Abstract
Morphine is used as an anesthetic supplement. Its disposition in surgical patients under enflurane-nitrous oxide anesthesia has not been determined. Available data on morphine concentrations in plasma after equivalent i.v. doses are conflicting, possibly as a result of varying degrees of specificity of the analytical methods for the unchanged, pharmacologically active form of the drug. This study determined the pharmacokinetics of morphine (0.05, 0.1, 0.14 or 0.2 mg/kg) injected i.v. in 10 surgical patients anesthetized with enflurane-N2O-O2. Arterial plasma was analyzed for unchanged morphine and conjugated morphine. Specificity of the analytical procedure for unchanged morphine was achieved by the combination of solvent extraction and radioimmunoassay techniques. Kinetic indices were derived by nonlinear least-squares analysis of log concentration (ng/ml) vs. time relationships. Morphine disposition was independent of dose in this 4-fold range and was best described by a 3-compartment model with a mean elimination half-time (t1/2.beta.) of 104 .+-. 5 min. The apparent volumes of distribution (Vd) and of the central compartment (Vl) were 3.4 .+-. 0.2 and 0.13 .+-. 0.02 l/kg, respectively, while the clearance (ClB) was 23 .+-. 1 ml/min per kg. Extraction of morphine by the liver appeared to be complete. Conjugated morphine was eliminated from plasma with a t1/2.beta. of 169 .+-. 15 min. The ultimate elimination of morphine from the body was dependent upon its reuptake from slowly perfused peripheral tissues, k10 > k31 (P < 0.001).