Thermal degradation of long-chain polyunsaturated fatty acids during deodorization of fish oil

被引:99
|
作者
Fournier, V
Destaillats, F
Juanéda, P
Dionisi, F
Lambelet, P
Sébédio, JL
Berdeaux, O
机构
[1] INRA, UMR FLAVIC, F-21065 Dijon, France
[2] Nestle Res Ctr, Vers Chez Les Blancs, France
[3] INRA, Clermont Ferrand, France
关键词
deodorization; fish oil; geometrical isomerization; long-chain polyunsaturated fatty acids; thermal degradation;
D O I
10.1002/ejlt.200500290
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Long-chain polyunsaturated fatty acids (LC-PUFA) of the n-3 series, particularly eicosapentaenoic (EPA) and docosahexaenoic (DHA) acid, have specific activities especially in the functionality of the central nervous system. Due to the occurrence of numerous methylene-interrupted ethylenic double bonds, these fatty acids are very sensitive to air (oxygen) and temperature. Non-volatile degradation products, which include polymers, cyclic fatty acid monomers (CFAM) and geometrical isomers of EPA and DHA, were evaluated in fish oil samples obtained by deodorization under vacuum of semi-refined fish oil at 180, 220 and 250 degrees C. Polymers are the major degradation products generated at high deodorization temperatures, with 19.5% oligomers being formed in oil deodorized at 250 degrees C. A significant amount of CFAM was produced during deodorization at temperatures above or equal to 220 degrees C. In fact, 23.9 and 66.3 mg/g of C20 and C22 CFAM were found in samples deodorized at 220 and 250 degrees C, respectively. Only minor changes were observed in the EPA and DHA trans isomer content and composition after deodorization at 180 degrees C. At this temperature, the formation of polar compounds and CFAM was also low. However, the oil deodorized at 220 and 250 degrees C contained 4.2% and 7.6% geometrical isomers, respectively. Even after a deodorization at 250 degrees C, the majority of geometrical isomers were mono- and di-trans. These results indicate that deodorization of fish oils should be conducted at a maximal temperature of 180 degrees C. This temperature seems to be lower than the activation energy required for polymerization (intra and inter) and geometrical isomerization.
引用
收藏
页码:33 / 42
页数:10
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