Roberts W L, Annesley T M, De B K, Moulton L, Juenke J M, Moyer T P
Department of Pathology at University of Utah Health Sciences Center, Salt Lake City, USA.
Ther Drug Monit. 2001 Apr;23(2):148-54. doi: 10.1097/00007691-200104000-00009.
The measurement of the unbound or free phenytoin concentration is indicated in several situations, including uremia. In patients with uremia, metabolites of phenytoin and other substances accumulate and can displace phenytoin from its protein binding sites, with a consequent increase in the free fraction of drug. Some of the phenytoin metabolites that accumulate in uremia can cross-react with phenytoin immunoassays. In this study the authors evaluated four free phenytoin immunoassays compared with a high-performance liquid chromatography (HPLC) method: the Roche COBAS Integra, the Syva EMIT 2000, the Opus INNOFLUOR, and the Abbott TDx. All four methods demonstrated good precision, with interday coefficients of variation of < or = 5% and comparable recoveries using quality control material. Two of the methods, the EMIT 2000 and COBAS Integra, showed excellent agreement with the HPLC method using samples from patients both with normal renal function and with renal insufficiency. The other two methods, the INNOFLUOR and TDx, showed average positive biases for the therapeutic range of 3-7% and 21-22%, respectively, compared with the HPLC method for samples from patients with normal renal function, and average positive biases of 24-32% and 75-81%, respectively, with samples from patients with uremia.
在几种情况下需要测定游离苯妥英浓度,包括尿毒症。在尿毒症患者中,苯妥英及其他物质的代谢产物会蓄积,并可将苯妥英从其蛋白质结合位点上置换出来,从而导致药物的游离分数增加。一些在尿毒症中蓄积的苯妥英代谢产物可与苯妥英免疫测定法发生交叉反应。在本研究中,作者评估了四种游离苯妥英免疫测定法,并与高效液相色谱(HPLC)法进行比较:罗氏COBAS Integra、Syva EMIT 2000、Opus INNOFLUOR和雅培TDx。所有四种方法均显示出良好的精密度,日间变异系数≤5%,并且使用质控材料时回收率相当。其中两种方法,即EMIT 2000和COBAS Integra,在使用肾功能正常和肾功能不全患者的样本时,与HPLC法显示出极好的一致性。另外两种方法,即INNOFLUOR和TDx,与HPLC法相比,对于肾功能正常患者样本的治疗范围平均正偏差分别为3 - 7%和21 - 22%,对于尿毒症患者样本的平均正偏差分别为24 - 32%和75 - 81%。