Herkner K, Nowotny P, Waldhäusl W
J Chromatogr. 1978 Sep 1;146(2):273-81.
The method described permits an exact and rapid determination of aldosterone in urine and plasma. The reliability of the method is based on the separation of aldosterone from contaminating steroids by thin-layer chromatography. The mobile phase used was: cyclohexane--ethyl acetate (20:80). The steroids were extracted by dichloromethane. Plasma was extracted directly, and urine after hydrolysis with sulfuric acid (pH = 1). Recovery before radioimmunological analysis of aldosterone was 54.8 +/- 7.2 (S.D.)%(N = 40) for urine samples, and 39.1 +/- 4.4% (n = 60) for plasma samples. The coefficient of variation for multiple determinations of aldosterone was for urine 8.2% for low (n = 10) and 7.8% (n = 10). The sensitivity of the determination of aldosterone was for urine 0.04 microgram per 24-h volume (n = 10) and for plasma 4.4 ng per 100 ml (n = 10). The method avoids pitfalls due to the cross-reaction of anti-aldosterone serum with other materials.
所述方法可精确、快速地测定尿液和血浆中的醛固酮。该方法的可靠性基于通过薄层色谱法将醛固酮与污染性类固醇分离。所用流动相为:环己烷 - 乙酸乙酯(20:80)。类固醇用二氯甲烷萃取。血浆直接萃取,尿液用硫酸(pH = 1)水解后萃取。醛固酮放射免疫分析前,尿液样本的回收率为54.8±7.2(标准差)%(N = 40),血浆样本的回收率为39.1±4.4%(n = 60)。醛固酮多次测定的变异系数,尿液低浓度时(n = 10)为8.2%,高浓度时(n = 10)为7.8%。醛固酮测定的灵敏度,尿液为每24小时尿量0.04微克(n = 10),血浆为每100毫升4.4纳克(n = 10)。该方法避免了因抗醛固酮血清与其他物质交叉反应而产生的问题。