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使用同位素稀释液相色谱-串联质谱法测定人血清中总3,3',5-三碘甲状腺原氨酸的参考测量程序的开发与评估

Development and evaluation of a reference measurement procedure for the determination of total 3,3',5-triiodothyronine in human serum using isotope-dilution liquid chromatography-tandem mass spectrometry.

作者信息

Tai Susan S-C, Bunk David M, White Edward, Welch Michael J

机构信息

Analytical Chemistry Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8392, USA.

出版信息

Anal Chem. 2004 Sep 1;76(17):5092-6. doi: 10.1021/ac049516h.

Abstract

3,3',5-Triiodothyronine (T3) is an important diagnostic marker for thyroid function. A reference measurement procedure (RMP) for total T3 in serum involving isotope dilution coupled with liquid chromatography-tandem mass spectrometry (LC/MS/MS) has been developed and critically evaluated. The method uses solid-phase extraction with mixed-mode retention mechanisms of reversed phase and ion exchange prior to reversed-phase LC/MS/MS. In addition to a labeled T3 internal standard (T3-13C9), labeled thyroxine (T4-d5) is also added to serum samples in order to monitor the degradation of T4 to T3. The accuracy of the measurement was evaluated by a recovery study for added T3 and was supported by a comparison study with the other RMP. The recovery of the added T3 ranged from 98.9% to 99.4%. The results of this method and the other RMP agreed to within 1%. Samples of frozen serum pools were prepared and measured in three separate sets. Excellent reproducibility was obtained with within-set coefficients of variation (CVs) ranging from 0.8% to 1.6% and between-set CVs ranging from 1.9% to 2.6%. Excellent linearity was also obtained with correlation coefficients of all linear regression lines (measured intensity ratios vs mass ratios) ranging from 0.9995 to 0.9996. The detection limit at a signal-to-noise ratio of approximately 3 was 1 pg of T3. The T4 degradation during sample preparation was minimized to a small percentage (no more than 3% of the T3 values) by use of antioxidants (ascorbic acid, dithiothreitol, citric acid) and can be accounted for in the T3 measurement process. This well-characterized LC/MS/MS method for total serum T3, which demonstrates good accuracy and precision, low susceptibility to interferences, accountability of the conversion of T4 to T3, and comparability with the other RMP, qualifies as a reference measurement procedure and can be used to provide an accuracy base to which routine methods for T3 can be compared.

摘要

3,3',5-三碘甲状腺原氨酸(T3)是甲状腺功能的重要诊断标志物。已开发并严格评估了一种用于血清总T3的参考测量程序(RMP),该程序涉及同位素稀释结合液相色谱-串联质谱法(LC/MS/MS)。该方法在反相LC/MS/MS之前使用具有反相和离子交换混合模式保留机制的固相萃取。除了标记的T3内标(T3-13C9)外,还向血清样品中添加标记的甲状腺素(T4-d5),以监测T4向T3的降解。通过对添加的T3进行回收率研究评估测量的准确性,并通过与其他RMP的比较研究得到支持。添加的T3的回收率在98.9%至99.4%之间。该方法和其他RMP的结果在1%以内一致。制备了冷冻血清库样品并分三组进行测量。组内变异系数(CV)范围为0.8%至1.6%,组间CV范围为1.9%至2.6%,获得了出色的重现性。所有线性回归线(测量强度比与质量比)的相关系数范围为0.9995至0.9996,也获得了出色的线性。在信噪比约为3时的检测限为1 pg T3。通过使用抗氧化剂(抗坏血酸、二硫苏糖醇、柠檬酸),样品制备过程中T4的降解被最小化至小百分比(不超过T3值的3%),并且可以在T3测量过程中予以考虑。这种针对血清总T3的特征明确的LC/MS/MS方法,具有良好的准确性和精密度,对干扰的敏感性低,T4向T3转化的可追溯性,以及与其他RMP的可比性,符合参考测量程序标准,可用于为T3的常规方法提供可比较的准确性基础。

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