Determination of Corticosteroids in Fish Plasma by High Performance Liquid Chromatography: Evaluation of the Method Using Striped Bass (Morone saxatilis)

1984 ◽  
Vol 41 (9) ◽  
pp. 1280-1286 ◽  
Author(s):  
R. Bruce MacFarsane

A sensitive, specific, and reproducible technique for the simultaneous determination of cortisol, cortisone, and corticosterone in fish plasma was developed using high performance liquid chromatography (HPLC). Corticosteroids were extracted from plasma by methylene chloride and Sep-Pak cartridges for comparative purposes. The Sep-Pak method proved more convenient and efficient. Chromatography was accomplished on a nitrile bonded phase using a methanol–water mobile phase. Steroids were identified and quantified by monitoring absorbance at 254 and 280 nm simultaneously. Sensitivity is approximately 5 ng for each steroid. An evaluation of the technique using subadult striped bass (Morone saxatilis) revealed that cortisol was the only corticosteroid detected. Plasma cortisol concentrations increased in response to brief confinement and crowding, supporting the efficacy of this measurement as an evaluator of stress in striped bass. The HPLC technique provides specific determination of each corticosteroid (thus eliminating cross-reactivity problems inherent in radioimmunoassay methods), resolves corticosteroids from androgens and estrogens, and permits the isolation and purification of individual steroids.

1981 ◽  
Vol 64 (5) ◽  
pp. 1055-1059
Author(s):  
Wray Winterlin ◽  
Gregory Hall ◽  
Charles Mourer

Abstract A simple and sensiiive procedure is presented for the I determination of furazolidone in turkey tissues, j using liquid partitioning followed by high performance liquid chromatography (HPLC). Fat, liver, kidney, skin, and muscle tissues are ground with methylene chloride in a Polytron homogenizer, followed by solvent removal, partitioning in hexane-0.01M acetic acid, and back-partitioning the 0.01M acetic acid with methylene chloride. The determination by HPLC used a reverse phase Ultrasphere- ODS 5 μm column. The method is sensitive to 0.5 ppb, with a standard deviation of 6.39% at the 2 ppb fortification level. Recovery from fortified tissues j averaged 84% from samples fortified with 0.5-10 ppb furazolidone. An alternative cleanup procedure I using a Sep-Pak C18 cartridge is also presented.


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