pH-dependent solubility profile of Desipramine hydrochloride (Ds.HCl) was studied using pH-ramp shake flask method. First, the pH value of DsHCl stock solution in 0.15 M phosphate buffer was adjusted to 11.7 in order to minimize supersaturation effect. Then, the pH value in separate samples was adjusted downwards with HCl, to prepare solutions in the pH 1.7-11.7 region. After stirring (6 h) and sedimentation (18 h), PTFE (hydrophobic, pore size 0.22 µm) filters or centrifugation were used for phase separation. Concentration was measured using HPLC with UV/Vis detection. The computer program pDISOL-X was used for data processing and refinement of equilibrium constants. Different techniques were used for solid phase characterization
The purpose of the study was to assess the stoichiometries of phosphate precipitates and determine t...
The objectives of the research work undertaken are; 1. Development of fast dissolving tablets of t...
Drug solubility plays an important role during formulation development; it affects drug delivery and...
Although solubility-pH data for desipramine hydrochloride (DsHCl) have been reported previously, the...
The aim of this study was to examine solubility-pH behavior of desipramine structural analogues: im...
Aims: The aqueous solubility of two polymorphic forms of venlafaxine hydrochloride was investigated....
The solubilities of five sparingly soluble drug-compounds in water have been measured at constant...
Experimental studies of solubility are important in all phases of drug design and development. Solub...
The solubility of a model basic drug, nortriptyline (Nor), was investigated as a function of pH in p...
Related to published version: [http://cherry.chem.bg.ac.rs/handle/123456789/2924]Related to accepted...
A novel general approach was described to address many of the challenges of salt solubility determin...
In the present study the solubility-pH profiles of sibutramine free base and its hydrochloride salt ...
The purpose of the study was to assess the stoichiometries of phosphate precipitates and determine t...
The ionization constants (pKa) and the pH-dependent solubility (log S-pH) of six phenothiazine deriv...
The solubilities of five sparingly soluble drug-compounds in water were mea-sured at constant temper...
The purpose of the study was to assess the stoichiometries of phosphate precipitates and determine t...
The objectives of the research work undertaken are; 1. Development of fast dissolving tablets of t...
Drug solubility plays an important role during formulation development; it affects drug delivery and...
Although solubility-pH data for desipramine hydrochloride (DsHCl) have been reported previously, the...
The aim of this study was to examine solubility-pH behavior of desipramine structural analogues: im...
Aims: The aqueous solubility of two polymorphic forms of venlafaxine hydrochloride was investigated....
The solubilities of five sparingly soluble drug-compounds in water have been measured at constant...
Experimental studies of solubility are important in all phases of drug design and development. Solub...
The solubility of a model basic drug, nortriptyline (Nor), was investigated as a function of pH in p...
Related to published version: [http://cherry.chem.bg.ac.rs/handle/123456789/2924]Related to accepted...
A novel general approach was described to address many of the challenges of salt solubility determin...
In the present study the solubility-pH profiles of sibutramine free base and its hydrochloride salt ...
The purpose of the study was to assess the stoichiometries of phosphate precipitates and determine t...
The ionization constants (pKa) and the pH-dependent solubility (log S-pH) of six phenothiazine deriv...
The solubilities of five sparingly soluble drug-compounds in water were mea-sured at constant temper...
The purpose of the study was to assess the stoichiometries of phosphate precipitates and determine t...
The objectives of the research work undertaken are; 1. Development of fast dissolving tablets of t...
Drug solubility plays an important role during formulation development; it affects drug delivery and...