Wallace S, Brodie M J
Eur J Clin Pharmacol. 1976 Mar 22;09(5-6):429-32. doi: 10.1007/BF00606560.
The binding of 3 drugs to serum proteins of patients with chronic hepatic disease has been studied by an ultrafilitration technique, and compared to that of normal subjects. The binding of phenylbutazone was reduced in all patients, salicylate in patients with inactive liver disease and sulphadiazine in patients whose disease was active. Analysis of binding data showed a real reduction in the capacity of albumin to bind the drugs in the majority of patients. Addition of bilirubin to normal plasma caused a reduction in sulphadiazine binding, but had no effect on the binding of salicylate or phenylbutazone. The possible causes of this reduction in binding are discussed.
采用超滤技术研究了三种药物与慢性肝病患者血清蛋白的结合情况,并与正常受试者进行了比较。所有患者中保泰松的结合率均降低,非活动性肝病患者中水杨酸盐的结合率降低,而活动性肝病患者中磺胺嘧啶的结合率降低。结合数据的分析表明,大多数患者中白蛋白结合药物的能力确实下降。向正常血浆中添加胆红素会导致磺胺嘧啶结合率降低,但对水杨酸盐或保泰松的结合没有影响。讨论了结合率降低的可能原因。