General theory for rapidly establishing steady state drug concentrations using two consecutive constant rate intravenous infusions
- 1 January 1975
- journal article
- Published by Springer Nature in European Journal of Clinical Pharmacology
- Vol. 9 (2-3) , 235-238
- https://doi.org/10.1007/bf00614023
Abstract
Steady state plasma drug concentrations can be achieved rapidly and safely by a drug input mode consisting of two consecutive constant rate intravenous infusions. A general method for calculating the relative rates of the two infusions is presented. The derivation is independent of the concepts of compartmental distribution and elimination of drugs within the body.Keywords
This publication has 15 references indexed in Scilit:
- Pharmacokinetics of pentazocine in the rhesus monkeyJournal of Pharmaceutical Sciences, 1974
- Pharmacokinetics of intravenous theophyllineClinical Pharmacology & Therapeutics, 1973
- The pharmacokinetics of inulin and urea: a comparison of the dose eliminated from a compartmental model and that eliminated in urineJournal of Pharmacy and Pharmacology, 1972
- General Treatment of Linear Mammillary Models with Elimination from any Compartment as Used in PharmacokineticsJournal of Pharmaceutical Sciences, 1972
- Pharmacokinetics of absorption, distribution and elimination of fenfluramine and its main metabolite in manJournal of Pharmacy and Pharmacology, 1972
- Pharmacokinetic Aspects of Intravenous Regional AnesthesiaAnesthesiology, 1971
- Pharmacokinetics of lidocaine in manClinical Pharmacology & Therapeutics, 1971
- Digoxin Metabolism in the ElderlyCirculation, 1969
- Some Pharmacokinetic Aspects of 5-(Dimethyltriazeno)-imidazole-4-carboxamide in the DogJournal of Pharmaceutical Sciences, 1968
- Comparative Pharmacokinetics of Coumarin Anticoagulants IVJournal of Pharmaceutical Sciences, 1968