The study demonstrates the application of QbD based on historical data for a product at a later development stage - retrospective QbD (rQbD). More specifically, it is investigated the root-cause for the observed slower drug release in Orodispersible Films (ODFs) during storage. Risk assessment tools were used to identify parameters affecting ODFs critical quality attributes, namely percent drug release and residual water content. The parameters room temperature, room relative humidity, drying temperature and mixing equipment were used in the statistical modeling of the available data. The estimated models were then used to define the feasible working region. Statistical modeling indicates that initial residual water content of the ODFs is mainly affected by 2nd order interactions of room temperature, room relative humidity and drying temperature, while the stability of drug release profile is mostly influenced by room temperature and an interaction between room relative humidity and drying temperature. Depending on the drying temperature employed the effect of room temperature and room relative humidity change significantly. This work shows that it is possible to apply rQbD to achieve a greater understanding of the manufacturing process of ODFs and to define a proper design space.

译文

:研究证明了基于历史数据的QbD在后期产品开发中的应用-回顾性QbD(rQbD)。更具体地说,研究了在储存过程中观察到的较慢的药物在口腔分散膜(ODF)中释放的根本原因。风险评估工具用于确定影响ODF关键质量属性的参数,即药物释放百分比和残留水分。在可用数据的统计模型中,使用了室温,室内相对湿度,干燥温度和混合设备等参数。然后,将估计的模型用于定义可行的工作区域。统计模型表明,ODFs的初始残留水含量主要受室温,室温相对湿度和干燥温度的二阶相互作用影响,而药物释放曲线的稳定性主要受室温以及室温相对湿度与干燥温度之间相互作用的影响。干燥温度。取决于所采用的干燥温度,室温和室内相对湿度的影响会显着变化。这项工作表明,有可能应用rQbD来更好地理解ODF的制造过程并定义适当的设计空间。

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