Ferreri L F, Raisys V A, Opheim K E
J Anal Toxicol. 1984 May-Jun;8(3):138-40. doi: 10.1093/jat/8.3.138.
The Abbott TDx fluorescence polarization immunoassay was evaluated for the determination of serum digoxin concentrations. Within-assay precision was less than 4% coefficient of variation (CV) for concentrations ranging from 0.64 to 3.75 ng/mL. Between-assay precision was 14.5% CV at 0.75 ng/mL, 5.7% CV at 1.50 ng/mL, and 4.9% CV at 3.48 ng/mL. Sensitivity to 0.2 ng/mL digoxin was confirmed. Correlation of 86 patient specimens assayed by radioimmunoassay (RIA) with the TDx showed the following: correlation coefficient r = 0.94, slope = 0.93, intercept = 0.11, and Sy/x = 0.19. Recovery from serum at concentrations of 0.97 ng/mL and 4.50 ng/mL averaged 98%. No significant interference from lipemia, icteria, or hemolysis was observed. Spironolactone showed no cross-reactivity with the antibody, while digitoxin exhibited significant cross-reactivity. Compared to the RIA procedure, the TDx assay was more rapid, reliable and, in this clinical situation, more cost effective.
对雅培TDx荧光偏振免疫分析法进行了评估,以测定血清地高辛浓度。对于浓度范围为0.64至3.75 ng/mL的样本,批内精密度变异系数(CV)小于4%。在0.75 ng/mL时批间精密度CV为14.5%,在1.50 ng/mL时为5.7%,在3.48 ng/mL时为4.9%。已证实对0.2 ng/mL地高辛具有敏感性。通过放射免疫分析法(RIA)检测的86份患者样本与TDx的相关性如下:相关系数r = 0.94,斜率 = 0.93,截距 = 0.11,且Sy/x = 0.19。在0.97 ng/mL和4.50 ng/mL浓度下从血清中的回收率平均为98%。未观察到脂血、黄疸或溶血产生的显著干扰。螺内酯与抗体无交叉反应,而洋地黄毒苷表现出显著的交叉反应。与RIA方法相比,TDx分析法更快、更可靠,并且在这种临床情况下更具成本效益。