Piafsky K M, Borgå O
Clin Pharmacol Ther. 1977 Nov;22(5 Pt 1):545-9. doi: 10.1002/cpt1977225part1545.
The protein binding of two basic drugs, alprenolol and imipramine, and the acidic drug, naproxen, was determined in plasma obtained from 23 healthy subjects. A 2-fold variation was found between individuals in the free fraction of the two bases, while the range was even greater with naproxen. The free fraction correlated with the plasma concentration of alpha 1-acid glycoprotein for alprenolol (r = -0.75, p less than 0.001) and imipramine (r = -0.78, p less than 0.001), while there was no correlation for naproxen (r - 0.24, p greater than 0.1). This confirms recent experiments which showed that isolated alpha 1-acid glycoprotein avidly bound both alprenolol and imipramine. Drug binding, however, did not correlate with albumin concentration, although experiments with isolated albumin demonstrated its unusually high affinity for naproxen.
在从23名健康受试者获取的血浆中,测定了两种碱性药物阿普洛尔和丙咪嗪以及酸性药物萘普生的蛋白结合率。发现两种碱性药物的游离分数在个体间存在2倍的差异,而萘普生的差异范围更大。阿普洛尔(r = -0.75,p < 0.001)和丙咪嗪(r = -0.78,p < 0.001)的游离分数与α1-酸性糖蛋白的血浆浓度相关,而萘普生则无相关性(r = 0.24,p > 0.1)。这证实了最近的实验,该实验表明分离出的α1-酸性糖蛋白能 avidly 结合阿普洛尔和丙咪嗪。然而,药物结合与白蛋白浓度无关,尽管分离白蛋白的实验表明其对萘普生具有异常高的亲和力。