Comparison of Plasma Concentration of Linezolid's Detection by FICA and LC-MS/MS.

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Jing Chen, Chenxia Zhu, Yangjin He, Hengbin Cao
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引用次数: 0

Abstract

Linezolid was the first totally synthetic oxazolidinone antibiotic that was approved for clinical use against Mycobacterium tuberculosis. Our study investigated the correlation and consistency of fluorescence immunochromatography assay (FICA) and high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) in measuring linezolid levels in the plasma. Plasma samples were collected from 80 to 100 tuberculosis patients. The samples were analyzed by FICA and LC-MS/MS, and linezolid levels measured by the two methods were compared by outlier test, correlation coefficient, Bland-Altman scatter plot, Deming regression analysis and bias evaluation. A total of 83 plasma samples were collected, all of which were non-outlier. The correlation coefficient of FICA and LC-MS/MS results was 0.9845. Deming regression analysis showed that the regression equation of FICA and LC-MS/MS was y = 0.2229 + 1.0076x. The medical decision levels of 2 and 7 μg/mL were taken into the regression equation, and the 95% CI of 2- and 7-μg/mL bias were both within the allowed error range. The findings indicated a strong correlation between the results obtained from FICA and LC-MS/MS were consistent showed good correlation, demonstrating their equivalence in measurement.

通过 FICA 和 LC-MS/MS 检测利奈唑胺血浆浓度的比较
来奈唑胺是第一种完全合成的噁唑烷酮类抗生素,已被批准用于临床治疗结核分枝杆菌。我们的研究调查了荧光免疫层析(FICA)和高效液相色谱-串联质谱(LC-MS/MS)在测量血浆中利奈唑胺水平时的相关性和一致性。从 80 至 100 名肺结核患者中采集了血浆样本。通过离群值检验、相关系数、Bland-Altman 散点图、戴明回归分析和偏差评估对两种方法测定的利奈唑胺水平进行比较。共收集了 83 份血浆样本,所有样本均无异常值。FICA 与 LC-MS/MS 结果的相关系数为 0.9845。戴明回归分析表明,FICA 与 LC-MS/MS 的回归方程为 y = 0.2229 + 1.0076x。将 2 和 7 μg/mL 的医疗决策水平纳入回归方程,2 和 7 μg/mL 偏差的 95% CI 均在允许误差范围内。研究结果表明,FICA 和 LC-MS/MS 得出的结果之间具有很强的相关性,显示出两者在测量上的等效性。
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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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