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开发一种新型连续过滤装置用于药物工艺开发和生产。

Development of a Novel Continuous Filtration Unit for Pharmaceutical Process Development and Manufacturing.

机构信息

EPSRC Centre for Innovative Manufacturing in Continuous Manufacturing and Crystallisation, University of Strathclyde, Glasgow, G1 1RD, UK.

EPSRC Centre for Innovative Manufacturing in Continuous Manufacturing and Crystallisation, University of Strathclyde, Glasgow, G1 1RD, UK; Department of Chemical and Process Engineering, University of Strathclyde, Glasgow, G1 1RD, UK.

出版信息

J Pharm Sci. 2019 Jan;108(1):372-381. doi: 10.1016/j.xphs.2018.07.005. Epub 2018 Sep 6.

DOI:10.1016/j.xphs.2018.07.005
PMID:30009797
Abstract

The lack of a commercial laboratory, pilot and small manufacturing scale dead end continuous filtration and drying unit it is a significant gap in the development of continuous pharmaceutical manufacturing processes for new active pharmaceutical ingredients (APIs). To move small-scale pharmaceutical isolation forward from traditional batch Nutsche filtration to continuous processing a continuous filter dryer prototype unit (CFD20) was developed in collaboration with Alconbury Weston Ltd. The performance of the prototype was evaluated by comparison with manual best practice exemplified using a modified Biotage VacMaster unit to gather data and process understanding for API filtration and washing. The ultimate objective was to link the chemical and physical attributes of an API slurry with equipment and processing parameters to improve API isolation processes. Filtration performance was characterized by assessing filtrate flow rate by application of Darcy's law, the impact on product crystal size distribution and product purity were investigated using classical analytical methods. The overall performance of the 2 units was similar, showing that the prototype CFD20 can match best manual lab practice for filtration and washing while allowing continuous processing and real-time data logging. This result is encouraging and the data gathered provides further insight to inform the development of CFD20.

摘要

缺乏商业化实验室、中试和小规模生产,使连续过滤和干燥单元陷入僵局,这是新型活性药物成分(API)连续药物制造工艺开发中的一个重大空白。为了将小型制药分离从传统的分批氮洗过滤推进到连续处理,与 Alconbury Weston Ltd 合作开发了连续过滤干燥器原型单元(CFD20)。通过与使用经过修改的 Biotage VacMaster 单元收集 API 过滤和洗涤数据和工艺理解的手动最佳实践进行比较,评估了原型的性能。最终目标是将 API 料浆的化学和物理特性与设备和工艺参数联系起来,以改进 API 分离工艺。通过应用达西定律评估滤液流速来表征过滤性能,使用经典分析方法研究产品粒度分布和产品纯度的影响。这 2 个单元的整体性能相似,表明原型 CFD20 可以匹配最佳手动实验室实践的过滤和洗涤,同时允许连续处理和实时数据记录。这一结果令人鼓舞,所收集的数据提供了进一步的见解,以指导 CFD20 的开发。

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