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在连续双螺杆湿法造粒过程中管理原料药 API 的变异性。

Managing API raw material variability during continuous twin-screw wet granulation.

机构信息

Laboratory of Pharmaceutical Process Analytical Technology, Ghent University, Ghent, Belgium.

Laboratory of Pharmaceutical Technology, Ghent University, Ghent, Belgium.

出版信息

Int J Pharm. 2019 Apr 20;561:265-273. doi: 10.1016/j.ijpharm.2019.03.012. Epub 2019 Mar 6.

Abstract

Very few studies have investigated the impact of raw material variability upon the granule critical quality attributes (CQAs) produced via twin-screw wet granulation (i.e., granule size distribution, density, flowability). In this study, the impact of the raw material variability of an active pharmaceutical ingredient (API) in a high dose formulation on the twin-screw wet granulation process and on the resulting granule quality attributes was investigated. In a previous study (Stauffer et al., 2018), eight API batches were characterized to determine the API batch-to-batch variability. Principal component analysis (PCA) was then used to analyse the raw material property differences between the API batches and to determine the causes of the batch-to-batch variability. In current study, the three principal components from that PCA model were used as factors together with twin-screw granulation process parameters (i.e., screw speed and liquid-to-solid ratio) in a D-optimal screening design of experiments to understand the influence of these factors upon the granule CQAs. It was found that the API particle size distribution and related properties (e.g., density, agglomeration profile) were critical for the granule CQAs. In a next step, the significant factors from the screening design results were used to determine the design space of the twin-screw granulation process for the studied formulation via a D-optimal optimisation design, herewith controlling the risk of failure for the potential API raw material variability. The possibility to obtain suitable granule CQAs with a risk of failure of 1% for all API batches was demonstrated. It was thus possible to identify a combination of process parameters that can manage the API batch-to-batch variability leading to granules with pre-defined suitable CQAs.

摘要

很少有研究调查原料药变异性对通过双螺杆湿法造粒(即颗粒粒径分布、密度、流变性)生产的颗粒关键质量属性(CQAs)的影响。在本研究中,考察了高剂量配方中活性药物成分(API)的原料药变异性对双螺杆湿法造粒工艺和所得颗粒质量属性的影响。在之前的一项研究(Stauffer 等人,2018 年)中,对八个 API 批次进行了表征,以确定 API 批次间的变异性。然后使用主成分分析(PCA)来分析 API 批次之间的原材料属性差异,并确定批次间变异性的原因。在当前研究中,将来自该 PCA 模型的三个主成分与双螺杆造粒工艺参数(即螺杆速度和液固比)一起用作因素,在 D-最优筛选实验设计中,以了解这些因素对颗粒 CQAs 的影响。结果发现,API 粒径分布和相关性质(例如,密度、团聚体形态)对颗粒 CQAs 至关重要。在下一步中,筛选设计结果中的显著因素用于通过 D-最优优化设计确定所研究配方的双螺杆造粒工艺的设计空间,从而控制潜在 API 原料药变异性的失败风险。结果证明,有可能获得具有所有 API 批次失败风险为 1%的合适颗粒 CQAs。因此,可以确定一组工艺参数,这些参数可以管理 API 批次间的变异性,从而获得具有预定义合适 CQAs 的颗粒。

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