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首页> 外文期刊>Pharmaceutics >A Novel Framework to Aid the Development of Design Space across Multi-Unit Operation Pharmaceutical Processes—A Case Study of Panax Notoginseng Saponins Immediate Release Tablet
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A Novel Framework to Aid the Development of Design Space across Multi-Unit Operation Pharmaceutical Processes—A Case Study of Panax Notoginseng Saponins Immediate Release Tablet

机译:一个新的框架,可帮助跨多单元操作的制药工艺开发设计空间—以三七总皂苷速释片为例

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The fundamental principle of Quality by Design (QbD) is that the product quality should be designed into the process through an upstream approach, rather than be tested in the downstream. The keystone of QbD is process modeling, and thus, to develop a process control strategy based on the development of design space. Multivariate statistical analysis is a very useful tool to support the implementation of QbD in pharmaceutical process development and manufacturing. Nowadays, pharmaceutical process modeling is mainly focused on one-unit operations and system modeling for the development of design space across multi-unit operations is still limited. In this study, a general procedure that gives a holistic view for understanding and controlling the process settings for the entire manufacturing process was investigated. The proposed framework was tested on the Panax Notoginseng Saponins immediate release tablet (PNS IRT) production process. The critical variables and the critical units acting on the process were identified according to the importance of explaining the variability in the multi-block partial least squares path model. This improved understanding of the process by illustrating how the properties of the raw materials, the process parameters in the wet granulation and the compaction and the intermediate properties affect the tablet properties. Furthermore, the design space was developed to compensate for the variability source from the upstream. The results demonstrated that the proposed framework was an important tool to gain understanding and control the multi-unit operation process.
机译:设计质量(QbD)的基本原理是,应通过上游方法将产品质量设计到过程中,而不是在下游进行测试。 QbD的重点是过程建模,因此,根据设计空间的发展来开发过程控制策略。多元统计分析是非常有用的工具,可支持在制药过程开发和制造中实施QbD。如今,制药过程建模主要集中于一个单元的操作,而用于跨多个单元的设计空间开发的系统建模仍然受到限制。在这项研究中,研究了提供整体视图以了解和控制整个制造过程的过程设置的一般过程。在三七总皂苷速释片(PNS IRT)的生产过程中测试了拟议的框架。根据解释多块局部最小二乘路径模型中的可变性的重要性,确定了作用于过程的关键变量和关键单元。通过说明原材料的特性,湿法制粒中的工艺参数以及压实和中间特性如何影响片剂特性,从而改善了对工艺的理解。此外,开发了设计空间以补偿上游的可变性来源。结果表明,所提出的框架是了解和控制多单元操作过程的重要工具。

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