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Mianserin kinetics in depressed patients
Clinical Pharmacology and Therapeutics
|June 1, 1983
Summary
Mianserin kinetics show significant patient variability in plasma levels and elimination half-life. Its pharmacokinetic profile is comparable to tricyclic antidepressants like imipramine and maprotiline.
Area of Science:
- Pharmacology
- Clinical Pharmacy
- Psychopharmacology
Background:
- Mianserin is an antidepressant medication.
- Understanding drug kinetics is crucial for effective treatment.
- Variability in drug metabolism can impact therapeutic outcomes.
Purpose of the Study:
- To investigate the pharmacokinetic profile of mianserin.
- To compare mianserin kinetics with other antidepressant drugs.
Main Methods:
- Single 60 mg dose administration of mianserin to eight depressed inpatients.
- Measurement of plasma mianserin levels over time.
- Analysis of pharmacokinetic parameters including peak plasma levels, elimination half-life, first-pass loss, volume of distribution, and total body clearance.
Main Results:
- Considerable interpatient variability in plasma mianserin levels was observed.
- Mean peak plasma levels were 114 +/- 26 ng/ml, reached between 1-3 hours.
- The mean elimination half-life (t 1/2) was 21.6 +/- 3.1 hours.
- Estimated first-pass loss ranged from 26% to 48% (mean 37%).
- Mean apparent volume of distribution was 15.7 +/- 2.2 l/kg.
- Apparent total body clearance ranged from 0.33 to 0.81 l/hr/kg (mean 0.52 +/- 0.05 l/hr/kg).
Conclusions:
- Mianserin exhibits significant interpatient variability in its pharmacokinetic parameters.
- Mianserin's kinetics are generally similar to tertiary amine tricyclic antidepressants (e.g., imipramine) and the tetracyclic maprotiline.
- These findings contribute to understanding mianserin's behavior in the body and its comparison to other antidepressants.