Thermal degradation kinetics of myrtle leaves ethanol extract (Myrtus communis L.): effect on phenolic compounds content and antioxidant activity

化学 阿布茨 原花青素 桃金娘属 DPPH 槲皮素 杨梅素 抗氧化剂 类黄酮 酚类 乙醇 食品科学 色谱法 有机化学 多酚 精油 山奈酚
作者
Ahmed Snoussi,Saoussen Bouacida,Milan Mitić,Biljana Arsić,Hayet Ben Haj Koubaier,Moncef Chouaibi,Sonja Janković,Ivana Zlatanović,Jelena Mrmošanin,Gordana Stojanović,Nabiha Bouzouita
出处
期刊:Journal of Food Measurement and Characterization [Springer Nature]
卷期号:16 (3): 2119-2130 被引量:4
标识
DOI:10.1007/s11694-022-01341-1
摘要

This study was designed to examine the effect of thermal treatment at different temperatures (70, 90 and 110 °C) over time (0–120 min) on the phenolic content and antioxidant activity of Myrtus communis L. ethanol extract in acetate buffer (pH = 3). Total phenols, flavonoids and proanthocyanidins contents and the radical scavenging activity, monitored during the treatment, were significantly influenced by the applied temperature (p < 0.05). The higher the temperature and the duration of the treatment, the greater the degradation and the loss of these compounds. Likewise, DPPH⋅ radical scavenging activity decreased, in a temperature-depending manner, during thermal treatment. Nonetheless, the results of the ABTS⋅+ test showed that the activity remained almost stable during the treatment. Furthermore, the kinetics of degradation of compounds analysed by HPLC-DAD, namely myricetin-3-O-galactoside, quercetin-3-O-glucoside and quercetin-3-O-rhamnoside was investigated and their energy of activation was determined. Degradation rate in case of quercetin-3-O-rhamnoside was the most sensitive to temperature (20.536 kJ/mol) followed by myricetin-3-O-galactoside (12.268 kJ/mol) and quercetin-3-O-glucoside (2.838 kJ/mol). The use of the discriminant analysis has shown that some other factors other than temperature and time of thermal treatment might also have a minor influence on the content of total phenolics, total flavonoids, proanthocyanidins and values of the antioxidant tests (DPPH⋅, ABTS⋅+) in the investigated extracts of M. communis L.
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