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

IF 3.1 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
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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.

人血清中头孢吡肟的同位素稀释-LC-MS/MS 候选参考测量程序
背景参考测量程序是实验室医学分析测量结果标准化和可比性的基本要素。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 参考测量程序,用于测量人血清中头孢吡肟的浓度。未知样品的定值基于确定的测量系列验证。每个系列可测量六个未知样品。运行和样品的通过标准是根据性能评估经验确定的。为此,对包含六个头孢吡肟样品的已定义测量系列的五次运行进行了运行间测定和评估。目的是确定严格、实际的目标限值,并将测量的不确定性降至最低。最终确定的目标限值用于基于系列的验证和赋值。结果经广泛研究发现,所开发的血清中头孢吡肟定量测量程序切实可行,符合其目的。六份头孢吡肟样品的运行间平均不精确度≤ 2.0%,质控品的运行间平均不精确度≤ 2.3%,质控品的运行间平均不准确度在 ± 1.1% 以内。结论符合 ISO 15193 标准的新型同位素稀释-LC-MS/MS 测量程序可推荐用作人血清中头孢吡肟浓度定值的候选参考测量程序。
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来源期刊
Journal of Mass Spectrometry and Advances in the Clinical Lab
Journal of Mass Spectrometry and Advances in the Clinical Lab Health Professions-Medical Laboratory Technology
CiteScore
4.30
自引率
18.20%
发文量
41
审稿时长
81 days
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