The main objective of this study was to prepare a solid self-microemulsifying drug delivery
system (S-SMEDDS) by spray drying liquid SMEDDS with an inert solid carrier Aerosil 200 …

The current research aims to improve the solubility of the poorly soluble drug, ie, ibuprofen,
by developing self-emulsifying drug delivery systems (SEDDS) utilizing a twin screw melt …

The objective of the present study was to design and optimized chlordiazepoxide solid self
microemulsifying drug delivery system prepared via spray drying for oral administration …

Objective: Gliclazide (GCZ) is a widely prescribed anti-diabetic drug belongs to class IΙ
under BCS and exhibit low and variable oral bioavailability due to its poor aqueous …

The aim of this study was to develop self emulsifying drug delivery systems (SEDDS) of
glipizide and to convert it into solid SEDDS (S-SEDDS) using Syloid® 244 FP as adsorbent …

A solid self emulsifying formulation (S-SEF) has been developed with an intention to
improve the dissolution characteristics of poorly water soluble lercanidipine hydrochloride …

The objective of the present study was to develop a self micro-emulsifying drug delivery
system (SMEDDS) of chlorthalidone (CTD) to improve its solubility and dissolution. CTD is a …

The aim of the present study was to develop a novel semi-solid self-microemulsifying drug
delivery system (SMEDDS) using Gelucire® 44/14 as oil with strong solid character to …

Objectives: To formulate a poorly water-soluble, antidiabetic drug, gliclazide, in the
vegetable oil-based self-emulsifying delivery system (SEDDS), as a trial to improve its …