Purpose: To develop a novel preparation approach of solid Self-Emulsifying Drug Delivery
System (s-SEDDS) based on spray congealing as potential drug delivery technology for …

The aim of present study was to investigate the impact of various excipients (oil type and
nonionic surfactants) having same composition on physicochemical characterization and …

Aim of present study was to develop solid self micro emulsifying drug delivery system (S-
SEDDS) with Aerosil 200 for enhancement of dissolution rate of model drug Glibenclamide …

Objective: To develop and characterize self-nanoemulsifying drug delivery system
(SNEDDS) of the poorly water-soluble drug, glibenclamide (GBD). Methods: Solubility of …

Self-nanoemulsifying drug delivery systems (SNEDDS) were developed with the objective to
overcome problems associated with the delivery of Gliclazide, a poorly bioavailable, anti …

A solid self-nanoemulsifying drug-delivery system (solid SNEDDS) has been explored to
improve the solubility and dissolution profile of glipizide. SNEDDS preconcentrate was …

The aim of this work was to develop effective fast-dissolving tablet formulations of glyburide,
endowed with improved dissolution and technological properties, investigating the actual …

Context: An adequate drug dissolution behavior is essential for the therapeutic effectiveness
of all solid dosage forms. Objective: To develop a new solid self-micro-emulsifying drug …

Background The present research was aimed to develop a self-microemulsifying drug
delivery system (SMEDDS) pellet to increase the dissolution rate and in vivo hypoglycemic …

Abstract Development of self-nanoemulsifying drug delivery systems (SNEDDS) of
glimepiride is reported with the aim to achieve its oral delivery. Lauroglycol FCC, Tween-80 …