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采用 PAT 手段,通过使用 FBRM C35 进行在线颗粒测量,改善高剪切湿法制粒过程的理解。

A PAT approach to improve process understanding of high shear wet granulation through in-line particle measurement using FBRM C35.

机构信息

Pharmaceutical Development Center, Wyeth Pharmaceuticals, 401 N Middletown Road, Pearl River, New York 10965, USA.

出版信息

J Pharm Sci. 2010 Jul;99(7):3205-12. doi: 10.1002/jps.22089.

DOI:10.1002/jps.22089
PMID:20186936
Abstract

This article summarizes the investigation of in-line particle characterization during high shear wet granulation (HSWG) using focused beam reflectance measurement (FBRM) for enhanced process understanding, which is part of an effort to develop this drug product within the framework of quality by design (QbD) and process analytical technology (PAT). Traditionally, the effectiveness of in-line monitoring of HSWG processes is hindered by wet and sticky material fouling the probe resulting in inconsistent and erroneous data collection. For this study, a FBRM C35 probe was used which incorporates a scraping mechanism to maintain a clean probe window ensuring consistent measurements throughout each batch. The evaluations were conducted on nine scale-up DOE development batches and eight clinical sub-lots. In the DOE campaign, the purpose of FBRM was used to study the impact of varying water amount and wet massing time on granule dimension and count during granulation, while batch-to-batch variation or batch reproducibility was evaluated under the same process conditions for the clinical batches. In addition, a preliminary investigation of the most optimal probe position was conducted. The results indicate that FBRM is capable of monitoring the rate and degree of change to granule dimension/count during HSWG, and could be a potential technique for granulation endpoint determination.

摘要

本文总结了在高剪切湿法制粒(HSWG)过程中使用聚焦光束反射测量(FBRM)进行在线颗粒特性分析的研究,以增强对工艺的理解,这是在质量源于设计(QbD)和过程分析技术(PAT)框架内开发该药物产品的努力的一部分。传统上,HSWG 过程的在线监测的有效性受到湿粘性材料污染探头的阻碍,导致数据收集不一致和错误。对于这项研究,使用了 FBRM C35 探头,其中包含刮削机构,以保持探头窗口清洁,确保每次批量测量的一致性。评估在九个放大设计实验(DOE)开发批次和八个临床亚批次上进行。在 DOE 活动中,FBRM 的目的是研究在制粒过程中不同水量和湿混时间对颗粒尺寸和数量的影响,而在相同的工艺条件下评估临床批次的批间变化或批重复性。此外,还进行了最佳探头位置的初步研究。结果表明,FBRM 能够监测 HSWG 过程中颗粒尺寸/数量的变化速度和程度,并且可能是确定制粒终点的潜在技术。

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