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改良的INCSTAR Epo-trac 125/RIA在精英运动员血清促红细胞生成素浓度测定中的应用。

Application of a modified INCSTAR Epo-trac 125/RIA for measurement of serum erythropoietin concentration in elite athletes.

作者信息

Roberts D, Schuh D, Smith D J

机构信息

Faculty of Kinesiology, University of Calgary, Alberta, Canada.

出版信息

Clin Biochem. 1995 Dec;28(6):573-80. doi: 10.1016/0009-9120(95)00039-7.

Abstract

OBJECTIVES

To evaluate the analytical performance of a radioimmunoassay for measurement of erythropoietin.

DESIGN AND METHODS

The INCSTAR Epo-trac 125I radioimmunoassay was examined for applications requiring sensitivity and precision within the normal range.

RESULTS

Sensitivity was improved by increasing sample volume to 300 microL. Minimal detectable concentration was determined at 5.3 U/L, %CV ranged from 4.8-5.8 and 13.3-6.4 for intra- and inter-assay imprecision, respectively. Accuracy was maximized by controlling for lipemic and hemolyzed samples and ensuring serum was separated from the clot within 1 h of collection. Values demonstrated good correlation to the Diagnostic Systems Laboratory RIA-kit.

CONCLUSIONS

With sample volume increased to 300 microL and control of sample preparation, the INCSTAR Epo-trac 125/RIA showed improved precision. Assay sensitivity at lower values allows resolution of changes in erythropoietin within the normal reference range. Age was not found to influence erythropoietin concentration. Within 10 days sojourn at moderate altitude an increase in circulating erythropoietin and reticulocytosis was observed in swimmers.

摘要

目的

评估一种用于测定促红细胞生成素的放射免疫分析方法的分析性能。

设计与方法

对INCSTAR Epo-trac 125I放射免疫分析方法进行检测,以用于在正常范围内需要灵敏度和精密度的应用。

结果

将样本体积增加至300微升可提高灵敏度。最低检测浓度为5.3 U/L,批内不精密度的变异系数(%CV)范围为4.8 - 5.8,批间不精密度的变异系数范围为13.3 - 6.4。通过控制脂血和溶血样本并确保在采集后1小时内将血清与血凝块分离,可使准确性最大化。结果显示与诊断系统实验室的放射免疫分析试剂盒具有良好的相关性。

结论

随着样本体积增加至300微升并控制样本制备过程,INCSTAR Epo-trac 125/RIA的精密度得到提高。较低值时的分析灵敏度可分辨正常参考范围内促红细胞生成素的变化。未发现年龄会影响促红细胞生成素浓度。在中等海拔停留10天内,游泳者的循环促红细胞生成素增加且出现网织红细胞增多。

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