Roberts W L, Rainey P M
Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06510.
Clin Chem. 1993 Sep;39(9):1872-7.
Accumulation of phenytoin metabolites in uremia has been shown to interfere with some immunoassay methods for phenytoin measurement. We evaluated the effects of uremia (serum creatinine > 13 mg/L) on free and total phenytoin concentrations measured by the Abbott TDx fluorescence polarization immunoassay, and the DuPont aca and Syva EMIT homogeneous enzyme-multiplied immunoassay methods, using HPLC as the comparison method. In uremic patients, the TDx assay showed both fixed and proportional bias in comparison with the HPLC for both total phenytoin concentration (TDx = 1.24 x HPLC + 1.9 mg/L) and free phenytoin concentration (TDx = 1.52 x HPLC + 0.24 mg/L). The total bias was as great as 100% for both total and free phenytoin. Cross-reactive substances other than 5-(p-hydroxyphenyl)-5-phenylhydantoin (HPPH) and HPPH-glucuronide appeared to be responsible. In contrast, there was minimal interference with aca and EMIT assays.
已证实在尿毒症患者体内苯妥英代谢物的蓄积会干扰某些用于测定苯妥英的免疫分析方法。我们以高效液相色谱法(HPLC)作为对照方法,评估了尿毒症(血清肌酐>13mg/L)对采用雅培TDx荧光偏振免疫分析法、杜邦aca和Syva EMIT均相酶放大免疫分析法所测定的游离及总苯妥英浓度的影响。在尿毒症患者中,与HPLC相比,TDx分析法在总苯妥英浓度(TDx = 1.24×HPLC + 1.9mg/L)和游离苯妥英浓度(TDx = 1.52×HPLC + 0.24mg/L)方面均显示出固定偏差和比例偏差。总偏差和游离苯妥英的偏差高达100%。除5 -(对羟基苯基)-5-苯乙内酰脲(HPPH)和HPPH - 葡萄糖醛酸苷外的交叉反应物质似乎是造成偏差的原因。相比之下,aca和EMIT分析所受干扰极小。