Sensitive method for measuring tissue α-tocopherol and α-tocopheryloxybutyric acid by high-performance liquid chromatography with fluorometric detection

被引:19
|
作者
Tirmenstein, MA
Watson, BW
Haar, NC
Fariss, MW [1 ]
机构
[1] Washington State Univ, Coll Pharm, Dept Pharmaceut Sci, Pullman, WA 99164 USA
[2] Virginia Commonwealth Univ, Med Coll Virginia, Dept Pathol, Richmond, VA 23298 USA
来源
JOURNAL OF CHROMATOGRAPHY B | 1998年 / 707卷 / 1-2期
关键词
alpha-tocopherol; alpha-tocopheryloxybutyric acid;
D O I
10.1016/S0378-4347(97)00592-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The monhydrolysable tocopherol ether analog, d-alpha-tocopheryloxybutyric acid (TSE), and its tocopherol ester counterpart, d-alpha-tocopheryl hemisuccinate (TS), have been shown to possess anti-tumor activity. In the present study, a sensitive high-performance liquid chromatography (HPLC) method using fluorometric detection is described for the simultaneous determination of TSE and alpha-T in biological specimens. Maximal sensitivity for the measurement of TSE and alpha-T was observed with the wavelengths, 210 nm excitation and 300 nm emission. Using an internal standard (I.S.) method, the amount of these tocopherol compounds was determined in standards, liver homogenates isolated from rats administered TSE-tris salt or vehicle (saline) and in HL-60 human leukaemia cells incubated with TSE-tris salt or saline. Treatment with TSE resulted in the significant accumulation of TSE, but no alpha-T in the liver and HL-60 cells. (C) 1998 Elsevier Science B.V.
引用
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页码:308 / 311
页数:4
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