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采用放射免疫分析法测定妊娠血清中未结合雌三醇。

Measurement by radioimmunoassay of unconjugated estriol in pregnancy serum.

作者信息

Zucchelli G C, Piro M A, Grosso P, Malvano R

出版信息

Clin Chim Acta. 1975 Nov 15;65(1):57-66. doi: 10.1016/0009-8981(75)90334-4.

Abstract

Antisera to estriol 6--onjugates were tested for suitability in the direct radioimmunoassay of unconjugated estriol in extracts of pregnancy serum. Assessment of specificity through titration with competing steroids allowed a selection to be made within the group of antisera. The measurement was then standardized by checking the absence of analytical blank (solvent and sample blank) and the extent of binding variability associated with the use of charcoal-dextran as a separating agent. Validation was made by means of the usual recovery and dilution tests, and by a cross-comparison of analytical data obtained with different antisera; reproducibility of calibration curve and within-and between-assay variability was evaluated under routine conditions. The validity of the clinical information was assessed by assaying 202 samples randomly collected throughout normal pregnancy from the 16th week to term: both trend and levels of unconjugated estriol concentration were found to be in good agreement with the literature data.

摘要

检测了抗雌三醇6-缀合物抗血清在直接放射免疫分析法中用于检测妊娠血清提取物中游离雌三醇的适用性。通过与竞争性甾体进行滴定来评估特异性,从而在抗血清组中进行选择。然后通过检查分析空白(溶剂和样品空白)的不存在以及与使用活性炭-葡聚糖作为分离剂相关的结合变异性程度来对测量进行标准化。通过常规的回收率和稀释试验以及对用不同抗血清获得的分析数据进行交叉比较来进行验证;在校准曲线的重现性以及测定内和测定间变异性方面在常规条件下进行了评估。通过对在整个正常妊娠期间从第16周直至足月随机收集的202份样本进行检测来评估临床信息的有效性:游离雌三醇浓度的趋势和水平均与文献数据高度一致。

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