| Literature DB >> 7324829 |
J Kanto, R Virtanen, E Iisalo, K Mäenpää, P Liukko.
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.Entities:
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Year: 1981 PMID: 7324829 DOI: 10.1111/j.1399-6576.1981.tb01613.x
Source DB: PubMed Journal: Acta Anaesthesiol Scand ISSN: 0001-5172 Impact factor: 2.105