The purpose of this study was to investigate solid self-microemulsifying drug delivery system (SSMEDDS), as potential delivery system for poorly water soluble drug carbamazepine (CBZ). Self-microemulsifying drug delivery system (SMEDDS) was formulated using the surfactant polyoxyethylene 20 sorbitan monooleate [Polysorbate 80] (S), the cosurfactant PEG-40 hydrogenated castor oil [Cremophor (R) RH40
Aim of present study was to develop solid self micro emulsifying drug delivery system (S-SEDDS) with...
Nashik. 422 003 (M.S) India. Keywords: Self micro-emulsifying, E-mail: aryanparakh57@gmail.com ABST...
Approximately half of the new drug applicants that reach formulation have poor water solubility. Ora...
The majority of drugs have a low dissolution rate, which is a limiting step for their absorption. In...
The purpose of this study was to investigate the solid self-emulsifying drug delivery system (SSEDDS...
Development of self-dispersing drug delivery systems (SMEDDS) is a modern strategy for oral deliv...
Self-microemulsifying drug delivery system (SMEDDS) is a promising system for the Biopharmaceutics C...
Low aqueous solubility is attributed to the low oral bioavailability is a major problem for formulat...
The aim of present study was to develop solid and liquid self-microemulsifying drug delivery syste...
In order to compare the effects of hydrophilic and hydrophobic solid carrier on the formation of sol...
About 70-75 % of drugs is taken orally and is found not to be as useful as desired. A self-micro emu...
The purpose of the present study was to formulate and characterize carbamazepine loaded microemulsio...
Approximately half of the new drug applicants that reach formulation have poor water solubility. Ora...
AbstractThe purpose of the present study was to formulate and characterize carbamazepine loaded micr...
Objective of this study was to prepare, characterize and evaluate a self-microemulsifying drug deliv...
Aim of present study was to develop solid self micro emulsifying drug delivery system (S-SEDDS) with...
Nashik. 422 003 (M.S) India. Keywords: Self micro-emulsifying, E-mail: aryanparakh57@gmail.com ABST...
Approximately half of the new drug applicants that reach formulation have poor water solubility. Ora...
The majority of drugs have a low dissolution rate, which is a limiting step for their absorption. In...
The purpose of this study was to investigate the solid self-emulsifying drug delivery system (SSEDDS...
Development of self-dispersing drug delivery systems (SMEDDS) is a modern strategy for oral deliv...
Self-microemulsifying drug delivery system (SMEDDS) is a promising system for the Biopharmaceutics C...
Low aqueous solubility is attributed to the low oral bioavailability is a major problem for formulat...
The aim of present study was to develop solid and liquid self-microemulsifying drug delivery syste...
In order to compare the effects of hydrophilic and hydrophobic solid carrier on the formation of sol...
About 70-75 % of drugs is taken orally and is found not to be as useful as desired. A self-micro emu...
The purpose of the present study was to formulate and characterize carbamazepine loaded microemulsio...
Approximately half of the new drug applicants that reach formulation have poor water solubility. Ora...
AbstractThe purpose of the present study was to formulate and characterize carbamazepine loaded micr...
Objective of this study was to prepare, characterize and evaluate a self-microemulsifying drug deliv...
Aim of present study was to develop solid self micro emulsifying drug delivery system (S-SEDDS) with...
Nashik. 422 003 (M.S) India. Keywords: Self micro-emulsifying, E-mail: aryanparakh57@gmail.com ABST...
Approximately half of the new drug applicants that reach formulation have poor water solubility. Ora...