Faculty Publications

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    Probing the synergistic effects of rutin and rutin ester on the oxidative stability of sardine oil
    (Springer, 2022) Chandrasekar, V.; Arunachalam, S.S.; Hari, H.; Shinkar, A.; Belur, P.D.; Iyyaswami, R.
    Multicomponent antioxidant mixture is proved to be highly effective in imparting oxidative stability to the edible oil. It is believed that the high efficacy of those mixtures is due to the synergistic effect exhibited by two or more components. The current study aims to analyse the synergistic effect of a flavonoid and its corresponding ester in improving the oxidative stability of n-3 PUFA rich sardine oil. The oxidative stability of rutin, esterified rutin and their combinations at three different concentrations was studied in sardine oil stored at 37 ºC for 12 days in contact with air under darkness. The combination of rutin and rutin ester showed maximum reduction of 54.2% in oxidation at 100 mg/kg and 150 mg/kg. Perhaps this is the first report on the synergistic effect of a flavonoid and its lipophilized ester for improving the oxidative stability of n-3 PUFA rich oil. © 2022, Association of Food Scientists & Technologists (India).
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    Synthesis and characterization of 3,4-dihydroxyphenyl acetic acid esters and study of their efficacy in bulk fish oil
    (Elsevier Ltd, 2024) Arunachalam, S.S.; Chandrasekar, V.; Belur, P.D.
    Lipophilization of natural antioxidants is a proven strategy to enhance the solubility in bulk oil systems, thereby increasing their efficacy against oxidative degradation. This study aims to synthesize esters of 3,4-dihydroxyphenylacetic acid (3,4-DHPA) using Amberlyst-15 and to study the application of these esters in refined fish oil. Lipophilic esters were synthesized by esterification and transesterification of 3,4-DHPA in various solvent systems. Esters of methanol, butanol and hexanol were obtained with percent conversion of 81.1, 69.3 and 78.8 respectively, and were subjected to molecular characterization and in vitro oxidant assays. The 3,4-DHPA and its methyl ester showed 36% reduction in the TOTOX value over 30 days of storage. The length of the acyl chain in the ester was found to exert a high influence on its efficacy and lipophilicity. This is the first report of 3,4-DHPA and its lipophilic esters studied for enhancing the oxidative stability of fish oil. © 2024 Elsevier Ltd
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    Effect of combinations of 3,4-dihydroxyphenylacetic acid and its esters on the oxidative stability of fish oil–containing trace water
    (John Wiley and Sons Inc, 2024) Arunachalam, S.S.; Chandrasekar, V.; Belur, P.D.
    The current study aims to comprehend the effect of the various combinations of 3,4-dihydroxyphenylacetic acid (3,4-DHPA) and its esters in varying molar ratios on retarding oxidation in bulk refined fish oil in the presence of 0.3% w/w water. All the esters and 3,4-DHPA exhibited better performance than the synthetic antioxidant butylated hydroxytoluene. In the presence of trace water, the parent compound was found to have a synergistic effect with hexyl ester when used at a molar ratio of 2:1, respectively, exhibiting a higher percent reduction among all the esters and their combinations. The study also showed that the presence of extraneous water can significantly accelerate the oxidation (twofold) in a bulk fish oil system. This suggests that the microenvironment of the oil is altered when water is present and that association colloids play a key role in enhancing the rate of oxidation. Thus, while designing a competent mixture of antioxidants, the specific site of oxidation involved and the surface-active components should be taken into consideration to efficiently retard oxidation. Practical Applications: Analyzing the impact of trace amounts of water on the efficiency of natural antioxidants, including 3,4-DHPA and its lipophilic esters, helps to comprehend the required optimal antioxidant concentrations for such a dynamic bulk oil system. The study finds application in controlling oxidation in PUFA-rich oils containing surface-active minor components that can accelerate oxidation. The results of the study show that 3,4-DHPA and its esters could be a potential replacement for the synthetic antioxidant BHT in all aspects. © 2024 Wiley-VCH GmbH.