Diamandis E P, D'Costa M
Department of Clinical Biochemistry, Mount Sinai Hospital, Toronto, Ontario, Canada.
J Chromatogr. 1988 Apr 8;426(1):25-32. doi: 10.1016/s0378-4347(00)81923-4.
We have developed a selective and precise high-performance liquid chromatographic method for urinary free cortisol with an improved and efficient sample clean-up using C18 Sep-Pak cartridges. The urine sample (2 ml), with 11-deoxycortisol as internal standard, is applied to the Sep-Pak, which is then sequentially washed with acetone-water (1:4, v/v), water and hexane. Cortisol is eluted with diethyl ether, evaporated to dryness and redissolved in 2 ml of water. The wash cycle is repeated once using the same Sep-Pak cartridge. This double extraction greatly improves sample clean-up and allows modification of the mobile phase (tetrahydrofuran-methanol-water) so that cortisol is rapidly eluted as a single well resolved peak at 13 min. Chromatography is performed isocratically on a reversed-phase column with detection at 254 nm. Detection limits for urinary free cortisol by this procedure were two or three times lower than those obtained with two commercial radioimmunoassay kits. The chromatographic method was used successfully in the diagnosis of patients with hypercortisolism and Cushing's syndrome.
我们开发了一种选择性和精确性高的高效液相色谱法,用于测定尿游离皮质醇,该方法采用C18 Sep-Pak柱进行改进且高效的样品净化。将含有11-脱氧皮质醇作为内标的尿液样品(2 ml)加至Sep-Pak柱上,然后依次用丙酮-水(1:4,v/v)、水和己烷冲洗。皮质醇用乙醚洗脱,蒸发至干并重新溶解于2 ml水中。使用同一Sep-Pak柱重复洗涤一次。这种双重萃取极大地改善了样品净化效果,并允许对流动相(四氢呋喃-甲醇-水)进行调整,从而使皮质醇在13分钟时作为单一分离良好的峰快速洗脱。在反相柱上进行等度色谱分析,检测波长为254 nm。通过该方法测定尿游离皮质醇的检测限比使用两种商用放射免疫分析试剂盒所获得的检测限低两到三倍。该色谱法成功用于皮质醇增多症和库欣综合征患者的诊断。