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Evaluating the potential of adjusting axial back mixing in continuous manufacturing of solid oral dosage forms

机译：评估连续制造固体口服剂型调节轴向混合的电位

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M. Peterwitz; R. Loll; J. Jodwirschat; G. Schembecker;
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年度 2020
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1. Manufacturing classification system in the real world: factors influencing manufacturing process choices for filed commercial oral solid dosage formulations, case studies from industry and considerations for continuous processing [J] . Leane Michael, Pitt Kendal, Reynolds Gavin K., Pharmaceutical development and technology . 2018,第1a10期

机译：现实世界中的制造分类系统：影响制造工艺选择的因素，用于提交的商业口服固体剂量配方，行业和考虑因素的连续加工考虑
2. Recent progress in continuous manufacturing of oral solid dosage forms [J] . Vanhoorne V., Vervaet C. International Journal of Pharmaceutics . 2020,第1期

机译：近期制造口腔固体剂型的进展
3. Evaluating the potential for optimization of axial back-mixing in continuous pharmaceutical manufacturing [J] . Moritz Peterwitz, Gerhard Schembecker Computers & Chemical Engineering . 2021,第Apra期

机译：评估连续药物制造中轴向后搅拌优化的可能性
4. A Quality-by-Control Approach in Pharmaceutical Continuous Manufacturing of Oral Solid Dosage via Direct Compaction [C] . Qinglin Su, Sudarshan Ganesh, Dan Bao Le Vo European Symposium on Computer Aided Chemical engineering . 2019

机译：通过直接压实的口腔固体剂量的药物连续制造的一种质量控制方法
5. Model Development and Analysis of Solid Oral Dosage Manufacturing Processes Involving Particle Size Change [D] . ?Metta, Nirupaplava 2020

机译：模型开发和口服固体制剂制造的分析过程涉及粒度变化
6. The Use of Animated Videos to Illustrate Oral Solid Dosage Form Manufacturing in a Pharmaceutics Course [O] . Venkata Kashyap Yellepeddi, Charles Roberson 2016

机译：动画课程中动画视频的使用说明口服固体剂型的生产
7. Monitoring of Manufacturing Changes and Formulation Excipients on Solid Oral Dosage Forms of Furosemide Using Chemometrics and Laser-Induced Breakdown Spectroscopy (LIBS) [O] . Doucet Franue7ois R., St-Onge Louis, Tourigny M., 2006

机译：使用化学计量学和激光诱导击穿光谱法（LIBS）监测速尿的固体口服剂型上的制造变化和配制辅料
8. Guidance for Industry: SUPAC-MR: Modified Release Solid Oral Dosage Forms. Scale-Up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation [R] . 1997

机译：行业指南：sUpaC-mR：改良释放固体口服剂型。放大和批准后的变化：化学，制造和控制;体外溶出度测试和体内生物等效性文档

Evaluating the potential of adjusting axial back mixing in continuous manufacturing of solid oral dosage forms

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