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.     

Degradation and Nutritional Quality Changes of Oil During Frying

The changes in regular canola oil as affected by frying temperature were studied. French fries were fried intermittently in canola oil that was heated for 7 h daily over seven consecutive days. Thermo-oxidative alterations of the oil heated at 185 ± 5 or 215 ± 5 °C were measured by total polar components (TPC), anisidine value (AV), color components formation, and changes in fatty acid composition and tocopherols. Results showed that TPC, AV, color and trans fatty acid content increased significantly (P < 0.05) as a function of frying temperature and time. The oil polyunsaturated fatty acids (PUFA) decreased in direct proportion to frying temperature and time. After 7 days of frying, the amount of PUFA was reduced by half and the trans isomers contribution increased 2.5 times during frying at 215 °C. Of the parameters assessed, total polar component and color had the highest correlation, with correlation coefficients of 0.9650 and 0.9302 for frying at 215 and 185 °C, respectively. TPC formation correlated inversely with the reduction of tocopherols.     

The Effect of Type of Oil and Degree of Degradation on Glycidyl Esters Content During the Frying of French Fries

The aim of the study was to determine the effect of oil degradation on the content of glycidyl esters (GEs) in oils used for the frying of French fries. As frying media, refined oils such as rapeseed, palm, palm olein and blend were used. French fries were fried for 40 h in oils heated to 180 °C in 30‐min cycles. After every 8 h of frying, fresh oil and samples were analyzed for acid and anisidine values, color, refractive index, fatty acid composition, and content and composition of the polar fraction. GEs were determined by LC–MS. Hydrolysis and polymerization occurred most intensively in palm olein, while oxidation was reported for rapeseed oil. The degradation of oil caused increased changes in the RI of frying oils. Losses of mono‐ and polyunsaturated fatty acids were observed in all samples, with the largest share in blend. The highest content of GE found in fresh oil was in palm olein (25 mg kg^?1) and the lowest content of GE was found in rapeseed oil (0.8 mg kg^?1). The palm oil, palm olein and blend were dominated by GEs of palmitic and oleic acids, while rapeseed oil was dominated by GE of oleic acid. With increasing frying time, the content of GEs decreased with losses from 47 % in rapeseed oil to 78 % in palm oil after finishing frying.     

Formation of Alkylbenzenes and Tocochromanols Degradation in Sunflower Oil and in Fried Potatoes during Deep‐Frying and Pan‐Frying

Formation of toxic alkylbenzenes, total polar compounds (%TPC) and degradation of tocochromanol are monitored. Analyses of the oil extracted from fried potatoes confirm the trend observed in the frying oil. The fresh oil has a TPC content of 3%, which increases with the frying time, exceeding the acceptable value (25%) after about 25 h for deep‐frying and 1.5 h for pan‐frying. During deep‐frying, total tocochromanol decreases to about half (25 mg per 100 g) of the initial value, pan‐frying shows faster, degradation (complete after 1.5 h). Toluene concentration increases with the frying time reaching a maximum, and afterwards gradually decreases. Except for butylbenzene during pan‐frying, pentylbenzene and butylbenzene concentration, increase with the frying time, but remain much lower than toluene. Practical Applications: This is the first systematic work comparing alkylbenzenes evolution under different frying conditions. Different from previous works, frying experiments are carried out following the indication of many European countries that recommend using temperature lower than 180 °C. The amount of alkylbenzenes assumed through a standard portion of fried potatoes (200 g) is assessed, which is relevant for evaluating dietary exposure to these contaminants.     

Effect of Hydrothermal Treatment of Rapeseed on Antioxidant Capacity of the Pressed Rapeseed Oil

Response surface methodology (RSM) was used to evaluate the quantitative effects of two independent variables, rapeseed moisture content and conditioning temperature, on the antioxidant capacity (AC) and total phenolic (TPC), tocopherol (TTC), and phosphorus contents (PC) in the pressed rapeseed oils. The mean AC results for the crude rapeseed oils ranged from 199.8 to 947.2 μmolTE/100 g. TPC and PC in the crude rapeseed oils correlated significantly (P < 0.01) and positively with AC of oils (R ² = 0.9498 and 0.4396, respectively). The experimental results of AC, TPC, and PC were close to the predicted values calculated from the polynomial response surface model equations (R ² = 0.9801, 0.9747 and 0.9165, respectively). The effect of oil processing temperature on AC and TPC was about 1.5 times greater than the effect of moisture level in rapeseed.     

Stability and radical‐scavenging activity of heated olive oil and other vegetable oils

The effect of heating at 180 °C on the antioxidant activity of virgin olive oil (VOO), refined olive oil (ROO) and other vegetable oil samples (sunflower, soybean, cottonseed oils, and a commercial blend specially produced for frying) was determined by measuring the radical‐scavenging activity (RSA) toward 1,1‐diphenyl‐2‐picrylhydrazyl radical (DPPH^?). The RSA of the soluble (polar) and insoluble (non‐polar) in methanol/water fractions of olive oil samples was also measured. The stability of heated oils was assessed by determining their total polar compound (TPC) content. VOO was the most thermostable oil. Total polar phenol content and the RSA of VOO heated for 2.5 h decreased by up to 70 and 78%, respectively, of their initial values; an up to 84% reduction in RSA of VOO polar and non‐polar fractions also occurred. Similar changes were observed in the RSA of ROO and its non‐polar fraction after 2.5 h of heating. The other oils retained their RSA to a relatively high extent (up to 40%) after 10 h of heating, but in the meantime they reached the rejection point (25–27% TPC). The results demonstrate that VOO has a remarkable thermal stability, but when a healthful effect is expected from the presence of phenolic compounds, heating has to be restricted as much as possible.     

Quality Assessment of Heated Cooking Oil,Agab, Using a Simple Newly-Developed Spectrophotometric Method

Deep fat frying is one of the most widely used cooking practices but heat treatment produces many degradation products, some of which may cause health hazards. A simple, rapid, and inexpensive method for assessment of the quality of cooking oil used for frying was developed using a spectrophotometer. Potato slices were heated in Agab oil (soybean/sunflower:1/l volume) at 180 ± 5 °C for 8 h per day for 6 consecutive days. Heated samples were collected at 15-min intervals and UV absorbance at λ = 370–400 nm was measured; samples were also analyzed for anisidine value (AV), conjugated diene formation (CD), and total polar compounds (TPC). A systematic increase of absorbance in heated oil over frying time was observed. TPC was highest (R ² = 0.99) for the correlation with heating time followed by CD (0.93) and AV (0.89). The spectrophotometric method developed in the present study to assess the quality of heated oils is simple, quick, and reliable because its results were strongly correlated with the results from the TPC.     

Review of stability measurements for frying oils and fried food flavor

Measurements of degradation in frying oils based on oil physical properties and volatile and nonvolatile decomposition products were reviewed. Rapid methods by means of test kits were also considered. Factors that affect the analysis of total polar components (TPC) in frying oils were examined. Relationships between TPC, free fatty acid (FFA) content, Food Oil Sensor readings (FOS), color change (ΔE), oil fry life and fried-food flavor were evaluated. Flavor scores for codfish, fried in fresh and discarded commercial frying oil blends, were dependent upon individuals in the consumer panel (n=77). Part (n=29) of the panel preferred the flavor of fresh fat; others (n=24) didn't; the rest (n=24) had no preference. FFA, FOS and TPC were analyzed in two soybean oils and in palm olein during a four-day period in which french fries were fried. Flavor score and volatiles of potatoes fried on days 1 and 4 in each oil were also determined. TPC, FFA and FOS significantly increased (P<0.05) in all oils during the frying period. TPC and FFA were highest in the used palm olein, and flavor of potatoes fried in palm olein on day 1 was less desirable than those fried in the soybean oils. Potatoes fried in day-1 oils had significantly higher concentrations (P<0.10) of several pyrazines and aldehydes than those fried in day-4 oils. Presented at the 84th Annual Meeting of the American Oil Chemists' Society, Anaheim, California, April 25–29, 1993.     

Frying Stability of Canola Oil Blended with Palm Olein, Olive, and Corn Oils

The fatty acid composition, peroxide value (PV), acid value (AV), iodine value (IV), total tocopherols (TT) content, and total phenolics (TP) content of canola oil (CAO), palm olein oil (POO), olive oil (OLO), corn oil (COO), and the binary and ternary blends of the CAO with the POO, OLO, and COO were determined. The blends were prepared in the volume ratios of 75:25 (CAO/POO, CAO/OLO, CAO/COO) and 75:15:10 (CAO/POO/OLO, CAO/POO/COO). The CAO and its blends were used to fry potato pieces (7.0 × 0.5 × 0.3 cm) at 180 °C. During the frying process, the total polar compounds (TPC) content, AV, oil/oxidative stability index (OSI), and color index (CI) of the CAO/blends were measured. In general, frying stability of the CAO was significantly (P < 0.05) improved by the blending, and the frying performance of the ternary blends was found to be better than that of the binary blends.     

Anti-Rancidity Effects of Sesame and Rice Bran Oils on Canola Oil During Deep Frying

In this study, the effect of sesame oil (SEO) and rice bran oil (RBO) on the rancidity of canola oil (CAO) during the process of frying potato pieces at 180 °C was investigated. The SEO and RBO were added to the CAO at levels of 3 and 6%. Frying stability of the oil samples during the frying process was measured on the basis of total polar compounds (TPC) content, conjugated diene value (CDV), acid value (AV), and carbonyl value (CV). In general, frying stability of the CAO significantly (P < 0.05) improved in the presence of the SEO and RBO. The positive effect of the SEO on the stability of the CAO was more than that of the RBO. Increasing the amounts of SEO and RBO from 3 to 6% led to decreases in the TPC and AV, and increases in the CDV and CV of the CAO during the frying process. The best frying performance for the CAO was obtained by use of 3% of both SEO and RBO together (CAO/SEO/RBO, 94:3:3 w/w/w).     

Specific Heat Capacity Measurements of Frying Oil Using Modulated Differential Scanning Calorimetry

The specific heat capacity (c_p) of frying oils is of practical importance in engineering work associated with refining operations and the thermal resistance during application. The objective of this study was to use modulated differential scanning calorimetry (MDSC) to measure the specific heat capacity of frying oil. Samples were exposed to a cyclic heating profile that was generated by a linear heating rate while simultaneously superimposing a sinusoidally varying time–temperature wave. The c_p variation of three commercial frying oils during frying was tested over a temperature range between 0 and 250 °C, and the correlation of c_p with triacylglycerol (TAG) polymer contents, total polar compounds (TPC), and polar fractions was studied. Results indicated that the specific heat capacity of frying oils increased linearly as temperature increased. During frying, c_p had a positive relation with TAG polymers and TPC at the beginning, but finally decreased when frying ended. This was possibly associated with the variation of polar fractions as frying continued. The large molecular compounds and small molecular compounds of polar fractions were considered to contribute oppositely to c_p, which led to its final decrease.     

Formation and distribution of oxidized fatty acids during deep‐ and pan‐frying of potatoes

The formation of cis‐9,10‐epoxystearate, trans‐9,10‐epoxystearate, cis‐9,10‐epoxyoleate, cis‐12,13‐epoxyoleate, trans‐9,10‐epoxyoleate, trans‐12,13‐epoxyoleate and the co‐eluting 9‐ and 10‐ketostearates during eight successive pan‐ and deep‐frying sessions of pre‐fried potatoes in five different types of vegetable oils – namely cottonseed oil, sunflower oil, vegetable shortening, palm oil and virgin olive oil – was followed and quantified both in fried oils and in fried potatoes by GC/MS after derivatization to methyl esters. These oxidized fatty acids were present at relatively low concentrations in the fresh oils and pre‐fried potatoes while they increased linearly with frying time, reaching up to 1140.8 µg/g in virgin olive oil (VOO) and 186.9 µg/g in potatoes pan‐fried in VOO after eight pan‐frying sessions, with trans‐9,10‐epoxystearate predominating in all cases. The formation of polymerized triacylglycerols (PTG) was also quantified in frying oils by size exclusion HPLC. Pan‐frying caused higher oxidized fatty acid and PTG formation compared to deep‐frying. Epoxyoleates and PTG concentrations were increased after frying in polyunsaturated oils, while epoxystearate and 9‐ and 10‐ketostearate concentrations were increased after frying in monounsaturated oils. No specific absorption of the oxidized fatty acids by the fried potatoes seems to occur. The dietary intake of oxidized fatty acids and PTG by the consumption of fried potatoes was discussed.     

Plasma Modified Membrane for Daily Recovery of Oil from Repeated Frying Operation with Frequent Oil Replenishment

Sunflower oil was used for deep frying of potatoes at 170 ± 5 °C and for 8 h per day for 5 days in a fryer with an automatic oil filtration system. Three different frying operations were performed: operation (OP)-1, OP-2 and OP-3; that correspond to the oil unfiltered at the end of each frying day, the oil filtered through the fryer's own filter (passive filtration) and the oil firstly subjected to passive filtration and then filtered through a polyethersulfone membrane modified with hexamethyldisiloxane via radio frequency plasma (75 W-5 min, discharge power–time), respectively. The performance of each operation was investigated in terms of free fatty acids (FFA), conjugated dienoic acids (CD), TOTOX value, total polar content (TPC), Hunter color, viscosity, fatty acid composition, and tocopherol content. The results showed that OP-3 could decrease FFA, CD, TOTOX, TPC, L*a*b* value, viscosity and linoleic acid (18:2)/palmitic acid (16:0) ratio in 29.6, 11.7, 25, 30.8, 6.1*11.3*20.8*, 7.8, 12.2 %, respectively, compared to the unfiltered oil (OP-1). Regenerated oil from OP-3 had a frying life approximately 17 h more than oils from both OP-1 and OP-2.     

Pan-frying stability of NuSun oil,a mid-oleic sunflower oil

Pan-frying is a popular frying method at home and in many restaurants. Pan-frying stabilities of two frying oils with similar iodine values (IV)—mid-oleic sunflower oil (NuSun oil; IV=103.9) and a commercial canola oil (IV=103.4)—were compared. Each oil sample was heated as a thin film on a Teflon-coated frying pan at ∼180°C to a target end point of ≥20% polymer. High-performance size-exclusion chromatography analysis of the mid-oleic sunflower and canola oil samples indicated that the heated samples contained 20% polymer after approximately 18 and 22 min of heating, respectively. The food oil sensor values increased from zero to 19.9 for the canola sample and from zero to 19.8 for the mid-oleic sunflower sample after 24 min of heating. The apparent first-order degradation rate for the mid-oleic sunflower sample was 0.102±0.008 min⁻¹, whereas the rate for the canola sample was 0.092±0.010 min⁻¹. The acid value increased from approximately zero prior to heating to 1.3 for the canola sample and from zero to 1.0 for the mid-oleic sunflower sample after 24 min of heating. In addition, sensory and volatile analyses of the fried hash browns obtained from both oils indicated there were no significant differences between the two fried potato samples.     

Utilization of high‐oleic rapeseed oil for deep‐fat frying of French fries compared to other commonly used edible oils

Changes in chemical, physical and sensory parameters of high‐oleic rapeseed oil (HORO) (NATREON?) during 72 h of deep‐fat frying of potatoes were compared with those of commonly used frying oils, palm olein (PO), high‐oleic sunflower oil (HOSO) and partially hydrogenated rapeseed oil (PHRO). In addition to the sensory evaluation of the oils and the potatoes, the content of polar compounds, oligomer triacylglycerols and free fatty acids, the oxidative stability by Rancimat, the smoke point and the anisidine value were determined. French fries obtained with HORO, PO and HOSO were still suitable for human consumption after 66 h of deep‐fat frying, while French fries fried in PHRO were inedible after 30 h. During the frying period, none of the oils exceeded the limit for the amount of polar compounds, oligomer triacylglycerols and free fatty acids recommended by the German Society of Fat Science (DGF) as criteria for rejection of used frying oils. After 72 h, the smoke point of all oils was below 150 °C, and the amount of tocopherols was reduced to 5 mg/100 g for PHRO and 15 mg/100 g for HORO and HOSO. Remarkable was the decrease of the oxidative stability of HOSO measured by Rancimat. During frying, the oxidative stability of this oil was reduced from 32 h for the fresh oil to below 1 h after 72 h of frying. Only HORO showed still an oxidative stability of more than 2 h. From the results, it can be concluded that the use of HORO for deep‐fat frying is comparable to other commonly used oils.     

Deterioration Kinetics of Crude Palm Oil,Canola Oil and Blend During Repeated Deep-Fat Frying

The oxidation of vegetable oils is generally treated as an apparent first order kinetic reaction. This study investigated the deterioration of crude palm oil (CPO), refined canola oil (RCO) and their blend (CPO:RCO 1:1 w/w) during 20 h of successive deep‐fat frying at 170, 180 and 190 °C. Kinetics of changes in oil quality indices, namely, free fatty acid (FFA), peroxide value (PV), anisidine value (p‐AV), total polar compounds (TPC) and color index (CI) were monitored. The results showed that FFA and PV accumulation followed the kinetic first order model, while p‐AV, TPC and CI followed the kinetic zero order model. The concentration and deterioration rate constants k, increased with increasing temperatures. This effect of temperature was modeled by the Arrhenius equation. The results showed that PV had the least activation energies E_a (kJ/mol) values of 5.4 ± 1 (RCO), 6.6 ± 0.7 (CPO) and 11.4 ± 1 (blend). The highest E_a requirement was exhibited by FFA with a range of 31.7 ± 3–76.5 ± 7 kJ/mol for the three oils. The overall E_a values showed that the stability of the blend was superior and not just intermediate of CPO and RCO. The correlation of the other oil quality indices with TPC indicated a positive linear correlation. The p‐AV displayed the strongest correlation, with mean correlation coefficient r_s of 0.998 ± 0.00, 0.994 ± 0.00 and 0.999 ± 0.00 for CPO, RCO and blend, respectively.     

Rapid Determination of Total Polar Compounds in Frying Oil Using ATR‐FTIR Combined with Extended Partial Least Squares Regression

A method of rapidly determining the total polar compounds (TPCs) in frying oils using attenuated total reflectance‐Fourier transform infrared spectroscopy combined with partial least squares (PLS) regression is developed. Oils of various types and geographic origins are used to ensure that the proposed model is robust. The first derivative spectrum is selected as the spectral processing method. The interval PLS, forward interval PLS, and backward interval PLS algorithms are compared in terms of their performance. A correlation coefficient (R²) of 0.9942, a root mean square error of calibration (RMSEC) of 1.1, a root mean square error of prediction (RMSEP) of 2.30, a residual predictive deviation (RPD) of 4.1, and a limit of detection (LOD) of 1.65% are obtained by the fiPLS33 model with fewer latent variables and a lower spectral interval number. In addition, sub‐models using a single type of oil showed higher performance (R² 0.9957–0.9998, RMSEC 0.12–0.92, RMSEP 0.79–1.58, RPD 4.79–9.64, LOD 0.66–1.26%) than the general model. The TPC models developed are accurate, stable, and adaptable, and they can be used to analyze general frying oil samples quickly, regardless of the oil type, and to analyze samples of specific oil types accurately. Practical applications: The content of TPCs is an important indicator of whether the oil has been overused and whether it will be harmful during the frying process. However, traditional chemical methods are time‐consuming, and they have not been used to determine large‐sized samples. In addition, due to a lack of regional optimization, most studies on determining TPCs with FTIR give unsatisfactory model performance. A general TPC model that incorporates several oil types and regional optimization is expected to improve prediction performance. Therefore, the proposed method represents a rapid and accurate tool for measuring TPCs in edible fats and oils.     

Accumulation of 5-Hydroxymethylfurfural in Oil During Frying of Model Dough

5-Hydroxymethylfurfural (HMF), a thermal process contaminant, forms in food during frying as a result of the Maillard reaction and caramelization. Owing to its chemical properties, HMF formed in foods during frying partially transfers into frying oil. This study aimed to investigate the accumulation of HMF in oil during repetitive frying operations. A model dough composed of 25 % of glucose was fried at 160, 170, 180 °C for 50 frying cycles. Apart from total polar compounds (TPC), accumulation of HMF was determined in oils during repetitive frying operations. Increasing frying temperature also increased the amount of HMF formed in dough, and those transferred to oil. Prolonging frying cycles to 150, increasing amount of dough being fried to 100 g and frying time to 10 min caused the TPC content to reach 25 % at the 130th frying cycle at 180 °C. Under the same frying conditions, the concentration of HMF showed a rapid increase at the first 10th frying cycle. Its increase was at a slower rate until the 50th frying cycle reaching a plateau level exceeding 5.0 mg/L. The results revealed that HMF transferred and accumulated in the frying oil during repetitive frying. The HMF concentration exceeding 5.0 mg/L in oil may be considered as an indicator for heavily used frying oil. Correlation between TPC and HMF contents of frying oil showed no linear correlation.     

Determination of Deep Frying Soybean Oil Disposal Point by a Sensory Method

Measurements of degradation in frying oils are mainly based on physico-chemical properties. Total polar compounds (TPC) and free fatty acids (FFA) content in frying oils are used as a guide for discarding used oils. The purpose of this study was to evaluate the efficacy of a sensory method in detecting degradation in soybean oils used in potato chips deep frying. The sensory evaluation of oil samples was determined by a trained panel; after rigorous selection and training steps. Free fatty acid, TPC and Rancimat induction period (IP) were quantified in the same samples. The proposed sensory method was sensitive to small differences in rancidity. The selected and trained sensory panel discarded oil samples with 0.175% FFA as oleic acid, 18.92% TPC, and 0.20 h IP. According to the results achieved in this research sensorial trained panel response is sensitive and accurate in refusing deteriorated frying oils. Besides this, soybean oil can be used for deep frying procedures and safely discarded according to the panel response, although presenting up to 7% linolenic acid.     

A Chemometric Approach to Assess the Frying Stability of Cottonseed Oil Blends During Deep-Frying Process: I. Polar and Polymeric Compound Analyses

The main goal of the present study was (i) to determine the formation of degradation products in cottonseed oil (CSO) blends during deep frying process by adsorption and high performance size exclusion chromatography techniques and (ii) to evaluate the impacts of food additives on total polar (TPC) and polymeric compound (PTAG) formation using a chemometric approach. In order to prepare the frying CSO blends; ascorbic palmitate, mixed tocopherols, dimethylpolysiloxane, lecithin and sesame oils were used as additives. To determine the real impacts of additives, a quarter-fraction factorial experimental design with two levels and five factors was used. The changes in TPC and PTAG data were carefully evaluated during 10 h of frying at 170 ± 5 °C with normal distribution (ND) graphs and analyzed using a one-way analysis of variance (ANOVA), followed by Tukey’s Post-hoc test (α = 0.05). The results indicated that the increasing values for TPC and PTAG during the frying processes for all blends, TPC and PTAG contents reached maximum levels of 16.37 and 6.01 % respectively, which are below the limit values stated by official authorities for the quality assessment of frying oils. The ANOVA test results were in good agreement with ND graphs and data indicated that the impact of mixed tocopherols was significant for TPC formation, meanwhile the impact of lecithin and ascorbic palmitate × dimethylpolysiloxane were significant for PTAG formation. Thus, the present study should be considered to be a very useful guide for developing new frying oil formulations based on CSO by using food additives.