Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2487952 | Journal of Pharmaceutical Sciences | 2006 | 8 Pages |
Abstract
As a high throughput solubility assay, the solutionâprecipitation method using a dimethylsulfoxide (DMSO) sample stock solution (DMSOâSP) has been widely used in drug discovery. However, the solid form of the precipitant has not been investigated. In this study, we investigated the experimental conditions of the DMSOâSP, focusing on the solid form of the precipitant. The final concentration of DMSO was 1% (v/v). The precipitant of more than a half of the model compounds was observed as crystalline by polarized light microscopy analysis. When the incubation time was 20Â h and the precipitant was crystalline, the DMSOâSP solubility was similar to the solubility from a powder material (PWD). However, when the incubation time was 10Â min and/or the precipitant was not crystalline, the DMSOâSP solubility was higher than the PWD solubility. These results suggested that the information regarding the solid form of the precipitant is important in interpreting the solubility data. In addition, we developed an automated birefringence diagnose system for drug discovery usage.
Keywords
Related Topics
Health Sciences
Pharmacology, Toxicology and Pharmaceutical Science
Drug Discovery
Authors
Kiyohiko Sugano, Teruhisa Kato, Kentaro Suzuki, Kako Keiko, Tetsujo Sujaku, Takashi Mano,