Extraction of Lignan Compounds from Roasted Sesame Oil and their Effects on the Autoxidation of Methyl Linoleate
Jin‐Young Lee, Eunok Choe
Abstract
Jin‐Young Lee, Eunok Choe
Abstract
ABSTRACT: Lignan compounds were extracted from roasted sesame oil and their effects on the autoxidation of methyl linoleate (ML) were studied. Lignan compounds extracted from roasted sesame oil, sesamol, sesamin, and sesamolin, were added to ML, which was then oxidized at 60 o C for 18 h in the dark. Alpha‐tocopherol was separately added to ML for a reference antioxidant. Degree of ML oxidation was monitored by conjugated dienoic acid (CDA) contents and p ‐anisidine value (PAV) by AOCS methods, and ML retention by gas chromatography. CDA contents and PAV of samples increased with the oxidation time at 60 o C in the dark, and ML decreased. Sesamol‐, sesamin‐, or sesamolin‐added samples showed lower CDA contents, PAV, and ML loss than the samples without lignans during oxidation in the dark, which indicated that lignan compounds lowered the ML autoxidation. The antioxidant activity of sesamol was significantly higher ( P < 0.05) than that of sesamin, sesamolin, or α‐tocopherol. Lignan compounds added to ML were degraded during the autoxidation of ML, and the degradation rate was higher in sesamol‐ than in sesamin‐, or sesamolin‐added ML, but was lower than in tocopherol‐added samples. As the lignan compounds concentration in ML increased, the degradation rate of lignans decreased, and the inhibition of the ML autoxidation by lignan compounds increased. The results strongly suggested that the autoxidative stability of ML could be improved by the addition of sesamol, sesamin, or sesamolin extracted from the roasted sesame oil.
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ABSTRACT: Lignan compounds were extracted from roasted sesame oil and their effects on the autoxidation of methyl linoleate (ML) were studied. Lignan compounds extracted from roasted sesame oil, sesamol, sesamin, and sesamolin, were added to ML, which was then oxidized at 60 o C for 18 h in the dark. Alpha‐tocopherol was separately added to ML for a reference antioxidant. Degree of ML oxidation was monitored by conjugated dienoic acid (CDA) contents and p ‐anisidine value (PAV) by AOCS methods, and ML retention by gas chromatography. CDA contents and PAV of samples increased with the oxidation time at 60 o C in the dark, and ML decreased. Sesamol‐, sesamin‐, or sesamolin‐added samples showed lower CDA contents, PAV, and ML loss than the samples without lignans during oxidation in the dark, which indicated that lignan compounds lowered the ML autoxidation. The antioxidant activity of sesamol was significantly higher ( P < 0.05) than that of sesamin, sesamolin, or α‐tocopherol. Lignan compounds added to ML were degraded during the autoxidation of ML, and the degradation rate was higher in sesamol‐ than in sesamin‐, or sesamolin‐added ML, but was lower than in tocopherol‐added samples. As the lignan compounds concentration in ML increased, the degradation rate of lignans decreased, and the inhibition of the ML autoxidation by lignan compounds increased. The results strongly suggested that the autoxidative stability of ML could be improved by the addition of sesamol, sesamin, or sesamolin extracted from the roasted sesame oil.
Key concepts: Sesamin, Sesamol, Autoxidation, Lignan, Chemistry, Sesame oil, Chromatography, Food science