Hubert I L, Shaw W, Spierto F W
Am J Med Technol. 1977 Apr;43(4):329-35.
Problem areas within a proficiency testing (PT) program are performance evaluation and sample stability. The different units used in the various T3 uptake methodologies make performance evaluation complex. To facilitate this evaluation, a normalization method for T3 uptake performance evaluation has been developed. Sample stability studies for T3 uptake indicate that, at room temperature, sample values increase after storage for about seven days. Room temperature sample stability studies for T4 using a competitive protein binding (CPB) method indicate that the apparent T4 content of pooled serum increases after about one week. Fatty acids are shown to be an interfering substance in the T4 CPB method as well as the T4 radioimmunoassay (RIA) method. This interference increases with a decrease in carbon chain length from C18 to C12 and with an increase in unsaturation of fatty acids. The B/B0 ration for arachidonic acid at a concentration of 0.48 micronMoles per tube is 17.4 in a CPB method and 87.1 in a radioimmunoassay method indicating that the greater effect is in the CPB method. The increase in T3 uptake values are probably also due to the interfering effect of fatty acids.
能力验证(PT)项目中的问题领域包括性能评估和样本稳定性。各种T3摄取方法中使用的不同单位使得性能评估变得复杂。为便于进行这种评估,已开发出一种用于T3摄取性能评估的归一化方法。T3摄取的样本稳定性研究表明,在室温下,样本值在储存约七天后会增加。使用竞争性蛋白结合(CPB)方法对T4进行的室温样本稳定性研究表明,混合血清的表观T4含量在约一周后会增加。脂肪酸在T4 CPB方法以及T4放射免疫分析(RIA)方法中均显示为干扰物质。这种干扰随着碳链长度从C18减少到C12以及脂肪酸不饱和度的增加而增加。在CPB方法中,每管浓度为0.48微摩尔的花生四烯酸的B/B0比值为17.4,在放射免疫分析方法中为87.1,这表明在CPB方法中的影响更大。T3摄取值的增加可能也归因于脂肪酸的干扰作用。