在 Alinity i 分析仪上使用改进的 CMIA 与一家参考实验室的 LC-MS/MS 方法之间的他克莫司浓度具有良好的相关性,但与另一家参考实验室的 LC-MS/MS 方法之间却出现了意想不到的负偏差。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-07-05 DOI:10.1093/ajcp/aqae005
Kelsey Woodard, Tracey Kisler, Amitava Dasgupta
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引用次数: 0

摘要

研究目的我们比较了 Alinity i 分析仪(雅培实验室)上最新获得美国食品和药物管理局批准的他克莫司测定法(CMIA)和 2 家参考实验室基于液相色谱/串联质谱(LC-MS/MS)的方法得出的他克莫司浓度。我们还研究了 CMIA 他克莫司检测法与 Elecsys 他克莫司检测法之间的相关性:方法:使用 Alinity i 分析仪通过化学发光微粒子免疫分析法(CMIA)测定 EDTA 全血中他克莫司的浓度,然后将 2 份等分样品送至 2 个参考实验室,这 2 个实验室均使用阿霉素作为 LC-MS/MS 方法的内标:结果:CMIA 他克莫司测定法的总精密度非常高。将参考实验室 A 用 LC-MS/MS 方法获得的他克莫司浓度绘制在 x 轴上,相应的 CMIA 值绘制在 y 轴上,可观察到以下回归方程:y = 0.9721x + 1.005(r = 0.95),表明 CMIA 无明显偏差。然而,当使用参考实验室 B 的他克莫司值进行比较时,回归方程为 y = 0.7664x + 1.775(r = 0.93),表明 CMIA 存在明显的负偏差。当我们比较参考实验室 A 和 B 所获得的他克莫司浓度时,我们发现参考实验室 B 所获得的他克莫司浓度存在正偏差,但 CMIA 和 Elecsys 免疫测定法所获得的他克莫司浓度相当:由于使用 CMIA 和参考实验室 A(我们的长期药物分析参考实验室)的 LC-MS/MS 测得的他克莫司浓度具有良好的相关性,我们认为 Alinity i 上的 CMIA 可用于他克莫司的治疗药物监测。
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Good correlation between tacrolimus concentrations using improved CMIA on the Alinity i analyzer and LC-MS/MS method from a reference laboratory but unexpected negative bias with another LC-MS/MS method from a different reference laboratory.

Objectives: We compared tacrolimus concentrations obtained by the more recently US Food and Drug Administration-approved tacrolimus assay (CMIA) on the Alinity i analyzer (Abbott Laboratories) with a liquid chromatography/tandem mass spectrometry (LC-MS/MS)-based method from 2 reference laboratories. We also investigated the correlation between the CMIA tacrolimus and Elecsys tacrolimus assays.

Methods: Tacrolimus concentrations were measured in EDTA whole blood by the chemiluminescent microparticle immunoassay (CMIA) using the Alinity i analyzer, and then 2 aliquots were sent to 2 reference laboratories, both using ascomycin as the internal standard for the LC-MS/MS method.

Results: The total precision of the CMIA tacrolimus assay was excellent. When tacrolimus concentrations obtained by the LC-MS/MS method from reference laboratory A were plotted on the x-axis and corresponding CMIA values were plotted on the y-axis, the following regression equation was observed: y = 0.9721x + 1.005 (r = 0.95), indicating no significant bias with the CMIA. However, when tacrolimus values obtained from reference laboratory B were used for comparison, the regression equation was y = 0.7664x + 1.775 (r = 0.93), indicating significant negative bias with the CMIA. When we compared tacrolimus concentrations obtained by reference laboratories A and B, we observed positive bias with tacrolimus concentrations obtained by reference laboratory B. However, tacrolimus concentrations obtained by both CMIA and Elecsys immunoassays were comparable.

Conclusions: Because of good correlation of tacrolimus concentrations using the CMIA and LC-MS/MS from reference laboratory A, our long-term reference laboratory for drug analysis, we concluded that the CMIA on the Alinity i can be used for therapeutic drug monitoring of tacrolimus.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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