Distribution of antidepressants between plasma and red blood cells
Language English Country Sweden Media print
Document type Clinical Trial, Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
16816836
PII: NEL270306A14
Knihovny.cz E-resources
- MeSH
- Antidepressive Agents, Second-Generation blood pharmacokinetics MeSH
- Antidepressive Agents, Tricyclic blood pharmacokinetics MeSH
- Erythrocyte Membrane drug effects metabolism MeSH
- Neurotransmitter Uptake Inhibitors blood pharmacokinetics MeSH
- Plasma metabolism MeSH
- Humans MeSH
- Reference Values MeSH
- Tissue Distribution MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Antidepressive Agents, Second-Generation MeSH
- Antidepressive Agents, Tricyclic MeSH
- Neurotransmitter Uptake Inhibitors MeSH
OBJECTIVE: The distribution of different antidepressants between plasma and red blood cells (RBCs) or between water and erythrocyte membranes (ghosts) has not been sufficiently compared so far. MATERIALS AND METHODS: Distribution of seven antidepressants (amitriptyline, nortriptyline, imipramine, desipramine, didesmethylimipramine, dothiepin, and citalopram) was measured in vitro in small volumes of blood or erythrocyte membrane suspension using radiolabeled drugs. Blood samples were taken from healthy subjects. RESULTS: The distribution of antidepressants between plasma and RBCs is strongly affected by temperature; however, it does not depend on the antidepressant concentration in the range of their therapeutic concentrations. The data analysis proved that the ratio of RBCs to plasma volume concentrations is the suitable parameter characterizing antidepressant distribution in whole blood. Significantly higher ratios of RBCs to plasma concentrations were found for demethylated metabolites of tricyclic antidepressants and in the case of citalopram. Citalopram showed the highest accumulation in intact RBCs and at the same time the lowest binding to isolated membranes. The binding of drugs to isolated erythrocyte membranes was much higher than in whole blood. CONCLUSION: The concentration ratio of antidepressant in RBCs and in plasma is sensitive not only to the binding properties of plasma proteins and cell membranes, but also to changes in drug molecule, both in aminopropyl chain and in aromatic rings. This ratio is to a large extent characteristic of a particular antidepressant.
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