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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >An improved ultrafiltration method for determining free testosterone in serum.
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An improved ultrafiltration method for determining free testosterone in serum.

机译:一种测定血清中游离睾丸激素的改良超滤方法。

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In this method, we use the Amicon MPS-1 centrifugal ultrafiltration device and the YMB membrane in measuring free testosterone in serum. Two independent assays are combined: total testosterone and the ultrafiltrable fraction of added [3H]testosterone. The unbound fraction is determined in 0.15-0.5 mL ultrafiltrates of 0.6 to 1 mL of variably diluted serum that has been equilibrated with [3H]testosterone at 37 degrees C. The assay is rapid (less than 1 h), practicable (requires 0.6 mL of serum), and reproducible (CV 3.2% within assay, 3.9% between assays). Accuracy was evaluated as the fraction of free testosterone in the ultrafiltrate of dialyzed serum vs that in a prior dialysate; they were the same confirming the validity of the free testosterone measurement. Samples from ostensibly healthy men and women and from hirsute and pregnant women gave results that agreed with those obtained by equilibrium dialysis. Total testosterone concentrations for normal and hirsute women showed considerable overlap, but data on free testosterone concentrations in these populations were better resolved.
机译:在这种方法中,我们使用Amicon MPS-1离心超滤装置和YMB膜测量血清中的游离睾丸激素。结合了两个独立的检测方法:总睾丸激素和添加的[3H]睾丸激素的超滤级分。未结合部分的测定是在0.15-0.5 mL 0.6至1 mL可变稀释血清的超滤液中进行的,该血清已在[37H]睾丸激素中于37℃平衡。该测定快速(少于1小时),可行(需要0.6 mL血清)和可重复性(测定内CV为3.2%,测定间CV为3.9%)。准确性评估为透析血清超滤液中游离睾丸激素相对于先前透析液中游离睾丸激素的分数;它们相同,证实了游离睾丸激素测定的有效性。表面上健康的男女以及多毛和孕妇的样品所得到的结果与通过平衡透析获得的结果相吻合。正常妇女和多毛妇女的总睾丸激素浓度显示出相当大的重叠,但是这些人群中游离睾丸激素浓度的数据得到了较好的解析。

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