Lentjes E G, Romijn F, Maassen R J, de Graaf L, Gautier P, Moolenaar A J
Department of Clinical Chemistry, University Hospital Leiden, The Netherlands.
Clin Chem. 1993 Dec;39(12):2518-21.
A method is described for a temperature-controlled ultrafiltration procedure to measure free cortisol in serum. A special thermometer with a sensor was developed, measuring the temperature directly in the ultrafiltration device. The sensor is screwed on the axis of the centrifuge rotor, and the centrifuge is placed in a temperature-controlled box so that the temperature of the sample is kept at 37 degrees C +/- 0.1 degrees C. The overall CV of the free cortisol assay ranges from 2.2% to 11.4%, of which the ultrafiltration contributes only 2.2-3.6%. Increasing amounts of cortisol-binding protein, as found in women using estrogen-containing oral contraceptives, have minor but significant effects on the free cortisol concentrations in serum. Serum free cortisol concentrations in a reference population (n = 114; central 95 percentiles) were 12-43 nmol/L (4-9.5% of total cortisol); in the group of the oral-contraceptive users (n = 27), the reference interval was 11-53 nmol/L (1.5-4.5%).
描述了一种用于测量血清中游离皮质醇的温控超滤程序的方法。开发了一种带有传感器的特殊温度计,可直接在超滤装置中测量温度。该传感器拧在离心机转子的轴上,离心机置于温控箱中,以使样品温度保持在37℃±0.1℃。游离皮质醇测定的总变异系数在2.2%至11.4%之间,其中超滤仅占2.2 - 3.6%。在使用含雌激素口服避孕药的女性中发现,皮质醇结合蛋白量增加对血清中游离皮质醇浓度有轻微但显著的影响。参考人群(n = 114;中间95百分位数)的血清游离皮质醇浓度为12 - 43 nmol/L(占总皮质醇的4 - 9.5%);在口服避孕药使用者组(n = 27)中,参考区间为11 - 53 nmol/L(1.5 - 4.5%)。