Nau H, Luck W, Kuhnz W
Br J Clin Pharmacol. 1984 Jan;17(1):92-8. doi: 10.1111/j.1365-2125.1984.tb05006.x.
The protein binding of diazepam (D) and its major active metabolite N-desmethyl diazepam (DD) was investigated in vitro in the serum of 14 mothers at birth, 21 foetuses at birth, in 100 neonates between 1 and 11 days of age and in 16 control subjects. The free (unbound) fractions of D and DD in the foetus were similar to those in the controls, but lower than those in the mothers. During the first day of life the free fractions of D and DD doubled in the neonates and subsequently declined slowly to reach near control levels at 1 week of age. The sharp increase and slow decrease of the free fractions of D and DD during the first postnatal week was closely paralleled by sharply increasing and decreasing free fatty acid (FFA) concentrations. Bilirubin and albumin levels were of lower importance in regard to the protein binding of D and DD. These results indicate that the greatly increased FFA levels shortly after birth result in increased free fractions of D and DD. Because of the known immaturity of the neonatal hepatic elimination capacity, these elevated free fractions may result in elevated free concentrations of the two compounds, which may help to explain the adverse effects observed clinically in some D-exposed neonates.
在体外研究了地西泮(D)及其主要活性代谢物N-去甲基地西泮(DD)在14例分娩时母亲的血清、21例分娩时胎儿的血清、100例1至11日龄新生儿的血清以及16例对照受试者血清中的蛋白结合情况。胎儿体内D和DD的游离(未结合)部分与对照组相似,但低于母亲体内的游离部分。在出生后的第一天,新生儿体内D和DD的游离部分增加了一倍,随后缓慢下降,在1周龄时接近对照水平。出生后第一周内D和DD游离部分的急剧增加和缓慢下降与游离脂肪酸(FFA)浓度的急剧上升和下降密切平行。胆红素和白蛋白水平对D和DD的蛋白结合影响较小。这些结果表明,出生后不久FFA水平的大幅升高导致D和DD的游离部分增加。由于已知新生儿肝脏消除能力不成熟,这些升高的游离部分可能导致这两种化合物的游离浓度升高,这可能有助于解释临床上在一些暴露于D的新生儿中观察到的不良反应。