Fortier R L, McGrath W P, Twomey S L
Clin Chem. 1979 Aug;25(8):1466-9.
We report our evaluation of a commercially available procedure and reagents for determination of ferritin in serum by enzyme-labeled immunosorbent assay (ELISA). Results by our procedure and the "Fer Iron" (Ramco Labs) procedure shows a degree of association (r) of 0.95 and a regression equation of y = 1.03x - 33. Similarly, our procedure compared to the "Gamma Dab" (Clinical Assays) ferritin procedure shows a degree of association of 0.98 and a regression equation of y = 0.93x - 11. Between-day standard deviations were 6 and 22 micrograms/L (n = 24 and 20) for ferritin concentrations of 20 and 300 micrograms/L, respectively. Ferritin values showed no correlation with total iron concentration, but show a broad inverse relationship with iron-binding capacities. The favorable correlation with existing procedures and the speed of the analysis commend the use of ELISA for measurement of ferritin in serum.
我们报告了对一种通过酶联免疫吸附测定法(ELISA)测定血清中铁蛋白的市售方法及试剂的评估。我们的方法与“Fer Iron”(Ramco实验室)方法的结果显示,关联度(r)为0.95,回归方程为y = 1.03x - 33。同样,我们的方法与“Gamma Dab”(临床检测)铁蛋白方法相比,关联度为0.98,回归方程为y = 0.93x - 11。对于铁蛋白浓度分别为20和300微克/升的情况,日间标准差分别为6和22微克/升(n = 24和20)。铁蛋白值与总铁浓度无相关性,但与铁结合能力呈广泛的负相关。与现有方法的良好相关性以及分析速度使得ELISA法适用于血清中铁蛋白的测定。