Oie S, Levy G
Clin Pharmacol Ther. 1977 May;21(5):627-32. doi: 10.1002/cpt1977215627.
The nonprotein-bound fraction of bilirubin was determined in undiluted plasma or serum from healthy adult volunteers and newborn infants after addition of unconjugated bilirubin, 12 mg/100 ml. There were significant interindividual difference (2-fold in 13 adults, 2.6-fold in 9 full-term newborn infants) in the free fraction value. Sulfisoxazole, salicylic acid, and salicyluric acid had a pronounced displacing effect on bilirubin in the 10 to 30 mg/100 ml drug concentration range. Aspirin had only a small effect at concentrations below 20 mg/100 ml. There was a very strong correlation between the free fraction value of bilirubin in individual samples of drug-free plasma and in the same plasmas after addition of any one of the 4 drugs studied. This shows that the relative increase of the free fraction of bilirubin induced by any one of the drugs was essentially the same but that the absolute increase varied greatly between subjects. It may be possible, therefore, to predict quanitatively the bilirubin-displacing effect of drugs in individual patients before drug administration by determining the free fraction of bilirubin in a plasma or serum sample obtained prior to initiation of drug therapy.
在健康成年志愿者和新生儿的未稀释血浆或血清中加入12mg/100ml未结合胆红素后,测定胆红素的非蛋白结合部分。游离部分的值存在显著的个体间差异(13名成年人中为2倍,9名足月新生儿中为2.6倍)。在10至30mg/100ml的药物浓度范围内,磺胺异恶唑、水杨酸和水杨尿酸对胆红素具有显著的置换作用。阿司匹林在浓度低于20mg/100ml时只有很小的作用。在不含药物的血浆个体样本以及加入所研究的4种药物中任何一种后的相同血浆中,胆红素的游离部分值之间存在非常强的相关性。这表明任何一种药物诱导的胆红素游离部分的相对增加基本相同,但个体间的绝对增加差异很大。因此,在给药前通过测定药物治疗开始前获得的血浆或血清样本中胆红素的游离部分,有可能定量预测个体患者中药物的胆红素置换作用。