Model Study of Different Antioxidant Properties of α‐ and γ‐Tocopherol in Fats

作者: T. Gottstein , W. Grosch

DOI: 10.1002/LIPI.19900920404

关键词:

摘要: A model study using 2,2,5,7,8-pentamethyl-6-hydroxychroman (α-COH) and 2,2,7,8-tetramethyl-6-hydroxychroman (γ-COH) as antioxidants, linoleic acid its methyl ester (both in bulk phase) the lipids was performed. After having demonstrated that antioxidative activities of substances did agree with those corresponding tocopherols (α-T, γ-T), stability α-COH γ-COH determined, products arising from α-COH, γ-COH, were identified. oxidize to different major (quinone, trimer) depending on reaction temperature (37°C 47°C) antioxidant concentration, whereas obtained by oxidation (diphenyl ether dimer, biphenyl dimer) not seem be affected differences conditions. It concluded γ-T superior α-T because it appears more stable and, also, being oxidized compounds which are still effective antioxidants. Modellversuche uber die unterschiedlichen antioxidativen Eigenschaften von α- und γ-Tocopherol Fetten Es wurden Modellversuche mit 2,2,5,7,8-Pentamethyl-6-hydroxychroman 2,2,7,8-Tetramethyl-6-hydroxychroman als Antioxidantien Linolsaure ihr Methylester Lipide durchgefuhrt. Nach dem Beweis, das der Modellsubstanzen denen entsprechenden Tocopherole γ-T) ubereinstimmen, wurde Stabilitat gemessen Produkte identifiziert, aus ihrem hervorgehen. Bei Erhohung Temperatur Antioxidanskonzentration ergab unterschiedliche Hauptprodukte (Chinon, Trimer), wahrend des (Diphenyletherdimer, Biphenyldimer) nicht durch Unterschiede den Reaktionsbedingungen beeinflust wurden. Es gefolgert, Antioxidans uberlegen ist, weil es stabiler ist zu Produkten oxidiert wird, noch antioxidativ wirksam sind.

参考文章(39)
E Niki, A Kawakami, M Saito, Y Yamamoto, J Tsuchiya, Y Kamiya, Effect of phytyl side chain of vitamin E on its antioxidant activity. Journal of Biological Chemistry. ,vol. 260, pp. 2191- 2196 ,(1985) , 10.1016/S0021-9258(18)89536-9
Masao FUJIMAKI, Koichiro KANAMARU, Tadao KURATA, Osamu IGARASHI, Studies on the Oxidation Mechanism of Vitamin E Agricultural and biological chemistry. ,vol. 34, pp. 1781- 1786 ,(1970) , 10.1271/BBB1961.34.1781
J.F. O'Brien, W.E. Klopfenstein, Gas-liquid chromatographic analysis of diglycerides Chemistry and Physics of Lipids. ,vol. 6, pp. 1- 7 ,(1971) , 10.1016/0009-3084(71)90052-1
C. H. Lea, R. J. Ward, Relative antioxidant activities of the seven tocopherols Journal of the Science of Food and Agriculture. ,vol. 10, pp. 537- 548 ,(1959) , 10.1002/JSFA.2740101007
J. Cillard, P. Cillard, Behavior of alpha, gamma, and delta tocopherols with linoleic acid in aqueous media Journal of the American Oil Chemists' Society. ,vol. 57, pp. 39- 42 ,(1980) , 10.1007/BF02675523
H. W. Gardner, K. Eskins, G. W. Grams, G. E. Inglett, Radical addition of linoleic hydroperoxides to α-tocopherol or the analogous hydroxychroman Lipids. ,vol. 7, pp. 324- 334 ,(1972) , 10.1007/BF02532650
L. Telegdy Kováts, E. Berndorfer-Kraszner, Über den Antioxydationsmechanismus der Tocopherole (α, β, γ, δ) in Schweinefett Food / Nahrung. ,vol. 12, pp. 407- 414 ,(1968) , 10.1002/FOOD.19680120414