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 self emulsifying drug delivery system (SEDDS) is considered to be the novel technique
for the delivery of lipophillic plant actives. The self emulsifying (SE) formulation significantly …

Solubility is one of the most important parameter to achieve desired concentration of drug in
systemic circulation for therapeutic response. As a consequence of modern drug discovery …

The main object of the self-emulsifying drug-delivery system (SEDDS) is oral bioavailability
(BA) enhancement of a poorly water-soluble drug. Low aqueous solubility and low oral BA …

The oral delivery of lipophilic drugs presents a major challenge because of the low aqueous
solubility and less bioavailability. Self-micro emulsifying drug delivery systems (SMEDDSs) …

Introduction: Oral administration of a drug is the most common, ideal and preferred route of
administration. The main problem of oral drug formulations is their low bioavailability arises …

The oral route is one of the most preferred ways for chronic drug therapy; but the drug
dissolution is usually a rate determining step of the absorption processes for poorly water …

The oral delivery of hydrophobic drug presents a major challenge because of the low
aqueous solubility of such compounds. Self-emulsifying/microemulsifying drug delivery …

Self-emulsifying drug delivery system (SEDDS) is an isotropic mixture of lipid, surfactant and
co-surfactant, which forms a fine emulsion when comes in contact of an aqueous medium …

In modern drug discovery techniques, there has been a consistent increase in the number of
poor water soluble drug candidate compounds, and currently more than 50% of new …