AbstractPurpose: To evaluate the physicochemical and in vitro characteristics of solid dispersions using BCS II model drugs with Soluplus® and one of its component homopolymers, PEG 6000. Methods: Nifedipine (NIF) and sulfamethoxazole (SMX) of 99.3% and 99.5% purity, respectively, were selected as BCS II model drugs, such that an improved dissolution rate and concentration in the gastrointestinal tract should increase oral bioavailability. Soluplus® is an amorphous, tri-block, graft co-polymer with polyvinyl caprolactam, polyvinyl acetate, and polyethylene glycol (PCL:PVAc:PEG6000) in the ratio 57:30:13. PEG 6000 (BASF) is a waxy material with melting point of about 60°C. Solid dispersions were prepared using lyophilization or spray drying ...
PURPOSE: This study is to design a sustained release solid dispersion using swellable polymer by mel...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
The poor water solubility of many drugs has emerged as one of the major challenges in the pharmaceut...
Purpose: To evaluate the physicochemical and in vitro characteristics of solid dispersions using BCS...
AbstractPurpose: To evaluate the physicochemical and in vitro characteristics of solid dispersions u...
The present study deals with characterization of dispersions of a poorly water-soluble drug, celecox...
Background and Objective: One of the established strategies to improve solubility and dissolution ra...
Amorphous solid dispersion (ASD) of a poorly soluble active pharmaceutical ingredient (API) in a pol...
The tyrosine kinase inhibitor nilotinib has a very low aqueous solubility and a low and variable ora...
AbstractPoor solubility and bioavailability of an existing or newly synthesized drug always pose cha...
Ibuprofen solid dispersions were prepared by the solvent and fusion-solventmethods using polyethylen...
The objective of this study was to compare the dissolution behavior of tablets prepared from solid d...
NoOBJECTIVES: To compare the properties of solid dispersions of felodipine for oral bioavailability ...
With the advent of combinatorial chemistry and high throughput screening of drug molecules, poorly w...
To improve its solubility, dissolution, and bioavailability; Ibuprofen-polyethylene glycol 8000 (PEG...
PURPOSE: This study is to design a sustained release solid dispersion using swellable polymer by mel...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
The poor water solubility of many drugs has emerged as one of the major challenges in the pharmaceut...
Purpose: To evaluate the physicochemical and in vitro characteristics of solid dispersions using BCS...
AbstractPurpose: To evaluate the physicochemical and in vitro characteristics of solid dispersions u...
The present study deals with characterization of dispersions of a poorly water-soluble drug, celecox...
Background and Objective: One of the established strategies to improve solubility and dissolution ra...
Amorphous solid dispersion (ASD) of a poorly soluble active pharmaceutical ingredient (API) in a pol...
The tyrosine kinase inhibitor nilotinib has a very low aqueous solubility and a low and variable ora...
AbstractPoor solubility and bioavailability of an existing or newly synthesized drug always pose cha...
Ibuprofen solid dispersions were prepared by the solvent and fusion-solventmethods using polyethylen...
The objective of this study was to compare the dissolution behavior of tablets prepared from solid d...
NoOBJECTIVES: To compare the properties of solid dispersions of felodipine for oral bioavailability ...
With the advent of combinatorial chemistry and high throughput screening of drug molecules, poorly w...
To improve its solubility, dissolution, and bioavailability; Ibuprofen-polyethylene glycol 8000 (PEG...
PURPOSE: This study is to design a sustained release solid dispersion using swellable polymer by mel...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
The poor water solubility of many drugs has emerged as one of the major challenges in the pharmaceut...