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一种用于测定血清中游离睾酮的改良超滤方法。

An improved ultrafiltration method for determining free testosterone in serum.

作者信息

Vlahos I, MacMahon W, Sgoutas D, Bowers W, Thompson J, Trawick W

出版信息

Clin Chem. 1982 Nov;28(11):2286-91.

PMID:7127776
Abstract

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.

摘要

在该方法中,我们使用Amicon MPS-1离心超滤装置和YMB膜来测定血清中的游离睾酮。该方法结合了两种独立的测定方法:总睾酮和添加的[³H]睾酮的可超滤部分。未结合部分是在0.6至1 mL不同稀释度且已在37℃下与[³H]睾酮平衡的血清的0.15 - 0.5 mL超滤物中测定的。该测定方法快速(少于1小时)、可行(需要0.6 mL血清)且可重复(批内变异系数为3.2%,批间变异系数为3.9%)。通过比较透析血清超滤物中游离睾酮的比例与先前透析液中游离睾酮的比例来评估准确性;二者相同,证实了游离睾酮测量的有效性。表面健康的男性和女性、多毛症患者以及孕妇的样本结果与通过平衡透析获得的结果一致。正常女性和多毛症女性的总睾酮浓度有相当大的重叠,但这些人群中游离睾酮浓度的数据得到了更好的区分。

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