Skin and Mucosal Delivery (Focus Group – SMD)
Barbara Mikolaszek, n/a
PhD
Medical University og Gdansk
Gdansk, Pomorskie, Poland
The diffusivity of pressure-sensitive adhesive (PSA) matrix is considered as a crucial parameter for the transdermal delivery system (TDS) performance. While incorporating excipients into the polymer matrix is a conventional strategy for modifying active pharmaceutical ingredient (API) release kinetics and skin permeation, this approach is often limited by complex excipient-PSA-drug interactions and effects physicochemical stability or mechanical properties (peel adhesion or tack) [1,2]. The present study evaluates matrix surface microstructure as a formulation parameter to modulate the in vitro and in vivo biopharmaceutical performance of transdermal patch.