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Evaluation of a new immunoassay to measure sirolimus blood concentrations compared to a tandem mass-spectrometric chromatographic analysis.

机译:与串联质谱分析相比较,评估了一种新的用于测定西罗莫司血药浓度的免疫测定方法。

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A new immunoassay of sirolimus based on the microparticle enzyme immunoassay (MEIA) principle has been developed with collaboration of Abbott Diagnostics. Laboratories and Axis-Shield. Our laboratory evaluated this new assay on 153 whole blood samples (EDTA) drawn from a population of renal (n = 141) and hepatic (n = 12) transplant patients. Each blood sample was analyzed simultaneously by MEIA (Y) and by a reference method (X) used routinely in our laboratory, namely, liquid chromatography tandem mass spectrometry (LC-MS/MS). The statistical analysis of Passing-Bablok produced the following results: Spearman r value = 0.95, slope = 1.15 and intercept with the Y axis = +0.2 ng/mL. The observed global overestimation of 15% compared to the reference method could be explained by the cross-reactivity of sirolimus metabolites with the antibody. A complementary analysis taking into account the transplanted organ (kidney versus hepatic) did not show any significant difference between the populations, most likely owing to the low number of hepatic transplantation samples. The analytical performance of the MEIA method showed CV
机译:与Abbott Diagnostics合作开发了一种基于微粒酶免疫测定(MEIA)原理的新的西罗莫司免疫测定。实验室和轴盾。我们的实验室对从肾脏(n = 141)和肝(n = 12)移植患者人群中提取的153个全血样品(EDTA)进行了评估。通过MEIA(Y)和本实验室常规使用的参考方法(X)同时分析每个血液样本,即液相色谱串联质谱法(LC-MS / MS)。 Passing-Bablok的统计分析得出以下结果:Spearman r值= 0.95,斜率= 1.15,Y轴截距= +0.2 ng / mL。西罗莫司代谢产物与抗体的交叉反应可以解释与参考方法相比,观察到的全球高估了15%。考虑移植器官(肾脏与肝脏)的补充分析并未显示出人群之间的任何显着差异,这很可能是由于肝移植样本数量少所致。 MEIA方法的分析性能显示CV≤10%,定量限为1.5 ng / mL,这对于常规临床监测是可以接受的。总而言之,MEIA方法显示出鲁棒,稳定,可重现的特征,与参考LC-MS / MS方法具有极好的相关性。

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