Olanzapine Plexis formulation release data
Olanzapine particles were coated with successive laminations of biocompatible polymers. The final formulation (filled triangles) consists of a “sandwich” of polymers. The apparent half life of dissolution is ca. 10 days.
In vitro release of olanzapine formulations
These “sandwich” coated particles (6mg) were injected subcutaneously into Sprague-Dawley rats (n=6). Serum samples (open circles) were taken at times indicated and HPLC performed.
For reference, data from Aravigiri et al showing PK after oral dosing in rats (closed circles) is shown.
