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基于 PAT 的制药膏剂生产过程批统计过程控制。

PAT-based batch statistical process control of a manufacturing process for a pharmaceutical ointment.

机构信息

Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.

Global Technical Operations, Pharmaceutical Mfg (PM) Platform, Division of Janssen Pharmaceutica, Johnson & Johnson, Turnhoutseweg 30, 2340 Beerse, Belgium.

出版信息

Eur J Pharm Sci. 2019 Aug 1;136:104946. doi: 10.1016/j.ejps.2019.05.024. Epub 2019 Jun 3.

Abstract

In this study, a process analytical technology (PAT)-based batch statistical process control (BSPC) model was developed for the laboratory-scale manufacturing process of a commercially available pharmaceutical ointment. The multivariate BSPC model was developed based on the in-line measured viscosity (viscometer), product temperature (viscometer), particle size distribution (PSD) (focused beam reflectance measurement (FBRM)) and active pharmaceutical ingredient (API) concentration (Raman spectroscopy) of four reference batches using a partial least squares (PLS) approach. From this in-line collected data, the characteristic trajectory of the batch process under normal operating conditions was acquired. To assess the capability of the process analyzers and BSPC model to detect deviations from the expected batch trajectory, two test batches with induced process and formulation disturbances were monitored in-line. The elevated process temperature in test batch 1 resulted in a deviating viscosity, product temperature and number of small particles (<100 μm). After correcting the process temperature, the viscosity and product temperature were within the control interval, while the particle size was smaller compared to the reference batches. For test batch 2, API was added at three different time points, whereas the same amount of API was added in one step during manufacturing of the reference batches. The induced disturbance was reflected in the in-line measured viscosity, PSD and API concentration. The combination of process analyzers and multivariate batch modelling enabled early fault detection and real-time process adjustments, thereby preventing batch loss or reprocessing. In addition, the feasibility of the investigated process analyzers to measure certain quality attributes in-line during manufacturing of an ointment was demonstrated.

摘要

在这项研究中,开发了一种基于过程分析技术(PAT)的批统计过程控制(BSPC)模型,用于商业化制药软膏的实验室规模制造过程。该多变量 BSPC 模型是基于在线测量的粘度(粘度计)、产品温度(粘度计)、粒度分布(PSD)(聚焦光束反射测量(FBRM))和活性药物成分(API)浓度(拉曼光谱)开发的四个参考批次使用偏最小二乘(PLS)方法。从这些在线收集的数据中,获得了正常操作条件下批处理过程的特征轨迹。为了评估过程分析仪和 BSPC 模型检测与预期批处理轨迹偏离的能力,两个具有诱导过程和配方干扰的测试批次在线进行了监测。测试批次 1 中的升高的过程温度导致粘度、产品温度和小颗粒(<100μm)数量偏离。在纠正过程温度后,粘度和产品温度在控制间隔内,而粒度与参考批次相比较小。对于测试批次 2,API 分三个不同的时间点添加,而在参考批次的制造过程中,API 一次添加相同的量。诱导的干扰反映在在线测量的粘度、PSD 和 API 浓度中。过程分析仪和多变量批处理建模的组合实现了早期故障检测和实时过程调整,从而防止了批处理损失或重新处理。此外,还证明了所研究的过程分析仪在制造软膏时在线测量某些质量属性的可行性。

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