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Evaluation of the EMIT Mycophenolic Acid Assay from Dade Behring.

机译:Dade Behring对EMIT霉酚酸含量的评估。

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摘要

The Emit Mycophenolic Acid Assay, a new homogeneous enzyme immunoassay for the quantitative analysis of mycophenolic acid (MPA) in human plasma, was evaluated and compared to a high-performance liquid chromatography (HPLC) method. Coefficients of variation (CV) of the within-run imprecision (n = 10) varied from 2.5% to 4.4% and from 1.3% to 4.9% for the Emit and the HPLC, respectively. The CV's of between-day imprecision (n = 10) ranged from 7.9% to 10.8% for the Emit and from 4.7% to 12.1% for the HPLC. Mean recoveries were 95.6% and 100.1% for Emit and HPLC, respectively. Serial dilution of a patient pool demonstrated a linear relationship between expected (x) and measured (y) concentrations: Emit, y = 0.998x + 0.086; HPLC, y = 1.006x - 0.016. The detection limit and the lower limit of quantification were 0.087 mg/L and 0.20 mg/L for Emit. The detection limit for HPLC was 0.08 mg/L using a signal-to-noise ratio of three. Sample stability under various storage conditions was satisfactory, although storage at -20 degrees C is recommended for storage longer than one day. No cross-reactivity from the major metabolite mycophenolic acid glucuronide (MPAG) was found. A correlation study on 261 patient samples yielded the following regression equation (bivariate Deming procedure): Emit = 1.012HPLC + 0.244, r = 0.970.
机译:Emit霉酚酸含量测定是一种用于定量分析人血浆中霉酚酸(MPA)的新型均相酶免疫测定,并与高效液相色谱(HPLC)方法进行了比较。批处理内不精确度(n = 10)的变异系数(CV)对于Emit和HPLC分别从2.5%至4.4%和从1.3%至4.9%不等。日间不精确度(n = 10)的CV对于Emit为7.9%至10.8%,对于HPLC为4.7%至12.1%。 Emit和HPLC的平均回收率分别为95.6%和100.1%。一系列患者稀释液表明预期(x)浓度与测得(y)浓度之间呈线性关系:发射,y = 0.998x + 0.086; HPLC,y = 1.006x-0.016。 Emit的检出限和定量下限分别为0.087 mg / L和0.20 mg / L。 HPLC的检出限为0.08 mg / L,信噪比为3。尽管建议在-20摄氏度下存储超过一天,但在各种存储条件下的样品稳定性仍令人满意。没有发现与主要代谢产物麦考酚酸葡糖醛酸(MPAG)的交叉反应性。对261个患者样品的相关性研究得出以下回归方程(双变量Deming程序):Emit = 1.012HPLC + 0.244,r = 0.970。

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