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 …

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 current investigation was aimed to improve the solubility of poorly soluble lercanidipine
hydrochloride as self emulsifying powder (SEP). Liquid SEDDS of LCH was formulated with …

Objective: The objective of this work was to improve the solubility and dissolution rate of
Nifedipine by preparing a solid-self micro emulsifying drug delivery system (Solid-smedds) …

Oral bioavailability of drugs is significantly low due to poor solubility. Approximately 40% of
newly discovered drugs are poorly water soluble. To increase the bioavailability, various …

In the current research work, losartan potassium (LP) loaded Self Emulsifying Drug Delivery
System (SEDDS) was formulated using various ratios of lipids, surfactants and co …

The main objective of present work was to prepare a solid SEDDS for enhancement of oral
bioavailability of Valsartan, poorly water soluble drug. The solubility of the drug was …

The present work was aimed at improving dissolution rate of poorly soluble drug nifedipine
by developing and characterizing self-micro emulsifying delivery systems (SMEDDS). The …

The main purpose of this work was to formulate and evaluate co-surfactant free self-
emulsifying drug delivery system (SEDDS) for poorly soluble drug for enhance oral …

Self nano-emulsifying system drug delivery system (SNEDDS) is promising for drugs of BCS
class II. The objective of present study to develop self nano-emulsifying drug delivery system …