Skin and Mucosal Delivery (Focus Group – SMD)
Katie Ollerton, n/a
Ms
University of Liverpool
Liverpool, England, United Kingdom
Nanoformulation of non-water soluble, lipophilic Docetaxel (DCTX) into solid drug nanoparticles (SDNs) allows the generation of an aqueous dispersion to facilitate its transdermal delivery (TD).1 To reduce reliance on biological tissue in such TD studies, in vitro skin mimics such as Strat-M, are increasingly used.2 However, their ability to predict the permeation of nanoformulated actives within complex formulations remains uncertain. Radioanalytics were used to conduct comparative permeation experiments through Strat-M and human skin to assess the model’s predictive capabilities.