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用于规范环境的分析型毛细管电泳方法的验证

Validation of analytical capillary electrophoresis methods for use in a regulated environment.

作者信息

Wielgos T, Turner P, Havel K

机构信息

Baxter International, Round Lake, IL, USA.

出版信息

J Capillary Electrophor. 1997 Nov-Dec;4(6):273-8.

PMID:9827417
Abstract

Since its introduction into the analytical laboratory, CE has had to prove that it was capable of generating results comparable to HPLC or GC techniques in the six areas (specificity, precision, accuracy, linearity, ruggedness, and range) typically required of validated methods intended for submission to governmental agencies. This paper will showcase the development and validation of two analytical methods: one for specific identification of HEPES (N-[2-hydroxyethyl]piperazine-N'-[2-ethane sulfonic acid]) and the other to quantitate millimolar concentrations of tris (tris[hydroxymethyl]aminomethane) in high electrolyte solutions. Utilizing neutral markers and internal standards, results for HEPES demonstrate that migration time reproducibility, expressed as %RSD of 2% or less on a variety of capillaries, is obtainable. Additionally, for quantitation of tris, the values obtained for accuracy (%relative mean bias), precision (%RSD), and linearity (r2) over multiple days and capillaries meet the rigorous standards we require of HPLC or GC methods.

摘要

自毛细管电泳(CE)引入分析实验室以来,它必须证明自己能够在通常要求用于提交给政府机构的经过验证的方法的六个领域(特异性、精密度、准确度、线性、耐用性和范围)中产生与高效液相色谱(HPLC)或气相色谱(GC)技术相当的结果。本文将展示两种分析方法的开发和验证:一种用于特异性鉴定4-(2-羟乙基)-1-哌嗪乙磺酸(HEPES),另一种用于定量高电解质溶液中毫摩尔浓度的三(羟甲基)氨基甲烷(tris)。利用中性标记物和内标,HEPES的结果表明,在各种毛细管上,迁移时间重现性(以%相对标准偏差表示,为2%或更低)是可以实现的。此外,对于tris的定量,在多天和多个毛细管上获得的准确度(%相对平均偏差)、精密度(%相对标准偏差)和线性(r2)值符合我们对HPLC或GC方法要求的严格标准。

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