Introduction: Oral administration of most therapeutic peptides and proteins is mainly
restricted due to the enzymatic and absorption membrane barrier of the GI tract. In order to …

Objective: The aim of this study was to develop self-emulsifying drug delivery systems
(SEDDS) for oral delivery of therapeutic proteins through hydrophobic ion pairing. Method …

Aim The aim of this study was to evaluate the protective effect of self-emulsifying drug
delivery systems (SEDDS) for therapeutic peptides towards intestinal proteases and …

Introduction: Oral administration of a drug is the most common, ideal and preferred route of
administration. The main problem of oral drug formulations is their low bioavailability arises …

One of the biggest challenges confronting the contemporary drug delivery science today is
to improve on the oral bioavailability of a vast number of drugs exhibiting poor and …

It was the aim of this study to evaluate the impact of lipases on the release behaviour of a
peptide drug from oral self-nanoemulsifying drug delivery systems. Octreotide was ion …

The aim of the study was to create a self-emulsifying drug delivery system (SEDDS) with
mucolytic properties based on incorporated papain for improved mucus permeation. In order …

Aim It was the aim of this study to evaluate the mucus permeating properties of self-
emulsifying drug delivery systems (SEDDS) exhibiting different size and zeta potential …

Since the development of self-emulsifying drug delivery systems (SEDDS) in 1980's, they
attract the attention of researchers in order to confront the challenge of poor water-solubility …

Self-emulsifying drug delivery systems (SEDDS) have been widely employed to improve the
oral bioavailability of poorly soluble drugs. In the past few years, SEDDS were extensively …