Analytical and Computational Methods for the Estimation of Drug-Polymer Solubility and Miscibility in Solid Dispersions Development
The development of stable solid dispersion formulations that maintain desired improvement of drug dissolution rate during the entire shelf life requires the analysis of drug-polymer solubility and miscibility. Only if the drug concentration is below the solubility limit in the polymer, the physical...
Main Authors: | Djordje Medarević, Jelena Djuriš, Panagiotis Barmpalexis, Kyriakos Kachrimanis, Svetlana Ibrić |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2019-08-01
|
Series: | Pharmaceutics |
Subjects: | |
Online Access: | https://www.mdpi.com/1999-4923/11/8/372 |
Similar Items
-
An effective algorithm to identify the miscibility gap in a binary substitutional solution phase
by: Fu T., et al.
Published: (2020-01-01) -
Miscibility and Solubility of Caffeine and Theophylline in Hydroxypropyl Methylcellulose
by: Edyta Leyk, et al.
Published: (2021-11-01) -
A Novel Rheological Method to Assess Drug-Polymer Interactions Regarding Miscibility and Crystallization of Drug in Amorphous Solid Dispersions for Oral Drug Delivery
by: Georgia Tsakiridou, et al.
Published: (2019-11-01) -
Selection of appropriate dapsone and poly(1-vinylpyrrolidone-co-vinyl acetate) ratios for the preparation of amorphous solid dispersions
by: Dinesh Choudhury, et al.
Published: (2023-03-01) -
Effect of Hypromellose Acetate Succinate Substituents on Miscibility Behavior of Spray-dried Amorphous Solid Dispersions: Flory–Huggins Parameter Prediction and Validation
by: Durgesh K. Jha, et al.
Published: (2021-12-01)