Oral Delivery (Focus Group – OrD)
Adriana O. Santos, n/a
Assistant Professor
University of Beira Interior
Covilhã, Castelo Branco, Portugal
Nanoemulsions (NE) improve drugs stability and bioavailability through several administration routes by providing solubilization, protection from physiological degradation and facilitating permeation, but do not ensure prolonged drug release [1,2]. Recently, we reported an innovative NE produced by low energy with extreme homogeneity, despite the low percentage of hydrophilic surfactants [2,3]. Envisioning a prolonged release of our NE containing lipophilic drugs, we sought the development of a promising strategy based on the encapsulation of the NE in calcium alginate particles [3].