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具有不同载脂蛋白A-I和B水平的冻干人血清基参考物质的制备

Preparation of lyophilized human serum based reference materials with graded levels of apolipoproteins A-I and B.

作者信息

Henderson L O, Hazlehurst J S, Taylor L, Hannon W H

机构信息

Division of Environmental Health Laboratory Sciences, Centers for Disease Control, Atlanta, Georgia 30333.

出版信息

Clin Biochem. 1988 Aug;21(4):219-23. doi: 10.1016/s0009-9120(88)80004-3.

Abstract

Surveys of national and international laboratories indicate that among-laboratory and between-laboratory sources of variance account for the majority of variability in laboratories measuring apolipoproteins A-I and B. These sources of variance are amenable to correction through the use of common quality control and reference materials. We utilized proven techniques employing ethyl alcohol and acetate buffer to precipitate either apolipoprotein A-I rich or apolipoprotein B rich fractions that were blended with whole or delipidated serum producing five pilot-sized pools containing graded levels of apolipoproteins. After lyophilization the pools were tested and each pool contained levels of analytes similar to frozen serum and contained varied amounts of apolipoproteins A-I and B. Temporal and accelerated thermal stability testing demonstrated stability of the analytes in the pools with time (three years) and temperature (up to 56 degrees C). This technology provides a preparative procedure for apolipoprotein reference materials over the extended range needed in clinical applications.

摘要

对国内和国际实验室的调查表明,实验室间和实验室内的变异来源占测量载脂蛋白A-I和B的实验室中大部分变异性。这些变异来源可通过使用通用质量控制和参考物质进行校正。我们采用了经过验证的技术,使用乙醇和醋酸盐缓冲液沉淀富含载脂蛋白A-I或富含载脂蛋白B的部分,将其与全血清或脱脂血清混合,制成五个中试规模的样本池,其中载脂蛋白水平呈梯度变化。冻干后对样本池进行检测,每个样本池中的分析物水平与冷冻血清相似,且含有不同量的载脂蛋白A-I和B。时间和加速热稳定性测试表明,样本池中的分析物在时间(三年)和温度(高达56摄氏度)下具有稳定性。该技术为临床应用所需的扩展范围内的载脂蛋白参考物质提供了一种制备程序。

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