Perucca E
Ther Drug Monit. 1980;2(4):331-44.
It is generally accepted that only the unbound drug in plasma is in equilibrium with drug in the biophase. Under these circumstances, routine measurement of total drug levels in plasma can be justified only if the interpatient variability in protein binding is small. In the case of phenytoin, this is not always true. Important alterations in the plasma protein binding of phenytoin may occur in the perinatal period, in late pregnancy, in hepatic disease, in renal failure, in the nephrotic syndrome and other conditions associated with hypoalbuminemia, and in the presence of displacing agents such as valproic acid, phenylbutazone, and salicylic acid. Changes in protein binding may alter substantially the relationship between the plasma concentration of total drug and the magnitude of pharmacological effect. This possibility needs to be taken into account when interpreting serum phenytoin levels in clinical practice.
一般认为,只有血浆中游离的药物才与生物相中药物处于平衡状态。在这种情况下,只有当患者间蛋白质结合的变异性较小时,常规测量血浆中总药物水平才合理。就苯妥英而言,情况并非总是如此。苯妥英血浆蛋白结合的重要改变可能发生在围产期、妊娠晚期、肝脏疾病、肾衰竭、肾病综合征以及其他与低白蛋白血症相关的疾病中,以及存在如丙戊酸、保泰松和水杨酸等置换剂的情况下。蛋白质结合的变化可能会显著改变总药物血浆浓度与药理效应大小之间的关系。在临床实践中解读血清苯妥英水平时需要考虑到这种可能性。