Aim of present study was to develop solid self micro emulsifying drug delivery system (S-SEDDS) with Aerosil 200 for enhancement of dissolution rate of model drug Glibenclamide (GBM). SEDDS was prepared using Capmul MCM C8TM, Cremophor RH 40TM, and Transcutol PTM as oil, surfactant and cosurfactant respectively. For formulation of stable SEDDS, micro emulsion region was identified by constructing pseudo ternary phase diagram containing different proportion of surfactant: co-surfactant (1:1, 2:1 and 3:1), oil and water. Prepared SEDDS was evaluated for turbidity measurement, globule size and zeta potential, viscosity determination and % transmittance. S-SEDDS was prepared by adsorption technique using Aerosil 200 as solid carrier. Prepared S...
Approximately half of the new drug applicants that reach formulation have poor water solubility. Ora...
A study was conducted to formulate a semi-solid SEDDS with enhanced bioavailability using Gelucire® ...
CThe objective of the present study was to prepare solid self-nanoemulsifying drug delivery system (...
Objective: The present study was aimed to develop a novel o/w self-emulsifying drug delivery system ...
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...
The objective of our investigation was to formulate a self-emulsifying drug delivery system (SEDDS) ...
Poorly Solubility of orally administered drug is major challenge of pharmaceutical industry as nearl...
Low aqueous solubility of the newly discovered drug possesses a great challenge for the development ...
The objective of present study was to develop self-emulsifying drug delivery system (SEDDS) of model...
The aim of present study was to develop solid and liquid self-microemulsifying drug delivery syste...
Approximately half of the new drug applicants that reach formulation have poor water solubility. Ora...
Self-emulsifying drug delivery systems (SEDDS) have been mainly investigated to enhance the oral bio...
Objective: Gliclazide (GCZ) is a widely prescribed anti-diabetic drug belongs to class IΙ under BCS...
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...
A study was conducted to formulate a semi-solid SEDDS with enhanced bioavailability using Gelucire® ...
CThe objective of the present study was to prepare solid self-nanoemulsifying drug delivery system (...
Objective: The present study was aimed to develop a novel o/w self-emulsifying drug delivery system ...
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...
The objective of our investigation was to formulate a self-emulsifying drug delivery system (SEDDS) ...
Poorly Solubility of orally administered drug is major challenge of pharmaceutical industry as nearl...
Low aqueous solubility of the newly discovered drug possesses a great challenge for the development ...
The objective of present study was to develop self-emulsifying drug delivery system (SEDDS) of model...
The aim of present study was to develop solid and liquid self-microemulsifying drug delivery syste...
Approximately half of the new drug applicants that reach formulation have poor water solubility. Ora...
Self-emulsifying drug delivery systems (SEDDS) have been mainly investigated to enhance the oral bio...
Objective: Gliclazide (GCZ) is a widely prescribed anti-diabetic drug belongs to class IΙ under BCS...
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...
A study was conducted to formulate a semi-solid SEDDS with enhanced bioavailability using Gelucire® ...
CThe objective of the present study was to prepare solid self-nanoemulsifying drug delivery system (...