Kinetic evaluation of 3 beta-hydroxycholest-5-en-7-one (7-ketocholesterol) stability during saponification

被引:57
作者
Park, PW
Guardiola, F
Park, SH
Addis, PB
机构
[1] UNIV MINNESOTA, DEPT FOOD SCI & NUTR, ST PAUL, MN 55108 USA
[2] UNIV BARCELONA, FAC PHARM, NUTR & FOOD SCI UNIT, BARCELONA, SPAIN
[3] ANALTEK, EVANSVILLE, IN 47711 USA
关键词
degradation; first-order kinetics; gas chromatography; 6-ketocholestanol; 7-ketocholesterol stability; mass spectrometry; saponification; tautomerization; trimethylsilyl ether;
D O I
10.1007/BF02518118
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
To clarify conflicting information regarding 7-ketocholesterol (7-KC) recovery from saponification, we evaluated the stability of 7-KC in methanolic alkaline medium. We added 1 N alcoholic KOH to 7-KC or lard spiked with 7-KC and held the mixtures at 45, 55, 65, and 75 degrees C for different times to simulate various saponification conditions. Gas-chromatographic determination of residual 7-KC with 5 alpha-cholestane as the internal standard (IS) showed that the higher the saponification temperature, the greater the 7-KC degradation. Hot saponification at 75 degrees C for 30 min caused extensive destruction and left only 31% 7-KC. 7-KC loss during saponification could be described by pseudo first-order kinetics, and the dependence of degradation rate on temperature (T, K) by k (h(-1)) = (2.6 x 10(17)) exp (-1.36 x 10(4)/T). As predicted by the kinetic equation, 7-KC loss during room-temperature saponification (21 degrees C) was practically negligible; following the exposure of 7-KC or lard spiked with 7-KC to 1 N alcoholic KOH for 18 h, about 97% 7-KC was recovered. 6-Ketocholestanol, when used as an IS, should be looked at carefully because of potential tautomerization, leading to the formation of two enol isomers when in extended contact with trimethylsilyl derivatization reagents.
引用
收藏
页码:623 / 629
页数:7
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