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阿斯特拉邻甲酚酞络合酮钙法的评估。

Evaluation of the ASTRA o-cresolphthalein complexone calcium method.

作者信息

Hartmann A E, Lewis L R

出版信息

Am J Clin Pathol. 1984 Aug;82(2):182-7. doi: 10.1093/ajcp/82.2.182.

Abstract

An automated calcium method based on o-cresolphthalein complexone chemistry and designed to be used in conjunction with the Beckman ASTRA systems (Beckman Instruments, Inc., Brea, CA) was evaluated. Day-to-day reproducibility studies yielded coefficients of variation ranging from 1.2 to 3.1%. Linearity was 5.0-15.5 mg/dL, and recovery of calcium averaged 98%. Bilirubin, creatinine, hemoglobin, and turbidity did not cause significant interference while there was a positive interference due to magnesium. The throughput is 70 samples per hour, and a single stat result can be obtained in 9 minutes from the standby mode. Very little sample (12 microL) or reagent (150 microL) is required. There was excellent correlation between the ASTRA calcium method and atomic absorption spectrophotometry (Y = 1.047x - 0.39, r = 0.9941). Analytic performance was judged acceptable according to Westgard's medical usefulness criteria of the observed total analytic errors being less than the limit of allowable error.

摘要

对一种基于邻甲酚酞络合酮化学原理、设计用于与贝克曼ASTRA系统(贝克曼仪器公司,加利福尼亚州布雷亚)联合使用的自动钙检测方法进行了评估。日常重复性研究得出的变异系数在1.2%至3.1%之间。线性范围为5.0 - 15.5mg/dL,钙的回收率平均为98%。胆红素、肌酐、血红蛋白和浊度不会引起显著干扰,而镁会产生正干扰。通量为每小时70个样本,从待机模式开始9分钟内可获得单个急诊结果。所需样本量极少(12微升)或试剂极少(150微升)。ASTRA钙检测方法与原子吸收分光光度法之间具有极好的相关性(Y = 1.047x - 0.39,r = 0.9941)。根据韦斯特加德关于观察到的总分析误差小于允许误差限度的医学实用性标准,分析性能被判定为可接受。

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