Solubility Prediction of Different Forms of Pharmaceuticals in Single and Mixed Solvents Using Symmetric Electrolyte Nonrandom Two-Liquid Segment Activity Coefficient Model
Author:
Affiliation:
1. Process and Systems Engineering Center (PROSYS), Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, DK-2800 Kgs. Lyngby, Denmark
2. LEO-Pharma A/S, Industriparken 55, DK-2750 Ballerup, Denmark
Funder
Det Frie Forskningsråd
Publisher
American Chemical Society (ACS)
Subject
Industrial and Manufacturing Engineering,General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.iecr.8b04268
Reference35 articles.
1. Solubility Modeling with a Nonrandom Two-Liquid Segment Activity Coefficient Model
2. Solvent selection for pharmaceuticals
3. High-throughput crystallization: polymorphs, salts, co-crystals and solvates of pharmaceutical solids
4. A microfluidic device based on droplet storage for screening solubility diagrams
5. Group-contribution estimation of activity coefficients in nonideal liquid mixtures
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