Oral Delivery
Oral lipid-based drug delivery systems, especially self-nanoemulsifying drug delivery systems (SNEDDS) are able to increase absorption of poorly soluble drugs. SNEDDS are isotropic systems based on lipids and surfactants and form nanoemulsion droplets upon dispersion in aqueous media. For many BCS Class 2 or 4 drugs, however, the solubility in SNEDDS is low, thus reducing the potential of using SNEDDS, due to the large amount of lipid that has to administered with the drug dose. The aim was to assess the effect of increasing the apparent solubility of drugs in SNEDDS by different means.
Anette Müllertz, n/a (she/her/hers)
Professor
University of Copenhagen
Copenhagen, Hovedstaden, Denmark