Taylor G, Houston J B
J Pharm Pharmacol. 1983 May;35(5):284-8. doi: 10.1111/j.2042-7158.1983.tb02935.x.
Promethazine blood concentration-time curves have been determined in 7 rabbits following intravenous, oral and hepatic portal vein administration of promethazine. This phenothiazine has a large volume of distribution and a high metabolic clearance resulting in low blood concentrations particularly when the oral route is used. Analysis of the areas under the blood concentration-time curves indicates that hepatic first-pass metabolism is the major determinant of promethazine's low oral availability. Absorption from the gastrointestinal tract is essentially complete in most rabbits and the contribution of metabolism by the intestinal mucosa is minimal. The present findings are compared with the literature on other phenothiazines.
在7只兔子中,分别通过静脉注射、口服和肝门静脉给药后测定了异丙嗪的血药浓度-时间曲线。这种吩噻嗪类药物分布容积大,代谢清除率高,导致血药浓度较低,尤其是采用口服途径给药时。对血药浓度-时间曲线下面积的分析表明,肝脏首过代谢是异丙嗪口服生物利用度低的主要决定因素。在大多数兔子中,胃肠道的吸收基本完全,肠黏膜代谢的贡献最小。将目前的研究结果与其他吩噻嗪类药物的文献进行了比较。