The knowledge of the solubility of pharmaceuticals in pure solvents and solvent mixtures is crucial for designing the crystallization process of drug substances. The first step in finding optimal crystallization conditions is usually a solvent screening. Since experiments are very time consuming, a
✦ LIBER ✦
The E and C model for predicting the solubility of drugs in pure solvents
✍ Scribed by Pilar Bustamante; Manuel Jiménez-Durán; Begoña Escalera
- Book ID
- 113368273
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 268 KB
- Volume
- 129
- Category
- Article
- ISSN
- 0378-5173
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