Introduction: To develop self-emulsifying drug delivery system (SEDDS) of nateglinide to
convert it into solid SEDDS (S-SEDDS) aerosil-200 as adsorbent. Materials and Methods …

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 …

Improvement of bio-availability of poorly water soluble drugs presents one of the furthermost
challenge in drug formulations. One of the most admired and commercially viable …

This study was undertaken to improve solubility and bioavailability of nateglinide by
preparation of stable self-emulsifying solid dispersions (SESDs). The influence of …

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 …

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 objective of the study is to formulate Solid Self Emulsifying Drug Delivery System
(SEDDS) for improvement of solubility and dissolution of poorly water-soluble drug …

The most common route of the drug administration is oral route despite the fact that most
drugs have low oral aqueous solubility and bioavailability especially for BCS class II and …

Objectives: To develop a stable formulation for self emulsifying drug delivery systems
(SEDDS) in order to enhance the solubility, rate and extent of drug release and oral …

In order to compare the effects of a solid carrier on the formulation of a solid self-
microemulsifying drug delivery system (s-SMEDDS), a liquid SMEDDS was prepared with …