Kushinsky S, Mirrasoul M, Bennett G
Clin Biochem. 1977 Apr;10(2):52-5. doi: 10.1016/s0009-9120(77)80001-5.
Convenient methodology based on separation of testosterone from non-alcoholic neutral steroids by means of a sulfation procedure has been developed for the radioimmunoassay (RIA) of testosterone in male and in female serum. When coordinated with our previously published non-chromatographic procedure (1) for the RIA of estrone and 17 beta-estradiol in serum all 3 steroids can be determined in the same specimen. With only minor modification (14) progesterone also can be determined. Validation of the procedure was based on: 1. agreement between results obtained using TLC and sulfation to fractionate testosterone (r=0.99; b=1.03), 2. accurate recovery of different quatities of testosterone added to serum, 3. independence of the concentration of testosterone and volume of serum used for assay, 4. low procedural blanks (1.1+/-0.7 pg), 5. low intra-assay (4.7-4.8%) and interassay (4.8-8.8%) variability and 6. correspondence of observed values for testosterone in male serum (7.00+/-2.03 ng/ml) and in femal serum (420+/-115 pg/ml) with those reported previously by others.
基于通过硫酸化程序从非酒精性中性类固醇中分离睾酮的便捷方法已被开发出来,用于男性和女性血清中睾酮的放射免疫分析(RIA)。当与我们之前发表的血清中雌酮和17β-雌二醇RIA的非色谱程序(1)配合使用时,所有3种类固醇都可以在同一样本中进行测定。只需进行微小修改(14),孕酮也可以被测定。该程序的验证基于:1. 使用薄层层析(TLC)和硫酸化分离睾酮所获得的结果之间的一致性(r = 0.99;b = 1.03),2. 准确回收添加到血清中的不同量的睾酮,3. 睾酮浓度与用于测定的血清体积无关,4. 低程序空白值(1.1±0.7 pg),5. 低批内变异(4.7 - 4.8%)和批间变异(4.8 - 8.8%),以及6. 男性血清(7.00±2.03 ng/ml)和女性血清(420±115 pg/ml)中观察到的睾酮值与其他人先前报道的值相符。