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同位素稀释质谱法作为测定血清中总甘油酯和甘油三酯的候选决定性方法。

Isotope dilution mass spectrometry as a candidate definitive method for determining total glycerides and triglycerides in serum.

作者信息

Ellerbe P, Sniegoski L T, Welch M J

机构信息

National Institute of Standards and Technology, Gaithersburg, MD 20899.

出版信息

Clin Chem. 1995 Mar;41(3):397-404.

PMID:7882515
Abstract

A new isotope dilution mass spectrometric method for total glycerides and triglycerides in human serum is described. Total glycerides are defined as the sum of tri-, di-, and monoglycerides plus free glycerol; triglycerides are defined as the pure triglyceride species. In both determinations, serum samples are supplemented by addition of [13C3]tripalmitin, processed, derivatized, and the abundance ratios of selected ions are determined. Bias is investigated by quantifying the analyte in the same samples under different chromatographic and ionization conditions. The analytes were determined in two human serum pools. The CV for a single measurement ranged from 0.35% to 0.72%, and the relative SEM ranged from 0.10% to 0.34%; there was no significant bias in the measurements. The combination of high precision and absence of significant bias in the results qualify this method for consideration as a Definitive Method as defined by the National Committee for Clinical Laboratory Standards.

摘要

本文描述了一种用于测定人血清中总甘油酯和甘油三酯的新的同位素稀释质谱法。总甘油酯定义为甘油三酯、甘油二酯、甘油单酯与游离甘油之和;甘油三酯定义为纯甘油三酯。在这两种测定中,血清样品通过添加[13C3]三棕榈酸甘油酯进行补充,经过处理、衍生化,然后测定选定离子的丰度比。通过在不同的色谱和电离条件下对相同样品中的分析物进行定量来研究偏差。在两个人血清混合样本中测定了分析物。单次测量的变异系数范围为0.35%至0.72%,相对标准误范围为0.10%至0.34%;测量中无显著偏差。结果具有高精度且无显著偏差,这使得该方法有资格被视为美国国家临床实验室标准委员会定义的决定性方法。

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