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游离血清皮质醇:采用平衡透析或超滤及自动化免疫分析系统进行定量测定。

Free serum cortisol: quantification applying equilibrium dialysis or ultrafiltration and an automated immunoassay system.

作者信息

Vogeser Michael, Möhnle Patrick, Briegel Josef

机构信息

Institute of Clinical Chemistry, Hospital of the University of Munich, Munich, Germany.

出版信息

Clin Chem Lab Med. 2007;45(4):521-5. doi: 10.1515/CCLM.2007.104.

Abstract

BACKGROUND

Quantification of bioactive, free serum cortisol concentrations can characterize adrenocortical function more appropriately compared to total serum cortisol measurement. Ultrafiltration or equilibrium dialysis of serum samples allow direct measurement of free serum cortisol concentrations but respective methods have poorly been validated so far. The aim of our study was to investigate the analytical performance of free serum cortisol measurement employing equilibrium dialysis and ultrafiltration.

METHODS

Two commercially available ultrafiltration devices and self-assembled dialysis cells, respectively, were studied. Cortisol was quantified in filtrate or dialysate using an automated immunoassay system. Using two serum pools, the inter-assay coefficient of variation was determined for the three methods and a method comparison was performed.

RESULTS

Inter-assay coefficients of variation (n=10) between 3.2% and 14.8% were observed in the imprecision study. Method comparison demonstrated close agreement between free serum cortisol results obtained by ultrafiltration and equilibrium dialysis, respectively (equilibrium dialysis=1.2xultrafiltration+3.9 nmol/L; r=0.99; n=35).

CONCLUSIONS

Direct quantification of free serum cortisol after equilibrium dialysis or ultrafiltration of the samples offers acceptable reproducibility and results in close agreement can be obtained. Both methods can potentially be introduced into a routine laboratory setting.

摘要

背景

与总血清皮质醇测量相比,生物活性游离血清皮质醇浓度的定量分析能更恰当地表征肾上腺皮质功能。血清样本的超滤或平衡透析可直接测量游离血清皮质醇浓度,但目前各自的方法验证程度较低。我们研究的目的是调查采用平衡透析和超滤测量游离血清皮质醇的分析性能。

方法

分别研究了两种市售超滤装置和自行组装的透析池。使用自动免疫分析系统对滤液或透析液中的皮质醇进行定量。使用两个血清池,测定三种方法的批间变异系数并进行方法比较。

结果

在精密度研究中观察到批间变异系数(n = 10)在3.2%至14.8%之间。方法比较表明,超滤和平衡透析分别获得的游离血清皮质醇结果之间具有密切一致性(平衡透析 = 1.2×超滤 + 3.9 nmol/L;r = 0.99;n = 35)。

结论

样本经平衡透析或超滤后直接定量游离血清皮质醇具有可接受的重现性,且结果高度一致。这两种方法都有可能引入常规实验室检测。

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