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单次母体静脉注射和肌肉注射后阿托品的胎盘转运及药代动力学

Placental transfer and pharmacokinetics of atropine after a single maternal intravenous and intramuscular administration.

作者信息

Kanto J, Virtanen R, Iisalo E, Mäenpää K, Liukko P

出版信息

Acta Anaesthesiol Scand. 1981 Apr;25(2):85-8. doi: 10.1111/j.1399-6576.1981.tb01613.x.

Abstract

The placental transfer and pharmacokinetics of atropine were studied in 44 healthy parturients undergoing caesarean section. The concentrations in the plasma were determined by a new radioimmunoassay after intravenous (n=32) or after intramuscular (n=12) administration of 0.01 mg/kg of atropine. A fast placental transfer with apparent foetal uptake of the drug was found after intravenous injection. There was also a difference in the umbilical vein and artery concentrations after intramuscular administration. The maternal pharmacokinetics of i.v. atropine obeyed and two-compartment open model with a fast distribution phase (mean ta1/2=1.02 min) and quite fast elimination (t1/2=2.56h). The total apparent volume of distribution was 1.01/kg and the total plasma clearance 6.36 ml/min/kg. The mean peak maternal plasma levels after i.m. atropine administration were found at 1.59 h and the mean calculated half-life of elimination was then 2.1 h. No atropine was found in the amniotic fluid.

摘要

在44例接受剖宫产的健康产妇中研究了阿托品的胎盘转运和药代动力学。静脉注射(n = 32)或肌肉注射(n = 12)0.01mg/kg阿托品后,采用一种新的放射免疫分析法测定血浆浓度。静脉注射后发现药物有快速的胎盘转运及明显的胎儿摄取。肌肉注射后脐静脉和脐动脉的浓度也存在差异。静脉注射阿托品的母体药代动力学符合二室开放模型,分布相快(平均tα1/2 = 1.02分钟),消除较快(t1/2 = 2.56小时)。总表观分布容积为1.01/kg,血浆总清除率为6.36ml/(分钟·kg)。肌肉注射阿托品后母体血浆平均峰值出现在1.59小时,计算得出的平均消除半衰期为2.1小时。羊水中未发现阿托品。

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