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

The objective of the present investigation was to develop and characterize the self-
nanoemulsifying drug delivery system (SNEDDS) of glimepiride, a poorly soluble drug …

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

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 objective of the present study was to improve solubility, dissolution rate and therapeutic
efficacy of a BCS Class II drug, glibenclamide by using oral self nano emulsifying powder …

The primary object of self-nanoemulsifying drug delivery system (SNEDDS) is to enhance
the oral bioavailability of poorly water soluble drugs. The major problem in oral formulations …

The current investigation was aimed to improve the solubility of poorly soluble drug,
cilostazol (CLZ). Self-nanoemulsifying drug delivery system (SNEDDS) composed of oil …

Surface adsorbed chitosan-loaded solid self-nanoemulsifying drug delivery system (S-
SNEDDS) of glibenclamide (GBN) was developed. Low cost coffee husk was investigated as …

The oral drug delivery is fraught with low and erratic bioavailability owing to enzymatic
degradation of drug, poor permeability, poor solubility and dissolution, intestinal efflux and …

The aim of study was to develop self-nanoemulsifying pellets (SNEP) for oral delivery of
poorly water soluble drug, repaglinide (RPG). Solubility of RPG in oily phases and …