Dolezalová M
University Hospital, Motol, Prague, Czech Republic.
Clin Chim Acta. 1994 Dec 16;231(2):129-37. doi: 10.1016/0009-8981(94)90197-x.
An HPLC method with solid-phase extraction for the specific determination of urinary free cortisol is described. A 3-ml urine sample is cleaned up on a disposable cartridge C 18. After successive washing with 0.025 mol/l borate buffer (pH 7.5) and a mixture of acetone and water, retained cortisol and 6 alpha-methylprednisolone (internal standard) are eluted with ethyl acetate. The recovery of cortisol is 92.9 +/- 4.4%. The reversed-phase chromatographic procedure uses an octadecyl-bonded column with a mobile phase composed of methanol, tetrahydrofuran and water with UV detection at 245 nm. The calibration curve is linear up to a cortisol concentration of 356 nmol/l. Coefficients of variation show good reproducibility of the assay. The detection limit is 9 nmol/l (16 pmol injected). The normal range of urinary free cortisol excretion was found to be 17-132 nmol/24 h. This simple and convenient method is suitable for routine use.
描述了一种采用固相萃取法特异性测定尿游离皮质醇的高效液相色谱法。取3 ml尿样在一次性C 18柱上进行净化处理。依次用0.025 mol/l硼酸盐缓冲液(pH 7.5)以及丙酮和水的混合液洗涤后,保留的皮质醇和6α-甲基泼尼松龙(内标)用乙酸乙酯洗脱。皮质醇的回收率为92.9±4.4%。反相色谱程序采用十八烷基键合柱,流动相由甲醇、四氢呋喃和水组成,在245 nm处进行紫外检测。校准曲线在皮质醇浓度达356 nmol/l时呈线性。变异系数表明该测定具有良好的重现性。检测限为9 nmol/l(进样16 pmol)。尿游离皮质醇排泄的正常范围为17 - 132 nmol/24 h。这种简单便捷的方法适用于常规检测。