Disposition of pethidine in man under acidic urinary PH. I. Plasma level and urinary elimination of pethidine and norpethidine.

K Chan
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引用次数: 3

Abstract

A detailed study on the plasma and urine levels of pethidine and its major basic metabolite, norpethidine, was carried out after intravenous and oral administration of pethidine, under conditions of controlled acidic urinary pH, to two healthy subjects who had previously shown significant difference in the urinary recovery of pethidine after the intramuscular administration of a standard dose. Utilizing the data of area under plasma concentration-time curve and cumulative urinary excretion of pethidine, similar values of renal clearance of the drug were obtained after separate intravenous and oral administration to the same subject. There is an overall difference in the renal clearance and metabolic pattern of the drug between these two subjects under conditions of controlled acidic urinary pH. It is postulated that variation in the overall elimination of pethidine and other weakly basic drugs can only be elucidated under conditions and may be interpreted in terms of differences in the renal clearance and hepatic biotransformation of the drug.

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酸性尿ph下哌替啶在人体内的分布。血浆水平和尿中哌替啶和去甲哌替啶的消除。
在控制尿液酸性pH值的条件下,静脉和口服哌替啶后,对两名健康受试者进行了哌替啶及其主要基础代谢物去甲哌替啶的血浆和尿液水平的详细研究,这两名受试者在肌肉注射标准剂量哌替啶后尿恢复有显著差异。利用哌替啶的血药浓度-时间曲线下面积和尿累积排泄数据,对同一受试者分别静脉给药和口服给药后,获得了相似的肾脏清除率。在控制酸性尿ph的条件下,这两名受试者对药物的肾脏清除率和代谢模式存在总体差异。我们假设,只有在这种条件下才能阐明哌替啶和其他弱碱性药物的整体消除的差异,并可能通过药物的肾脏清除率和肝脏生物转化的差异来解释。
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