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荧光偏振免疫分析法与液相色谱法对尿液中普鲁卡因胺和N-乙酰普鲁卡因胺定量分析的比较。

Comparison of fluorescence polarization immunoassay with liquid chromatography for quantification of procainamide and N-acetylprocainamide in urine.

作者信息

Tisdale J E, Padhi I D, Ware J A, Svensson C K

机构信息

Department of Pharmacy Practice, Wayne State University, Detroit, Michigan 48202, USA.

出版信息

Ther Drug Monit. 1996 Dec;18(6):693-7. doi: 10.1097/00007691-199612000-00011.

Abstract

The objective of this study was to compare the precision and accuracy of fluorescence polarization immunoassay (FPIA) with high-performance liquid chromatography (HPLC) for measurement of procainamide (PA) and N-acetylprocainamide (NAPA) concentrations in urine. To determine the correlation between FPIA and HPLC, urine PA and NAPA concentrations were assayed using both techniques in samples obtained from study patients receiving PA and in spiked samples. In samples from patients, FPIA-determined PA and NAPA concentrations were 19 +/- 9% lower and 28 +/- 31% higher, respectively, than those determined by HPLC. The slope of the FPIA-HPLC regression lines for PA and NAPA differed significantly from that of the line of unity (the slope that would result if FPIA and HPLC yielded identical concentrations). In spiked samples, FPIA-determined PA and NAPA concentrations were 15 +/- 2% and 11 +/- 2% lower than HPLC-determined concentrations, respectively, and the slopes of the FPIA-HPLC regression lines differed significantly from the line of unity. Therefore, FPIA cannot be recommended as a urine assay method when quantitative assessment of urine PA or NAPA excretion is needed for pharmacokinetic studies.

摘要

本研究的目的是比较荧光偏振免疫分析法(FPIA)与高效液相色谱法(HPLC)在测定尿液中普鲁卡因胺(PA)和N - 乙酰普鲁卡因胺(NAPA)浓度时的精密度和准确性。为了确定FPIA与HPLC之间的相关性,在接受PA治疗的研究患者的样本以及加标样本中,使用这两种技术测定尿液中PA和NAPA的浓度。在患者样本中,FPIA测定的PA和NAPA浓度分别比HPLC测定的浓度低19±9%和高28±31%。PA和NAPA的FPIA - HPLC回归线斜率与单位线(如果FPIA和HPLC产生相同浓度时的斜率)有显著差异。在加标样本中,FPIA测定的PA和NAPA浓度分别比HPLC测定的浓度低15±2%和11±2%,且FPIA - HPLC回归线斜率与单位线有显著差异。因此,当药代动力学研究需要对尿液中PA或NAPA排泄进行定量评估时,不推荐将FPIA作为尿液检测方法。

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