Laurino J P, McKay J, Fischberg E, Schwenzer K, Kaufman R
Department of Pathology, Brown University, Providence, Rhode Island.
Ther Drug Monit. 1994 Jun;16(3):312-5. doi: 10.1097/00007691-199406000-00013.
The performance of the ROCHE FP NAPA reagent, a newly reformulated monoclonal antibody-based fluorescence polarization immunoassay (FPIA) for N-acetylprocainamide, was compared with two commercially available polyclonal antibody-based immunoassays, the Abbott TDx and Syva EMIT. Although excellent correlation was observed between the ROCHE FP NAPA reagent and the Syva EMIT reagent, a positive bias was observed in the correlation between the ROCHE FP NAPA reagent and the Abbott TDx reagent. The bias in the TDx method was investigated further by the concurrent high-performance liquid chromatography (HPLC) analysis of patient samples. Insignificant differences (p < 0.05) were observed between the HPLC and ROCHE FP values. The TDx system, however, yielded significantly higher (p < 0.0005) results than did HPLC.
将罗氏公司新配制的基于单克隆抗体的N - 乙酰普鲁卡因胺荧光偏振免疫分析法(FPIA)即ROCHE FP NAPA试剂的性能,与两种市售的基于多克隆抗体的免疫分析法,即雅培TDx和希瓦EMIT进行了比较。尽管在ROCHE FP NAPA试剂和希瓦EMIT试剂之间观察到了极好的相关性,但在ROCHE FP NAPA试剂和雅培TDx试剂之间的相关性中观察到了正偏差。通过对患者样本同时进行高效液相色谱(HPLC)分析,进一步研究了TDx方法中的偏差。在HPLC和ROCHE FP值之间未观察到显著差异(p < 0.05)。然而,TDx系统产生的结果比HPLC显著更高(p < 0.0005)。