Najmeh Molaahmadibahraseman; Reza Farhoosh; Ali Sharif
Abstract
Introduction: Medical benefits of Omega 3 fatty acids have appealeda lot of research to be done on of fish oil. Among marine fish, kilka has the most industrial application. Kilka oil contains significant amount of omega-3 fatty acids. In this study, physiochemical properties, fatty acid composition ...
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Introduction: Medical benefits of Omega 3 fatty acids have appealeda lot of research to be done on of fish oil. Among marine fish, kilka has the most industrial application. Kilka oil contains significant amount of omega-3 fatty acids. In this study, physiochemical properties, fatty acid composition and stabilization of kilka oil were investigated. p- hydroxy benzoic asid, its methyl ester and alpha-tocopherol as control were compared to each other.Materials and Methods: Crude Kilka fish oil was supplied by Khazarcompany (Babolsar, Iran). All chemicals and solvents used in this study were of analytical reagent grade and purchased from Merck (Darmstadt, Germany) and Sigma–Aldrich (St. Louis, MO). 200 ppm of the mentioned antioxidants was added to the purified oil and kinetic regime of oxidation at temperatures of 35, 45 and 55°C was prepared. After monitoring theoxidation over time using peroxide test, graph of peroxide changes over time was plotted and induction period and kinetic parameters (F, ORR and A) were calculated. In order to compare the performance of antioxidants in oil and water, 10% emulsion of Kilka oil-in-water was prepared and 200 ppm of antioxidant was added to it and its oxidation process was monitored at 55°C.Results and Discussion: Results showed that the fatty acid composition of this oil contains a variety of unsaturated fatty acids, saturated and polyunsaturated (mainly linoleic, eicosapentaenoic and docosahexaenoic acids). Temperature had significant effect on oxidation. p-hydroxymethylbenzoate, a little more than p-hydroxybenzoic asid, could increase oxidative stability of oil. Alpha-tocopherol had better performance as compared with other antioxidants. Performance of methylp-hydroxybenzoatewas better in emulsion than oil. In general, the emulsifier and emulsion preparation as compared with antioxidant had a more prominent role in the oxidative stability of Kilka oil.
Najmeh Molaahmadibahraseman; Reza Farhoosh; Saeid Johny; Ali Sharif
Abstract
Introduction: Medical benefits of omega-3 fatty acids have led to a lot of research on fish oil. Among marine fish, Kilka has the highest industrial applications. Kilka oil contains significant amounts of omega-3 fatty acids. In the present study, oxidative stability of Kilka fish oil based on the Schaal ...
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Introduction: Medical benefits of omega-3 fatty acids have led to a lot of research on fish oil. Among marine fish, Kilka has the highest industrial applications. Kilka oil contains significant amounts of omega-3 fatty acids. In the present study, oxidative stability of Kilka fish oil based on the Schaal oven test and the use of two phenolic acid derivatives (syringic and vanillic acids) was investigated.Materials and methods: Crude Kilka fish oil was supplied by Khazar company (Babolsar, Iran). All chemicals and solvents used in this study were of analytical reagent grade and purchased from Merck (Darmstadt, Germany) and Sigma–Aldrich (St. Louis, MO). Free radical scavenging activities of phenolic compounds was measured by reading the absorbance of methanolic solutions of the antioxidants containing 1,1-diphenyl-2-picrylhdrazyl (DPPH)at 517 nm. The partition coefficient (log P) of the antioxidants was measured in terms of the maximal UV absorbance of aqueous (0.3 mM) and 50:50 aqueous/acetate buffer (0.1M, pH =5.5) solutions. In order to study the antioxidant activity in lipid systems, peroxide value of the chromatographically purified Kilka fish oil as well as its 10% oil-in-water emulsion containing 200 mg/kg of antioxidants was monitored at 55 °C. Results and discussion: Syringic acid with two methoxy groups showed higher scavenging activity (IC50) than vanillic acid with one methoxy group (54.2 vs. 418.2). Radical scavenging activity in phenolic acids had direct relationship with the type and number of electron donor groups on phenolic ring. Peroxide values changed exponentially. Despite the relatively high polarity (Log P = – 0.65) and high scavenging activity, the performance of syringic acid in Kilkafish oil was degraded as affected by inter-molecular interactions and was not in accordance with the "polar paradox" hypothesis. Antioxidant activity of syringic acid in emulsion increased significantly as compared with oil and it was similar to α-tocopherol. It was concluded that the type of emulsifier and also the way of emulsion preparation as compared with antioxidant had a more prominent role in the oxidative stability of Kilka fish oil.Introduction: Medical benefits of omega-3 fatty acids have led to a lot of research on fish oil. Among marine fish, Kilka has the highest industrial applications. Kilka oil contains significant amounts of omega-3 fatty acids. In the present study, oxidative stability of Kilka fish oil based on the Schaal oven test and the use of two phenolic acid derivatives (syringic and vanillic acids) was investigated.Materials and methods: Crude Kilka fish oil was supplied by Khazar company (Babolsar, Iran). All chemicals and solvents used in this study were of analytical reagent grade and purchased from Merck (Darmstadt, Germany) and Sigma–Aldrich (St. Louis, MO). Free radical scavenging activities of phenolic compounds was measured by reading the absorbance of methanolic solutions of the antioxidants containing 1,1-diphenyl-2-picrylhdrazyl (DPPH)at 517 nm. The partition coefficient (log P) of the antioxidants was measured in terms of the maximal UV absorbance of aqueous (0.3 mM) and 50:50 aqueous/acetate buffer (0.1M, pH =5.5) solutions. In order to study the antioxidant activity in lipid systems, peroxide value of the chromatographically purified Kilka fish oil as well as its 10% oil-in-water emulsion containing 200 mg/kg of antioxidants was monitored at 55 °C. Results and discussion: Syringic acid with two methoxy groups showed higher scavenging activity (IC50) than vanillic acid with one methoxy group (54.2 vs. 418.2). Radical scavenging activity in phenolic acids had direct relationship with the type and number of electron donor groups on phenolic ring. Peroxide values changed exponentially. Despite the relatively high polarity (Log P = – 0.65) and high scavenging activity, the performance of syringic acid in Kilkafish oil was degraded as affected by inter-molecular interactions and was not in accordance with the "polar paradox" hypothesis. Antioxidant activity of syringic acid in emulsion increased significantly as compared with oil and it was similar to α-tocopherol. It was concluded that the type of emulsifier and also the way of emulsion preparation as compared with antioxidant had a more prominent role in the oxidative stability of Kilka fish oil.
