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Published on: November 27, 2016
Comparative Preclinical Pharmacokinetics and Bioavailability of Antidepressant GSB-106 Tablet Form
G B Kolyvanov1, V P Zherdev2, O G Gribakina2
1Laboratory of Pharmacokinetics, Moscow, Russia. litbiopharm@yandex.ru.
The bioavailability of the new antidepressant GSB-106 was studied in rabbits. The tablet form showed a relative bioavailability of over 160%.
Area of Science:
- Pharmacology
- Drug Development
- Biochemistry
Background:
- Antidepressant drug development is crucial for mental health treatment.
- Understanding drug pharmacokinetics is essential for efficacy and safety.
- GSB-106 is a novel compound under investigation for antidepressant properties.
Purpose of the Study:
- To determine the pharmacokinetics of GSB-106 in rabbits.
- To assess the relative bioavailability of an oral tablet formulation of GSB-106 compared to the active pharmaceutical substance.
- To establish a basis for further clinical development of GSB-106.
Main Methods:
- Single oral administration of GSB-106 (pharmaceutical substance and tablet form) to rabbits.
- Blood plasma sampling at determined intervals post-administration.
- Quantification of GSB-106 concentrations using High-Performance Liquid Chromatography (HPLC) coupled with mass spectrometry (MS).
Main Results:
- GSB-106 concentrations in rabbit blood plasma were successfully measured.
- The relative bioavailability of the GSB-106 tablet formulation was calculated to be 160.79% ± 24.33%.
- This indicates enhanced absorption of the tablet form compared to the substance alone.
Conclusions:
- The oral tablet formulation of GSB-106 demonstrates favorable bioavailability in rabbits.
- The pharmacokinetic profile supports further investigation into GSB-106 as a potential oral antidepressant.
- HPLC-MS is a suitable method for quantifying GSB-106 in biological matrices.
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