Phenacetin concentrations in portal and hepatic venous blood in man.

T Inaba, W A Mahon, R M Stone
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Abstract

After intra-gastric or intra-duodenal administration of phenacetin (200 mg in solution), concentrations of phenacetin and its 0-dealkylated metabolite, acetaminophen, in portal and hepatic veins and in peripheral blood were monitored. A sharp increase in the portal concentration of phenacetin indicated rapid absorption. The concentration ratio of acetaminophen to phenacetin in early portal blood was 0.01--0.11 and lower than the ratio in hepatic vein. The hepatic extraction ratio of phenacetin was calculated to be 0.59--0.78. It is concluded that 0-dealkylation occurs mainly in the liver and only to a limited extent in the gastrointestinal wall.

非那西丁在人门静脉和肝静脉血中的浓度。
胃内或十二指肠内给药非那西丁(溶液200 mg)后,监测非那西丁及其0-脱烷基代谢物对乙酰氨基酚在门脉、肝静脉和外周血中的浓度。非那西丁门静脉浓度急剧升高表明吸收迅速。早期门静脉血对乙酰氨基酚与非那西丁的浓度比为0.01 ~ 0.11,低于肝静脉的浓度比。经计算,非那西丁的肝提取比为0.59 ~ 0.78。由此可见,0-脱烷基主要发生在肝脏中,仅在肠壁中有少量发生。
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