Ara K, Ahmad K
Bangladesh Med Res Counc Bull. 1980 Dec;6(2):39-44.
The time- and dose-dependent uptake of paracetamol into the brain and liver of rats was investigated and correlated with the serum levels of the drug. The results showed a rapid entry of paracetamol into the brain and liver: peak concentration of the drug was reached in these organs at 45 min after oral administration. The concentrations in the brain and liver were significantly higher (P less than 0.01) than in serum. The quick attainment of high concentration in the liver may explain the rapid onset of hepatotoxicity with a single large dose of the drug.
研究了对乙酰氨基酚在大鼠脑和肝脏中的时间和剂量依赖性摄取,并将其与药物的血清水平相关联。结果显示对乙酰氨基酚迅速进入脑和肝脏:口服给药后45分钟,这些器官中药物达到峰值浓度。脑和肝脏中的浓度显著高于血清中的浓度(P小于0.01)。肝脏中迅速达到高浓度可能解释了单次大剂量药物导致肝毒性迅速发作的原因。