Background High lipophilicity and poor aqueous solubility are the endemic problems of new
drug molecules. Sixty to seventy percent of these drugs are unable to solubilize completely …

Self-emulsifying drug delivery systems (SEDDSs) originated as an oral lipid-based drug
delivery system with the sole purpose of improving delivery of highly lipophilic drugs …

Aim To evaluate the impact of the surface decoration of cannabidiol (CBD) loaded self-
emulsifying drug delivery systems (SEDDS) on the efficacy of the formulations to cross the …

Resveratrol is a promising neuroprotective agent against neurodegenerative disorders such
as Alzheimer's disease. Resveratrol-loaded transferosomes and nanoemulsions were …

In the present study, various surfactants were combined with insulin (INS), bovine serum
albumin (BSA) and horseradish peroxidase (HRP) via hydrophobic ion pairing to increase …

A quality-by-design and characterization approach was followed to ensure development of
self-emulsifying drug delivery systems (SEDDSs) destined for topical delivery of the highly …

Aim Evaluation of different polyhydroxy surfaces in SEDDS to overcome the limitations
associated with conventional polyethylene glycol (PEG)-based SEDDS surfaces for …

It was the aim of this study to evaluate the potential of reverse micelles (RM) and
hydrophobic ion pairs (HIP) for incorporation of semaglutide into self-emulsifying oral drug …

Self-emulsifying drug delivery systems (SEDDS) are lipid-based isotropic mixtures that
enhance the bioavailability of poorly water-soluble drugs and reduce the possible side …

To date, buccal administration of lipophilic drugs is still a major challenge due to their poor
solubility in saliva and limited penetration into mucosal tissues. To overcome these …