Optimization of Freeze-Drying Cycles of Pharmaceutical Organic Co-Solvent-Based Formulations Using the Design Space Methodology
Author:
Publisher
Informa UK Limited
Subject
Physical and Theoretical Chemistry,General Chemical Engineering
Link
http://www.tandfonline.com/doi/pdf/10.1080/07373937.2012.689590
Reference20 articles.
1. Quality by design in formulation and process development for a freeze-dried, small molecule parenteral product: a case study
2. Advanced approach to build the design space for the primary drying of a pharmaceutical freeze‐drying process
3. On the Use of Mathematical Models to Build the Design Space for the Primary Drying Phase of a Pharmaceutical Lyophilization Process
4. Pikal , M.J. Freeze-drying.Encyclopedia of Pharmaceutical Technology;Marcel Dekker : New York , 2002;1299–1326.
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1. Freeze-Drying of Thermosensible Pharmaceuticals with Organic Co-solvent + Water Formulations;Principles and Practices of Lyophilization in Product Development and Manufacturing;2023
2. A review on experimental determination and optimization of physical quality factors during pharmaceuticals freeze-drying cycles;Drying Technology;2017-07-21
3. On the Design of a Fuzzy Logic–Based Control System for Freeze-Drying Processes;Journal of Pharmaceutical Sciences;2016-12
4. Noninvasive Monitoring of a Freeze-Drying Process for tert-Butanol/Water Cosolvent-Based Formulations;Industrial & Engineering Chemistry Research;2016-05-09
5. Risk-Based Design of a Freeze-Drying Cycle for Pharmaceuticals;Industrial & Engineering Chemistry Research;2015-12-17
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