23 Full factorial design for optimization of stable amorphous host–guest-based mirabegron complex for extended-release action
Author:
Publisher
Springer Science and Business Media LLC
Subject
Condensed Matter Physics,General Chemistry,Food Science
Link
http://link.springer.com/content/pdf/10.1007/s10847-019-00955-1.pdf
Reference28 articles.
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2. Martínez, L.M., Videa, M., Silva, T.L., Castro, S., Caballero, A., Lara-Díaz, V.J., Castorena-Torres, F.: Two-phase amorphous-amorphous solid drug dispersion with enhanced stability, solubility and bioavailability resulting from ultrasonic dispersion of an immiscible system. Eur. J. Pharm. Biopharm. 119, 243–252 (2017). https://doi.org/10.1016/j.ejpb.2017.06.021
3. Mesallati, H., Conroy, D., Hudson, S., Tajber, L.: Preparation and characterization of amorphous ciprofloxacin-amino acid salts. Eur. J. Pharm. Biopharm. 121, 73–89 (2017). https://doi.org/10.1016/j.ejpb.2017.09.009
4. Pokharkar, V.B., Mandpe, L.P., Padamwar, M.N., Ambike, A.A., Mahadik, K.R., Paradkar, A.: Development, characterization and stabilization of amorphous form of a low Tg drug. Powder Technol. 167(1), 20–25 (2006). https://doi.org/10.1016/j.powtec.2006.05.012
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