Selvig K
Eur J Clin Pharmacol. 1981 Jan;19(2):149-55. doi: 10.1007/BF00568402.
Serum concentrations and urinary excretion of proxyphylline have been measured in five healthy adults after intravenous (29 mumol/kg), single oral (21 mumol/kg) and multiple oral (21 mumol/kg three times a day) doses to produce steady state. The mean peak time after oral administration was 29 min. The mean fraction absorbed was 1.09 calculated from serum concentrations, and 1.05 calculated from urinary excretion of the drug. The apparent volume of distribution was 0.61 1/kg (0.53--0.72 1/kg), 26% higher in males than in females. A two-compartment open model was found to describe the decline in the serum concentrations, giving a mean distribution half-life of 6 min. The intersubject ranges of biological half-life were 8.1--12.1 h and 8.3--12.6 h calculated from serum and urine data, respectively. 24% (18--29%) of the dose was excreted unchanged in urine, which agreed with the relationship between the calculated total body clearance and the renal clearance of the drug.
在五名健康成年人中,分别静脉注射(29 μmol/kg)、单次口服(21 μmol/kg)和多次口服(21 μmol/kg,每日三次)以达到稳态后,测定了茶碱的血清浓度和尿排泄量。口服给药后的平均达峰时间为29分钟。根据血清浓度计算的平均吸收分数为1.09,根据药物尿排泄量计算的平均吸收分数为1.05。表观分布容积为0.61 l/kg(0.53 - 0.72 l/kg),男性比女性高26%。发现用二室开放模型可描述血清浓度的下降情况,平均分布半衰期为6分钟。根据血清和尿液数据计算的生物半衰期的个体间范围分别为8.1 - 12.1小时和8.3 - 12.6小时。24%(18 - 29%)的剂量以原形经尿液排泄,这与计算出的药物总体清除率和肾清除率之间的关系相符。