| Literature DB >> 7061181 |
M L Aitio, R Virtanen, R Lammintausta.
Abstract
The saliva and plasma concentrations of disopyramide and its main metabolite, mono-N-dealkyldisopyramide, and the protein binding of disopyramide were studied in ten healthy volunteers after a single oral 400-mg dose of disopyramide. Disopyramide had a concentration-dependent inhibitory effect on the salivary flow rate. The correlations between the salivary and total plasma concentrations of disopyramide (r = 0.774 linear, 0.890 exponential, p less than 0.0001), of the metabolite (r - 0.700, p less than 0.001), and between the salivary and free plasma concentrations of disopyramide (r = 0.785, p less than 0.001) were relatively good. The fraction of disopyramide not bound to plasma proteins varied from not measurable to 0.35, was concentration-dependent, and showed intersubject variation. The ratio of disopyramide concentrations in saliva and plasma (S/P ratio) varied from 0.08 to 1.51 and was highest when the salivary and plasma levels were high. No significant correlation existed between S/P ratio and salivary pH, and the correlation was poor (r = 0.546) between the measured salivary concentrations and those calculated theoretically. A wide interindividual variation was seen in all parameters measured. The salivary concentrations of disopyramide are unreliable for predicting the corresponding total or free plasma concentrations.Entities:
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Year: 1982 PMID: 7061181
Source DB: PubMed Journal: Int J Clin Pharmacol Ther Toxicol ISSN: 0174-4879