Premium
Capabilities of different cooking oils in prevention of cholesterol oxidation during heating
Author(s) -
Xu Zhimin,
Zhang Ting,
Prinyawiwatkul Witoon,
Samuel Godber J.
Publication year - 2005
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/s11746-005-1062-9
Subject(s) - cholesterol , chemistry , soybean oil , canola , food science , bran , corn oil , olive oil , degradation (telecommunications) , lipid oxidation , biochemistry , antioxidant , organic chemistry , raw material , telecommunications , computer science
The potential of various cooking oils to prevent cholesterol degradation and/or oxidation, as measured by the production of 7‐ketocholesterol during heating at different temperatures, was studied using a cholesterol model system. In the control group (without cooking oil), cholesterol was relatively stable, and 73% of its initial concentration was present after 30 min of heating at 125°C. Less than 30 and 10% of cholesterol remained at 150 and 175°C after 30 min, respectively, and 10% at 200°C after 10 min. In the treatment group, cholesterol mixed with corn, canola, soybean, or olive oil had significantly improved thermal stability. More than 60 and 40% of cholesterol remained at 150 and 175°C after 30 min, respectively. In the control group, 7‐ketocholesterol was produced when samples were heated above 150°C, and levels increased consistently during 30 min of heating. At 175 or 200°C, the level of 7‐ketocholesterol did not increase further after reaching the highest level after 10 min of heating. 7‐Ketocholesterol is not stable above 175°C, and its degradation rate could be much faster than its production at 200°C. 7‐Ketocholesterol was not found in samples of cholesterol mixed with corn oil or laboratory‐prepared soybean and rice bran oils until the heating temperature was raised to 175°C for 20 min. The levels of 7‐ketocholesterol in those treatment groups were greater than that in the control group at 175°C for 30 min. These oils may increase the thermal stability of 7‐ketocholesterol and retard its degradation rate.