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药物蛋白结合与肾病综合征

Drug protein binding and the nephrotic syndrome.

作者信息

Gugler R, Azarnoff D L

出版信息

Clin Pharmacokinet. 1976;1(1):25-35. doi: 10.2165/00003088-197601010-00003.

Abstract

A reduction in plasma albumin concentration, as seen in patients with the nephrotic syndrome, is usually associated with a decrease in plasma protein binding of highly bound drugs. Therefore, the fraction of the unbound drug increases, but the absolute free concentration remains essentially unchanged due to a compensatory reduction in the steady state total plasma concentration. With phenytoin, protein binding and plasma albumin concentration are closely related, so that the degree of binding can be estimated without specific binding techniques. To be able to correctly interprete plasma levels the degree of protein binding should be known, since a reduced total concentration may be fully effective, if the free drug fraction is increased in hypoalbuminaemic patients. Although the mean steady state plasma concentration of highly bound drugs is not affected in the nephrotic syndrome, a greater fluctuation of the unbound level is observed between doses, offering a possible explanation for the increased incidence of toxicity in hypoalbuminaemic patients. As a consequence, shorter dosing intervals of these drugs seems to be advisable, rather than a reduction in the total daily dose. Reduced protein binding is accompanied by an increase in the total plasma clearance which is a function of the elimination rate constant and the volume of distribution.

摘要

正如在肾病综合征患者中所见,血浆白蛋白浓度降低通常与高度结合药物的血浆蛋白结合减少有关。因此,未结合药物的比例增加,但由于稳态总血浆浓度的代偿性降低,绝对游离浓度基本保持不变。对于苯妥英,蛋白结合与血浆白蛋白浓度密切相关,因此无需特定的结合技术即可估计结合程度。为了能够正确解释血浆水平,应了解蛋白结合程度,因为在低白蛋白血症患者中,如果游离药物比例增加,总浓度降低可能仍具有充分疗效。虽然肾病综合征中高度结合药物的平均稳态血浆浓度不受影响,但在给药间隔期间观察到游离水平有更大波动,这可能解释了低白蛋白血症患者中毒发生率增加的原因。因此,这些药物似乎建议采用更短的给药间隔,而不是减少每日总剂量。蛋白结合减少伴随着总血浆清除率增加,总血浆清除率是消除速率常数和分布容积的函数。

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