Saliva Concentrations of Disopyramide Cannot Substitute the Drug's Plasma Concentrations
- 30 June 1987
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Analytical Toxicology
- Vol. 11 (4) , 179-181
- https://doi.org/10.1093/jat/11.4.179
Abstract
For many drugs the salivary concentration corresponds to the free plasma drug concentration, which may be more closely related to drug activity or toxicity than the total plasma drug concentration. In this study a preliminary investigation was undertaken to determine the feasibility of monitoring saliva levels of disopyramlde, an antiarrhythmic drug, for clinical and toxicological purposes. Single oral doses of this compound were administered to healthy volunteers. Stimulated mixed saliva and plasma levels were measured by the EMIT technique. The concentrations of disopyramlde in the stimulated mixed saliva tended to be lower than those found in the corresponding plasma sample (fp 0.3–0.5), and the saliva-to-plasma concentration ratio increased with a decreasing salivary pH (pH 6.89, S/P=0.25; pH 8.15, S/P=0.08). The correlation between the saliva and the total plasma concentrations was significant but relatively poor, however. Consequently, mixed salivary disopyramide concentrations are a poor indicator of plasma concentrations, even if correction is made for pH change.This publication has 7 references indexed in Scilit:
- Monitoring Saliva Concentrations of Methaqualone, Codeine, Secobarbital, Diphenhydramine and Diazepam After Single Oral DosesJournal of Analytical Toxicology, 1983
- Saliva Concentrations of Lidocaine and Its Metabolites in ManTherapeutic Drug Monitoring, 1982
- Measurement of Phencyclidine in SalivaJournal of Analytical Toxicology, 1980
- Quantitative High-Performance Liquid-Chromatographic Method for Determining Disopyramide (Norpace) in SerumClinical Toxicology, 1979
- Drug concentration in salivaClinical Pharmacology & Therapeutics, 1978
- Use of saliva in therapeutic drug monitoring.Clinical Chemistry, 1977
- Pharmacokinetic interpretation of data gathered during therapeutic drug monitoring.Clinical Chemistry, 1976