FLUOROMETRIC DETECTION OF SERUM CORTICOSTERONE USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY
被引:34
作者:
MASON, SR
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机构:Department of Biochemistry, Molecular Biosciences, University of Queensland, Brisbane
MASON, SR
WARD, LC
论文数: 0引用数: 0
h-index: 0
机构:Department of Biochemistry, Molecular Biosciences, University of Queensland, Brisbane
WARD, LC
REILLY, PEB
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h-index: 0
机构:Department of Biochemistry, Molecular Biosciences, University of Queensland, Brisbane
REILLY, PEB
机构:
[1] Department of Biochemistry, Molecular Biosciences, University of Queensland, Brisbane
来源:
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS
|
1992年
/
581卷
/
02期
关键词:
D O I:
10.1016/0378-4347(92)80280-4
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
A simple, sensitive, specific and reproducible method for the determination of corticosterone concentrations in rat serum using high-Performance liquid chromatography (HPLC) with fluorimetric detection is described. Corticosterone is detectable down to 0.1 ng injected onto the HPLC column. Cortisol is used as an internal standard. Ethyl acetate was used for both initial serum corticosteroid extraction and the subsequent fluorophore extraction after sulfuric acid hydrolysis; thus sulfuric acid does not enter the HPLC system. The resultant fluorophores for both corticosterone and cortisol are stable for at least two weeks at ambient temperature not requiring storage at -20-degrees-C. The procedure is highly suitable for use with HPLC systems utilising automatic sample injectors. The method is specific for corticosterone; dexamethasone, cortisone and gonadal steroids are not detectable and do not interfere in this assay.