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 …

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

In the study, self emulsifying drug delivery system (SEDDS) of gliclazide, a poorly soluble
drug, was developed and evaluated by in-vitro, ex-vivo and in-vivo techniques. Oil and …

The objective of this study was to develop a novel solid self-nanoemulsifying drug delivery
system (SNEDDS) using a membrane emulsification technique involving Shirasu porous …

Oral route is preferred for drug administration. More than 40% of New Chemical Entities
exhibit poor aqueous solubility resulting in unsatisfactory oral drug delivery. Low aqueous …

The main objective of drug (s) formulation is to enhance the bioavailability of the drug within
the body. Some of the challenging issues associated with poorly water-soluble drugs …

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 …

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 …

Background The oral route is the most popular route for the clinical administration of drugs to
treat various diseases. Before a drug is absorbed into the blood circulation, it must undergo …