation of EVOO adulteration.     

28份国产特级初榨橄榄油中多酚含量及其变化规律北大核心CSCD

为了对我国油橄榄产业提供基础数据支持,采用国际油橄榄理事会推荐的HPLC法检测特级初榨橄榄油中的多酚含量,分析了我国不同产地的28份市售食用特级初榨橄榄油样品的多酚含量,并对不同生产年度和不同产地单果级特级初榨橄榄油中多酚含量变化规律进行了分析。结果表明:市售国产特级初榨橄榄油中均含有较为丰富的多酚类化合物,多酚含量范围为(63.885±2.345)mg/kg~(307.325±6.865)mg/kg;特级初榨橄榄油中多酚含量受贮存时间的影响较大,同时不同产地中适合生产高多酚含量特级初榨橄榄油的品种具有差异。不同特级初榨橄榄油样品之间多酚含量波动较大,需要通过多种方法来防止油脂中多酚类化合物的降解,以保证油品的质量,并因地制宜对油橄榄品种进行优化筛选。     

Authentication of extra virgin olive oils by Fourier-transform infrared spectroscopy

Fourier-transform infrared spectroscopy (FTIR), followed by multivariate treatment of the spectral data, was used to classify vegetable oils according to their botanical origin, and also to establish the composition of binary mixtures of extra virgin olive oil (EVOO) with other low cost edible oils. Oil samples corresponding to five different botanical origins (EVOO, sunflower, corn, soybean and hazelnut) were used. The wavelength scale of the FTIR spectra of the oils was divided in 26 regions. The normalized absorbance peak areas within these regions were used as predictors. Classification of the oil samples according to their botanical origin was achieved by linear discriminant analysis (LDA). An excellent resolution among all categories was achieved using an LDA model constructed with eight predictors. In addition, multiple linear regression models were used to predict the composition of binary mixtures of EVOO with sunflower, corn, soybean and hazelnut oils. For all the binary mixtures, models capable of detecting a low cost oil content in EVOO as low as 5% were obtained.     

Impact of olive oil phenolic concentration on human plasmatic phenolic metabolites

Three different functional phenol-enriched virgin olive oils (FVOO) were prepared with a phenolic content of 250 (L-FVOO), 500 (M-FVOO), and 750 mg (H-FVOO) total phenols/kg. In a randomised, cross-over study with 12 healthy volunteers, the pharmacokinetics of phenolic biological metabolites was assessed. An increasing linear trend was observed for hydroxytyrosol sulfate, the main phenolic metabolite quantified in plasma, with C_max values of 1.35, 3.32, and 4.09 μmol/l, and AUC mean values of 263.7, 581.4, and 724.4 μmol/min for L-FVOO, M-FVOO, and H-FVOO, respectively. From our data an acute intake of phenol-enriched olive oils promotes a dose-dependent response of phenol conjugate metabolites in human plasma. Also, we point out for the first time hydroxytyrosol acetate sulfate as a main biological metabolite of hydroxytyrosol from olive oil ingestion.     

Oxidation Processes in Sicilian Olive Oils Investigated by a Combination of Optical and EPR Spectroscopy

Abstract: Extra virgin olive oil (EVOO) is recognized as one of the healthiest foods for its high content of antioxidants, which forestall and slow down radical formation. Free radical‐initiated oxidation is considered one of the main causes of rancidity in fats and oils. As a consequence, reliable protocols for the investigation of oil oxidation based on selective, noninvasive, and fast methods are highly desirable. Here we report an experimental approach based on UV‐Vis absorbance, steady‐state fluorescence, and electron paramagnetic resonance (EPR) spectroscopy for studying oxidation processes induced by temperature for a period up to 35 d on Sicilian EVOO samples. We followed the decrease in β‐carotene content during incubation time and observed changes in polyphenols and tocopherols during the oxidation processes, focusing on the time scale of those changes. Using EPR spectroscopy, the free radical formation in different oil samples is reported, providing a fingerprint for both the antioxidant content and temporal features of the oxidation process at its early stage. Practical Application: We monitor β‐carotene and chlorophyll in an auto‐oxidation process. A protocol based on spectroscopic measurements is presented and can be used for the quality control process of commercial olive oil.     

Classification of extra virgin olive oils according to their geographical origin using phenolic compound profiles obtained by capillary electrochromatography

A simple and reliable method for the evaluation of the phenolic fraction of extra virgin olive oils (EVOO) by capillary electrochromatography (CEC) with UV–Vis detection, using lauryl acrylate (LA) ester-based monolithic columns, has been developed. The percentages of the porogenic solvents in the polymerization mixture, and the mobile phase composition, were optimized. The optimum monolith was obtained with a monomers/porogens ratio of 40:60% (wt/wt) using a LA/1,3-butanediol diacrylate ratio of 70:30% (wt/wt) and a 1,4-butanediol/1-propanol ratio of 25:75% (wt/wt). A satisfactory resolution between the phenolic compounds was achieved in less than 25 min with a 15:85 (v/v) ACN–water buffer containing 5 mM formic acid at pH 3.0. The method was applied to the analysis of the phenolic fraction of EVOO samples. Using linear discriminant analysis of the CEC phenolic profiles, the EVOO samples belonging to three different geographical origins (Croatia, Italy and Spain) were correctly classified with an excellent resolution among all the categories.     

Are virgin olive oils obtained below 27 °C better than those produced at higher temperatures?

Within the European Union, indications of ‘first cold pressing’ and ‘cold extraction’ can only be used for virgin olive oil (VOO) obtained below 27 °C from mechanical processing. Three different malaxing temperatures (25, 35 and 45 °C) are here evaluated for the quality of the VOO obtained in a continuous industrial plant. The oils were stored at room temperature in the dark for 12 months. Initially, oil obtained from a blend of Frantoio/Leccino cultivars (F/L) had higher acidity and peroxide levels and lower phenolic content than a Coratina cultivar (Cor). The oxidative stability of the oils positively correlated with malaxation temperature (F/L, R² = 0.818; Cor, R² = 0.987) as the phenolic content was directly proportional to the temperature (F/L, R² = 0.887; Cor, R² = 0.992). Only oils obtained at 45 °C were rejected because of ‘heated or burnt’ off-flavour. Decarboxymethylation of secoiridoids and further hydrolysis of phenolic esters occurred during storage. The oxidation products of derivatives of tyrosol and hydroxytyrosol were detected after nine months in both the F/L and Cor samples. Thus, VOO obtained at a processing temperature lower than 27 °C does not show higher chemical and sensory qualities than VOO obtained at 35 °C.     

Characterisation and phenolic profiles of two rare olive oils from southern Tunisia: Dhokar and Gemri‐Dhokar cultivars

BACKGROUND: The aim of this work was to study the chemical characteristics of two Tunisian cultivars, namely Dhokar and Gemri‐Dhokar, to analyse the fatty acids, sterols, triacylglycerols, triterpenic alcohols, and to determine the phenolic composition and oxidative stability. RESULTS: Among the rare varieties, Gemri‐Dhokar olive oil had the highest value of oleic acid (69.39%) whereas Dhokar oil was noteworthy for its lower content of phenolic compounds (94.56 mg kg^?1 gallic acid equivalents of oil) and presented the highest level of palmitic acid (19.37%). The main sterols found in all olive oil samples were β‐sitosterol and Δ5‐avenasterol, whereas cholesterol and 24‐methylenecholesterol were also found in all samples but in lower amounts. Two triterpenic dialcohols (erythrodiol and uvaol) were also detected and their content ranged from 1.45 to 2.30%, in Gemri‐Dhokar and Dhokar olive oil, respectively. Ten phenolic compounds were identified. In all samples, the main phenols found were oleuropein aglycon and pinoresinol. These phenolic compounds showed significant correlations with oxidative stability. CONCLUSION: The analytical parameters of two oils that were determined in this study were greatly influenced by genetic factors (cultivar). © 2012 Society of Chemical Industry     

Role of vitamin E and phenolic compounds in the antioxidant capacity,measured by ESR,of virgin olive,olive and sunflower oils after frying

The effect of lipid profile, vitamin E and total phenolic content was studied in relation to the antioxidant capacity (measured by ESR) of three edible oils (virgin olive, sunflower and olive oils), using short-time deep fat frying as a model. Physico-chemical changes in the oils were also studied. Samples were analysed before and after 15, 30, 45 and 60 min fryings. Determination of free radicals, by electron spin resonance spectroscopy, revealed the highest antioxidant capacity in virgin olive oil and sunflower oil. This parameter was mainly influenced by vitamin E content, followed by lipid profile and phenolic content. The frying procedure decreased the antioxidant capacity in all tested oils. Sunflower oil underwent more chemical changes by frying than did olive and virgin olive oils. Antioxidant capacity of the edible oils was correlated with polar components and ultraviolet indices but not with peroxide index or acidity value. The use of ESR, as a rapid and very sensitive method for determining antioxidant capacity of edible oils, is suggested.     

Using Lipid Profiles for the Characterization of Turkish Monocultivar Olive Oils Produced by Different Systems

The aim of this study was to characterize the biochemical profiles of the virgin olive oils produced in various districts of Aegean and South East Anatolia regions of Turkey over two growing seasons (2001–2002). The olive oils were extracted by classic hydraulic pressing, three phase continuous system, Abencor oil method at laboratory scale, and foot oil process from monocultivar Turkish olives, including Ayvalik, Memecik, Nizip Yaglik, Gemlik, Domat, and Uslu. Total phenolics, ortho-diphenols, oxidative stability, and total chlorophylls of the oils differed by location. The cis-trans fatty acids, triacylglycerols, and the actual versus theoretical equivalent carbon number of 42 (ECN 42) triglycerol content (ΔECN42) were within national and international averages. Oil samples from the three phase continuous system had higher total phenolic contents than those of the hydraulic pressure system. Turkish monocultivar virgin olive oil samples were classified by biochemical profiles using the principal component and hierarchical cluster analyses multivariate statistical methods. Clustering analysis defined groups according to growing location. Triacylglycerols and fatty acid profiles can be used for identification of monocultivar olive oils with regard to authenticity and classification.     

MALDI-TOF mass spectrometry detection of extra-virgin olive oil adulteration with hazelnut oil by analysis of phospholipids using an ionic liquid as matrix and extraction solvent

The adulteration of extra virgin olive oil (EVOO) with hazelnut oil (HO) is frequent and constitutes a serious concern both for oil suppliers and consumers. The high degree of similarity between the two oils as regards triacylglycerol, total sterol and fatty acid profile, complicates the detection of low percentages of HO in EVOO. However, phospholipids (PLs) are usually present in seed oils at a concentration range of 10–20 g/kg, while the amounts of PLs in VOOs are 300–400 times lower. Thus, in this work a sample pretreatment procedure focused towards the selective PLs extraction was developed; the Bligh–Dyer extraction procedure was modified introducing the ionic liquid resulting from the combination of TBA (tributylamine) and CHCA (α-Cyano-4-hydroxycinnamic acid) as extraction solvent. The selective extraction and enrichment of phospholipids from EVOO and HO samples was then achieved. The relevant extracts were analyzed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) using the same ionic liquid TBA-CHCA as MALDI matrix, that was found to be very suitable for PLs analysis. In fact, a remarkable increase of the phospholipids signals, with a simultaneous decrease of those relevant to triacylglycerols and diacylglycerols, was observed in the relevant mass spectra. The applicability of the whole method to the individuation of the presence of HO in EVOO was demonstrated by the analysis of EVOO samples progressively adulterated with variable quantities of HO, that was still detectable at a 1% contamination level.