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人血清中头孢吡肟的同位素稀释液相色谱-串联质谱候选参考测量程序

Isotope-dilution-LC-MS/MS candidate reference measurement procedure for cefepime in human serum.

作者信息

Schäffler Judith, Vogeser Michael, Habler Katharina

机构信息

Institute of Laboratory Medicine, LMU University Hospital, LMU Munich, Germany.

出版信息

J Mass Spectrom Adv Clin Lab. 2024 Aug 8;33:43-48. doi: 10.1016/j.jmsacl.2024.08.001. eCollection 2024 Aug.

Abstract

BACKGROUND

Reference measurement procedures are an essential element in the standardization and comparability of analytical measurement results in laboratory medicine. No LC-MS/MS-based reference measurement procedure for cefepime in serum has been published previously.

MATERIALS AND METHODS

An isotope-dilution based two-dimensional LC-MS/MS reference measurement procedure for cefepime concentrations in human serum was developed and tested. The value assignment of unknown samples is based on a defined measurement series validation. Six unknown samples can be measured per series. Pass criteria for the run and the samples were determined empirically based on a performance evaluation. For this purpose, a between-run determination of five runs of the defined measurement series with six cefepime samples was carried out and evaluated. The goal was to define rigorous, realistic target limits and minimize measurement uncertainty. The final defined target limits are used for series-based validation and value assignment. The results for the six unknown samples are provided with the associated measurement uncertainty for this series.

RESULTS

The developed and extensively studied measurement procedure for the quantification of cefepime in serum was found to be practicable and fit for its purpose. The between-run mean imprecision of the six cefepime samples was ≤ 2.0 %, for the QCs it was ≤ 2.3 % and the between-run mean inaccuracy of the QCs was within ± 1.1 %.

CONCLUSION

The novel isotope-dilution-LC-MS/MS measurement procedure in accordance to ISO 15193 can be recommended as candidate reference measurement procedure for the value assignment of cefepime concentrations in human serum.

摘要

背景

参考测量程序是检验医学分析测量结果标准化和可比性的关键要素。此前尚未发表基于液相色谱 - 串联质谱法(LC-MS/MS)的血清中头孢吡肟参考测量程序。

材料与方法

开发并测试了一种基于同位素稀释的二维LC-MS/MS人血清中头孢吡肟浓度参考测量程序。未知样品的值赋值基于定义的测量系列验证。每个系列可测量六个未知样品。运行和样品的通过标准基于性能评估凭经验确定。为此,对包含六个头孢吡肟样品的定义测量系列进行了五次运行的批间测定并进行评估。目标是定义严格、现实的目标限值并最小化测量不确定度。最终定义的目标限值用于基于系列的验证和值赋值。为六个未知样品的结果提供了该系列相关的测量不确定度。

结果

所开发并经过广泛研究的血清中头孢吡肟定量测量程序被认为是可行的且符合其用途。六个头孢吡肟样品的批间平均不精密度≤2.0%,质控品的批间平均不精密度≤2.3%,质控品的批间平均偏差在±1.1%以内。

结论

符合ISO 15193的新型同位素稀释 - LC-MS/MS测量程序可推荐作为人血清中头孢吡肟浓度值赋值的候选参考测量程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2790/11396040/5d194963bb0a/gr1.jpg

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