Many articles have been published in the last two decades demonstrating improvement in the dissolution and absorption of low solubility drugs when formulated into self-emulsifying drug delivery systems (SEDDS). Several such pharmaceutical products have appeared in the market for medium dose (Neoral® for Cyclsoprin A, Kaletra® for Lopinavir and Ritonavir), or low dose medications (Rocaltrol® for Calcitriol and Avodart® for Dutasteride). However, these are in the form of viscous liquids or semisolid presentations, characterized by the disadvantages of high production cost, stability problems and the requirement of large quantities of surfactants. Solid SEDDS (S-SEDDS), as coarse powders, granules or pellets, besides solubility improvement, ca...
Self-emulsifying drug delivery system (SEDDS), a type of lipid-based technology which are isotropic ...
Purpose To develop tablet formulations by adsorbing liquid self-emulsifying drug delivery systems (S...
CThe objective of the present study was to prepare solid self-nanoemulsifying drug delivery system (...
Many articles have been published in the last two decades demonstrating improvement in the dissoluti...
the preparation of solid self-emulsifying drug delivery systems (solid-SEDDS) by means of awet granu...
The review focused on technique of solid self-emulsifying pellets (SEPs) for solubility enhancement ...
Low aqueous solubility is attributed to the low oral bioavailability is a major problem for formulat...
Low aqueous solubility of the newly discovered drug possesses a great challenge for the development ...
none4noPurpose: to develop a novel preparation approach of solid Self-Emulsifying Drug Delivery Syst...
Oral route is the easiest and most convenient route for drug administration. Oral drug delivery syst...
Drug development in the past used to be initiated after the identification of most active molecule. ...
A method of producing self-emulsifying pellets by wet granulation of powder mixture composed of micr...
A study was conducted to formulate a semi-solid SEDDS with enhanced bioavailability using Gelucire® ...
The purpose of present study was aimed at developing self emulsifying drug delivery system in liquid...
Self-emulsifying drug delivery system is mixture of oils, surfactant, cosurfactant, which are emulsi...
Self-emulsifying drug delivery system (SEDDS), a type of lipid-based technology which are isotropic ...
Purpose To develop tablet formulations by adsorbing liquid self-emulsifying drug delivery systems (S...
CThe objective of the present study was to prepare solid self-nanoemulsifying drug delivery system (...
Many articles have been published in the last two decades demonstrating improvement in the dissoluti...
the preparation of solid self-emulsifying drug delivery systems (solid-SEDDS) by means of awet granu...
The review focused on technique of solid self-emulsifying pellets (SEPs) for solubility enhancement ...
Low aqueous solubility is attributed to the low oral bioavailability is a major problem for formulat...
Low aqueous solubility of the newly discovered drug possesses a great challenge for the development ...
none4noPurpose: to develop a novel preparation approach of solid Self-Emulsifying Drug Delivery Syst...
Oral route is the easiest and most convenient route for drug administration. Oral drug delivery syst...
Drug development in the past used to be initiated after the identification of most active molecule. ...
A method of producing self-emulsifying pellets by wet granulation of powder mixture composed of micr...
A study was conducted to formulate a semi-solid SEDDS with enhanced bioavailability using Gelucire® ...
The purpose of present study was aimed at developing self emulsifying drug delivery system in liquid...
Self-emulsifying drug delivery system is mixture of oils, surfactant, cosurfactant, which are emulsi...
Self-emulsifying drug delivery system (SEDDS), a type of lipid-based technology which are isotropic ...
Purpose To develop tablet formulations by adsorbing liquid self-emulsifying drug delivery systems (S...
CThe objective of the present study was to prepare solid self-nanoemulsifying drug delivery system (...