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推荐的 2021 年冻干验证最佳实践——第一部分:工艺设计和建模。

Recommended Best Practices for Lyophilization Validation-2021 Part I: Process Design and Modeling.

机构信息

Abbvie, North Chicago, IL, USA.

Birck Nanotechnology Center, Purdue University, 1205 W State St., West Lafayette, IN, 47907, USA.

出版信息

AAPS PharmSciTech. 2021 Aug 18;22(7):221. doi: 10.1208/s12249-021-02086-8.

Abstract

This work describes lyophilization process validation and consists of two parts. Part I focuses on the process design and is described in the current paper, while part II is devoted to process qualification and continued process verification. The intent of these articles is to provide readers with recent updates on lyophilization validation in the light of community-based combined opinion on the process and reflect the industrial prospective. In this paper, the design space approach for process design is described in details, and examples from practice are provided. The approach shows the relationship between the process inputs; it is based on first principles and gives a thorough scientific understanding of process and product. The lyophilization process modeling and scale-up are also presented showing the impact of facility, equipment, and vial heat transfer coefficient. The case studies demonstrating the effect of batch sizes, fill volume, and dose strength to show the importance of modeling as well as the effect of controlled nucleation on product resistance are discussed.

摘要

这项工作描述了冷冻干燥工艺验证,由两部分组成。第一部分侧重于工艺设计,在当前的论文中进行了描述,而第二部分则致力于工艺确认和持续工艺验证。这些文章的目的是为读者提供冷冻干燥验证的最新信息,以反映社区对该工艺的综合意见,并反映出工业的前瞻性。在本文中,详细描述了工艺设计的设计空间方法,并提供了实际应用的示例。该方法展示了工艺输入之间的关系;它基于第一性原理,对工艺和产品有透彻的科学理解。还介绍了冷冻干燥工艺的建模和放大,展示了设备、设备和瓶传热系数的影响。通过案例研究,展示了批量大小、填充量和剂量强度对产品阻力的影响,说明了建模的重要性以及控制成核对产品阻力的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d092/8373746/24896079af14/12249_2021_2086_Fig1_HTML.jpg

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